Bähr C, Baum B, Hewicker-Trautwein M, Scholz H, Distl O
Institut für Tierzucht und Vererbungsforschung, Tierärztliche Hochschule Hannover.
Dtsch Tierarztl Wochenschr. 2005 Jan;112(1):28-32.
In two different dairy farms six calves exhibiting bilateral flexion of the fetlock joints in front or rear legs were born in 2000 to 2002. Four of the affected calves from the same farm were crossbred between German Holstein cows with red and white coat colour and a bull of the breed Limousin. The other two affected calves born on another farm were purebred German Holsteins with a black and white coat colour. The tests for BVD virus antigen and antibodies were negative in all affected calves. Three of the calves showed a lower selen and a higher glutamate dehydrogenase concentration in the analyses of blood metabolites. Two crossbred calves showed a degeneration of the liver with a progressive periportal fibrosis in a histological examination. In one calf an edema of astrocytes of the central nervous system was seen. The analysis of the pedigrees revealed for the four crossbred calves the Limousin bull as common ancestor and the mothers of the calves as relatives. For the affected purebred German Holstein calves also a sire was identified as a common ancestor. The pedigrees support inheritance through a monogenic autosomal recessive locus or more recessive gene loci with variable expressivity. However, the analysis could not clarify whether different gene loci are responsible for the congenital anomalies observed in the calves from the two farms and thus, the observed anomalies may be different genetic entities. Obvious environmental reasons were not found.
2000年至2002年期间,在两个不同的奶牛场出生了6头犊牛,它们的前腿或后腿跗关节出现双侧屈曲。来自同一农场的4头患病犊牛是德国红白花荷斯坦奶牛与利木赞公牛的杂交后代。在另一个农场出生的另外2头患病犊牛是纯种德国黑白花荷斯坦奶牛。所有患病犊牛的牛病毒性腹泻病毒抗原和抗体检测均为阴性。在血液代谢产物分析中,3头犊牛的硒含量较低,谷氨酸脱氢酶浓度较高。在组织学检查中,2头杂交犊牛出现肝脏退化,并伴有进行性门静脉周围纤维化。在1头犊牛中,观察到中枢神经系统星形胶质细胞水肿。系谱分析显示,4头杂交犊牛的共同祖先为利木赞公牛,犊牛的母亲为亲属。对于患病的纯种德国荷斯坦犊牛,也确定了1头公牛为共同祖先。系谱支持通过单基因常染色体隐性位点或更多具有可变表达性的隐性基因位点进行遗传。然而,分析无法阐明两个农场犊牛中观察到的先天性异常是否由不同的基因位点引起,因此,观察到的异常可能是不同的遗传实体。未发现明显的环境原因。