A liquid phase blocking ELISA for the detection of antibodies against infectious bronchitis virus

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Brazilian Humoral Journal response of against Medical infectious and Biological bronchitis Research virus (1999) 32: 747-752 ISSN 0100-879X Short Communication 747 A liquid phase blocking ELISA for the detection of antibodies against infectious bronchitis virus T.C. Cardoso 1, R.L. Mouro-Sousa 2, C. Oliveira 3, G. Stringhini 1 and A. Augusto-Pinto 2 1 Departamento de Apoio, Produção e Saúde Animal, Faculdade de Odontologia, Universidade Estadual Paulista, Araçatuba, SP, Brasil 2 Departamento de Microbiologia, Faculdade de Ciências Agrárias e Veterinárias, Universidade Estadual Paulista, Jaboticabal, SP, Brasil 3 Merial Laboratories, Setor de Biologia Aviária, Campinas, SP, Brasil Correspondence T.C. Cardoso Departamento de Apoio, Produção e Saúde Animal Curso de Medicina Veterinária Rua Clóvis Pestana, 793 16015-050 Araçatuba, SP Brasil Fax: +55-18-622-6487 E-mail: tcardoso@ fmva.unesp.br Reasearch supported by FAPESP (No. 1997/10877-2). Abstract Key words Liquid phase blocking ELISA Humoral response Infectious bronchitis virus Received June 18, 1998 Accepted February 26, 1999

748 T.C. Cardoso et al. Virus antigen Capture antibody g g g Detector antibody Serum samples Serum neutralization test

Humoral response against infectious bronchitis virus 749 Development of LPB-ELISA Application of LPB-ELISA

750 T.C. Cardoso et al. Figure 1 - Correlation and linear regression of antibody titers obtained by liquid phase blocking ELISA (LPB-ELISA) (log 10 ) and by serum neutralization test (SNT) (log 2 ). The equation for the line is: LPB y = 0.2322x + 0.3419; r 2 = 0.892. Statistical analysis Reproducibility of LPB-ELISA LPB-ELISA (log10) 5 4 3 2 1 0 0 2 4 6 8 SNT (log 2 ) Table 1 - Specificity and sensitivity of LPB-ELISA for the determination of IBV-antibodies in vaccinated and nonvaccinated chickens. a Total number of serum samples from vaccinated chickens. b Total number of serum samples from nonvaccinated SPF chickens. Specificity = 156-0/ 156 x 100 = 100%. Sensitivity = 100-12/100 x 100 = 88%. Agreement = 156 + 88/256 x 100 = 95.31%. Serum neutralization test LPB-ELISA Positive Negative Positive 156 12 Negative 0 88 Total number of serum 156 a 100 b samples according to source g ³ g ³ ³

Humoral response against infectious bronchitis virus 751 g Acknowledgments References 1. Ignjatovic J & Galli L (1995). Immune responses to structural proteins of avian infectious bronchitis virus. Avian Pathology, 24: 313-332. 2. Box PG, Holmes HC, Finney PM & Froymann R (1988). Infectious bronchitis in laying hens: The relationship between haemagglutination inhibition antibody levels and resistance to experimental challenge. Avian Pathology, 17: 349-361. 3. Cavanagh D (1983). Coronavirus IBV glycopolypeptides: size of their polypeptide moieties and nature of their oligosaccharides. Journal of General Virology, 64: 1187-1191. 4. Witt JJ, Mekkes DR, Kouwenhoven B & Verheijden JHM (1997). Sensitivity and specificity of serological tests for infectious bronchitis virus antibodies in broilers. Avian Pathology, 26: 105-118. 5. Cardoso TC, Montassier HJ, Galletti MCM & Pinto AA (1996). Evaluation of indirect ELISA for monitoring antibodies against infectious bronchitis virus. Revista de Microbiologia, 27: 64-69. 6. Cardoso TC, Montassier HJ, Galletti MCM & Pinto AA (1996). Development and application of a sandwich ELISA to measure chicken antibodies to infectious bronchitis virus. Virus Reviews and Research, 1: 75-80. 7. Cardoso TC, Sousa RLM, Alessi AC, Montassier HJ & Pinto AA (1998). A double antibody sandwich ELISA for rapid diagnosis of virus infections and to measure the humoral response against infectious bursal disease on clinical material. Avian Pathology, 27: 450-454. 8. Ann Hebert G, Pelham PL & Pittman B (1973). Determination of the optimal ammonium sulfate concentration of fractionation of rabbit, sheep, horse and goat anti-

752 T.C. Cardoso et al. sera. Applied Microbiology, 25: 26-36. 9. Esterhuysen JJ, Prehaud C & Thomson GR (1995). A liquid phase blocking ELISA for the detection of antibodies to rabies virus. Journal of Virological Methods, 51: 31-42. 10. McCullough KC, Bruckner L, Schaffiner R, Werner F, Heinz KM & Ulrich K (1992). Relationship between the anti FMDV antibody reaction as measured by different assays and protection in vivo against challenge infection. Veterinary Microbiology, 30: 99-112. 11. Araujo JP, Montassier HJ & Pinto AA (1996). Liquid phase blocking sandwich enzyme linked immunosorbent assay for the detection of antibodies against footand-mouth disease virus in water buffalo sera. American Journal of Veterinary Research, 57: 840-843. 12. Cornaglia E, Chretien N, Charara S & Elazhary Y (1994). Detection of porcine respiratory coronavirus and transmissible gastroenteritis virus by an enzyme linked immunosorbent assay. Veterinary Microbiology, 42: 349-359. 13. Hamblin C, Barnett ITR & Hedger RS (1986). A new enzyme linked immunosorbent assay (ELISA) for the detection of antibodies against foot-and-mouth disease virus. I. Development and method of ELISA. Journal of Immunological Methods, 93: 123-129. 14. Michalski WP, O Rourke D & Bagust TJ (1996). Chicken anaemia virus antibody ELISA: problems with non specific reactions. Avian Pathology, 25: 245-254. 15. De Jonge N, Fillié YE & Deelder AM (1987). A simple and rapid treatment (trichloroacetic acid precipitation) of serum samples to prevent non specific reactions in the immunoassay of proteoglycan. Journal of Immunological Methods, 99: 195-197.