Chamois, healthier as more diverse
The Pyrenean chamois (Rupicapra pyrenaica pyrenaica) is a mountain ungulate which inhabits the Pyrenees. Its populations are managed through hunting and may be affected by several diseases, as keratoconjunctivitis and chamois pestivirosis, caused by a virus similar to that of border disease of sheep. This last disease has decimated the population of chamois in the Catalan Pyrenees during the last years, causing mortalities ranging between 40 and 85%.
The Major Histocompatibility Complex (MHC) is a sensitive marker of population genetic variability, and studying MHC may help to understand the evolution of the chamois populations in the different areas of the Pyrenees as related to their relative isolation and diseases.
In this study the exon 2 of the DRB gene of the class II MHC of 81 Pyrenean chamois from the National Game Reserves (NGR) of Cadí, Alt Pallars-Aran, Freser-Setcases i Cerdanya-Alt Urgell was analyzed. Twenty-nine haplotypes were identified, 26 of them for the first time. Genetic variability was higher in the NGR of Freser-Setcases than in Cadí, and the pestivirus-affected chamois had overall less genetic variability than healthy chamois. Interestingly, No chamois pestivirosis-related mortality has been registered in the NGR of Freser-Setcases, although the causal pestivirus has been detected in this NGR. Perhaps the higher genetic variability in this NGR could explain the resistance of this chamois population to this disease, together with other immunological, epidemiological and ecological factors.
This study was supported by the research project CGL 2009-11631, of the Ministerio de Ciencia e Innovación, and by the Direcció General del Medi Natural i Biodiversitat of the Departament d’Agricultura, Ramaderia, Pesca, Alimentació i Medi Natural of the Generalitat de Catalunya.
References
Cavallero S, Marco I, Lavín S, D'Amelio S, López-Olvera JR. "Polymorphisms at MHC class II DRB1 exon 2 locus in Pyrenean chamois (Rupicapra pyrenaica pyrenaica)" Infect Genet Evol. 2012 Jul;12(5):1020-6.