Skip to main content
Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1988 Sep;26(9):1853–1858. doi: 10.1128/jcm.26.9.1853-1858.1988

Identification of a group-reactive epitope of group B rotaviruses recognized by monoclonal antibody and application to the development of a sensitive immunoassay for viral characterization.

R Yolken 1, S B Wee 1, J Eiden 1, J Kinney 1, S Vonderfecht 1
PMCID: PMC266729  PMID: 2460499

Abstract

Group B rotaviruses (GBRs) are fastidious agents which cause enteric disease in humans and a number of other animal species. Detailed study of the role of GBRs in human disease has been hampered by the lack of immunoreagents suitable for large-scale studies. We developed a monoclonal antibody which recognizes a group-reactive antigen contained in a number of strains of GBRs. When utilized in conjunction with a hyperimmune guinea pig antiserum to GBR, this monoclonal antibody can be used in an enzyme immunoassay system to detect a wide range of GBRs. Alternatively, this monoclonal antibody can be combined with sera obtained from GBR-infected animals to devise assays which are largely specific for the homologous strain of GBR. Reactivity was not noted in either system with strains of group A or group C rotaviruses or with other members of the family Reoviridae. These results indicate that GBRs contain both group-reactive and species-specific antigens which are distinct from those found in group A rotaviruses. The availability of well-defined immunoreagents will facilitate detailed studies of GBR infections in humans and animals.

Full text

PDF
1853

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ashley C. R., Caul E. O. Potassium tartrate-glycerol as a density gradient substrate for separation of small, round viruses from human feces. J Clin Microbiol. 1982 Aug;16(2):377–381. doi: 10.1128/jcm.16.2.377-381.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Askaa J., Bloch B. Infection in piglets with a porcine rotavirus-like virus. Experimental inoculation and ultrastructural examination. Arch Virol. 1984;80(4):291–303. doi: 10.1007/BF01311220. [DOI] [PubMed] [Google Scholar]
  3. Black R. E., Merson M. H., Rahman A. S., Yunus M., Alim A. R., Huq I., Yolken R. H., Curlin G. T. A two-year study of bacterial, viral, and parasitic agents associated with diarrhea in rural Bangladesh. J Infect Dis. 1980 Nov;142(5):660–664. doi: 10.1093/infdis/142.5.660. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bridger J. C. Detection by electron microscopy of caliciviruses, astroviruses and rotavirus-like particles in the faeces of piglets with diarrhoea. Vet Rec. 1980 Dec 6;107(23):532–533. [PubMed] [Google Scholar]
  5. Chen C. M., Hung T., Bridger J. C., McCrae M. A. Chinese adult rotavirus is a group B rotavirus. Lancet. 1985 Nov 16;2(8464):1123–1124. doi: 10.1016/s0140-6736(85)90710-x. [DOI] [PubMed] [Google Scholar]
  6. Eiden J., Vonderfecht S., Theil K., Torres-Medina A., Yolken R. H. Genetic and antigenic relatedness of human and animal strains of antigenically distinct rotaviruses. J Infect Dis. 1986 Dec;154(6):972–982. doi: 10.1093/infdis/154.6.972. [DOI] [PubMed] [Google Scholar]
  7. Eiden J., Vonderfecht S., Yolken R. H. Evidence that a novel rotavirus-like agent of rats can cause gastroenteritis in man. Lancet. 1985 Jul 6;2(8445):8–11. doi: 10.1016/s0140-6736(85)90057-1. [DOI] [PubMed] [Google Scholar]
  8. Espejo R. T., Puerto F., Soler C., González N. Characterization of a human pararotavirus. Infect Immun. 1984 Apr;44(1):112–116. doi: 10.1128/iai.44.1.112-116.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Flewett T. H., Woode G. N. The rotaviruses. Arch Virol. 1978;57(1):1–23. doi: 10.1007/BF01315633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Herring A. J., Inglis N. F., Ojeh C. K., Snodgrass D. R., Menzies J. D. Rapid diagnosis of rotavirus infection by direct detection of viral nucleic acid in silver-stained polyacrylamide gels. J Clin Microbiol. 1982 Sep;16(3):473–477. doi: 10.1128/jcm.16.3.473-477.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Hung T., Chen G. M., Wang C. G., Yao H. L., Fang Z. Y., Chao T. X., Chou Z. Y., Ye W., Chang X. J., Den S. S. Waterborne outbreak of rotavirus diarrhoea in adults in China caused by a novel rotavirus. Lancet. 1984 May 26;1(8387):1139–1142. [PubMed] [Google Scholar]
  12. Kapikian A. Z., Flores J., Hoshino Y., Glass R. I., Midthun K., Gorziglia M., Chanock R. M. Rotavirus: the major etiologic agent of severe infantile diarrhea may be controllable by a "Jennerian" approach to vaccination. J Infect Dis. 1986 May;153(5):815–822. doi: 10.1093/infdis/153.5.815. [DOI] [PubMed] [Google Scholar]
  13. McNulty M. S., Allan G. M., Todd D., McFerran J. B., McCracken R. M. Isolation from chickens of a rotavirus lacking the rotavirus group antigen. J Gen Virol. 1981 Aug;55(Pt 2):405–413. doi: 10.1099/0022-1317-55-2-405. [DOI] [PubMed] [Google Scholar]
  14. Mebus C. A., Rhodes M. B., Underdahl N. R. Neonatal calf diarrhea caused by a virus that induces villous epithelial cell syncytia. Am J Vet Res. 1978 Jul;39(7):1223–1228. [PubMed] [Google Scholar]
  15. Nakata S., Estes M. K., Graham D. Y., Loosle R., Tao H., Wang S. H., Saif L. J., Melnick J. L. Antigenic characterization and ELISA detection of adult diarrhea rotaviruses. J Infect Dis. 1986 Sep;154(3):448–455. doi: 10.1093/infdis/154.3.448. [DOI] [PubMed] [Google Scholar]
  16. Nakata S., Estes M. K., Graham D. Y., Wang S. S., Gary G. W., Melnick J. L. Detection of antibody to group B adult diarrhea rotaviruses in humans. J Clin Microbiol. 1987 May;25(5):812–818. doi: 10.1128/jcm.25.5.812-818.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Pedley S., Bridger J. C., Brown J. F., McCrae M. A. Molecular characterization of rotaviruses with distinct group antigens. J Gen Virol. 1983 Oct;64(Pt 10):2093–2101. doi: 10.1099/0022-1317-64-10-2093. [DOI] [PubMed] [Google Scholar]
  18. Pereira H. G., Azeredo R. S., Leite J. P., Barth O. M., Sutmoller F., de Farias V., Vidal M. N. Comparison of polyacrylamide gel electrophoresis (PAGE), immuno-electron microscopy (IEM) and enzyme immunoassay (EIA) for the rapid diagnosis of rotavirus infection in children. Mem Inst Oswaldo Cruz. 1983 Oct-Dec;78(4):483–490. doi: 10.1590/s0074-02761983000400012. [DOI] [PubMed] [Google Scholar]
  19. Rodger S. M., Bishop R. F., Holmes I. H. Detection of a rotavirus-like agent associated with diarrhea in an infant. J Clin Microbiol. 1982 Oct;16(4):724–726. doi: 10.1128/jcm.16.4.724-726.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Shmilovitz M., Kretzer B., Levi S. A new provisional serovar of Shigella dysenteriae. J Clin Microbiol. 1985 Feb;21(2):240–242. doi: 10.1128/jcm.21.2.240-242.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Snodgrass D. R., Herring A. J., Campbell I., Inglis J. M., Hargreaves F. D. Comparison of atypical rotaviruses from calves, piglets, lambs and man. J Gen Virol. 1984 May;65(Pt 5):909–914. doi: 10.1099/0022-1317-65-5-909. [DOI] [PubMed] [Google Scholar]
  22. Steele A. D., Alexander J. J. Molecular epidemiology of rotavirus in black infants in South Africa. J Clin Microbiol. 1987 Dec;25(12):2384–2387. doi: 10.1128/jcm.25.12.2384-2387.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Viscidi R., Laughon B. E., Hanvanich M., Bartlett J. G., Yolken R. H. Improved enzyme immunoassays for the detection of antigens in fecal specimens. Investigation and correction of interfering factors. J Immunol Methods. 1984 Feb 24;67(1):129–143. doi: 10.1016/0022-1759(84)90092-9. [DOI] [PubMed] [Google Scholar]
  24. Vonderfecht S. L., Eiden J. J., Miskuff R. L., Yolken R. H. Kinetics of intestinal replication of group B rotavirus and relevance to diagnostic methods. J Clin Microbiol. 1988 Feb;26(2):216–221. doi: 10.1128/jcm.26.2.216-221.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Vonderfecht S. L., Eiden J. J., Torres A., Miskuff R. L., Mebus C. A., Yolken R. H. Identification of a bovine enteric syncytial virus as a nongroup A rotavirus. Am J Vet Res. 1986 Sep;47(9):1913–1918. [PubMed] [Google Scholar]
  26. Vonderfecht S. L., Miskuff R. L., Eiden J. J., Yolken R. H. Enzyme immunoassay inhibition assay for the detection of rat rotavirus-like agent in intestinal and fecal specimens obtained from diarrheic rats and humans. J Clin Microbiol. 1985 Nov;22(5):726–730. doi: 10.1128/jcm.22.5.726-730.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Wang S. S., Cai R. F., Chen J., Li R. J., Jiang R. S. Etiologic studies of the 1983 and 1984 outbreaks of epidemic diarrhea in Guangxi. Intervirology. 1985;24(3):140–146. doi: 10.1159/000149633. [DOI] [PubMed] [Google Scholar]
  28. Woode G. N., Bridger J. C., Jones J. M., Flewett T. H., Davies H. A., Davis H. A., White G. B. Morphological and antigenic relationships between viruses (rotaviruses) from acute gastroenteritis of children, calves, piglets, mice, and foals. Infect Immun. 1976 Sep;14(3):804–810. doi: 10.1128/iai.14.3.804-810.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Yolken R. H. Enzyme immunoassays for the detection of infectious antigens in body fluids: current limitations and future prospects. Rev Infect Dis. 1982 Jan-Feb;4(1):35–68. doi: 10.1093/clinids/4.1.35. [DOI] [PubMed] [Google Scholar]
  30. Yolken R. H., Stopa P. J. Analysis of nonspecific reactions in enzyme-linked immunosorbent assay testing for human rotavirus. J Clin Microbiol. 1979 Nov;10(5):703–707. doi: 10.1128/jcm.10.5.703-707.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. de StGroth S. F., Scheidegger D. Production of monoclonal antibodies: strategy and tactics. J Immunol Methods. 1980;35(1-2):1–21. doi: 10.1016/0022-1759(80)90146-5. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Clinical Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES