\r\n\tThis book will address the various modern, technical, and practical aspects of smart technology for capturing solar radiation and converting it into different forms of energy, as well as enabling it for renewables integration in energy generation and transformation, built environment, transportation, buildings, and agriculture.
\r\n
\r\n\tThe book will cover the most recent developments, innovations and applications concerning the following topics: \r\n\t• Solar radiation – Smart and enabling technologies for measurement, modelling, and forecasting \r\n\tHigh-resolution measurement sensor and instrument technology (Pyranometers, Albedometers, Pyrheliometers, UV Radiometers, Sun Trackers, Spectroradiometer, Pyrgeometers, etc.), Artificial intelligence techniques for modelling and forecasting of solar radiation, Solar Irradiance forecast with satellite data, Solar potential analysis, Short-term forecasting of photovoltaic power and solar irradiance prediction with sky imagers. \r\n\t• Renewable energy integration – Smart solutions for integration of RE in distributed generation, energy storage, and demand-side management. \r\n\tIntegrated Photovoltaics: Smart technology for vehicle-integrated PV, Building Integrated PV, Agrivoltaics, Road-Integrated PV, Floating PV, Product-integrated PV. \r\n\tRenewable Energy Applications in Built Environment and mobility: Solar cars, solar-powered electric charging stations, passive solar systems, solar heating, and cooling systems, building-integrated vegetation, multifunctional solar systems, solar pumps, solar lighting, solar shading, Natural lighting, Solar dryer, Greenhouse.
",isbn:null,printIsbn:null,pdfIsbn:null,doi:null,price:0,priceEur:0,priceUsd:0,slug:null,numberOfPages:0,isOpenForSubmission:!0,isSalesforceBook:!1,hash:"0400d540d2b8fb55d4cc8590e1e58844",bookSignature:"Dr. Mohammadreza Aghaei and Associate Prof. Amin Moazami",publishedDate:null,coverURL:"https://cdn.intechopen.com/books/images_new/11493.jpg",keywords:"High-Resolution Measurement Technology, Solar Irradiance Prediction, Integrated Photovoltaics, Energy Storage, Photovoltaics Technology, Nano Materials, Life Cycle Assessment, Photovoltaic Power Plants, UAV-Based Aerial Inspection, Bankability, Blockchain Technology, Circular Solar Economy",numberOfDownloads:null,numberOfWosCitations:0,numberOfCrossrefCitations:null,numberOfDimensionsCitations:null,numberOfTotalCitations:null,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"May 5th 2022",dateEndSecondStepPublish:"June 2nd 2022",dateEndThirdStepPublish:"August 1st 2022",dateEndFourthStepPublish:"October 20th 2022",dateEndFifthStepPublish:"December 19th 2022",remainingDaysToSecondStep:"12 days",secondStepPassed:!1,currentStepOfPublishingProcess:2,editedByType:null,kuFlag:!1,biosketch:"Dr. Aghaei is a pioneering researcher in Renewable Energy, Solar photovoltaics, Energy systems, Autonomous and Smart Monitoring, Aerial Robotics, and Artificial Intelligence. 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He is the coordinator of the COLLECTiEF project and was actively involved in several national and international projects.",coeditorTwoBiosketch:null,coeditorThreeBiosketch:null,coeditorFourBiosketch:null,coeditorFiveBiosketch:null,editors:[{id:"317230",title:"Dr.",name:"Mohammadreza",middleName:null,surname:"Aghaei",slug:"mohammadreza-aghaei",fullName:"Mohammadreza Aghaei",profilePictureURL:"https://mts.intechopen.com/storage/users/317230/images/system/317230.jpg",biography:"Mohammadreza Aghaei is a senior researcher in the field of photovoltaic solar energy and energy system. \nHe received the Ph.D. degree in electrical engineering from Politecnico di Milano, Italy, in 2016. He was a Postdoctoral Scientist with Fraunhofer ISE and Helmholtz-Zentrum Berlin (HZB)-PVcomB, Germany, in 2017 and 2018, respectively. He is a Guest Scientist with the Department of Microsystems Engineering (IMTEK)/Department of Sustainable Systems Engineering (INATECH), Solar Energy Engineering, the University of Freiburg since 2017. He also fulfilled another two years postdoc in the Design of Sustainable Energy Systems Group, at Eindhoven University of Technology (TU/e), The Netherlands. Dr. Aghaei is currently a senior scientist with the Faculty of Engineering, Norwegian University of Science and Technology Norwegian (NTNU), Norway. He is also co-coordinator of EU-project 'COLLECTiEF” - Collective Intelligence for Energy Flexibility.\nHe has authored numerous publications in international refereed journals, book chapters, and conference proceedings. Main his research interests include Energy transition, Energy flexibility, Solar Energy, Photovoltaics, predictive and autonomous monitoring, solar cells, Artificial intelligence (AI), and Unmanned Aerial vehicle (UAV). 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1. Introduction
Radiation sources are known to be basically of two origins, that is, the natural or background radiation and artificial or man-made radiation. Natural or background radiation sources are grouped as those from cosmic; these are radiation from the space. The dose from cosmic source of radiation could vary from one location to another, i.e., the dose values vary in different parts of the world and also change with altitude. The exposure also decreases in intensity with depth in the atmosphere or increase with increase altitude [1].
Other natural source group is the terrestrial radiation, which is from soil, water and vegetation. These are radionuclides such as 238U, 234Th and 40K, and they contribute mostly to the external dose to human body. Radon is another example of naturally occurring radionuclide which is found in rock formations and can release higher levels of radiation that can pose health risks particularly lung cancer.
The third source of natural radiation is the internal radiation, and these are 40K, 14C and 210Pb inside the body. These radionuclides enter the body through the ingestion of food, milk and water or by inhalation.
The artificial or man-made radiations are those that originate from various activities of man such as in consumer products, examples which include building materials, television receivers and tobacco products. Other activities are nuclear power plants for electricity/power generation, testing and using of nuclear bombs, decommissioning of radioactive waste, and industrial activities such as mining, security inspection systems use in cargo scanners and personnel security systems and medical purposes.
Also radiation can be categorized into types; they are ionizing and nonionizing radiation. Nonionizing radiation is the type of electromagnetic radiation with no enough energy to ionize atom, while ionizing radiation is radiation that carries enough energy to detach electrons from atoms causing the atom to become charged or ionized. Ionizing radiation has more energy than nonionizing radiation, that is, enough to cause chemical changes, and thereby causing damage to tissue. The ionizing radiation is further categorized into four types: alpha particles, beta particles, gamma rays and X-rays. The effects of ionizing radiation at high-dose levels are well known, while the effects of ionizing radiation at low doses are not yet clear. Ionizing radiation is used for diagnostic and therapeutic medical purposes, and there are advantages and disadvantages attached to the use of ionizing radiation for this purpose; the advantage lies in being able to diagnose and treat diseases; however, it can damage human cells and cause harm. Radiation doses of about 10 Sv and above received in a short period can cause the organs and tissues in the body to cease to function and may lead to death [2].
These two categories of radiation, ionizing and nonionizing, can cause damage to humans. Ionizing radiation can cause cancer, heart and brain problems, while nonionizing radiation can cause burning of retinas, skin cancer as a result of long exposure to the sun [3].
Examples of natural sources of ionizing radiation include metal mining, radon exposure, cosmic rays from the sun and radioactive rocks and soils, while examples of artificial sources of ionizing radiation includes nuclear reactors, medical equipment such as X-rays. Sources of natural nonionizing radiation are sunlight and thermal radiation, while man-made sources of nonionizing radiation are microwave oven, cell phones and power lines.
Most of the man-made exposure to radiation is from medical procedures. This can be shown from the NCRP Report No. 93, 1987, on the ionizing radiation exposure of the population of the United States. Natural sources of radiation accounted for 82%, and medical sources are responsible for 11% of the remaining and 18% from man-made radiation (NCRP Report No. 160), and most of the exposure is from diagnostic X-rays such as examinations of computed tomography, conventional radiography and fluoroscopy and interventional fluoroscopy. The average dose from the use of radiation for treatment purposes is much less than that from diagnostic purposes even though quite a number of exposures may be used in certain treatments such as cancer; only a small number of people are involved, and exposures are limited to small areas where treatment is necessary [4].
Medical use of radiation is known to be the greatest artificial source of doses to human beings at large. Following the improvement in technology and healthcare, this has led to an increase in the usage of radiation; this can be measured by the frequency of procedures and by the levels of individual and collective doses. Medical X-rays are responsible, in Western countries, for at least some 300 man Sv per million inhabitants, representing approximately 90% of man-made source. The common sources of radiation exposure to the population are the natural sources and medical irradiation [5].
The risk of radiation exposure from X-ray such as malignancy, skin damage and cataract is high with increasing number of examination performed. There is an increase in the number of procedures performed and the possibility of more complicated procedures such as interventional procedures that can lead to higher doses to patients and staff. The increasing number of computed tomography (CT) procedures performed also can lead to increase in the collective dose.
Since the diagnostic X-rays take the highest portion of the medical use of radiation or in which human are exposed apart from the natural sources, it is therefore necessary that people or the population are protected which therefore necessitate the need for a radiation protection to be considered in order to eliminate the damage from unnecessary exposure. Even though, the doses from diagnostic radiology are much less than in the treatment of diseases, there is a need to monitor that the dose to the patient is not too low or too high for a particular procedure. According to the International Commission on Radiation Protection (ICRP), radiation protection involves the use of three techniques, and these are justification of practices, optimization of protection and the use of dose limits/levels. Since dose limits do not apply to medical exposure, optimization and justification are therefore important in patients using radiation for medical purposes.
The European Union Council Directive 97/43/Euratom (the Council of the European Union, 1997) also laid emphasis on the need of these two principles of justification and optimization. The principle of justification implies that the advantages to the patient and the society during a radiological procedure must be more than the risks for the patient and the need to consider alternative techniques that do not involve medical radiation exposure [6].
The principle of optimization is to keep the dose ‘as low as reasonably achievable’ (ALARA principle) economic and social factors being taken into consideration (ICRP 60) [7]. Also ICRP in its recommendation in Publication 73 (ICRP 73) introduced the need for establishment and use of diagnostic reference levels (DRLs) to ensure that implementation guidance is available. The purpose of DRLs is not to be used when considering the dose to individual patients but to prevent delivery of unnecessary high doses as well as to be used in estimating radiation doses as a form of quality assurance [7].
The International Commission on Radiological Protection (ICRP) defined DRL as ‘a form of investigation level, applied to an easily measured quantity, usually the absorbed dose in air, or tissue-equivalent material at the surface of a simple phantom or a representative patient,’ while the Council of the European Union defined DRL as ‘dose levels in medical radiodiagnostic practices or, in case of radiopharmaceuticals, levels of activity, for typical examinations for groups of standard-sized patients or standard phantoms for broadly defined types of equipment.’
DRLs settings for diagnostic radiology should not be based on patient’s doses measured from only well-equipped hospitals but in all types of different hospitals, clinics and practices. DRL values are to be established by using the 75th percentile, taking into account of values that are too low or too high. DRLs are to be set locally, regionally or nationally and recorded on regular basis to allow for comparison over some time and also for the purpose of establishing database. According to Vassileva and Rehani [8], DRLs are indicators for a typical practice in a country or in a region, and since equipment and procedures can vary between different facilities in countries or regions, it is therefore a good practice to establish national or regional DRLS. DRLs should be reviewed wherever DRLs are constantly exceeded and that corrective actions are taken when appropriate.
In most countries with established National Diagnostic Reference Levels (nDRLs), the responsibility lies with the government national authorities and institutes responsible for radiological protection and nuclear safety. They perform the function of collecting data from different hospitals or clinics with medical imaging facilities, analysis of the data and then give update on the DRL values. The established DRL values are reviewed periodically, and recommendations are made based on the findings.
2. Reason for DRLs
From the article on historical background on DRLs, Wall and Shrimpton [9] reported that national surveys of patient doses on X-ray examinations conducted in Europe and the USA in the 1950s showed high variations in doses from different hospitals which came about the need for quantitative guidance on patient exposure. It was reported that in the late 1980s, the dose guidelines started first in the USA and then in the UK and then followed in Europe, and the reference doses were incorporated into working documents giving Quality Criteria for Diagnostic Radiographic Images for adult and pediatric by European countries study groups of radiologists and physicists.
In 1997, the need to develop the DRLs then followed, (Council Directive 97/43/EURATOM, 1997) which is defined as dose levels in diagnostic radiology to patients of standard-sized groups or standard phantoms, for particular examinations and as well considering different types of equipment [6]. The DRL values should not be exceeded for standard procedures when good and normal practice is applied. The main aim of a DRL is to serve as a control in using radiation for diagnostic purposes and by avoiding unnecessary exposure to radiation. In 1989, national reference doses were first suggested for some radiographic examinations. This was followed by the investigation in the levels in patient doses by ICRP in 1990 and further developed into development of DRLs in ICRP Publication 73.
The list of medical exposure according to the United Kingdom nDRLs required by the Ionizing Radiation Regulations in 2000 include adult and pediatric computer tomography examinations, general radiography and fluoroscopy which include diagnostic examinations on adult and pediatrics and interventional procedures on adult and dental radiography.
3. Regulatory bodies on the use of ionizing radiation and DRLs
The regulatory bodies on the use of radiation include the following organizations:
3.1 United Nations Scientific Committee on the Effects of Atomic Radiation, UNSCEAR
UNSCEAR, which was established in 1955 with the mandate to undertake broad assessments of the sources of ionizing radiation and its effects on human health and the environment, provides the service of assessing global levels and effects of ionizing radiation as well as providing scientific basis for radiation protection. The use of radiation for medical purposes could be of positive applications; it is a reality that X-rays can cause biological harm or injury to humans [10]. Reports from developed countries indicated that the use of ionizing radiation for diagnostic purpose is estimated to be about 1 mSv per capital annual. At this dose level, the estimated annual additional cancer mortality is 0.5 per 10,000 persons of a general population basing on the additive risk model of the United Nations Scientific Committee on the Effect of Atomic Radiation (UNSCEAR). In its report in 2008, UNSCEAR Report No. 1 reported an increase in the total number of diagnostic medical examinations from 2.4 to 3.6 billion; this is an increase of almost 50% from its previous study in 1991–1996. The use of high-dose X-ray techniques such as the computed tomography scanning is leading to growth in the annual number of procedures in many countries thereby increasing the collective dose. It is estimated that the total collective effective dose from medical diagnostic examinations have increased by 1.7 million man Sv, that is, it rises from about 2.3 million to about 4 million man Sv, which gives an increase of about 70% [11].
3.2 International Atomic Energy Agency (IAEA)
IAEA develops safety standards to protect the health and minimize the danger to people’s life and property associated with the use of ionizing radiation in medicine, etc. IAEA focuses on ensuring that radiation doses to patients commensurate with the medical purpose, thereby preventing patients from being exposed to unnecessary and unintended radiation. To ensure that radiation protection and safety of radiation sources in medical uses of ionizing radiation, the IAEA Safety Guide on Radiation Protection and Safety in Medical Uses of Ionizing Radiation (2018) was published to provide recommendations and guidance on fulfilling the requirements of IAEA Safety Standards series No GSR Part 3 [12].
According to the report from the IAEA office of Public Information and Communication, DRLs is a tool for comparing diagnostic imaging procedures in a country which include adults and children of different ages and weights in examinations in X-rays, CT, image-guided interventional procedures or nuclear medicine procedure. Each facility needs to set their DRL and then compare with local, national or regional doses. The newsletter report also mentioned the need to track radiation dose data to improve practice and reduce doses without loss of diagnostic quality. As well as prevent unnecessary exposures.
International Atomic Energy Agency also states that DRLs should be set locally, regionally or even nationally. IAEA also agreed to set the nDRLs at the third quartile values, and they could not be considered as optimum dose but in identifying unusual practices. According to IAEA, the government is responsible for the establishment of DRLs and to involve health authority, the professional bodies and the regulatory body. IAEA also identifies DRLs as a tool in radiation protection of the patients.
3.3 The International Commission on Radiological Protection (ICRP)
The primary aim of radiological protection, as stated in ICRP Publication 60, is ‘to provide an appropriate standard of protection for mankind without unduly limiting the beneficial practices giving rise to radiation exposure’ [13].
According to the International Commission on Radiological Protection (ICRP) in its international recommendations, ICRP 60, (ICRP 19), the focus is on the principles of justification and optimization of all radiation exposures in diagnostic radiology. Another recommendation, which is the ICRP 85, [14], focused on the risk of skin damage from interventional radiology. In 2007 in its publication (ICRP Publication 103), ICRP presented the revised recommendations for radiological protection followed by ICRP Publication 118 (2012) published on deterministic effects of ionizing radiation. ICRP makes recommendations only, and it is the responsibility of government of individual countries to implement those recommendations through legislation appropriate for their own country.
3.4 World Health Organization (WHO)
According to the World Health Organization (WHO), there are established relevant guidelines that have to be considered in each type of diagnostic procedure [15, 16, 17]. Human exposure to radiation for medical research is considered as not justified unless it is in accordance with the provisions of the Helsinki Declaration [18] and follows the guidelines for its application prepared by the Council for International Organizations of Medical Sciences [19] and WHO [20].
The WHO in 2008 launched a Global Initiative on Radiation Safety in Health Care Settings (GIRSHCS), thereby facilitating the adoption and applications of regulations, in the evaluation of radiation medicine and medical imaging procedures. WHO also facilitates training on the use of appropriate technologies as well as publishing and disseminating guidance tools and technical documents. In 2012, the WHO presented report of its Radiation Risk Communication in pediatric imaging workshop on the need to develop and implement a risk communication tool in order to create the awareness of radiation risks and exposure in pediatric procedures [21].
3.5 National Council on Radiation Protection and Measurements (NCRP)
National Council on Radiation Protection and Measurements Report No. 160 (1993) focused on the biological effects of ionizing radiation such as cancer, cardiovascular disease and cataracts, while its Report No. 180 focused on the management of exposure to ionizing radiation and expressed radiation protection principles as justification, optimization of protection and numeric protection criteria, i.e., the management of dose to an individual. This means that the protection criteria is the first objective when there is a numeric protection for a specific exposure; then the optimization of protection should follow [22, 23].
4. Conclusion
The use and exposure of humans to ionizing and nonionizing form of radiation is of various purposes. Radiation exposure cannot be entirely avoided on this planet, taking into account how much radiation people receive from natural sources. The proper use of radiation can be of immense benefits. The sources and categories of radiation exposure, the various use of ionizing radiation and the principles of radiation protection to avoid unnecessary exposure to high level of radiation dose from the use of ionizing radiation have been discussed in this chapter.
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Introduction",level:"1"},{id:"sec_2",title:"2. Reason for DRLs",level:"1"},{id:"sec_3",title:"3. Regulatory bodies on the use of ionizing radiation and DRLs",level:"1"},{id:"sec_3_2",title:"3.1 United Nations Scientific Committee on the Effects of Atomic Radiation, UNSCEAR",level:"2"},{id:"sec_4_2",title:"3.2 International Atomic Energy Agency (IAEA)",level:"2"},{id:"sec_5_2",title:"3.3 The International Commission on Radiological Protection (ICRP)",level:"2"},{id:"sec_6_2",title:"3.4 World Health Organization (WHO)",level:"2"},{id:"sec_7_2",title:"3.5 National Council on Radiation Protection and Measurements (NCRP)",level:"2"},{id:"sec_9",title:"4. Conclusion",level:"1"}],chapterReferences:[{id:"B1",body:'United States Environmental Protection Agency. Radiation sources and doses. Available from: https://www.epa.gov/radiation/radiation-sources-and-doses'},{id:"B2",body:'Australian radiation protection and Nuclear Safety- Health Effects of Ionizing Radiation. 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Adopted by the 18th World Medical Assembly and as amended by the 29th World Medical Assembly, Tokyo, 1975, the 35th World Medical Assembly, Venice, 1983, and the 41st World Medical Assembly, Hong Kong'},{id:"B19",body:'Council for International Organizations of Medical Sciences (CIOMS), in collaboration with World Health Organization. International Ethical Guidelines for Biomedical Research Involving Human Subjects. Geneva; 1993'},{id:"B20",body:'World Health Organization (WHO). Use of ionizing radiation and radionuclides on human beings for medical research, training and non-medical purposes. Technical Report Series No. 611. Geneva: WHO; 1977'},{id:"B21",body:'World Health Organization. Radiation risk communication in paediatric imaging. 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Department of Mathematics and Physics, Cape Peninsula University of Technology, Cape Town, South Africa
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1. Introduction
The ruminants sector plays an important role in global socioeconomic directions. Therefore, it is necessary to research, to discover and to innovate and transfer knowledge to the farmer, for practices and alternatives that improve ruminants reproduction and production.
Increasing the efficiency of breeding and production of a farm herd is one of the great challenges for large ruminant producers. Recently and now, genetic selection programs have sought the characteristics needed to increase milk production, with gains by increasing the quantity and quality of milk. However, reproductive efficiency was neglected. In recent years, various publications have presented strategies to further increase milk and meat production and also to increase reproductive performance, which is a key factor for the efficient growth of ruminants [1].
In farmers, importance of a sustainable, economically viable production system can be obtained by maximizing reproductive efficiency of the ruminants herd.
This reproduction management can determine the profitability from the number of offspring produced, the genetic progress and the shorter interval between lactations periods.
The essential importance of precision reproductive care is therefore highlighted. This reproductive biotechnology (ET, AI) applied is capable of produce maximum production efficiency in animal farms with vulnerable populations, or in limited areas, in addition to improving animal welfare.
The first biotechnology of reproduction represented by artificial insemination (AI) is known as the simplest and lowest cost of reproductive biotechnology. This technique enhances the male’s genetics, bringing slow genetic progress. However, dairy breeds in conditions of seasonality and climate change exhibit failures in estrus cycling and demonstration, which compromises AI results. In other words, with the discovery and description of FTAI protocols that synchronize follicular growth and induce ovulation, it is possible to achieve a high rate of inseminated animals without the need to observe the clinical and behavioral signs of estrus. [2], thus providing an increase in the conception rate and avoiding the occurrence of human errors in the detection of estrus, and calculating the optimal time for insemination. However, gametes an embryo can undergo degeneration in the extreme temperatures of summer [3]. The transfer of embryos produced in vivo (ET) became a strategy to avoid the deleterious effects of this period and provide a higher productive index than with AI [4].
With the beginning of the evolution of modern biotechnologies, the next step as major commercial progress in reproductive biotechnology was the transfer of embryos that appeared in the late 1970s. The ability to preserve, freeze and transport bovine embryos around the world has made ET an extremely useful technology for disease control, genetic rescue of valuable individuals and the development of new lines or breeds of animals.
ET is a multifactorial protocol that depends on several carefully and correctly performed sequential steps. Poor performance in any of the steps directly affects the success rate of the final result, the conception rate and the number of weaned products.
The use of embryo transfer as a breeding technique is growing throughout Europe, even in countries with less embryo transfer tradition. Historically the entire embryo transfer process was carried out at a specialist centres but now experienced reproduction vets are starting to carry out the artificial insemination (AI), flushing and searching as ambulatory procedures for transfer into a suitable recipient. The most time consuming and difficult part of the in vivo embryo transfer process is synchronizing recipients and transferring the embryo into the most suitable recipient. Receptors must be selected with with the best chance of maintaining the pregnancy [5, 6].
Embryo transfer provided a means by which the number of conception products could be multiplied rapidly, with the same origin. However, embryo transfer veterinarians have developed technology for commercial use and taken techniques from the laboratory to the farm. There have been countless practical difficulties for practitioners in uniting and setting up the International Embryo Transfer Society (IETS) in order to facilitate the discussions and steps deemed necessary for progress. Currently, the vast majority of countries in the European Union have one or more embryo transfer associations, where these actions are reported and come to support and develop ET biotechnology (eg AETE, SIET, AET-d, AETF, ARET and others).
Embryo transfer (ET) is now commonly used to produce AI sires from the top producing cows and proven bulls for the dairy industry [7]. As a perspective, the new genomic techniques presented are increasingly used for the selection of embryo donors, and genomic analysis has become essential for the selection of bull dams that will be used in embryo transfer [8]. Although the economy sometimes seems to exclude the use of embryo transfer techniques for anything other than gamete production, the commercial cattle industry benefits from the use of commercial males produced through well-designed MOET programs [9].
With the explosive development of this biotechnology, the techniques for obtaining embryos have been improved, the materials and consumables have become more efficient, the equipment more efficient, which makes the production cost of the embryo decrease and be higher quality. This desideratum is fully accepted by farmers and who apply this ET biotechnology more and more frequently [10].
Although there has been no appreciable increase the embryo production per poliovulated donor in last years, the importance of follicle wave dynamics [11] and methods for the synchronization of follicular wave emergence [12, 13], they simplified the protocols by which female poiliovulation could be achieved, leading to increased embryo production per application session. Currently, donor cows are hyper-stimulated more frequently than in the past (at an interval of 30–60 days) and thus more embryos can be produced per year, without changes in the current superstimulation protocol [14]. Other authors [15] have been interested in various factors that affect the viable production of embryos in animals and especially in dairy cows.
Potential embryo donors can be inseminated naturally or artificially (AI) and the embryos are normally collected non-surgically from 6 to 8 days after fertilization. After collection, the embryos must be identified and then evaluated morphologically. The evaluation procedure is done in an appropriate environment before the transfer. At this stage, they can be subjected to manipulations, such as splitting and sexing, and can be cooled or frozen for shorter periods or longer storage [16]. Discussion of donor superovulation, recipient synchronization, and embryo transfer should begin with a review of recent information on the physiology of female reproduction and the estrous cycle.
The reproductive genetic potential of every normal newborn calf is enormous. It is said that there are about 150,000 “eggs” or potential oocytes in a female and many billions of sperm produced by each male. We can say that through natural reproduction, only a small part of the reproductive potential of a valuable individual could be realized. The bull will be able to produce an average of 15 to 50 calves per year, and the cow will have an average calf per year. With the use of artificial insemination biotechnology, it is possible to exploit the large number of sperm produced by a genetically superior bull; however, the reproductive potential of the female with superior genetics was largely unused. It will produce on average 5–8-10 calves in its entire biological life through normal management programs. As artificial insemination has done for bulls, embryo transfer is a technique that can greatly increase the number of offspring that a genetically important cow can prove and produce. The main reason for the development of embryo transfer in cattle was to further the increase in genetic progress of the female.
2. Advantages of embryo transfer (ET)
Increase the small population of valuable animals [17, 18].
Helps in the genetic improvement of animal, decreases the generation interval, increases selection intensity [19].
It helps to get more many calves from a genetically superior single female as against a few calves which can be produced naturally in its lifetime
An possibilites tool to produce breeding bulls from a limited number of superior females for use in AI [20].
May increase the numbers of the existing purebred herd.
Possible to obtain offspring from the genetically valuable female that has become infertile due to disease, injury, or age [21].
With the improvement in cryopreservation and the advancement of technologies, it is economical and easier to transport (import/export) embryos instead of living animals.
Endangered animals can be saved from extinction by embryo production and cryopreservation [22].
Avoids transmission of diseases from infected donors to their offspring-Genetic defects [20].
Decreases the risk of transmitting infectious agents. Embryo collected from cows with bovine leukemia virus, blue tongue virus, FMD virus if washed properly before transfer (Trypsin treatment) to unaffected recipients does not transmit disease.
ET allows differentiation between normal and abnormal fertilization [23].
An important tool for disease control, genetic salvage of valuable animals, biosecurity program, development of new lines/breeds of animal.
Helps in the proliferation of femele genetic material from dam and sire [24].
Associated reproductive technologies (ART) such as embryo splitting, sexing of embryos, cloning, transgenesis further broadens the horizons of ET [25].
The males produced by ET out of superior donors by using elite bull semen can be used as future elite sires on the AI network and females produced would serve as the future bull mother. Therefore the existing demand of elite sires especially in cattle and buffalo breeding programs can be largely met [24].
Can be used to evaluate the contribution of the aging oocyte to decreased reproduction in geriatric animals [23].
Infertility treatment, ET serves as an important tool in the treatment of infertility in cows.
3. Sexual cycle physiology
The intrinsic control of the bovine estrous cycle is coordinated by the interdependent secretion of hormones from structures such as: hypothalamus, anterior pituitary, ovaries and uterus [26]. These include gonadotropin-releasing hormone (GnRH) from the hypothalamus, folliculostimulating hormone (FSH) and luteinizing hormone (LH) from the anterior pituitary gland, estrogen, progesterone and inhibin from the ovary and prostaglandin F2a (PGF) from the uterus.
During gestation, the multiplication phase of the oogonia results in the constitution at the birth of a stock of primordial follicles, the number of which in the cow is between 200 and 250,000. These primordial follicles have a diameter of between 30 and 40 microns. At the secondary and especially tertiary stage, a cavity appears. It then becomes possible to identify by ultrasound these follicles with a diameter of between 2 and 4 mm.
In cows, as in many other mammals, follicular growth develops in the form of waves. In a 21-day cycle, there are two waves. The presence of a third wave is not uncommon. It has the effect of lengthening the average length of a cycle by a few days (24 vs. 21 days). When the cycle has two waves (Figure 1), the emergence of one wave occurs on days 0–1 and 10–11 of the cycle. Day 0 corresponds to that of estrus. By emergence we mean the moment or by ultrasound, it is possible to distinguish in the mass of follicles recruited the one which will become dominant. During the 2.5 days after the emergence of a wave, the selected future dominant and dominated follicles continue to grow. The dominant follicle reaches at this time the average diameter of 8 or even 9 mm. This moment is called “follicular deviation” and characterizes the moment when the dominant follicle will be able to clearly distinguish itself from other growing follicles. Its diameter is therefore 2 mm greater than that of the other selected follicles. The follicle continues to grow until it reaches a diameter of 10 mm. Clinically, this dominance can be identified by ultrasound, or by Doppler ultrasound to identify changes in the vascularization of the follicle or by assaying hormones such as estradiol or follicular fluid inhibin. This dominance is therefore both morphological, ie exerted by the largest follicle and physiological, because it brings about an arrest in the development of the dominated follicles which go through a static phase before settling down. This physiological dominance also implies the appearance at the granular level of LH hormone receptors which will take over from FSH to ensure further growth of the dominant follicle. The period of physiological dominance is shorter than that of morphological dominance. Clinically, the identification of more than 10 follicles with a diameter of between 3 and 8 mm makes it possible to exclude the presence of a physiologically dominant follicle. Growth of the dominant follicle will continue until it reaches a maximum diameter of 16 mm.
Figure 1.
Physiology of the sexual cycle in cows, with two follicular waves.
This is followed by a so-called static plateau phase lasting more or less 6 days at the end of which the dominant follicle will begin to regress. Due to the gradual decrease in estradiol synthesis by the dominant follicle, there is a new release of FSH and the appearance on day 10 of new follicular emergence. This cannot be observed as long as the dominant follicle from the previous wave is in the growth or plateau phase. This new wave develops like the previous one through the dominance of a new follicle which will suppress the growth of the subordinate follicles which will become saturated. The follicle continues to grow. In proestrus he is no longer under the progesterone influence, so given the massive release of LH he can stop growing and then ovulate.
During the cycle, the follicular population is therefore distributed into several classes except that of the follicles in the reserve. A first class consists of recruited follicles. Their diameter is 2 to 4 mm. A second class is made up of growing follicles. These follicles can potentially become the ovulatory follicle. Their diameter is between 6 and 10 mm. The third class refers to the dominant follicle. Its diameter is between 10 and 16 mm. Finally, can we also identify the preovulatory follicle with a diameter greater than 15 mm. It will persist on the ovary for 5 to 6 days before regressing or ovulating (Figures 1 and 2) [5, 6, 10, 27].
In a cycle with three waves (Figure 2), the emergence of cows occurs on days 1, 10 and 17 respectively, with day 0 being estrus and therefore day 1 ovulation. The general wave pattern is comparable to that described for a cycle with two waves. Waves 1 and 2 are anovulatory. Only the third is normally ovulatory. It will be seen that the luteal phase like the cycle is of longer duration than for a cycle with two waves. Likewise, the interval between the onset of the ovulatory wave and ovulation is shorter (7 vs. 11 days).
Figure 2.
Physiology of the sexual cycle in cows, with three follicular waves.
The main mechanism of synchronization of the estrous cycle is ovulation, when the first follicular wave occurs [11]. A new hormone-secreting endocrine gland is formed instead of the ovulatory follicle and is called the corpus luteum (CL) it is formed in the following days (3–5) and in the absence of pregnancy, it wraps around day 16 or 17 of the cycle [26]. The most common hypothesis for CL regression is that the non-pregnant uterus secretes a luteolytic factor into the uterine venous blood. This substance is transferred through a local blood (veno-arterial) pathway to the ovarian artery through which it reaches the ovary and causes luteolysis [27].
After CL regression, a rapid decrease in serum progesterone concentrations to values lower than 1 ng/ml results, at the same time, the frequency of LH pulse increases and follicular development is further stimulated. The growth and maturation of the follicle that becomes preovulatory results in increased estradiol secretion, which causes local estrogenic changes in the oviduct and uterus, behavioral estrus and a preovulatory release of LH (around the time of estrus manifestation). The preovulatory LH peak results in the resumption of the oocyte meiosis process, and ovulation 24 to 32 hours later and the luteinization of the ovulated follicle to form a secretory corpus luteum hemoragicum. The growth and development of the hemorrhagic corpus in a fully functional CL results in progestative changes in the oviduct and uterus that are favorable for embryonic development and pregnancy. If pregnancy does not occur, the cycle resumes again with the disappearance of CL [6, 11, 23, 27].
3.1 Estrus synchronization, superovulation
Estrus synchronization and superovulation are critical components of an embryo transfer program. These techniques involve the manipulation of the basic endocrine patterns, presented and described in this document [28]. The key to successful estrus synchronization is synchronous growth and ovulation of a viable dominant follicle and closely synchronized, rapid declines in circulating progesterone to values <1 ng/ml [29]. If properly implemented, within the physiological constraints of their mechanism of action, current techniques for synchronization of estrus and ovulation are highly successful [30]. However, the variation in the dynamics of ovarian follicular waves makes it difficult to control the exact time of estrus and ovulation.
The goal of superstimulation treatments in cows is to obtain the maximum number of fertilized and transferable embryos with the highest possible probability of inducing and sustaining a pregnancy.
The variability of the ovarian response was related to differences in super-stimulatory treatments, such as gonadotropin preparation, gonadotropin type, duration of treatment, timing of previous estrus treatment, total gonadotropin dose, and use of additional hormones in superstimulation. Protocol [4]. Additional, equally important, sources of variability are factors inherent in the animal and its environment. These factors may include nutritional status, reproductive history, age, season, breed, ovarian status at the time of treatment and perhaps most importantly, inherent numbers of antral follicles [5]. While considerable recent progress has been made in the study of bovine reproductive physiology, factors inherent to the donor animal that affect superovulatory response are only partially understood [13, 25, 30].
4. Embryo transfer procedures
In farm animals, fertilized ova is removed from the uterus of their dam (the donor) and transferred to the uterus of other females (recipients) for development to term. Almost all commercial embryo transfers now use nonsurgical methods to recover the embryos rather than surgical methods (only for small ruminants). The procedure requires multiple steps (Figure 3), a large amount of time, and a variable cost.
Figure 3.
Stages of in vivo embryo transfer in large ruminants.
The stages of a direct/in vivo ET protocol are highlighted in the following mandatory steps [31]:
Donor cows, selection of embryo donors.
Poliovulatory treatment of donors,
Artificial insemination/mounting,
Collection of embryos and classification,
Selection and preparation of receptors,
Synchronization of estrus and ovulation with the donor,
Direct transfer/preservation,
Gestation and parturition.
4.1 Donor selection
The selection of the embryo donor candidate is based on two major criteria: (1) the genetic merit, generally evaluated by the owner and based on performance, and (2) the reproduction criteria interpreted and evaluated by the veterinarian. The donor must be in good physical condition, an average but growing BCS. It should be free of underlying conditions, be at least 50 to 60 days after calving and have a regular cycle. In general, cows with a history of reproductive problems, even minor ones, do not make good embryo donor animals.
Donors are further evaluated by careful examination of the cervix, uterus, and ovaries per rectum to determine if they lack adhesions to neighboring organ structures, and the presence of other palpable lesions. It is recommended to test the permeability of the cervical canal with a cervical dilator, especially if the donor is before the first calving - heifer. This prevents the occasional of being unable to negotiate the cervix after a series of costly hormonal injections.
Single or multiple embryos can be collected from ovulating or naturally superovulated cows. For optimal efficiency, 2 to 4 donors should be treated and synchronized with their recipients for each attempt/session; this allows the sharing of the recommended potential of 8–10 recipients per donor.
4.2 Superovulation
Superovulation is and remains one of the least anticipated steps in the process of embryo production. The objective of superstimulation treatments in the cow is to obtain the maximum number of fertilized and transferable embryos with a high probability of producing pregnancies [32].
In the bovine tremendous variation in response occurs with age, breed, lactational status, nutritional status, season, and stage of the cycle at which treatment is initiated. Follicle stimulating hormone (FSH), which has a short half-life (Pluset, Folltropin-V, and others), necessitates twice-daily injections over a period of 4 to 5 days. Synthetic hormones with a long half-life (like PMSG), are administered in a single dose, but have other drawbacks. Treatment is start in the mid-luteal phase (day 8 to 12) of the donor’s estrus cycle and white use of prostaglandins (PGF) to synchronize the estrus of the donors and the recipients. Alternatively, treatment may be induced on day 16 or 17 (day 0 = estrus) of the donor’s natural estrous cycle, or with progesterone administration (which mimics a progesterone phase). Ultrasonography and palpation of the ovaries per rectum have been shown to have similar accuracy for determination of the number of follicles (in estrus fase) or CL (at the time of embryo recovery). However, the number of anovulatory follicles can be counted more accurately [1, 4, 33, 34].
4.3 Artificial insemination/mounting
Donors should be artificially inseminated twice with a 10–12 hour interval, beginning 6 hours after the occurrence of oestrus, to ensure the time interval in which ovulation occurs. Depending on the quality of the frozen/sexed semen, a dose with a higher sperm concentration, even a double dose, can be used for each insemination. Ultrasonography is helpful in assessing the potential superovulatory response on the day prior to ovulation or at the time of AI.
4.4 Collection of embryos and classification
The donor animal is kept in a standing position in a trevis. The first step in the non-surgical recovery of embryos is to determine the numbers of corpus luteum in the ovary [21]. This step is important to rule out that the superovulation response in the animal; if less or no CL is found-indicates the poor response of superovulation-flushing not to be done in such animals. The donor was given an epidural anesthesia, then a wash and disinfection of the ano-vulvar region (Figure 4).
Figure 4.
Recovery of bovine embryos by flushing method. A. Scheme of catheter placement and reservoir-uterus-filter fluid flow, ultrasound images with catheter guidance through the cervix and visualization of uterine lavage, see white arrow. B. Inserting the stylus through the cervical lumen, C. inflating the balloon from the catheter and obtaining the dam at the top of the uterine horn, D. flow of flushing fluid and recovery of embryos.
A two-way round tip balloon catheter (Fr. size 16 to 24) with a tul inflatable balloon is used. Once the instruments has been made ready (two/tree-way catheter), the vulvar lips are parted and the catheter with stylet is inserted into the vagina and advanced towards the lumen of the cervix. It is further advanced to the horn of the uterus until the balloon is situated at the base of the uterine horn. By blowing air, a dam is created with the tip of the uterine horn, there are located the embryonic formations between days 5–8 after ovulation. The amount of air used depends upon the size of the uterus. Basically, there are two methods of embryo collection [35]: the continuous or interrupted flow, closed-circuit system and the interrupted-syringe technique. The most commonly used medium for embryo recovery is Dulbecco’s phosphate buffered saline (PBS), but there are many others ready to use (Euroflush, Vigro). Uterine horn is flushed with 30–60 ml of media and repeated until 300–800 ml of media is used up. The same process is repeated for the other horn as well [36].
Embryos are found with a 10 X magnification stereoscope after filtering the collection/washing medium through a pore filter with a diameter between 50 and 70 μm. The identified embryos are usually transferred as soon as possible, sometimes if desired it is possible to keep the embryos in that environment for a few hours at room temperature. It is also possible to cool the bovine embryos in storage medium and store them in the refrigerator for 2 or 3 days. Most often, embryos can be frozen for use at a later date.
A good response and an appropriate recovery rate results in getting a 4–5 embryos are recovered with each flush. This can lead to 50 freezable embryos per donor per year resulting in the birth of 30 calves after the transfer of the embryo to a recipient [24].
After the fecundation, the single-celled embryo now called the zygote undergoes rapid mitotic divisions (cell number increases, cytoplasm remaining same) called cleavage [37]. Bovine embryo descends into the uterus around day 4.5 days (estrus day 0) [38]. According to the standards, embryos are recovered from six to eight days after the onset of estrus (day 0). Embryos can be recovered even earlier from four days when the embryos arrive from the salpinx in the uterus, but before day 6 the recovery rates are lower than on days 6–8 (Table 1).
Species
Days from estrus
Cattle
7
Buffalo
6
Sheep
3–6
Goat
3–4
Table 1.
Day of collection of embryo.
However, embryos can also be recovered on days 9–14, although they leave the pellucid area on days 9–10, making them more difficult to identify and isolate from cellular detritus and more susceptible to infection [39].
Identification and evaluation of embryos is one of the most important and delicate stage, the practitioner needs experience to get used to the procedure. Embryo quality and poor handling techniques can directly affect pregnancy rates. A step-by-step procedure for looking for embryos is presented in the content of this section.
Evaluation of the embryo in the uterine effluent is based on identification of several morphologic features of the embryo using light microscopy. These methods are subjective and depend on experience. The embryo is spherical and is composed of blastomeres surrounded by a gelatin-like shell and zona pellucid (Figure 5).
Figure 5.
Schematic diagram of a transferable embryo (expanded blastocyst phase).
Embryos recovered 5 to 8 days after estrus are classified morphologically into the following groups, based on their stage of development. Proper evaluation requires rolling of the embryos along the bottom of the dish.
Morula. The blastomeres are round and not tightly joined together. Individual blastomeres are difficult to identify with each other. The blastomere cell mass of the embryo occupies most of the perivitellin space.
Compact morula (tight morula). The shape and appearance of a tight mill is similar to a golf ball, in that the outer edge is slightly wavy (curly) given due to compaction. Individual blastomeres grow and become indistinguishable. The cells on the surface of the mass have a polygonal shape. The embryonic cell mass occupies 60–70% of the perivitellin space.
Early blastocyst. A tiny transparent (clear) space that contains fluid is visible. This area is the beginning of the blastocele (cavity). The embryo occupies 70–80% of the perivitelline space [6, 14, 37].
Blastocyst. The blastocele cavity becomes prominent and represents more than 70% of the embryo’s volume. Inside, two groups of cells are separated and differentiated. They can be clearly recognized as a trophoblastic layer below the pellucid area and the darker cell mass occupying part of the embryo. The perivitellin space is still visible, but it is very small.
Expanding or expanded blastocyst. There is no more perivitelline space between the trophoblastic cell layer and the interior of the area. The area of the pellucida stretches becomes thinner as the blastocyst expands. A small, well-compacted internal cell mass is observed positioned in one part of the embryo. The color of the embryo becomes pale to clear and is due to the large amount of fluid present inside.
Collapsed blastocyst. A perivitelline space can be identified together with a very thin pellucid area. The blastocyst may be partially collapsed, with a smaller blastocyst cavity, or completely collapsed and have the appearance of a compact morula.
Hatched blastocyst. After a continuous growth, the blastocyst expands to rupture and the embryo escapes from the pellucid area. From this moment the embryos pass into the gastrulation phase. The hatched blastocysts can be spherical with a well-defined blastocyst or they can be collapsed, similar to cellular detritus. Identifying embryos at this stage is especially difficult for the inexperienced operator.
When blastocysts/gastrules without areas or hatching are collected, there is a higher risk of damage due to handling. In addition, hatched blastocysts are sticky and can adhere to micropipette handling tubes. Therefore, the use of embryonic filters is not recommended when there is a suspicion that hatched embryos will be recovered (> day 7.5).
Embryos are then classified according to quality based on morphologic appearance. Excellent/good, fair, and poor quality embryos are considered transferable into recipients. Excellent or good quality embryos (Code 1) are freezable (Figure 5).
4.4.1 Codes for embryo quality
Code 1: Excellent or good. The mass of the embryo is symmetrical and spherical with individual blastomeres (cells) they are uniform in size, color and density. The embryo was in accordance with the expected stage of development (collection day). The irregularities are usually minor and more than 85% of the cellular material should be a compact and intact embryonic mass. This is based on the observation of the percentage of embryonic cells represented by the extruded material in the perivitelline space. The pellucid area should be smooth and smooth and could adhere to a micro-plate or a straw.
Code 2: Fair. Some irregularities can be observed in the general shape of the embryo mass or in the size, color and density of individual cells. At least 50% of the cellular material must be an intact, viable mass of embryos.
Code 3: Poor. Some major irregularities in the shape of the embryo mass, or the size, color and density of blastomeres, are identified. At least 25% of the cellular material should be like an intact, viable mass of embryos.
Code 4: Dead or degenerating. Degenerate embryos, oocytes, or I-cell embryos are nonviable.
Embryos of fair quality can be transferred fresh, if the receptors are available and synchronized. The category of good and excellent quality embryos have a high probability of surviving cryopreservation. The EITS considers that the export of embryos of poor and fair quality is inadequate [40]. The assessment of bovine embryos has recently been revised and is constantly improving [41], but the IETS manual has the most comprehensive library of embryonic images useful to practitioners.
Loading the Straw. Immediately before direct transfer, the embryos are individually aspirated into sterile 0.25 ml French straw. The embryo is usually loaded from the support vessel into the straw using a 1 ml syringe attached to the end of the straw stopper. First, a 3 cm medium column is aspirated into the straw, then a 0.5 cm air column is aspirated, then a 3 cm medium column containing the embryo, followed by another air bubble.
Selection and preparation of receptor. The recipient should be non-pregnant, cyclic (minimum of two normal cycles), should have CL on at least one of the ovaries. The embryo stage should match the uterine age of the recipient for a successful pregnancy to occur. While perfect synchrony is desirable, recipients that are 1 day out of phase can be considered acceptable; this means that a 7-day embryo can be transferred into a recipient who showed heat 6–8 days earlier. The lower quality embryo is more sensitive to asynchrony. The recipient should not have any pathological condition which can hinder its pregnancy. Pregnancy rates following embryo transfer are best when the recipient is in estrus from 36 hours before to 12 hours after the donor [42].
Synchronous recipients can be produced in three ways:
Selection from a large pool of cycling females. This strategy limits the number of embryos and time when embryos can be collected. Approximately five percent of the herd will be in heat on any given day.
Estrous cycles of any number of recipients can be synchronized with PGF2alpha or its analogues, or with CIDR devices, to exhibit heat the same day as or just ahead of the donor.
Timed ET, analogous to timed AI (Ov-Sync), can also be used. The importance of close synchrony between the age and the stage of development of the embryo, and the endocrine status of the endometrium of the recipient must be emphasized. Pregnancy rates following embryo transfer are best when the recipient is in estrus from 36 hours before to 12 hours after the donor [43].
Embryo transfer to the recipient can be done surgical or non-surgically. However non-surgical is more ethical to use. The recipient is secured in a Travis and the vulvar area is cleaned. As the animal is in the luteal phase. Epidural anesthesia is induced to prevent straining and defecation. The insertion of the tip of the instrument into the desired uterine horn should be done quickly, and smoothly. Trauma to the delicate endometrium causes bleeding, and blood (complement in the serum) is embryocidal. Ruminants embryos are transferred to the uterine horn and the same procedure as A.I. is followed except that in ET embryos are deposited deep in the horn ipsilateral to CL [44].
Pregnancy rates for IVP embryos were lower in commercial embryo transfer programs than for in vivo embryos [45].
Pregnancy rates are 10% lower in frozen embryos than the fresh ones [37]. Using heifers as recipients, there have been reports that in some 10% of such animals (heifers) it is difficult, if not impossible, to carry out ET via the cervix.
Any kind of stress to the recipient should be avoided. Any other routine treatments scheduled (eg antiparasitic) must take place at least 3 weeks before the transfer; also changes in the feeding regime should be prohibited for 3–4 weeks before and after embryo transfer. Beneficiaries must be accommodated where they can be easily and quietly handled on the day of transfer [23]. Any stressors should be removed.
5. Embryonic mortality
It is said that about 25–40% of embryonic losses are produced in the first few days after transfer to the cow [46, 47]. It has been observed that most of these females return to heat at an interval after 20–22 days, presenting a complete and normal sexual cycle [48]; Therefore, it is believed that embryonic mortality (EM) could occur between days 7 and 17, the period from embryo transfer (ET) until it settles at maternal recognition of pregnancy [49]. In a lower proportion, but just as important, is the pregnancy losses that occur between days 28 and 98, after the transfer and the percentages between 7% and 33% have been reported [50].
The critical nature of the period and the phenomenon of recognition and survival of the embryo at the maternal uterine endometrium during implantation requires a very careful synchronization between the transferred embryo and the recipient. Thus, the importance of both the biochemistry of the uterine environment and the signals of the embryo that generates the recognition and implantation is highlighted [51, 52]. These embryonic signals must be released at the time and concentration necessary to maintain CL morphology and maintenance of function, thus generating a continuous production of P4. Progesterone levels play an essential role in maintaining the embryotrophic environment and supporting the normal development of the concept (the embryo and all adjacent cell structures) [48].
In connection with the influence of P4 (progesterone) on certain events related to pregnancy maintenance from the early stages and the ability of PGF2α to trigger luteolysis, a number of hormonal strategies for maintaining pregnancy have been researched, developed and supported [53, 54]. These strategies tend to be based on the increased efficiency and secretion capacity of P4 by CL: secretion must occur in a timely manner, thus ensuring a suitable uterine environment for the development of the embryo transferred to the recipient bovine female. All these strategies aim to increase the load rate in ET programs [48].
In order to prevent the mortality of the transferred embryos, and the loss of the pregnancies during embryo transfer sessions, two main objectives are considered: - Maintaining the corpus luteum function, even inducing a new one; and Inhibition of the appearance/secretion of luteolytic factor. All procedures apply to female embryo recipients.
In the first case, it is recommended to administer a treatment with Gn-RH, more precisely HCG to develop and support the luteal tissue, or even to form another CL (by causing ovulation of the follicle, if any). In the second case, the administration of non-steroidal anti-inflammatory drugs is considered, which is said to block the synthesis of PGF.
6. Embryo production biosecurity and contamination risks
The procedures for embryo production, in MOET programs, include several steps where contamination with pathogen agents may occur. For instance, the first source of potential contamination comes from the donor itself. Before ovulation, an oocyte could be contaminated by its contact with a given pathogen shed in granulosa cells or follicular fluid during infection (viremia or bacteremia). For example, in bovines, viruses were detected in follicular fluid a few days after experimental exposure to bovine viral diarrhea virus [55]. Hence, the recovery of cumulus–oocyte complexes at this moment might lead to production of contaminated embryos [6, 37].
Disease Risk Management. Success in embryo production by either MOET or IVEP relies on the capacity to correctly perform all technical steps, eliminating or reducing factors recognized to have negative effects. It is essential to select donors and recipients with good general health and adequate nutrition. In addition to those issues, considering that the first source of potential contamination comes from the donor itself, an important measure is to select these females, taking into account their sanitary status. When incorporating animals into the flock, their health status should be checked before and quarantine should be respected. Vaccination and deworming must be employed as prescribed, depending on the location and system of production, but always before their use as donors. Testing should be conducted for some infectious diseases, and those positive should be culled. All technicians in direct contact with the animals must be careful and well trained to ensure familiarity with and safety in the procedures. The technique must be aseptic and all labware sterile. The equipment should be cleaned and all devices that are in contact with the animals should be sterilized before reuse. Clothing should be completely cleaned before reuse [56].
In general, in IVEP, the risk of potential hazards associated with oocyte collection from slaughterhouses are higher than those collected by laparoscopic ovum pickup. Consequently, when using these ovaries, it is important to determine their origin, particularly whether ovaries came from a herd depopulated for any health cause [57]. Care must be taken in the transportation of this material to the laboratory to avoid any external contamination. For media preparation and gamete or embryo manipulation or culture, all biological products should be avoided. These reagents could be replaced by those derived from plant origin or amino acids. When cell culture is preferred for IVEP, the use of controlled cell lines, confirmed to be pathogen-free, is recommended. From a sanitary point of view, safer strategies include the use of chemically defined media that do not contain serum or somatic cells [57].
For MOET, pathogens could be present in the female genital tract and can adhere to either oocytes before fertilization or embryos before collection. Intact zona pellucida is a natural barrier to penetration of pathogen into the oocyte or prehatching embryos. However, some pathogens may adhere to the zona pellucida of oocytes and embryos; thus, the zona pellucida represents a vector for disease transmission to recipients and to embryos after hatching (once transferred). For IVEP, the magnitude of this risk may vary according to the source of ovaries or oocytes that are being used: either from laparoscopic ovum pickup when the donor health status is well known or from the slaughterhouse [57].
Follicular aspiration by laparoscopy, instead of transvaginally, practically eliminates the chance of contamination by microorganisms being carried into the follicle from the vagina via the collection needle, as has been reported in humans [58].
On the other hand, ovaries collected from slaughterhouses provide an inexpensive and abundant source of oocytes, which is usually helpful for research projects and cloning. However, considering that these ovaries are generally transported in containers together, the presence of just a few ovaries from infected animals could represent a potential source of contamination. Other general sources of possible contamination involve the presence of environmental pathogens associated with the technician, slaughterhouse, equipment for laparoscopic ovum pickup or embryo collection, or even in the laboratory, such as glassware, culture dishes, media, and incubators. Regarding media, it is known that any biological product such as fetal calf serum and bovine serum albumin used in the recovery, culture, and cryopreservation of oocytes, sperm, and embryos may constitute a risk of contamination [6, 37, 55, 56, 57, 58].
The semen used in a ET protocol (MOET or IVEP program) must be collected from males managed under appropriate sanitary protocols that ensure their good health status. Although AI represents a useful tool for disease control when best practices are applied, a further source of risk in an embryo production program is the semen. Numerous viral, bacterial, and parasite agents may be present in semen, which may adhere to the surface of spermatozoa or they could be present in the seminal fluid or in the semen extender.
In general, the studies are in agreement when the sanitary procedures recommended by IETS are correctly implemented. The risk of disease transmission from donor to recipient and to offspring for most pathogens is negligible or, at least, is much lower than that associated with live animals. These facts confirm that embryo transfer represents a safe strategy for global genetics trade and a valuable tool for the control and eradication of several diseases in small ruminants [59, 60].
Various publications [57] describe the possibility of transmitting diseases and the management of prevention procedures. The procedures for managing these risks have been described in the OIE Terrestrial Code [61], which explicitly refers to the specifications published in the IETS manual. These procedures are included in national regulations for the transfer of embryos between herds.
Adherence to these procedures ensures that embryo transfers contribute to improving the animal health of a population by controlling the movement of genetic material between herds. The basic concept behind these regulations is the official validation of embryo transfer teams. This approval is a very important method of veterinary regulations, as they are usually based more on animals coordinated in protocols and their products. However, in this case, the safety of embryo transfer procedures is based on the correct ethics and technique of the head of the embryo transfer team [62].
The criteria used by national veterinary services for the approval of embryo transfer teams are based on the Terrestrial Code. For example, in Chapter 4.7. it is stated that: “the embryo collection team is a group of competent technicians-operators, including at least one veterinarian, who carry out the production, collection, processing and storage of embryos”.
It is recommended that the following conditions be met:
the team should be approved by the competent national authority;
the team should be supervised and ordered by a team veterinarian;
the team veterinarian should be responsible for all operations of his team, including:
checking the health of the embryo donor
implementation of appropriate disease control measures when handling or operating donors
disinfection and hygiene procedures;
team staff should be regularly trained appropriately in disease control techniques and principles. High standards of hygiene must be practiced to prevent the spread of infection;
the embryo collection team should have adequate equipment for:
induction and collection of embryos
processing and treatment of embryos in a permanent laboratory or in a mobile laboratory
conservation and storage of embryos;
These facilities do not necessarily have to be in the same location;
the embryo collection team must draw up a correct record of its sessions, which should be kept for verification by the Veterinary Authority for a period of at least two years after the export/movement of the embryos;
the embryo collection team should be periodically inspected and checked at least once a year by an official veterinarian, to ensure compliance with the procedures and sessions for the proper collection, processing and storage of embryos.
7. Conclusion
Embryotransfer in vivo, (IVD by MOET) is a procedure that can significantly increase the amount of offspring a genetically significant ruminants can carry. This it is a multistep procedure involving superovulation, synchronization of donor and recipient, insemination of donor, collection, isolation, evaluation, genetic testing freezing and transfer of embryo. This is the shortest path to genetic progress on economic efficiency in large and small ruminant farms.
Conflict of interest
The authors declare no conflict of interest.
\n',keywords:"embryotransfer (ET), ruminant, cow, estrus, IVEP, MOET, ART",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/78116.pdf",chapterXML:"https://mts.intechopen.com/source/xml/78116.xml",downloadPdfUrl:"/chapter/pdf-download/78116",previewPdfUrl:"/chapter/pdf-preview/78116",totalDownloads:256,totalViews:0,totalCrossrefCites:1,dateSubmitted:"July 17th 2021",dateReviewed:"July 28th 2021",datePrePublished:"August 17th 2021",datePublished:null,dateFinished:"August 16th 2021",readingETA:"0",abstract:"Assisted reproductive technologies (ART) have made tremendous advances, in last years. Artificial insemination is a method for achieving slow genetic progress in populations of animals. Many large and small ruminants are bred by AI, and more than a half million embryos are transferred every year around the world. Most of the ruminants sires used for artificial insemination were derived from embryo transfer. Improvements of reproductive biotechnologies of controlling the estrous cycle and ovulation have resulted in more effective programs for AI, superovulation of donor, and the management of ET. In the ruminants, ET procedure is a timely alternative that can allow good conception rates to be obtained constant in a year. There have been great advances of this biotechnique with on aimed to intensify the genetic progress between generations of farm. The gains is possible with the development of advanced reproductive biotechnique. The best current strategy in applying biotechnology to farmers is to use AI with sexed semen, so farmers will enjoy and benefit. The use of ET together with cryopreserved sexed embryos has a very specific potential for donor replacement and genetic improvement of the herd. In this chapter, procedures of the MOET protocol were described step by step.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/78116",risUrl:"/chapter/ris/78116",signatures:"Ștefan Gregore Ciornei",book:{id:"10664",type:"book",title:"Animal Reproduction",subtitle:null,fullTitle:"Animal Reproduction",slug:null,publishedDate:null,bookSignature:"Prof. Yusuf Bozkurt and Prof. Mustafa Numan Bucak",coverURL:"https://cdn.intechopen.com/books/images_new/10664.jpg",licenceType:"CC BY 3.0",editedByType:null,isbn:"978-1-83969-515-5",printIsbn:"978-1-83969-514-8",pdfIsbn:"978-1-83969-516-2",isAvailableForWebshopOrdering:!0,editors:[{id:"90846",title:"Prof.",name:"Yusuf",middleName:null,surname:"Bozkurt",slug:"yusuf-bozkurt",fullName:"Yusuf Bozkurt"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:null,sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_2",title:"2. Advantages of embryo transfer (ET)",level:"1"},{id:"sec_3",title:"3. Sexual cycle physiology",level:"1"},{id:"sec_3_2",title:"3.1 Estrus synchronization, superovulation",level:"2"},{id:"sec_5",title:"4. Embryo transfer procedures",level:"1"},{id:"sec_5_2",title:"4.1 Donor selection",level:"2"},{id:"sec_6_2",title:"4.2 Superovulation",level:"2"},{id:"sec_7_2",title:"4.3 Artificial insemination/mounting",level:"2"},{id:"sec_8_2",title:"4.4 Collection of embryos and classification",level:"2"},{id:"sec_8_3",title:"4.4.1 Codes for embryo quality",level:"3"},{id:"sec_11",title:"5. Embryonic mortality",level:"1"},{id:"sec_12",title:"6. Embryo production biosecurity and contamination risks",level:"1"},{id:"sec_13",title:"7. Conclusion",level:"1"},{id:"sec_17",title:"Conflict of interest",level:"1"}],chapterReferences:[{id:"B1",body:'Fonseca-Zangirolamo A, Kemmer Souza A, Zamparone Bergamo L, Applications of embryo transfer biotechnology in dairy cattle. SPERMOVA. 2018; 8(1): 29 – 32, DOI. 10.18548/aspe/0006.03.'},{id:"B2",body:'Colazo MG, Mapletoft RJ. A review of current timed-AI (TAI) programs for beef and dairy cattle. Canadian Veterinary Journal. 2014; 55: 772-780.'},{id:"B3",body:'Chebel RC, Demetrio DGB, Metzger J. Factors affecting success of embryo collection and transfer in large dairy herds. Theriogenology. 2008; 69(1): 98-106'},{id:"B4",body:'Vasconcelos JLM, Jardina DTG, Sá Filho OG, Aragon FL, Veras MB. Comparison of progesterone-based protocols with gonadotropin releasing hormone or estradiol benzoate for timed artificial insemination or embryo transfer in lactating dairy cows. Theriogenology. 2011; 75(6): 1153-1160.'},{id:"B5",body:'Ciornei Şt.G., Drugociu D., Rosca P, Ghinet Liliana, 2018, Polyovulatory response and in vivo embryo production at the omanian indigenous buffalo, out of breeding season in ne of Romania Lucrări Științifice, vol. 61 -IV, Medicină Veterinară, Ed. “Ion Ionescu de la Brad”, Iași 286 - 291.'},{id:"B6",body:'Mircu C., coord. coordinator. Treatise on assisted reproduction (in Romanian), Ed agroprint, Timisoara, 2020, chapter 3, pages 139-168, ISBN 978-606-785-136-6'},{id:"B7",body:'Teepker G, Keller DS. Selection of sires originating from a nucleus breeding unit for use in a commercial dairy population. Can J Anim Sci 1989; 69:595-604.'},{id:"B8",body:'Seidel GE Jr. Brief introduction to whole genome selection in cattle using single nucleotide polymorphisms. Reprod Fertil Dev 2010; 22:138-144.'},{id:"B9",body:'Christensen LG. Use of embryo transfer in future cattle breeding schemes. Theriogenology 1991; 35:141-156.'},{id:"B10",body:'Pall Emoke and Cenariu M., Reproductive biotechnology, Biotehnici în reproducție (Romanian) Ed. Colorama, Cluj-Napoca, Romania, 2020.'},{id:"B11",body:'Adams GP. Control of ovarian follicular wave dynamics in cattle; Implications for synchronization and superstimulation. Theriogenology, 1994; 4:19-24.'},{id:"B12",body:'Bó GA, Adams GP, Pierson RA, et al. Exogenous control of follicular wave emergence in cattle. Theriogenology, 1995; 43:31-40.,'},{id:"B13",body:'Bó GA, Baruselli PS, Moreno D, et al. The control of follicular wave development for self-appointed embryo transfer programs in cattle. Theriogenology 2002; 57, 53-72'},{id:"B14",body:'Bó Gabriel A, Mapletoft Reuben J. Historical perspectives and recent research on superovulation in cattle. Theriogenology 2014; 81:38-48'},{id:"B15",body:'Sartori R, Bastos MR, Wiltbank MC. Factors affecting fertilisation and early embryo quality in single-and superovulated dairy cattle. Reprod Fertil Dev 2009; 22:151-158.'},{id:"B16",body:'Hasler JF. The current status and future of commercial embryo transfer in cattle. Anim Reprod Sci 2003; 79:245-264.'},{id:"B17",body:'Manisha Sethi, Nadeem Shah, Pratyush Kumar, Neeraj Bhatia, Anju Rohilla and Tushar Kumar Mohanty . Chapter - 5 Embryo Transfer Technology: Non-Surgical Collection, Evaluation and Transfer of the Embryo in Cow, pg 83-105'},{id:"B18",body:'Selk G. Embryo transfer in cattle, 2002. (https://hdl.handle.net/11244/49938)'},{id:"B19",body:'Gengler N, Druet T. Impact of biotechnology on animal breeding and genetic progress. In Biotechnology in Animal Husbandry. Springer, Dordrecht, 2001, 33-45.'},{id:"B20",body:'Mapletoft RJ. Embryo transfer in the cow: General procedures. Revue Scientifique et Technique de l\'OIE (France), 1985'},{id:"B21",body:'Seidel GE, Seidel SM. Training manual for embryo transfer in cattle. FAO animal production and health paper, 1991, 77.'},{id:"B22",body:'Dresser BL. Cryobiology, embryo transfer, and artificial insemination in ex situ animal conservation programs. Biodiversity, 1988, 296.'},{id:"B23",body:'Gordon I. Reproductive technologies in farm animals. 2nd Edition. University College Dublin. Ireland, 2017.'},{id:"B24",body:'Pickles AC. Current therapy in theriogenology, 2nd edn, edited by David A. Morrow, WB Saunders Co, Philadelphia, 1987.'},{id:"B25",body:'Mapletoft RJ, Hasler JF. Assisted reproductive technologies in cattle: a review. Revue scientifique et technique (International Office of Epizootics). 2005; 24(1):393-403'},{id:"B26",body:'Senger PL. Pathways to pregnancy and parturition. 2nd ed. Current Conceptions, Inc., Washington State University, Pullman, WA, USA, 2003'},{id:"B27",body:'Hanzen Ch., and Lourtie PVD, Follicular development in the cow. I. Morphological aspects and dynamic growth pattern, July 2000, Annales de Médecine Vétérinaire 144(4):223-+'},{id:"B28",body:'Wiltbank MC. How information of hormonal regulation of the ovary has improved understanding of timed breeding programs. In: Proceedings of the Ann Meet Soc Theriogenol 1997; 83-97.'},{id:"B29",body:'Adams GP. Control of ovarian follicular wave dynamics in mature and prepubertal cattle for synchronization and superstimulation. In: Proceeding of the XX Congress of the World Association of Buiatrics; Sydney, Australia 1998; 595-605.'},{id:"B30",body:'Mapletoft RJ, Martinez MF, Colazo MG, et al. The use of controlled internal drug release devices for the regulation of bovine reproduction. J Anim Sci 2003; 81(E. Suppl. 2):E28-E36.'},{id:"B31",body:'Ciornei S., Drugociu D., Rosca P., Ciornei Liliana. Poliovulatory response and embryo recovery rate in beef sheep in Romania, as apossibility for genetic development - A case report. Anim Reprod. 2020; 17(3), OPU/IVF and ET p.10'},{id:"B32",body:'BEAM S.W., BUTLER W.R. Energy balance, metabolic hormones and early postpartum follicular development in dairy cows fed prilled lipid. J.Dairy Sci., 1998, 81, 121-131.'},{id:"B33",body:'Verma-Kumar S, Srinivas SV, Muraly P, et al. 2004, Cloning of buffalo (Bubalus bubalis) prostaglandin F2a receptor: changes in its expression and concentration in the buffalo cow corpus luteum. Reprod; 127:705-715.'},{id:"B34",body:'Ciornei Ş. G, Drugociu D., Rosca P, Ghinet Liliana (Ciornei) 2020 - Caesarean section in uterine torsion at Buffalo (RIB) – a case study, Rev Rom Med Vet (2020) 30 | 2: 53-56, ISSN: 1220-3173; E-ISSN: 2457-7618'},{id:"B35",body:'Mapletoft Reuben J, Bó GA. Superovulation in Cattle. In: Bovine Reproduction 1st Edition, RM Hopper, (Editor), Wiley-Blackwell Publishing, Ames, Iowa. Chapter 75; 2015; 696-702'},{id:"B36",body:'Curtis JL. Cattle embryo transfer procedure. An instruction manual for the rancher, dairyman, artificial insemination technician, animal scientist, and veterinarian. Academic Press, Inc., 1991'},{id:"B37",body:'Hafez ESE, Hafez B. Fertilization and cleavage. Reproduction in farm animals, 2000, 110-125.'},{id:"B38",body:'Valadão L, Da Silva HM, Da Silva FM. Bovine Embryonic Development to Implantation. In Embryology-Theory and Practice. Intech Open, 2018.'},{id:"B39",body:'Duran PG, Center PC. Technical Aspects of the Recovery, Handling and Transfer of Embryos. ASPAC Food & Fertilizer Technology Center, 2000.'},{id:"B40",body:'Manual of the International Embryo Transfer Society. Fourth Edition. DA Stringfellow and MD Givens (eds). Savoy, IL: IETS, 2010. Available from the International Embryo Transfer Society website.'},{id:"B41",body:'Bó Gabriel A, Mapletoft Reuben J. Evaluation and classification of bovine embryos. Anim Reprod 2013; 10:344-348'},{id:"B42",body:'Phillips PE, Jahnke MM. Embryo transfer (techniques, donors and recipients). Veterinary Clinics: Food Animal Practice. 2016; 32(2):365-385'},{id:"B43",body:'Youngquist Robert S., and Walter R. Current Therapy in Large Animal Theriogenology, 2nd Edition, Saunders. 2007'},{id:"B44",body:'Tervit HR, Cooper MW, Goold PG, Haszard GM. Non-surgical embryo transfer in cattle. Theriogenology. 1980; 13(1):63-71'},{id:"B45",body:'Hasler JF. In vitro production of cattle embryos: problems with pregnancies and parturition. Human Reproduction. 2000; 15(5):47-58.'},{id:"B46",body:'Néstor Isaías Tovío Luna, Arturo Duica Amaya and Henry Alberto Grajales Lombana. Chapter 10,Antiluteolytic Strategy for Bovine Embryo Transfer Programmes, in: http://dx.doi.org/10.5772/60425'},{id:"B47",body:'Santos J, Thatcher W, Chebel R et al. The effect of embryonic death rates in cattle on the efficacy of estrus synchronization programs. Animal Reproduction Science. 2004; 83: pp. 513-535'},{id:"B48",body:'Grajales H, Tovío N, Duica A. Fundamentos de fisiología reproductiva en la hembra bovina.1 ed. Bogota, D.C: Editorial Universidad Nacional de Colombia; 2011'},{id:"B49",body:'Binelli M, Thatcher W, Mattos R, Baruselli P. Antiluteolytic Strategies to Improve Fertility in Cattle. Theriogenology. 2001; 56: pp. 1451-1463.'},{id:"B50",body:'Silke V, Diskin M, Kenny D et al. Extent, pattern and factors associated with late embryonic loss in dairy cows. Animal Reproduction Science. 2002; 71: pp. 1-12.'},{id:"B51",body:'Tovío N, Duica A, Grajales H. Desarrollo embrionario y estrategias antiluteoliticas hormonales en programas de transplante de embriones bovinos. Revista MVZ Córdoba. 2008; 13 (1): pp. 1240-1251'},{id:"B52",body:'Silva R, Rodriguez C, Marques M et al. Efeito do eCG e do GnRH na taxa de prenhez de vacas Nelore lactantes inseminadas em tempo fixo. Acta Scientiae Veterinariae. 2004; 32 (Suplemento): pp. 221.'},{id:"B53",body:'Duica A, Tovío N, Grajales H. Factores que afectan la eficiencia reproductiva de la hembra receptora en un programa de transplante de embriones bovinos. Journal de Medicina Veterinaria Universidad de la Salle. 2007 Jul; 14: pp. 107-124'},{id:"B54",body:'Baruselli P, Bó G, Reis E et al. Introducción de la IATF en el manejo reproductivo de rebaños de ganado de engorde en Brasil. Congreso Internacional de Reproducción Bovina Intervet. 2005; Bogotá, Colombia.'},{id:"B55",body:'Bielanski, A, and C Dubuc. 1995. In vitro fertilization of ova from cows experimentally infected with a non-cytopathic strain of bovine viral diarrhea virus. Anim. Reprod. Sci. 38:215-221. https://doi.org/10.1016/0378-4320(95)98107-F.'},{id:"B56",body:'Menchaca, A. 2020. Procedures for small ruminant embryo technology. Part 1: In vivo embryo production. Manual of the International Embryo Transfer Society. 5th ed. IETS, Champaign, IL.'},{id:"B57",body:'Thibier, M 2011. Embryo transfer: A comparative biosecurity advantage in international movements of germplasm. Rev. Sci. Tech. 30:177-188.'},{id:"B58",body:'Cottell, E, J McMorrow, B Lennon, M Fawsy, M Cafferkey, and R Harrison. 1996. Microbial contamination in an in vitro fertilization-embryo transfer system. Fertil. Steril. 66:776-780. https://doi.org/10.1016/S0015-0282(16)58635-X.'},{id:"B59",body:'Joanna Maria Gonçalves Souza-Fabjan1 and Alejo Menchaca, In: 5th Edition IETS Manual,Volume 1: 13-Supplement. Small ruminant specificity for disease control or transmission via embryos).'},{id:"B60",body:'Stringfellow D.A. (2009). – Recommendations for the sanitary handling of in vivo derived embryos. In Manual of the International Embryo Transfer Society: a procedural guide and general information for the use of embryo transfer technology emphasizing sanitary procedures, 4th Ed. IETS, Savoy, Illinois, 65-68.'},{id:"B61",body:'World Organisation for Animal Health (OIE) (2010). – Terrestrial Animal Health Code. OIE, Paris. Available at: www.oie.int/en/international-standard-setting/terrestrialcode/ access-online/ (accessed in Jun 2021).'},{id:"B62",body:'Thibier M. (2006). – Biosecurity and the various types of embryos transferred. Reprod. domestic Anim., 41, 260-267.'}],footnotes:[],contributors:[{corresp:"yes",contributorFullName:"Ștefan Gregore Ciornei",address:"stefan_ciornei@yahoo.com",affiliation:'
Department Clinics, Biotechnology of Reproduction, Faculty of Veterinary Medicine, Iasi University of Life Sciences (IULS), Iasi, Romania
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Cartilage struts under the anterior half of the alae of a pinched nose tip were popularised and the cartilage of the auricular concha became the donor site of choice for nasal procedures. Recently, some surgeons pointed to its potential role in aesthetic cases and added some technical refinements. These grafts are used for open and closed rhinoplasties. They usually consist of a rod of septal or auricular cartilage that we lay as reinforcement inside a pocket along the alar margin. Indications include the following: congenital or traumatic asymmetry, dynamic alar collapse, alar flare, primary retraction or notching, secondary (surgical or traumatic) retraction and malposition of the lateral cartilages (upwards or downwards). Harvesting and implanting techniques as well as the possible drawbacks are discussed.",book:{id:"8616",slug:"contemporary-rhinoplasty",title:"Contemporary Rhinoplasty",fullTitle:"Contemporary Rhinoplasty"},signatures:"Pedro S. Arquero, Wenceslao M. 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Rollin Daniel stated that rhinoplasty is the most difficult of all cosmetic operations for three reasons: (a) nasal anatomy is highly variable, (b) the procedure must correct form and function and (c) patients’ expectations. With this in mind, a study was planned on learning curve in septorhinoplasty based on a surgeon questionnaire. The aims of the study were to extract the idea of learning curve from different surgeons across experience about septorhioplasty, to calculate certain parameters of the learning curve in rhinoplasty and to prepare a roadmap for an early rhinoplasty surgeon. The conclusion derived from the study was the concept of the learning curve in rhinoplasty should not be generalised as certain factors, for example, minimum number to achieve proficiency has a wide range. It is thought that each type of rhinoplasty should be dealt with separately and learning curve calculated accordingly. A roadmap for a novice surgeon is hereby charted out.",book:{id:"8616",slug:"contemporary-rhinoplasty",title:"Contemporary Rhinoplasty",fullTitle:"Contemporary Rhinoplasty"},signatures:"Aditya Yeolekar",authors:[{id:"266750",title:"Associate Prof.",name:"Aditya",middleName:null,surname:"Yeolekar",slug:"aditya-yeolekar",fullName:"Aditya Yeolekar"}]},{id:"64668",title:"Cleft Lip and Palate Patient Rhinoplasty",slug:"cleft-lip-and-palate-patient-rhinoplasty",totalDownloads:1787,totalCrossrefCites:0,totalDimensionsCites:2,abstract:"Cleft lip and palate patients represent one of the most difficult groups of patients for septorhinoplasty. Prior surgery at younger ages resulting in severe scar tissue is a major obstacle in most cleft rhinoplasties along with substantial asymmetries especially in the unilateral cleft patient. Replacement of missing and asymmetric cartilages and even bone is a key component for rhinoplasty in the cleft patient. Use of very sturdy cartilage typically from rib is almost always required to adequately resist the fibrotic soft tissues in the noses. Plus, rib cartilage can be carved into ideal septal extension and batten grafts that are required.",book:{id:"8616",slug:"contemporary-rhinoplasty",title:"Contemporary Rhinoplasty",fullTitle:"Contemporary Rhinoplasty"},signatures:"Angelo Cuzalina and Ahmed Tamim",authors:[{id:"270232",title:"Dr.",name:"Angelo",middleName:null,surname:"Cuzalina",slug:"angelo-cuzalina",fullName:"Angelo Cuzalina"},{id:"278087",title:"Dr.",name:"Ahmed",middleName:null,surname:"Tamim",slug:"ahmed-tamim",fullName:"Ahmed Tamim"}]},{id:"64721",title:"Saddle Nose: A Systematic Approach",slug:"saddle-nose-a-systematic-approach",totalDownloads:1046,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"The saddle nose deformity is always associated to cartilaginous or bone defects. It could have congenital, traumatic, infectious or iatrogenic origin. Its correction consists not only in a camouflage, but also it is important to reconstruct the missing structure. In this chapter, we will discuss about all aspect of the saddle nose and we will propose a different therapeutical approach (septum, concha or costal grafts) in relation to the severity of the defects (with a personal classification). The classification is also based on the presence or absence of the nasal septum, which is a fundamental aspect that we must take into account when approaching nasal reconstruction. We will discuss the technical aspect of the rib graft harvesting and its use to reconstruct the nasal structure.",book:{id:"8616",slug:"contemporary-rhinoplasty",title:"Contemporary Rhinoplasty",fullTitle:"Contemporary Rhinoplasty"},signatures:"Marianetti Tito Matteo",authors:[{id:"177687",title:"Dr.",name:"Tito",middleName:null,surname:"Marianetti",slug:"tito-marianetti",fullName:"Tito Marianetti"}]},{id:"36343",title:"A Review of Stimulating Strategies for Cochlear Implants",slug:"stimulating-strategies-for-cochlear-implants",totalDownloads:4448,totalCrossrefCites:1,totalDimensionsCites:0,abstract:null,book:{id:"652",slug:"cochlear-implant-research-updates",title:"Cochlear Implant Research Updates",fullTitle:"Cochlear Implant Research Updates"},signatures:"Charles T. M. Choi and Yi-Hsuan Lee",authors:[{id:"107160",title:"Prof.",name:"Charles T. M.",middleName:null,surname:"Choi",slug:"charles-t.-m.-choi",fullName:"Charles T. M. 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Dr. Summers is a systems ecologist and began his career at the EPA in 1989 and has worked in various programs and capacities. This includes leading the National Coastal Assessment in collaboration with the Office of Water which culminated in the award-winning National Coastal Condition Report series (four volumes between 2001 and 2012), and which integrates water quality, sediment quality, habitat, and biological data to assess the ecosystem condition of the United States estuaries. He was acting National Program Director for Ecology for the EPA between 2004 and 2006. He has authored approximately 150 peer-reviewed journal articles, book chapters, and reports and has received many awards for technical accomplishments from the EPA and from outside of the agency. Dr. Summers holds a BA in Zoology and Psychology, an MA in Ecology, and Ph.D. in Systems Ecology/Biology.",institutionString:null,institution:{name:"Environmental Protection Agency",institutionURL:null,country:{name:"United States of America"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:4,paginationItems:[{id:"38",title:"Pollution",coverUrl:"https://cdn.intechopen.com/series_topics/covers/38.jpg",isOpenForSubmission:!0,editor:{id:"110740",title:"Dr.",name:"Ismail M.M.",middleName:null,surname:"Rahman",slug:"ismail-m.m.-rahman",fullName:"Ismail M.M. Rahman",profilePictureURL:"https://mts.intechopen.com/storage/users/110740/images/2319_n.jpg",biography:"Ismail Md. Mofizur Rahman (Ismail M. M. Rahman) assumed his current responsibilities as an Associate Professor at the Institute of Environmental Radioactivity, Fukushima University, Japan, in Oct 2015. He also has an honorary appointment to serve as a Collaborative Professor at Kanazawa University, Japan, from Mar 2015 to the present. \nFormerly, Dr. Rahman was a faculty member of the University of Chittagong, Bangladesh, affiliated with the Department of Chemistry (Oct 2002 to Mar 2012) and the Department of Applied Chemistry and Chemical Engineering (Mar 2012 to Sep 2015). Dr. Rahman was also adjunctly attached with Kanazawa University, Japan (Visiting Research Professor, Dec 2014 to Mar 2015; JSPS Postdoctoral Research Fellow, Apr 2012 to Mar 2014), and Tokyo Institute of Technology, Japan (TokyoTech-UNESCO Research Fellow, Oct 2004–Sep 2005). \nHe received his Ph.D. degree in Environmental Analytical Chemistry from Kanazawa University, Japan (2011). He also achieved a Diploma in Environment from the Tokyo Institute of Technology, Japan (2005). 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Saxena",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRET3QAO/Profile_Picture_2022-05-10T10:10:26.jpeg",institutionString:"King George's Medical University",institution:{name:"King George's Medical University",institutionURL:null,country:{name:"India"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null}]},subseriesFiltersForPublishedBooks:[{group:"subseries",caption:"Bacterial Infectious Diseases",value:3,count:2},{group:"subseries",caption:"Parasitic Infectious Diseases",value:5,count:4},{group:"subseries",caption:"Viral Infectious Diseases",value:6,count:7}],publicationYearFilters:[{group:"publicationYear",caption:"2022",value:2022,count:2},{group:"publicationYear",caption:"2021",value:2021,count:4},{group:"publicationYear",caption:"2020",value:2020,count:3},{group:"publicationYear",caption:"2019",value:2019,count:3},{group:"publicationYear",caption:"2018",value:2018,count:1}],authors:{paginationCount:301,paginationItems:[{id:"116250",title:"Dr.",name:"Nima",middleName:null,surname:"Rezaei",slug:"nima-rezaei",fullName:"Nima Rezaei",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/116250/images/system/116250.jpg",biography:"Professor Nima Rezaei obtained an MD from Tehran University of Medical Sciences, Iran. He also obtained an MSc in Molecular and Genetic Medicine, and a Ph.D. in Clinical Immunology and Human Genetics from the University of Sheffield, UK. He also completed a short-term fellowship in Pediatric Clinical Immunology and Bone Marrow Transplantation at Newcastle General Hospital, England. Dr. Rezaei is a Full Professor of Immunology and Vice Dean of International Affairs and Research, at the School of Medicine, Tehran University of Medical Sciences, and the co-founder and head of the Research Center for Immunodeficiencies. He is also the founding president of the Universal Scientific Education and Research Network (USERN). Dr. Rezaei has directed more than 100 research projects and has designed and participated in several international collaborative projects. He is an editor, editorial assistant, or editorial board member of more than forty international journals. He has edited more than 50 international books, presented more than 500 lectures/posters in congresses/meetings, and published more than 1,100 scientific papers in international journals.",institutionString:"Tehran University of Medical Sciences",institution:{name:"Tehran University of Medical Sciences",country:{name:"Iran"}}},{id:"180733",title:"Dr.",name:"Jean",middleName:null,surname:"Engohang-Ndong",slug:"jean-engohang-ndong",fullName:"Jean Engohang-Ndong",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/180733/images/system/180733.png",biography:"Dr. Jean Engohang-Ndong was born and raised in Gabon. After obtaining his Associate Degree of Science at the University of Science and Technology of Masuku, Gabon, he continued his education in France where he obtained his BS, MS, and Ph.D. in Medical Microbiology. He worked as a post-doctoral fellow at the Public Health Research Institute (PHRI), Newark, NJ for four years before accepting a three-year faculty position at Brigham Young University-Hawaii. Dr. Engohang-Ndong is a tenured faculty member with the academic rank of Full Professor at Kent State University, Ohio, where he teaches a wide range of biological science courses and pursues his research in medical and environmental microbiology. Recently, he expanded his research interest to epidemiology and biostatistics of chronic diseases in Gabon.",institutionString:"Kent State University",institution:{name:"Kent State University",country:{name:"United States of America"}}},{id:"188773",title:"Prof.",name:"Emmanuel",middleName:null,surname:"Drouet",slug:"emmanuel-drouet",fullName:"Emmanuel Drouet",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/188773/images/system/188773.png",biography:"Emmanuel Drouet, PharmD, is a Professor of Virology at the Faculty of Pharmacy, the University Grenoble-Alpes, France. As a head scientist at the Institute of Structural Biology in Grenoble, Dr. Drouet’s research investigates persisting viruses in humans (RNA and DNA viruses) and the balance with our host immune system. He focuses on these viruses’ effects on humans (both their impact on pathology and their symbiotic relationships in humans). He has an excellent track record in the herpesvirus field, and his group is engaged in clinical research in the field of Epstein-Barr virus diseases. He is the editor of the online Encyclopedia of Environment and he coordinates the Universal Health Coverage education program for the BioHealth Computing Schools of the European Institute of Science.",institutionString:null,institution:{name:"Grenoble Alpes University",country:{name:"France"}}},{id:"131400",title:"Prof.",name:"Alfonso J.",middleName:null,surname:"Rodriguez-Morales",slug:"alfonso-j.-rodriguez-morales",fullName:"Alfonso J. Rodriguez-Morales",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/131400/images/system/131400.png",biography:"Dr. Rodriguez-Morales is an expert in tropical and emerging diseases, particularly zoonotic and vector-borne diseases (especially arboviral diseases). He is the president of the Travel Medicine Committee of the Pan-American Infectious Diseases Association (API), as well as the president of the Colombian Association of Infectious Diseases (ACIN). He is a member of the Committee on Tropical Medicine, Zoonoses, and Travel Medicine of ACIN. He is a vice-president of the Latin American Society for Travel Medicine (SLAMVI) and a Member of the Council of the International Society for Infectious Diseases (ISID). Since 2014, he has been recognized as a Senior Researcher, at the Ministry of Science of Colombia. He is a professor at the Faculty of Medicine of the Fundacion Universitaria Autonoma de las Americas, in Pereira, Risaralda, Colombia. He is an External Professor, Master in Research on Tropical Medicine and International Health, Universitat de Barcelona, Spain. He is also a professor at the Master in Clinical Epidemiology and Biostatistics, Universidad Científica del Sur, Lima, Peru. In 2021 he has been awarded the “Raul Isturiz Award” Medal of the API. Also, in 2021, he was awarded with the “Jose Felix Patiño” Asclepius Staff Medal of the Colombian Medical College, due to his scientific contributions to COVID-19 during the pandemic. He is currently the Editor in Chief of the journal Travel Medicine and Infectious Diseases. His Scopus H index is 47 (Google Scholar H index, 68).",institutionString:"Institución Universitaria Visión de las Américas, Colombia",institution:null},{id:"332819",title:"Dr.",name:"Chukwudi Michael",middleName:"Michael",surname:"Egbuche",slug:"chukwudi-michael-egbuche",fullName:"Chukwudi Michael Egbuche",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/332819/images/14624_n.jpg",biography:"I an Dr. Chukwudi Michael Egbuche. I am a Senior Lecturer in the Department of Parasitology and Entomology, Nnamdi Azikiwe University, Awka.",institutionString:null,institution:{name:"Nnamdi Azikiwe University",country:{name:"Nigeria"}}},{id:"284232",title:"Mr.",name:"Nikunj",middleName:"U",surname:"Tandel",slug:"nikunj-tandel",fullName:"Nikunj Tandel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/284232/images/8275_n.jpg",biography:'Mr. Nikunj Tandel has completed his Master\'s degree in Biotechnology from VIT University, India in the year of 2012. He is having 8 years of research experience especially in the field of malaria epidemiology, immunology, and nanoparticle-based drug delivery system against the infectious diseases, autoimmune disorders and cancer. He has worked for the NIH funded-International Center of Excellence in Malaria Research project "Center for the study of complex malaria in India (CSCMi)" in collaboration with New York University. The preliminary objectives of the study are to understand and develop the evidence-based tools and interventions for the control and prevention of malaria in different sites of the INDIA. Alongside, with the help of next-generation genomics study, the team has studied the antimalarial drug resistance in India. Further, he has extended his research in the development of Humanized mice for the study of liver-stage malaria and identification of molecular marker(s) for the Artemisinin resistance. At present, his research focuses on understanding the role of B cells in the activation of CD8+ T cells in malaria. Received the CSIR-SRF (Senior Research Fellow) award-2018, FIMSA (Federation of Immunological Societies of Asia-Oceania) Travel Bursary award to attend the IUIS-IIS-FIMSA Immunology course-2019',institutionString:"Nirma University",institution:{name:"Nirma University",country:{name:"India"}}},{id:"334383",title:"Ph.D.",name:"Simone",middleName:"Ulrich",surname:"Ulrich Picoli",slug:"simone-ulrich-picoli",fullName:"Simone Ulrich Picoli",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/334383/images/15919_n.jpg",biography:"Graduated in Pharmacy from Universidade Luterana do Brasil (1999), Master in Agricultural and Environmental Microbiology from Federal University of Rio Grande do Sul (2002), Specialization in Clinical Microbiology from Universidade de São Paulo, USP (2007) and PhD in Sciences in Gastroenterology and Hepatology (2012). She is currently an Adjunct Professor at Feevale University in Medicine and Biomedicine courses and a permanent professor of the Academic Master\\'s Degree in Virology. She has experience in the field of Microbiology, with an emphasis on Bacteriology, working mainly on the following topics: bacteriophages, bacterial resistance, clinical microbiology and food microbiology.",institutionString:null,institution:{name:"Universidade Feevale",country:{name:"Brazil"}}},{id:"229220",title:"Dr.",name:"Amjad",middleName:"Islam",surname:"Aqib",slug:"amjad-aqib",fullName:"Amjad Aqib",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/229220/images/system/229220.png",biography:"Dr. Amjad Islam Aqib obtained a DVM and MSc (Hons) from University of Agriculture Faisalabad (UAF), Pakistan, and a PhD from the University of Veterinary and Animal Sciences Lahore, Pakistan. Dr. Aqib joined the Department of Clinical Medicine and Surgery at UAF for one year as an assistant professor where he developed a research laboratory designated for pathogenic bacteria. Since 2018, he has been Assistant Professor/Officer in-charge, Department of Medicine, Manager Research Operations and Development-ORIC, and President One Health Club at Cholistan University of Veterinary and Animal Sciences, Bahawalpur, Pakistan. He has nearly 100 publications to his credit. His research interests include epidemiological patterns and molecular analysis of antimicrobial resistance and modulation and vaccine development against animal pathogens of public health concern.",institutionString:"Cholistan University of Veterinary and Animal Sciences",institution:null},{id:"62900",title:"Prof.",name:"Fethi",middleName:null,surname:"Derbel",slug:"fethi-derbel",fullName:"Fethi Derbel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/62900/images/system/62900.jpeg",biography:"Professor Fethi Derbel was born in 1960 in Tunisia. He received his medical degree from the Sousse Faculty of Medicine at Sousse, University of Sousse, Tunisia. He completed his surgical residency in General Surgery at the University Hospital Farhat Hached of Sousse and was a member of the Unit of Liver Transplantation in the University of Rennes, France. He then worked in the Department of Surgery at the Sahloul University Hospital in Sousse. Professor Derbel is presently working at the Clinique les Oliviers, Sousse, Tunisia. His hospital activities are mostly concerned with laparoscopic, colorectal, pancreatic, hepatobiliary, and gastric surgery. He is also very interested in hernia surgery and performs ventral hernia repairs and inguinal hernia repairs. He has been a member of the GREPA and Tunisian Hernia Society (THS). During his residency, he managed patients suffering from diabetic foot, and he was very interested in this pathology. For this reason, he decided to coordinate a book project dealing with the diabetic foot. Professor Derbel has published many articles in journals and collaborates intensively with IntechOpen Access Publisher as an editor.",institutionString:"Clinique les Oliviers",institution:null},{id:"300144",title:"Dr.",name:"Meriem",middleName:null,surname:"Braiki",slug:"meriem-braiki",fullName:"Meriem Braiki",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/300144/images/system/300144.jpg",biography:"Dr. Meriem Braiki is a specialist in pediatric surgeon from Tunisia. She was born in 1985. She received her medical degree from the University of Medicine at Sousse, Tunisia. She achieved her surgical residency training periods in Pediatric Surgery departments at University Hospitals in Monastir, Tunis and France.\r\nShe is currently working at the Pediatric surgery department, Sidi Bouzid Hospital, Tunisia. Her hospital activities are mostly concerned with laparoscopic, parietal, urological and digestive surgery. She has published several articles in diffrent journals.",institutionString:"Sidi Bouzid Regional Hospital",institution:null},{id:"229481",title:"Dr.",name:"Erika M.",middleName:"Martins",surname:"de Carvalho",slug:"erika-m.-de-carvalho",fullName:"Erika M. de Carvalho",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/229481/images/6397_n.jpg",biography:null,institutionString:null,institution:{name:"Oswaldo Cruz Foundation",country:{name:"Brazil"}}},{id:"186537",title:"Prof.",name:"Tonay",middleName:null,surname:"Inceboz",slug:"tonay-inceboz",fullName:"Tonay Inceboz",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/186537/images/system/186537.jfif",biography:"I was graduated from Ege University of Medical Faculty (Turkey) in 1988 and completed his Med. PhD degree in Medical Parasitology at the same university. I became an Associate Professor in 2008 and Professor in 2014. I am currently working as a Professor at the Department of Medical Parasitology at Dokuz Eylul University, Izmir, Turkey.\n\nI have given many lectures, presentations in different academic meetings. I have more than 60 articles in peer-reviewed journals, 18 book chapters, 1 book editorship.\n\nMy research interests are Echinococcus granulosus, Echinococcus multilocularis (diagnosis, life cycle, in vitro and in vivo cultivation), and Trichomonas vaginalis (diagnosis, PCR, and in vitro cultivation).",institutionString:"Dokuz Eylül University",institution:{name:"Dokuz Eylül University",country:{name:"Turkey"}}},{id:"71812",title:"Prof.",name:"Hanem Fathy",middleName:"Fathy",surname:"Khater",slug:"hanem-fathy-khater",fullName:"Hanem Fathy Khater",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/71812/images/1167_n.jpg",biography:"Prof. Khater is a Professor of Parasitology at Benha University, Egypt. She studied for her doctoral degree, at the Department of Entomology, College of Agriculture, Food and Natural Resources, University of Missouri, Columbia, USA. She has completed her Ph.D. degrees in Parasitology in Egypt, from where she got the award for “the best scientific Ph.D. dissertation”. She worked at the School of Biological Sciences, Bristol, England, the UK in controlling insects of medical and veterinary importance as a grant from Newton Mosharafa, the British Council. Her research is focused on searching of pesticides against mosquitoes, house flies, lice, green bottle fly, camel nasal botfly, soft and hard ticks, mites, and the diamondback moth as well as control of several parasites using safe and natural materials to avoid drug resistances and environmental contamination.",institutionString:null,institution:{name:"Banha University",country:{name:"Egypt"}}},{id:"99780",title:"Prof.",name:"Omolade",middleName:"Olayinka",surname:"Okwa",slug:"omolade-okwa",fullName:"Omolade Okwa",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/99780/images/system/99780.jpg",biography:"Omolade Olayinka Okwa is presently a Professor of Parasitology at Lagos State University, Nigeria. She has a PhD in Parasitology (1997), an MSc in Cellular Parasitology (1992), and a BSc (Hons) Zoology (1990) all from the University of Ibadan, Nigeria. She teaches parasitology at the undergraduate and postgraduate levels. She was a recipient of a Commonwealth fellowship supported by British Council tenable at the Centre for Entomology and Parasitology (CAEP), Keele University, United Kingdom between 2004 and 2005. She was awarded an Honorary Visiting Research Fellow at the same university from 2005 to 2007. \nShe has been an external examiner to the Department of Veterinary Microbiology and Parasitology, University of Ibadan, MSc programme between 2010 and 2012. She is a member of the Nigerian Society of Experimental Biology (NISEB), Parasitology and Public Health Society of Nigeria (PPSN), Science Association of Nigeria (SAN), Zoological Society of Nigeria (ZSN), and is Vice Chairperson of the Organisation of Women in Science (OWSG), LASU chapter. She served as Head of Department of Zoology and Environmental Biology, Lagos State University from 2007 to 2010 and 2014 to 2016. She is a reviewer for several local and international journals such as Unilag Journal of Science, Libyan Journal of Medicine, Journal of Medicine and Medical Sciences, and Annual Research and Review in Science. \nShe has authored 45 scientific research publications in local and international journals, 8 scientific reviews, 4 books, and 3 book chapters, which includes the books “Malaria Parasites” and “Malaria” which are IntechOpen access publications.",institutionString:"Lagos State University",institution:{name:"Lagos State University",country:{name:"Nigeria"}}},{id:"273100",title:"Dr.",name:"Vijay",middleName:null,surname:"Gayam",slug:"vijay-gayam",fullName:"Vijay Gayam",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/273100/images/system/273100.jpeg",biography:"Dr. Vijay Bhaskar Reddy Gayam is currently practicing as an internist at Interfaith Medical Center in Brooklyn, New York, USA. He is also a Clinical Assistant Professor at the SUNY Downstate University Hospital and Adjunct Professor of Medicine at the American University of Antigua. He is a holder of an M.B.B.S. degree bestowed to him by Osmania Medical College and received his M.D. at Interfaith Medical Center. His career goals thus far have heavily focused on direct patient care, medical education, and clinical research. He currently serves in two leadership capacities; Assistant Program Director of Medicine at Interfaith Medical Center and as a Councilor for the American\r\nFederation for Medical Research. As a true academician and researcher, he has more than 50 papers indexed in international peer-reviewed journals. He has also presented numerous papers in multiple national and international scientific conferences. His areas of research interest include general internal medicine, gastroenterology and hepatology. He serves as an editor, editorial board member and reviewer for multiple international journals. His research on Hepatitis C has been very successful and has led to multiple research awards, including the 'Equity in Prevention and Treatment Award” from the New York Department of Health Viral Hepatitis Symposium (2018) and the 'Presidential Poster Award” awarded to him by the American College of Gastroenterology (2018). He was also awarded 'Outstanding Clinician in General Medicine” by Venus International Foundation for his extensive research expertise and services, perform over and above the standard expected in the advancement of healthcare, patient safety and quality of care.",institutionString:"Interfaith Medical Center",institution:{name:"Interfaith Medical Center",country:{name:"United States of America"}}},{id:"93517",title:"Dr.",name:"Clement",middleName:"Adebajo",surname:"Meseko",slug:"clement-meseko",fullName:"Clement Meseko",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/93517/images/system/93517.jpg",biography:"Dr. Clement Meseko obtained DVM and PhD degree in Veterinary Medicine and Virology respectively. He has worked for over 20 years in both private and public sectors including the academia, contributing to knowledge and control of infectious disease. Through the application of epidemiological skill, classical and molecular virological skills, he investigates viruses of economic and public health importance for the mitigation of the negative impact on people, animal and the environment in the context of Onehealth. \r\nDr. Meseko’s field experience on animal and zoonotic diseases and pathogen dynamics at the human-animal interface over the years shaped his carrier in research and scientific inquiries. He has been part of the investigation of Highly Pathogenic Avian Influenza incursions in sub Saharan Africa and monitors swine Influenza (Pandemic influenza Virus) agro-ecology and potential for interspecies transmission. He has authored and reviewed a number of journal articles and book chapters.",institutionString:"National Veterinary Research Institute",institution:{name:"National Veterinary Research Institute",country:{name:"Nigeria"}}},{id:"158026",title:"Prof.",name:"Shailendra K.",middleName:null,surname:"Saxena",slug:"shailendra-k.-saxena",fullName:"Shailendra K. Saxena",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRET3QAO/Profile_Picture_2022-05-10T10:10:26.jpeg",biography:"Professor Dr. Shailendra K. Saxena is a vice dean and professor at King George's Medical University, Lucknow, India. His research interests involve understanding the molecular mechanisms of host defense during human viral infections and developing new predictive, preventive, and therapeutic strategies for them using Japanese encephalitis virus (JEV), HIV, and emerging viruses as a model via stem cell and cell culture technologies. His research work has been published in various high-impact factor journals (Science, PNAS, Nature Medicine) with a high number of citations. He has received many awards and honors in India and abroad including various Young Scientist Awards, BBSRC India Partnering Award, and Dr. JC Bose National Award of Department of Biotechnology, Min. of Science and Technology, Govt. of India. Dr. Saxena is a fellow of various international societies/academies including the Royal College of Pathologists, United Kingdom; Royal Society of Medicine, London; Royal Society of Biology, United Kingdom; Royal Society of Chemistry, London; and Academy of Translational Medicine Professionals, Austria. He was named a Global Leader in Science by The Scientist. He is also an international opinion leader/expert in vaccination for Japanese encephalitis by IPIC (UK).",institutionString:"King George's Medical University",institution:{name:"King George's Medical University",country:{name:"India"}}},{id:"94928",title:"Dr.",name:"Takuo",middleName:null,surname:"Mizukami",slug:"takuo-mizukami",fullName:"Takuo Mizukami",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/94928/images/6402_n.jpg",biography:null,institutionString:null,institution:{name:"National Institute of Infectious Diseases",country:{name:"Japan"}}},{id:"233433",title:"Dr.",name:"Yulia",middleName:null,surname:"Desheva",slug:"yulia-desheva",fullName:"Yulia Desheva",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/233433/images/system/233433.png",biography:"Dr. Yulia Desheva is a leading researcher at the Institute of Experimental Medicine, St. Petersburg, Russia. She is a professor in the Stomatology Faculty, St. Petersburg State University. She has expertise in the development and evaluation of a wide range of live mucosal vaccines against influenza and bacterial complications. Her research interests include immunity against influenza and COVID-19 and the development of immunization schemes for high-risk individuals.",institutionString:'Federal State Budgetary Scientific Institution "Institute of Experimental Medicine"',institution:null},{id:"238958",title:"Mr.",name:"Atamjit",middleName:null,surname:"Singh",slug:"atamjit-singh",fullName:"Atamjit Singh",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/238958/images/6575_n.jpg",biography:null,institutionString:null,institution:null},{id:"333753",title:"Dr.",name:"Rais",middleName:null,surname:"Ahmed",slug:"rais-ahmed",fullName:"Rais Ahmed",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/333753/images/20168_n.jpg",biography:null,institutionString:null,institution:null},{id:"252058",title:"M.Sc.",name:"Juan",middleName:null,surname:"Sulca",slug:"juan-sulca",fullName:"Juan Sulca",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/252058/images/12834_n.jpg",biography:null,institutionString:null,institution:null},{id:"191392",title:"Dr.",name:"Marimuthu",middleName:null,surname:"Govindarajan",slug:"marimuthu-govindarajan",fullName:"Marimuthu Govindarajan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/191392/images/5828_n.jpg",biography:"Dr. M. Govindarajan completed his BSc degree in Zoology at Government Arts College (Autonomous), Kumbakonam, and MSc, MPhil, and PhD degrees at Annamalai University, Annamalai Nagar, Tamil Nadu, India. He is serving as an assistant professor at the Department of Zoology, Annamalai University. His research interests include isolation, identification, and characterization of biologically active molecules from plants and microbes. He has identified more than 20 pure compounds with high mosquitocidal activity and also conducted high-quality research on photochemistry and nanosynthesis. He has published more than 150 studies in journals with impact factor and 2 books in Lambert Academic Publishing, Germany. He serves as an editorial board member in various national and international scientific journals.",institutionString:null,institution:null},{id:"274660",title:"Dr.",name:"Damodar",middleName:null,surname:"Paudel",slug:"damodar-paudel",fullName:"Damodar Paudel",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/274660/images/8176_n.jpg",biography:"I am DrDamodar Paudel,currently working as consultant Physician in Nepal police Hospital.",institutionString:null,institution:null},{id:"241562",title:"Dr.",name:"Melvin",middleName:null,surname:"Sanicas",slug:"melvin-sanicas",fullName:"Melvin Sanicas",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/241562/images/6699_n.jpg",biography:null,institutionString:null,institution:null},{id:"337446",title:"Dr.",name:"Maria",middleName:null,surname:"Zavala-Colon",slug:"maria-zavala-colon",fullName:"Maria Zavala-Colon",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Puerto Rico, Medical Sciences Campus",country:{name:"United States of America"}}},{id:"338856",title:"Mrs.",name:"Nur Alvira",middleName:null,surname:"Pascawati",slug:"nur-alvira-pascawati",fullName:"Nur Alvira Pascawati",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"Universitas Respati Yogyakarta",country:{name:"Indonesia"}}},{id:"441116",title:"Dr.",name:"Jovanka M.",middleName:null,surname:"Voyich",slug:"jovanka-m.-voyich",fullName:"Jovanka M. 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