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. 2002 Nov 13;17(2):133–138. doi: 10.1016/0147-9571(94)90038-8

Cellular immune status of coronavirus-infected neonatal calves

Sanjay Kapil 1, Sagar M Goyal 1,, Ava M Trent 2
PMCID: PMC7134123  PMID: 7924246

Abstract

A preliminary study was conducted to determine the cellular immune status of neonatal, colostrum-deprived calves following inoculation with either attenuated or virulent bovine coronavirus (BCV). Uninfected calves served as controls. To determine the intestinal and systemic cellular immune status, we performed MHC-restricted cytotoxic lymphocyte (CTL) assay on mesenteric lymphocytes, enumerated T cell subsets in peripheral blood lymphocytes, and examined histopathological alterations in mesenteric lymph nodes and gut-associated lymphoid tissue. Target cells for the CTL assay were autologous testicular cells and effector cells were mesenteric lymphocytes from calves infected with BCV. No appreciable specific lysis was observed in any group of calves indicating the absence of demonstrable CTL responses. The TC/TS population was severely depressed in the calf inoculated with the virulent virus but not in those inoculated with either the attenuated virus or placebo. The mesenteric lymph nodes and Peyer's patches of calves inoculated with the virulent virus showed severe depletion of lymphocytes. These calves developed intestinal antibody responses in the acute phase of infection (1 week after infection) but were immunosuppressed in the later stage of infection.

Keywords: Bovine coronavirus, cellular immunity, T lymphocytes, calf scours, immunosuppression

References

  • 1.Saif L.J., Heckert R.A. Enteric coronaviruses. In: Saif L.J., Theil K.W., editors. Viral Diarrheas of Man and Animals. CRC Press; Boca Raton, Fla: 1990. pp. 185–252. [Google Scholar]
  • 2.Torres-Medina A, Schlafer D.H., Mebus C.A. Rotaviral and coronaviral diarrhea. Vet. Clin. N. Am., Food Anim. Pract. 1985;1:471–493. doi: 10.1016/S0749-0720(15)31297-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Saif L.J. Development of nasal, fecal, and serum isotype-specific antibodies in calves challenged with bovine coronavirus or rotavirus. Vet. Immunol. Immunopathol. 1987;17:425–439. doi: 10.1016/0165-2427(87)90159-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Kapil S., Trent A.M., Goyal S.M. Antibody responses in spiral colon, ileum, and jejunum of bovine coronavirus infected calves. Comp. Immunol. Microbial. Infect. Dis. 1994;17:139–149. doi: 10.1016/0147-9571(94)90039-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Kapil S., Pomeroy K.A., Goyal S.M., Trent A.M. Experimental infection with a virulent pneumoenteric isolate of bovine coronavirus. J. Vet. Diagn. Invest. 1991;3:88–89. doi: 10.1177/104063879100300123. [DOI] [PubMed] [Google Scholar]
  • 6.Kapil S., Trent A.M., Goyal S.M. Excretion and persistence of bovine coronavirus in neonatal calves. Arch. Virol. 1990;115:127–132. doi: 10.1007/BF01310629. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Baldwin C.L., Teale A.J., Naessens J.G., Goddeeris B.M., MacHugh N.D., Morrison W.I. Characterization of a subset of bovine T lymphocytes that express BoT4 by monoclonal antibodies and function: Similarity to lymphocytes defined by human T4 and murine L3T4. J. Immunol. 1986;136:4385–4391. [PubMed] [Google Scholar]
  • 8.Ellis J.A., Baldwin C.L., MacHugh N.D., Bensaid A., Teale A.J., Goddeeris B.M., Morrison W.I. Characterization by a monoclonal antibody and functional analysis of a subset of bovine T lymphocytes that express BoT8, a molecule analogous to human CD8. Immunology. 1986;58:351–358. [PMC free article] [PubMed] [Google Scholar]
  • 9.Rose N.R., Friedman H. Manual of Clinical Immunology. American Society for Microbiology; Washington, D.C: 1980. [Google Scholar]
  • 10.Huegin A.W., Cerny A., Zinkernagel R.M., Neftel K.A. Suppressive effects of beta-lactam-antibiotics on in vitro generation of cytotoxic T cells. Int. J. Immunopharmacol. 1986;8:723–729. doi: 10.1016/0192-0561(86)90008-1. [DOI] [PubMed] [Google Scholar]
  • 11.Campos M., Rossi C.R. In vitro induction of cytotoxic lymphocytes from infectious bovine rhinotracheitis virus hyperimmune cattle. Am. J. Vet. Res. 1986;47:2411–2414. [PubMed] [Google Scholar]
  • 12.Godson D.L., Campos M., Babiuk L.A. Non-major histocompatibility complex-restricted cytotoxicity of bovine coronavirus-infected target cells mediated by bovine intestinal intraepithelial leukocytes. J. Gen. Virol. 1991;72:2457–2465. doi: 10.1099/0022-1317-72-10-2457. [DOI] [PubMed] [Google Scholar]
  • 13.Shimizu M., Shimizu Y. Demonstration of cytotoxic lymphocytes to virus-infected target cells in pigs inoculated with transmissible gastroenteritis virus. Am. J. Vet. Res. 1979;40:208–213. [PubMed] [Google Scholar]
  • 14.Carman P.S., Ernst P.B., Rosenthal K.L., Clark D.A., Befus A.D., Bienenstock J. Intraepithelial leukocytes contain a unique subpopulation of NK-like cytotoxic cells active in the defense of gut epithelium to enteric murine coronavirus. J. Immunol. 1986;136:1548–1553. [PubMed] [Google Scholar]
  • 15.Mebus C.A., Stair E.L., Rhodes M.B., Twiehaus M.J. Pathology of neonatal calf diarrhea induced by a coronavirus-like agent. Vet. Pathol. 1973;10:45–64. doi: 10.1177/030098587301000105. [DOI] [PubMed] [Google Scholar]
  • 16.Sharma J.M., Dupuy J.M., Lamontagnel L. Immunosuppression by avian infectious bursal disease virus and mouse hepatitis virus. In: Spector S., Bendinelli M., Friedman H., editors. Virus Induced Immunosuppression. Plenum Press; New York: 1990. pp. 201–216. [Google Scholar]

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