Rice fungicides registered in India (Source: Central Insecticide Board, Govt. of India)
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IntechOpen Book Series will also publish a program of research-driven Thematic Edited Volumes that focus on specific areas and allow for a more in-depth overview of a particular subject.
\\n\\nIntechOpen Book Series will be launching regularly to offer our authors and editors exciting opportunities to publish their research Open Access. We will begin by relaunching some of our existing Book Series in this innovative book format, and will expand in 2022 into rapidly growing research fields that are driving and advancing society.
\\n\\nLaunching 2021
\\n\\nArtificial Intelligence, ISSN 2633-1403
\\n\\nVeterinary Medicine and Science, ISSN 2632-0517
\\n\\nBiochemistry, ISSN 2632-0983
\\n\\nBiomedical Engineering, ISSN 2631-5343
\\n\\nInfectious Diseases, ISSN 2631-6188
\\n\\nPhysiology (Coming Soon)
\\n\\nDentistry (Coming Soon)
\\n\\nWe invite you to explore our IntechOpen Book Series, find the right publishing program for you and reach your desired audience in record time.
\\n\\nNote: Edited in October 2021
\\n"}]',published:!0,mainMedia:{caption:"",originalUrl:"/media/original/132"}},components:[{type:"htmlEditorComponent",content:'With the desire to make book publishing more relevant for the digital age and offer innovative Open Access publishing options, we are thrilled to announce the launch of our new publishing format: IntechOpen Book Series.
\n\nDesigned to cover fast-moving research fields in rapidly expanding areas, our Book Series feature a Topic structure allowing us to present the most relevant sub-disciplines. Book Series are headed by Series Editors, and a team of Topic Editors supported by international Editorial Board members. Topics are always open for submissions, with an Annual Volume published each calendar year.
\n\nAfter a robust peer-review process, accepted works are published quickly, thanks to Online First, ensuring research is made available to the scientific community without delay.
\n\nOur innovative Book Series format brings you:
\n\nIntechOpen Book Series will also publish a program of research-driven Thematic Edited Volumes that focus on specific areas and allow for a more in-depth overview of a particular subject.
\n\nIntechOpen Book Series will be launching regularly to offer our authors and editors exciting opportunities to publish their research Open Access. We will begin by relaunching some of our existing Book Series in this innovative book format, and will expand in 2022 into rapidly growing research fields that are driving and advancing society.
\n\nLaunching 2021
\n\nArtificial Intelligence, ISSN 2633-1403
\n\nVeterinary Medicine and Science, ISSN 2632-0517
\n\nBiochemistry, ISSN 2632-0983
\n\nBiomedical Engineering, ISSN 2631-5343
\n\nInfectious Diseases, ISSN 2631-6188
\n\nPhysiology (Coming Soon)
\n\nDentistry (Coming Soon)
\n\nWe invite you to explore our IntechOpen Book Series, find the right publishing program for you and reach your desired audience in record time.
\n\nNote: Edited in October 2021
\n'}],latestNews:[{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"}]},book:{item:{type:"book",id:"1362",leadTitle:null,fullTitle:"Numerical Simulations of Physical and Engineering Processes",title:"Numerical Simulations of Physical and Engineering Processes",subtitle:null,reviewType:"peer-reviewed",abstract:"Numerical Simulations of Physical and Engineering Process is an edited book divided into two parts. Part I devoted to Physical Processes contains 14 chapters, whereas Part II titled Engineering Processes has 13 contributions.\nThe book handles the recent research devoted to numerical simulations of physical and engineering systems. It can be treated as a bridge linking various numerical approaches of two closely inter-related branches of science, i.e. physics and engineering. Since the numerical simulations play a key role in both theoretical and application oriented research, professional reference books are highly needed by pure research scientists, applied mathematicians, engineers as well post-graduate students. In other words, it is expected that the book will serve as an effective tool in training the mentioned groups of researchers and beyond.",isbn:null,printIsbn:"978-953-307-620-1",pdfIsbn:"978-953-51-4427-4",doi:"10.5772/1828",price:159,priceEur:175,priceUsd:205,slug:"numerical-simulations-of-physical-and-engineering-processes",numberOfPages:614,isOpenForSubmission:!1,isInWos:1,isInBkci:!0,hash:"5cd4c772ac313082f094190ade16e150",bookSignature:"Jan Awrejcewicz",publishedDate:"September 26th 2011",coverURL:"https://cdn.intechopen.com/books/images_new/1362.jpg",numberOfDownloads:98956,numberOfWosCitations:244,numberOfCrossrefCitations:183,numberOfCrossrefCitationsByBook:8,numberOfDimensionsCitations:261,numberOfDimensionsCitationsByBook:11,hasAltmetrics:0,numberOfTotalCitations:688,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"November 24th 2010",dateEndSecondStepPublish:"December 22nd 2010",dateEndThirdStepPublish:"April 28th 2011",dateEndFourthStepPublish:"May 28th 2011",dateEndFifthStepPublish:"July 27th 2011",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6,7,8",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"68338",title:"Prof.",name:"Jan",middleName:null,surname:"Awrejcewicz",slug:"jan-awrejcewicz",fullName:"Jan Awrejcewicz",profilePictureURL:"https://mts.intechopen.com/storage/users/68338/images/system/68338.jpeg",biography:"Full Professor, Head of the Department of Automation, Biomechanics and Mechatronics of Lodz University of Technology (Poland). Multiple doctor honoris causa, recipient of the Humboldt Award, member of the Polish Academy of Sciences. Author/co-author of over 780 journal and conference papers and 50 monographs. Editor of 28 books and 36 journal special issues. Principal investigator of numerous research grants. Member of Editorial Boards of 88 Journals (17 with IF). Organizer and Head of 14 International Conferences 'Dynamical Systems – Theory and Applications” (Lodz, 1992-2017) and 3 International Conferences 'Mechatronics: Ideas for Industrial Applications' (Warsaw, 2012; Lodz, 2014; Gdansk, 2015). 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by",editors:[{id:"50017",title:"Prof.",name:"Sylvie",surname:"Manguin",slug:"sylvie-manguin",fullName:"Sylvie Manguin"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}}]},chapter:{item:{type:"chapter",id:"44741",title:"Impact of Fungicides on Rice Production in India",doi:"10.5772/51009",slug:"impact-of-fungicides-on-rice-production-in-india",body:'Rice is the most economically important staple food crop in India, China, East-Asia, South East Asia, Africa and Latin America catering to nutritional needs of 70% of the population in these countries (FAO, 1995). In several developed countries such as North America and European Union (EU) also, rice consumption has increased due to food diversification and immigration (Faure and Mazaud, 1996). Worldwide, rice is grown on 161 million hectares, with an annual production of about 678.7 million tons of paddy (FAO, 2009). About 90% of the world’s rice is grown and produced (143 million ha of area with a production of 612 million tons of paddy) in Asia (FAO, 2009). Rice provides 30–75% of the total calories to more than 3 billion Asians (Khush, 2004; von Braun and Bos, 2004). To meet the global rice demand, it is estimated that about 114 million tons of additional milled rice needs to be produced by 2035, which is equivalent to an overall increase of 26% in the next 25 years. The possibility of expanding the area under rice in the near future is limited. Therefore, this extra rice production needed has to come from a productivity gain (Kumar and Ladha, 2011). Maximum yields per unit area of land can be achieved and sustained only if along with high yielding crop varieties there is also a provision for protection of the crop against its enemies (Srivastava et al., 2010). Amongst the various biotic factors affecting rice production and productivity, rice diseases are one of the most important ones. The annual losses due to rice diseases are estimated to be 10-15% on an average basis worldwide. Therefore, judicious management of rice diseases can result in improved productivity and additional grain harvested. Rice diseases are caused by wide variety of pathogen including fungus, bacteria, virus and nematodes (Ling, 1980). In the pre-war period, diseases of rice were practically unimportant in Tropical Asia where ancient varieties were traditionally grown on soils of low fertility (Areygunawardena, 1968). However, with the increasing demand for world rice supplies and advent of green revolution resulting in use of improved varieties, high fertilization, irrigation and intensive cultural practices have resulted in great increase in the occurrence and severity of diseases infesting rice in several countries (Teng, 1990). The major rice diseases that often cause great economic losses are rice blast (
The various methods used for managing rice disease includes, use of resistant varieties, cultural practices, biological and chemical control. All these methods have varied degrees of success in managing rice diseases. The most important control tactics used worldwide includes use of resistant varieties and chemical control. Breeding for disease resistant varieties has been long used for managing the rice diseases and is one of the most economical methods which contributed immensely to world’s rice productivity (Mew, 1991; Bonman,
Rice blast and brown spot were the major diseases noticed during pre independent India and before introduction of high yielding varieties. After introduction of HYV, along with them, BLB, tungro and sheath blight have become major diseases. Recently diseases like sheath rot, false smut, stem rot and grain discolouration which were minor and occurring sporadically are emerging and causing considerable yield loss. This is primarily due to climate change, crop intensification and changes in practice. Out of the total yield loss due to diseases in rice, 35% is by blast, 25% by sheath blight, 20% by BLB, 10% by tungro and remaining 10% by other diseases.
The market share of fungicide used on rice in India during 2010-11 is Rs 380 crores, of which blast and sheath blight fungicides alone constitute 280 crores and the share of fungicides used against brown spot, BLB, grain discoloration, stem rot and false smut is 100 crores.
Fungicides prevent rice diseases which can result in severe damage to the crop in terms of both quality and quantity. Globally 8.4 % of fungicides market share is for rice (Collins, 2007). Synthesizing and characterizing a new molecule to be used as fungicide involves several steps. Initially the new lead molecule is tested in-vitro for its efficacy against the target pathogen and then it is characterized under field condition to ascertain its efficacy against the target disease and to finalize the most effective dose/rate that can be used for the control of the target disease. Several fungicides belonging to different groups have been synthesized and evaluated for use in rice ecosystem. More than 30 fungicides have been registered for use in rice (Table 1) and several new molecules are under testing. The rice fungicides can be broadly classified in two categories.
Rice fungicides registered in India (Source: Central Insecticide Board, Govt. of India)
These fungicides have narrow to moderate spectrum of control and are highly specific. These are applied on the seed surface before sowing. The seed is dressed with either a dry formulation or wet treated with a slurry or liquid formulation. Low cost earthen pots can be used for mixing pesticides with seed or seed can be spread on a polythene sheet and required quantity of chemical can be sprinkled on seed lot and mixed mechanically by the farmers (http://agritech.tnau.ac.in/seed_certification/seed_treatment_Insecticides%20&%20Fungicides. html). The major advantage is that it provides high level of control at low dose and with low residue. In the greenhouse study, tricyclazole at 0.2g/kg of seed effectively controlled leaf blast upto 21 days after planting and resulted in 8.2 μg/g tricylazole in the leaves at that time according to GLC assay (Froyd et al., 1976). Anwar and Bhat (2005) evaluated few fungicides
Metalaxyl 28.35% | 0.75 - 1.5 fl. oz. per 100 lbs. of seed. | For |
Trifloxystrobin 22% | 0.32 - 0.64 fl. oz./cwt | For |
Mefenoxam 33.3% | Apply 0.0425 to 0.085 oz. per 100 lbs. of seed for | For |
Thiram 42% | 1.5 fl oz/bu | For seed decay, damping off, and seedling blights caused by Pythium and Rhizoctonia |
Mancozeb 50% | 4 oz. per 100 lbs. of seed. | For control of damping-off, seed rots, and seedling blights caused by Drechslera and Pythium. Drill box treatment. |
Mancozeb 37% | 3.4 to 6.7 oz. per 100 lbs. of seed. | For control of soil borne and seed borne fungi causing seed rot and reduced seedling vigor. Apply before, during, or after soaking in water. |
Carboxin 10% + Thiram 10% | 5 to 6.8 fl. oz. per 100 lbs. of seed. | For control of various seed and seedling diseases. The higher rate is recommended for control of |
Carboxin 5.7% + Thiram 5.7% | 9 to 12 fl. oz. per 100 lbs. of seed. | To control various seed and seedling diseases, especially effective against |
Carbendazim 50 WP | 4 g/kg of seeds | To control blast, brown spot and udbatta disease of rice |
Tricyclazole 75 WP | 3 g/kg of seeds | To control rice blast disease |
Rice Seed treatment fungicides:
These fungicides are applied as spray using power or back pack sprayers directed towards the plant foliage. These fungicides may be contact (surface acting) or systemic (translocated inside plant) in action. They are highly effective in controlling foliar rice diseases with good residuality. Based on their chemical class and mode of action, rice fungicides can be further grouped into following categories;
Some of the new fungicides as per the AgroProjects and Agranova database are mentioned below:
Fungicide timing is a very critical component in disease control and management. The disease needs to be present in order to justify any fungicide application and its effectiveness. This is not the case in every field and the variety grown greatly influences the disease impact, even if present. The geographical and sometimes micro-climatic conditions of the cropping area also greatly influence the incidence and intensity of any plant disease. Thus scouting and sound decision-making are worthwhile, compared to “blanket” preventative fungicide applications (Cartwright et al, 2004). Application of right chemical (Hexaconazole 5SC) at a right time (maximum tillering stage) was very important in control of sheath blight (Swamy et al., 2009). While, Pencycuron 250 EC was very effective under Punjab and West Bengal rice growing conditions against sheath blight when sprayed at maximum tillering stage(Lore et al., 2005; Biswas, 2002).
Several studies have revealed that many new fungicides have been identified for managing sheath blight in rice which differs in their efficacy from place to place and time of application. Dithane M-45 (Das and Mishra, 1990), Carbendazim and Mancozeb (Thangaswamy and Ranagswamy, 1989; Roy and Saikia, 1976) Iprodione (Izadyar and Baradaram, 1989) Triazole (Suryadi
The major consideration for the design of fungicide use strategies is the threat of fungicide resistance. Fungicide resistance can occur when a
Considerable efforts have been made by industry to conduct research in the areas of mode of action, resistance risk, field monitoring for baseline sensitivity and sensitivity variations in treated fields. Numerous pathogens that attack the highly maintained grasses, such as those found on golf courses, frequently require weekly spray applications through out the summer. This has led to resistance development in
The first report of practical resistance to fungicides in rice crop was recorded in 1971 on blast pathogen (
Bennett (2012), reported a suspected mutation of the
Kim et al., 2010, reported on Bakanae disease pathogen
Studying the case histories of resistance development by considering the genetic, biochemical and epidemiological process which explains the complex interaction and changing factors determining the rate and severity of development of fungicide resistance
Acquired fungicide resistance is a major threat to plant disease control by chemicals. Pathogens respond to fungicides by evolving resistance against them. Fungicides which provide maximum control also create maximum selection pressure on the pathogen to acquire resistance. Resistance results from one or more changes at genetic level of pathogen population due to mutations occurring in nature. Fungicide itself does not induce resistance. It selects resistant propagules already present at low frequency in natural population of pathogen.
Fungicides may be categorised based on resistance development by the pathogen as low resistant risk fungicides –dithiocarbamate which are protectant fungicides and have multisite action, medium risk fungicedes- SBI’s where mutation of several genes is required and high risk fungicides – benzimidazole and strobulins where resistance is controlled by single gene. Thus, a major consideration for the design of fungicide use strategies is the threat of fungicide resistance. There have been considerable efforts by industry to conduct research in the areas of mode of action, resistance risk and field monitoring.
Blast is the most important fungal disease of rice and occurs in all the rice growing regions of the world. Fungicidal control is largely practised for blast disease in temperate or subtropical rice cultivation, mainly in Japan, China, South Korea, Taiwan and, increasingly, Vietnam. The majority of the fungicides used in blast control are protectants. In early years, copper and mercury compounds were recommended against blast but were found not suitable because of phytotoxicity and mammalian toxicity. Current major products are mainly systemics with a residual activity of at least 15 days, although older organophosphorous products such as edifenphos are still widely used. The modern rice fungicides include isoprothiolane, probenazole, pyroquilon and tricyclazole (Anon., 1992; Filippi and Prabhu, 1997), and are applied as foliar sprays, as granules into water or seed-box treatments (irrigated lowland rice), or as seed dressings for upland rice. In recent years, newer melanin biosynthesis inhibitors such as carpropamid (Motoyama et al., 1999; Thieron et al., 1999) or broad-spectrum fungicides like azoxystrobin (strobilurin)(Lee and Beaty, 1999) have gained favour.
According to Kapoor and Singh (1982) benomyl seed treatment (1:400 w/w) gives protection to seedlings in nursery for 24-25 days. It inhibits spore germination and appressorium formation. Venkata Rao and Muralidharan (1983) found benomyl, carbendazim, MBC, edifenphos (all 0.1%) and 0.25% mancozeb effective against the blast in the order listed, and significantly better than other fungicides. Tewari and Kameshwar Rao (1983) applied carbendazim through mud balls, soil drench and foliar spray at the rate of 0.5 kg a i/ha and found effective control of the disease. Three sprays were given at the tillering stage at 10 day interval and two sprays at the neck emergence stage at 5 days interval. Saikia (1991) has confirmed the same number and timing of sprays of edifenphos, thiophanate methyl and carbendazim at 0.1% effectively reducing the leaf blast by 71.3-81% and neck blast by 60-65% with corresponding increase in yield. Studies on efficacy of fungicides indicated that tricyclazole and isoprothiolane are highly effective resulting in 87.9 and 83.8% reduction in neck blast and 33.8 and 29.9% increase in grain yield over check, respectively (Sachin and Rana, 2011). Sood and Kapoor (1997) evaluated seven fungicides and found that tricyclozole 75 WP was most effective and reduced the leaf and neck blast by 89.2% and 94.5% respectively. Muhammad Saifulla
Prasanna Kumar et. al. (2011c) evaluated three new QoI fungicides (Kresoxim methyl, Metaminostrobin and Trifloxystrobin) in combinations with other groups for two seasons against against blast and sheath blight of rice. All the QoI group fungicides were very effective in controlling leaf and neck blast and also improved the growth of the plant in terms of height, test weight and yield. Kresoxim methyl 40% + Hexaconazole 8% SC @ 200+40 g ai/ha was effective against leaf blast (5.18% and 11.11%) and neck blast (11.11% and 11.85%) with highest yield of 45.75 and 53.42 q/ha respectively during Kharif 2010 and summer 2011. Similar effectiveness was recorded in Kresoxim methyl 50% @ 200 g ai/ha against leaf blast (5.18% and 11.11%) and neck blast (11.85% and 11.11%) which was found on par with tricyclozole @ 225 g ai/ha. Application of Metaminostrobin 20% SC + hexaconazole 5% SC and Metaminostrobin alone gave higher grain yield 41.26 and 41.23 q/ha respectively and was on par with tricylcozole 75%WP. The combination was effective against leaf blast (21.11 and 18.89%) and neck blast (25.56 and 33.89%) during Kharif 2009 and summer 2010.
Nine combinations of fungicides and insecticides were tested for their efficacy and compatibility on major pests and disease of rice (Prasanna Kumar et. al., 2011a). The combination treatments involving the insecticides and fungicide treatment recorded moderate severity ranged from 12.1 to 18.5%. Combination of tricylcazole 75% WP + Fipronil 5% SC recorded least disease severity and insect infestation (17% neck blast) and highest yield of 5190 kg/ha, followed by isoprothiolane 40% EC + fipronil 5% SC compared to untreated check which recorded highest neck blast incidence(34%).
Similar results regarding the efficacy of various fungicides have been reported by different researchers globally. Varier
Sheath blight is one of the most important rice diseases worldwide and ranks number two position after blast disease. Common fungicides used earlier against sheath blight were copper, organomercury and organo-aresenic compounds (Ou 1985). Carbendazim, benomyl, ediphenfos and kitazin have been reported to be the most effective chemicals recorded by various Indian workers (Premalatha Dath 1990). The fungicidal control of sheath blight in India was attempted by Kannaiyan and Prasad (1976) and Bhaktavatsalam et. al. (1977). The rhizosphere population of the pathogen of rice seedlings was drastically reduced through foliar sprays of the fungicides such as kitazin, edifenphos, benomyl, carboxin and carbendazim. The efficacy of benomyl (Das and Panda, 1984) and carbendazim (Bhaktavatsalam et. al., 1977; Rajan and Alexander, 1988) in the management of sheath blight was studied. Benomyl and captan at 0.2% were highly effective in reducing the seedling infection while soil drenching with edifenphos, kitazin and benomyl during tillering stage was also effective in controlling the disease. Seed treatment with carbendazim, chloroneb, chlorotholonil, carboxin, benomyl and phenyl mercury acetate (PMA) reduced the seed borne infection of the pathogen and improved the seed germination, shoots and root growth, seedling vigour and prolonged the viability of the seeds. Again, 0.2% sprays of benomyl, kitazin, edifenphos and chlorotholonil were highly effective in controlling sheath blight and increased the grain yield in field trials. Roy and Saikia (1976) obtained the best control of sheath blight with carbendazim or by benomyl sprays (0.05%) both in green house and field tests. In field trials with six fungicides, kitazin granule was the most effective in reducing the disease severity, followed by edifenphos (Verma and Menon, 1977) but Mathai and Nair (1977) showed that edifenphos was the best as it increased the yield.
Flutolanil, a new systemic fungicide developed with both protective and curative properties is very effective to control various Rhizoctonia groups of fungi including rice sheath blight (Araki, 1985; Hirooka et. al., 1989). However, sheath blight disease was effectively controlled by 80% at low concentration of 1.6 to 3.2µg/g of plant. Foliar spray, soil drenching and seed treatment have been tried effectively under green house and field studies. Sundravadana et al., 2007, reported that for controlling sheath blight disease, the optimum rate of azoxystrobin was 125 g/ha. Field trials in 2008 and 2009 conducted by Parsons et al., (2009) showed that a newly formulated mixture of azoxystrobin and propiconazole called Quilt Xcel™ was highly effective in controlling sheath blight and protecting rice yield and milling quality.
PrasannaKumar et. al. (2011c) evaluated three new QoI fungicides (Kresoxim methyl, Metaminostrobin and Trifloxystrobin) and combinations with other groups were evaluated for two seasons against blast and sheath blight of rice. All the QoI group fungicides were very effective in controlling sheath blight and also improved the growth of the plant in terms of height, test weight and yield. Kresoxim methyl 40% + Hexaconazole 8% SC @ 200+40 g ai/ha was effective against sheath blight (12.59% and 20.74%) with highest yield of 45.75 and 53.42 q/ha respectively during Kharif 2010 and summer 2011. During summer 2010, application of Metaminostrobin 20% SC+hexaconazole 5% SC and Metaminostrobin alone gave higher grain yield 41.26 and 41.23 q/ha respectively. The combination was effective against sheath blight (25 and 16.11%) during Kharif 2009 and summer 2010. They also found that Trifloxystrobin 50% WG @ 200 g ai/ha recorded higher yield (47.66 q/ha and 50.17 q/ha) in both the seasons (Kharif 2010 and summer 2011). The stand alone formulation of trifloxystrobin 50% WG @ 200 g ai/ha was effective against sheath blight with PDI of 15 and 11.11% during Kharif 2010 and summer 2011 respectively.
PrasannaKumar et. al. (2011b) also reported that application of hexaconazole 75% WG @ 50g ai/ha, tetraconazole 11.6% w/w ME @ 1.0 L/ha and thifluzamide 24% SC @ 110 ai/ha were found highly effective in controlling sheath blight with increased yield when compared to untreated check. Thifluzamide a new fungicide group of carboxynilide was tested for its efficacy against sheath blight in three seasons (PrasannaKumar et. al., 2012). They found that among different concentrations, thifluzamide 24% SC at 110 g ai/ha was effective in reducing the disease severity [12 % (2005), 19.33% (2006) and 21.33 (2009)] when compared to uncontrolled check [47% (2005), 62.33 (2006) and 59.67 (2009). Carboxynilide group fungicide was both preventive and curative in effect without phytotoxicity.
A combination of fungicide and insecticide were evaluated against important diseases and insects in rice during kharif 2007, 2008, 2009 and 2010 (PrasannaKumar et. al., 2011a). They found that during 2009, the ready mix formulation of flubendiamide 3.5% + hexaconazole 5% WG @ 85 g/ha were effective in controlling rice pests to maximum extent. The combination treatment recorded least sheath blight severity of 13.9% with the yield of 4190 kg/ha when compared to the standard check (40.6% and 2409 kg/ha).
Swamy et. al. (2009) reported that new fungicide formulations tricyclozole 400g + propiconazole 125g @ 0.25% and trifloxystrobin 25g + tebuconazole 50g @ 0.04% was on par with the standard checks hexaconazole 5% EC @ 0.2% and validamycin 3L @ 0.25%. Similarly, a new formulation Captan 70% + Hexaconazole 5% WP @ 0.2% was significantly effective in reducing the sheath blight of rice (Kiran Kumar and PrasannaKumar, 2011).
Foliar sprays of fungicides such as validamycin A in Vietnam, Thailand, Korea, Malaysia and Japan and pencycuron in Malaysia have been widely used (IRRI, 1993). First spray is applied between the stage of early internode elongation and the development of 2.5- to 5-cm panicle in the boot, and the second on 80-90% of emerging panicles from 10-14 days later. The best time to apply chemicals was at the jointing stage, during which time the percentage tiller infected was highly correlated with sheath blight at wax ripeness stage: percentage yield loss depended on disease index at wax ripeness (CPC, 2005).
Brown spot is one of the most important rice diseases in India. The disease affects the yield and milling quality of the grain. Sulpha drugs like sulphanilamide and antibiotics like nyastatin and griseofulvin have been used for seed treatment to control brown spot in rice. Spraying with captafol, edifenphos and zineb was also found to be effective (Chakrabarthi et. al. (1975). A new formulation Captan 70% + Hexaconazole 5% WP @ 0.2% was significantly effective in reducing the brown spot of rice (Kiran Kumar and PrasannaKumar, 2011). According to Sunder
Sheath rot of rice occurs in most rice-growing regions of the country. Chemical control of sheath rot has been intensively studied in India. Murty (1986) found that carbendazim, edifenphos and mancozeb (seed treatment and two foliar sprays around the booting stage) reduced sheath rot incidence significantly. Benomyl and copper oxychloride have also been reported to be effective in the field. However, studies by Lewin and Vidhyasekaran (1987) indicated that all fungicides they tested (captafol, carbendazim, carboxin, copper oxychloride, edifenphos, iprobenfos, iprodione, mancozeb, tridemorph, thiophanate-methyl and validamycin) were ineffective. Seed treatment with benlate and panoctine improves germination of sheath rot infected seeds (Alagarsamy and Bhaskaran, 1987). For field control of the disease, hinosan, bavistin, and dithane M-45 proved to be effective. Fungicides like kitazin, benlate, difolatan, miltox, NF-48 and deconil were sprayed @ 0.2% separately on plants twice at 10 days interval during the flowering stage, could control the disease effectively. According to Raina and Singh (1980) and Chinnaswamy et. al. (1981), the most effective fungicide for the control of sheath rot was carbendazim followed by MBC, aureofungin and difolatan.
Effective combinations of fungicides (carbendazim) and insecticides (monocrotophos) to control sheath rot and leaf-folder, Cnaphalocrocis medinalis (Raju et al., 1988) resulted in lower incidence of sheath rot. Combined spraying of monocrotophos with any of the fungicides edifenphos, mancozeb and carbendazim resulted in reduced sheath rot and highest yields. Tridemorph + phosphamidon followed by carbendazim + phosphamidon and tridemorph + neem oil provided the best control and increased yield against sheath rot and rice mealybug, Brevennia rehi, (Lakshmanan, 1992). Two sprays of either thiophanate-methyl (Das et al., 1997), carbendazim (Das et al., 1997; Dodan et al., 1996) or propiconazole (Dodan et al., 1996) were highly effective in controlling rice sheath rot and significantly increased grain yield.
False smut has recently become an important disease of rice in India. Hybrids are more prone for this disease and fungicides have been extensively tested to manage the disease. Singh (1984) identified aureofungin, captan, captafol, fentin hydroxide, furcarbanil, mancozeb, and thiocyanomethylthiobenzothiozole to be effective in inhibiting conidial germination. Seed treatment with fungicides did not check the disease, but spraying the rice crop with carbendazim and copper fungicides at the time of tillering and pre-flowering effectively controlled the disease and yields increased (Anon., 1990). Copper oxychloride was most effective in decreasing disease incidence by 95.5 and 96.1% on the basis of infected tillers and grains, respectively, with a corresponding increase of 7.2% in grain yield (Dodan et al., 1997). Propiconazole or azoxystrobin applied during the boot stage of rice reduced the number of false smut balls in harvested rice grain by 50-75% but yield was not affected. Copper hydroxide fungicides reduced false smut balls in harvested rice by 80% but yield was also often reduced significantly. Barnwal (2011) observed that two sprays of propiconazole (0.1%) was found effective which recorded least false smut disease with number of affected florets panicle (1 of 4.13) with disease severity of 22.2 per cent and disease control over check of 77.6 per cent.
Singh and Singh (1985) have reported that 0.4% Bordeaux mixture or 0.25% COC sprayed thrice at 10 days interval starting when the crop is 60-65 days old gave about 90% reduction in disease incidence.
Stem rot disease is becoming more serious mainly in rain-fed crop. In India under field conditions, foliar application of mercurial fungicides like merculin and agrosan GN were found to be better than non mercurial like captan and thiram (Kang et. al., 1970). Hinosan, kitazin and brassicol were also found effective in reducing the disease with corresponding increase in yield (Jain, 1975).
Bakanae or foot rot disease is not widely distributed in all rice-growing areas of the country. However, the disease more serious in some endemic areas. Seed treatment with organo-mercury compounds is highly effective in controlling
Seed treatment with wettable powder containing ipconazole offered protection against seedborne diseases including bakanae (Tateishi et al., 1998). Seed treatments with benomyl + thiram and thiophanate methyl + thiram were more effective than carboxin + thiram. A drench treatment on seedlings did not provide significant control of the disease (Padasht et al., 1996). Seed soaking for 8 h in a suspension of emisan alone or emisan + streptocycline gave effective control of soil microflora including
Narrow brown spot is generally not considered economically important, and no crop loss information is available on the disease. The commonly used fungicides
From past three decades several fungicedes have been tested at All India Co-ordinated Research Centres in India for their efficacy against important diseases of rice (Table 3).
The ability of the pathogens to adopt to intensive cultivation of cereals and need to feed the increasing population will lead to increase in area of intensive cropping along with increase in consumption of fungicides. The key change in fungicide use have usually been associated with changes in the spectra of pathogens as well as in crop intensities, practices or prices. Shift in pathogen spectra could not be predicted and will continue to occur in the future due to increase in free trade. The R&D expenditures of major Agro companies on fungicides is > 60 % as against 40% for seed and traits. This ensures that new fungicides will continue to be developed to protect the cultivars species with no genetic disease resistance. Efforts are made develop a new strategy for environmentally friendly control of fungal plant diseases with the development of proteomics-based fungicides.
The trend towards a more judicious use of fungicides in combination with disease forecasting done would be continued which will help reduce the risk of adaptation by the target pathogen and at the same time will reduce residues in the environment and on the produce. The efforts of breeding for disease resistance will increase along with tools of genetic engineering. Both genetic resistance and selective fungicides are prone to adaptation by the pathogen. Another new area of research is the use of antimicrobial peptides (AMP) for improving resistance to pathogens using transgenic plants as bio-factories for fungicides or bactericides. The balance between genetic and chemical control will continue and research on both areas will complement each other to assure the availability of effective combinations of host resistance and fungicides for crops to produce higher and quality produce.
Veterinary pharmaceuticals include drugs, medications, and other substances in use to treat or prevent animal diseases for health, growth promotion, and productivity [1]. These drugs can be broadly divided into categories according to the different pathogens or targeted infections. They include antiparasitic drugs, antiinflammatory, reproductive medication, surgical medications, anesthetics, nutritional drugs, and feed additives sometimes used as growth promoters (Table 1). Among commonly used drug in veterinary medicine are antibiotics. These drugs and medicaments can be administered in form of injectable, tablet, bolus, drench, and bath/wash or added to feed and drinking water. There are documented evidence of earlier norms and practices of animal husbandry regarding how shepherd and nomads provide medication for livestock. Some were written document by priests in monasteries, such as the use of garlic (
Antibiotics | Antiparasitic | Antiinflammatory | Anesthetics | Growth promoters |
---|---|---|---|---|
Terramycin | Banminth | Ibuprofen | Phenobarbital | Feed grade antibiotics |
Penicillin | Ivermectin | Meloxicam | Thiamylal | Probiotics |
Streptomycin | Diminazene aceturate | Dexamethasone | Xylazine hydrochloride | Dihydropyridine |
Colistin | Amprolium | Prednisone | Chlorpromazine | Organic acids |
Erythromycin | Piperazine | Prednisolone | Diazepam | Amino acids |
Doxycycline | Albendazole | Aspirin | Thiopental sodium | Racto-amine |
Enrofloxacin | Closantel | Phenylbutazone | Pentobarbital | Sodium-bicarbonate |
Tylosin | Dermatocide | Dimethylsulfoxide | Chloral hydrate | Potassium chloride |
Oxytetracycline | Diazinon | Flunixin | Methohexital | Fatty acids |
Amoxycillin | Nitroxynil | Meglumine | Methoxyflurane | Zytomil |
Gentamycin | Cypermethrin | Cortisone | Halothane | Renature-Z oral powder |
Chloramphenicol | Pyrantel pamoate | Methimazole | Diethyl ether | Vita-Sel-E oral solution |
Ciprofloxacin | Praziquantel | Celecoxib | Isoflurane | Eucament plus oral solution |
Griseofulvin | Mectizan | Colchicine | Enflurane | Chicktonic |
Norfloxacin | Nitroxyl | Cyclooxygenase | Nitrous oxide | Aminogrow WS |
Rifampin | Diclazuril | Pylorus | Glyceryl quiacolate | Electromix WS |
Novidium chloride | Mavacoxib | Succinyl choline | Introvit A+ WS | |
Isomethadone | Tepoxalin | Curare | Introvit-ES-200 WS | |
Furazolidone | Homidium chloride | Piroxicam | Lidocaine | Introvit-K-200 WS |
Some veterinary pharmaceuticals distributed in Nigeria.
Source: survey of commonly use veterinary antimicrobials in Nigeria, courtesy of Dr. Jolly Amoche of National Veterinary Research Institute, Vom.
Globally, there are more livestock in the world than human, with livestock systems occupying about 30% of the planet’s ice-free terrestrial surface area [6]. Most of these animals are kept in free range husbandry systems in under-developed countries where the enterprise supports the livelihood of about 600 million small holders [7]. The livestock sector in developing countries is also evolving in response to rapidly increasing demand for livestock products with changes in the demand for livestock products being driven among other factors by human population growth, urbanization, and increasing income [8, 9].
A major limiting factor in profitable livestock production in developing country is the burden of infectious diseases. These livestock diseases cause great socioeconomic impact, and the burdens are most of the time exasperated by poor biosecurity in both intensive and open production systems. This has made the use of antimicrobials for treatment of diseases indispensable [10]. It is important to emphasize that the reduction in the burden of infectious livestock diseases has been possible due in part to the use of a wide range effective drugs and vaccines and improvements in diagnostic techniques and services [11].
Therapeutic treatments are targeted at animals that are diseased. In food animals, it is usually often more convenient to treat entire groups by administering medication through feed or water, though individual animals may also be treated. For animals like poultry and fish, mass medication is the most feasible means of treatment but with the possibility of drug dispersal into the environment via leaching and agricultural wastewater [12]. Furthermore, certain mass-medication procedures called metaphylaxis, aimed at treatment of sick animals while medicating others in the group that may not be sick but exposed, can also be counterproductive. Other prophylactic antimicrobial treatments are typically used during high-risk periods for infectious diseases even, while the animals may not be infected also described as nonspecific infection prevention [13]. These practices, however plausible, are currently considered as contributing to emergence of antimicrobial resistance due to subtherapeutic exposure to veterinary pharmaceuticals by both infected and noninfected animals, as well as the environment [14].
Antimicrobial resistance has been described as the ability of bacterial, parasites, viruses, and fungi to survive and spread despite treatment with specific and combination therapy that are normally used against them [15]. The World Health Organization also emphasized that resistance happens when microorganisms change when they are exposed to antimicrobial drugs (such as antibiotics, antifungals, antivirals, antimalarials, and antihelmintics). These microorganisms that develop antimicrobial resistance are sometimes referred to as “superbugs”. Antimicrobial resistance may be spontaneous and occur as a natural process, and resistance to antimicrobials dates back as far as when the first generations of antibiotics including penicillin were introduced in 1943/44 by Alexander Fleming [13]. In evolution, selection pressure is bound to cause subpopulation of microorganism with resistance genes to emerge [16]. This selective pressure has been ascribed to appropriate and inappropriate use of antimicrobials but aggravated by (1) intensity of usage, (2) persistence of usage, (3) under usage and subtherapeutic doses that animals are exposed to in prophylactic treatment, and (4) unintended human exposure through antimicrobials in food residues and the environment [10].
The burden of infectious diseases in developing countries and intensive use of antimicrobials to combat this has also been stressed in a study that suggested that up to a third of the global increase (67%) in antibiotic consumption will be in food animals, over the period 2010–2030 and attributable to low-middle income countries [17]. This challenge is in view of the high burden of foodborne infectious and zoonotic diseases especially also in developing countries [18]. Veterinary practices use drugs for mitigating these diseases in animals, including food animals that have to be maintained in health and productivity (meat, egg, and milk). To prevent these drugs from getting into the food chain and being consumed by humans, “withdrawal time,” which is the last time any drug may be administered before egg/milk and meat from such animals are collected and consumed is specified. The withdrawal time for antimicrobials is intended to prevent harmful drug residues in meat, milk, and eggs [19]. These waiting periods need to be observed from the time of treatment to when the animals are slaughtered for food. This is important because food products that contain antimicrobial residues not metabolized leaves residues beyond permissible limits at the end of the withdrawal period may be considered unwholesome for consumption and may contribute to antimicrobial resistance in humans [20].
Veterinary pharmaceuticals, therefore, contribute in many ways to the emergence of antimicrobial resistance either directly in suboptimal usage in animals or indirectly in human who consume subtherapeutic doses in animal products [13]. When resistant organism emerges, it has also been argued that human sources also seed these resistant bacteria to animals and the environment through sewage [21]. A recent study by Marcelino et al. [22] described high levels of antibiotic resistance gene expression among birds living in a wastewater treatment plants. The study observed that birds feeding at a wastewater treatment plant carried greatest resistance gene burden, suggesting that human waste, even after treatment, contributes to the spread of antibiotic resistance genes to the wild. Domestic and wild animals, including rodents, and birds, can acquire these environmental contaminants and pass them on via their excreta to grazing land or feed of food animals, which may in turn end up in human through the food chain [23]. While it is imperative to canvass AMR stewardship through rational and circumspect usage of antimicrobial in animals, it is important to bear in mind that human also present risk to animals. The USFD described the phenomenon of antimicrobial resistance as a very complex and nonvictimless phenomenon, affecting both human and animal health [13].
In the management of infectious and noninfectious diseases of livestock in developing countries, a number of veterinary pharmaceuticals are administered. The choice of drugs is often determined by efficacy, availability, and cost. These factors are explored by manufacturers mostly based in developed countries from where the drugs are exported to developing countries. This distribution chain is also largely driven by business interest such that drug companies sell volumes that are targeted at frequent, intensive usage that may have deleterious effect such as emergence of AMR.
Intensive use of veterinary chemotherapy on the other hand may be justifiable considering that many bacterial, viral, and parasitic diseases like mycoplasmosis, Newcastle disease, avian influenza, anthrax, coccidiosis, brucellosis, foot and mouth disease (FMD), rift valley fever, etc. threatens socioeconomics, instills fear that shock systems, either by suddenly and rapidly killing large number of animals or causes large-scale drop in demand through fear of zoonotic diseases [24, 25]. On the other hand, the growing concern that animals are major sources of human diseases and that around 60% of all animal diseases are zoonotic [26] make treatment of such diseases in animals an essential control measure before it is transmitted to human, and to reduce their capacity to cause epidemics and pandemics.
The livability and economic impacts of animal disease disaster is well documented, for instance, highly pathogenic avian influenza recently killed millions of poultry birds in Nigeria (including other countries in West Africa) and wiped out entire farms [27]. The costs of epidemic African swine fever in Cote d’Ivoire was estimated at $9.2 million; Nipah virus in Malaysia $114 million, while contagious bovine pleuropneumonia in Botswana costs about $300 million [25]. In the absence of preventive measures such as biosecurity and vaccination, the use of antimicrobial especially for nonviral infections is essential for profitable livestock production and to prevent infections that may be transmitted from animals to human as attested to by WHO [28].
The global antimicrobial resistance (AMR) crisis is predicted to kill roughly 10 million people annually by 2050 due to antibiotic-resistant infections, with Africa alone accounting for about 4.15 million [29]. This is estimated to cost the global economy about $100 trillion [30] with about 28.3 million people pushed into extreme poverty [31]. The alarming rate of AMR in developing countries can be attributed to gross misuse of antimicrobials in human and animals [32]. Although resistance can still develop even at an appropriate antimicrobial use, however the situation can be made worse whenever there is excessive and unnecessary usage [33]. The global revolution in livestock and aquaculture is an underlying factor for frequent antimicrobial use and subsequent development of AMR. This is also driven by population increase, urbanization, improving economic conditions, and globalization. Countries like Brazil, China, and India are currently the hotspots for livestock intensification, while Nigeria, Myanmar, Peru, and Vietnam are future spots (Van [17]). In developing countries, most nonhuman-medical use of antimicrobials is almost certainly in livestock and farmed fish production and it is likely that most veterinary use is in intensive production rather than pastoralist or small-holder systems [34]. In Nigeria and other developing countries in sub-Saharan Africa, Asia and Middle East, there is paucity of information on antimicrobial drug resistance in farm animals, although little information exists on residue level [35, 36, 37, 38]. However, there is information on antimicrobial drug resistant microbes isolated from human patients from different parts of Nigeria [39, 40]. Previous report by Adesokan et al. [41] on pattern of antimicrobial usage in livestock production in three states of South-Western Nigeria between the period of 2010 and 2012 showed an increased use of tetracyclines (33.6%) followed by fluoroquinolones (26.5%) and beta-lactams/aminoglycosides (20.4%). Similar trend was also reported in Africa for tetracycline & beta-lactams [42]. However, studies by Idowu et al. [35] showed level of tetracycline residues between the ranges of 0.1–1.0% in chicken eggs.
The process of AMR development is very complex, and all of the factors that contributed to the events are not fully understood. It is clear that genetic change or mutation in microbial DNA may often cause resistance to antimicrobial agents, and this change might also be passed to the offspring or transferred to other related or even unrelated microorganisms [43]. This is known as “selection pressure” where the use of antimicrobial drugs in health care, agriculture, or industrial settings favor the survival of resistant strains (or genes) over susceptible ones, thus leading to a relative increase in resistant bacteria within microbial communities [44]. This is because no matter how effective an antimicrobial is, it rarely kills 100% of the organisms, meaning some may still survive due to genetic change, which can be passed forward. Currently, science has not fully proved the causes of different types of AMR that are causing great public health risks. The widespread use of antimicrobials in food production system especially in food-producing animals is another cause of AMR [45]. The extensive use of antimicrobials in animal production as growth promoters widely exposes the microbes to the drugs, thus enhancing the development of microbial resistance causing health consequences in both animals and humans. However, the scientific evidence of how and to what extent such drug exposure affects human health still remains unclear. It is interesting to note that antimicrobial resistance would not develop in animals if antimicrobial drugs were never used in them [12].
There is danger to public health if resistant organism from animals can also cause disease in human exposed by a way of food consumption or direct contact with food-producing animals, companion animals, or through environmental spread [46]. The threat to public health also exists even if the organisms do not cause disease in human, because they may still be able to transfer the resistant genes from food-producing animals to unrelated human pathogenic bacteria as well as normal commensals [47]. It is then clear that the increase use of antimicrobials in animal production for variety of purposes such as for therapeutic and nontherapeutic use has contributed to increasing AMR in bacteria affecting man and animals [48]. In Africa and other developing countries, studies have suggested a strong correlation between the use of antimicrobials in veterinary practice and the development of AMR [49], because it is shown that a larger proportion of antimicrobial medications have been used in animals than humans mainly for food production purposes [50]. There is presence of high antimicrobial residue in meat and milk meant for human consumption correlating with the detection of multidrug resistance (MDR) bacteria in animals and their products [51] as well as in humans in contact with the animals [52, 53, 54]. This is also because a large proportion of the population in developing countries lives in close proximity with livestock, which enhance the chances of transfer of resistant microorganisms from animals to humans [55, 56]. Similarly, the increasing use of antimicrobials as prophylaxis in aquaculture in developing countries further contributed to the emergence of AMR causing problems in human, animal, and environmental health [57]. The risk to humans further exists especially when similar antimicrobial is used in both animals and humans, or there is presence of cross resistance between antimicrobial used in human and veterinary practice. Using antimicrobials that are also used in human medicine for growth promotion is especially conducive to AMR because exposure of many animals to low dosages makes resistance more likely to emerge [34].
For some antimicrobials, there is development of resistance by bacteria through plasmid-mediated transferable resistance [58]. The minimum inhibitory concentrations (MIC) for a target pathogen might be considerably different from those of commensals, and thus, the resistance gene in commensals may be selected and transferred to humans and then to human pathogens leading to development of AMR [59]. Despite the fact that the exchange of genetic materials and the short generation time of organism contributed to the development of AMR by many bacteria [60], some drugs such as penicillin still retains excellent activity on certain organism (e.g.,
AMR development can often be caused by inhibition of specific antimicrobial pathways such as cell wall synthesis, nucleic acid synthesis, ribosome function, protein synthesis, foliate metabolism, and cell membrane function by the organism [62, 63, 64]. The various steps involved in the production, distribution, prescription, dispensing, and finally consumption of the drug by human patient or its use in animal production often contributed to the emergence of AMR especially when there is imprudent or irresponsible practice along the supply chain [65]. Part of veterinary medical education is to understand how antimicrobials affect microorganisms, and how they can be used responsibly to protect human and animal health [66]. In food production systems, veterinarians are on the frontline when it comes to keeping nation’s food supply safe. Advances in animal health care and management have greatly improved food safety over the years and have reduced the need for antimicrobials in food production systems [67]. Nevertheless, antimicrobials are an important part of the veterinarian’s toolkit, and so veterinarians are aware that they should be used judiciously and in the best interest of animal and public health [66]. More importantly in the development of AMR is the quality of antimicrobials. Though difficult to implement, it has been suggested that incidence of microbial resistance can be reduced if the antimicrobials that are used in human health are not used in veterinary practice [68]. Moreover, the practices of mass treatment of all animals in a group when only one animal is sick (metaphylaxis) as well as the treatment of all animals when they are exposed to conditions that can make them likely to be ill (prophylaxis) will result in an increased antimicrobial use and as such would encourage the development of resistance [69].
Although the development of animal-related AMR is associated with the quality and quantity of antimicrobial usage in veterinary practice, there are other underlining factors that can influence AMR development:
Lack of awareness: in developing countries, there is little or no awareness or concern in the use of antimicrobials as compared to developed nations who recognize AMR as a global challenge. Omulo et al. [70] showed that only 24% of studies in Africa are related to AMR in animals or their products. In East Africa for example, despite the relevance of antibiotic procurement in health budgets, there was still a slow progress in research focusing on AMR of enteric pathogens. There is still lack of awareness among many veterinarians and other food producing personnel on the negative impact to human health as a result of extensive use of antimicrobials in animals [71].
Lack of information: the information is lacking in developing countries concerning the existence and prevalence of AMR in animals and animal products and the negative health consequence as well as the cost of AMR illness in people and animals.
Fake and substandard drugs: there is much concern over counterfeits and substandard drugs in animal health care, but there is insufficient data to understand its importance. Counterfeits and substandard products, which contain active ingredient at a lower level, will increase the chance of developing resistance. There is no comprehensive information on fake/substandard veterinary drugs.
Lack of adequate ‘One Health’ integration between animal and human healthcare: in developing countries, there is poor collaboration in healthcare sectors between human and veterinary practice especially on collection and sharing of data on antimicrobial usage. However, at international level, good collaboration exists in the area of AMR between human and animal world health bodies like WHO, OIE, and FAO.
Lack of substitution to the use of antimicrobials: alternative to the use of antimicrobials is lacking in developing countries unlike the developed nations that had successfully banned the use of antimicrobials as growth promoters and replaced with alternative growth promoters and good practice without having negative impact on the performance of their livestock industries. This could hardly be achieved in developing nations that have propensity to source antimicrobials from the black markets, which may be of poor quality, thus exacerbating the problem and creating a considerable increase in disease, with consequent mortality and morbidity losses [34].
In a bid to ensure measurable containment of AMR, there is a global formal declaration on AMR calling for the development of action plans on AMR by both international and national bodies. The Global Action Plan on Antimicrobial Resistance was approved in May 2015 by the World Health Assembly with the key strategies to increase global AMR awareness as well as developing policies that will attract more investment in the area of new medical interventions [72]. There is also a call to all Member States for establishing National Action Plans for AMR by 2017 of which about 57 countries have formalized such plans so far. The 2016 meeting of the UN General Assembly was another milestone focusing on multidisciplinary solution to the problems of AMR [73]. Moreover, the G20 called for the creation of a Global Research and Development (R&D) Collaboration Hub on AMR in July 2017 that could coordinate international funding efforts [74], and the search for the appropriate individuals to lead that hub began early this year. In line with the global agreement to develop National Action Plan on AMR, Nigeria (with some other developing nations) keyed into this agreement in 2017 through a ‘One Health’ approach [75] and then enrolled into a Global Antimicrobial Resistance Surveillance System (GLASS). The Action Plan addresses five strategic objectives:
improving awareness and understanding of AMR through effective communication, education, and training
strengthening the knowledge and evidence base through surveillance and research
reducing the incidence of infection through effective sanitation, hygiene, and preventive measures
optimizing the use of antibiotics in human and animal health
preparing the economic case for sustainable investment and increasing investment in new medicine, diagnostic tools, vaccines, and other interventions
Several challenges exist regarding AMR containment in developing country like Nigeria; however, the development of this action plan is an important positive step in the right direction as it aims to address the problem at all level of governance and society [75].
Veterinarians play an important role in limiting and minimizing the spread of antimicrobial resistance (AMR). Because vets are often the first point of contact for livestock owners seeking animal medical attention, they can therefore play a part in addressing the problem of AMR [45]. One of the ways to reduce the risk of transfer of AMR from animals to humans is by minimizing the zoonotic transfer of bacteria [76]. This could be achieved by practicing stringent hygiene in the farms and any meat processing plants including the abattoirs and the markets. Thorough and effective cooking of meat product can also reduce the risk of AMR [77]. There is need to strengthen the information resources in developing countries to support health workers, patients, animal owners, and attendants as well as the general public to help in reducing the risk of AMR arising from the use of antimicrobials in animals. This will enable the society to better understand the importance and value of antimicrobials. The excessive and inappropriate use of antimicrobials in veterinary practice should be discouraged. Because antimicrobials are an extremely valuable resource in livestock production, their prudent use in animals will continue to provide benefits to society and will help ensure high standards of welfare for those animals in the care of veterinarians [78]. Since exposure of bacteria to subtherapeutic concentrations of antimicrobials is thought to increase the speed of the selection of resistance, this should always be avoided [14, 15, 79]. Appropriate pharmacokinetic and pharmacodynamic relations for antimicrobials used in animals should be developed [12]. Optimal dosage strategies for eliminating zoonotic organisms in animals will reduce the risk of transferring resistance to humans [80].
According to Delia [34], broad consensus on the management of AMR in human and animal healthcare will require to:
reduce antibiotic use in humans and animals through public health improvement such as hygiene and sanitation, immunization, infection control, as well as good housing and environment.
regulate the sale and use of antibiotics through prescription.
encourage research and development of new antimicrobials.
minimize the level of environmental contamination of antimicrobials emanating from manufacturing process as well as agricultural, hospital, and community use.
develop integrated global policies on the use of antibiotics.
ban the nontherapeutic use of antimicrobials as growth promoters in agriculture.
Currently, there is no adequate information on animal production losses due to disease burden and the extent at which it could be prevented through proper use of antibiotics or their alternatives.
Although in Europe and other developed nations, the use of alternatives to antimicrobials as growth promoters is a success; their applicability in developing countries is not fully understood.
Despite the huge investments in the control of diseases in developing countries through vaccination, vector control, and the use of resistant breeds, evaluation from the angle of reduction in the usage of veterinary drug is lacking. In developing countries, the incidence and composition of substandard and fake drugs as well as their effects on treatment failure and resistance development is not well known. Similarly, the level of resilience of livestock farmers in developing countries to ban or restrict access to antimicrobials is equally not well known. It should be noted that policy and regulation alone is unlikely to improve use of vet drugs and the options for improving the use of vet drugs in agriculture and their effectiveness, feasibility, and affordability are not well understood.
There have been success factors in the improvement of drug use in human health through wide range of intervention studies. Similarly, the World Animal Health Organization (OIE) and other world veterinary bodies also developed frameworks on rational use of vet drugs to which there is a limit veterinarians can make profit from antimicrobial sale for food animal production [71]. This is not the case in developing countries where the sale and use of veterinary antimicrobials is facing challenges for improvement. It was found from series of intervention studies that training remains the most common strategy for improving drug use, but this gave little success unless when combined with other strategies like changing the market condition [1].
Antimicrobial use in human and veterinary practice requires holistic approach in order to improve drug governance. There is need to list the critical or essential drugs in human and veterinary practice with requirement for prescription and guidelines such as banning the use of medically important antibiotics in agricultural practice and off-label use of antimicrobials as well as monitoring antimicrobial use and resistance. Not much success has been recorded in this regard in developing countries especially in livestock production and aquaculture due to little investments. According to OIE, better governance of veterinary antimicrobials comes from empowering veterinarians and limiting prescription to them. Most of the private veterinary service providers in developing countries are not operating at a significant scale and as such are often employed directly by agriculture and agro-allied companies making them to be less independent. The few that are successful are not operating with the guidelines of current OIE policy [81]. The community animal health workers (CAHWs), that have proven to be effective, are very expensive to train and may not be politically acceptable [82]. This is because there is lack of resources to support them by public veterinary services, and the private veterinarians often see them as potential competitors. A study investigated rational drug use by farmers and found that farmers in West Africa were mainly responsible for buying and using antimicrobials, and providing simple information on correct drug use could lead to improved drug usage as well as reduced amount of underdosages, which is an important factor for the development of AMR [83].
As previously mentioned, developed countries banned the use of medically important antibiotics as well as growth promoters in animal production, which has led to better farming practices as well as reduction in AMR of medically important microbes found in farm animals. With this natural experiment, it demonstrated that routine antimicrobial usage is not a precondition for healthy animals as long as there is better hygiene and sanitation with good housing condition, and the use of antibiotics is only limited to clinical condition. The benefit of antimicrobials as growth promoters may sound reasonable only under poor management and hygiene situations [71]. Although the type of intensive livestock production in developing countries makes them rely more on nontherapeutic use of antimicrobials, there are many other promising innovations that could support profitable and productive agriculture with less reliance on antimicrobials use such as:
The use of nonantibiotic growth promoters like enzymes in feed, competitive exclusion products as well as probiotics and prebiotics
The use of other animal health technologies such as vaccines, vector control, disinfectants, phyto-therapy, as well as phage-therapy, which are underutilized in developing countries. The phage products can readily be designed to thwart development of resistance. They have been used as antibacterial agents for nearly 100 years in the former Soviet Union, and they are now undergoing a renaissance in other countries due to the growing AMR problem [33, 84, 85, 86, 87].
The use of robust diagnostic techniques for improved drug selection and identification of AMR pathogens
The management and bio-security innovations like all-in-all-out systems, pathogen-free systems, stocking density reduction, and improved waste management systems.
The use of genetically disease resistant animals as well as avoidance of monocultures of genetically similar animals.
All these intervention strategies will improve animal welfare as well as reducing environmental externalities of animal agriculture. A more radical suggestion is to decrease the amount of consumption of animal source food or shift from intensive to organic animal production.
The safeguarding of antimicrobial agents for future generations is of utmost priority as AMR threatens the very core of modern medicines and the sustainability of an effective, global public health response to the enduring threats from infectious diseases [72]. In many developing countries of the world, gaps exist among health care professionals on the current status of antibiotic resistance in their area due to lack of a systematic surveillance at country, provincial, and district level [88]. There is a paucity of clinical data on antibiotic resistance, and this is particularly the case in resource-poor settings. Tons of antibiotics are used annually in clinical and agricultural settings worldwide. The estimates of the total annual global consumption of antimicrobials in animal production vary considerably due to poor surveillance and data collection in many countries [89]. In 2013, food animals alone consumed over 130,000 tons of antibiotics [90]. It cannot be ignored that two-thirds of the estimated future growth of usage of antimicrobials is estimated to be within the animal production sector, with use in pig and poultry production predicted to double [89]. Nigeria, Pakistan, India, Bangladesh, China, and Egypt are the developing countries with massive consumption of antibiotics [88].
The implementation of rational and restricted use of antibiotics is lacking in most developing countries where you have the largest market of antimicrobial drugs and reports of the highest rate of antibiotic resistance [86, 87]. Due to these developments, antimicrobial stewardship programs have emerged as an essential means to attenuate the threat of a real possibility of the specter of a “postantibiotic era” [91, 92].
Antimicrobial stewardship is a harmonized program (the optimal selection, dosage, and drug regimen) that fosters the proper use of antimicrobials (including antibiotics) with the goal of optimizing clinical outcomes, reducing microbial resistance, and lessening the spread of infections produced by multidrug-resistant organisms. The main objectives of antimicrobial stewardship are to attain excellent patient outcomes associated with antimicrobial use while reducing toxicity and other unfavorable events, thereby curbing the discriminatory pressure on bacterial population that propels the emergence of multidrug-resistant strains [93, 94].
Antimicrobial stewardship programs (ASPs) are a cornerstone of the response to the AMR crisis in human medicine but are still largely underdeveloped in veterinary medicine [95]. Antimicrobial stewardship is important to both animal health and food safety. Just like humans, animals get infections that require treatment with antibiotics. The rise of antimicrobial resistance is a serious threat to public health [30]. It is imperative that antibiotic stewardship programs seeking to preserve the effectiveness of existing antibiotics in human health also consider strategies that reduce overuse of antibiotics in the agricultural sector as antimicrobials are used in terrestrial animal production practices to preserve animal and public health, but also as growth promoters at a subtherapeutic level [89]. Other aspects to be considered with regard to antimicrobial use include the distinction between therapeutic and nontherapeutic use, between the diverse existing production systems and between specifics related to the different animal species and their eco-geographical location [72, 89].
According to the WHO, FAO, and OIE global tripartite database for antimicrobial resistance country self-assessment in 2016–2017, 42% of the countries on question regarding antimicrobial stewardship and regulation in animals and crop production responded that no national policy or legislation regarding the quality and efficacy of antimicrobials and their use in animals, and crops was available [101]. Responses to other veterinary-related questions showed a huge gap in the preparedness for combating AMR and also the lack of policy making and implementation of a successful antimicrobial stewardship program.
Various strategies have been shown to improve appropriateness of antimicrobial use and cure rates, decrease failure rates, and reduce healthcare-related costs in human hospitals [96, 97, 98]. According to Guardabassi & Prescott [95], the following successful strategies used in human hospitals can be adopted with focus on their implementation in veterinary practice.
educational approaches
development and implementation of guidelines
preprescription approval
postprescription review
computer-based decision support
It should be noted that one strategy does not exclude the other and that multiple strategies can be successfully used in combination.
A good antimicrobial stewardship program (ASP) needs remarkable input in research and training by all stakeholders including national and international veterinary organizations, funding concerns, and animal health industries [95]. At governmental levels, the growth and execution of ASPs need coordination of the task of national public health and veterinary authorities, veterinary clinics, organizations, and private practitioners. The concept of antimicrobial stewardship and of its continuous improvement is in its relative infancy in various sectors of veterinary practice in developing countries, but every veterinary component of the agricultural sector has the responsibility and access to a wide range of resources to develop an ASP.
Stewardship of antimicrobial drugs in human healthcare and veterinary settings is essential to slow the emergence of resistance and extending the useful life of effective antimicrobials according to FDA Center for Veterinary Medicine [99]. All developing countries should be committed to advancing efforts to implement good antimicrobial stewardship practices in veterinary settings as part of their role to protect human and animal health. Each program must be region-specific and constantly under review given that resistance patterns change, requiring changes to local policy of, for example, empirical antibiotic choice [100].
Therefore, the goals in all countries should be to align antimicrobial drug product use with the principles of antimicrobial stewardship, foster antimicrobial stewardship in veterinary settings, and enhance monitoring of antimicrobial resistance and use in animals to further preserve antimicrobial drugs to ensure human and animal health [99].
Resistance to antimicrobial agents arises in some instance through excessive use in animals as chemotherapeutics, and as subtherapeutic additives in feeds. Prolong exposure of microorganisms to sublethal doses of antimicrobials can result in spontaneous emergence of resistance gene and its subsequent transfer among animals, environment and animal products in food chain, and transfer of resistance to human. A pragmatic approach to slow down the development of antimicrobial resistance is to control abuse of antimicrobials through a number of measures. First, it is important to recognize that veterinary pharmaceuticals are important beyond animals and include human health and the environment, hence the need for “One Health” guidiance and regulation. Secondly, it is necessary to reduce drugs that are used as prophylaxis and should rather improve research and innovation for vaccine development, application and explore other alternatives to chemotherapies. The use of feed grade antibiotics and additives in feed as growth promoters also need to be discouraged in developing countries and instead promote organic, home grown livestock husbandry to complement intensive and factory farming. Alternatives to growth-promoting and prophylactic uses of antimicrobials in agriculture include improved management practices, wider use of vaccines, probiotics, and phage virus. Monitoring programs, prudent usage that are controlled, and educational campaigns are some of the approaches that can minimize further development of antimicrobial resistance in developing countries especially. These can be achieved through mutual and ‘One Health’ understanding of the challenges and informed solution through antibiotic stewardship by promoting collective action of all parties with interest including producers, consumers, and mediators.
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\\n\\nThe Author, on his/her own behalf and on behalf of the Co-Authors, will not assert any rights under the Copyright, Designs and Patents Act 1988 to object to derogatory treatment of the Work as a consequence of IntechOpen's changes to the Work arising from the translation of it, corrections and edits for house style, removal of problematic material and other reasonable edits as determined by IntechOpen.
\\n\\nAUTHOR'S DUTIES
\\n\\nWhen distributing or re-publishing the Work, the Author agrees to credit the Monograph/Compacts as the source of first publication, as well as IntechOpen. The Author guarantees that Co-Authors will also credit the Monograph/Compacts as the source of first publication, as well as IntechOpen, when they are distributing or re-publishing the Work.
\\n\\nThe Author agrees to:
\\n\\nThe Author will be held responsible for the payment of the agreed Open Access Publishing Fee before the completion of the project (Monograph/Compacts publication).
\\n\\nAll payments shall be due 30 days from the date of issue of the invoice. The Author or whoever is paying on behalf of the Author and Co-Authors will bear all banking and similar charges incurred.
\\n\\nThe Author shall obtain in writing all consents necessary for the reproduction of any material in which a third-party right exists, including quotations, photographs and illustrations, in all editions of the Work worldwide for the full term of the above licenses, and shall provide to IntechOpen, at its request, the original copies of such consents for inspection or the photocopies of such consents.
\\n\\nThe Author shall obtain written informed consent for publication from those who might recognize themselves or be identified by others, for example from case reports or photographs.
\\n\\nThe Author shall respect confidentiality during and after the termination of this Agreement. The information contained in all correspondence and documents as part of the publishing activity between IntechOpen and the Author and Co-Authors are confidential and are intended only for the recipients. The contents of any communication may not be disclosed publicly and are not intended for unauthorized use or distribution. Any use, disclosure, copying, or distribution is prohibited and may be unlawful.
\\n\\nAUTHOR'S WARRANTY
\\n\\nThe Author and Co-Authors confirm and warrant that the Work does not and will not breach any applicable law or the rights of any third party and, specifically, that the Work contains no matter that is defamatory or that infringes any literary or proprietary rights, intellectual property rights, or any rights of privacy.
\\n\\nThe Author and Co-Authors confirm that: (i) the Work is their original work and is not copied wholly or substantially from any other work or material or any other source; (ii) the Work has not been formally published in any other peer-reviewed journal or in a book or edited collection, and is not under consideration for any such publication; (iii) Authors and any applicable Co-Authors are qualifying persons under section 154 of the Copyright, Designs and Patents Act 1988; (iv) Authors and any applicable Co-Authors have not assigned, and will not during the term of this Publication Agreement purport to assign, any of the rights granted to IntechOpen under this Publication Agreement; and (v) the rights granted by this Publication Agreement are free from any security interest, option, mortgage, charge or lien.
\\n\\nThe Author and Co-Authors also confirm and warrant that: (i) he/she has the power to enter into this Publication Agreement on his or her own behalf and on behalf of each Co-Author; and (ii) has the necessary rights and/or title in and to the Work to grant IntechOpen, on behalf of themselves and any Co-Author, the rights and licences in this Publication Agreement. If the Work was prepared jointly by the Author and Co-Authors, the Author confirms that: (i) all Co-Authors agree to the submission, license and publication of the Work on the terms of this Publication Agreement; and (ii) the Author has the authority to enter into this biding Publication Agreement on behalf of each Co-Author. The Author shall: (i) ensure each Co-Author complies with all relevant provisions of this Publication Agreement, including those relating to confidentiality, performance and standards, as if a party to this Publication Agreement; and (ii) remain primarily liable for all acts and/or omissions of each Co-Author.
\\n\\nThe Author agrees to indemnify IntechOpen harmless against all liabilities, costs, expenses, damages and losses, as well as all reasonable legal costs and expenses suffered or incurred by IntechOpen arising out of, or in connection with, any breach of the agreed confirmations and warranties. This indemnity shall not apply in a situation in which a claim results from IntechOpen's negligence or willful misconduct.
\\n\\nNothing in this Publication Agreement shall have the effect of excluding or limiting any liability for death or personal injury caused by negligence or any other liability that cannot be excluded or limited by applicable law.
\\n\\nTERMINATION
\\n\\nIntechOpen has the right to terminate this Publication Agreement for quality, program, technical or other reasons with immediate effect, including without limitation (i) if the Author and/or any Co-Author commits a material breach of this Publication Agreement; (ii) if the Author and/or any Co-Author (being a private individual) is the subject of a bankruptcy petition, application or order; or (iii) if the Author and/or any Co-Author (as a corporate entity) commences negotiations with all or any class of its creditors with a view to rescheduling any of its debts, or makes a proposal for, or enters into, any compromise or arrangement with any of its creditors.
\\n\\nIn the event of termination, IntechOpen will notify the Author of the decision in writing.
\\n\\nIntechOpen’s DUTIES AND RIGHTS
\\n\\nUnless prevented from doing so by events beyond its reasonable control, IntechOpen, at its discretion, agrees to publish the Work attributing it to the Author and Co-Authors.
\\n\\nUnless prevented from doing so by events beyond its reasonable control, IntechOpen agrees to provide publishing services which include: managing editing (editorial and publishing process coordination, Author assistance); publishing software technology; language copyediting; typesetting; online publishing; hosting and web management; and abstracting and indexing services.
\\n\\nIntechOpen agrees to offer free online access to readers and use reasonable efforts to promote the Publication to relevant audiences.
\\n\\nIntechOpen is granted the authority to enforce the rights from this Publication Agreement on behalf of the Author and Co-Authors against third parties, for example in cases of plagiarism or copyright infringements. In respect of any such infringement or suspected infringement of the copyright in the Work, IntechOpen shall have absolute discretion in addressing any such infringement that is likely to affect IntechOpen's rights under this Publication Agreement, including issuing and conducting proceedings against the suspected infringer.
\\n\\nIntechOpen has the right to include/use the Author and Co-Authors names and likeness in connection with scientific dissemination, retrieval, archiving, web hosting and promotion and marketing of the Work and has the right to contact the Author and Co-Authors until the Work is publicly available on any platform owned and/or operated by IntechOpen.
\\n\\nMISCELLANEOUS
\\n\\nFurther Assurance: The Author shall ensure that any relevant third party, including any Co-Author, shall execute and deliver whatever further documents or deeds and perform such acts as IntechOpen reasonably requires from time to time for the purpose of giving IntechOpen the full benefit of the provisions of this Publication Agreement.
\\n\\nThird Party Rights: A person who is not a party to this Publication Agreement may not enforce any of its provisions under the Contracts (Rights of Third Parties) Act 1999.
\\n\\nEntire Agreement: This Publication Agreement constitutes the entire agreement between the parties in relation to its subject matter. It replaces all prior agreements, draft agreements, arrangements, collateral warranties, collateral contracts, statements, assurances, representations and undertakings of any nature made by, or on behalf of, the parties, whether oral or written, in relation to that subject matter. Each party acknowledges that in entering into this Publication Agreement it has not relied upon any oral or written statements, collateral or other warranties, assurances, representations or undertakings which were made by or on behalf of the other party in relation to the subject matter of this Publication Agreement at any time before its signature (known as the "Pre-Contractual Statements"), other than those which are set out in this Publication Agreement. Each party hereby waives all rights and remedies which might otherwise be available to it in relation to such Pre-Contractual Statements. Nothing in this clause shall exclude or restrict the liability of either party arising out of any fraudulent pre-contract misrepresentation or concealment.
\\n\\nWaiver: No failure or delay by a party to exercise any right or remedy provided under this Publication Agreement or by law shall constitute a waiver of that or any other right or remedy, nor shall it preclude or restrict the further exercise of that or any other right or remedy. No single or partial exercise of such right or remedy shall preclude or restrict the further exercise of that or any other right or remedy.
\\n\\nVariation: No variation of this Publication Agreement shall have effect unless it is in writing and signed by the parties, or their duly authorized representatives.
\\n\\nSeverance: If any provision, or part-provision, of this Publication Agreement is, or becomes invalid, illegal or unenforceable, it shall be deemed modified to the minimum extent necessary to make it valid, legal and enforceable. If such modification is not possible, the relevant provision or part-provision shall be deemed deleted. Any modification to, or deletion of, a provision or part-provision under this clause shall not affect the validity and enforceability of the rest of this Publication Agreement.
\\n\\nNo partnership: Nothing in this Publication Agreement is intended to, or shall be deemed to, establish or create any partnership or joint venture or the relationship of principal and agent or employer and employee between IntechOpen and the Author or any Co-Author, nor authorize any party to make or enter into any commitments for, or on behalf of, any other party.
\\n\\nGoverning law: This Publication Agreement and any dispute or claim, including non-contractual disputes or claims arising out of, or in connection with it, or its subject matter or formation, shall be governed by and construed in accordance with the law of England and Wales. The parties submit to the exclusive jurisdiction of the English courts to settle any dispute or claim arising out of, or in connection with, this Publication Agreement, including any non-contractual disputes or claims.
\\n\\nPolicy last updated: 2018-09-11
\\n"}]'},components:[{type:"htmlEditorComponent",content:'When submitting a manuscript, the Author is required to accept the Terms and Conditions set out in our Publication Agreement – Monographs/Compacts as follows:
\n\nCORRESPONDING AUTHOR'S GRANT OF RIGHTS
\n\nSubject to the following Article, the Author grants to IntechOpen, during the full term of copyright, and any extensions or renewals of that term, the following:
\n\nThe foregoing licenses shall survive the expiry or termination of this Publication Agreement for any reason.
\n\nThe Author, on his or her own behalf and on behalf of any of the Co-Authors, reserves the following rights in the Work but agrees not to exercise them in such a way as to adversely affect IntechOpen's ability to utilize the full benefit of this Publication Agreement: (i) reprographic rights worldwide, other than those which subsist in the typographical arrangement of the Work as published by IntechOpen; and (ii) public lending rights arising under the Public Lending Right Act 1979, as amended from time to time, and any similar rights arising in any part of the world.
\n\nThe Author, and any Co-Author, confirms that they are, and will remain, a member of any applicable licensing and collecting society and any successor to that body responsible for administering royalties for the reprographic reproduction of copyright works.
\n\nSubject to the license granted above, copyright in the Work and all versions of it created during IntechOpen's editing process, including all published versions, is retained by the Author and any Co-Authors.
\n\nSubject to the license granted above, the Author and Co-Authors retain patent, trademark and other intellectual property rights to the Work.
\n\nAll rights granted to IntechOpen in this Article are assignable, sublicensable or otherwise transferrable to third parties without the specific approval of the Author or Co-Authors.
\n\nThe Author, on his/her own behalf and on behalf of the Co-Authors, will not assert any rights under the Copyright, Designs and Patents Act 1988 to object to derogatory treatment of the Work as a consequence of IntechOpen's changes to the Work arising from the translation of it, corrections and edits for house style, removal of problematic material and other reasonable edits as determined by IntechOpen.
\n\nAUTHOR'S DUTIES
\n\nWhen distributing or re-publishing the Work, the Author agrees to credit the Monograph/Compacts as the source of first publication, as well as IntechOpen. The Author guarantees that Co-Authors will also credit the Monograph/Compacts as the source of first publication, as well as IntechOpen, when they are distributing or re-publishing the Work.
\n\nThe Author agrees to:
\n\nThe Author will be held responsible for the payment of the agreed Open Access Publishing Fee before the completion of the project (Monograph/Compacts publication).
\n\nAll payments shall be due 30 days from the date of issue of the invoice. The Author or whoever is paying on behalf of the Author and Co-Authors will bear all banking and similar charges incurred.
\n\nThe Author shall obtain in writing all consents necessary for the reproduction of any material in which a third-party right exists, including quotations, photographs and illustrations, in all editions of the Work worldwide for the full term of the above licenses, and shall provide to IntechOpen, at its request, the original copies of such consents for inspection or the photocopies of such consents.
\n\nThe Author shall obtain written informed consent for publication from those who might recognize themselves or be identified by others, for example from case reports or photographs.
\n\nThe Author shall respect confidentiality during and after the termination of this Agreement. The information contained in all correspondence and documents as part of the publishing activity between IntechOpen and the Author and Co-Authors are confidential and are intended only for the recipients. The contents of any communication may not be disclosed publicly and are not intended for unauthorized use or distribution. Any use, disclosure, copying, or distribution is prohibited and may be unlawful.
\n\nAUTHOR'S WARRANTY
\n\nThe Author and Co-Authors confirm and warrant that the Work does not and will not breach any applicable law or the rights of any third party and, specifically, that the Work contains no matter that is defamatory or that infringes any literary or proprietary rights, intellectual property rights, or any rights of privacy.
\n\nThe Author and Co-Authors confirm that: (i) the Work is their original work and is not copied wholly or substantially from any other work or material or any other source; (ii) the Work has not been formally published in any other peer-reviewed journal or in a book or edited collection, and is not under consideration for any such publication; (iii) Authors and any applicable Co-Authors are qualifying persons under section 154 of the Copyright, Designs and Patents Act 1988; (iv) Authors and any applicable Co-Authors have not assigned, and will not during the term of this Publication Agreement purport to assign, any of the rights granted to IntechOpen under this Publication Agreement; and (v) the rights granted by this Publication Agreement are free from any security interest, option, mortgage, charge or lien.
\n\nThe Author and Co-Authors also confirm and warrant that: (i) he/she has the power to enter into this Publication Agreement on his or her own behalf and on behalf of each Co-Author; and (ii) has the necessary rights and/or title in and to the Work to grant IntechOpen, on behalf of themselves and any Co-Author, the rights and licences in this Publication Agreement. If the Work was prepared jointly by the Author and Co-Authors, the Author confirms that: (i) all Co-Authors agree to the submission, license and publication of the Work on the terms of this Publication Agreement; and (ii) the Author has the authority to enter into this biding Publication Agreement on behalf of each Co-Author. The Author shall: (i) ensure each Co-Author complies with all relevant provisions of this Publication Agreement, including those relating to confidentiality, performance and standards, as if a party to this Publication Agreement; and (ii) remain primarily liable for all acts and/or omissions of each Co-Author.
\n\nThe Author agrees to indemnify IntechOpen harmless against all liabilities, costs, expenses, damages and losses, as well as all reasonable legal costs and expenses suffered or incurred by IntechOpen arising out of, or in connection with, any breach of the agreed confirmations and warranties. This indemnity shall not apply in a situation in which a claim results from IntechOpen's negligence or willful misconduct.
\n\nNothing in this Publication Agreement shall have the effect of excluding or limiting any liability for death or personal injury caused by negligence or any other liability that cannot be excluded or limited by applicable law.
\n\nTERMINATION
\n\nIntechOpen has the right to terminate this Publication Agreement for quality, program, technical or other reasons with immediate effect, including without limitation (i) if the Author and/or any Co-Author commits a material breach of this Publication Agreement; (ii) if the Author and/or any Co-Author (being a private individual) is the subject of a bankruptcy petition, application or order; or (iii) if the Author and/or any Co-Author (as a corporate entity) commences negotiations with all or any class of its creditors with a view to rescheduling any of its debts, or makes a proposal for, or enters into, any compromise or arrangement with any of its creditors.
\n\nIn the event of termination, IntechOpen will notify the Author of the decision in writing.
\n\nIntechOpen’s DUTIES AND RIGHTS
\n\nUnless prevented from doing so by events beyond its reasonable control, IntechOpen, at its discretion, agrees to publish the Work attributing it to the Author and Co-Authors.
\n\nUnless prevented from doing so by events beyond its reasonable control, IntechOpen agrees to provide publishing services which include: managing editing (editorial and publishing process coordination, Author assistance); publishing software technology; language copyediting; typesetting; online publishing; hosting and web management; and abstracting and indexing services.
\n\nIntechOpen agrees to offer free online access to readers and use reasonable efforts to promote the Publication to relevant audiences.
\n\nIntechOpen is granted the authority to enforce the rights from this Publication Agreement on behalf of the Author and Co-Authors against third parties, for example in cases of plagiarism or copyright infringements. In respect of any such infringement or suspected infringement of the copyright in the Work, IntechOpen shall have absolute discretion in addressing any such infringement that is likely to affect IntechOpen's rights under this Publication Agreement, including issuing and conducting proceedings against the suspected infringer.
\n\nIntechOpen has the right to include/use the Author and Co-Authors names and likeness in connection with scientific dissemination, retrieval, archiving, web hosting and promotion and marketing of the Work and has the right to contact the Author and Co-Authors until the Work is publicly available on any platform owned and/or operated by IntechOpen.
\n\nMISCELLANEOUS
\n\nFurther Assurance: The Author shall ensure that any relevant third party, including any Co-Author, shall execute and deliver whatever further documents or deeds and perform such acts as IntechOpen reasonably requires from time to time for the purpose of giving IntechOpen the full benefit of the provisions of this Publication Agreement.
\n\nThird Party Rights: A person who is not a party to this Publication Agreement may not enforce any of its provisions under the Contracts (Rights of Third Parties) Act 1999.
\n\nEntire Agreement: This Publication Agreement constitutes the entire agreement between the parties in relation to its subject matter. It replaces all prior agreements, draft agreements, arrangements, collateral warranties, collateral contracts, statements, assurances, representations and undertakings of any nature made by, or on behalf of, the parties, whether oral or written, in relation to that subject matter. Each party acknowledges that in entering into this Publication Agreement it has not relied upon any oral or written statements, collateral or other warranties, assurances, representations or undertakings which were made by or on behalf of the other party in relation to the subject matter of this Publication Agreement at any time before its signature (known as the "Pre-Contractual Statements"), other than those which are set out in this Publication Agreement. Each party hereby waives all rights and remedies which might otherwise be available to it in relation to such Pre-Contractual Statements. Nothing in this clause shall exclude or restrict the liability of either party arising out of any fraudulent pre-contract misrepresentation or concealment.
\n\nWaiver: No failure or delay by a party to exercise any right or remedy provided under this Publication Agreement or by law shall constitute a waiver of that or any other right or remedy, nor shall it preclude or restrict the further exercise of that or any other right or remedy. No single or partial exercise of such right or remedy shall preclude or restrict the further exercise of that or any other right or remedy.
\n\nVariation: No variation of this Publication Agreement shall have effect unless it is in writing and signed by the parties, or their duly authorized representatives.
\n\nSeverance: If any provision, or part-provision, of this Publication Agreement is, or becomes invalid, illegal or unenforceable, it shall be deemed modified to the minimum extent necessary to make it valid, legal and enforceable. If such modification is not possible, the relevant provision or part-provision shall be deemed deleted. Any modification to, or deletion of, a provision or part-provision under this clause shall not affect the validity and enforceability of the rest of this Publication Agreement.
\n\nNo partnership: Nothing in this Publication Agreement is intended to, or shall be deemed to, establish or create any partnership or joint venture or the relationship of principal and agent or employer and employee between IntechOpen and the Author or any Co-Author, nor authorize any party to make or enter into any commitments for, or on behalf of, any other party.
\n\nGoverning law: This Publication Agreement and any dispute or claim, including non-contractual disputes or claims arising out of, or in connection with it, or its subject matter or formation, shall be governed by and construed in accordance with the law of England and Wales. The parties submit to the exclusive jurisdiction of the English courts to settle any dispute or claim arising out of, or in connection with, this Publication Agreement, including any non-contractual disputes or claims.
\n\nPolicy last updated: 2018-09-11
\n'}]},successStories:{items:[]},authorsAndEditors:{filterParams:{},profiles:[{id:"396",title:"Dr.",name:"Vedran",middleName:null,surname:"Kordic",slug:"vedran-kordic",fullName:"Vedran Kordic",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/396/images/7281_n.png",biography:"After obtaining his Master's degree in Mechanical Engineering he continued his education at the Vienna University of Technology where he obtained his PhD degree in 2004. He worked as a researcher at the Automation and Control Institute, Faculty of Electrical Engineering, Vienna University of Technology until 2008. His studies in robotics lead him not only to a PhD degree but also inspired him to co-found and build the International Journal of Advanced Robotic Systems - world's first Open Access journal in the field of robotics.",institutionString:null,institution:{name:"TU Wien",country:{name:"Austria"}}},{id:"441",title:"Ph.D.",name:"Jaekyu",middleName:null,surname:"Park",slug:"jaekyu-park",fullName:"Jaekyu Park",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/441/images/1881_n.jpg",biography:null,institutionString:null,institution:{name:"LG Corporation (South Korea)",country:{name:"Korea, South"}}},{id:"465",title:"Dr",name:"Christian",middleName:null,surname:"Martens",slug:"christian-martens",fullName:"Christian Martens",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:null},{id:"479",title:"Dr.",name:"Valentina",middleName:null,surname:"Colla",slug:"valentina-colla",fullName:"Valentina Colla",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/479/images/358_n.jpg",biography:null,institutionString:null,institution:{name:"Sant'Anna School of Advanced Studies",country:{name:"Italy"}}},{id:"494",title:"PhD",name:"Loris",middleName:null,surname:"Nanni",slug:"loris-nanni",fullName:"Loris Nanni",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/494/images/system/494.jpg",biography:"Loris Nanni received his Master Degree cum laude on June-2002 from the University of Bologna, and the April 26th 2006 he received his Ph.D. in Computer Engineering at DEIS, University of Bologna. On September, 29th 2006 he has won a post PhD fellowship from the university of Bologna (from October 2006 to October 2008), at the competitive examination he was ranked first in the industrial engineering area. He extensively served as referee for several international journals. He is author/coauthor of more than 100 research papers. He has been involved in some projects supported by MURST and European Community. His research interests include pattern recognition, bioinformatics, and biometric systems (fingerprint classification and recognition, signature verification, face recognition).",institutionString:null,institution:null},{id:"496",title:"Dr.",name:"Carlos",middleName:null,surname:"Leon",slug:"carlos-leon",fullName:"Carlos Leon",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Seville",country:{name:"Spain"}}},{id:"512",title:"Dr.",name:"Dayang",middleName:null,surname:"Jawawi",slug:"dayang-jawawi",fullName:"Dayang Jawawi",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",biography:null,institutionString:null,institution:{name:"University of Technology Malaysia",country:{name:"Malaysia"}}},{id:"528",title:"Dr.",name:"Kresimir",middleName:null,surname:"Delac",slug:"kresimir-delac",fullName:"Kresimir Delac",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/528/images/system/528.jpg",biography:"K. Delac received his B.Sc.E.E. degree in 2003 and is currentlypursuing a Ph.D. degree at the University of Zagreb, Faculty of Electrical Engineering andComputing. His current research interests are digital image analysis, pattern recognition andbiometrics.",institutionString:null,institution:{name:"University of Zagreb",country:{name:"Croatia"}}},{id:"557",title:"Dr.",name:"Andon",middleName:"Venelinov",surname:"Topalov",slug:"andon-topalov",fullName:"Andon Topalov",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/557/images/1927_n.jpg",biography:"Dr. Andon V. Topalov received the MSc degree in Control Engineering from the Faculty of Information Systems, Technologies, and Automation at Moscow State University of Civil Engineering (MGGU) in 1979. He then received his PhD degree in Control Engineering from the Department of Automation and Remote Control at Moscow State Mining University (MGSU), Moscow, in 1984. From 1985 to 1986, he was a Research Fellow in the Research Institute for Electronic Equipment, ZZU AD, Plovdiv, Bulgaria. In 1986, he joined the Department of Control Systems, Technical University of Sofia at the Plovdiv campus, where he is presently a Full Professor. He has held long-term visiting Professor/Scholar positions at various institutions in South Korea, Turkey, Mexico, Greece, Belgium, UK, and Germany. And he has coauthored one book and authored or coauthored more than 80 research papers in conference proceedings and journals. His current research interests are in the fields of intelligent control and robotics.",institutionString:null,institution:{name:"Technical University of Sofia",country:{name:"Bulgaria"}}},{id:"585",title:"Prof.",name:"Munir",middleName:null,surname:"Merdan",slug:"munir-merdan",fullName:"Munir Merdan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/585/images/system/585.jpg",biography:"Munir Merdan received the M.Sc. degree in mechanical engineering from the Technical University of Sarajevo, Bosnia and Herzegovina, in 2001, and the Ph.D. degree in electrical engineering from the Vienna University of Technology, Vienna, Austria, in 2009.Since 2005, he has been at the Automation and Control Institute, Vienna University of Technology, where he is currently a Senior Researcher. His research interests include the application of agent technology for achieving agile control in the manufacturing environment.",institutionString:null,institution:null},{id:"605",title:"Prof",name:"Dil",middleName:null,surname:"Hussain",slug:"dil-hussain",fullName:"Dil Hussain",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/605/images/system/605.jpg",biography:"Dr. Dil Muhammad Akbar Hussain is a professor of Electronics Engineering & Computer Science at the Department of Energy Technology, Aalborg University Denmark. Professor Akbar has a Master degree in Digital Electronics from Govt. College University, Lahore Pakistan and a P-hD degree in Control Engineering from the School of Engineering and Applied Sciences, University of Sussex United Kingdom. Aalborg University has Two Satellite Campuses, one in Copenhagen (Aalborg University Copenhagen) and the other in Esbjerg (Aalborg University Esbjerg).\n· He is a member of prestigious IEEE (Institute of Electrical and Electronics Engineers), and IAENG (International Association of Engineers) organizations. \n· He is the chief Editor of the Journal of Software Engineering.\n· He is the member of the Editorial Board of International Journal of Computer Science and Software Technology (IJCSST) and International Journal of Computer Engineering and Information Technology. \n· He is also the Editor of Communication in Computer and Information Science CCIS-20 by Springer.\n· Reviewer For Many Conferences\nHe is the lead person in making collaboration agreements between Aalborg University and many universities of Pakistan, for which the MOU’s (Memorandum of Understanding) have been signed.\nProfessor Akbar is working in Academia since 1990, he started his career as a Lab demonstrator/TA at the University of Sussex. After finishing his P. hD degree in 1992, he served in the Industry as a Scientific Officer and continued his academic career as a visiting scholar for a number of educational institutions. In 1996 he joined National University of Science & Technology Pakistan (NUST) as an Associate Professor; NUST is one of the top few universities in Pakistan. In 1999 he joined an International Company Lineo Inc, Canada as Manager Compiler Group, where he headed the group for developing Compiler Tool Chain and Porting of Operating Systems for the BLACKfin processor. The processor development was a joint venture by Intel and Analog Devices. In 2002 Lineo Inc., was taken over by another company, so he joined Aalborg University Denmark as an Assistant Professor.\nProfessor Akbar has truly a multi-disciplined career and he continued his legacy and making progress in many areas of his interests both in teaching and research. 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