Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-28T01:38:49.287Z Has data issue: false hasContentIssue false

Resistance and resilience to gastro-intestinal nematode parasites and relationships with productivity of Red Maasai, Dorper and Red Maasai ✕ Dorper crossbred lambs in the sub-humid tropics

Published online by Cambridge University Press:  18 August 2016

R.L. Baker*
Affiliation:
International Livestock Research Institute (ILRI), PO Box 30709, Nairobi, Kenya
S. Nagda
Affiliation:
International Livestock Research Institute (ILRI), PO Box 30709, Nairobi, Kenya
S.L. Rodriguez-Zas
Affiliation:
Department of Animal Science, University of Illinois, Urbana-Champaign, USA
B.R. Southey
Affiliation:
Department of Animal Science, University of Illinois, Urbana-Champaign, USA
J.O. Audho
Affiliation:
International Livestock Research Institute (ILRI), PO Box 30709, Nairobi, Kenya
E.O. Aduda
Affiliation:
International Livestock Research Institute (ILRI), PO Box 30709, Nairobi, Kenya
W. Thorpe
Affiliation:
International Livestock Research Institute (ILRI), PO Box 30709, Nairobi, Kenya
*
Get access

Abstract

Resistance and resilience to naturally acquired gastro-intestinal (GI) nematode parasite infections (predominantly Haemonchus contortus) were studied in 1785 lambs born over six lambings (1991 to 1996) consisting of 212 Red Maasai, 311 Dorper and 1262 crossbred (Red Maasai-Dorper) lambs in the sub-humid coastal region of Kenya. These lambs were the progeny of 41 Dorper and 35 Red Maasai rams. Live weights (LWT), blood packed cell volume (PCV) and faecal egg counts (FEC) were recorded at 1- to 2-monthly intervals from birth until the lambs were about one year of age. Red Maasai were more resistant and resilient post weaning to infections with GI nematodes than Dorper lambs as shown by their significantly lower FEC and their significantly higher PCV, respectively. An increasing proportion of Red Maasai genes in the crossbred lambs was associated with decreased FEC and higher PCV, but there was no heterosis for logarithm-transformed FEC (LFEC) or PCV. From one month of age Red Maasai lambs were significantly lighter than Dorper lambs by about 1 kg, but Red Maasai lambs had significantly lower lamb mortality rate from birth to 12 months of age (proportionately 0·30 and 0·66, respectively). Heritability estimates from a repeated measures analysis for records taken at 6 and 8 months of age were 0·14 (s.e. 0·05) for PCV from an animal model and 0·12 (s.e. 0·05) for LFEC from a sire model. The heritability estimate for LFEC from a repeated measures analysis including the four measurements recorded between 6 and 12 months of age was significantly higher (P < 0·05) for Dorper-sired lambs (0·15, s.e. 0·05 for an animal model and 0·19, s.e. 0·07 for a sire model) than for Red Maasai-sired lambs (0·00 and 0·01, s.e. 0·02). The phenotypic and genetic correlations between PCV and LFEC were moderately to highly negative and averaged –0·34 and –0·81, respectively. None of the genetic correlation estimates between LWT and PCV and LWT and LFEC for lambs post weaning were significantly different from zero. The heritability estimates for PCV and LFEC have important implications for within-breed genetic improvement programmes: for the Red Maasai, improvement should concentrate on resilience (e.g. selection for high PCV); for the Dorper, selection should be feasible for both improved resistance (low FEC) and resilience (high PCV).

Type
Research Article
Copyright
Copyright © British Society of Animal Science 2003

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

Albers, G.A.A., Gray, G.D., Piper, L.R., Barker, J.S.F., Le Jambre, L.F. and Barger, I.A. 1987. The genetics of resistance and resilience to Haemonchus contortus in young Merino sheep. International Journal for Parasitology 17: 13551363.Google Scholar
Amarante, A.F.T., Craig, T.M., Ramsey, W.S., Davis, S.K. and Bazer, F.W. 1999a. Nematode burdens and cellular responses in the abomasal mucosa and blood of Florida Native, Rambouillet and crossbreed lambs. Veterinary Parasitology 80: 311324.CrossRefGoogle ScholarPubMed
Amarante, A.F.T., Craig, T.M., Ramsey, W.S., El-Sayed, N.M, Desouki, A.Y. and Bazer, F.W. 1999b. Comparison of naturally acquired parasite burdens among Florida Native, Rambouillet and crossbreed ewes. Veterinary Parasitology 85: 6169.CrossRefGoogle ScholarPubMed
Axford, R.F.E., Bishop, S.C., Nicholas, F.W. and Owen, J.B. 1999. Breeding for disease resistance in farm animals, second edition. CAB International, Wallingford.Google Scholar
Bahirathan, M., Miller, J.E., Barras, S.R. and Kearney, M.T. 1996. Susceptibility of Suffolk and Gulf Coast Native suckling lambs to naturally acquired strongylate nematode infections. Veterinary Parasitology 65: 259268.Google Scholar
Baker, R.L. 1998. A review of genetic resistance to gastrointestinal nematode parasites in sheep and goats in the tropics and evidence for resistance in some sheep and goat breeds in sub-humid coastal Kenya. Animal Genetics Resources Information Bulletin 24: 1330.CrossRefGoogle Scholar
Baker, R.L., Lahlou Kassi, A., Rege, J.E.O., Reynolds, L., Bekele, T., Mukassa-Mugerwa, E. and Rey, B. 1992. A review of genetic resistance to endoparasites in small ruminants and an outline of ILCA’s research programme in this area. Proceedings of the tenth scientific workshop of the small ruminant collaborative research support program, Nairobi, vol. 10, pp. 79104.Google Scholar
Baker, R.L., Mugambi, J.M., Audho, J.O., Carles, A.B. and Thorpe, W. 2002. Comparison of Red Maasai and Dorper sheep for resistance to gastro-intestinal nematode parasites, productivity and efficiency in a humid and a semi-arid environment in Kenya. Proceedings of the seventh world congress on genetics applied to livestock production, Montpellier, vol 31, pp. 639642.Google Scholar
Baker, R.L., Mwamachi, D.M., Audho, J.O., Aduda, E.O. and Thorpe, W. 1999. Genetic resistance to gastro-intestinal nematode parasites in Red Maasai, Dorper and Red Maasai ✕ Dorper ewes in the sub-humid tropics. Animal Science 69: 335344.Google Scholar
Baker, R.L., Mwamachi, D.M., Audho, J.O. and Thorpe, W. 1994. Genetic resistance to gastrointestinal nematode parasites in Red Maasai sheep in Kenya. Proceedings of the fifth world congress on genetics applied to livestock production, Guelph, vol. 20, pp. 277280.Google Scholar
Baker, R.L., Rege, J.E.O., Tembely, S., Mukasa-Mugerwa, E., Anindo, D., Mwamachi, D.M., Thorpe, W. and Lahlou-Kassi, A. 1998. Genetic resistance to gastrointestinal nematode parasites in some indigenous breeds of sheep and goats in East Africa. Proceedings of the sixth world congress on genetics applied to livestock production, Armidale, vol. 25, pp. 269272.Google Scholar
Barger, I.A. 1996. Prospects for integration of novel parasite control options into grazing systems. International Journal for Parasitology 26: 10011007.CrossRefGoogle ScholarPubMed
Barger, I.A. 1999. The role of epidemiological knowledge and grazing management for helminth control in small ruminants. International Journal for Parasitology 29: 4147.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.Google Scholar
Bisset, S.A. and Morris, C.A. 1996. Feasibility and implications of breeding sheep for resilience to nematode challenge. International Journal for Parasitology 26: 857868.CrossRefGoogle ScholarPubMed
Bisset, S.A., Vlassoff, A., West, C.J. and Morison, L. 1997. Epidemiology of nematodosis in Romney lambs selectively bred for resistance or susceptibility to nematode infections. Veterinary Parasitology 70: 255269.Google Scholar
Bouix, J., Krupinski, J., Rzepecki, R., Nowosad, B., Skrzyala, I., Roborzynski, M., Fudalewicz-Niemczyk, W., Skalska, M., Malczewski, A. and Gruner, L. 1998. Genetic resistance to gastrointestinal nematode parasites in Polish long-wool sheep. International Journal for Parasitology 28: 17971804.Google Scholar
Bouix, J., Vu Tien Khang, J., Mandonnet, N. and Gruner, L. 1995. Response to artificial infections with Teladorsagia circumcincta in sheep bred for resistance to natural infection. International conference on novel approaches to the control of helminth parasites of livestock, Armidale, Australia. Abstract booklet, p. 33.Google Scholar
Boujenane, I., Berrada, D., Mihi, S. and Jamai, M. 1998. Reproductive performance of ewes and pre-weaning growth of lambs from three native Moroccan breeds mated to rams from Moroccan and improved breeds. Small Ruminant Research 27: 203208.Google Scholar
Boujenane, I. and Kansari, J. 2002. Lamb production and its components from purebred and crossbred mating types. Small Ruminant Research 43: 115120.CrossRefGoogle Scholar
Bullerdiek, P. 1996. Appraisal of various management interventions in a sheep production system with high gastrointestinal parasite challenge in a subhumid tropical environment. Ph. D. thesis, Humboldt University, Berlin, Germany.Google Scholar
Carke, J.N. 1982. The utilization of breed resources in the improvement of sheep productivity. Proceedings of the second world congress on genetics applied to livestock production, Madrid, vol. 5, pp. 635654.Google Scholar
Cloete, S.W.P., Snyman, M.A. and Herselman, M.J. 2000. Productive performance of Dorper sheep. Small Ruminant Research 36: 119135.Google Scholar
Clunies-Ross, I. 1932. Observations on the resistance of sheep to infestation by the stomach worm Haemonchus contortus . Journal of the Council for Scientific and Industrial Research 5: 7380.Google Scholar
Colditz, I.G., Watson, D.L., Gray, G.D. and Eady, S.J. 1996. Some relationships between age, immune responsiveness and resistance to parasites in ruminants. International Journal for Parasitology 26: 869877.Google Scholar
Dickerson, G.E. 1969. Experimental approaches in utilising breed resources. Animal Breeding Abstracts 37: 191202.Google Scholar
Falconer, D.S. 1989. Introduction to quantitative genetics. Longman Scientific and Technical, United Kingdom.Google Scholar
Fogarty, N.M. 1995. Genetic parameters for live weight, fat and muscle measurements, wool production and reproduction in sheep: a review. Animal Breeding Abstracts 63: 101144.Google Scholar
Gamble, H.R. and Zajac, A.M. 1992. Resistance of St Croix lambs to Haemonchus contortus in experimentally and naturally acquired infections. Veterinary Parasitology 41: 211225.Google Scholar
Geary, T.M., Thompson, D.P. and Klein, R. 1999. Mechanism-based screening: discovery of the next generation of anthelmintics depends upon more basic research. International Journal for Parasitology 29: 105112.CrossRefGoogle ScholarPubMed
Gilmour, A.R., Cullis, B.R., Welham, S.J. and Thompson, R. 1999. ASREML reference manual. New South Wales (NSW) agriculture biometrics bulletin no. 3. NSW Agriculture, Orange, NSW, Australia.Google Scholar
Gray, G.D. 1991. Breeding for resistance to Trichostrongyle nematodes in sheep. In Breeding for disease resistance in farm animals (ed. Owen, J.B. and Axford, R.F.E.), pp. 139161. CAB International, Wallingford.Google Scholar
Gray, G.D. and Woolaston, R.R. 1991. Breeding for disease resistance in sheep. Wool Research and Development Corporation, Melbourne.Google Scholar
Gray, G.D., Woolaston, R.R. and Eaton, B.T. 1995. Breeding for resistance to infectious diseases of small ruminants. Australian Centre for International Agricultural Research (ACIAR) monograph no. 34. ACIAR, Canberra.Google Scholar
Hansen, J. and Perry, B. 1994. The epidemiology, diagnosis and control of helminth parasites of ruminants, second edition. International Laboratory for Research on Animal Diseases (ILRAD), Nairobi, Kenya.Google Scholar
International Livestock Centre for Africa. 1991. Proceedings of the research planning workshop on resistance to endoparasites in small ruminants, 5-7 February, 1991, Addis Ababa, Ethiopia.Google Scholar
Inyangala, B.A.O., Rege, J.E.O. and Itulya, S. 1992. The performance of Dorper and Dorper x Red Maasai sheep. Discovery and Innovation 4: 7682.Google Scholar
Jaetzold, R. and Schmidt, H. 1983. Farm management handbook of Kenya. Natural conditions and farm information-part C, East Kenya (eastern and coast provinces), vol. 2. Ministry of Agriculture in cooperation with the German Agricultural Team of the Germany Agency for Technical Cooperation (GTZ).Google Scholar
Johnson, D.L. and Thompson, R. 1995. Restricted maximum likelihood estimation of variance components for univariate animal models using sparse matrix techniques and average information. Journal of Dairy Science 78: 449456.Google Scholar
Kiriro, P.M. 1994. Estimate of genetic and phenotypic parameters for the Dorper, Red Maasai and their crosses. In Second biennial conference of the African small ruminant research network (ed. Lebbie, S.H.B., Rey, B. and Irungu, E.K.), pp. 229234. International Livestock Centre for Africa (ILCA), Addis Ababa, Ethiopia.Google Scholar
Kosgey, I.S., Arendonk, J.A.M. van and Baker, R.L. 2001. Breeding objectives for meat sheep in smallholder production systems in the tropics. Proceedings of 52nd annual conference of the European Association for Animal Production, Budapest, 26-29, August 2001 ().Google Scholar
Li, Y., Miller, J.E. and Franke, D.E. 2001. Epidemiological observations and heterosis analysis of gastrointestinal nematode parasitism in Suffolk, Gulf Coast Native and crossbred lambs. Veterinary Parasitology 98: 273283.Google Scholar
Liga, Ch., Gabriilidis, G., Papadopoulos, Th., Georgoudis, A. 2000. Investigation of direct and maternal genetic effects on birth and weaning weights of Chios lambs. Livestock Production Science 67: 7580.Google Scholar
Lopez-Villalobos, N. and Garrick, D.J. 1999. Genetic parameter estimates for lamb survival estimates in Romney sheep. Proceedings of the New Zealand Society of Animal Production 59: 121124.Google Scholar
Maria, G.A., Boldman, K.G., Van Vleck, L.D. 1993. Estimates of variances due to direct and maternal effects for growth traits of Romanov sheep. Journal of Animal Science 71: 845849.CrossRefGoogle ScholarPubMed
Milne, C. 2000. The history of the Dorper sheep. Small Ruminant Research 36: 99102.Google Scholar
Morris, C.A., Vlassoff, A., Bissett, S.A., Baker, R.L., Watson, T.G., West, C.J. and Wheeler, M. 2000. Continued selection of Romney sheep for resistance or susceptibility to nematode infection: estimates of direct and correlated responses. Animal Science 70: 1727.Google Scholar
Morris, C.A., Watson, T.G., Bisset, S.A., Vlassoff, A. and Douch, P.G.C. 1995. Breeding sheep in New Zealand for resistance or resilience to nematode parasites. In Breeding for resistance to infectious diseases in small ruminants (ed. Gray, G.D., Woolaston, R.R. and Eaton, B.T.), pp. 7798. Australian Centre for International Agricultural Research monograph no. 34. ACIAR, Canberra, Australia.Google Scholar
Mugambi, J.M., Bain, R.K., Wanyangu, S.W., Ihiga, M.A., Duncan, J.L., Murray, M. and Stear, M.J. 1997. Resistance of four sheep breeds to natural and subsequent artificial Haemonchus contortus infection. Veterinary Parasitology 69: 265273.Google Scholar
Mugambi, J.M., Wanyangu, S.W., Bain, R.K., Owango, M.O., Duncan, J.L. and Stear, M.J. 1996. Response of Dorper and Red Maasai lambs to trickle Haemonchus contortus infections. Research in Veterinary Science 61: 218221.Google Scholar
Mwamachi, D.M., Audho, J.O., Thorpe, W. and Baker, R.L. 1995. Evidence for multiple anthelmintic resistance in sheep and goats reared under the same management in coastal Kenya. Veterinary Parasitology 60: 303313.Google Scholar
Nguti, R., Janssen, P., Rowlands, G.J., Audho, J.O. and Baker, R.L. 2003. Survival of Red Maasai, Dorper and crossbred lambs in the sub-humid tropics. Animal Science 76: 317.CrossRefGoogle Scholar
Nitter, G. 1978. Breed utilisation for meat production in sheep. Animal Breeding Abstracts 46: 131143.Google Scholar
Owen, J.B. and Axford, R.F.E. 1991. Breeding for disease resistance in farm animals. CAB International, Wallingford.Google Scholar
Paris, J., Murray, M. and McOdimba, F.A. 1982. An evaluation of the sensitivity of current parasitological techniques for the diagnosis of bovine African trypanosomiasis. Acta Tropica 39: 307316.Google Scholar
Payne, R.W., Lane, P.W., Digby, P.G.N., Harding, S.A., Leech, P.K., Morgan, G.W., Todd, A., Thompson, R., Tunncliffe Wilson, G., Welham, S.J. and White, R.P. 1997. Genstat 5 release 3 reference manual. Clarendon Press, Oxford.Google Scholar
Preston, J.M. and Allonby, E.W. 1978. The influence of breed on the susceptibility of sheep and goats to a single experimental infection with Haemonchus contortus . Veterinary Record 103: 509512.Google Scholar
Preston, J.M. and Allonby, E.W. 1979. The influence of breed on the susceptibility of sheep to Haemonchus contortus infection in Kenya. Research in Veterinary Science 26: 134139.Google Scholar
Rege, J.E.O., Tembely, S., Mukasa-Mugerwa, E., Sovani, S., Anindo, D., Lahlou-Kassi, A., Nagda, S. and Baker, R.L. 2002. The effect of breed and season on production and response to infections with gastro-intestinal nematode parasites in sheep in the highlands of Ethiopia. Livestock Production Science 78: 159174.Google Scholar
Robison, O.W., McDaniel, B.T. and Rincom, E.J. 1981. Estimation of direct and maternal additive and heterotic effects from crossbreeding experiments in animals. Journal of Animal Science 52: 4450.CrossRefGoogle ScholarPubMed
Ross, J.G. 1970. Genetic differences in the susceptibility of sheep to infection with Trichostrongylus axei. A comparison of Scottish Blackface and Dorset breeds. Research in Veterinary Science 11: 465468.Google Scholar
Schoeman, S.J. 2000. A comparative assessment of Dorper sheep in different production environments and systems. Small Ruminant Research 36: 137146.Google Scholar
Smith, W.D. 1999. Prospects for vaccines of helminth parasites of grazing ruminants. International Journal for Parasitology 29: 1734.CrossRefGoogle ScholarPubMed
Southey, B.R., Rodriguez-Zas, S.L. and Leymaster, K.A. 2001. Survival analysis of lamb mortality in a terminal sire composite population. Journal of Animal Science 79: 22982306.CrossRefGoogle Scholar
Tosh, J.J. and Kemp, R.A. 1994. Estimation of variance components for lamb weights in three sheep populations. Journal of Animal Science 72: 11841190.Google Scholar
Waller, P.J. 1997a. Anthelmintic resistance. Veterinary Parasitology 72: 391412.Google Scholar
Waller, P.J. 1997b. Sustainable helminth control of ruminants in developing countries. Veterinary Parasitology 71: 195207.Google Scholar
Wanyangu, S.W., Mugambi, J.M., Bain, R.K., Duncan, J.L., Murray, M. and Stear, M.J. 1997. Response to artificial and subsequent natural infection with Haemonchus contortus in Red Maasai and Dorper ewes. Veterinary Parasitology 69: 275282.Google Scholar
Whitlock, J.H. 1948. Some modifications of the McMaster helminth egg-counting technique and apparatus. Journal of the Council for Scientific and Industrial Research of Australia 21: 177180.Google Scholar
Wilson, R.T. 1991. Small ruminant production and the small ruminant genetic resource in tropical Africa. Food and Agriculture Organization animal production and health paper no. 88. FAO, Rome.Google Scholar
Woolaston, R.R. and Baker, R.L. 1996. Prospects of breeding small ruminants for resistance to internal parasites. International Journal for Parasitology 26: 845855.Google Scholar
Woolaston, R.R. and Eady, S.J. 1995. Australian research on genetic resistance to nematode parasites. In Breeding for resistance to infectious diseases in small ruminants (ed. Gray, G.D., Woolaston, R.R. and Eaton, B.T.), pp. 5375. Australian Centre for International Agricultural Research (ACIAR) monograph no. 34. ACIAR, Canberra, Australia.Google Scholar
Woolaston, R.R. and Piper, L.R. 1996. Selection of Merino sheep for resistance to Haemonchus contortus: genetic variation. Animal Science 62: 451460.Google Scholar
Young, L.D., Dickerson, G.E., Ch’ang, T.S. and Evans, R. 1986. Heterosis retention in sheep crossbreeding. Proceedings of the third world congress on genetics applied to livestock production, Lincoln, vol. 9, pp. 497508.Google Scholar