Myostatin mutation causing double muscling could affect increased psoroptic mange sensitivity in dual purpose Belgian Blue cattle.

peer reviewed ; Belgian Blue cattle are known for their high degree of muscling and good carcass qualities. This high degree of muscling is mainly caused by a mutation in the myostatin gene (MSTN). Although the MSTN mutation is considered as fixed in the Belgian Blue breed, segregation is occurring in a sub-population bred for dual purpose. In the latter population, we observed an association between the mutation in MSTN and susceptibility to psoroptic mange, a skin disease caused by Psoroptes ovis mites that heavily plagues Belgian Blue cattle. In total, 291 animals were sampled and screened... Mehr ...

Verfasser: Meyermans, R
Janssens, S
Coussé, A
Gorssen, W
Hubin, X
Mayeres, P
Veulemans, W
Claerebout, E
Charlier, Carole
Buys, N
Dokumenttyp: journal article
Erscheinungsdatum: 2022
Verlag/Hrsg.: Elsevier B.V.
Schlagwörter: Ectoparasitic susceptibility / GDF8 / Mites / Psoroptes ovis / Scabies / Animal Science and Zoology / Life sciences / Animal production & animal husbandry / Genetics & genetic processes / Sciences du vivant / Productions animales & zootechnie / Génétique & processus génétiques
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26927123
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://orbi.uliege.be/handle/2268/288881

peer reviewed ; Belgian Blue cattle are known for their high degree of muscling and good carcass qualities. This high degree of muscling is mainly caused by a mutation in the myostatin gene (MSTN). Although the MSTN mutation is considered as fixed in the Belgian Blue breed, segregation is occurring in a sub-population bred for dual purpose. In the latter population, we observed an association between the mutation in MSTN and susceptibility to psoroptic mange, a skin disease caused by Psoroptes ovis mites that heavily plagues Belgian Blue cattle. In total, 291 animals were sampled and screened for their susceptibility for mange lesions and their MSTN genotype. Via linear mixed modelling, we observed that homozygous mutant animals had a significant increase in the size of mange lesions (+2.51% lesion extent) compared to homozygous wild type. These findings were confirmed with zero-inflated modelling, an animal model and odds analysis. Risk ratios for developing severe mange lesions were 5.9 times as high for homozygous mutant animals. All analyses confirmed an association between the MSTN genotype and psoroptic mange lesion size.