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Isotype-specific antibody responses to foot-and-mouth disease virus in sera and secretions of ‘carrier’ and ‘non-carrier’ cattle

Published online by Cambridge University Press:  15 May 2009

J. S. Salt
Affiliation:
Institute for Animal Health, Pirbright Laboratory, Ash Road, Pirbright, Surrey GU24 ONF, UK
R. P. Kitching
Affiliation:
Institute for Animal Health, Pirbright Laboratory, Ash Road, Pirbright, Surrey GU24 ONF, UK
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Summary

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Isotype-specific antibody responses to foot-and-mouth disease virus (FMDV) were measured in the sera and upper respiratory tract secretions of vaccinated and susceptible cattle challenged with FMDV by direct contact or by intranasal inoculation. A comparison was made between cattle that eliminated FMDV and those that developed and maintained a persistent infection. Serological and mucosal antibody responses were detected in all animals after challenge. IgA and 1gM were detected before the development of IgG1 and IgG2 responses. 1gM was not detected in vaccinated cattle. Challenge with FMDV elicited a prolonged biphasic secretory antibody response in FMDV ‘carrier’ animals only. The response was detected as FMDVspecific IgA in both mucosal secretions and serum samples, which gained statistical significance (P < 0·05) by 5 weeks after challenge. This observation could represent the basis of a test to differentiate vaccinated and/or recovered convalescent cattle from FMDV ‘carriers’.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1996

References

1.Belsham, GJ. Distinctive features of foot-and-mouth disease virus, a member of the picornavirus family; aspects of virus protein synthesis, protein processing and structure. Prog Biophys Molec Biol 1993; 60: 241–60.CrossRefGoogle ScholarPubMed
2.McCullough, KC, de Simone, F, Brocchi, E, Capucci, L, Crowther, JR, Khim, U. Protective immune response against foot-and-mouth disease. J Virol 1992; 66: 1835–40.CrossRefGoogle ScholarPubMed
3.Sutmoller, P, Gaggero, A. Foot and mouth disease carriers. Vet Rec 1965; 77: 968–9.CrossRefGoogle Scholar
4.Burrows, R. Studies on the carrier state of cattle exposed to foot and mouth disease virus. J Hyg 1966; 64: 8190.CrossRefGoogle ScholarPubMed
5.Hargreaves, SK. The control of foot and mouth disease in Zimbabwe. O.I.E. Scientific Conference on the Control of Foot and Mouth Disease, African Horse Sickness and Contagious Bovine Pleuropneumonia; Gabarone, Botswana, 202304, 1994.Google Scholar
6.Burrows, R. The persistence of FMDV in sheep. J Hyg 1968; 66: 633–40.Google Scholar
7.Bengis, RG, Thomson, GR, Hedger, RS, de Vos, V. Pini, A. Foot and mouth disease and the African buffalo (Syncerus caffer). Onderstepoort J Vet Res 1986; 53: 6973.Google ScholarPubMed
8.Hedger, RS, Condy, JB. Transmission of foot and mouth disease from African buffalo virus carriers to bovines. Vet Rec 1985; 117: 205.CrossRefGoogle ScholarPubMed
9.Dawe, PS, Sorenson, K, Ferris, NP, Barnett, ITR, Armstrong, RM, Knowles, NJ. Experimental transmission of foot-and-mouth disease virus from carrier African buffalo (Syncerus caffer) to cattle in Zimbabwe. Vet Rec 1994; 134: 211–5.CrossRefGoogle ScholarPubMed
10.Gebauer, F, de la Torre, JC, Gomes, I, et al. The rapid selection of genetic and antigenic variants of foot and mouth disease virus during persistence in cattle. J Virol 1988; 62: 2041–9.CrossRefGoogle Scholar
11.Prato Murphy, ML, Meyer, RF, Mebus, C, Schudel, AA, Rodriguez, M. Analysis of sites of foot and mouth disease virus persistence in carrier cattle via the polymerase chain reaction. Arch Virol 1994; 136: 299307.CrossRefGoogle Scholar
12.Sutmoller, P, Cottral, GE. Improved techniques for the detection of foot and mouth disease virus in carrier cattle. Arch fur ges Virusforsch 1967; 21:–7.CrossRefGoogle ScholarPubMed
13.Donn, A, Martin, LA, Donaldson, AI. Improved detection of persistent foot-and-mouth disease infection in cattle by the polymerase chain reaction. J Virol Meth 1994; 49: 179–86.CrossRefGoogle ScholarPubMed
14.Hyslop, NStG. Secretion of foot-and-mouth disease virus and antibody in the saliva of infected and immunised cattle. J Comp Path 1965; 75: 111–7.CrossRefGoogle Scholar
15.Kaaden, O, Matthaeus, W. Detection and some characteristics of foot-and-mouth disease (FMD) antibodies in bovine saliva. Arch fur ges Virusforsch 1970; 30: 263–6.CrossRefGoogle ScholarPubMed
16.Figueroa, F, Ohlbaum, A, Contreras, G. Neutralising antibody response in bovine serum and nasal and salivary secretions after immunisation with live or inactivated foot-and-mouth disease virus. Infect Imm 1973; 8: 296–8.CrossRefGoogle ScholarPubMed
17.McVicar, JW. Sutmoller, P. Neutralising activity in the serum and oro-pharyngeal fluid of cattle after exposure to foot and mouth disease virus and subsequent reexposure. Arch ges Virusforsch 1974; 44: 173–6.CrossRefGoogle Scholar
18.Garland, AJM. The inhibitory activity of secretions in cattle against foot and mouth disease virus [dissertation]. London, England: University of London, 1974.Google Scholar
19.Sellers, RF. Quantitative aspects of the spread of foot and mouth disease. Vet Bull 1971; 41: 431–9.Google Scholar
20.McVicar, JW, Graves, JH, Sutmoller, P. Growth of foot- and-mouth disease virus in the bovine pharynx. 74th Ann Mtg US Anim Hlth Assoc 1970; 230–4.Google Scholar
21.Burrows, R, Mann, JA, Garland, AJM, Greig, A, Goodridge, D. The pathogenesis of natural and simulated natural foot-and-mouth disease infection in cattle. J Comp Pathol 1981; 91: 599609.CrossRefGoogle ScholarPubMed
22.Abu Elzein, EME, Crowther, JR. Detection and quantification of 1gM, IgA, IgG1 and IgG2 antibodies against FMDV from bovine sera using an ELISA. J Hyg 1981; 86: 7985.CrossRefGoogle Scholar
23.Francis, MJ, Ouldridge, EJ, Black, L. The antibody response in bovine pharyngeal fluid following foot and mouth disease vaccination and, or, exposure to live virus. Res Vet Sci 1983; 35: 206–10.CrossRefGoogle ScholarPubMed
24.Matsumoto, M, McKercher, PD, Nusbaum, KE. Secretory antibody responses in cattle infected with foot and mouth disease virus. Am J Vet Res 1978; 39: 1081–7.Google ScholarPubMed
25.Archetti, IL, Amadori, M, Donn, A, Salt, J, Lodetti, E. Detection of foot-and-mouth disease virus-infected cattle by assessment of antibody response in oropharyngeal fluids. J Clin Microbiol 1995; 33: 7984.CrossRefGoogle ScholarPubMed
26.van Zaane, D, Ijzerman, J. Monoclonal antibodies against bovine immunoglobulins and their use in isotype-specific ELISA's for rotavirus antibody. J Immunol Meth 1984; 72: 427–41.CrossRefGoogle ScholarPubMed
27.Madic, J, Magdalena, J, Quak, J, van Oirschot, JT. Isotype-specific antibody responses in sera and mucosal secretions of calves experimentally infected with bovine herpesvirus 1. Vet Immunol Immunopath 1995; 46: 267–83.CrossRefGoogle ScholarPubMed
28.Sutmoller, P, McVicar, JW. Pathogenesis of foot-and- mouth disease: clearance of the virus from the circulation of cattle and goats during experimental viraemia. J Hyg 1976; 77: 245–53.CrossRefGoogle ScholarPubMed
29.Snowdon, WA.Growth of foot-and-mouth disease virus in monolayer cultures of calf thyroid cells. Nature 1966; 210: 1079–80.CrossRefGoogle ScholarPubMed
30.Roeder, PL, Le Blanc Smith, PM. Detection and typing of foot-and-mouth disease virus by enzyme-linked immunosorbent assay: a sensitive, rapid and reliable technique for primary diagnosis. Res Vet Sci 1987; 43: 225–32.CrossRefGoogle ScholarPubMed
31.Mulcahy, G, Gale, C, Robertson, P, lyisan, S, DiMarchi, RD, Doel, TR. Isotype responses of infected, virus- vaccinated and peptide-vaccinated cattle to foot and mouth disease virus. Vaccine 1990; 8: 249–56.CrossRefGoogle ScholarPubMed
32.Butler, JE. Bovine immunoglobulins – an augmented review. Vet Immunol Immunopath 1983; 4: 4352.CrossRefGoogle ScholarPubMed
33.Kimman, TG, Westenbrink, F, Straver, PJ, van Zaane, D. Isotype-specific ELISA's for the detection of antibodies to bovine respiratory syncytial virus. Res Vet Sci 1987; 43: 180–7.CrossRefGoogle ScholarPubMed
34.Kimman, TG, Brouwers, RAM, Daus, FJ, van Oirschot, JT, van Zaane, D. Measurement of isotype-specific antibody responses to Aujeszky's disease virus in sera and mucosal secretions of pigs. Vet Immunol Immunopath 1992; 31:95113.CrossRefGoogle ScholarPubMed
35.Sutmoller, P, McVicar, JW, Cottral, GE. The epizootiological importance of foot-and-mouth disease carriers. Arch fur ges Virusforsch 1968; 23: 227–35.CrossRefGoogle ScholarPubMed
36.Hedger, RS. Observations on the carrier state and related antibody titres during an outbreak of foot and mouth disease. J Hyg 1970; 68: 5360.CrossRefGoogle ScholarPubMed
37.Sellers, RF, Herniman, KAJ, Gumm, ID. The airborne dispersal of foot-and-mouth disease virus from vaccinated and recovered pigs, cattle and sheep after exposure to infection. Res Vet Sci 1977; 23: 70–5.CrossRefGoogle ScholarPubMed
38.McVicar, JW, Sutmoller, P. Growth of foot-and-mouth disease virus in the upper respiratory tract of nonimmunised, vaccinated and recovered cattle after intranasal inoculation. J Hyg 1976; 76: 467–81.CrossRefGoogle Scholar
39.Donaldson, AI, Kitching, RP. Transmission of foot and mouth disease by vaccinated cattle following natural challenge. Rev Vet Sci 1989; 46: 914.CrossRefGoogle ScholarPubMed
40.Butler, JE, Peterson, L, McGivern, PL. A reliable method for the preparation of bovine secretory immunoglobulin A (SIgA) which circumvents problems posed by IgGl dimers in colostrum. Molec Immunol 1980; 17: 757–68.CrossRefGoogle Scholar
41.Butler, JE. Biochemistry and biology of ruminant immunoglobulins. In: Pandey, R, ed. Progress in veterinary microbiology and immunology. Vol 2. Basel: Karger Press, 1986: 153.Google Scholar
42.Thomas, HIJ, Morgan-Capner, P, Cradock-Watson, JE, Enders, G, Best, JM, O'Shea, S. Slow maturation of IgG1 avidity and persistence of specific 1gM in congenital rubella: Implications for diagnosis and immunopathology. J Med Virol 1993; 41: 196200.CrossRefGoogle Scholar
43.Sjogren, M, Hoofnagle, JH. Immunoglobulin M antibody to hepatitis B core antigen in patients with chronic type B hepatitis. Gastroenterol 1985; 89: 252–8.CrossRefGoogle ScholarPubMed
44.Brillanti, S, Foli, M, Perini, P, Masci, C, Miglioli, M, Barbara, L. Long-term persistence of 1gM antibodies to HCV in chronic hepatitis C. J Hepatol 1993; 19: 185–7.CrossRefGoogle Scholar
45.Hedger, RS. The isolation and characterisation of foot- and-mouth disease virus from clinically normal herds of cattle in Botswana. J Hyg 1968; 66: 2736.CrossRefGoogle ScholarPubMed
46.Auge de Mello, P, Honigman, MH, Fernandez, MV, Gomes, I. Further information on the survival of modified foot and mouth disease virus in cattle. Bull Off Int Epiz 1970; 73: 489505.Google ScholarPubMed
47.Armstrong, SJ, Dimmock, NJ. Neutralization of influenza virus by low concentrations of hemagglutininspecific polymeric immunoglobulin A inhibits viral fusion activity, but activation of the ribonucleoprotein is also inhibited. J Virol 1992; 66: 3823–32.CrossRefGoogle ScholarPubMed
48.Renegar, KB, Small, PA. Passive transfer of local immunity to influenza virus infections by IgA antibody. J Immunol 1992; 146: 1972–8.CrossRefGoogle Scholar
49.Israel, BA, Herber, R, Gao, Y, Letchworth, GJ III. Induction of a mucosal barrier to bovine herpesvirus I replication in cattle. Virology 1992; 188: 256–64.CrossRefGoogle ScholarPubMed
50.Heckert, RA, Saif, LJ, Mengel, JP, Myers, GW. Isotypespecific antibody responses to bovine coronavirus structural proteins in serum, feces, and mucosal secretions from experimentally challenge-exposed colostrum-deprived calves. Am J Vet Res 1991; 52: 692–9.CrossRefGoogle ScholarPubMed
51.Butchaiah, G, Card, JL, Morgan, DO. Antigenic relationships of foot-and-mouth disease virus serotype Asia-Isolates demonstrated by monoclonal antibodies. Vet Immunol Immunopath 1992; 30: 275–92.CrossRefGoogle Scholar
52.Tessler, J. Reactivation of antibody-neutralised foot- and-mouth disease virus by organic chemicals and inhibition by 1-butanol. Am J Vet Res 1966; 27: 917–22.Google ScholarPubMed
53.Crouch, CF, Bielefeldt Ohmann, H, Watts, TC, Babiuk, LA. Chronic shedding of bovine enteric coronavirus antigen-antibody complexes in clinically normal cows. J Gen Virol 1985; 66: 1489–500.CrossRefGoogle ScholarPubMed
54.Kaetzel, CS, Robinson, JK, Chintalacharuvu, KR, Vaerman, J-P, Lamm, ME. The polymeric immunoglobulin receptor (secretory component) mediates transport of immune complexes across epithelial cells: A local defence function of IgA. Proc Natl Acad Sci 1991; 88: 8796–800.CrossRefGoogle ScholarPubMed
55.Mazanec, MB, Nedrud, JG, Kaetzel, CS, Lamm, ME. A three-tiered view of the role of IgA in mucosal defence. Imm Today 1993; 14: 430–5.CrossRefGoogle Scholar
56.Tucker, SP, Compans, RW. Virus infection of polarised epithelial cells. Adv Vir Res 1993; 42: 187247.CrossRefGoogle Scholar
57.Sixbey, JW, Yao, Q-Y. Immunoglobulin A-induced shift of Epstein-Barr virus tissue tropism. Science 1992; 255: 1578–80.CrossRefGoogle ScholarPubMed
58.Baxt, B, Mason, PW. Foot-and-mouth disease virus undergoes restricted replication in macrophage cell cultures following Fc receptor-mediated adsorption. Virol 1995; 207: 503–9.CrossRefGoogle ScholarPubMed
59.Berinstein, A, Roivainen, M, Hovi, T, Mason, PW, Baxt, B. Antibodies to the vitronectin receptor (integrin αvβ3) inhibit binding and infection of foot-and-mouth disease virus to cultured cells. J Virol 1995; 69: 2664–6.CrossRefGoogle Scholar
60.Hedger, RS, Stubbins, AGJ. The carrier state in foot- and-mouth disease, and the probang test. State Vet J 1971; 26; 4550.Google Scholar
61.Stites, DP, Siiteri, PK. Steroids as immunosuppressants in pregnancy. Immunol Rev 1983; 75: 117–38.CrossRefGoogle Scholar
62.Wira, CR, Sandoe, CP, Steele MG. Glucocorticoid regulation of the humoral immune system. 1. In vivo effects of dexamethasone on IgA and IgG in serum and at mucosal surfaces. J Immunol 1990; 144: 142–6.CrossRefGoogle ScholarPubMed
63.Madic, J, Magdalena, J, Quak, J, van Oirschot, JT. Isotype-specific antibody responses to bovine herpes- virus 1 in sera and mucosal secretions of calves after experimental reinfection and after reactivation. Vet Immunol Immunopath 1995; 47: 8192.CrossRefGoogle ScholarPubMed