Variation and covariation in strongyle infection in East African shorthorn zebu calves

Parasite burden varies widely between individuals within a population, and can covary with multiple aspects of individual phenotype. Here we investigate the sources of variation in faecal strongyle eggs counts, and its association with body weight and a suite of haematological measures, in a cohort...

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Detalles Bibliográficos
Autores principales: Callaby, R., Hanotte, Olivier H., Wyk, Ilana Conradie van, Kiara, Henry K., Toye, Philip G., Mbole-Kariuki, Mary N., Jennings, A., Thumbi, Samuel M., Coetzer, Jacobus A.W., Bronsvoort, B.M. de C., Knott, S.A., Woolhouse, Mark E.J., Kruuk, L.E.B.
Formato: Journal Article
Lenguaje:Inglés
Publicado: Cambridge University Press 2015
Materias:
Acceso en línea:https://hdl.handle.net/10568/67376
Descripción
Sumario:Parasite burden varies widely between individuals within a population, and can covary with multiple aspects of individual phenotype. Here we investigate the sources of variation in faecal strongyle eggs counts, and its association with body weight and a suite of haematological measures, in a cohort of indigenous zebu calves in Western Kenya, using relatedness matrices reconstructed from single nucleotide polymorphism (SNP) genotypes. Strongyle egg count was heritable (h2 = 23·9%, s.e. = 11·8%) and we also found heritability of white blood cell counts (WBC) (h2 = 27·6%, s.e. = 10·6%). All the traits investigated showed negative phenotypic covariances with strongyle egg count throughout the first year: high worm counts were associated with low values of WBC, red blood cell count, total serum protein and absolute eosinophil count. Furthermore, calf body weight at 1 week old was a significant predictor of strongyle EPG at 16–51 weeks, with smaller calves having a higher strongyle egg count later in life. Our results indicate a genetic basis to strongyle EPG in this population, and also reveal consistently strong negative associations between strongyle infection and other important aspects of the multivariate phenotype.