Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
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We wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
IntechOpen is proud to announce that 179 of our authors have made the Clarivate™ Highly Cited Researchers List for 2020, ranking them among the top 1% most-cited.
\n\n
Throughout the years, the list has named a total of 252 IntechOpen authors as Highly Cited. Of those researchers, 69 have been featured on the list multiple times.
\n\n\n\n
Released this past November, the list is based on data collected from the Web of Science and highlights some of the world’s most influential scientific minds by naming the researchers whose publications over the previous decade have included a high number of Highly Cited Papers placing them among the top 1% most-cited.
\n\n
We wish to congratulate all of the researchers named and especially our authors on this amazing accomplishment! We are happy and proud to share in their success!
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Adj. of Instituto de Física Aplicada (INFAP) – CONICET – UNSL and Associate Professor at the National University of San Luis (UNSL), Argentina. He holds a Master’s degree and a Ph.D. and Master's thesis in Membrane Technology from the National University of San Luis. He is the Director of Physics Chemistry Service Laboratory at UNSL. He is an expert in polysaccharides and physics chemistry of macromolecules. He is an author or co-author of more than 30 peer-reviewed international publications, 8 book chapters, 75 communications in national and international congresses and editor of 8 books. He is a member of the Sociedad Argentina de Ciencia y Tecnología Ambiental, Asociación Argentina de Fisicoquímica y Química Inorgánica and Asociación Argentina de Tecnólogos Alimentarios. Since July 2013, he is the Editor in Chief and Founder of the Journal of Polymer and Biopolymers Physics Chemistry, Science and Education Publishing. 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1. Introduction
Staphylococci are natural residents on the skin and mucous membranes of a wide range of host species [1]. Many of the bacterial species have a benign or symbiotic relationship with their host; however, the bacteria may become pathogenic if they gain entry into the host tissue through trauma of the cutaneous barrier [2, 3]. Staphylococcus aureus is the most significant species within this genus by virtue of its versatility as a pathogen in humans and animals [4, 5]. In humans, S. aureus is responsible for a variety of conditions, ranging from superficial skin infections to life-threatening diseases [6]. In addition, through the production of potent superantigens and other toxins, S. aureus can cause specific toxin-mediated conditions such as toxic shock syndrome, scalded skin syndrome and food poisoning [6]. In animals, S. aureus is a common cause of intramammary infections (IMIs), or mastitis [7]. Worldwide, the dairy industry incurs significant financial losses annually due to intramammary infections [8–10].
Other Staphylococcus species, collectively termed coagulase-negative staphylococci (CNS), are responsible for a variety of opportunistic infections in humans and animals [11]. Due to the ubiquity of many of the species within this group, their clinical significance has traditionally been dismissed, and when isolated from clinical specimens, the bacteria have merely been regarded as contaminants [12]. This perception is, however, changing as many species have emerged as important causes of nosocomial infections, particularly in relation to foreign-device-related infections and infections in immunocompromised patients [1, 13].
The propensity for staphylococci to develop antimicrobial resistance is a cause for great concern in both human and veterinary medicine [14]. As the efficacy of antimicrobials declines, the morbidity and mortality in infected patients increase [15, 16]. Moreover, in the case of human medicine, the costs associated with the treatment of infections caused by antimicrobial-resistant bacteria represent a serious public health burden in hospital and community settings [10].
2. The genus Staphylococcus
2.1. Classification of staphylococci
Before the 1970s, S. aureus and S. epidermidis, or S. albus as it was originally named, were the only recognized Staphylococcus species [17]. Staphylococcus aureus was considered a pathogen and S. epidermidis, when isolated from clinical material, was regarded as a contaminant [17]. In the mid-1970s, Kloos and Schleifer [17–19] conducted comprehensive systematic studies of staphylococci and micrococci and described a number of new species. To date, 49 species and 26 subspecies have been described and with improvements in the accuracy of genotyping methods the number of species is still increasing [20, 21].
The genus Staphylococcus is classified along with the genera Jeotgalicoccus, Macrococcus, Nosocomiicoccus and Salinicoccus in the family Staphylococcaceae [12, 21]. The full Linnaean classification for the genus and the type species, S. aureus, is shown in Table 1.
The current Linnaean classification scheme for the genus Staphylococcus [21].
In diagnostic laboratories, staphylococci are historically differentiated by their ability to produce the enzyme coagulase, which mediates the conversion of fibrinogen to fibrin resulting in the clotting of blood [22]. The production of coagulase has long been recognized as an important indicator of pathogenicity [23, 24], and the coagulation of rabbit plasma provides a rapid in vitro method for differentiating pathogenic coagulase-positive staphylococci (CPS) and ‘non-pathogenic’ coagulase-negative staphylococci [1, 24].
Seven CPS are currently recognized, namely S. aureus, S. lutrae, S. schleiferi subsp. coagulans, the coagulase-variable, S. hyicus and the S. intermedius group (SIG), which comprises S. intermedius, S. pseudintermedius and S. delphini [25, 26]. Staphylococcus aureus, which is known to be pathogenic in both humans and animals, is considered to be the most important of all the CPS. Other CPS, particularly S. hyicus and members of the SIG group, are important veterinary pathogens and are responsible for infections in a number of different animal species [2, 25, 26].
The CNS comprise a biochemically heterogeneous group of bacteria which have, for convenience, been grouped together by virtue of their inability to produce the enzyme coagulase [23, 24]. The susceptibility of CNS isolates to novobiocin has been shown to be a useful phenotypic characteristic in diagnostic laboratories to differentiate S. saprophyticus from other clinically important species [2, 27]. The phylogenetic relationship between the coagulase-negative staphylococcal species has recently been clarified through the analysis of four gene loci, namely the 16S rRNA gene and the three protein-encoding genes, dnaJ, rpoB and tuf, which code for heat shock protein 40, the β-subunit of RNA polymerase and elongation factor Tu, respectively [12, 28]. The molecular analysis resolved the CNS into 14 cluster groups, which are depicted in Figure 1.
Figure 1.
Phylogenetic separation of staphylococcal species and subspecies. Coagulase-positive Staphylococcus spp. are shown in green font [12, 28].
2.2. General characteristics of staphylococci
Staphylococci are non-motile, non-sporeforming Gram-positive coccus-shaped bacteria [29]. The cocci may occur singly, in pairs and in tetrads, and they characteristically divide in more than one plane to form irregular ‘grape-like’ clusters [2, 29]. In fact, the name Staphylococcus is derived from the Greek words ‘staphyle’ and ‘kokkos’ meaning ‘bunch of grapes’ and ‘berry’, respectively [1, 29]. Most staphylococci are facultative anaerobes and catalase positive with the exception of S. aureus subsp. anaerobius and S. saccharolyticus [1]. Staphylococci can grow in a wide pH range (4.8–9.4) and can survive temperatures of up to 60°C for 30 minutes [29]. Many Staphylococcus species are tolerant of high salt concentrations (7.5–10%) due to the production of osmoprotectants [29]. The ability to grow in the presence of above-average salt concentrations explains the predilection of many staphylococcal species for the sebaceous surfaces of mammals [1]. This phenotypic trait is exploited in diagnostic laboratories by incorporating high concentrations of sodium chloride into agar media to selectively isolate staphylococci from contaminated samples [1, 5].
Staphylococcus aureus is able to exist as a commensal on the skin and mucous membranes of different hosts, but when the opportunity presents, the bacterium is able to become pathogenic [1]. Staphylococcus aureus can colonize a number of sites on the human body with the anterior nares being the preferred site [30, 31]. Approximately 20% of healthy humans are persistent nasal carriers of S. aureus, about 30% are intermittent carriers and around 50% of individuals are never colonized with S. aureus [31, 32]. Individuals who are colonized by S. aureus are at a higher risk of becoming infected and are also an important source for the dissemination of S. aureus among individuals in the community [1, 33]. The primary means of transmission of S. aureus is by direct contact, usually skin-to-skin contact with colonized or infected individuals, although indirect means, via fomites, is also thought to play a role [33]. Various host factors, including loss of the normal skin barrier, the presence of underlying diseases, such as diabetes and acquired immunodeficiency syndrome, predispose individuals to infection [33].
The success of S. aureus as a pathogen is attributed in part to the capacity of the bacteria to produce a diverse array of virulence factors [1, 14]. Some of these factors may be more important than others in different diseases or at different stages of pathogenesis as not all factors are produced by each strain [34, 35]. Based on structure and functionality, the virulence factors can be broadly divided into two general groups, namely surface-associated factors and degradative enzymes, including exotoxins [36]. The microbial surface components of S. aureus recognizing the adhesive matrix molecular components (MSCRAMMs) comprise surface proteins that promote colonization by binding to host cells [36]. This group, which includes fibrinogen-, fibronetin- and collagen-binding proteins, is important during the initial stage of infection [37]. Once infection is established, the expression of tissue-binding proteins is downregulated, whilst the synthesis of extracellular toxins and tissue-degrading enzymes is induced to aid the acquisition of nutrients and the dissemination of the bacteria [38].
The CNS constitute a significant proportion of the natural microflora colonizing the skin and mucous membranes of humans and animals [12, 39]. The different staphylococcal species display apparent site or niche preferences on their hosts and occur more frequently at these sites [2, 12]. Staphylococcus epidermidis is the most abundant and widely distributed species on human skin and can occur in densities of 103 to 104 cells cm−2 [12, 40, 41]. Staphylococcus epidermidis is particularly prevalent in moist areas, such as the axillae, inguinal and perineal areas, anterior nares, conjunctiva and toe webs [12]. Staphylococcus haemolyticus and S. hominis are preferentially isolated from areas of the skin where there are numerous apocrine glands such as the axillae and pubic areas, whereas S. capitis is typically located around the sebaceous glands on the forehead and scalp following puberty [2, 12]. Staphylococcus warneri is commonly recovered from human hands, whilst S. lugdunensis has a preference for the inguinal and breast areas [41–43].
Coagulase-negative staphylococci are typically less pathogenic than S. aureus possessing a smaller array of virulence factors [12]. However, CNS often exhibit greater resistance to antimicrobials and also have a greater tendency to develop multidrug resistance [44]. Coagulase-negative staphylococci are believed to serve as reservoirs of antimicrobial resistance genes, which can transfer and integrate into the S. aureus genome leading to the emergence of new, potentially more resistant strains [45, 46].
3. Genomic organization and genetic flexibility of S. aureus
The staphylococcal genome consists of a closed circular molecule of double-stranded DNA between two and three megabase pairs in length and encoding between 2 509 and 2 892 open-read frames [1, 47]. Whole genome sequencing of a number of S. aureus strains has revealed that approximately 75% of the bacterium’s genome comprises a core component, common to all strains [6]. The majority of the genes comprising the core genome are those associated with central metabolism and other housekeeping functions [48]. The remaining 25% of the S. aureus genome, termed the accessory genome, contains genes that encode a diverse array of non-essential functions ranging from virulence, antimicrobial and metal resistance, to substrate utilization and miscellaneous metabolism [49]. Many of the regions making up the accessory genome are, or once were, mobile genetic elements (MGEs), such as chromosomal cassettes, pathogenicity islands, plasmids, prophages and transposons [50]. Mobile genetic elements can be transferred horizontally between bacteria of the same or different species, leading to the evolution of bacterial strains [50, 51]. The distribution of these elements is therefore important from a clinical perspective, as it may lead to the evolution of bacterial strains that are potentially more virulent or resistant to antimicrobials [50].
3.1. Host specificity and host switching of S. aureus
Devriese and Oeding [52] were amongst the first researchers to note the occurrence of phenotypic differences between S. aureus strains isolated from humans and different animal hosts. A simplified biotyping scheme was developed by Devriese and co-workers to differentiate S. aureus isolates into ecological variants, or ecovars, that delineated along human, poultry or ruminant associations [53, 54]. Many strains, however, were found not to belong to any of the host-specific biotypes and instead were classed as non-host-specific biotypes which are usually associated with several hosts [55]. The use of phenotyping techniques such as multilocus enzyme electrophoresis (MLEE) [56] and later more discriminatory genotyping methods, such as pulsed-field gel electrophoresis (PFGE) [55, 57], multilocus sequence typing (MLST) [56, 58] and whole genome sequencing [59], has clearly demonstrated the existence of specialized host-specific S. aureus clones [54].
Microarray studies of animal and human S. aureus isolates have shown that strains that are isolated from one host species tend to be uncommon in other species [60], although this delineation is not always absolute [54]. In many respects, the host range of S. aureus should be considered an evolving trait [61]. Adaptation to a particular host species does not prevent S. aureus strains from causing occasional infections in other species [62]. Wherever there is an interface between different host species, the opportunity exists for bacterial exchange. In most cases, these exchanges lead to transient infections which are short lived due to the failure of the S. aureus strain to establish transmission pathways in the new host species [62]. However, sustained interspecies events are known to occur albeit at a lower frequency [62].
A number of independent studies have investigated specific S. aureus host-switching events. All of the described host-switch events highlight the significant role that the transfer of MGEs plays in host adaptation and specialization [56, 62, 63]. It is believed that if the conditions under which S. aureus host switches occur is understood, then strategies could be developed to curb future host jumps and the emergence of new human pathogens [63].
4. Staphylococcal infections in humans
Infections caused by S. aureus are often acute and pyogenic and, if left untreated, may spread to surrounding tissue or via bacteremia to metastatic sites [2]. Some of the most common infections caused by S. aureus involve the skin, and include furuncles or boils, cellulitis, impetigo and post-operative wound infections of various sites [2]. Mastitis is one of a variety of skin and soft tissue infections that may be caused by S. aureus. Unlike other S. aureus infections in humans, staphylococcal mastitis has not been extensively studied [60, 64]. It is estimated that mastitis develops in approximately 1–3% of nursing mothers [65]. Infection usually presents within two to three days after giving birth, with symptoms ranging from cellulitis to abscess formation [65]. In severe cases, systemic symptoms such as fever and chills may arise [65]. Staphylococcus aureus may also cause more serious infections such as bacteremia, pneumonia, osteomyelitis, acute endocarditis, myocarditis, pericarditis, cerebritis, meningitis and abscesses of the muscle, urogenital tract, central nervous system and various intra-abdominal organs [2].
Staphylococcal diseases that arise exclusively from the production of staphylococcal toxins include staphylococcal scalded skin syndrome (SSSS), toxic shock syndrome (TSS) and staphylococcal food poisoning [65]. Staphylococcal food poisoning occurs following the ingestion of food contaminated with enterotoxins [66]. Enterotoxins are heat stable and can survive conditions that would ordinarily kill bacteria [67]. Furthermore, enterotoxins are tolerant to low pH conditions and the activity of proteolytic enzymes and are thus able to retain their activity in the digestive tract following ingestion [5, 67]. Following ingestion of contaminated food and a short incubation period (two to eight hours), nausea and vomiting ensue [66]. Diarrhea, hypotension and dehydration may also occur [65]. Staphylococcal food poisoning is usually self-limiting and typically resolves within 24 to 48 hours following the onset of symptoms [3]. Occasionally, the symptoms may be severe enough to warrant hospitalization, particularly in the case of infants, the elderly or immunocompromised individuals [66]. Staphylococcal food poisoning is a common disease but the true incidence is considered to be underestimated due to misdiagnosis, unreported outbreaks, improper specimen collection and laboratory examination [66]. The disease represents a considerable burden in terms of loss of productivity, medical and hospital expenses and financial losses to food industries [66]. Enterotoxin production is not limited to S. aureus but has been documented in a number of other staphylococci including S. hyicus, S. pseudintermedius,S. chromogenes, S. cohnii, S. epidermidis, S. lentus, S. lugdunensis, S. saprophyticus, S. sciuri, S. warneri and S. xylosus [3, 5, 68, 69].
Almost half of all the CNS species that have been identified to date have been implicated in human infections [65]. Coagulase-negative staphylococci, in particular S. epidermidis, are frequently responsible for nosocomial infections and prosthetic-device-related infections [27, 70]. The increased infection rate is correlated with increase in the use of prosthetic and indwelling devices in hospitals as well as the larger number of immunocompromised patients [39, 41]. Staphylococcus epidermidis is uniquely adapted to colonize prosthetic devices by virtue of the ability of the bacterium to produce an extracellular polysaccharide, also referred to as a glycocalyx or slime layer, which facilitates the formation of a protective biofilm on the surface of the implanted device [39, 65]. The process of biofilm formation and the protective effects conferred upon the bacteria are discussed in further detail below.
Staphylococcus haemolyticus is the second most frequently encountered CNS associated with human infections [2]. Staphylococcus haemolyticus has been implicated in native valve endocarditis, septicemia, peritonitis, urinary tract infections and wound and bone and joint infections [2]. Staphylococcus saprophyticus is another opportunistic pathogen, which is frequently responsible for causing human urinary tract infections, particularly in young, sexually active females [2, 12].
Two staphylococcal species, S. lugdunensis and S. schleferi, have been described as emerging zoonotic pathogens [71]. Staphylococcus lugdunensis, which is known to cause skin infections and invasive infections, such as endocarditis, osteomyelitis and sepsis in humans, has more recently been described as an animal pathogen implicated in respiratory and skin infections [71, 72]. Staphylococcus schleiferi, which has typically been associated with skin infections in pet animals, has also been found associated with endocarditis and metastatic infection as well as endophthalmitis in humans [73, 74]. Both bacterial species have been reported to cause more serious infections than other CNS, but the exact reasons for this enhanced virulence are not known [43, 71].
5. Staphylococcal infections in animals
Amongst all of the described staphylococcal species, only S. aureus, S. epidermidis, S. hyicus and S. pseudintermedius are responsible for significant disease conditions in animals [75, 76]. Other Staphylococcus spp. are predominantly associated with opportunistic infections in different animal species [75].
In poultry, S. aureus is responsible for several infectious conditions including septic arthritis, subdermal abscesses (‘bumblefoot’), gangrenous dermatitis and bacterial chrondronecrosis with osteomyelitis [58, 77]. In sheep and goats, S. aureus is a common cause of dermatitis whilst in horses and pigs S. aureus may cause botryomycosis, a chronic, suppurative granulomatous condition [24]. In companion animals, S. aureus causes suppurative conditions similar to those produced by S. pseudintermedius [24].
Staphylococcus hyicus is responsible for causing exudative epidermitis in pigs, also known as greasy pig disease, as well as sporadic joint infections and cystitis [24]. In companion animals S. pseudintermedius is commonly isolated from cases of pyoderma, otitis externa and other suppurative conditions including mastitis, endometritis, cystitis, osteomyelitis and wound infections [24]. Methicillin-resistant S. pseudintermedius is emerging as an important clinical problem in veterinary medicine in many countries [78, 79].
Staphylococcus species can cause intramammary infections in a variety of animal species [24]. Bovine IMIs are the most economically significant, but in areas where sheep and goats are maintained for milking purposes, IMIs caused by staphylococci can cause substantial losses [80]. Similarly, in countries where milk is sourced from buffalo or camels, significant financial losses due to mastitis have been reported [81, 82]. The direct, or obvious, financial losses incurred as a result of IMIs include treatment costs (veterinary fees and drugs); milk that is discarded due to poor quality, or milk lost during the required withdrawal period before and after drug administration; increased labor costs and animal fatalities or euthanasia [83, 84]. In addition to the direct financial losses incurred due to IMIs, a number of indirect costs exist, which are harder to quantify and are often overlooked. Subclinical infections usually proceed undetected in a herd resulting in a gradual decrease in milk production and a decline in overall milk quality [83]. This leads to a gradual erosion of profit margins, which, even when detected, can take significant time and financial input to rectify [83].
Staphylococcus aureus is possibly the most notorious of all mastitis pathogens by virtue of the fact that infections caused by this species are difficult to treat and tend to become chronic [36]. Coagulase-negative staphylococci are considered to be emerging pathogens, as in many countries the CNS have become the most common bacteria isolated from intramammary infections [9]. The species most commonly isolated from intramammary infections include S. chromogenes, S. epidermidis, S. haemolyticus, S. simulans and S. xylosus [85, 86].
6. Antimicrobial resistance in staphylococci
Staphylococcus aureus is intrinsically susceptible to all antimicrobials that have been developed [33]. Antimicrobial resistance may be acquired through mutation and selection of resistant bacterial strains or through horizontal transfer of resistance genes from other bacteria of the same or different species [33]. Common mechanisms which are used to circumvent the action of antimicrobials include (i) the production of enzymes that inactivate or destroy the antimicrobial; (ii) a reduction of the bacterial cell wall permeability limiting the antimicrobial access into the cell; (iii) the development of alternative metabolic pathways to those inhibited by the antimicrobial; and (iv) active elimination of the antimicrobial from the bacterial cell or the target site [87, 88]. The mechanisms responsible for antimicrobial resistance in CNS are identical to those occurring in S. aureus [89].
6.1. The emergence of resistance in S. aureus
Shortly after the introduction of penicillin in human medicine in 1946, reports of S. aureus strains exhibiting resistance to this antimicrobial began emerging [90]. Penicillin-resistant staphylococci were first recognized in hospitals and then subsequently in the community [91]. By the late 1960s, more than 80% of both community- and hospital-associated staphylococcal isolates were resistant to penicillin [92]. It is estimated that more than 90% of staphylococcal isolates now produce penicillinase, regardless of the clinical setting [93].
A similar clinical scenario was observed following the introduction of methicillin, the first semisynthetic penicillin resistant to the action of penicillinase [90]. Shortly after the introduction of methicillin in 1959, methicillin-resistant strains were reported [94]. Once again, resistant strains initially presented in the hospital environment; and then by the late 1990s, virulent methicillin-resistant clones emerged in the community [91].
During the 1960s, a number of non-β-lactam antibiotics, such as chloramphenicol, erythromycin, streptomycin and tetracycline, were introduced [89]. Although initially effective against S. aureus, resistance to these antimicrobials was eventually observed [89]. By 1976, resistance to gentamicin and kanamycin had been reported, and by the early 1980s, multidrug-resistant S. aureus strains were reportedly responsible for nosocomial outbreaks in many countries [47, 95].
Vancomycin and teicoplanin, both glycopeptide antibiotics, have been the frontline treatment for serious methicillin-resistant Staphylococcus aureus (MRSA) infections for the last 15 years [47, 96]. Due to the increasing burden of MRSA infections and the concomitant increase in the usage of vancomycin, bacterial isolates showing intermediate susceptibility (not inhibited in vitro at concentrations below 4–8 µg/ml, vancomycin-intermediate S. aureus (VISA)) were reported in Japan in 1997 [97]. By 2002, vancomycin-resistant S. aureus (VRSA; isolates only inhibited at antimicrobial concentrations of 16 µg/ml or more) were encountered in Michigan, United States [33, 98].
A timeline showing the emergence of resistance in S. aureus relative to the introduction of significant antimicrobial classes is shown in Figure 2. Several antimicrobials with good anti-staphylococcal activity have been introduced in recent years, including ceftaroline, ceftobiprole, dalbavancin, daptomycin, linezolid, telavancin and tigecycline [99, 100]. Isolates showing reduced susceptibility to daptomycin and resistance to linezolid have already been documented [101]. Undoubtedly, as the use of these drugs becomes more widespread, bacterial resistance will become more common [102].
Figure 2.
The emergence of antibiotic resistance in S. aureus (VISA, vancomycin-intermediate S. aureus; VRSA, vancomycin-resistant S. aureus; CA-MRSA, community-associated methicillin-resistant S. aureus; LA-MRSA, livestock-associated methicillin-resistant S. aureus) Adapted from [33, 47].
The distinct lack of novel antimicrobials for future use is a serious cause for concern [93, 103]. Current strategies are aimed at prudent and strategic use of antimicrobials to delay the emergence of resistance and ensure the longevity of antimicrobials in clinical practice [104, 105].
6.2. Mechanism of penicillin resistance in staphylococci
Resistance to penicillin is primarily mediated by the blaZ gene, which is responsible for the production of beta-lactamase (penicillinase), an enzyme that hydrolyzes the β-lactam ring of the penicillin molecule [93]. The blaZ gene is part of a transposable element located on a large plasmid, which often carries additional antimicrobial resistance genes, which confer resistance to erythromycin, fusidic acid and gentamicin [93]. The plasmid may also carry genes encoding resistance to disinfectants (quaternary ammonium compounds), dyes (acriflavine and ethidium bromide) or heavy metals (cadmium, lead and mercury) [106].
6.3. Mechanism of methicillin resistance in staphylococci
Methicillin resistance arises due to the acquisition of the mecA gene, which encodes an alternative penicillin-binding protein, PBP2a (or PBP2\'), which has a low affinity for β-lactam antibiotics [14, 100, 107]. The synthesis of PBP2a allows bacterial cell cell wall synthesis to proceed uninterrupted in the presence of β-lactam antibiotics despite the inactivation of the native penicillin-binding protein of the cells [93, 100]. The mecA gene confers resistance to all β-lactam antibiotics, including cephalosporins, cefamycins and carbapenems [103, 107].
The mecA gene is part of a large mobile genetic element designated the staphylococcal cassette chromosome mec (SCCmec) [31, 100]. The SCCmec integrates into the staphylococcal chromosome of methicillin-sensitive S. aureus at a specific site (attBscc) which is located at the 3’ end of an open reading frame of a gene with an unknown function (orfX) [33, 108]. In addition to the mecA gene, SCCmec also carries the genes that control the transcription of the mecA gene (mecI and mecR1) and chromosomal cassette recombinase genes (ccrA, ccrB or ccrC), which mediate the integration and excision of the cassette into the host chromosome [31]. The SCCmec element may also contain other genes encoding resistance to antimicrobials, such as aminoglycosides or macrolides and resistance to heavy metal ions [109, 110]. According to their genetic structure and contents, SCCmec elements are categorized into several types and subtypes [14, 31]. To date, the website of the International Working Group on the Classification of Staphylococcal Cassette Chromosome elements (IWCC) lists 11 types of SCCmec elements (I to XI) [111].
Staphylococcal chromosomal cassettes containing the mec gene have been identified not only in S. aureus but also in other CPS and CNS [112]. In CNS, SCCmec elements exhibit a more polymorphous structure with a larger number of ccr–mec combinations being encountered, which have not been described for MRSA [113]. The higher frequency and diversity of SCCmec elements in CNS suggest that CNS are a potential reservoir of SCCmec elements, which may facilitate and drive the emergence of new MRSA clones [114]. The possible mechanism(s) involved in the horizontal transfer of SCCmec elements from CNS to S. aureus are currently not known [115].
The origin of the mecA gene has been a source of speculation for many years. Homologues of the mecA gene have been found in S. sciuri and S. vitulinus, but in both cases, the mecA gene is not located in a mecA complex as with SCCmec [116]. Tsubakishita and co-workers [108] identified a mecA gene homologue in S. fleuretti, which shared almost 100% sequence homology with MRSA strain N315 and which resided on a structure almost identical to the mecA complex. Staphylococcus fleuretti is a member of the S. sciuri group of staphylococci and is a commensal bacterium of animals [108]. The occurrence of a direct precursor of the methicillin resistance determinant in a Staphylococcus species, which normally resides on animals, suggests that staphylococci of animal origin may be a reservoir for the evolution of novel SCCmec elements [116].
Molecular investigations of a S. aureus isolate, which was found to be phenotypically resistant to methicillin but negative for the mecA gene when tested with a standard diagnostic polymerase chain reaction (PCR) assay, led to the discovery of a novel mecA homologue [117]. The mecA homologue, initially designated mecALGA251 after S. aureus LGA251, the bacterial strain in which the gene was first sequenced, shares 70% nucleotide identity with the conventional mecA gene [118]. The work of Garcίa-Álvarez and co-workers [117] showed that mecALGA251 was found in S. aureus lineages typically associated with cattle, namely clonal complex (CC)130, CC1943 and sequence type (ST)425, suggesting the existence of a zoonotic MRSA reservoir. Furthermore, evidence of animal-to-human transmission of MRSA strains harboring mecALGA251 has been documented [119]. In 2012, the IWCC renamed the mecA variant, mecC [120]. The mecC gene resides on a novel SCCmec element designated SCCmec XI [121]. Methicillin-resistant S. aureus strains carrying the mecC gene have been shown to cause a range of infections in humans and appear to be predominantly community associated [118, 119]. The prevalence of mecC in CNS has not been extensively explored as yet [60], but an allotype of the mecC gene has been detected in a S. xylosus strain [118].
6.3.1. Healthcare-associated MRSA
Traditionally, MRSA has been considered a hospital- or healthcare-associated pathogen (HA-MRSA) primarily infecting people who are immunocompromised or who have had surgery or medical device implants [122, 123]. Healthcare-associated MRSA strains usually carry SCCmec types I, II and III and are multidrug resistant [14]. Worldwide, the majority of HA-MRSA strains belong to CC5, CC8, CC22, CC30 and CC45 [14, 122].
6.3.2. Community-associated MRSA
Since the mid-1990s, MRSA strains were increasingly reported in healthy people without any healthcare-associated risk factors [31, 122]. These cases were termed community-associated MRSA (CA-MRSA), and genetic analyses revealed that these S. aureus isolates were genetically distinct from the typical HA-MRSA strains [31]. Community-associated MRSA strains are primarily associated with SCCmec types IV and V, which typically lack non-β-lactam resistance genes [124]. Most CA-MRSA strains belong to sequence type (ST)1, ST8, ST30, ST59, ST80 and ST93 [14, 122] with ST8 (‘USA300’) being the most common clonal lineage in the USA and ST80 the most common in Europe [125, 126]. Carriage of the gene encoding the Panton–Valentine leukocidin appears to be epidemiologically associated with certain CA-MRSA strains [14, 123].
6.3.3. Livestock-associated MRSA
The emergence of a third group of MRSA strains was witnessed in the last decade, which was described following investigations that began on a pig farm in the Netherlands [54, 127]. Pig farmers and other close human contacts were found to be at a higher risk of carrying MRSA than members of the population who did not frequent pig farms [128]. This group of MRSA strains, initially referred to as ‘non-typeable MRSA’ or ‘pig MRSA’, was found to belong to a single clonal complex, CC398, with the majority of strains belonging to sequence type (ST)398 [31]. Methicillin-resistant S. aureus ST398 has subsequently been isolated from other animal species, including dogs, horses, veal calves and poultry [125, 129–131], and it has therefore been designated livestock-associated MRSA (LA-MRSA) [125]. It has been shown that persons in direct (occupational) contact with LA-MRSA-positive animals, such as farmers, laborers, veterinarians and abattoir staff, have an increased risk of becoming MRSA carriers [31]. Methicillin-resistant S. aureus ST398 strains can cause infections in both animals [31] and humans [117]. Furthermore, certain strains belonging to an independent clade within CC398 have been associated with direct human-to-human transmission without prior exposure to livestock [132].
Livestock-associated MRSA ST398 carries SCCmec element IV or V [133]. These strains are generally resistant to tetracycline while resistance to aminoglycosides, lincosamides, macrolides and trimethoprim has also been documented [31]. Fluoroquinolone resistance has also been reported in isolates from Germany [14]. The LA-MRSA ST398 strains have been found to carry previously unidentified resistance genes, such as dfrK, a novel, plasmid-borne trimethoprim resistance gene [134]. This gene is located close to tetL, which would allow for the selection of either gene by the use of tetracycline or trimethoprim, both of which are used in veterinary medicine [135]. A novel ABC efflux pump encoding gene, vgaC, which confers resistance to lincosamides and streptogramins, was also found on the same plasmid [134]. The multidrug resistance gene, cfr, was found in two porcine S. aureus isolates from Germany, one MRSA ST398 and one MSSA ST9 [136]. The cfr gene confers resistance to a number of antimicrobials including lincosamides, oxazolidinones, phenicols pleuromutilins and streptogramin A [133].
Molecular typing and whole genome sequencing have revealed that LA-MRSA CC398 strains originated from human-methicillin-sensitive S. aureus strains, which crossed the species barrier and in the process lost phage-carrying virulence genes that are usually found in human isolates [137]. The host switch from humans to livestock was further accompanied by the acquisition of methicillin and tetracycline resistance genes [137], suggesting that an antibiotic selective pressure exists in the livestock industry [138].
6.4. Mechanisms of vancomycin resistance in staphylococci
The molecular mechanisms underlying VISA and VRSA are different [139, 140]. Intermediate vancomycin resistance is associated with the presence of a thickened and/or poorly cross-linked peptidoglycan bacterial cell wall [140]. The altered cell wall structure traps the antimicrobial molecules reducing cellular penetration and preventing the antimicrobial from reaching its target site [140]. Heteroresistant VISA isolates (hVISA) have been described by Hiramatsu and co-workers [141]. Heteroresistant strains are susceptible to vancomycin but contain a small subpopulation of cells, approximately one in every 106 cells, which exhibit resistance. It is proposed that hVISA may be a precursor to VISA and, as such, needs to be detected so that appropriate control measures can be implemented to limit the spread of the bacterium [142].
Vancomycin-resistant S. aureus strains do not arise from VISA but have acquired the complete genetic apparatus mediating resistance to glycopeptides from vancomycin-resistant enterococci [51, 93, 98]. The genes encoding vancomycin resistance, collectively referred to as the vanA gene complex, reside on a transposon, Tn1546 [139]. The transposon is carried by a conjugative plasmid and is transmissible to a number of Gram-positive bacterial genera including Bacillus, Staphylococcus and Streptococcus [139].
7. Alternate bacterial strategies to circumvent the action of antimicrobials
In addition to the challenges posed by antimicrobial resistance, the treatment of staphylococcal infections is further complicated by a number of strategies that staphylococci have developed, which enable the bacteria to evade the host immune response and the activity of antimicrobials [12, 143]. Two strategies, namely the formation of biofilms and the development of small-colony variants, will be discussed in further detail.
7.1. The formation of biofilms
Biofilms can be described as large, amorphous aggregates of bacterial cells encased in extracellular material comprising inter alia, bacterial by-products, polysaccharides and proteins [12]. Biofilms may form on abiotic surfaces, such as implanted medical devices as well as biotic surfaces, such as host tissue [12, 39]. The formation of biofilms can be visualized as being a four-step process: (i) the attachment of bacteria to the surface; (ii) proliferation of the bacterial cells; (iii) biofilm growth and maturation; and finally (iv) dissociation and dissemination of bacterial cells to new sites [12, 39].
The formation of biofilms affords bacterial cell protection from a multitude of chemical, cellular and physical antagonists [143]. The bacteria encased in biofilms are able to tolerate significantly higher concentrations of antimicrobials and disinfectants than free-floating bacterial cells [39, 143, 144]. Furthermore, the bacterial cells residing in biofilms are more resistant to phagocytosis and are protected from pH extremes and physical desiccation [143]. The protective effect of biofilms is in part attributable to the physiological changes that the bacterial cells undergo whilst growing en masse. Bacteria existing within biofilms grow more slowly than exponential-phase bacteria [143]. This is partly due to restricted diffusion of gases and nutrients within the biofilm environment, but this is also affected by alterations in bacterial gene expression [145]. Beenken and co-workers [145] revealed a change in the expression of 580 genes (more than 20% of the genome) when using microarrays to study differences between S. aureus cells growing in biofilm and planktonic cultures.
The close contact between bacterial cells residing in biofilm communities facilitates and promotes the exchange of MGEs [146]. The horizontal transfer of plasmids in biofilms is typically higher than observed between cells existing in a planktonic state and, in fact, studies have shown that biofilms promote plasmid stability and may enhance the host range of MGEs [146]. As previously discussed, the exchange of MGEs plays a significant role in the emergence of new, potentially more virulent, staphylococcal strains.
7.2. Intracellular persistence and the formation of small-colony variants
The ability of staphylococci to persist intracellularly in non-professional phagocyctic cells following ingestion affords protection to the bacteria from the host immune system as well as the action of antimicrobials [12]. The adaptation to an intracellular environment is accompanied by the formation of ‘small-colony variants’ (SCVs), which represent an alternate phenotypic and metabolic state of the normal, wild-type, staphylococcal phenotype [12, 147]. The SCV phenotype is characterized by a reduced growth rate as well as substantial changes in gene expression [12]. The altered phenotypic state also affects the susceptibility of the bacteria to antimicrobials [144]. In addition to phagocytes, internalization of S. epidermidis in human endothelial cells and bone cells has been demonstrated [12].
The formation of biofilms and small-colony variants is implicated in persistent and relapsing infections, and, as such, it poses a significant challenge for the treatment staphylococcal infections [12, 147].
8. Use of antimicrobials in animal health and food animal production operations and implications for human health
Antimicrobials are used in animal health and food production to treat and prevent disease and, more contentiously, for growth promotion in food production animals [148, 149]. The volume of antimicrobials used in animals is larger than the volumes used in human medicine even in countries where strict regulations regarding antimicrobials are enforced [148]. Exact data on antimicrobial consumption in animals are scarce and only available for a few countries [148]. Recent data from the USA suggest that almost 80% of antimicrobials produced are used in food-producing animal operations [150–152] and 70% hereof are used for non-therapeutic purposes [153, 154]. The largest users of antimicrobials are typically the poultry and swine producers due to the intensive nature of these production systems [155].
The use and administration of antimicrobials in companion animals (cats, dogs and horses) fall largely under the control of veterinary practitioners [148, 156]. Individual animals are examined and diagnosed, following which the appropriate therapeutic recourse is selected [148, 156]. In the event that antimicrobials are administered, this is done in accordance with the manufacturer’s recommendations ensuring the prudent use of antimicrobials [148]. In contrast, the use of antimicrobials in food production animals (livestock and poultry) is often done with little or no veterinary consultation [148]. Many antimicrobials are accessible to producers as ‘over-the-counter’ remedies from local retailers, thereby limiting the control over the use of these products [148, 157]. In food production animals, antimicrobials may be applied therapeutically to treat sick individuals, but it is more common for producers to apply antimicrobials to entire herds or flocks in order to treat sick animals and to curb the spread of infectious organisms to healthy animals [148, 156]. The administration of antimicrobials in this manner is termed metaphylaxis [148, 158].
In food production systems, antimicrobials are often intentionally administered to animals in sub-therapeutic doses to promote growth and enhance feed efficiency [148]. The benefits of using antimicrobials as ‘growth promoters’ were recognized as early as the 1940s [149, 158]. Researchers observed that poultry that were administered vitamin B12 in the form of crude Streptococcus aureofaciens fermentations showed improved growth compared to birds given purified vitamin B12 [159]. It was speculated that the crude fermentations contained an unidentified growth factor, which enhanced growth [158]. The growth factor in the fermentation product was subsequently identified as chlortetracycline [158]. Shortly after this observation, the US Food and Drug Administration (FDA) approved the inclusion of certain antimicrobials into animal feed to enhance animal growth and production as well as prevent disease [158]. Some of the antimicrobials which have been utilized as growth promoters in some countries include: avilamycin (everninomycin), avoparcin (glycopeptide), bacitracin (polypeptide), bambermycin (glycolipid), carbadox and olaquindox (quinoxalines), lincomycin (lincosamides), pencillin (β-lactams), streptomycin (aminoglycosides), tetracycline and chlortetracycline (tetracyclines), tylosin and spiramycin (macrolides) and virginiamycin (streptogramin) [156, 159, 160].
The use of antimicrobials in animals, particularly as growth promoters in food producing animals, has been subjected to intense scrutiny and is frequently criticized as a driving force behind the emergence, maintenance and horizontal transfer of antimicrobial-resistant determinants in bacteria [161, 162]. The principle concern is the potential zoonotic transmission of antimicrobial-resistant pathogenic and non-pathogenic bacteria to humans either through direct contact with animals or indirectly through contact with the animals’ environment or through the food chain [161, 163]. Due to public concerns and increasing scientific evidence, stricter regulations regarding the use of growth promoters have been implemented [164]. The European Union began phasing out the use of antimicrobials for growth promotion in the late 1990s [163]. By the year 2000, Denmark had successfully implemented a complete ban of antimicrobial growth promoters in food animal production [157, 160]. Stakeholders in favor of restrictions have argued that in countries like Denmark, where bans have been introduced, there has been a concomitant decrease in antimicrobial resistance in animal and human bacterial isolates [164]. Opponents to the ban of growth promoters have, however, questioned the evidence provided by supporters of the ban and have argued that a decline in the use of growth promoters will negatively affect productivity and animal health, which will in turn lead to an increase in the therapeutic use of antimicrobials [149, 164]. A number of excellent reviews have examined the complexity and debate surrounding the use of growth promoters in livestock production, and the reader is referred to these texts for further information [148, 149, 157, 165–167].
9. The interface between human and animal populations
The dynamics of staphylococcal antimicrobial resistance and bacterial transmission at the human–animal interface will be considered separately for companion animals (cats, dogs and horses) and food production animals (livestock and poultry). Consideration will also be given to the intersection of humans and animal carcasses further along the food chain in the abattoir.
9.1. Companion animals
It is common in developed countries for humans to own companion animals [126]. Due to the close contact between humans and their pets, the opportunity for the transmission of bacteria between hosts is high [126]. Numerous reports have documented the transmission of MRSA strains between humans and dogs [168–174], humans and cats [175, 176] and humans and horses [177, 178]. Bacterial transmission of MRSA leads to both hosts becoming colonized, which places the hosts at a higher risk of being infected by the colonizing strain when the opportunity presents [78]. Furthermore, the colonized hosts serve as reservoirs of MRSA for other members of the household [179, 180].
Molecular genotyping of MRSA isolates recovered from companion animals has revealed that the S. aureus strains recovered from colonized and infected animals usually belong to clonal complexes implicated in human infections [126, 171, 173, 174, 177, 181, 182]. An investigation conducted in the United Kingdom examined the occurrence and the genetic relatedness of MRSA recovered from veterinary personnel and hospitalized animals in a small animal hospital [171]. Eighty-two percent (23/28) of the MRSA isolates recovered from the nasal mucosa of staff, hospitalized dogs and the environment were genetically related to EMRSA-15 (ST22), the predominant MRSA clone responsible for nosocomial infections in the United Kingdom [171]. In the USA, the most common MRSA clone recovered from companion animals is the ST5 clone, which is also the most common HA-MRSA clone in humans [171]. These data have suggested that the transmission of MRSA usually occurs from the human host to their respective pet [78, 179].
In general, prevalence studies seem to suggest that MRSA colonization amongst healthy pets is low [126, 176]. Higher MRSA colonization rates have been documented amongst companion animals in settings like animal shelters and veterinary hospitals [126, 171, 183]. Presumably, due to the relatively low MRSA colonization of companion animals there is currently no significant evidence indicating that pet owners are at an increased risk of MRSA colonization or infection compared with humans who do not own pets [107]. However, it is suggested that the lack of evidence may be partly attributed to the paucity of studies examining this particular aspect of animal ownership [107].
Since 2006, there has been a significant increase in the number of documented cases involving the isolation of methicillin-resistant S. pseudintermedius (MRSP) strains from surgical wound infections of dogs and cats [79]. A few studies have reported the occurrence of indistinguishable strains of MRSP from humans and their canine companions [176] and amongst animals and workers in veterinary clinics [184]. In Japan, a study investigating the prevalence of MRSP in a veterinary teaching hospital, cultured MRSP from 17 dogs and a staff member [25]. The isolate recovered from the employee had an antimicrobial susceptibility pattern and a PFGE profile similar to isolates recovered from dogs handled at the facility, indicating zoonotic transmission [25]. A study investigating the prevalence of MRSP in staff working at a veterinary dermatology practice reported that 5.3% (9/171) of the staff tested positive [185]. In general, owners of infected pets and veterinarians handling infected animals seem to have a higher risk of being MRSP positive [79]. In all documented cases, MRSP-positive individuals have been asymptomatic [79].
9.2. Food production animals
Livestock and poultry production has, over the past few decades, intensified in order to keep abreast with the food demands posed by a burgeoning human population [138, 148]. Larger numbers of animals are maintained under confined conditions in order to maximize productivity and improve profit margins. Accompanying these changes in farming practices has been an increase in the use of antimicrobials as well as increase in the proximity in which animals and humans co-exist [137, 138]. The close proximity of animal and human hosts has in turn increased opportunities for the transmission and exchange of microbial flora [56, 138]. It is well established that individuals such as farmers, veterinarians, farm laborers and abattoir workers working in close contact with animals have a greater risk of being colonized or even infected with zoonotic bacteria carried by animals than individuals that do not interact with animals [31]. The relatively recent description of zoonotic LA-MRSA ST398 and the novel methicillin resistance gene, mecC, has once again highlighted the implications associated with the horizontal transmission of pathogenic bacteria between animal and human hosts and the role of animals in the epidemiology and the evolution of human disease [118, 186].
Since the description of LA-MRSA, a plethora of studies have been conducted to estimate the prevalence of MRSA in different food animals, and a number of reviews have been published [14, 31, 107, 125]. Livestock-associated MRSA has been extensively described in pig production systems with many investigations documenting the transmission of CC398 between animals and close human contacts [187–193]. A study conducted in Germany found 86% (97/113) of people who worked with pigs to be asymptomatic carriers of CC398 MRSA [190]. Interestingly, in the same study, sampling of the family members of CC398 MRSA carriers showed that 4.3% (5/116) of these individuals, who had no direct exposure to pigs, were colonized by the same MRSA strain [190]. Nasal colonization was also found in 45% (22/49) of veterinarians frequenting pig farms in the study area and in 9% (4/44) of their family members who had not been exposed to pigs [190]. A pilot study conducted in two large pig production systems in the USA revealed an overall MRSA prevalence of 49% (147/299) in the animals sampled and 45% (9/20) of the farm workers [194]. All MRSA isolates belonged to ST398 [194]. In Belgium, 37.8% (48/129) of close human contacts sampled from 50 pig farms were found to be colonized by MRSA ST398 [191]. An identical MRSA strain was recovered from the skin lesions of one worker who was sampled at the time of the study [191]. In some geographical settings, other MRSA clones have been found to colonize pigs. In China, MRSA strains belonging to ST9 were commonly isolated from pigs and close human contacts [195, 196]. In Italy, pigs sampled at abattoirs were found to be colonized by MRSA ST9, ST(CC)97 and ST398 [197]. Further, the presence of human-associated CA-MRSA t127, ST1 and SCCmec type V was detected [197]. Despite the high rate of LA-MRSA colonization in pigs, this S. aureus clone has only been implicated in sporadic clinical infections in pigs [107]. Livestock-associated MRSA has been isolated from skin infections such as exudative epidermidis and infections of the urogenital tract and the uterus and mammary gland of pigs [14].
In the Netherlands, MRSA ST398 colonization has been documented in veal calves and close human contacts [131]. From the 102 farms sampled in one study, MRSA was isolated from animals on 88% (90/102) of the farms investigated [131]. Overall, 28% (602/2151) of the animals and 33% (32/97) of the farmers sampled tested positive for MRSA [131]. The MRSA strains recovered from the human and animal samples included ST398 as well as ST5, ST15, ST45 and CC34 from the human specimens and ST97, ST239, ST1159 and CC425 from the calves [131]. The data clearly demonstrated that MRSA colonization of human contacts was strongly associated with the intensity of animal contact and with the number of MRSA-positive animals on the farm [131]. Furthermore, a direct correlation was observed between MRSA prevalence and farm hygiene practices [131].
In dairy cattle operations, LA-MRSA ST398 has been isolated from clinical and subclinical milk samples. One of the first reports, emanating from Belgium, recovered LA-MRSA from 9.3% (11/118) of the dairy farms surveyed [198]. The prevalence on positive farms varied between 3.9% and 7.4% [198]. Methicillin-resistant S. aureus ST398 has also been reported from dairy herds in Germany [199] and Switzerland [61, 200]. Juhász-Kaszanyitzky and co-workers [201] published the first report documenting the transmission of MRSA between dairy cows with mastitis and a close contact worker on the farm. In this study, identical MRSA strains, belonging to MLST ST1, were recovered from both animal and human hosts. The direction of transmission, from bovine to human or human to bovine could, however, not be established [201].
One of the first reports of LA-MRSA in poultry emerged following a study conducted in Belgium [130]. The researchers reported that 12% (10/81) of the S. aureus isolates recovered from the nasal and cloacal swabs of healthy broiler chickens belonged to spa types associated with CC398 [130]. A further study in Belgium identified a new spa type, t1456, within CC398 following a random sampling of broiler farms [202]. Despite sporadic reports on the isolation of CC398 from poultry operations, the epidemiology of LA-MRSA in poultry is still unclear [14].
According to Schwabe [203], a zoonosis is described as a ‘shared infection’ of animals and man, without ascribing direction of transmission from one host to the other. Inasmuch as bacterial transfer and colonization, or infection, of humans are of significant concern to human medicine, the reverse scenario, which is often overlooked, warrants consideration. Humans may represent an important source of new bacterial strains, which can cause disease in livestock and, as such, pose a potential threat to food security [138]. Several molecular genotyping studies, which have traced the origins of epidemic S. aureus clones in human and animal hosts, have reported that the majority of host-switch events have involved the movement and adaptation of bacteria from human to animal hosts [62]. Both LA-MRSA ST398 and the major pathogenic S. aureus ST5 clone, responsible for lameness in poultry, have been shown to originate from humans but have now adapted and diversified to spread in animal hosts [58, 137].
Irrespective of the direction of bacterial transmission, it is of mutual benefit to both human and animal health that bacterial populations at the interface between different host species are monitored. Surveillance is therefore advocated in order to monitor changes in the epidemiology and virulence of bacterial strains and to enable appropriate pre-emptive measures to be taken [138].
9.3. Food animal products
The abattoir environment presents a dynamic interface between humans and animals largely due to the fact that abattoirs process large numbers of animals originating from different farms across a relatively broad geographic expanse. During slaughtering and subsequent processing, it is quite plausible for carcasses to become contaminated with staphylococcal strains originating from animals, abattoir workers or the environment [14]. Numerous reports have documented the occurrence of CA-MRSA, HA-MRSA and LA-MRSA strains from different meat products [14, 204, 205, 206]. An extensive study conducted in the Netherlands demonstrated the presence of LA-MRSA on a variety of raw meat products collected from retail outlets [204]. In this study, 11.9% (264/2217) of the raw meat products analyzed were found to be positive for MRSA [204]. It was further shown that 85% (224/264) of the MRSA strains belonged to spa types associated with CC398 [204]. A survey conducted in the USA found 39.2% (47/120) of the retail meat samples analyzed to be positive for S. aureus. Five percent (6/120) of the S. aureus isolates were resistant to methicillin. Molecular typing identified the isolates as belonging to the ST5 and ST8 lineages [205]. A similar survey conducted in Canada found 7.7% (31/402) of the meat samples analyzed contained MRSA [206, 207]. The three major sequence types obtained were ST5 (29%), ST8 (39%) and ST398 (32%) [206, 207].
The principal concern arising from the presence of MRSA in food is the development of food poisoning following ingestion of preformed staphylococcal enterotoxins [207]. The best preventative measure is to ensure the correct handling and storage of food to reduce the risk of enterotoxins being produced [207]. Another concern regarding the presence of MRSA on meat is that people may become colonized or infected from handling or eating contaminated meat [205, 207]. Regarding the latter, there is, at present, no substantial data to support or refute this concern. More intensive surveillance is needed to elucidate the true role of food contamination in the development of human diseases [107].
10. Monitoring antimicrobial resistance in staphylococci at the human–animal interface
In addition to direct contact between animal and human hosts, the transmission of antimicrobial-resistant bacteria and resistance genes may occur through a number of routes [76, 149]. Figure 3 presents some of the potential routes of bacterial transmission taking into consideration the role of the environment as well as aspects related to the movement of animals, food products and human contacts. The globalized trade of live animals and/or meat products is one of the features of modern food production systems, which has the potential to elaborate the impact of antimicrobial-resistant bacteria of animal origin [138].
In order to be able to accurately assess the impact of antimicrobial use in animal health and food production operations on human medicine, integrated surveillance programmes are needed [148]. The formulation and implementation of surveillance programmes require a concerted effort from role-players in multiple disciplines. Funding, infrastructure, political ‘buy-in’ and the support of several role-players are key to the success of these programs [148]. Currently, only a few countries have been able to implement successful monitoring programmes [148]. One of the longest running and most successful programmes is the Danish Integrated Antimicrobial Resistance Monitoring and Research Programme (DANMAP), which has been systematically collecting and analyzing data since 1995 [163]. The programme utilizes a ‘one-health’ approach and entails the monitoring of the entire food chain from ‘farm to fork to sickbed’ [208]. The objectives of DANMAP are summarized as follows:
to monitor the use of antimicrobial agents in food animals and humans;
to monitor the occurrence of antimicrobial resistance in bacteria isolated from food animals, food of animal origin and humans;
to study associations between antimicrobial consumption and antimicrobial resistance; and
to identify routes of transmission of resistant bacteria and/or resistance determinants and areas for further research [163, 208].
Results from DANMAP are reported annually and are accessible online [163]. The data accumulated from long-term surveillance programmes should enable resistance trends to be monitored over periods of time as well as identify emerging problems so that adequate intervention strategies can be implemented [148, 208].
In accordance with Office International des Epizooties (OIE) guidelines, surveillance programmes should investigate antimicrobial resistance in the following groups of bacteria:
Human and animal pathogens that cause infections. These bacteria are thought to reflect resistance caused by the use of antimicrobials in the respective reservoirs.
Zoonotic bacteria that can develop resistance in the animal reservoir and which can be transmitted to humans via direct contact or consumption of contaminated food. These bacteria may subsequently compromise treatment when causing infection in humans.
Sentinel or indicator bacteria, such as enterococci and Escherichia coli, are selected for monitoring purposes due to their ubiquity in animals, foods and humans. Furthermore, these bacteria readily develop or transfer antimicrobial resistance in response to selective pressure in both human and animals and are considered reservoirs of resistance determinants [148, 208, 209].
The staphylococci of animal origin which are commonly monitored as part of surveillance programmes include S. aureus and coagulase-negative staphylococci from bovine mastitis cases as well as S. hyicus isolates from cases of exudative epidermitis in pigs [148, 163]. From human health laboratories, S. aureus isolates derived from blood, urine and CSF samples are used for surveillance purposes [208, 209]. Some surveillance programmes, such as the British Society for Antimicrobial Chemotherapy Resistance Surveillance project, extend monitoring to include CNS species [209].
11. Evaluating the antimicrobial susceptibility of staphylococcal isolates
In a clinical context, evaluating the antimicrobial susceptibility of bacterial isolates is an important aid for practitioners needing to make decisions regarding the appropriate therapeutic treatment of infected patients [88]. Antimicrobial susceptibility testing of bacterial isolates also provides essential data for surveillance programs as previously discussed. Several methodologies exist for evaluating the in vitro susceptibility of bacterial isolates to different classes of antimicrobials. The two principal methods used are agar disk diffusion and the broth micro-dilution minimum inhibitory concentration (MIC) method [148, 210]. The agar disk diffusion method provides qualitative results that categorize isolates as susceptible, intermediate or resistant to the antimicrobial(s) under evaluation [135, 210]. The method is relatively cost-effective and flexible with respect to the panel of antimicrobials that can be selected for testing [135]. The MIC method may be performed in a variety of formats ranging from in-house prepared plates or broths to commercially available micro-dilution plates or gradient strips [210]. The MIC method provides a quantitative result expressed in micrograms per milliliter as well as a categorization of the bacterium as susceptible or resistant [135, 210]. Since the method is able to quantify antimicrobial susceptibility, the MIC is the preferred method for use in surveillance or epidemiological programs [148].
Irrespective of the test methodology selected, it is imperative that all antimicrobial susceptibility tests are conducted in accordance with the international standard being followed, namely the Clinical Laboratory Standards Institute (CLSI), the European Committee on Antimicrobial Susceptibility Testing (EUCAST) or other recognized national standards [210]. Furthermore, it should be ensured that all of the appropriate quality control measures advocated by the standard are implemented and rigorously followed [210].
In vitro methods for analyzing the antimicrobial susceptibility do not take into consideration the protective effect afforded by biofilm growth, which commonly occurs during the course of staphylococcal infections [143]. Due to the protective environment afforded by biofilm growth and the accompanying changes in bacterial physiology, bacterial cells growing in biofilms are typically able to tolerate antimicrobial concentrations 10-fold to 1000-fold higher than planktonic bacterial populations [143]. A few methods have evolved to investigate the antimicrobial susceptibility of isolates growing in biofilms, with the commercially available method from Innovotech Inc. (Edmonton, Canada) gaining wide acceptance. The Innovotech MBECTM P&G system is a uniquely designed microtiter plate with 96 identical pegs protruding from the plastic lid (Innovotech Inc., 2012). The system facilitates the generation of 96 identical biofilms on the pegs which can be subjected to varying concentrations of antimicrobial or disinfectant to calculate the minimum biofilm eradication concentration (MBEC) and MIC values for each test isolate (Innovotech Inc., 2012). The Innovotech MBECTM P&G system (formerly called the Calgary biofilm device) has been used in a number of applications to examine the effect of different chemicals on staphylococcal biofilms [211–215].
11.1. Detection of antimicrobial resistance genes in staphylococcal isolates
A complementary approach to phenotypically evaluating the susceptibility of staphylococcal isolates is to screen test isolates for specific antimicrobial resistance genes using molecular assays, such as PCR and real-time PCR [24, 216]. This approach is still only infrequently used in routine clinical diagnostic work, but from a research perspective, molecular screening has provided a wealth of information with respect to the distribution and spread of resistance genes amongst bacteria [88].
An obstacle to using DNA-based assays for resistance testing is the formidable complexity of resistance mechanisms that exist [217]. It is common for resistance to an antimicrobial to involve multiple genes and, in some cases, not all of the mechanisms involved have been identified [217]. The use of microarrays is one manner in which this limitation has been overcome [216]. Microarray analysis enables bacterial isolates to be simultaneously screened for a large number of gene targets [216]. A DNA microarray consists of an orderly arrangement of DNA probes which have been spotted onto a solid support, such as a silicon chip, glass slide or nylon membrane [216]. Bacterial DNA or cDNA is labelled with a fluorescent dye and allowed to hybridize to the microarray [216]. One of the microarrays currently available commercially, the StaphyType Kit (Alere Technologies, Jena, Germany) permits the simultaneous screening of 334 S. aureus gene targets. In addition to screening for a multitude of antimicrobial resistance genes, the kit screens bacterial isolates for species-specific gene markers, toxin-encoding genes and genes encoding specific tissue-binding proteins [218].
12. Epidemiological molecular typing systems for staphylococci
Bacterial typing is important for both clinical and epidemiological investigations to determine the source(s) of infection, routes of transmission in disease outbreaks or the analysis of the genetic relatedness or specific characteristics of bacterial strains [219]. A number of different typing techniques have been developed, each with specific advantages and drawbacks. It is therefore imperative that the most appropriate method, or combination of methods, be selected depending on the purpose of the investigation on hand [219].
Pulsed-field gel electrophoresis is a highly discriminatory technique and is considered to be the ‘gold standard’ for typing S. aureus isolates of both human and animal origin [14]. Pulsed-field gel electrophoresis is also the recommended strain typing technique for S. epidermidis and other CNS [220]. Pulsed-field gel electrophoresis detects rapidly accumulating genetic variation and is therefore useful for distinguishing strains for the investigation of an outbreak or for examining the phylogeny of a small bacterial population [60]. The PFGE technique is based on the digestion of bacterial DNA with restriction enzymes that cleave specific recognition sites along the chromosome [221]. The restriction enzyme digestion generates a number of DNA fragments, which are resolved by electrophoresis in an electric field, which is pulsed at different angles across the gel. The resulting banding patterns are analyzed using specific software and interpretations made according to the criteria of Tenover and co-workers [222]. The principal drawbacks of this technique are the fact that this method is technically demanding and time consuming and requires several days before results are available [223]. Furthermore, specialized equipment is required to perform the gel electrophoresis [122, 223]. Inter-laboratory reproducibility of results has also been problematic, making the comparison of data generated by different laboratories quite difficult [122].
Multilocus sequence typing (MLST) is a sequence-based genotyping method, which is performed by sequence analysis of approximately 450-bp internal fragments of seven housekeeping genes [224]. The DNA sequences for each locus are assigned distinct allele identification numbers, and the combination of the numbers defined for all loci is used to generate the sequence type (ST) [33, 122]. Isolates that have identical sequences at all seven loci are considered a clone, whereas sequence types that differ by single nucleotide polymorphisms at fewer than three loci are considered closely related and are grouped in clonal complexes (CC) [14, 33]. In contrast to PFGE, MLST indexes genetic variations that accumulate slowly over time [125]. Multilocus sequence typing is, therefore, better suited to measure evolutionary changes over a relatively long time span and is the best method for studying the global epidemiology and frequency of specific bacterial lineages [60, 125]. The method is highly discriminatory and has the distinct advantage of enabling results from other laboratories and studies to be compared using the Internet [122, 224]. At present, the greatest limitation to using MLST is the high cost associated with the sequencing of multiple gene loci [125].
Typing of the spa gene is also widely used for the epidemiological study of S. aureus isolates [1]. The spa gene encodes protein A, an important virulence factor of S. aureus [225]. The typing method entails the DNA amplification and sequencing of a polymorphic 24-bp variable-number tandem repeat (VNTR) within the coding region of the spa gene followed by the assessment of the data using a central online server. Typing of the spa gene has been found to be a suitable typing method for conducting both local and global epidemiological studies [226]. This method has been found to have a greater discriminatory power than MLST but it is less discriminatory than PFGE [122, 227, 228]. Since spa typing involves the sequencing of only a single locus compared with MLST, it is cheaper, less laborious and less time consuming to perform [125, 228]. A potential problem, however, is that unrelated lineages can sometimes contain similar spa types [125].
Typing of the SCCmec element is one of the most important epidemiological tools for studying methicillin-resistant staphylococci [228]. A number of multiplex PCR and real-time PCR assays have been developed to classify the different SCCmec types and subtypes [229–234]. An overview of the scope and drawback of various SCCmec typing methods, which have been developed, can be found elsewhere [91]. At present, there is no universally accepted assay which can identify and differentiate all of the mec types and subtypes [122]. Furthermore, since the described PCR assays target different regions of the SCCmec element, it is not uncommon for discrepant results to be obtained when different methods are used to test the same isolates [228].
13. Concluding remarks
Staphylococci are ubiquitous in the environment and occur commensally on the skin and mucous membranes of humans and animal hosts. The genetic flexibility of bacteria in this genus, particular S. aureus, is the primary evolutionary driving force behind the emergence of new strains exhibiting enhanced virulence and antimicrobial resistance. The use of antimicrobials in animal health and food animal production operations has been implicated as a driving force behind the development of antimicrobial-resistant bacteria, which can transfer to humans through direct contact or indirectly through the food chain or environment. However, much of the evidence put forward to corroborate the argument against the use of antimicrobials in food animal production operations is tenuous and, if anything, it supports the need for further surveillance data. The implementation and maintenance of national and international integrated antimicrobial resistance surveillance systems are required. Through active monitoring, potential problems can be identified and appropriate guidelines and policies put in place to ensure the longevity of clinically important antimicrobials.
\n',keywords:"Staphylococci, Antimicrobial Resistance, MRSA, LA-MRSA, Animals",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/49455.pdf",chapterXML:"https://mts.intechopen.com/source/xml/49455.xml",downloadPdfUrl:"/chapter/pdf-download/49455",previewPdfUrl:"/chapter/pdf-preview/49455",totalDownloads:1938,totalViews:765,totalCrossrefCites:1,totalDimensionsCites:1,hasAltmetrics:0,dateSubmitted:"December 3rd 2014",dateReviewed:"October 19th 2015",datePrePublished:null,datePublished:"November 26th 2015",dateFinished:null,readingETA:"0",abstract:"The widespread and often indiscriminate use of antimicrobials in animals is considered an important driving force behind the emergence and spread of antimicrobial-resistant bacteria. The emergence of livestock-associated methicillin-resistant Staphylococcus aureus and the description of a novel methicillin-resistant gene, mecC, have renewed concerns regarding the role of animals as reservoirs and a source for the evolution of novel, virulent zoonotic pathogens. The transfer of antimicrobial-resistant bacteria residing in, or on, animals to close human contacts or the introduction of the bacteria into the food supply chain is a cause for concern. The purpose of this mini-review is to provide a background to the genus Staphylococcus and the emergence of antimicrobial resistance as well as a discussion on the most significant antimicrobial resistance mechanisms. The use of antimicrobials in animal husbandry is discussed and the interface between humans and different animal populations is closely examined. Finally, the need for antimicrobial monitoring programmes is discussed and is supplemented with information pertaining to antimicrobial susceptibility testing and molecular typing of staphylococcal isolates.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/49455",risUrl:"/chapter/ris/49455",book:{slug:"antimicrobial-resistance-an-open-challenge"},signatures:"Tracy Schmidt, Marleen M. Kock and Marthie M. Ehlers",authors:[{id:"82278",title:"Prof.",name:"Marthie",middleName:null,surname:"Ehlers",fullName:"Marthie Ehlers",slug:"marthie-ehlers",email:"marthie.ehlers@up.ac.za",position:null,institution:{name:"University of Pretoria",institutionURL:null,country:{name:"South Africa"}}},{id:"82606",title:"Dr.",name:"Marleen",middleName:null,surname:"Kock",fullName:"Marleen Kock",slug:"marleen-kock",email:"marleen.kock@up.ac.za",position:null,institution:{name:"University of Pretoria",institutionURL:null,country:{name:"South Africa"}}},{id:"175149",title:"Ph.D. Student",name:"Tracy",middleName:null,surname:"Schmidt",fullName:"Tracy Schmidt",slug:"tracy-schmidt",email:"tracy.schmidt@kzndard.gov.za",position:null,institution:{name:"University of Pretoria",institutionURL:null,country:{name:"South Africa"}}}],sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_2",title:"2. The genus Staphylococcus",level:"1"},{id:"sec_2_2",title:"2.1. Classification of staphylococci",level:"2"},{id:"sec_3_2",title:"2.2. General characteristics of staphylococci",level:"2"},{id:"sec_5",title:"3. Genomic organization and genetic flexibility of S. aureus",level:"1"},{id:"sec_5_2",title:"3.1. Host specificity and host switching of S. aureus",level:"2"},{id:"sec_7",title:"4. Staphylococcal infections in humans",level:"1"},{id:"sec_8",title:"5. Staphylococcal infections in animals",level:"1"},{id:"sec_9",title:"6. Antimicrobial resistance in staphylococci",level:"1"},{id:"sec_9_2",title:"6.1. The emergence of resistance in S. aureus",level:"2"},{id:"sec_10_2",title:"6.2. Mechanism of penicillin resistance in staphylococci",level:"2"},{id:"sec_11_2",title:"6.3. Mechanism of methicillin resistance in staphylococci",level:"2"},{id:"sec_11_3",title:"6.3.1. Healthcare-associated MRSA",level:"3"},{id:"sec_12_3",title:"6.3.2. Community-associated MRSA",level:"3"},{id:"sec_13_3",title:"6.3.3. Livestock-associated MRSA",level:"3"},{id:"sec_15_2",title:"6.4. Mechanisms of vancomycin resistance in staphylococci",level:"2"},{id:"sec_17",title:"7. Alternate bacterial strategies to circumvent the action of antimicrobials",level:"1"},{id:"sec_17_2",title:"7.1. The formation of biofilms",level:"2"},{id:"sec_18_2",title:"7.2. Intracellular persistence and the formation of small-colony variants",level:"2"},{id:"sec_20",title:"8. Use of antimicrobials in animal health and food animal production operations and implications for human health",level:"1"},{id:"sec_21",title:"9. The interface between human and animal populations",level:"1"},{id:"sec_21_2",title:"9.1. Companion animals",level:"2"},{id:"sec_22_2",title:"9.2. Food production animals",level:"2"},{id:"sec_23_2",title:"9.3. Food animal products",level:"2"},{id:"sec_25",title:"10. Monitoring antimicrobial resistance in staphylococci at the human–animal interface",level:"1"},{id:"sec_26",title:"11. Evaluating the antimicrobial susceptibility of staphylococcal isolates",level:"1"},{id:"sec_26_2",title:"11.1. Detection of antimicrobial resistance genes in staphylococcal isolates",level:"2"},{id:"sec_28",title:"12. Epidemiological molecular typing systems for staphylococci",level:"1"},{id:"sec_29",title:"13. Concluding remarks",level:"1"}],chapterReferences:[{id:"B1",body:'Mathema B., Mediavilla J., Chen L., Kreiswirth B. Evolution and taxonomy of Staphylococci. In: Crossley D., Jefferson K., Archer G., Fowler V., editors. Staphylococci in Human Disease. 2nd ed. Singapore: Wiley-Blackwell; 2009. pp. 31–64.'},{id:"B2",body:'Kloos W., Bannerman T. Staphylococcus and Micrococcus. In: Murray P., Baron E., Pfaller M., Tenover F., Yolken R., editors. Manual of Clinical Microbiology. 7th ed. Washington: American Society of Microbiology; 1999. pp. 264–282.'},{id:"B3",body:'Cunha M., Calsolari M. 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Molecular techniques for MRSA typing: current issues and perspectives. The Brazil Journal of Infectious Diseases. 2003; 7: 32–43.'},{id:"B222",body:'Tenover F.C., Arbeit R.D., Goering R.V., Mickelsen P.A., Murray B.E., Persing D.H., et al. Interpreting chromosomal DNA restriction patterns produced by pulsed field gel electrophoresis: criteria for bacterial strain typing. Journal of Clinical Microbiology. 1995; 33(9): 2233–2239.'},{id:"B223",body:'Weller T. Methicillin-resistant Staphylococcus aureus typing methods: which should be the international standard? Journal of Hospital Infection. 2000; 44: 160–172.'},{id:"B224",body:'Enright M.C., Day N.P.J., Davies C.E., Peacock S.J., Spratt B.G. Multilocus sequence typing for characterization of methicillin-resistant and methicillin-susceptible clones of Staphylococcus aureus. Journal of Clinical Microbiology. 2000; 38(3): 1008–1015.'},{id:"B225",body:'Wright, J.S. Virulence mechanisms in MRSA pathogenesis. In: Fluit A.C., Schmitz F.-J., editors. MRSA: Current Perspectives. Wymondham: Caister Academic Press.'},{id:"B226",body:'Koreen L., Ramaswamy S.V., Graviss E.A., Naidich S., Musser M.M., Kreiswirth B.N. spa typing method for discriminating among Staphylococcus aureus isolates: implication for use of a single marker to detect genetic micro-and macrovariation. Journal of Clinical Microbiology. 2004; 42(2): 792–799.'},{id:"B227",body:'Malachowa N., Saba A., Gniadkowski M., Krzyszton-Russjan J., Empel J., Miedzobrodzki J., et al. Comparison of multiple-locus variable-number tandem-repeat analysis with pulsed-field gel electrophoresis, spa typing, and multilocus sequence typing for clonal characterization of Staphylococcus aureus isolates. Journal of Clinical Microbiology. 2005; 43: 3095–3100.'},{id:"B228",body:'Deurenberg R.H., Stobberingh E.E. The evolution of Staphylococcus aureus. Infection, Genetics and Evolution. 2008; 8: 747–763.'},{id:"B229",body:'Oliveira D.C., de Lencastre H. 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Combination of multiplex PCRs for staphylococcal cassette chromosome mec type assignment: rapid identification system for mec, ccr, and major differences in junkyard regions. Antimicrobial Agents and Chemotherapy. 2007; 51: 264–274.'},{id:"B233",body:"Milheiriço C., Oliveira, D.C., de Lencastre H. Multiplex PCR strategy for subtyping the staphylococcal cassette chromosome mec type IV in methicillin-resistant Staphylococcus aureus: 'SCCmec IV multiplex'. Journal of Antimicrobial Chemotherapy. 2007; 60: 42–48."},{id:"B234",body:'Milheiriço C., Oliveira D.C., de Lencastre H. Update to the multiplex PCR strategy for assignment of mec element types in Staphylococcus aureus. Antimicrobial Agents and Chemotherapy. 2007; 51: 3374–3377.'}],footnotes:[],contributors:[{corresp:"yes",contributorFullName:"Tracy Schmidt",address:"Tracy.Schmidt@kzndard.gov.za",affiliation:'
Allerton Provincial Veterinary Laboratory, Pietermaritzburg, South Africa
Department of Medical Microbiology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa
'},{corresp:null,contributorFullName:"Marleen M. Kock",address:null,affiliation:'
Department of Medical Microbiology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa
Department of Medical Microbiology, National Health Laboratory Services, Tshwane Academic Division (NHLS/TAD), Pretoria, South Africa
'},{corresp:null,contributorFullName:"Marthie M. Ehlers",address:null,affiliation:'
Department of Medical Microbiology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa
Department of Medical Microbiology, National Health Laboratory Services, Tshwane Academic Division (NHLS/TAD), Pretoria, South Africa
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1. Introduction
1.1 Amaranthus sp. taxonomy and distribution
Amaranthus L. is a eudicot genus in the Amaranthaceae family of the order Caryophyllales and is commonly known as the pigweeds or amaranths. The genus comprises about 75 species, which are generally annuals, and are distributed throughout the world’s temperate and tropical regions [1, 2]. The genus Amaranthus is further divided into three subgenera, Acnida, Albersia, and Amaranthus [3], with Acnida being dioecious and subgenera Albersia and Amaranthus being monoecious but with distinctive floral morphology. The three main domesticated species of Amaranthus (Amaranthus caudatus L., A. cruentus L., and A. hypochondriacus L.) originated in the Americas and are primarily cultivated for grain, as potherbs and ornamentals [2, 4].
Amaranth is an ancient crop in which scientific and commercial interest has recently been renewed. The grain amaranths (A. hypochondriacus, A. caudatus, A. cruentus) have many favorable agronomic properties and are highly adaptable to various ecological zones, with better resistance to biotic and abiotic stresses than many conventional other food crops [2]. These species also have advantages of being protein-rich C4 pseudo-cereals that can be adapted to cultivation in a wide range of environments, with good tolerance of drought and salinity [2, 5]. Amaranths also exhibit superior water use efficiency compared to many other C3 and C4 crops [6].
1.2 Amaranth use in the ancient times
The grain amaranth was an important crop for the Aztecs and the Incas [1, 2]. In the pre-Columbian period, it was one of the major crops like beans and corn in the New World and carried religious importance [1]. During the various dates of the religious calendar, Aztec people ground amaranth seeds mixed with honey or human blood and make different shapes of animals, birds, mountains, and gods, and they were eaten during the ceremonies [1, 2].
Prior to the conquest by Spaniards, Mexicans had a culture where a ceremonial paste called Zoale was prepared from amaranth grains and was fed to the slaves before they were sacrificed to the gods [1, 7]. From the Christian viewpoint, the use of grain amaranth was the very symbol of heathen idolatry [1], and therefore Spaniards discouraged the cultivation of Amaranthus [1, 7]. Although the cultivation was highly suppressed by the Spanish conquistadors, small patches of A. hypochondriacus were still grown inside maize fields [1, 2].
Along with the widespread use in food products, grain amaranths also gained religious significance in India and Nepal. In Uttar Pradesh, India, the crop amaranth is recognized as Ramdana (seed given by Lord Ram) [7]. In the states of Madhya Pradesh and Gujarat, India, amaranth is recognized as Rajgira (Rajgira, a seed given by King, an incarnation of Lord Vishnu). In Hindu culture, popped amaranth grain is soaked in milk and is one of the food items permitted to be eaten during religious festivals after a long fasting [2, 7]. In different parts of Nepal, India, and Pakistan, popped amaranth seed is used to make laddoos and confections like alegria in Mexico. Laddoos carries an important religious significance. It is considered a pure food and can be offered to Hindu gods. Around the Nilgiri Hills in India, Badagas peoples have a ritual that they offer a basket of puffed amaranths on Badagas funeral pyre [7, 8]. Looking at those cultural instances, grain amaranths may have been migrated from the Americas to the Old World only about 500 years ago; but it is quite astonishing to get strong evidences on the connection of amaranth grain to Hindu culture in the Old World.
2. Nutritional facts of amaranths
2.1 Amaranth proteins
Based on the solubility and extractability, there are four major seed storage proteins in plants: albumins, globulins, prolamins, and glutelins. In pseudo-cereals, including amaranth, the major seed storage proteins are composed of albumin, globulin, and glutelin [9, 10, 11, 12, 13]. However, there are some reports showing traces of prolamins in some of the amaranth species [10, 12]. Storage proteins accumulate in developing seeds and store nitrogen, carbon, and sulfur [14]. These proteins are hydrolyzed and mobilized during seed germination and early seedling growth [14, 15]. They do not carry any enzymatic functions and are found only in seeds. However, some storage proteins may also be involved in defense or metabolism. These proteins are synthesized in the rough endoplasmic reticulum. As seeds mature, they are collected in the protein bodies that are derived from vacuole [15]. They may also act as a sink for excess nitrogen.
Chief distinction between the major proteins is outlined as follows: albumin storage proteins are water soluble with low molecular weight 10–18 kDa and low isoelectric point between pH 4.0 and 5.0 [16]. Based on the sedimentation coefficients (S20w), albumin has the coefficient of approximately 2S; therefore it is defined as 2S albumin [17]. However, in the case of pseudo-cereals, the sedimentation coefficients of 1.7S comprised of polypeptides with Mr. ranging from 4000 to 20,000, and they are high in sulfur-containing amino acids, including cysteine and methionine [17]. Majority of albumins consists of two polypeptide chains linked by four disulfide bonds [18]. They are found in dicot plants and account for 20–60% of the total proteins in seed [16]. Globulin storage proteins are soluble in salt with their molecular weights in the range of 150–190 kDa [16]. They have an isoelectric point of pH 5–10 [19]. Based on the sedimentation coefficients, (S20w), globulin has the coefficients ranging from 7S to 12S [16]. They lack cysteine residues and lack disulfide bonds [16]. Glutelin storage proteins are soluble in borate buffer but poorly soluble in water. They have molecular weights in the range of 45–150 kDa and an isoelectric point range between the pH range of 4.8 and 8.7 and are highly hydrophobic in nature [16]. They are high in proline and glutamine content [16]. One of the distinctive signal peptides that is distinguished from other storage proteins is the 37 amino acid sequence at the NH2 terminus that is followed by 269 amino acid acidic subunit (Mr = 32,489) and a 193 amino acid basic unit (Mr = 19,587) [20].
2.2 Lysine content
Amaranth grain and leaves are popular for their nutritional value. Protein content is about 15% in grains [21], and it has a well-balanced amino acid composition with high lysine content [22]. Lysine is the limiting amino acid in most of the cereal crops including wheat, sorghum, and rice, but it is abundant in amaranth; only the first limiting amino acid in amaranth is leucine [21], and it is also abundant in most of our staple food sources. Therefore, amaranth is considered as a complete protein supplier when it is consumed with another cereal.
2.3 Seed properties and nutrient content
Grain amaranth plant produces millions of seeds that are small (≈1 mm) in diameter and has not been analyzed for detailed morphological features [23, 24]. The color of the seeds is highly variable from white, gold, brown, and pink to black [24]. Coons [25] reported that black color is dominant over white and a single gene controls the inheritance. It is possible that the seed coat colors, perisperm type, and seed shape in Amaranthus species are controlled by different gene loci. Seed shape changes based on angle of view; in lateral view seeds appear lenticular in shape, and in front view seeds appear circular or obovate [23]. Adhikary [24] reported white-vitreous and white-opaque type of seeds. Although seed shape and size may not have a significant impact in the nutrient content of a seed, some pigmented seeds have been reported to contain different amounts of nutrient components. For instance, [21] reported that pale-colored seeds of A. caudatus contain about 14% of protein, 10% of fat, 64% of starch, and 8% of dietary fiber, while black-pigmented seeds were reported to contain 16% of dietary fiber, with lysine concentration ranged between 5.2 and 6.0 g/16 g N in the grains [21]. Moreover, protein digestibility was found to be higher in pale seeds than in the black seeds [21].
Starch is formed by two glucan polymers, amylose and amylopectin [26], and is stored in the perisperm of amaranth seed [27]. Like the grasses, amaranth starch can be classified as either glutinous (waxy) or non-glutinous (starchy) [27]. Non-glutinous (starchy) seeds contain both amylose and amylopectin, and glutinous (waxy) seeds lack amylose [24, 26]. Both perisperm forms are found in all three species of the grain Amaranthus [26]. Amaranth seeds contain 65–75% of starch [28], and the digestibility of cooked amaranth seeds resulted in a similar response to white bread; however, flaked and roasted seeds responded with a slightly increased glycemic response [29, 29].
2.4 Squalene content
Squalene is a unique triterpene compound that has a biological and pharmacological importance. Although squalene is an intermediate product in the cholesterol biosynthesis process [30], earlier work has predicted that daily consumption can decrease cholesterol levels [31]. It can inhibit chemically induced breast and colon cancer [32]. There are also evidences of a lower frequency of heart diseases in the Mediterranean region [33], as people in this region consume more olive oil, which is rich in squalene [34]; thus it is believed that squalene consumption in the diet has a positive impact on human health. It originates partly from cholesterol synthesis process and partly from dietary sources such as plant oils or shark liver. Among the different types of plant oils, oil extracted from olive and amaranth has a higher concentration of squalene [34, 35]. Especially, grain amaranths have been suggested as an alternative natural source of squalene. The chemical content in five different accessions of A. cruentus was reported in the range of 2.26–5.67% [36]. Furthermore, in other domesticated species, [37] reported 3.6% in A. hypochondriacus and 6.1% in A. tricolor.
2.5 Gluten-free grain
Amaranthus is a gluten-free grain [38], and hence it is a suitable diet for a person with celiac disease (CD) [39, 40]. CD is an autoimmune condition or inflammatory disease, which affects the small intestine triggered by the gluten protein [41, 42] and can lead to weight loss, fatigue, malabsorption, abdominal pain, vomiting, and diarrhea [43]. The main sources of gluten protein are wheat, barley, and rye [42]. CD patients must follow a strict gluten-free diet, and this can potentially lead to nutrient deficiency [43]. Generally, gluten-free products are made with refined flours and starch and require specific packaging material and frequent use of chemical preservatives [44, 45]. This makes a challenge for both producer and consumer. One of the biggest challenges for food technologist is to enrich the nutritional value of gluten-free products with balanced dietary fibers and proteins [44, 46]. Hence, amaranths can be an alternative to address the challenge. In fact, amaranth has become one of the greatest supplements in gluten-free food commodities to enhance nutritional values [47]. Amaranth contains similar macronutrients as wheat and 2–3 times higher than other gluten free crops [42]. Seed protein of amaranth is greater than cereals and legumes [22]. Besides, amaranth has higher lysine and starch than in other cereals [40]. Monosaccharide composition of dietary fiber present in amaranth is well known [48, 24], and amaranth could serve as a significant source of dietary fiber [48]. Moreover, amaranth has higher fiber and mineral content than other gluten-free grains [21]. In today’s context, amaranth is one of the few gluten-free pseudo-cereals that has been used in a wide variety of gluten-free food commodities. Amaranth is usually combined with other gluten-free cereals such as rice, corn, and cassava in a variety of food products. For example, blending of amaranth with other flours such as cassava [46] and rice [47] in pasta formulation and rice and maize in bakery items [49, 42] has been introduced to enhance the nutritional value of the pasta and bakery items [46]. Because of its higher nutritional profile, genetic diversity, and high adaptability, amaranth can be considered as an excellent supplement to produce gluten-free food products.
One of the most common and costly problems affecting bakery products is fungal contamination. Rizzello et al. [45] reported that the use of amaranth in bakery products can enhance antifungal activity in bread. Amaranth seeds contain some antifungal peptides, which can show a defensive response toward pathogenic fungi [50]. It is noteworthy to mention that amaranth is rich in betalain pigment, which has also been shown to exhibit antimicrobial activities. Thus, betalain is a high demand in the food coloring industry. These pigments with a strong hue not only color the food products but also provide strong antimicrobial response. Thus, amaranth can be an excellent natural additive in the food industry.
2.6 Antioxidant properties of amaranth
To date, 75 different betalains have been reported from 17 of the 34 families in the Caryophyllales order [51]. Interestingly, no species outside Caryophyllales has been found to produce betalains naturally [52]. Most species in the Amaranthaceae have detectable betalains in organs including root, stem, leaves, and flowers. The ecological functions of betalains are presumed to include attracting pollinators to flowers and possibly protect vegetative cells from stresses. There is a long-standing speculation that these pigments are involved in response to abiotic and biotic stresses, but evidence in support of this idea is scant.
Red beetroot (B. vulgaris) is the only commercial betalain source [52], although amaranths have also been proposed as commercial sources of betalains [53, 54]. These betalains have some limited use in food coloring and also have several reported health benefits [55]. Chemical and biological experiments have demonstrated the antioxidant capacity of betalains [56]. Cai et al. [53] showed that the betalains from Amaranthaceae were stronger antioxidants than ascorbic acid, rutin, and catechins. Betalains have also been reported to have anticancer properties [57]. As these chemicals scavenge free radicals, it is expected that they may help prevent cancer and cardiovascular disease [55]. Sreekanth et al. [58] showed that betalain induces dose- and time-dependent cell deaths of the human chronic myeloid leukemia cell line (K562). Moreover, betalain extract from A. spinosus has a significant antimalarial activity in mice [59]. Pigment extract from beetroot pomace also inhibited the growth of gram-negative bacteria [59, 60] and induced zones of reduced growth in Salmonella typhimurium and Bacillus cereus [61]. Thus, amaranth plant is enriched with both nutritional and nutraceutical properties and is a wholesome crop for the future generation.
3. Concluding remarks
Amaranth was a staple of the Aztec diet and is described now as a “superfood” in part because of its high protein content and balanced amino acid profile. It produces a large number of seeds loaded with high-quality protein components, squalene, lysine, and many other health benefitting nutritional and nutraceutical components. Amaranth grain is gluten-free, which makes it a desirable food crop for millions of peoples all over the world. This widely distributed and protein-rich pseudo-cereal has a potential to support food security. However, this crop is still not in the mainstream cultivation practices in North America and in many parts of the world. With the increasing understanding of molecular and biological information of this crop, there is a strong basis for amaranth to be considered for our future generation. As we are witnessing the massive increase in human population in the next few decades and global climate change, we strongly believe amaranth has a huge potential to support the global food system.
Conflict of interest
All authors have read and approved the manuscript for submission. There is no competing interest.
\n',keywords:"amaranth, lysine, complete protein, gluten-free, ancient crop",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/68165.pdf",chapterXML:"https://mts.intechopen.com/source/xml/68165.xml",downloadPdfUrl:"/chapter/pdf-download/68165",previewPdfUrl:"/chapter/pdf-preview/68165",totalDownloads:249,totalViews:0,totalCrossrefCites:1,dateSubmitted:"March 28th 2019",dateReviewed:"June 17th 2019",datePrePublished:"January 7th 2020",datePublished:"March 18th 2020",dateFinished:null,readingETA:"0",abstract:"Amaranth was a staple of the Aztec diet and is described as a “superfood” in part because of its high protein content and well-balanced amino acid profile. In terms of nutrient content, amaranth surpasses many staple crops such as rice, corn, and wheat. Additionally, lysine content is twice as much than in rice and thrice as much than in corn. Along with desirable agronomic traits, this crop has been hugely applauded for its gluten-free nature. Not only can it benefit vegan and gluten allergy personals, but it also has the potential to supply high-quality proteins and at the same time provides antimicrobial activities in the packaged food items. Despite all of these properties, this crop is still not in the mainstream cultivation practices in North America and in many parts of the world. As the planet is expecting massive increase in human population and global climate change, we firmly believe that this widely distributed, ancient, protein-rich pseudo-cereal has a potential to augment our food system. In this book chapter, we aim to report the nutritional properties of grain amaranth.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/68165",risUrl:"/chapter/ris/68165",signatures:"Dinesh Adhikary, Upama Khatri-Chhetri and Jan Slaski",book:{id:"8949",title:"Nutritional Value of Amaranth",subtitle:null,fullTitle:"Nutritional Value of Amaranth",slug:"nutritional-value-of-amaranth",publishedDate:"March 18th 2020",bookSignature:"Viduranga Y. Waisundara",coverURL:"https://cdn.intechopen.com/books/images_new/8949.jpg",licenceType:"CC BY 3.0",editedByType:"Edited by",editors:[{id:"194281",title:"Dr.",name:"Viduranga Yashasvi",middleName:null,surname:"Waisundara",slug:"viduranga-yashasvi-waisundara",fullName:"Viduranga Yashasvi Waisundara"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:[{id:"299993",title:"Dr.",name:"Dinesh",middleName:null,surname:"Adhikary",fullName:"Dinesh Adhikary",slug:"dinesh-adhikary",email:"dinesh.adhikary@ubc.ca",position:null,institution:null},{id:"300684",title:"Ms.",name:"Upama",middleName:null,surname:"Khatri-Chhetri",fullName:"Upama Khatri-Chhetri",slug:"upama-khatri-chhetri",email:"upama@ualberta.ca",position:null,institution:null},{id:"308380",title:"Dr.",name:"Jan",middleName:null,surname:"Slaski",fullName:"Jan Slaski",slug:"jan-slaski",email:"Jan.Slaski@innotechalberta.ca",position:null,institution:null}],sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_1_2",title:"1.1 Amaranthus sp. taxonomy and distribution",level:"2"},{id:"sec_2_2",title:"1.2 Amaranth use in the ancient times",level:"2"},{id:"sec_4",title:"2. Nutritional facts of amaranths",level:"1"},{id:"sec_4_2",title:"2.1 Amaranth proteins",level:"2"},{id:"sec_5_2",title:"2.2 Lysine content",level:"2"},{id:"sec_6_2",title:"2.3 Seed properties and nutrient content",level:"2"},{id:"sec_7_2",title:"2.4 Squalene content",level:"2"},{id:"sec_8_2",title:"2.5 Gluten-free grain",level:"2"},{id:"sec_9_2",title:"2.6 Antioxidant properties of amaranth",level:"2"},{id:"sec_11",title:"3. Concluding remarks",level:"1"},{id:"sec_15",title:"Conflict of interest",level:"1"}],chapterReferences:[{id:"B1",body:'Sauer JD. The grain amaranths: A survey of their history and classification. Annals of the Missouri Botanical Garden. 1950;37:561-632'},{id:"B2",body:'Sauer JD. Revision of the dioecious amaranths. 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Anthropos. 1965;60:262-272'},{id:"B9",body:'Konishi Y, Fumita Y, Ikeda K, Okuno K, Fuwa H. Isolation and characterization of globulin from seeds of Amaranthus hypochondriacus L. Agricultural and Biological Chemistry. 1965;49:1453-1459'},{id:"B10",body:'Gorinstein S, Moshe R, Greene LJ, Paulo A. Evaluation of four Amaranthus species through protein electrophoretic patterns and their amino acid composition. Journal of Agricultural and Food Chemistry. 1991;39:851-854'},{id:"B11",body:'Barba de la Rosa AP, Gueguen J, Paredos-Lopez O, Viroben G. Fractionation procedures, electrophoretic characterization, and amino acid composition of amaranth seed proteins. Journal of Agricultural and Food Chemistry. 1992;40:931-936'},{id:"B12",body:'Leyva-Lopez NE, Vasco N, Barba de la Rosa AP, Paredes-Lopez O. Amaranth seed proteins: Effect of defatting on extraction yield and on electrophoretic patterns. Plant Foods for Human Nutrition. 1995;47:49-53'},{id:"B13",body:'Shewry PR, Pandya MJ. The 2S albumin storage proteins. In: Shewry PR, Casey R, editors. Dordrecht, The Netherlands: Kluwer Academic Publishers; 1999. pp. 563-586'},{id:"B14",body:'Fujiwara T, Nambara E, Yamagishi K, Goto DB, Naito S. Storage proteins. The Arabidopsis book. American Society of Plant Biologists. 2002. pp. 1-12'},{id:"B15",body:'Higgins TJV. Synthesis and regulation of major proteins in seeds. Annual Review in Plant Physiology. 1984;35:191-221'},{id:"B16",body:'Gonzalez-Perez S, Arellano B. In: Phillips GO, Williams PA, editors. Handbook of Hydrocolloids. 2nd ed. Sawston, Cambridge: Woodhead Publishing in Food Science, Technology and Nutrition; 2009. pp. 0-27'},{id:"B17",body:'Youle RJ, Huang AHC. Albumin storage proteins in the protein bodies of Castor bean. Plant Physiology. 1978;61:13-16'},{id:"B18",body:'Mylne JS, Hara-Nishimura I, Rosengren KJ. Seed storage albumins: Biosynthesis, trafficking and structures. 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Gluten-free breads and cookies of raw and popped amaranth flours with attractive technological and nutritional qualities. Plant Foods for Human Nutrition. 2010;65:241-246'},{id:"B43",body:'Shewry PR, Hey SJ. Do we need to worry about eating wheat? Nutrition Bulletin. 2016;41:6-13'},{id:"B44",body:'Gallagher E, Kunkel A, Gormley TR, Arendt EK. The effect of dairy and rice powder addition on loaf and crumb characteristics, and on shelf life (intermediate and long-term) of gluten-free breads stored in a modified atmosphere. European Food Research and Technology. 2003;218:44-48'},{id:"B45",body:'Rizzello CG, Coda R, De Angelis M, Di Cagno R, Carnevali P, Gobbetti M. Long-term fungal inhibitory activity of water-soluble extract from Amaranthus spp. seeds during storage of gluten-free and wheat flour breads. International Journal of Food Microbiology. 2009;131:189-196'},{id:"B46",body:'Fiorda FA, Soares MS, da Silva FA, Grosmann MVE, Souto LRF.Microstructure, texture and colour of gluten-free pasta made with amaranth flour, cassava starch and cassava bagasse. Food Science and Technology. 2013;54:132-138'},{id:"B47",body:'Cabrera-Chávez F, Calderón de la Barca AM, Islas-Rubio AR, Marti A, Marengo M, Pagani MA, et al. Molecular rearrangements in extrusion processes for the production of amaranth-enriched, gluten-free rice pasta. LWT-Food Science and Technology. 2012;47:421-426'},{id:"B48",body:'Kurek MA, Karp S, Wyrwisz J, Niu Y. Physicochemical properties of dietary fibers extracted from gluten-free sources: Quinoa (Chenopodium quinoa), amaranth (Amaranthus caudatus) and millet (Panicum miliaceum). Food Hydrocolloids. 2018;85:321-330'},{id:"B49",body:'Salcedo-Chávez B, Osuna-Castro JA, Guevara-Lara F, Domínguez-Domínguez J, Paredes-López O. Optimization of the isoelectric precipitation method to obtain protein isolates from amaranth (Amaranthus cruentus) seeds. Journal of Agricultural and Food Chemistry. 2002;50:6515-6520'},{id:"B50",body:'Lyapkova NS, Loskutova NA, Maisuryan AN, Mazin VV, Korableva NP, Platonova TA, et al. Transformed potato plants carrying the gene of the antifungal peptide of Amaranthus caudatus. Applied Biochemistry and Microbiology. 2001;37:349-354'},{id:"B51",body:'Khan MI, Giridhar P. Plant betalains: Chemistry and biochemistry. Phytochemistry. 2015;117:267-295'},{id:"B52",body:'Strack D, Vogt T, Schliemann W. Recent advances in betalain research. Phytochemistry. 2003;62:247-269'},{id:"B53",body:'Cai Y, Sun M, Corke H. Antioxidant activity of betalains from plants of the Amaranthaceae. Journal of Agricultural and Food Chemistry. 2003;51:2288-2294'},{id:"B54",body:'Cai Y-Z, Sun M, Corke H. Characterization and application of betalain pigments from plants of the Amaranthaceae. Trends in Food Science & Technology. 2005;16:370-376'},{id:"B55",body:'Gengatharan A, Dykes GA, Choo WS. Betalains: Natural plant pigments with potential application in functional foods. LWT-Food Science and Technology. 2015;64:645-649'},{id:"B56",body:'Borkowski T, Szymusiak H, Gliszczyńska-Rwigło A, Rietjens IMCM, Tyrakowska B. Radical scavenging capacity of wine anthocyanins is strongly pH-dependent. Journal of Agricultural and Food Chemistry. 2005;53:5526-5534'},{id:"B57",body:'Esatbeyoglu T, Wagner AE, Motafakkerazad R, Nakajima Y, Matsugo S, Rimbach G. Free radical scavenging and antioxidant activity of betanin: Electron spin resonance spectroscopy studies and studies in cultured cells. Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research Association. 2014;73:119-126'},{id:"B58",body:'Sreekanth D, Arunasree MK, Roy KR, Chandramohan Reddy T, Reddy GV, Reddanna P. Betanin a betacyanin pigment purified from fruits of Opuntia ficus indica induces apoptosis in human chronic myeloid leukemia cell line-K562. Phytomedicine. 2007;14:739-746'},{id:"B59",body:'Hilou A, Nacoulma OG, Guiguemde TR. In vivo antimalarial activities of extracts from Amaranthus spinosus L. and Boerhaavia erecta L. in mice. Journal of Ethnopharmacology. 2006;103:236-240'},{id:"B60",body:'Čanadanović-Brunet JM, Savatović SS, Gordana S. Antioxidant and antimicrobial activities of beet root pomace extracts. Science. 2011;29:575-585'},{id:"B61",body:'Velićanski AS, Cvetković DD, Markov SL, Vulić JJ, Djilas SM. Antibacterial activity of Beta vulgaris L. pomace extract. Acta Periodica Technologica. 2011;42:263-269'}],footnotes:[],contributors:[{corresp:"yes",contributorFullName:"Dinesh Adhikary",address:"dinesh.adhikary@ubc.ca",affiliation:'
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The Open Access Publishing Fee (OAPF) is payable only after your full chapter, monograph or Compacts monograph is accepted for publication.
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An online manuscript tracking system to facilitate your work
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Personal contact and support throughout the publishing process from your dedicated Author Service Manager
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Assurance that your manuscript meets the highest publishing standards
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English language copyediting and proofreading, including the correction of grammatical, spelling, and other common errors
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XML Typesetting and pagination - web (PDF, HTML) and print files preparation
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Discoverability - electronic citation and linking via DOI
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Permanent and unrestricted online access to your work
What isn't covered by the Open Access Publishing Fee?
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If your manuscript:
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Exceeds 20 pages (for chapters in Edited Volumes), an additional fee of 40 GBP per page will be required
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If a manuscript requires Heavy Editing or Language Polishing, this will incur additional fees.
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Your Author Service Manager will inform you of any items not covered by the OAPF and provide exact information regarding those additional costs before proceeding.
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Open Access Funding
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To explore funding opportunities and learn more about how you can finance your IntechOpen publication, go to our Open Access Funding page. IntechOpen offers expert assistance to all of its Authors. We can support you in approaching funding bodies and institutions in relation to publishing fees by providing information about compliance with the Open Access policies of your funder or institution. We can also assist with communicating the benefits of Open Access in order to support and strengthen your funding request and provide personal guidance through your application process. You can contact us at oapf@intechopen.com for further details or assistance.
\n\n
For Authors who are still unable to obtain funding from their institutions or research funding bodies for individual projects, IntechOpen does offer the possibility of applying for a Waiver to offset some or all processing feed. Details regarding our Waiver Policy can be found here.
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Added Value of Publishing with IntechOpen
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Choosing to publish with IntechOpen ensures the following benefits:
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Indexing and listing across major repositories, see details ...
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Long-term archiving
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Visibility on the world's strongest OA platform
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Live Performance Metrics to track readership and the impact of your chapter
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Dissemination and Promotion
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Benefits of Publishing with IntechOpen
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Proven world leader in Open Access book publishing with over 10 years experience
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+4,800 OA books published
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Most competitive prices in the market
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Fully compliant with OA funding requirements
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Optimized processes, enabling publication between 8 and 12 months
\n\t
Personal support during every step of the publication process
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+146,150 citations in Web of Science databases
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Currently strongest OA platform with over 130 million downloads
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