Hostname: page-component-76fb5796d-25wd4 Total loading time: 0 Render date: 2024-04-25T10:25:02.472Z Has data issue: false hasContentIssue false

Role of enteric pathogens in the aetiology of neonatal diarrhoea in lambs and goat kids in Spain

Published online by Cambridge University Press:  15 May 2009

M. Muñoz
Affiliation:
Departamento de Sanidad Animal (Enfermedades Infecciosas y Epidemiologia), Facultad de Veterinaria, Universidad de León, Campus de Vegazana, E-24071 León, Spain
M. Álvarez
Affiliation:
Departamento de Sanidad Animal (Enfermedades Infecciosas y Epidemiologia), Facultad de Veterinaria, Universidad de León, Campus de Vegazana, E-24071 León, Spain
I. Lanza
Affiliation:
Departamento de Sanidad Animal (Enfermedades Infecciosas y Epidemiologia), Facultad de Veterinaria, Universidad de León, Campus de Vegazana, E-24071 León, Spain
P. Cármenes
Affiliation:
Departamento de Sanidad Animal (Enfermedades Infecciosas y Epidemiologia), Facultad de Veterinaria, Universidad de León, Campus de Vegazana, E-24071 León, Spain
Rights & Permissions [Opens in a new window]

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Faeces samples from diarrhoeic and non-diarrhoeic lambs and goat kids aged 1–45 days were examined for enteric pathogens. Cryptosporidium parvum was detected in both diarrhoeic lambs (45%) and goat kids (42%) but not in non-diarrhoeic animals. F5+ (K99+) and/or F41+Escherichia coli strains were isolated from 26% and 22% of the diarrhoeic lambs and goat kids, respectively, although these strains, which did not produce enterotoxins ST I or LT I, were found with similar frequencies in non-diarrhoeic animals. A F5F41ST I+E. coli strain was isolated from a diarrhoeic lamb (0·6%). Verotoxigenic E. coli was isolated from both diarrhoeic and non-diarrhoeic lambs (4·1% and 8·2%, respectively) and there was no association between infection and diarrhoea. The prevalence of group A rotavirus infection in diarrhoeic lambs was very low (2·1%). Groups A and B rotaviruses were detected in three (8·1%) and five (13·5%) diarrhoeic goat kids from two single outbreaks. Group C rotaviruses were detected in four non-diarrhoeic goat kids. An association of diarrhoea and infection was demonstrated only for group B rotavirus. Clostridium perfringens was isolated from 10·8% of the diarrhoeic goat kids but not from non-diarrhoeic goat kids or lambs. Salmonella arizonae was isolated from a diarrhoeic goat kid (2·7%) and the clinical characteristics of the outbreaks where these two latter enteropathogens were found different from the rest. Picobirnaviruses were detected in a diarrhoeic lamb. No coronaviruses were detected using a bovine coronavirus ELISA. No evidence was found of synergistic effect between the agents studied. Enteric pathogens were not found in four (8·7%) and three (20%) outbreaks of diarrhoea in lambs and goat kids, respectively.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1996

References

1.Smith, MC, Sherman, DM. Goat medicine. Pennsylvania: Lea & Febiger, 1994: 342.Google Scholar
2.Fassi-Fehri, MM, Johnson, DW, Taoudi, A, Berrada, J. Epidémiologie des diarrhées à Escherichia coli et á rotavirus chez le veau et l'agneau au Maroc. Ann Rech Vét 1988; 19: 5964.Google Scholar
3.Nagy, B, Nagy, G, Palfi, V, Bozsó, M. Occurrence of Cryptosporidia, rotaviruses, coronavirus-like particles and K99+Escherichia coli in goat kids and lambs. Proceedings of the third international symposium of the World Association of Veterinary Laboratory Diagnosticians. Ames, Iowa, USA, 1983: 525–31.Google Scholar
4.Ramisse, J, Lepareur, F, Poudelet, M, Brebion, M, Moinet, I. Mise en évidence de rotavirus et de cryptosporidies dans les diarrnées des jeunes agenaux. Le Point Vétérinaire 1984; 16: 73–5.Google Scholar
5.Yvore, P, Esnault, A, Naciri, M, et al. Enquête épidémiologique sur les diarrhées néonatales des chevreaux dans les élevages de Touraine. In: Yvore, Perrin G, eds. Les maladies de la chévre. Niort, France: Les colloques de l'INRA, 1984: 437–42.Google Scholar
6.Nagy, B, Palfi, V, Nagy, G, Hajtos, I, Merenyi, L. Infectious gastrointestinal diseases of young goats. Proceedings of the fourth international conference on goats.Brasilia,Brasil, 1987: 373–8.Google Scholar
7.Snodgrass, DR, Herring, JA, Reid, HW, Scott, FMM, Gray, EW. Virus infections in cattle and sheep in Scotland 1975–1978. Vet Rec 1980: 106: 193–5.CrossRefGoogle ScholarPubMed
8.Adesiyun, AA, Kaminjolo, JS. Prevalence and epidemiology of selected enteric infections of livestock in Trinidad. Prev Vet Med 1994; 19: 151–65.CrossRefGoogle Scholar
9.Beutin, L, Geier, D. Steinrück, H, Zimmermann, S, Scheutz, F. Prevalence and some properties of verotoxin (shiga-like toxin)-producing Escherichia coli in seven different species of healthy domestic animals. J Clin Microbiol 1993; 31: 2483–8.CrossRefGoogle ScholarPubMed
10.Cid, D, Ruiz Santa Quiteria, JA, de la Fuente, R. F17 fimbriae in Escherichia coli from lambs and kids. Vet Rec 1993; 132: 251.CrossRefGoogle ScholarPubMed
11.Drolet, R, Fairbrother, JM, Vaillancourt, D. Attaching and effacing Escherichia coli in a goat with diarrhoea. Can Vet J 1994; 35: 122–3.Google Scholar
12.García-Pastor, L, Ferrer-Mayayo, LM, Cebrián-Yagüe, LM. Casuística de procesos patológicos en 3 agrupaciones de defensa sanitaria de ganado ovino de la princia de Zaragoza. Sextas jornadas sobre producción animal. Información Técnica Económica Agrarie 1995; 16: 592–4.Google Scholar
13.Muñoz, M, Lanza, I, Alvarez, M, Cármenes, P. Rotavirus excretion by kids in a naturally infected goat herd. Small Rum Res 1994; 14: 83–9.CrossRefGoogle Scholar
14.De Leeuw, PW, Tiessink, JWA, Straver, PJ, Moerman, A. Bovine coronavirus infections in calves and their detection in the laboratory. Proceedings of the twelfth world congress of diseases of cattle.The Netherlands, 1982; 1: 222–7.Google Scholar
15.Guinée, PAM, Jansen, WH, Agterberg, C. Detection of K99 antigen by means of agglutination and immuno-electrophoresis in Escherichia coli isolated from calves and its correlation with enterotoxigenicity. Infect Immun 1976; 8: 731–5.Google Scholar
16.Evans, DJ, Evans, DG, Gorbach, SL. Production of vascular permeability by enterotoxigenic Escherichia coli isolated from man. Infect Immun 1973; 8: 725–30.CrossRefGoogle ScholarPubMed
17.Henriksen, SA, Polenz, JFL. Staining of Cryptosporidia by a modified Ziehl-Neelsen technique. Acta Vet Scand 1981; 22: 594–6.CrossRefGoogle ScholarPubMed
18.Muñoz, M, Álvarez, M, Lanza, I, Cármenes, P. An outbreak of diarrhoea associated with atypical rotaviruses in goat kids. Res Vet Sci 1995; 59: 180–2.CrossRefGoogle ScholarPubMed
19.Gómez-Bautista, M, Ortega-Mora, LM, Gass, A, Troncoso, JM, Rojo-Vazquez, FA. Epizootiología de la cryptosporidiosis en rumiantes (terneros, corderos y cabritos). Cuarto congreso nacional y primer congreso ibérico de parasitología, Cáceres, España: 1989: 253.Google Scholar
20.Gouet, P. Pathologie digestive du chevreau nouveau-né. In: Yvore, P, Perrin, G, eds. Les maladies de la chèvre. Niort, France: Les colloques de l'INRA, 1984: 433–6.Google Scholar
21.Tzipori, S. Diarrhoea in goat kids attributed to Cryptosporidium infection. Vet Rec 1982; 111: 35–6.CrossRefGoogle ScholarPubMed
22.Cid, D, Orden, JARuiz Santa-Quiteria, JA, de la Fuente, R. Detección de los antígenos fimbriales (F5 y F41) y de enterotoxina termoestable (STa) en cepas de E. coli aisladas de procesos diarreicos de corderos y cabritos recién nacidos. Décimotercer congreso nacional de microbiologia. Salamanca, España: Sociedad Española de Microbiología, 1991: 243.Google Scholar
23.Mainil, JG, Bex, F, Jacquemin, E, Pohl, P. Prevalence of four enterotoxin (STaP, STaH, STb, and LT) and four adhesin subunit (K99, K88, 987P, and F41) genes among Escherichia coli isolates from cattle. Am J Vet Res 1990; 2: 187–90.CrossRefGoogle Scholar
24.Woodward, MJ, Wray, C. Nine DNA probes for detection of toxin and adhesin genes in Escherichia coli isolated from diarrhoeal disease in animals. Vet Microbiol 1990; 25: 5565.CrossRefGoogle ScholarPubMed
25.Carrol, PJ, Woodward, MJ, Wray, C. Detection of LT and STIa toxins by latex and EIA tests. Vet Rec 1990; 127: 335–6.Google Scholar
26.Reynolds, DI, Morgan, IH, Chanter, N, et al. Microbiology of calf diarrhoea in southern Britain. Vet Rec 1986; 119: 34–9.CrossRefGoogle ScholarPubMed
27.Snodgrass, DR, Terzolo, HR, Sherwood, D, Campbell, I, Menzies, JD, Synge, BA. Aetiology of diarrhoea in young calves. Vet Rec 1986; 119: 31–4.CrossRefGoogle ScholarPubMed
28.Dorn, CR, Scotland, SM, Smith, HR, Willshaw, GA, Rowe, B. Properties of vero cytotoxin-producing Escherichia coli of human and animal origin belonging to serotypes other than 0157:H7. Epidemiol Inflet 1989; 103: 8395.CrossRefGoogle Scholar
29.Chanter, N, Morgan, JH, Bridger, JC, Hall, GA, Reynolds, DJ. Dysentery in gnotibiotic calves caused by atypical Escherichia coli. Vet Rec 1984; 114: 71.CrossRefGoogle ScholarPubMed
30.Smith, HW. A search for transmissible pathogenic characters in invasive strains of Escherichia coli: the discovery of a plasmid-controlled toxin and a plasmid-controlled lethal character closely associated, or identical, with colicine V. J Gen Microbiol 1974; 83: 95111.CrossRefGoogle ScholarPubMed
31.Berrios, P, Celedón, MO, Ramírez, V. Rotavirus en ovinos: detección mediante ELISA y aislamiento en cultivos celulares MA-104. Arch Med Vet 1988; 20: 108–12.Google Scholar
32.Snodgrass, DR, Herring, JA. A survey of rotaviruses in sheep in Scotland. Vet Rec 1977; 100: 341.CrossRefGoogle ScholarPubMed
33.Muñoz, M, Lanza, I, Alvarez, M, Cármenes, P. Prevalence of neutralizing antibodies to 9 rotavirus strains representing 7 G-serotypes in sheep sera. Vet Microbiol 1995; 45: 351–61.CrossRefGoogle ScholarPubMed
34.Möstl, K, Nowotny, N. Abnehmende Häufigkeit der Beteiligung von Rotaviren an Ferkeldurchfällen in Österreich. Wien Tierärztl Mschr 1990; 77: 314–7.Google Scholar
35.Bridger, JC. Rotavirus: the present situation in farm animals. Vet Annual 1980; 20: 172–9.Google Scholar
36.Chasey, D, Banks, J. The commonest rotaviruses from neonatal lamb diarrhoea in England and Wales have atypical electropherotypes. Vet Rec 1984; 115: 326–7.CrossRefGoogle ScholarPubMed
37.Tzipori, S, Makin, TJ, Smith, ML, Krautil, FL. Clinical manifestation of diarrhoea in calves infected with rotavirus and enterotoxigenic Escherichia coli J Clin Microbiol 1981; 13: 1011–6.CrossRefGoogle ScholarPubMed
38.Tzipori, S, Sherwood, D, Angus, KW, Campbell, I, Gordon, M. Diarrhoea in lambs: experimental infection with enterotoxigenic E. coli, rotavirus and Cryptosporidium sp. Infect Immun 1981; 33: 401–6.CrossRefGoogle ScholarPubMed
39.Berrios, P, Nuñez, F, Celedón, MO, Fiegehen, P, Santibáñez, MC. Detección de rotavirus en caprinos de San José de Maipo, Región Metropolitana, Chile. Avances en Ciencias Veterinarias 1988; 3: 98101.Google Scholar
40.Gatti, MSV, Pestana de Castro, AF, Ferraz, MMG. Viruses with bisegmented double-stranded RNA in pig faeces. Res Vet Sci 1989; 47: 397–9.CrossRefGoogle ScholarPubMed
41.Van Opdenbosch, E, Wellemans, G. Birna-type virus in diarrhoea calf faeces. Vet Rec 1989; 125: 610.Google Scholar