Hostname: page-component-848d4c4894-75dct Total loading time: 0 Render date: 2024-05-17T15:55:07.529Z Has data issue: false hasContentIssue false

Genetic relationships between indicator traits and nematode parasite infection levels in 6-month-old lambs

Published online by Cambridge University Press:  09 March 2007

G. Davies*
Affiliation:
Roslin Institute (Edinsburgh), Roslin, Midlothian EH25 9PS, UK Department of Veterinary Clinical Studies, Glasgow University, Bearsden Road, Glasgow G61 1QH, UK
M. J. Stear
Affiliation:
Department of Veterinary Clinical Studies, Glasgow University, Bearsden Road, Glasgow G61 1QH, UK
S. C. Bishop
Affiliation:
Roslin Institute (Edinsburgh), Roslin, Midlothian EH25 9PS, UK
Get access

Abstract

This study investigated traits that could be used to aid selective breeding for increased nematode resistance in sheep. Data were collected on approximately 1000 Scottish Blackface lambs over a 5-year period (1992–6). The animals were continually exposed to mixed nematode infection by grazing. Anthelmintic treatment was administered and blood samples were collected every 28 days from 4 to 24 weeks of age. Approximately 500 of the lambs were necropsied at 6 to 7 months of age and their worm burdens were recorded. The traits measured were the number of adult males, adult females, fifth-stage larvae and fourth-stage larvae for all species present. In addition, the mean length of adult females and the number of eggs in utero were estimated for Teladorsagia circumcincta. Several indicator traits were also measured on some of the animals, including : faecal egg counts, immunoglobulin A activity and eosinophil count as markers of the local immune response, and plasma pepsinogen activity and fructosamine concentration as indicators of the pathological consequence of infection. The heritabilities for worm length, eggs in utero and worm burden were 0.53±0.17, 0.50±0.16 and 0.13±0.10 respectively. At a mean age of 22 weeks the heritabilities for fructosamine concentration, IgA activity, eosinophil count and pepsinogen activity were 0.39±0.16, 0.57±0.15, 0.35±0.15 and 0.56±0.16 respectively. Strong negative genetic correlations (< −0.6) were often observed between necropsy traits and eosinophil count, IgA activity and pepsinogen activity. Substantial genetic correlations were also observed between fructosamine concentration and worm length (0.67) and number of fourth-stage larvae (−0.80). The genetic and environmental correlations between indicators and necropsy traits were often opposite in sign. The indicator traits studied could aid selection for increased resistance to gastrointestinal nematodes in sheep.

Type
Research Article
Copyright
Copyright © British Society of Animal Science 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Armour, J., Jarrett, W.F.H. and Jennings, F.W. 1966. Experimental Ostertagia circumcincta infections in sheep: development and pathogenesis of a single infection. American Journal of Veterinary Research 27: 12671278.Google Scholar
Bairden, K. 1991. Ruminant parasitic gastroenteritis: some observations on epidemiology and control. University of Glasgow.Google Scholar
Bishop, S. C., Bairden, K., McKellar, Q. A., Park, M. and Stear, M. J. 1996. Genetic parameters for faecal egg count following mixed, natural, predominantly Ostertagia circumcincta infection and relationships with live weight in young lambs. Animal Science 63: 423428.CrossRefGoogle Scholar
Bishop, S. C. and Stear, M. J. 2000. The use of a gamma-type function to assess the relationship between the number of adult Teladorsagia circumcincta and total egg output. Parasitology 121: 435440.CrossRefGoogle ScholarPubMed
Coop, R. L., Graham, R. B., Jackson, F., Wright, S. E. and Angus, K. W. 1985. Effect of experimental Ostertagia circumcincta infection on the performance of grazing lambs. Research in Veterinary Science 38: 282287.CrossRefGoogle ScholarPubMed
Coop, R. L. and Holmes, P. H. 1996. Nutrition and parasite interaction. International Journal for Parasitology 26: 951962.CrossRefGoogle ScholarPubMed
Datta, F. U., Nolan, J. V., Rowe, J. B., Gray, G. D. and Crook, B. J. 1999. Long-term effects of short-term provision of protein-enriched diets on resistance to nematode infection, and live-weight gain and wool growth in sheep. International Journal for Parasitology 29: 479488.CrossRefGoogle ScholarPubMed
Dawkins, H. J. S., Windon, R. G. and Eagleson, G. K. 1989. Eosinophil responses in sheep selected for high and low responsiveness to Trichostrongylus colubriformis. International Journal for Parasitology 19: 199205.CrossRefGoogle ScholarPubMed
Doligalska, M., Moskwa, B. and Stear, M. J. 1999. Relationships among peripheral eosinophilia, eosinophil peroxidase activity, interleukin-5 concentration and faecal nematode egg count during natural, mixed gastrointestinal nematode infection. Veterinary Immunology and Immunopathology 70: 299308.CrossRefGoogle ScholarPubMed
Douch, P. G. C., Green, R. S., Morris, C. A., Bisset, S. A., Vlassof, A., Baker, R. L., Watson, T. G., Hurford, A. P. and Wheeler, M. 1995. Genetic and phenotypic relationships among anti-Trichostrongylus colubriformis antibody level, faecal egg count and body weight traits in grazing Romney sheep. Livestock Production Science 41: 121132.CrossRefGoogle Scholar
Egmond, M. Damen van, C. A., Spriel van, A. B. Vidarsson, G., Garderen van, E. and Winkel van de, J. G. J.. 2001. IgA and the IgA Fc receptor. Trends in Immunology 22: 205211.CrossRefGoogle ScholarPubMed
Fox, M. T., Gerrelli, D., Shivalkar, P. and Jacobs, D. E. 1989. Effect of omeprazole treatment on feed intake and blood gastrin and pepsinogen levels in the calf. Research in Veterinary Science 46: 280282.CrossRefGoogle ScholarPubMed
Gauly, M., Kraus, M., Vervelde, L., Leeuwen, M. A. W. van, and Erhardt, G. 2002. Estimating genetic differences in natural resistance in Rhön and Merinoland sheep following experimental Haemonchus contortus infection. Veterinary Parasitology 106: 5567.CrossRefGoogle ScholarPubMed
Gilmour, A. R., Thompson, R., Cullis, B. R. and Welham, S. 1996. ASREML. Biometrics bulletin no. 3, NSW Agriculture.Google Scholar
Gordon, H. M. and Whitlock, H. V. 1939. A new technique for counting nematode eggs in sheep faeces. Journal of the Council for Scientific and Industrial Research, Australia 12: 50.Google Scholar
Heath, M. F. and Connan, R. M. 1991. Interaction of Ostertagia and Nematodirus species in sheep and the potential of serum fructosamine determination in monitoring gastrointestinal parasitism. Research in Veterinary Science 51: 322326.CrossRefGoogle ScholarPubMed
McKellar, Q. A., Duncan, J. L., Armour, J. and McWilliam, P. 1986. Response to transplanted adult Ostertagia ostertagi in calves. Research in Veterinary Science 40: 367371.CrossRefGoogle ScholarPubMed
Morris, C. A., Green, R. S., Cullen, N. G. and Hickey, S. M. 2003. Genetic and phenotypic relationships among faecal egg count, antinematode antibody level and live weight in Angus cattle. Animal Science 76: 167174.CrossRefGoogle Scholar
Paynter, D. I. 1992. Australian standard diagnostic techniques for animal diseases. Standing Committee of Agriculture, CSIRO, Australia.Google Scholar
Sangster, N. C. 1999. Anthelmintic resistance: past, present and future. International Journal for Parasitology 29: 115124.CrossRefGoogle ScholarPubMed
Shaw, R. J., Morris, C. A., Green, R. S., Wheeler, M., Bisset, S. A., Vlassof, A. and Douch, P. G. C. 1999. Genetic and phenotypic relationships among Trichostrongylus colubriformis-specific immunoglobulin E, anti-Trichostrongylus colubriformis antibody, immunoglubulin G1, faecal egg count and body weight traits in grazing Romney lambs. Livestock Production Science 58: 2532.CrossRefGoogle Scholar
Sinski, E., Bairden, K., Duncan, J. L., Eisler, M. C., Holmes, P. H., McKellar, Q. A., Murray, M. and Stear, M. J. 1995. Local and plasma antibody-responses to the parasitic larval stages of the abomasal nematode Ostertagia circumcincta. Veterinary Parasitology 59: 107118.CrossRefGoogle Scholar
Smith, W. D. 1999. Prospects for vaccines of helminth parasites of grazing ruminants. International Journal for Parasitology 29: 1724.CrossRefGoogle ScholarPubMed
Smith, W. D., Jackson, F., Jackson, E. and Williams, J. 1985. Age immunity to Ostertagia circumcincta: comparison of the local immune responses of 4·5 and 10 month-old lambs. Journal of Comparative Pathology 95: 235245.CrossRefGoogle Scholar
Stear, M. J., Bairden, K., Duncan, J. L., Holmes, P. H., McKellar, Q. A., Park, M., Strain, S., Murray, M., Bishop, S. C. and Gettinby, G. 1997. How hosts control worms. Nature 389: 27.CrossRefGoogle ScholarPubMed
Stear, M. J., Bairden, K., McKellar, Q. A., Scott, I., Strain, S. and Bishop, S. C. 1999. The relationship between the number and size of nematodes in the abomasum and the concentration of pepsinogen in ovine plasma. Research in Veterinary Science 67: 8992.CrossRefGoogle ScholarPubMed
Stear, M. J., Bishop, S. C., Doligalska, M., Duncan, J. L., Holmes, P. H., Irvine, J., McCririe, L., McKellar, Q. A., Sinski, E. and Murray, M. 1995. Regulation of egg production, worm burden, worm length and worm fecundity by host responses in sheep infected with Ostertagia circumcincta. Parasite Immunology 17: 643652.CrossRefGoogle ScholarPubMed
Stear, M. J., Bishop, S. C., Henderson, N. G. and Scott, I. A. 2003. Key mechanism of pathogenesis in sheep infected with the nematode Teladorsagia circumcincta. Animal Health Research Reviews 4: 4552.CrossRefGoogle ScholarPubMed
Stear, M. J., Eckersall, P. D., Graham, P. A., McKellar, Q. A., Mitchell, S. and Bishop, S. C. 2001. Fructosamine concentration and resistance to infection with Teladorsagia circumcincta. Parasitology 123: 211218.CrossRefGoogle ScholarPubMed
Stear, M. J., McKellar, Q. A., Mitchell, S., Seeley, C. and Bishop, S. C. 2002. Eosinophilia as a marker of resistance to Teladorsagia circumcincta in Scottish Blackface lambs. Parasitology 124: 553560.CrossRefGoogle ScholarPubMed
Stevenson, L. M., Huntley, J. F., Smith, W. D. and Jones, D. G. 1994. Local eosinophil- and mast cell-related responses in abomasal nematode infections of lambs. FEMS Immunology and Medical Microbiology 8: 167174.CrossRefGoogle ScholarPubMed
Strain, S., Bishop, S. C., Henderson, N. G., Holmes, P. H., McKellar, Q. A., Mitchell, S. and Stear, M. J. 2002. The genetic control of IgA activity and its association with parasite resistance in naturally infected sheep. Parasitology 124: 545552.CrossRefGoogle ScholarPubMed
Woolaston, R. R. and Windon, R. G. 2001. Selection of sheep for response to Trichostrongylus colubriformis larvae: genetic parameters. Animal Science 73: 4148.CrossRefGoogle Scholar