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. 1970;31(3):293–302. doi: 10.1007/BF01253764

Rat coronavirus (RCV): A prevalent, naturally occurring pneumotropic virus of rats

J C Parker 1, S S Cross 1, W P Rowe 2
PMCID: PMC7086756  PMID: 4099196

Summary

A new virus isolated from the lungs of rats is prevalent in colony reared and wild rats and induces a fatal pneumonitis in newborn rats. The virus, designated as rat coronavirus (RCV), exhibits properties representative of the coronavirus group: characteristic surface structure, particles somewhat variable in size averaging approximately 90 mμ, apparent RNA content, essential lipid, heat sensitivity, and a close serologie relationship with the mouse hepatitis virus complex. RCV grows well in primary rat kidney cell cultures, exhibits a pathognomonic type CPE, and produces a complement fixing antigen which is sensitive for detection of antibody and useful in sero-epidemiologic studies.

Keywords: Hepatitis, Property Representative, Heat Sensitivity, Mouse Hepatitis Virus, Virus Complex

Footnotes

Supported by Public Health Service Contract No. SA-43-67-700 with the National Cancer Institute, National Institutes of Health, Bethesda, Md., U.S.A.

References

  • 1.Almeida J. D., Berry D. M., Cunningham C. H., Hamre D., Hofstad M. S., Mallucci L., Mcintosh K., Tyrrell D. A. J. Coronaviruses. Nature (Lond.) 1968;220:650. [Google Scholar]
  • 2.Ashe W. K., Scherp H. W., Fitzgerald R. J. Previously unrecognized virus from submaxillary glands of gnotobiotic and conventional rats. J. Bact. 1965;90:1719–1729. doi: 10.1128/jb.90.6.1719-1729.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Becker W. B., McIntosh K., Dees J. H., Chanock R. M. Morphogenesis of avian infectious bronchitis virus and a related human virus (Strain 229E) J. Virol. 1967;1:1019–1027. doi: 10.1128/jvi.1.5.1019-1027.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Berry D. M., Cruickshank J. G., Chu H. P., Wells R. J. H. The structure of infectious bronchitis virus. Virology. 1964;23:403–407. doi: 10.1016/0042-6822(64)90263-6. [DOI] [PubMed] [Google Scholar]
  • 5.Brennan P. C., Fritz T. E., Flynn R. J. Murine pneumonia: A review of the etiologic agents. Lab. Anim. Care. 1969;19:360–371. [PubMed] [Google Scholar]
  • 6.Hartley J. W., Rowe W. P. Tissue culture cytopathic and plaque assay for mouse hepatitis viruses. Proc. Soc. exp. Biol. (N.T.) 1963;113:403–406. doi: 10.3181/00379727-113-28378. [DOI] [PubMed] [Google Scholar]
  • 7.Hartley J. W., Rowe W. P., Bloom H. H., Turner H. C. Antibodies to mouse hepatitis viruses in human sera. Proc. Soc. exp. Biol. (N.Y.) 1964;115:414–418. doi: 10.3181/00379727-115-28928. [DOI] [PubMed] [Google Scholar]
  • 8.Joshi N. N., Dale D. G., Blackwood A. C. Etiology of murine endemic pneumonia. Rev. canad. Biol. 1965;24:169–178. [PubMed] [Google Scholar]
  • 9.Kapikian A. Z., Harvey J. D., Jr., Kelly S. J., Dees J. H., Turner H. C., McIntosh K., Kim Hyun Wha, Parrott R. H., Vincent M. M., Chanock R. M. Isolation from man of “Avian infectious bronchitis virus-like” viruses (Coronaviruses) similar to 229E virus, with some epidemiological observations. J. infect. Dis. 1969;119:282–290. doi: 10.1093/infdis/119.3.282. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Kaplan M. M., Wiktor T. J., Maes R. F., Campbell J. B., Koprowski H. Effect of polyions on the infectivity of rabies virus in tissue culture: Construction of a single-cycle growth curve. J. Virol. 1967;1:145–151. doi: 10.1128/jvi.1.1.145-151.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.McIntosh K., Kapikian A. Z., Hardison K. A., Hartley J. W., Chanock R. M. Antigenic relationships among the coronaviruses of man and between human and animal Coronaviruses. J. Immunol. 1969;102:1109–1118. [PubMed] [Google Scholar]
  • 12.Nelson J. B. Studies on endemic pneumonia of the albino rat. II. The nature of the causal agent in experimentally infected rats. J. exp. Med. 1946;84:15–22. [PubMed] [Google Scholar]
  • 13.Parker J. C., Tennant R. W., Ward T. G., Rowe W. P. Virus studies with germfree mice. I. Preparation of serologic diagnostic reagents and survey of germfree and monocontaminated mice for indigenous murine viruses. J. nat. Cancer Inst. 1965;34:371–380. [PubMed] [Google Scholar]
  • 14.Parkerr, J. C., J. I.Hercules, and E.Von Kaenel: The prevalence of some indigenous viruses of rat and hamster breeder colonies. Bact. Proc. 163 (1967).
  • 15.Rowe W. P., Hartley J. W., Capps W. I. Mouse hepatitis virus infection as a highly contagious, prevalent, enteric infection of mice. Proc. Soc. exp. Biol. (N.Y.) 1963;112:161–165. doi: 10.3181/00379727-112-27980. [DOI] [PubMed] [Google Scholar]
  • 16.Rowe W. P., Hartley J. W., Huebner R. J. Polyoma and other indigenous mouse viruses. In: Harris R. I. C., editor. The Problems of Laboratory Animal Disease. New York: Academic Press; 1962. pp. 131–142. [Google Scholar]
  • 17.Schell K., Huebner R. J., Turner H. C. Concentration of complement fixing viral antigens. Proc. Soc. exp. Biol. (N.Y.) 1966;121:41–46. doi: 10.3181/00379727-121-30692. [DOI] [PubMed] [Google Scholar]
  • 18.Ver B. A., Melnick J. L., Wallis C. Efficient filtration and sizing of viruses with membrane filters. J. Virol. 1968;2:21–25. doi: 10.1128/jvi.2.1.21-25.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]

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