Advances in Bioscience and Biotechnology
Vol.4 No.4A(2013), Article ID:30620,13 pages DOI:10.4236/abb.2013.44A008

Monoclonal antibody and its use in the diagnosis of livestock diseases

Rajib Deb1*, Sandip Chakraborty2, Belamaranahlly Veeregowda3, Amit Kumar Verma4, Ruchi Tiwari5, Kuldeep Dhama6

1Scientist, Division of Animal Genetics & Breeding, Project Directorate on Cattle (ICAR), Meerut, India

2Animal Resource Development Department, Pt. Nehru Complex, Agartala, India

3Veterinary College, Bengaluru, India

4Department of Veterinary Epidemiology and Preventive Medicine, Uttar Pradesh Pandit Deen Dayal Upadhayay Pashu Chikitsa Vigyan Vishvidhyalaya Ewam Go-Anusandhan Sansthan (DUVASU), Mathura, India

5Department of Veterinary Microbiology and Immunology Uttar Pradesh Pandit Deen Dayal Upadhayay Pashu Chikitsa Vigyan Vishvidhyalaya Ewam Go-Anusandhan Sansthan (DUVASU), Mathura, India

6Division of Pathology, Indian Veterinary Research Institute, Bareilly, India

Email: *

Copyright © 2013 Rajib Deb et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Received January 11th, 2013; revised March 14th, 2013; accepted April 16th, 2013

Keywords: Antibody; Cell Engineering; Diagnosis; Livestock; Microbes; Monoclonal; Parasites


Since the discovery of hybridoma cells by Kohler and Milstein, the uses of monoclonal antibody (mAb), the protein produced by such cells are in vogue. Such antibodies with single isotype have higher specificity, and the serological tests employied show higher reproducibility compared to those with use of polyclonal antisera. There are several procedures of mAb production which vary considerably but the principle remains the same which states that antigens introduced into animals generally result in the stimulation of lymphocytes, some of which produce antibody of only one type, although the isotype may change. The developments in the field of cell culture and transfection technology have lead to the production of improved qualities of mAbs. In general, monoclonal antibodies are important reagents used in biomedical research, such as, in the field of diagnostics and therapeutics as well as targeted drug delivery systems. They have got importance not only for infectious diseases caused by microbes and parasites, but also for cancer, metabolic and hormonal disorders, in the diagnosis of lymphoid and myeloid malignancies and tissue typing, enzyme linked immunosorbent assay (ELISA) (especially blocking ELISA), radio immunoassay (RIA), serotyping of pathogens and their immunological intervention with passive antibody, anti-idiotype inhibition or magic bullet therapy with cytotoxic agents coupled with antimouse specific antibody. The application of mAbs in diagnosis of vari- ous livestock diseases is an important area of concern as these diseases are a major and increasingly important factor reducing livestock productivity in various parts of the world. In this context, the application of mAbs for diagnosis of important bacterial diseases viz., Anthrax, Brucellosis, Paratuberculosis, Leptospirosis, Listeriosis, Clostridial infections and Mycoplasmosis (CBPP), fungal diseases viz., Zygomycosis, Cryptococcosis, Histoplasmosis and Paracoccidiodomycosis, viral diseases viz., Foot-and-mouth disease (FMD), Infectious bovine rhinotracheitis/Infectious pustular vulvovaginitis (IBR/IPV), Rota viral diarrhoea, Blue tongue, Rabies, Classical swine fever and re-emerging viral diseases like Hendra and Nipah viral infections and parasitic diseases viz., dirofilariosis, and Trichinellosis and haemportozoan diseases (including Trypanosomiasis, Leishmaniasis, Anaplasmosis, infections caused by Plasmodium spp. as well as tick borne diseases) have been discussed thoroughly along with the specifications of the diagnostic assays for each disease for the convenience of the diagnosticians, researchers, scientists and students to employ such assays, both in field and laboratories to strengthen the disease control programme.


In the year 1975, Köhler and Milstein discovered antibody producing cells, by fusing mouse myeloma cells with spleen cells of immunized mice. They found the hybridoma cells to have single specificity, characteristic of lymphocytes from immunized mice, but with the myeloma cells’ ability to multiply continuously [1]. The hybridoma cells express the property of specific antibody production specific to lymphocytes and the immortal characters of the myeloma cells that allow it to grow in tissue culture. Interestingly, hybridomas are monoclonal because the cells in culture originate from the division of one cell. The hybridoma can be injected into histocompatible mice to produce ascites cell tumours which become a source of high-titred monoclonal antibody and thereby can be frozen in liquid nitrogen for indefinite periods. When needed, the cells can be thawed and recultured for continued production of the identical specific antibody. Once established, a hybridoma cell line continues to produce identical antibody molecules, enabling us to have a technology for production of an unlimited standardized supply of a high specific antibody that can be used worldwide in antibody-mediated reactions.

We know that the hybridoma growing in tissue culture produces a monoclonal antibody (mAb), but the interesting fact is that the mAb thus produced is chemically, physically, and immunologically a distinct molecule specifically produced by all the cells of a clone. Importantly, a monoclonal antibody is an antibody directed against one antigenic determinant or epitope of an antigen and is a single isotype. By testing a number of different clones it is possible to select those producing mAb of an appropriate specificity and isotype suitable for a particular serological assay. Different animals make different antibodies against each determinant. There is no guarantee whatsoever of reproducibility from animal to animal in polyclonal serum production. If the animals are killed after a production lot, there is a limited supply of reagents as the next animal will produce antibodies of different specificity, affinity, isotype. The homogeneity, reproducibility and permanent availability of monoclonal antibodies are the attributes that are responsible for creating great interest and research fervour in this quickly developing field [2].


There are several procedures of mAb production and the methods vary considerably [3,4] but the principle remains the same which states that antigens introduced into animals generally result in the stimulation of lymphocytes, some of which produce antibody. Each lymphocyte produces only one type of antibody although the isotype may change and there may be variation in specificity. Thus, a polyclonal antibody response may be similar in specificity and physicochemical characteristics but not identical On the other hand, lymphoma (myeloma) cells multiply indefinitely in culture but it is rare to find a line that produces antibody of any known specificity. Strains of lymphoma cells can be selected or obtained that produce no immunoglobulin like molecules and which are deficient in hypoxanthine phosphoribosyltransferase and are therefore unable to survive in selective media like hypoxanthine, aminopentrin and thymidine (HAT). The hybrid cells thus generated inherit hypoxanthine phosphoribosyltransferase from the lymphocyte and have got the ability to multiply indefinitely from the lymphoma cell. Some of the hybrid cells will produce antibody of the desired specificity as well as isotype and subsequent cloning and recloning will result in a cell line that produces mAb i.e. hybridoma [1].


The development of improved production of mAbs and other recombinant proteins is often associated with progress in cell culture technology and particularly in mammalian cell culture [5]. Other cells commonly used for large-scale production are myeloma cells [6-8], such as SP 2/0, YB 2/0, NS0 and P3X63.Ag8.653 [12]. The production of mAbs in mammalian cells consists of a long process that involves steps of transfection of the gene of interest into the cells, wherein the two elements most widely used as promoters/enhancer are derived from the simian virus 40 (SV40) and cytomegalovirus (CMV). This is followed by the selection of clones and their adaptation to different culture conditions (usually suspension and serum-free medium), culture in bioreactors and scale-up to industrial level. Indeed, due to the high demands for mAbs, a large-scale process needs to be established having levels of production that meet the market needs (several kg/day) [9,10]. For this, the optimization of mAb production is usually performed in bioreactors by testing different bioreactor modes of operation and culture parameters [11].


In general, monoclonal antibodies (mAbs) are important reagents used in biomedical research, the field in which the use of mAbs has been and will still be necessary for identifying proteins, carbohydrates and nucleic acids, the uses of which have led to the elucidation of many molecules that control cell replication and differentiation. This has advanced our knowledge of the relationship between molecular structure and function, whose application in basic biologic sciences have improved our understanding of the host response to infectious-disease agents and transplanted organs, to toxins produced by infectious agents, to tissues and spontaneously transformed cells (tumors), and to endogenous antigens (involved in autoimmunity), in addition to which, the exquisite specificity of mAb allows them to be used in humans and animals for disease diagnosis and treatment. Thus, in a simplified manner, it can be said that mAbs have tremendous applications in the field of diagnostics and therapeutics as well as targeted drug delivery systems. This is true not only for infectious diseases caused by microbes and parasites, but also for cancer, metabolic and hormonal disorders, in the diagnosis of lymphoid and myeloid malignancies and tissue typing, enzyme linked immunosorbent assay (ELISA), radio immunoassay (RIA), serotyping of pathogens and their immunological intervention with passive antibody, antiidiotype inhibition or magic bullet therapy with cytotoxic agents coupled with anti-mouse specific antibody. Interestingly, the use of mAbs in competitive ELISA, also referred to as blocking ELISA, has come to the forefront as a method to detect the presence of anti-organism antibody. Since introduced by Anderson, the use of MAbs in a competitive ELISA is becoming widely used, a prominent advantage of which is the specificity of within monoclonal preparation. This feature allows the use of even crude antigen preparations [12]. Again, recombinant deoxyribonucleic acid technology through genetic engineering has successfully led to the possibility of reconstruction of mAbs viz., chimeric and humanized antibodies and complementarily determining region grafted antibodies and their enormous therapeutic use [13].

Importantly, there are three general areas in which mAbs are used in Veterinary medicine viz., 1) immunodiagnostic reagents directly as a tool to demonstrate the causative agent(s) or indirectly as reagent for serological detection of antibodies to the causative agent(s); 2) for experimental purposes ranging from molecular dissection of antigenic epitopes to monoclonal anti-idiotype antibody being utilized as a vaccine to induce protective immunity and 3) immunprophylaxis or immunotherapeutics applied to infectious diseases or as a vehicle for delivering toxic substances to, for example, tumors or as a tool to identify, locate and target tumors [1]. While discussing the uses of mAb, question always arises about what must be the exact amount required for carrying out different activities? The anticipated use of the mAbs will determine the amount required [14]. Only small amounts of mAb (less than 0.1 g) are required for carrying outmost research works and for many analytical purposes. Medium scale quantities (0.1 - 1 g) are used for production of diagnostic kits and reagents and for efficacy testing of new mAbs in animals. In this context, large-scale production of mAb is defined as over 1 g. These large quantities are used for routine diagnostic procedures and for therapeutic purposes.

Out of all the several applications of mAbs, the authors have found the application of mAbs in livestock diseases diagnosis as an important area of concern as these diseases are a major and increasingly important factor reducing livestock productivity [15,16] in various parts of the world.


Because of their specificity, mAbs have been widely used in the diagnosis of various diseases of livestock that are infectious in nature. Moreover, mAb-based immunodiagnostic assays have several advantages over polyclonally based assays that make the former likely to reduce such variability since they are readily available in unlimited quantities as appropriate and since monoclonal antibodies don’t exhibit much batch-to-batch variability.

5.1. Use of Mabs to Diagnose Microbial Diseases

5.1.1. For Detection of Antigen as Well as Antibodies against Bacterial Diseases of Livestock

Anthrax, a highly infectious and fatal disease of all warm blooded animals and human, is caused by a giant sporeforming rectangular shaped bacterium called Bacillus anthracis [17]. The similarity of endospore surface antigens between bacteria of the Bacillus cereus group complicates the development of selective antibody-based anthrax detection systems and interestingly, the surface of B. anthracis endospores exposes a tetrasaccharide containing the monosaccharide anthrose. Production of antitetrasaccharide mAbs and anti-anthrose-rhamnose disaccharide MAbs and testing for their fine specificities in a direct spore ELISA with inactivated spores of a broad spectrum of strains of B. anthracis and related species of the Bacillus genus revealed that although the two sets of mAbs have got different fine specificities, all of them can recognize the tested B. anthracis strains and show only a limited cross-reactivity with two B. cereus strains. The mAbs have been further tested for their ability to be implemented in a highly sensitive and specific beadbased Luminex assay, which detects spores from different strains of B. anthracis and two cross-reactive strains of B. cereus that correlates with the results obtained in direct spore ELISA. The detection limit of the Luminex assay is 103 to 104 spores per ml which is much more sensitive than the corresponding sandwich ELISA, instead of the fact that enzyme assay represents a useful first-line screening tool for the detection of B. anthracis spores [18].

Brucellosis is one of the most extended bacterial zoonoses causing economic losses, and has undoubtedly evolved as a disease since man first domesticated animals [19,20]. One application of mAbs is a test for brucellosis in cattle, caused by Brucella abortus that often causes cows to abort during late pregnancies, and it can be spread to farmers and people who drink milk from infected cows. Vaccinated cows may become carriers of the disease for which conventional diagnostic tests cannot distinguish between the disease-causing microbe and the vaccine (made from the microbe) and hence, these tests cannot help the diagnostician to detect the carriers [21]. But diagnostic tests using mAbs are so specific that they help in differentiation of infected and vaccinated animals (DIVA) and one can isolate carriers to prevent the spread of infection with the aid of these new tests. mAbs have been used from time to time for immunochemical identification of several B. abortus lipopolysaccharide (LPS) epitopes viz., A and M epitopes of smooth strains and R1 and R2 epitopes of rough strains [22]. It is quiet noteworthy that a method which is gaining prominence nowadays is the competitive ELISA (cELISA) [23], wherein, Brucella antigen is immobilised on the plate, following which, the serum under test and a mAb directed against an epitope on the antigen are coincubated. This anti-Brucella mAb is conjugated to an enzyme and the presence of this particular antibody is detected if it binds to the antigen. This will only occur if there is no antibody in the serum sample which is bound preferentially. Another test in which case mAb find its application is the Particle Concentration Fluorescence Immunoassay (PCFIA) [24], wherein, the mAb is conjugated with a fluorescent probe. Several attempts have been made to identify the main polypeptide specificities of the antibody response to outer-membrane protein (OMP) extracts of B. melitensis of sheep and goat by using either immunoblotting or c-ELISAs with specific mAbs [25]. The reactivity of mAb 12G12 has been analyzed in regard to the main biovars of Brucella species and is found to be strictly directed against the common specific epitope of the Brucella S-LPS, recognizes all of the smooth Brucella strains and biovars except B. suis biovar 2, and a cELISA has been developed with the horseradish peroxidase (HRPO)-conjugated mAbs 12G12 and S-LPS of B. melitensis Rev1 in order to improve the specificity of the serological diagnosis of brucellosis. Apart from that, mAbs in Brucellosis also finds its application in differentiating infected sheep and goat from those vaccinated with Rev. 1 vaccine, directed against the periplasmic protein coding the B. melitensis 16 M bp26 gene [26- 28].

Paratuberculosis (Johne’s disease) is a chronic infectious dreaded disease of domestic animals caused by Mycobacterium avium subsp. paratuberculosis (MAP), and causes huge production losses and has high impact on animal industry [29]. mAbs have been generated against the Ag85a complex of MAP, the sensitivity and specificity of the Ag85a antibody test has been compared with the ELISA and the fecal culture tests for the detection MAP and a serum bank has been established with a view to differentiate MAP-positive and negative cattle.

Leptospirosis is an economically important zoonotic bacterial infection of livestock that causes abortions, stillbirths, infertility along with loss of milk production [30]. Production of a murine mAb, designated as M553 that binds to an epitope on whole cell antigens prepared from Leptospira borgpetersenii serovar hardjo type hardjobovis and Leptospira interrogans serovar hardjo type hardjoprajitno has been reported. Such murine mAb based cELISA assay is found to be advantageous as comparative analysis with microscopic agglutination test (MAT) can also be done [31].

As far as the disease Listeriosis is concerned, colorimetric monoclonal ELISA is intended for the detection of Listeria spp. in dairy products, seafood and meats. However, the test is not confirmatory for L. monocytogenes as the MAbs used in the test may cross react with other Listeria spp [32-34].

Clostridial diseases are caused by bacteria of the genus Clostridium [35] that are widely recognized as enteric pathogens of livestock and wildlife. In spite of the ready availability of inexpensive, usually effective products for immunoprophylaxis, clostridial enteric infections remain a common presentation at Veterinary diagnostic laboratories. mAbs obtained from mouse immunized with Clostridium botulinum type D toxoid have been developed into a sandwich ELISA (sELISA) format that has got the capability to detect type D toxin and types C and D toxin complexes. and Its potential to replace the mouse bioassay as an alternative in vitro assay for the diagnosis of cattle botulism is under examination. The application of this procedure for screening intestinal samples for strains of C. botulinum that produce types C and D toxins from suspect cattle botulism cases would improve the diagnostic rate as well as significantly reduce the number of mice involved in diagnosis [36].

Contagious Bovine Pleuropneumonia (CBPP) is a respiratory infection caused by Mycoplasma mycoides sub species mycoides [37]. Difficulty in isolation requires conjunction with serological testing [38]. Ayling et al. (1998) [39] identified a mAb, M92/20, for use in indirect immunohistochemistry (IHC) for confirmation of suspected CBPP cases and this monoclonal shows no background noise but some cross-reactivity with other Mycoplasmas from the Mycoplasma mycoides cluster is known. Other monoclonals can also be evaluated in this test; in an examination of 11 CBPP affected lungs from Portuguese cattle, IHC has been found to detect all cases which illustrates that M92/20 based IHC is a sensitive and robust test for CBPP.

5.1.2. For Detection of Antigen as Well as Antibodies against Fungal Diseases of Livestock

The incidence of invasive fungal infections multiplied dramatically in recent decades [40]. Zygomycosis in animals is caused by the fungi of the class Zygomycetes. In most countries, infections are predominantly caused by Aspergillus fumigatus, Candida albicans, Absidia oryrnbifera and so also Rhizomucor (Mucor) pusillus. However, diagnosing these infections in a timely fashion is often very difficult as conventional microbiological and histopathological approaches generally are neither sensitive nor specific. Moreover, such approaches often do not detect invasive fungal infection until late in the course of disease for which there has been considerable interest in developing nonculture approaches to diagnose fungal infections wherein, mAb based diagnosis play an important role, since early diagnosis may guide appropriate treatment and prevent mortality [41]. A number of early studies focused on using cell wall components of fungal species as antigenic markers, among which mannan and galactomannans are useful in the diagnosis of invasive aspergillosis and candidiasis. Early efforts to detect antigenemia were often hampered by the use of insensitive methods with low detection limits [42]. Moreover, fungal mannans or galactomannans may be rapidly removed from circulation by the formation of immune complexes and by receptor-mediated endocytosis by Kupffer's cells in the liver [43], thereby limiting the sensitivity of these diagnostic approaches and hence, attempts have been made toward development of immunoassays based on mAbs with increased specificity and sensitivity. However, much less interest has been shown in diagnosis of other systemic fungal infections.

Invasive aspergillosis is an increasingly recognized condition in immunocompromised hosts and the major problem associated with it is the difficulty in diagnosing this infection. Antibody detection tests are used as an adjunct to microbiological methods for diagnosing invasive aspergillosis that are often negative due to fulminant nature of the disease and/or the poor immunological status of the host [44]. Therefore, the detection of various antigenic markers by mAb based assays for invasive aspergillosis is currently an area of great interest. Stynen and colleagues [45] have introduced a sandwich ELISA, known as Platelia Aspergillus (Bio-Rad, Marnes-la-Coquette, France) which employs rat monoclonal antibody EB-A2 and this test is one of the most sensitive methods currently available to detect galactomannan, whereas, a latex agglutination test (LAT) which employed the same mAb has got a threshold of 15 ng/ml [46]. Furthermore, the sandwich ELISA use to be positive earlier than the LAT and appeared to remain positive after the LAT had become negative. Thus, the development of the Platelia Aspergillus assay represents a marked improvement in the serological diagnosis of aspergillosis. The use of mannan antigenemia (otherwise known as mannanemia) detection for the immunodiagnosis of systemic candidiasis was suggested decades ago by Weiner and CoatsStephen [46], and it is now one of the most widely studied antigens in candidiasis. The detection of mannanemia in the past has been hampered by the use of insensitive methods that resulted in poor sensitivity and/or specificity [47]. Attempts to improve the immunological detection of mannan involved the use of immune complex dissociation by heating sera before performance of the test along with the use of a more-sensitive test format and mAbs that react with defined epitopes [48]. Several mAbs have been characterized and employed in the immunodiagnostic assays and AF1 is one of them that recognize an oligosaccharide shared by a number of mannoproteins from different pathogenic Candida species [49]. Another mAb, 3H8 (an IgG1), recognized only mannoproteins of high molecular mass present in the Candida albicans cell wall but not those of other Candida species [50]. Other mAbs include EB-CA1, for cases in which different species of the Candida genus share both the EB-CA1 epitope distributed on the mannan and mannoproteins of Candida tropicalis and other species of Candida like Candida glabrata, Candida parapsilosis, and C. krusei [51]. Two assays employing this monoclonal antibody have been marketed as the Pastorex Candida latex agglutination test (Bio-Rad) and the Platelia Candida Antigen test (a double-sandwich enzyme immunoassay) (Bio-Rad). The EIA is more sensitive than the LAT even supposing their specificities to be similar [52]. The etiological diagnosis can also be accomplished by indirect immunofluorescence staining and three-layered indirect enzyme immunohistochemical techniques using peroxidase anti-peroxidase (PAP) and alkaline phosphatase anti-alkaline phosphatase (APAAP) immunocomplexes with antifungal antibodies viz. a rat IgM monoclonal antibody (EB-A1) against Aspergillus galactomannan [53] and a murine IgG1 mAb (lA7B4) reacting with somatic antigens of A. corymblfera [54]. Monospecific hyper immune rabbit antisera raised against mannan from C. albicans and somatic antigens from A. fumigatus and A. corymblfera can also be applied. The reactivity of antibodies can be assessed on experimentally infected murine and bovine tissues [39]. Fungi that are stained only by the monoclonal rat anti-Aspergillus galactomannan antibody or the monospecific rabbit antibodies to somatic antigens of A. fumigatus are classified as Aspergillus spp., whereas fungi reacting only with the rabbit anti-Candida mannan antibodies are identified as Candida spp. Fungi that are stained with the murine mAb to somatic antigens of A. corymbijeru or by the monospecific rabbit antiserum to somatic antigens of A. corymbijeru were classified as zygomycetes in the family Mucoraceae.

As far as Cryptococcosis is concerned, the detection of cryptococcal capsular polysaccharide antigen is one of the most valuable rapid serodiagnostic tests for fungi performed on a routine basis. Murex Cryptococcus Test (Murex Diagnostics, Norcross, Ga.) (mouse monoclonal IgM-based latex agglutination assay) effectively eliminates false-positive reactions with rheumatoid factor [55].

Detection of Histoplasmosis (HPA) by RIA in a reference laboratory is an established method for the diagnosis of histoplasmosis and monitoring the response to treatment [56]. However, the limitations of using RIA include the requirement of radioactivity that may not be easily adaptable into a kit form, and the use of polyclonal antisera, which has shown interassay variability [57] as well as cross-reactivity with other dimorphic fungi such as B. dermatitidis, P. brasiliensis, and P. marneffei [58]. Thus, a more specific detection system through the application of mAb is likely to reduce the cross-reactivity with other dimorphic fungi and interassay variation, which led to raising a monoclonal antibody that recognizes a species-specific epitope on a 69- to 70-kDa antigen of histoplasmosis by inhibition ELISA [59]. Recently, Gomez et al. (1997) [60] have developed an inhibition ELISA for the detection of circulating antigen with a mAb P1B directed against an 87-kDa determinant of Paracoccidiodomyces brasiliensis [61], that appears to be a promising method.

Bovine mastitis is the most complex disease condition due to multiple causative agents, poor understanding of the early immune response and complexities associated with mammary epithelial cell damage by both the agents and the host factors and as an important matter of fact, decreased milk production accounts for approximately 70% of the total cost of mastitis [62]. So, diagnosis of mastitis is a centre of attraction for most dignosticians and clinicians and in this regard, mAb finds its application in direct capture ELISA that can be used to measure elevated polymorphonuclear granulocyte (PMN) antigens using mAb specific for PMN cells along with HRPO conjugated rabbit polyclonal anti-PMN antisera. The test gives an optical density (O.D.) which is found to be useful to predict the cell counts of milk samples [63].

5.1.3. For Detection of Antigen as Well as Antibodies against Viral Diseases of Livestock

Research and development on viruses with respect to diagnosis of virus infections need to be strengthened, an international network of databases of virus infections needs to be instituted and a global network for the diagnosis and containment of viral diseases is advocated [64] for containment and subsequent eradication of the other major infectious diseases of viral origin and in this regard mAb based diagnosis plays a crucial role.

Foot-and-mouth disease (FMD) is a highly contagious disease affecting Artiodactylae including cattle worldwide and is included in the notifiable disease list of the World Organization for Animal Health (OIE) [65-67]. It is recognized as a significant epidemic disease threatening the cattle industry since the sixteenth century and till date it is a major global animal health problem [68,69]. In India, annually there are 5000 outbreaks affecting nearly three lakh animals with an economic loss of Rs. 4300 cores. The losses are mainly due to reduction in milk yield, draught power, breeding capabilities etc. and it is a leading cause of loss of livestock economy (direct and indirect losses) due to its endemic nature in India where world’ largest livestock populations exist [70]. So, inclusion of mAb based diagnostic methods in the containment programme of FMD is an area of concern. In this regard, pen side diagnostic test, especially development of a rapid chromatographic strip test, the lateral flow device (LFD) based on a mAb that reacts against all seven serotypes of FMDV is available. The lateral flow assay (LFA) permits rapid diagnosis, thus allowing time for the early implementation of control measures to reduce the possibility of spread of FMD and the assay has been developed widely to support clinical diagnosis of FMD. Again a simple, rapid, colloidal gold-based immuno-chromatographic strip test based on mAb is also developed for easy clinical testing of serotype A of FMDV in field sites with high sensitivity and specificity [71].

Infectious bovine rhinotracheitis/infectious pustular vulvovaginitis (IBR/IPV) is caused by bovine herpesvirus 1 (BoHV-1). It is also an OIE listed disease affecting domestic and wild cattle. It is one of the most widespread respiratory/reproductive viral diseases of bovines in India [72], where massive cattle and buffalo populations are frequently exposed to IBR. To identify the recovered virus as BoHV-1, the supernatant of the culture where virus isolation has been done, should be neutralised with a monospecific BoHV-1 antiserum or neutralising monoclonal antibody (MAb). An alternative method of virus identification is the direct verification of BoHV-1 antigen in cells around the CPE by an immunofluorescence or immunoperoxidase test [73] with conjugated monospecific antiserum or MAb.

Amongst the various causes of neonatal diarrhoea, group A rotavirus has a world-wide distribution and is considered to be the single most important aetiological agent of acute viral gastroenteritis [74] in various new borne mammalian species that provoke economic losses [75]. In this regard, specific ELISA assays based on mAbs have been developed for identifying the genomic diversity and prevalence of rota virus [76].

Blue tongue virus (BTV) is the best studied member of the orbivirus genus in the Reoviridae family. The VP2 protein present in the outer layer of the neucleocapsid of the virus is an important component as far as the serogrouping of the virus is concerned. This is so because VP2 is involved in virus neutralization. For this purpose, several mAbs have been generated to identify the specific epitopes present on the VP2 protein [77]. Moreover, it is assumed that the VP7 protein, present in small number of viruses is accessible from the outer surface and can be targeted for the detection of BTV, for which gold-labelled mAbs to VP7 are used to give intense labelling with purified BTV core particles. Interestingly, these mAbs do not require any purification too [78].

Rabies, an acute viral encephalomyelitis that may affect all warm blooded animals including cattle, is caused by a lyssavirus. Rabies virus is the most important lyssavirus globally [79]. Although the number of antigenic sites on the rabies virus glycoprotein that have been described regularly increases with time, no attempt has been made earlier to carefully evaluate the relative importance of each of these sites before 1990s. Earlier attempts could identify at least three functionally independent antigenic sites, based on the grouping of the neutralization resistant variant rabies viruses [80]. However, Benmansour et al. (1991) [81] has provided a more precise description of the antigenicity of the protein in mice of the H-2d haplotype by using more than 250 newly isolated MAbs. Most of the mAbs recognize antigenic sites previously described as II and III and one minor antigenic site separated from site III by three amino acids, including a proline, has been identified as a minor site. Some of the mAbs are also found to neutralize the site III-specific mutant viruses and one of the mAbs, 1D1, has been found to react with sodium dodecyl sulfate-treated glycoprotein in Western blots (immunoblots) under reducing conditions and was therefore probably directed against a linear epitope, which is called G1 (G, Gif). As a general rule, from this study, it has been proposed to reserve the term “antigenic site” (either major or minor) for regions of the protein, defined by several mAbs originating from different fusions and to describe regions of the protein defined by a single mAb as epitopes. Over the years, investigators have found rabies virus in non-hematophagous bats in America, Africa, and Europe. So, in order to identify transmissibility of the virus, analysis of several European rabies virus isolates from various animal species by antinucleocapsid mAbs have been done that have indicated that transmission of the disease from bats to terrestrial animals is unlikely. Moreover, the antigenic profiles of two isolates from European bats have corresponded to that of European bat lyssavirus type 1 (EBL1). Comparisons of different isolates from bats with antinucleocapsid and antiglycoprotein mAbs along with direct sequencing of the polymerase chain reaction amplification product of the N gene have indicated that EBL1 and 2, Duvenhage virus (serotype 4 of lyssavirus) and the European fox rabies virus (serotype 1) are phylogenetically distant [82]. Many of the mAbs (Groups I-IV), having anti-P reactivity and generated by a recombinant rabies virus phosphoprotein fusion product (GST-P) recognizes linear epitopes. They have been judged by their reaction in immunoblots, following which the linear epitope recognized in each case has been mapped by using two series of Nand C-terminally deleted recombinant phosphoproteins. Assessment of the reactivities of representative mAbs to a variety of lyssavirus isolates by an indirect fluorescent antibody test indicates that group I mAbs, which recognize a highly conserved N-terminal epitope, are broadly cross-reactive with all lyssaviruses assayed, while group III mAbs, which react with a site overlapping that of group I mAbs, exhibit variable reactivities. Nevertheless, group IV mAbs react with most isolates of genotypes 1, 6, and 7 only. In contrast, group II mAbs recognize an epitope in a strain-specific manner located within a highly divergent central portion of the protein and these anti-P MAbs are potentially useful tools for lyssavirus discrimination [83].

A mAb based competition-ELISA has been described for the detection of pestivirus antibodies directed against conserved epitopes on the p80 viral protein. This particular method detects increases in serum antibody following experimentally induced infections of pigs and ruminants like cattle and sheep with a wide range of pestiviruses and is highly specific relative to virus neutralization tests. One added advantage of this mAb based assay is that sera from both ruminants and pigs can be assessed without any modification of the test [84]. The use of a panel of three mAbs, either HRPO or FITC conjugated or used in conjunction with an anti-mouse conjugate and specifically detecting all field strains of Classical Swine Fever Virus (CSFV), vaccine strains of CSFV and ruminant pestiviruses, respectively has been reported. A prerequisite is that the MAb against CSFV recognizes all field strains and that the anti-vaccine MAb recognizes all vaccine strains used in the country [85]. No single mAb selectively reacts with all ruminant pestiviruses. This test allows an unambiguous differentiation between field and vaccine strains of CSFV on the one hand and between CSFV and other pestiviruses on the other [86].

Hendra virus (HeV) and Nipah virus (NiV) are highly pathogenic paramyxoviruses that have recently emerged from flying fox populations to cause serious disease outbreaks in livestock in India and other Asian countries. two viral diseases is virus neutralization test (VNT) by the application of human mAbs that are exceptionally potent in cross-reactive neutralization of the viruses. In this context, neutralizing human mAbs against NiV and HeV have been previously identified by panning a large non-immune antibody library against a soluble form of the HeV attachment-envelope glycoprotein G (sGHeV). One of these antibodies, m102, has been found to exhibit the highest level of cross-reactive neutralization of both NiV and HeV G, thus has been affinity maturated by lightchain shuffling combined with random mutagenesis of its heavy-chain variable domain and panning against sGHeV. One of the selected antibody Fab clones (m102.4) has got affinity of binding to sGHeV that is equal to or higher than that of the other Fabs. It is converted to IgG1 and tested against infectious NiV and HeV and found to exhibit exceptionally potent and cross-reactive inhibitory activity. The virus-neutralizing activity correlates with the binding affinity of the antibody to sGHeV and sGNiV. m102.4 can neutralize NiV better than HeV which suggests that m102.4 has potential as a diagnostic and as a research reagent [88].

The review also requires a special mention of the works based on mAbs that have been carried out as far as the poultry disease diagnosis is concerned, especially in the Indian subcontinent [89-91], classical example being the antigenic characterization and subsequent detection of the minor antigenic differences of Indian isolates and vaccine strains of New Castle disease virus (NDV) [92, 93].

5.2. Use of mAbs to Diagnose Parasitic Diseases

Recent reports have shown that parasite antigens are detectable in the serum of Dirofilaria immitis-infected dogs by counter immuno electrophoresis (CIE). Hybridoma cell lines that produce mAbs specific for these antigens can be obtained by immunizing mice with a partially purified antigen preparation by fusing spleen cells with SP- 2 myeloma cells. By screening cell culture supernatants for antibody by ELISA and CIE inhibition, antibodies specific for two epitopes shared by the two major circulating parasite antigens have been identified [94]. For the identification of circulating parasite antigens associated with immune-complex glomerulonephritis in dogs infected with Dirofilaria immitis, mAbs have been generated against adult worms and selected for cloning because of their lack of cross-reactivity with Toxocara canis in indirect immunofluorescence tests. The ability of these mAbs to detect circulating antigens using an antigen-capture ELISA have shown that only few, out of many mAbs, like NAK-1, an IgG2a mAb, is capable of detecting circulating antigens in most of the infected dogs. However, this mAb is highly species-specific in its detection of circulating antigens and detects antigens at the same glomerular sites in which IgG and/or C3 are deposited [95].

mAbs may be a valuable tool in the early diagnosis of Trichinellosis by the detection of specific antigens even in small amounts whenever present in the circulation [96]. In this context, a sandwich ELISA based on IgY (egg yolk immunoglobulin) and mAb against excretorysecretory (ES) antigens (IgM type) of Trichinella spiralis muscle larvae has been developed for detection of circulating antigens (CAg) in serum from mice infected with T. spiralis, involving the use of chicken antibody IgY as a capture antibody and mouse mAb 35B9 as a detecting antibody. This method is able to detect as little as 1 ng/ mL of ES antigens added to normal mouse serum that shows high sensitivity of the assay. Moreover, it is also valuable as far as the early diagnosis and evaluation of the efficacy of chemotherapy in trichinellosis is concerned [97] and such IgM mAbs based assay can act as a complementary laboratory test for antibody detection [98].

Trypanosomiasis is the most widely distributed pathogenic mechanically transmitted vector borne haemoprotozoan disease prevalent in all livestock species and is a listed disease of OIE [99]. Species-specific mAbs developed against T. brucei, T. vivax, T. congolense [100] and T. evansi [101,102] allow isolation and purification of defined specific antigens for use in indirect ELISA.

Protozoan parasites of the genus Leishmania cause a spectrum of diseases, varying from self-healing cutaneous leishmaniasis to potentially fatal visceral leishmaniasis (VL) or kala-azar (KA). mAbs specific for selected species complexes of Leishmania have been employed for the characterization of several representative strains of Leishmania [102] including amastigote stage of Leishmania amazonensis. Moreover, mAb has been found to be suitable for isolation and purification of Leishmania antigens. mAb raised against pathogenic promastigotes of Leishmania donovani of Indian origin has been used for immuno-affinity purification of a 78 kDa membrane protein present in both the amastigote and promastigote forms of the parasite and for identification of a 57 kDa antigen of Leishmania infantum [103,104].

The molecular events underlying the commitment of Plasmodium spp. to invade RBC’s are not well understood. However, the interaction of two parasite proteins viz., RON2 and AMA1 is known to be critical for invasion and is essential to trigger junction formation. mAbs specific for the AMA1 pocket block junction formation and the induction of the parasitophorous vacuole. Using these mAbs that bind near the hydrophobic pocket of AMA1, RON2’s binding site on AMA1 can be identified, which helps in parasite identification and subsequent selection of potential vaccine candidate [105].

Babesiosis and anaplasmosis are tick-borne diseases of cattle caused by the organisms Babesia bovis, B. bigemina as well as Anaplasma marginale [106]. Validation of a B. bigemina mAb based competitive ELISA specific for B. bigemina has shown to have high sensitivity and specificity [107] and such mAbs are free from cross reaction to that of to B. bovis. This assay works well in the absence of any other workable test for B. bigemina. mAb also finds its application in a competitive ELISA using recombinant major surface protein 5 (rMSP5) of A. marginale which is available in kit form [108].


Biotechnological advancement has helped in the large scale production of mAbs that forms an integral component of many diagnostic assays viz., immunohistochemistry, immunofluorescence and ELISAs (indirect, competitive or sandwich) that are frequently employed either for detection of the infectious agent or any of its structural component (antigen) or the antibodies generated against the infectious agent. The specifications of the diagnostic assays for each of the many important diseases of livestock that has been discussed in this review will make it convenient for the diagnosticians, researchers, scientists and students to employ such assays, both under field and laboratory conditions to strengthen the disease diagnosis to benefit the disease control programmes and to provide better scope to facilitate eradication of most of them.


  1. Kohler, G. and Milstein, C. (1975) Continuous cultures of fused cells secreting antibody of predefined specificity. Nature, 256, 495-497. doi:10.1038/256495a0
  2. Nielsen, K.H., Henning, M.D. and Duncan, J.R. (1986) Monoclonal antibodies in veterinary medicine. Biotechnology and Genetic Engineering Reviews, 4, 311-353. doi:10.1080/02648725.1986.10647831
  3. Fazekas de St Groth, S. and Scheidegger, D. (1980) Production of monoclonal antibodies: Strategy and tactics. Journal of Immunological Methods, 35, 1-21. doi:10.1016/0022-1759(80)90146-5
  4. Prabhakar, B.S., Haspel, M.V. and Notkins, A.L. (1984) Monoclonal antibody techniques applied to viruses. In: Maramorosch, K. and Koprowski, H., Ed., Methods in Virology, Academic Press, New York, 7, 1-18.
  5. Costa, A.R., Rodriguez, M.E., Henriques, M. Azeredo, J. and Oliveira, R. (2010) Guidelines to cell engineering for monoclonal antibody production. European Journal of Pharmaceutics and Biopharmaceutics, 74, 127-138. doi:10.1016/j.ejpb.2009.10.002
  6. Chu, L. and Robinson, D.K. (2001) Industrial choices for protein production by large-scale cell culture. Current Opinion in Biotechnology, 12, 180-187. doi:10.1016/S0958-1669(00)00197-X
  7. Andersen, D.C. and Reilly, D.E. (2004) Production technologies for monoclonal antibodies and their fragments, Current Opinion in Biotechnology, 15, 456-462. doi:10.1016/j.copbio.2004.08.002
  8. Barnes, L.M., Bentley, C.M. and Dickson, A.J. (2000) Advances in animal cell recombinant protein production: GS-NS0 expression system. Cytotechnology, 32, 109- 123. doi:10.1023/A:1008170710003
  9. Jain, E. and Kumar, A. (2008) Upstream processes in antibody production: Evaluation of critical parameters. Biotechnology Advances, 26, 46-71. doi:10.1016/j.biotechadv.2007.09.004
  10. Das, R.C. (2001) Proteins and antibodies make advances as therapeutic products. American Clinical Laboratory, 20, 10-14.
  11. Li, F., Vijayasankaran, N., Shen, A., Kiss, R. and Amanullah, A. (2010) Cell culture processes for monoclonal antibody production. MAbs, 2, 466-477. doi:10.4161/mabs.2.5.12720
  12. Knowles, D.P. and Gorham, J.R. (1990) Diagnosis of viral and bacterial diseases. Review of Scientific Technology Office des’ International Epizootics, 9, 733-757.
  13. Siddiqui, M.Z. (2010) Monoclonal antibodies as diagnostics; an appraisal. Indian Journal of Pharmacological Science, 72, 12-17. doi:10.4103/0250-474X.62229
  14. Marx, U., Embleton, M.J., Fischer, R., Gruber, F.P., Hansson, U., Heuer, J., de Leeuw, W.A., Logtenberg, T., Merz, W., Portetelle, D., Romette, J.L. and Straughan, D.W. (1997) Monoclonal antibody production. The report and recommendations of ECVAM workshop 231. Alternatives to Laboratory Animals, 25, 121-137.
  15. Deb, R. and Chakraborty, S. (2012) Trends in veterinary diagnostics. Journal of Veterinary Science and Technology, 3, e103.
  16. Dhama, K., Gowthaman, V. and Singh, S.D. (2010) Animal disease diagnosis and control: The recent trends. Livestock Line, 4, 28-32.
  17. Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A. (2012) Anthrax. In: Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A. Eds., Infectious Diseases of Cattle, Satish Serial Publishing House, New Delhi, pp. 1-7.
  18. Tamborrini, M., Holzer, M., Seeberger, P.H., Schürch, N. and Pluschke, G. (2010) Anthrax spore detection by a Luminex assay based on monoclonal antibodies that recognize anthrose-containing oligosaccharides. Clinical and Vaccine Immunology, 17, 1446-1451. doi:10.1128/CVI.00205-10
  19. Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A. (2012) Brucellosis. In: Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A., Eds., Infectious Diseases of Cattle, Satish Serial Publishing House, New Delhi, pp. 7-15.
  20. Kumar, N., Pal, B.C., Yadav, S.K., Verma, A.K., Jain, U. and Yadav, G. (2009) Prevalence of bovine brucellosis in Uttar Pradesh, India. Journal of Veterinary Public Health, 7, 129-131.
  21. Report of the Scientific Committee on Animal Health and Animal Welfare (2001) Brucellosis in sheep and goats (Brucella melitensis). European commission health and consumer protection directorate-general, management of scientific health committees, scientific co-operation and networks. Veterinary Forum for South-East Europe, Vienna.
  22. Douglas, J.T. and Palmer, D.A. (1988) Use of monoclonal antibodies to identify the distribution of A and M epitopes on smooth Brucella species. Journal of Clinical Microbiology, 26, 1353-1356.
  23. Marín, C.M., Moreno, E., Moriyón, I., Díaz, R. and Blasco, J.M. (1999) Performance of competitive and indirect ELISAs, gel immunoprecipitation with Native Hapten Polysaccharide and standard serological tests in diagnosis of sheep brucellosis. Clinical Diagnostics and Laboratory Immunology, 6, 269-272.
  24. Greenlee, M.T., Farrar, J.A., Hird, D.W. and Holmes, J.C. (1994) Comparison of particle concentration fluorescence immunoassay to card complement fixation tests using isolation of Brucella abortus as the standard. Journal of Veterinary Diagnostics and Investigation, 6, 182-187. doi:10.1177/104063879400600208
  25. Tibor, A., Saman, E., Wergifosse (De), P., Cloeckaert, A., Limet, J. N. and Letesson, J. J. (1996) Molecular characterization, occurrence, and immunogenicity in infected sheep and cattle of two minor outer membrane proteins of Brucella abortus. Infection and Immunology, 64, 100- 107.
  26. Cloeckaert, A., Debbarh, H.S.A., Vizcaíno, N., Saman, E., Dubray, G. and Zygmunt, M. S. (1996) Cloning, nucleotide sequence, and expression of the Brucella melitensis bp26 gene coding for a protein immunogenic in infected sheep. FEMS Microbiology Letters, 140, 139-144. doi:10.1111/j.1574-6968.1996.tb08327.x
  27. Cloeckaert, A., Debbarh, H.S.A., Zygmunt, M.S. and Dubray, G. (1996) Production and characterisation of monoclonal antibodies to B. melitensis cytosoluble proteins that are able to differentiate antibody responses of infected sheep from Rev.1 vaccinated sheep. Journal of Mediacl Microbiology, 45, 206-213.
  28. Debbarh, H.S.A., Zygmunt, M., Dubray, G. and Cloeckaert, A. (1996) Competitive enzyme-linked immunosorbent assay using monoclonal antibodies to the B. melitensis BP26 protein to evaluate antibody responses in infected and B. melitensis Rev.1 vaccinated sheep. Veterinary Microbiology, 53, 325-337. doi:10.1016/S0378-1135(96)01265-5
  29. Deb, R., Saxena, V. K. and Goswami, P. P. (2011) Diagnostic tools against Mycobacterium avium subspecies paratuberculosis infection in animals: A review. Agricultural Review, 32, 46-54.
  30. Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A. (2012) Leptospirosis. In: Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A., Eds., Infectious Diseases of Cattle, Satish Serial Publishing House, New Delhi, pp. 37-42.
  31. Surujballi, O., Henning, D., Marenger, R. and Howlett, C. (1997) Development of a monoclonal-antibody based competitive enzyme-linked immunosorbent assay for the detection of Leptospira borgpetersenii serovar hardjo type hardjobovis antibodies in bovine sera. Canadian Journal of Veterinary Research, 61, 267-274.
  32. Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A. (2012) Listeriosis. In: Infectious Diseases of Cattle, Satish Serial Publishing House. 42-47.
  33. AOAC Official Method 994.03. (2000) Listeria monocytogenes in dairy products, seafoods, and meats. Colorimetric monoclonal enzyme-linked immunosorbent assay method (listeria-tek). Official methods of analysis of AOAC international. In: Horwitz W. Ed., Official Methods of Analysis of AOAC International, Volume I, Agricultural Chemicals, Contaminants, Drugs, AOAC International, Gaithersburg, MD, 150-152.
  34. Gouws, P.A. and Liedemann, I. (2005) Evaluation of diagnostic PCR for the detection of Listeria monocytogenes in food products. Food Technology and Biotechnology, 43, 201-205.
  35. Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A. (2012) Clostridial infections. In: Infectious Diseases of Cattle, Satish Serial Publishing House, 47-55.
  36. Brooks, C.E., Clarke, H.J., Finlay, D.A., McConnell, W., Graham, D.A. and Ball, H.J. (2010) Culture enrichment assists the diagnosis of cattle botulism by a monoclonal antibody based sandwich ELISA. Veterinary Microbiology, 144, 226-230. doi:10.1016/j.vetmic.2009.12.030
  37. Abdo, E.-M., Nicolet, J. and Frey, J. (2000) Antigenic and genetic characterisation of lipoprotein LppQ from Mycoplasma mycoides subsp. mycoides SC. Clinical Diagnostic and Laboratory Immunology, 7, 588-595.
  38. Saritha, N.S., Veeregowda, B.M., Reddy, G.R., Rathnamma, D., Leena, G., Vinay Kumar, Y.L., Sagar, M. and Nagraja, C.S. (2010) Isolation and molecular characterization of Mycoplasma synoviae from chicken. Indian Journal of Animal Sciences, 80, 497-499.
  39. Ayling, R.D., Regalla, J. and Nicholas, R.A.J. (1999) A field test for detecting antibodies to Mycoplasma mycoides subsp. mycoides small colony type using the latex slide agglutination test. In: Stipkovits, L., Rosengarten, R. and Frey, J. Eds., COST 826 Agriculture and Biotechnology. Mycoplasmas of Ruminants: Pathogenicity, Diagnostics, Epidemiology and Molecular Genetics Vol III, Office for official publications of the European Communities, Luxembourg, 155-158.
  40. Vanden Bergh, M.F., Verweij, P.E. and Voss, A. (1999) Epidemiology of nosocomial fungal infections: Invasive aspergillosis and the environment. Diagnostic Microbiology and Infectious Diseases, 34, 221-227. doi:10.1016/S0732-8893(99)00026-7
  41. Yeo, S.F. and Wong, B. (2002) Current status of nonculture methods for diagnosis of invasive fungal infections. Clinical Microbiology Review, 15, 465-484. doi:10.1128/CMR.15.3.465-484.2002
  42. Martins, T.B., Jaskowski, T.D., Mouritsen, C.L. and Hill, H.R. (1995) Comparison of commercially available enzyme immunoassay with traditional serological tests for detection of antibodies to Coccidioides immitis. Journal of Clinical Microbiology, 33, 940-943.
  43. De Repentigny, L. (1992) Serodiagnosis of candidiasis, aspergillosis, and cryptococcosis. Clinical Infectious Diseases, 14, S11-S22. doi:10.1093/clinids/14.Supplement_1.S11
  44. Latge, J.P. (1999) Aspergillus fumigatus and aspergillosis. Clinical Microbiology Review, 12, 310-350.
  45. Stynen, D., Goris, A., Sarfati, J. and Latge, J.P. (1995) A new sensitive sandwich enzyme-linked immunosorbent assay to detect galactofuran in patients with invasive aspergillosis. Journal of Clinical Microbiology, 33, 497-500.
  46. Loeffler, J., Henke, H., Hebart, H., Schmidt, D., Hagmeyer, L., Schumacher, U. and Einsele, H. (2000) Quantification of fungal DNA by using fluorescence resonance energy transfer and the light cycle system. Journal of Clinical Microbiology, 38, 586-590.
  47. Latge, J.P. (1995). Tools and trends in the detection of Aspergillus fumigatus. Current Topics in Medical Mycology, 6, 245-281.
  48. Jacquinot, P.M., Plancke, Y., Sendid, B., Strecker, G. and Poulain, D. (1998) Nature of Candida albicans-derived carbohydrate antigen recognized by a monoclonal antibody in patients sera and distribution over Candida species. FEMS Microbiology Letters, 166, 131-138. doi:10.1111/j.1574-6968.1998.tb13309.x
  49. Girmenia, C., Martino, P., De Bernardis, F. and Cassone, A. (1997) Assessment of detection of Candida mannoproteinemia as a method to differentiate central venous catheter-related candidemia from invasive disease. Journal of Clinical Microbiology, 35, 903-906.
  50. Marcilla, A., Monteagudo, C., Mormeneo, S. and Sentandreu, R. (1999) Monoclonal antibody 3H8: A useful tool in the diagnosis of candidiasis. Microbiology, 145, 695- 701. doi:10.1099/13500872-145-3-695
  51. Jacquinot, P.M., Plancke, Y., Sendid, B., Strecker, G. and Poulain, D. (1998) Nature of Candida albicans-derived carbohydrate antigen recognized by a monoclonal antibody in patients sera and distribution over Candida species. FEMS Microbiology Letters, 166, 131-138. doi:10.1111/j.1574-6968.1998.tb13309.x
  52. Sendid, B., Tabouret, M., Poirot, J.L., Mathieu, D., Fruit, J. and Poulain, D. (1999) New enzyme immunoassay for sensitive detection of circulating Candida albicans mannan and antimannan antibodies: Useful combined test for diagnosis of systemic candidiasis. Journal of Clinical Microbiology, 37, 1510-1517.
  53. Stynen, D., Sarfati, J., Goris, A., Prtvost, M.C., Lesourd, M., Kamphuis, H., Darras, V., Latge, J.P. (1992) Rat monoclonal antibodies against Aspergillus galactomannan. Infection Immunity, 60, 2237-2245.
  54. Jensen, H.E., Aalbzk, B., Lind, P., Frandsen, P.L., Krogh, H.V. and Stynen, D. (1993) Enzyme immunohistochemistry with mono and polyclonal antibodies in the pathological diagnosis of systemic bovine mycoses. Acta Pathologica Microbiologica et Immunologica Scandinavica, 101, 505-516. doi:10.1111/j.1699-0463.1993.tb00140.x
  55. Kiska, D.L., Orkiszewski, D.R., Howell, D. and Gilligan, P.H. (1994) Evaluation of new monoclonal antibodybased latex agglutination test for detection of cryptococcal polysaccharide antigen in serum and cerebrospinal fluid. Journal of Clinical Microbiology, 32, 2309-2311.
  56. Durkin, M.M., Connolly, P.A. and Wheat, L.J. (1997) Comparison of radioimmunoassay and enzyme-linked immunoassay methods for detection of Histoplasma capsulatum var. capsulatum antigen. Journal of Clinical Microbiology, 35, 2252-2255.
  57. Wheat, L.J., Connolly-Stringfield, P., Blair, R., Connolly, K., Garringer, T. and Katz, B.P. (1991) Histoplasmosis relapse in patients with AIDS. Detection using Histoplasma capsulatum variety capsulatum antigen levels. American Journal of International Medicine, 115, 936-941.
  58. Wheat, J., Wheat, H., Connolly, P., Kleiman, M., Supparatpinyo, K., Nelson, K., Bradsher, R. and Restrepo, A. (1997) Cross-reactivity in Histoplasma capsulatum variety capsulatum antigen assays of urine samples from patients with endemic mycoses. Clinical Journal of Infectious Diseases, 24, 1169-1171.
  59. Gomez, B.L., Figueroa, J.I., Hamilton, A.J., Diez, S., Rojas, M., Tobon, A.M., Restrepo, A. and Hay, R.J. (1999) Detection of the 70-kilodalton Histoplasma capsulatum antigen in serum of histoplasmosis patients: Correlation between antigenemia and therapy during follow-up. Journal of Clinical Microbiology, 37, 675-680.
  60. [61] Gomez, B.L., Figueroa, J.I., Hamilton, A.J., Ortiz, B., Robledo, M.A., Hay, R.J. and Restrepo, A. (1997). Use of monoclonal antibodies in diagnosis of paracoccidioidomycosis: New strategies for detection of circulating antigens. Journal of Clinical Microbiology, 35, 3278-3283.
  61. [62] Gomez, B.L., Figueroa, J.I., Hamilton, A.J., Diez, S., Rojas, M., Tobon, A.M., Hay, R.J. and Restrepo, A. (1998) Antigenemia in patients with paracoccidioidomycosis: Detection of the 87-kilodalton determinant during and after antifungal therapy. Journal of Clinical Microbiology, 36, 3309-3316.
  62. [63] Sailo, B. and Chakraborty, S. (2012) A brief overview of mastitis and other infectious diseases of cattle in India having public health concern. In: Singh, U., Deb, R., Kumar, S. and Sharma, A. Eds., Livestock Update, Satish Serial Publishing House, New Delhi, 91-122.
  63. [64] O’Sullivan, C.A., Joyce, P.J., Sloan, T. and Shattock, A.G. (1992) Capture immunoassay for the diagnosis of bovine mastitis using a monoclonal antibody to polymorphonuclear granulocytes. Journal of Dairy Research, 59, 123-133. doi:10.1017/S0022029900030375
  64. [65] Banerjee, K. (1996) Emerging viral infections with special reference to India. Indian Journal of Medical Research, 103, 177-200.
  65. [66] Verma, A.K., Pal, B.C., Singh, C.P., Jain, U., Yadav, S.K. and Mahima (2008) Studies of the outbreaks of foot-andmouth disease in Uttar Pradesh, India, between 2000 and 2006. Asian Journal of Epidemiology, 1, 40-46. doi:10.3923/aje.2008.40.46
  66. [67] Verma, A.K., Sahzad, Mehra, S., Kumar, A. and Yadav, S.K. (2009) LPB elisa based preand post-vaccination seroprevalence of foot and mouth disease virus. Indian Journal of Comparative Microbiology, Immunology and Infectious Diseases, 30, 130-132.
  67. [68] Verma, A.K., Raies, M., Jain, U., Yadav, S.K., Mahima and Pal, B.C. (2010) Differentiation of foot-and-mouth disease infected and vaccinated animals using 3ABC non-structural protein. Indian Journal of Veterinary Medicine, 30, 84-86.
  68. [69] Verma, A.K., Kumar, A., Mahima and Sahzad (2012) Epidemiology and diagnosis of foot and mouth disease: A review. Indian Journal of Animal Sciences, 82, 543-551.
  69. [70] Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A. (2012) Foot-and-mouth disease (FMD). In: Infectious Diseases of Cattle, Satish Serial Publishing House. 96-112.
  70. [71] Longjam, N., Deb, R., Sarmah, A. K., Tayo, T., Awachat, V. B. and Saxena, V. K. (2011). A brief review on the diagnosis of Foot-and-Mouth disease of livestock: Conventional to molecular tools. Veterinary Medicine International, 2011, Article ID: 905768. doi:10.4061/2011/905768
  71. [72] Reid, S. M., Ferris, N. P., Brüning, A., Hutchings, G. H., Kowalska, Z. and Akerbolm, L. (2001) Development of a rapid chromatographic strip test for the pen-side detection of foot-and-mouth disease virus antigen. Journal of Virological Methods, 96, 189-202. doi:10.1016/S0166-0934(01)00334-2
  72. [73] Kiran, K.K., Ravi, P. and Prabhudas, K. (2005) Infectious bovine rhinotracheitis national survey of IBR antibodies by AB-ELISA kit. Annual Report of Project Directorate on Animal Disease Monitoring and Surveillance, ICAR, Bangalore, 7-10.
  73. [74] Kaashoek, M.J., Moerman, A., Madic, J., Rijsewijk, F.A.M., Quak, J., Gielkens, A.L.J. and Van Oirschot, J.T. (1994) A conventionally attenuated glycoprotein E-negative strain of bovine herpesvirus type 1 is an efficacious and safe vaccine. Vaccine, 12, 439-444. doi:10.1016/0264-410X(94)90122-8
  74. [75] Dhama, K., Chauhan, R.S., Mahesh, M. and Malik, S.V.S. (2009) Rotavirus diarrhea in bovines and other domestic animals. Veterinary Research Communications, 33, 1-23. doi:10.1007/s11259-008-9070-x
  75. [76] Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A. (2012) Rota viral diarrhoea. In: Infectious Diseases of Cattle, Satish Serial Publishing House. 119-124.
  76. [77] Jindal, S.R., Maiti, N.K. and Oberoi, M.S. (2000) Genomic diversity and prevalence of Rotavirus in cow and buffalo calves in northern India. Review of Scientific Technology, Office des’ Scientific Technology, 19, 871- 876. doi:10.1099/0022-1317-71-6-1325
  77. [78] White, J.R. and Eaton, B.T. (1990) Conformation of the VP2 protein of blue tongue virus (BTV) determines the involvement in virus neutralization of highly conserved epitopes within the BTV serogroup. Journal of General Virology, 71, 1325-1332.
  78. [79] Hyatt, A.D. and Eaton, B.T. (1988). Ultrastructural distribution of the major capsid proteins within Bluetongue virus and infected cells. Journal of General Virology, 69, 805-815. doi:10.1099/0022-1317-69-4-805
  79. [80] Blanton, J.D., Palmer, D., Christian, K.A. and Rupprecht, C.E. (2010) Rabies surveillance in the United States during 2009. Journal of the American Veterinary and Medical Association, 237, 646-657. doi:10.2460/javma.237.6.646
  80. [81] Lafon, M., Wiktor, T.J. and MacFarlan, R.I. (1983) Antigenic sites on the CVS Rabies virus glycoprotein: Analysis with monoclonal antibodies. Journal of General Virology, 64, 843-851. doi:10.1099/0022-1317-64-4-843
  81. [82] Benmansour, A., Leblois, H., Coulon, P., Tuffereau, C., Gaudin, Y., Flamand, A. and Lafay, F. (1991) Antigenicity of rabies virus glycoprotein. Journal of Virology, 65, 4198-4203.
  82. [83] Bourhy, H., Kissi, B., Lafon, M., Sacramento, D. and Tordo, N. (1992) Antigenic and molecular characterization of bat rabies virus in Europe. Journal of Clinical Microbiology, 30, 2419-2426.
  83. [84] Nadin-Davis, S.A., Sheen, M., Abdel-Malik, M., Elmgren, M., Armstrong, J. and Wandeler, A.I. (2000) A panel of monoclonal antibodies targeting the Rabies virus phosphoprotein identifies a highly variable epitope of value for sensitive strain discrimination. Journal of Clinical Micobiology, 38, 1397-1403.
  84. [85] Paton, D.J., Ibata, G., Edwards, S. and Wensvoort, G. (1991) An ELISA detecting antibody to conserved pestivirus epitopes. Journal of Virological Methods, 31, 315- 324. doi:10.1016/0166-0934(91)90169-Z
  85. [86] Chakraborty, S. and Choudhury, S. (2012). Recent trends in the diagnosis of Classical Swine Fever. Advance Tropical Medicine and Public Health International, 2, 61-71.
  86. [87] Wensvoort, G., Terpstra, C., De Kluyver, E.P, Kraghten, C. and Warnaarm, J.C. (1989) Antigenic differentiation of pestivirus strains with monoclonal antibodies against hog cholera virus. Veterinary Microbiology, 21, 9-20. doi:10.1016/0378-1135(89)90014-X
  87. [88] Eaton, B.T., Broder, C.C., Middleton, D. and Wang, L.F. (2006) Hendra and Nipah viruses: Different and dangerous. Nature Reviews Microbiology, 4, 23-35. doi:10.1038/nrmicro1323
  88. [89] Zhu, Z., Bossart, K.N., Bishop, K.A., Crameri, G., Dimitrov, A.S., Mc Eachern, J.A., Feng, Y., Middleton, D., Wang, L.F., Broder, C.C. and Dimitrov, D.S. (2008) Exceptionally potent cross-reactive neutralization of Nipah and Hendra viruses by a human monoclonal antibody. The Journal of Infectious Diseases, 197, 846-853. doi:10.1086/528801
  89. [90] Dhama, K., Sawant, P.M., Kumar, D. and Kumar, R. (2011) Diagnostic applications of molecular tools and techniques for important viral diseases of poultry. Poultry World, 5, 32-40.
  90. [91] Kataria, J.M., Madan Mohan, C., Dey, S., Dash, B.B. and Dhama, K. (2005) Diagnosis and immunoprophylaxis of economically important poultry diseases: A Review. Indian Journal of Animal Sciences, 75, 555-567.
  91. [92] Mohaptra, N., Kataria, J.M., Dhama, K. and Senthil Kumar, N. (2002) Physicochemical and biological characterization of EDS-76 virus isolated from Japanese quails (Coturnix coturnix japonica). Indian Journal of Comparative Microbiology, Immunology and Infectious Diseases, 23, 127-135.
  92. [93] Swain, P., Verma, K.C., Kataria, J.M, Mohanty, S.K. and Dhama, K. (1998) Antigenic characterization of Indian isolates and vaccine strains of Newcastle disease virus (NDV). Tropical Animal Health and Production, 30, 295- 298. doi:10.1023/A:1005090805362
  93. [94] Swain, P., Dhama, K., Kataria, J.M. and Verma, K.C. (1998) Monoclonal antibodies in Newcastle disease virus research: A review. Indian Journal of Comparative Microbiology, Immunology and Infectious Diseases, 19, 1-7.
  94. [95] Weil, G.J., Malane, M.S., Powers, K.G. and Blair, L.S. (1985) Monoclonal antibodies to parasite antigens found in the serum of Dirofilaria immitis-infected dogs. Journal of Immunology, 134, 1185-1191.
  95. [96] Nakagaki, K., Nogami, S., Hayashi, Y., Hammerberg, B., Tanaka, H. and Ohishi, I. (1993) Dirofilaria immitis: Detection of parasite-specific antigen by monoclonal antibodies in glomerulonephritis in infected dogs. Parasitology Research, 79, 49-54. doi:10.1007/BF00931217
  96. [97] Youssef, M.Y., Barakat, R., Boulos, L.M. and el-Mansoury, S.T. (1989) Preparation and use of monoclonal antibodies in the detection of Trichinella spiralis circulating antigen. Journal of Egyptian Public Health Association, 64, 105-122
  97. [98] Wang, Z.Q., Fu, G.Y., Jing, F.J., Jin, J., Ren, H.J., Jiang, P. and Cui, J. (2012) Detection of Trichinella spiralis circulating antigens in serum of experimentally infected mice by an IgY-mAb sandwich ELISA. Foodborne Pathogens and Diseases, 9, 727-733.
  98. [99] Zumaquero-Ríos, J.L., García-Juarez, J., De-la-Rosa-Arana, J.L., Marcet, R. and Sarracent-Pérez, J. (2012) Trichinella spiralis: Monoclonal antibody against the muscular larvae for the detection of circulating and fecal antigens in experimentally infected rats. Experimental Parasitology, 132, 444-449. doi:10.1016/j.exppara.2012.09.016
  99. [100] Deb, R., Chakraborty, S., Singh, U., Kumar, S. and Sharma, A. (2012) Trypanosomiasis/Surra. In: Infectious Diseases of Cattle, Satish Serial Publishing House. 153- 159.
  100. [101] Nantulya, V.M. and Lindqvist, K.J. (1989) Antigen detection enzyme immunoassays for the diagnosis of Trypanosoma vivax, T. congolense and T. brucei infections in cattle. Tropical Medicine and Parasitology, 40, 267- 272.
  101. [102] Luckins, A.G. (1991) Antigen detection ELISA for Trypanosoma evansi using group-specific monoclonal antibodies. In: Improving the diagnosis and control of trypanosomiasis and other vector-borne diseases of African livestock using immunoassay methods, Third Research Co-ordination Meeting, Abidjan, 20-25.
  102. [103] Grimaldi, G. and Mc Mahon-Pratt, D. (1996) Monoclonal antibodies for the identification of new world Leishmania species. Memorias do Instituto Oswaldo Cruz, 91, 37-42.
  103. [104] Mukherjee, M., Bhattacharyya, A. and Duttagupta, S. (2002) Monoclonal antibody affinity purification of a 78 kDa membrane protein of Leishmania donovani of Indian origin and its role in host-parasite interaction. Journal of Bioscience, 27, 665-672. doi:10.1007/BF02708374
  104. [105] Nejad-Moghaddam, A. and Abolhassani, M. (2009) Production and characterization of monoclonal antibodies recognizing a common 57-kDa antigen of Leishmania species. Iranian Biomedical Journal, 13, 245-251.
  105. [106] Srinivasan, P., Beatty, W.L., Diouf, A., Herrera, R., Ambroggio, X., Moch, J.K., Tyler, J.S., Narum, D.L., Pierce, S.K., Boothroyd, J.C., Haynes, J.D. and Miller, L.H. (2011) Binding of Plasmodium merozoite proteins RON2 and AMA1 triggers commitment to invasion. Proceedings of the National Academy of Sciences, 1-6.
  106. [107] Bock, R.E., De Vos, A.J. and Molloy, J.B. (2006) Tickborne diseases of cattle. Part 1. Diagnostic overview. Australian and New Zealand Standard Diagnostic Procedures, 1-29.
  107. [108] Molloy, J.B., Bowles, P.M. and Jeston, P.J. (1998) Development of an enzyme-linked immunosorbent assay for detection of antibodies to Babesia bigemina in cattle. Parasitology Research, 84, 651-656. doi:10.1007/s004360050465
  108. [109] Mc Elwain, T.F. (2004) Bovine anaplasmosis. In: Manual of Standards for Diagnostic Tests and Vaccines for TerresTrial Animals, Office International des Épizooties, Paris, 494-506.


*Corresponding author.