Skip to main content
Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2002 Nov 12;11(1):11–20. doi: 10.1016/0147-9571(88)90003-3

Standardization and kinetics of in vitro bovine blood lymphocyte stimulation with bovine rotavirus

Denis Archambault 1,2, Guylaine Morin 1, Youssef Elazhary 1, Jean H Joncas 2,3, Raymond S Roy 1
PMCID: PMC7124774  PMID: 2838218

Abstract

Two groups of 3-month old calves were immunized intramuscularly with attenuated bovine rotavirus and boosted 21 and 42 days later. The first group of three calves were vaccinated with live virus emulsified with incomplete Freund's adjuvant (IFA) and the second group was immunized with live virus suspended in phosphate buffered saline (PBS). Three other calves, serving as controls, were inoculated with PBS emulsified with IFA. The specific cell-mediated and antibody responses of the animals were studied. Preliminary analysis of in vitro peripheral blood lymphocyte transformation to bovine rotavirus determined optimal conditions as: 96 h culture period, 5 × 105 cells per culture in RPMI 1640 medium containing 10% heat-inactivated bovine fetal serum and the use of inactivated virus in the cell culture at a concentration of 5 × 106 median tissue culture infective dose before inactivation. Specific blastic stimulation was observed on calves immunized with the rotavirus emulsified with IFA after the second and third vaccine inoculation with stimulation index values varying from 2.00 to 5.73. Serum neutralizing antibody titers of 125,600 were also induced in the same calves. Calves immunized with rotavirus-PBS suspension developed a mean antibody titer of 11,600, but showed no specific lymphocyte stimulation. No increase in specific immune responses was detected in the control animals.

Keywords: Bovine rotavirus, lymphocyte stimulation test, cellular immunity, neutralizing antibodies, vaccination, adjuvant

References

  • 1.Estes M.K., Palmer E.L., Obijeski J.F. Rotaviruses, a review. In: Cooper M., Hofschneider P.H., Koprowski H., Melchers F., Rott R., Schweiger H.G., Vogt P.K, Zinkernagel R, editors. 2nd edn. Vol. 105. Springer; Berlin: 1983. pp. 123–184. (Curr. Top. Microbiol. Immun.). [DOI] [PubMed] [Google Scholar]
  • 2.Flewett T.H., Woode G.N. The rotaviruses. Arch. Virol. 1978;57:1–23. doi: 10.1007/BF01315633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.McNulty M.S. Rotaviruses. J. gen. Virol. 1978;40:1–18. doi: 10.1099/0022-1317-40-1-1. [DOI] [PubMed] [Google Scholar]
  • 4.Bachmann P.A., Heiss R.G., Dirksen G., Schmid G. Kinetics of the local immune response to rotavirus infection in calves. 4th Int. Symp. Neonatal Diarrhea, Veterinary Infectious Disease Organization; Saskatoon; 1983. pp. 435–447. [Google Scholar]
  • 5.Mebus C.A., White R.G., Bass E.P., Twiehaus M.J. Immunity to neonatal calf diarrhea virus. J. Am. vet. med. Ass. 1973;163:880–883. [Google Scholar]
  • 6.Mebus C.A., Torres-Medina A., Twiehaus M.J., Bass E.P. Immune response to orally administered calf reovirus-like agent and coronavirus vaccine. In: Karger S., editor. 2nd edn. Vol. 33. International Association of Biological Standardization; Basel: 1976. pp. 396–403. (Develop. biol. Stand.). [PubMed] [Google Scholar]
  • 7.Van Zaane D., Ijzerman J., De Leew P.W. Intestinal antibody response after vaccination and infection with rotavirus of calves fed colostrum with or without rotavirus antibody. Vet. Immun. Immunopath. 1986;1:45–63. doi: 10.1016/0165-2427(86)90087-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Vonderfecht S.L., Osburn B.I. Immunity to rotavirus in conventional neonatal calves. J. clin. Microbiol. 1982;16:935–942. doi: 10.1128/jcm.16.5.935-942.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Castrucci G., Frigeri F., Ferrari M., Cilli V., Caleffi F., Aldrovandi V., Nigrelli A. The efficacy of colostrum from cows vaccinated with rotavirus in protecting calves to experimentally induced rotavirus infection. Comp. Immun. Microbiol. infect. Dis. 1984;7:11–18. doi: 10.1016/0147-9571(84)90011-0. [DOI] [PubMed] [Google Scholar]
  • 10.Saif L.J., Redman D.S., Smith K.L., Theil K.W. Passive immunity to bovine rotavirus in newborn calves fed colostrum supplements from immunized or nonimmunized cows. Infect. Immun. 1983;41:1118–1131. doi: 10.1128/iai.41.3.1118-1131.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Snodgrass D.R., Fahey K.J., Wells P.W., Campbell I., Whitelaw A. Passive immunity in calf rotavirus infections maternal vaccination increases and prolongs immunoglobulin G1 antibody secretion in milk. Infect. Immun. 1980;28:344–349. doi: 10.1128/iai.28.2.344-349.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Van Opdenbosch E., Wellemans G., Strobbe R. Evolution des anitcorps anti rota dans le lait de vaches traitées en fin de gestation soit par le vaccin anti rota complet, soit par l'adjuvant seul. Comp. Immun. Microbiol. infect. Dis. 1981;4:293–300. doi: 10.1016/0147-9571(81)90015-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Lawman M.J. Cell-mediated immunity: induction and expression of T-cell function. J. Am. vet. med. Ass. 1982;181:1022–1029. [PubMed] [Google Scholar]
  • 14.Onions D.E. The immune response to virus infections. Vet. Immun. Immunopath. 1983;4:237–277. doi: 10.1016/0165-2427(83)90059-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Rouse B.T., Horohov D.W. Cytotoxic T lymphocytes in Herpesvirus infections. Vet. Immun. Immunopath. 1984;6:35–66. doi: 10.1016/0165-2427(84)90048-5. [DOI] [PubMed] [Google Scholar]
  • 16.Bellanti J.A., Peters S.M., Rola-Pleszcynski M. Assays of cell-mediated immunity to viruses. In: Rose N.R., Friedman H., editors. Manual of Clinical Immunology. 2nd edn. American Society for Microbiology; Washington: 1980. pp. 316–326. [Google Scholar]
  • 17.Kristensen F., Kristensen B., Lazary S. The lymphocyte stimulation test in veterinary immunology. Vet. Immun. Immunopath. 1982;3:203–277. doi: 10.1016/0165-2427(82)90036-8. [DOI] [PubMed] [Google Scholar]
  • 18.Archambault D., Roy R.S., Dea S., Elazhary M.A.S.Y. Comparative study of bovine rotavirus isolated by plaque assay. Can. J. comp. Med. 1984;48:286–289. [PMC free article] [PubMed] [Google Scholar]
  • 19.Mebus C.A., Kono M., Underdahl N.R., Twiehaus M.J. Cell culture propagation of neonatal calf diarrhea (scours) virus. Can. vet. J. 1971;12:69–72. [PMC free article] [PubMed] [Google Scholar]
  • 20.Fauvel M., Spence L.S., Babiuk L.A., Petro R., Bloch S. Hemagglutination and hemagglutination-inhibition studies with a strain of Nebraska calf diarrhea virus (bovine rotavirus) Intervirology. 1978;9:95–105. doi: 10.1159/000148927. [DOI] [PubMed] [Google Scholar]
  • 21.Rodger S.M., Schnagl R.D., Holmes I.H. Further biochemical characterization including detection of surface glycoproteins of human, calf and simian rotavirus. J. Virol. 1977;24:91–98. doi: 10.1128/jvi.24.1.91-98.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Dea S., Roy R.S., Bégin M.E. Counterimmunoelectroosmophoresis for detection of neonatal calf diarrhea coronavirus: methodology and comparison with electron microscopy. J. clin. Microbiol. 1979;10:240–244. doi: 10.1128/jcm.10.2.240-244.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Reed L.J., Muench H. A simple method of estimation fifty percent end points. Am. J. Hyg. 1938;27:493–496. [Google Scholar]
  • 24.Bahnemann H.G. Binary ethylenimine as an inactivate for foot-and-mouth disease virus and its application for vaccine production. Arch. Virol. 1975;47:47–56. doi: 10.1007/BF01315592. [DOI] [PubMed] [Google Scholar]
  • 25.Rojas-Corona R.R., Skarnes R., Tangkuma S., Fire J. A comparison with other assay methods. 6th edn. Vol. 132. 1969. The limulus coagulation test for endotoxin; pp. 599–601. (Proc. Soc. exp. Biol. Med.). [DOI] [PubMed] [Google Scholar]
  • 26.Nozawa C.M., Fonseca M.E. An attempt to cultivate human rotavirus in human leukocytes culture. Rev. Int. Med. trop. Sao Paulo. 1984;26:228–229. doi: 10.1590/s0036-46651984000400008. [DOI] [PubMed] [Google Scholar]
  • 27.Barta O., Oyekan P.P. Lymphocyte transformation test in veterinary clinical immunology. Comp. Immun. Microbial. infect. Dis. 1981;4:209–221. doi: 10.1016/0147-9571(81)90006-0. [DOI] [PubMed] [Google Scholar]
  • 28.Brochier B., Pastoret P.P., Thiry E., Roupain J., Michaux C., Derboven G., Barta O. Le test de transformation lymphoblastique pour l'étude de l'immunocompétence du bétail. Ann. Méd. Vét. 1983;127:91–96. [Google Scholar]
  • 29.Woodard L.F., Renshaw H.W., Burger D. Cell-mediated immunity in neonatal calves: delayed-type hypersensitivity and lymphocyte blastogenesis following immunization with a mycobacterial immunopotentiating glycolipid and tuberculoproteins of Mycobacterium bovis. Am. J. vet. Res. 1978;39:579–584. [PubMed] [Google Scholar]
  • 30.Warren H.S., Vogel F.R., Chedid L.A. Current status of immunological adjuvants. In: Paul W.E., Fathman C.G., Metzger H., editors. 6th edn. Vol. 4. 1986. pp. 369–388. (Ann. Rev. Immun.). Palo Alto, California. [DOI] [PubMed] [Google Scholar]
  • 31.Reipenhoff-Talty, Suzuki H., Ogra P.L. Characteristics of the cell-mediated immune response to rotavirus in suckling mice. In: Karger S., editor. 6th edn. Vol. 53. International Association of Biological Standardization; Basel: 1983. pp. 263–268. (Develop. biol. Standard.). [PubMed] [Google Scholar]
  • 32.Sheridan J.F., Eydelloth R.J., Vonderfecht S.L., Aurelian L. 1983. Virus-specific immunity in neonatal and adult mouse rotavirus infection. Infect. Immun. 1983;39:917–927. doi: 10.1128/iai.39.2.917-927.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Kohl S., Harmon M.W., Tang J.P. Cytokine-stimulated human natural killer cytotoxicity: response to rotavirus-infected cells. Pediat. Res. 1983;17:868–872. doi: 10.1203/00006450-198311000-00006. [DOI] [PubMed] [Google Scholar]

Articles from Comparative Immunology, Microbiology and Infectious Diseases are provided here courtesy of Elsevier

RESOURCES