Skip to main content
Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2007 Nov 19;150(3):293–299. doi: 10.1016/S0007-1935(05)80009-0

Rotavirus infection in calves, piglets, lambs and goat kids in trinidad

JS Kaminjolo 1, AA Adesiyun 1
PMCID: PMC7130288  PMID: 8044669

Abstract

Faecal samples from diarrhoeic and non-diarrhoeic calves, piglets, lambs and goat kids were collected and screened by a latex agglutination test to detect the presence of group A rotavirus antigen. Of a total of 470 animals screened, 138 (29.4%) had faecal samples positive for rotavirus antigen. The prevalences of infection were 27.7% (73/264) in calves, 27.8% (45/162) in piglets, 48.6% (18/37) in lambs and 28.6% (2/7) in goat kids. Rotavirus antigen was not detected in calves and lambs <1 week old and in piglets <2 weeks old. The highest prevalence was found in calves between the ages 1–6 weeks (72.6%); piglets, 2–8 weeks (91.1%) and in lambs 1–8 weeks (88.9%). The overall prevalence of infection was 39.9% for diarrhoeic and 13.4% for non-diarrhoeic animals and the difference was statistically significant (P⩽0.001; X2). Differences among husbandry systems in relation to the prevalence of rotavirus infection were not statistically significant (P⩾0.05; X2).

The relatively high prevalence of rotavirus infection in the young animals tested, coupled with the detected significantly higher infection rates in diarrhoeic animals, indicate that rotavirus may be important in livestock diarrhoea in Trinidad.

Keywords: Rotavirus, diarrhoea, newborn, Trinidad

References

  1. Adesiyun A.A., Kaminjolo J.S., Loregnard R., Kitson-Piggot W. Campylobacter infections in calves, piglets, lambs and kids in Trinidad. British Veterinary Journal. 1992;148:547–556. doi: 10.1016/0007-1935(92)90011-O. [DOI] [PubMed] [Google Scholar]
  2. Archambault D., Morin G., Elazhary Y., Roy R.S. Study of virus excretion in faeces of diarrhoeic and asymptomatic calves infected with rotavirus. Zentralblatt für Veterindrmedizin Reihe B(Berlin) 1990;37:73–76. doi: 10.1111/j.1439-0450.1990.tb01028.x. [DOI] [PubMed] [Google Scholar]
  3. Blood D.C., Radostits O.M. 7th edn. Baillière Tindall; Philadelphia: 1989. Veterinary Medicine; pp. 864–873. (A Textbook of the Diseases of Cattle, Sheep, pigs, Goats and Horses.). [Google Scholar]
  4. Bohl E.H., Saif L.J., Theil K.E., Agnes A.G., Cross R.F. Porcine pararotavirus: detection, differentiation from rotavirus, and pathogenesis in gnotobiotic pigs. Journal of Clinical Microbiology. 1982;15:312–319. doi: 10.1128/jcm.15.2.312-319.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Brüssow H., Eichhorn W., Sotek J., Sidoti J. Prevalence of antibodies to four bovine rotavirus strains in different age groups of cattle. Veterinary Microbiology. 1990;25:143–151. doi: 10.1016/0378-1135(90)90073-5. [DOI] [PubMed] [Google Scholar]
  6. Chasey D., Davies P. Atypical rotavirus in pigs and cattle. Veterinary Record. 1984;114:16–17. doi: 10.1136/vr.114.1.16. [DOI] [PubMed] [Google Scholar]
  7. Chasey D., Banks J. The commonest rotaviruses from neonatal lamb diarrhoea in England and Wales have atypical electropherotypes. Veterinary Record. 1984;115:326–327. doi: 10.1136/vr.115.13.326. [DOI] [PubMed] [Google Scholar]
  8. Crouch C.F., Acres S.D. Prevalence of rotavirus and coronavirus antigens in the faeces of normal cows. Canadian Journal of Comparative Medicine. 1984;48:340–342. [PMC free article] [PubMed] [Google Scholar]
  9. De Leeuw P.W., Ellens D.J., Strayer P.J., Van Balken J.A.M., Moerman A., Baanvinger T. Rotavirus infections in calves in daily herds. Research in Veterinary Science. 1980;29:135–141. doi: 10.1016/S0034-5288(18)32653-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. De-Rycke J., Le Roux P., Melik N., Raimbault P. Frequency of entero-pathogenic K99 ST Echerichia coli and rotaviruses in neonatal diarrhoea of calves. Survey of a veterinarian's clientele in Sarthe. Annales de Recherches Veterinaires (Paris) 1982;12:403–411. [PubMed] [Google Scholar]
  11. Flewett T.H. Acute non-bacterial infectious gastroenteritis. In: Waterson A.P., editor. Vol. 1. Churchill Livingstone; London: 1977. pp. 151–169. (Recent Advances in Clinical Virology). [Google Scholar]
  12. Gelberg H.B., Woode G.N., Kniffen T.S., Hardy M., Hall W.F. The shedding of group A rotavirus antigen in a newly established closed specific pathogen-free swine herd. Veterinary Microbiology. 1991;28:213–229. doi: 10.1016/0378-1135(91)90077-s. [DOI] [PubMed] [Google Scholar]
  13. Gelberg H.B., Patterson J.S., Woods G.N. A longitudinal study of rotavirus antibody titers in swine in a closed specific pathogen-free herd. Veterinary Microbiology. 1991;28:231–242. doi: 10.1016/0378-1135(91)90078-t. [DOI] [PubMed] [Google Scholar]
  14. Gomwalk N.E., Mohammed I., Umoh J. Rotavirus infection in diarrhoeic and non-diarrhoeic calves in Zaria. Zariya Veterinaire. 1988;3:97–99. [Google Scholar]
  15. Hess R.G., Bachmann P.A., Baljer G., Mayr A., Pospischill A., Schmud G. Synergism in experimental mixed infections of newborn colostrum deprived calves with bovine rotavirus and entero-toxigenic Escherichia coli (ETEC) Zentralblallt für Veterinärmedizin Reihe B (Berlin) 1984;31:595–596. doi: 10.1111/j.1439-0450.1984.tb01339.x. [DOI] [PubMed] [Google Scholar]
  16. Hull B.P., Spence I., Bassett D., Swanston W.H., Tikasingh E.S. The relative importance of rotavirus and other pathogens in the aetiology of gastroenteritis in Trinidian children. American Journal of Tropical Medicine and Hygiene. 1982;31:142–148. doi: 10.4269/ajtmh.1982.31.142. [DOI] [PubMed] [Google Scholar]
  17. Kapikian A.Z., Kim H.W., Wyatt R.G. Human rotavirus-like agent as the major pathogen associated with “winter” gastroenteritis in hospitalized infants and young children. New England Journal of Medicine. 1976;294:965–972. doi: 10.1056/NEJM197604292941801. [DOI] [PubMed] [Google Scholar]
  18. Magar R., Robinson Y., Morin M. Identification of atypical rotaviruses in outbreaks of preweaning and postweaning diarrhoea in Quebec swine herds. Canadian Journal of Veterinary Research. 1991;55:260–263. [PMC free article] [PubMed] [Google Scholar]
  19. McNulty M.S. Rotaviruses. A review article. Journal of General Virology. 1978;40:1–18. doi: 10.1099/0022-1317-40-1-1. [DOI] [PubMed] [Google Scholar]
  20. McNulty M.S. The aetiology, pathology and epidemiology of viral gastroenteritis. Annales Recherches Veterinaires. 1983;14:427–432. [PubMed] [Google Scholar]
  21. McNulty M.S., Logan E.F. Longitudinal survey of rotavirus infection in calves. Veterinary Record. 1983;113:333–335. doi: 10.1136/vr.113.15.333. [DOI] [PubMed] [Google Scholar]
  22. McNulty M.S., Curran W.L., McFerran J.B., Collin D.S. Viruses and diarrhoea in dogs. Veterinary Record. 1980;106:350–351. doi: 10.1136/vr.106.15.350. [DOI] [PubMed] [Google Scholar]
  23. Mebus C.A., Underdahl N.R., Rhoades M.B., Twiehaus M.J. Calf diarrhoea (Scours) reproduced with a virus from a field outbreak. University of Nebraska Agricultural Experimental Station Research Bulletin. 1969;233:1–16. [Google Scholar]
  24. Moon H.W., McClurkin A.W., Isaacson R.E., Pohlenz J., Skartvedt S.M., Gillette K.G., Baetz A.L. Pathogenic relationship of rotavirus, Escherichia coli, and other agents in mixed infections in calves. Journal of the American Veterinary Medical Association. 1978;5:577–583. [PubMed] [Google Scholar]
  25. Perrin B., Martel J.L., Solsona M., Contrepois M., Dubourguier H.C., Girardeau J.P., Gouft P., Bordas C., Hayers F., Quilleriet-Eliez A., Ramisse J., Sendrai R. Incidence of rotavirus infection and in combined infection of rotavirus and enteropathogenic Escherichia coli in French calves. Annales Recherches Veterinaires. 1981;12:259–263. [PubMed] [Google Scholar]
  26. Saif L.J., Bohl E.H., Kohler E.M., Hughes J.H. Immune electron microscopy of transmissible gastroenteritis virus and rotavirus (Reovirus-like agent) of swine. American Journal of Veterinary Research. 1977;38:13–20. [PubMed] [Google Scholar]
  27. Sanekata T., Kishimoto E., Sato K., Honma H., Otsuki K., Tsubokura M. Detection of porcine rotavirus in stools by a latex agglutination test. Veterinary Microbiology. 1991;27:245–251. doi: 10.1016/0378-1135(91)90151-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Scott A.C., Luddington J., Lucas M., Gilbert F.R. Rotavrius in goats. Veterinary Record. 1978;103:145. doi: 10.1136/vr.103.7.145-b. [DOI] [PubMed] [Google Scholar]
  29. Sibalin M., Szekely H., Bürki F. Rotavirusinfektionen in einem grosseren Rhinderbestand. Wiener Tierärzlische Monatschrift. 1980;67:122–127. [Google Scholar]
  30. Snodgrass D.R., Smith W., Gray E.W., Herring J.A. Rotavirus in lambs with diarrhoea. Research in Veterinary Science. 1976;20:113–114. [PubMed] [Google Scholar]
  31. Sukura A., Neuvonen E. Latex test for rapid rotavirus diagnosis in calves. Acta Veterinaria Scandinavica. 1990;31:1–4. doi: 10.1186/BF03547571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Tzipori S. The actiology and diagnosis of calf diarrhoea. Veterinary Record. 1981;108:510–514. doi: 10.1136/vr.108.24.510. [DOI] [PubMed] [Google Scholar]
  33. Tzipori S., Sherwood D., Anges K.W., Campbell I., Gordon M. Diarrhoea in lambs: experimental infections with enterotoxigenic Escherichia coli, rotavirus, and Cryptosporidium sp. Infection and Immunity. 1981;33:401–406. doi: 10.1128/iai.33.2.401-406.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Tzipori S. The relative importance of enteric pathogens affecting neonates of domestic animals. Advances in Veterinary Science and Comparative Medicine (New York) 1985;29:103–206. [PubMed] [Google Scholar]
  35. Utrera V., Mazzali de Ilja R., Gorziglia M., Esparza J. Epidemiological aspects of porcine rotavirus infection in Venezuela. Research in Veterinary Science. 1984;36:310–315. [PubMed] [Google Scholar]
  36. Woode G.N. Epizootiology of bovine rotavirus infection. Veterinary Record. 1978;103:44–46. doi: 10.1136/vr.103.3.44. [DOI] [PubMed] [Google Scholar]
  37. Woode G.N., Bridger J., Hall G.A., Jones J.M., Jackson G. The isolation of reovirus-like agents (Rotaviruses) from acute gastroenteritis of piglets. Journal of Medical Microbiology. 1976;9:203–209. doi: 10.1099/00222615-9-2-203. [DOI] [PubMed] [Google Scholar]

Articles from The British Veterinary Journal are provided here courtesy of Elsevier

RESOURCES