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. 1990 Oct;64(10):5070–5075. doi: 10.1128/jvi.64.10.5070-5075.1990

Development of an adult mouse model for studies on protection against rotavirus.

R L Ward 1, M M McNeal 1, J F Sheridan 1
PMCID: PMC247999  PMID: 2168987

Abstract

Although mice have been used as an animal model for studies on rotavirus disease, these studies have been limited by the short time period after birth during which mice are susceptible to rotavirus illness (i.e., approximately 15 days). To overcome this limitation, an adult mouse model was developed in which the endpoint was infection rather than illness. The model developed utilized a strain of mouse rotavirus (EDIM) adapted to grow in culture by multiple passages in MA104 cells. The second cell culture passage of EDIM caused severe diarrhea in neonatal BALB/c mice, and little or no amelioration of disease was observed after nine cell culture passages, even when this preparation was plaque purified. Oral administration of 2 x 10(3) PFU of passage 9 also consistently caused infection of mice 4, 10, 15, 30, 60, 120, and 180 days of age as determined by viral shedding and seroconversion. Reinoculation of these mice with the same virus preparation at 2, 3, or 4 months after the first inoculation produced no evidence of reinfection. In contrast, infection of neonatal mice with the heterotypic WC3 bovine rotavirus did not prevent reinfection with culture-adapted EDIM. Thus, this strain of EDIM caused consistent infection of previously uninoculated neonatal and adult BALB/c mice and produced homotypic but not heterotypic protection against reinfection.

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Selected References

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  1. Bartz C. R., Conklin R. H., Tunstall C. B., Steele J. H. Prevention of murine rotavirus infection with chicken egg yolk immunoglobulins. J Infect Dis. 1980 Sep;142(3):439–441. doi: 10.1093/infdis/142.3.439. [DOI] [PubMed] [Google Scholar]
  2. Bell L. M., Clark H. F., O'Brien E. A., Kornstein M. J., Plotkin S. A., Offit P. A. Gastroenteritis caused by human rotaviruses (serotype three) in a suckling mouse model. Proc Soc Exp Biol Med. 1987 Jan;184(1):127–132. doi: 10.3181/00379727-184-rc2. [DOI] [PubMed] [Google Scholar]
  3. Bernstein D. I., Kacica M. A., McNeal M. M., Schiff G. M., Ward R. L. Local and systemic antibody response to rotavirus WC3 vaccine in adult volunteers. Antiviral Res. 1989 Dec;12(5-6):293–300. doi: 10.1016/0166-3542(89)90056-9. [DOI] [PubMed] [Google Scholar]
  4. Bohl E. H., Theil K. W., Saif L. J. Isolation and serotyping of porcine rotaviruses and antigenic comparison with other rotaviruses. J Clin Microbiol. 1984 Feb;19(2):105–111. doi: 10.1128/jcm.19.2.105-111.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bridger J. C., Brown J. F. Antigenic and pathogenic relationships of three bovine rotaviruses and a porcine rotavirus. J Gen Virol. 1984 Jul;65(Pt 7):1151–1158. doi: 10.1099/0022-1317-65-7-1151. [DOI] [PubMed] [Google Scholar]
  6. Bridger J. C., Pocock D. H. Variation in virulence of bovine rotaviruses. J Hyg (Lond) 1986 Apr;96(2):257–264. doi: 10.1017/s0022172400066031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Carpio M., Bellamy J. E., Babiuk L. A. Comparative virulence of different bovine rotavirus isolates. Can J Comp Med. 1981 Jan;45(1):38–42. [PMC free article] [PubMed] [Google Scholar]
  8. Clark H. F., Furukawa T., Bell L. M., Offit P. A., Perrella P. A., Plotkin S. A. Immune response of infants and children to low-passage bovine rotavirus (strain WC3). Am J Dis Child. 1986 Apr;140(4):350–356. doi: 10.1001/archpedi.1986.02140180084030. [DOI] [PubMed] [Google Scholar]
  9. Coelho K. I., Bryden A. S., Hall C., Flewett T. H. Pathology of rotavirus infection in suckling mice: A study by conventional histology, immunofluorescence, ultrathin sections, and scanning electron microscopy. Ultrastruct Pathol. 1981 Jan-Mar;2(1):59–80. doi: 10.3109/01913128109031504. [DOI] [PubMed] [Google Scholar]
  10. Eiden J., Lederman H. M., Vonderfecht S., Yolken R. T-cell-deficient mice display normal recovery from experimental rotavirus infection. J Virol. 1986 Feb;57(2):706–708. doi: 10.1128/jvi.57.2.706-708.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Eydelloth R. S., Vonderfecht S. L., Sheridan J. F., Enders L. D., Yolken R. H. Kinetics of viral replication and local and systemic immune responses in experimental rotavirus infection. J Virol. 1984 Jun;50(3):947–950. doi: 10.1128/jvi.50.3.947-950.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gouvea V. S., Alencar A. A., Barth O. M., de Castro L., Fialho A. M., Araújo H. P., Majerowicz S., Pereira H. G. Diarrhoea in mice infected with a human rotavirus. J Gen Virol. 1986 Mar;67(Pt 3):577–581. doi: 10.1099/0022-1317-67-3-577. [DOI] [PubMed] [Google Scholar]
  13. Greenberg H. B., Vo P. T., Jones R. Cultivation and characterization of three strains of murine rotavirus. J Virol. 1986 Feb;57(2):585–590. doi: 10.1128/jvi.57.2.585-590.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Ijaz M. K., Dent D., Haines D., Babiuk L. A. Development of a murine model to study the pathogenesis of rotavirus infection. Exp Mol Pathol. 1989 Oct;51(2):186–204. doi: 10.1016/0014-4800(89)90019-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. KRAFT L. M. Studies on the etiology and transmission of epidemic diarrhea of infant mice. J Exp Med. 1957 Nov 1;106(5):743–755. doi: 10.1084/jem.106.5.743. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Knowlton D. R., Ward R. L. Effect of mutation in immunodominant neutralization epitopes on the antigenicity of rotavirus SA-11. J Gen Virol. 1985 Nov;66(Pt 11):2375–2381. doi: 10.1099/0022-1317-66-11-2375. [DOI] [PubMed] [Google Scholar]
  17. Little L. M., Shadduck J. A. Pathogenesis of rotavirus infection in mice. Infect Immun. 1982 Nov;38(2):755–763. doi: 10.1128/iai.38.2.755-763.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Losonsky G. A., Vonderfecht S. L., Eiden J., Wee S. B., Yolken R. H. Homotypic and heterotypic antibodies for prevention of experimental rotavirus gastroenteritis. J Clin Microbiol. 1986 Dec;24(6):1041–1044. doi: 10.1128/jcm.24.6.1041-1044.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Matsui S. M., Offit P. A., Vo P. T., Mackow E. R., Benfield D. A., Shaw R. D., Padilla-Noriega L., Greenberg H. B. Passive protection against rotavirus-induced diarrhea by monoclonal antibodies to the heterotypic neutralization domain of VP7 and the VP8 fragment of VP4. J Clin Microbiol. 1989 Apr;27(4):780–782. doi: 10.1128/jcm.27.4.780-782.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Moreau M. C., Corthier G., Muller M. C., Dubos F., Raibaud P. Relationships between rotavirus diarrhea and intestinal microflora establishment in conventional and gnotobiotic mice. J Clin Microbiol. 1986 May;23(5):863–868. doi: 10.1128/jcm.23.5.863-868.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Offit P. A., Clark H. F., Kornstein M. J., Plotkin S. A. A murine model for oral infection with a primate rotavirus (simian SA11). J Virol. 1984 Jul;51(1):233–236. doi: 10.1128/jvi.51.1.233-236.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Offit P. A., Clark H. F., Plotkin S. A. Response of mice to rotaviruses of bovine or primate origin assessed by radioimmunoassay, radioimmunoprecipitation, and plaque reduction neutralization. Infect Immun. 1983 Oct;42(1):293–300. doi: 10.1128/iai.42.1.293-300.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Offit P. A., Clark H. F. Protection against rotavirus-induced gastroenteritis in a murine model by passively acquired gastrointestinal but not circulating antibodies. J Virol. 1985 Apr;54(1):58–64. doi: 10.1128/jvi.54.1.58-64.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Offit P. A., Dudzik K. I. Noninfectious rotavirus (strain RRV) induces an immune response in mice which protects against rotavirus challenge. J Clin Microbiol. 1989 May;27(5):885–888. doi: 10.1128/jcm.27.5.885-888.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Offit P. A., Shaw R. D., Greenberg H. B. Passive protection against rotavirus-induced diarrhea by monoclonal antibodies to surface proteins vp3 and vp7. J Virol. 1986 May;58(2):700–703. doi: 10.1128/jvi.58.2.700-703.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Ramig R. F. The effects of host age, virus dose, and virus strain on heterologous rotavirus infection of suckling mice. Microb Pathog. 1988 Mar;4(3):189–202. doi: 10.1016/0882-4010(88)90069-1. [DOI] [PubMed] [Google Scholar]
  27. Riepenhoff-Talty M., Lee P. C., Carmody P. J., Barrett H. J., Ogra P. L. Age-dependent rotavirus-enterocyte interactions. Proc Soc Exp Biol Med. 1982 Jun;170(2):146–154. doi: 10.3181/00379727-170-41410. [DOI] [PubMed] [Google Scholar]
  28. Sheridan J. F., Eydelloth R. S., Vonderfecht S. L., Aurelian L. Virus-specific immunity in neonatal and adult mouse rotavirus infection. Infect Immun. 1983 Feb;39(2):917–927. doi: 10.1128/iai.39.2.917-927.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Sheridan J. F., Smith C. C., Manak M. M., Aurelian L. Prevention of rotavirus-induced diarrhea in neonatal mice born to dams immunized with empty capsids of simian rotavirus SA-11. J Infect Dis. 1984 Mar;149(3):434–438. doi: 10.1093/infdis/149.3.434. [DOI] [PubMed] [Google Scholar]
  30. Starkey W. G., Collins J., Wallis T. S., Clarke G. J., Spencer A. J., Haddon S. J., Osborne M. P., Candy D. C., Stephen J. Kinetics, tissue specificity and pathological changes in murine rotavirus infection of mice. J Gen Virol. 1986 Dec;67(Pt 12):2625–2634. doi: 10.1099/0022-1317-67-12-2625. [DOI] [PubMed] [Google Scholar]
  31. Tajima T., Suzuki E., Ushijima H., Araki K., Kim B., Shinozaki T., Fujii R. Isolation of murine rotavirus in cell cultures. Brief report. Arch Virol. 1984;82(1-2):119–123. doi: 10.1007/BF01309375. [DOI] [PubMed] [Google Scholar]
  32. Tzipori S., Unicomb L., Bishop R., Montenaro J., Vaelioja L. M. Studies on attenuation of rotavirus. A comparison in piglets between virulent virus and its attenuated derivative. Arch Virol. 1989;109(3-4):197–205. doi: 10.1007/BF01311081. [DOI] [PubMed] [Google Scholar]
  33. Uhnoo I., Riepenhoff-Talty M., Dharakul T., Chegas P., Fisher J. E., Greenberg H. B., Ogra P. L. Extramucosal spread and development of hepatitis in immunodeficient and normal mice infected with rhesus rotavirus. J Virol. 1990 Jan;64(1):361–368. doi: 10.1128/jvi.64.1.361-368.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Ward R. L., Bernstein D. I., Shukla R., Young E. C., Sherwood J. R., McNeal M. M., Walker M. C., Schiff G. M. Effects of antibody to rotavirus on protection of adults challenged with a human rotavirus. J Infect Dis. 1989 Jan;159(1):79–88. doi: 10.1093/infdis/159.1.79. [DOI] [PubMed] [Google Scholar]
  35. Ward R. L., Knowlton D. R., Pierce M. J. Efficiency of human rotavirus propagation in cell culture. J Clin Microbiol. 1984 Jun;19(6):748–753. doi: 10.1128/jcm.19.6.748-753.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Ward R. L., Knowlton D. R., Schiff G. M., Hoshino Y., Greenberg H. B. Relative concentrations of serum neutralizing antibody to VP3 and VP7 proteins in adults infected with a human rotavirus. J Virol. 1988 May;62(5):1543–1549. doi: 10.1128/jvi.62.5.1543-1549.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Wolf J. L., Cukor G., Blacklow N. R., Dambrauskas R., Trier J. S. Susceptibility of mice to rotavirus infection: effects of age and administration of corticosteroids. Infect Immun. 1981 Aug;33(2):565–574. doi: 10.1128/iai.33.2.565-574.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Woode G. N., Zheng S., Melendy D. R., Ramig R. F. Studies on rotavirus homologous and heterologous active immunity in infant mice. Viral Immunol. 1989;2(2):127–132. doi: 10.1089/vim.1989.2.127. [DOI] [PubMed] [Google Scholar]

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