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首页> 外文期刊>Acta veterinaria scandinavica >Screening for bovine leukocyte adhesion deficiency, deficiency of uridine monophosphate synthase, complex vertebral malformation, bovine citrullinaemia, and factor XI deficiency in Holstein cows reared in Turkey
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Screening for bovine leukocyte adhesion deficiency, deficiency of uridine monophosphate synthase, complex vertebral malformation, bovine citrullinaemia, and factor XI deficiency in Holstein cows reared in Turkey

机译:在土耳其饲养的荷斯坦奶牛中筛选牛白细胞粘附缺乏,尿苷单磷酸合酶缺乏,复杂椎骨畸形,牛瓜氨酸血症和XI因子缺乏

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摘要

Background Bovine leukocyte adhesion deficiency (BLAD), deficiency of uridine monophosphate synthase (DUMPS), complex vertebral malformation (CVM), bovine citrullinaemia (BC) and factor XI deficiency (FXID) are autosomal recessive hereditary disorders, which have had significant economic impact on dairy cattle breeding worldwide. In this study, 350 Holstein cows reared in Turkey were screened for BLAD, DUMPS, CVM, BC and FXID genotypes to obtain an indication on the importance of these defects in Turkish Holsteins. Methods Genomic DNA was obtained from blood and the amplicons of BLAD, DUMPS, CVM, BC and FXID were obtained by using PCR. PCR products were digested with TaqI, AvaI and AvaII restriction enzymes for BLAD, DUMPS, and BC, respectively. These digested products and PCR product of FXID were analyzed by agarose gel electrophoresis stained with ethidium bromide. CVM genotypes were detected by DNA sequencing. Additionally, all genotypes were confirmed by DNA sequencing to determine whether there was a mutant allele or not. Results Fourteen BLAD, twelve CVM and four FXID carriers were found among the 350 Holstein cows examined, while carriers of DUMPS and BC were not detected. The mutant allele frequencies were calculated as 0.02, 0.017, and 0.006 for BLAD, CVM and FXID, respectively with corresponding carrier prevalence of 4.0% (BLAD), 3.4% (CVM) and 1.2% (FXID). Conclusion This study demonstrates that carriers of BLAD, CVM and FXID are present in the Turkish Holstein population, although at a low frequency. The actual number of clinical cases is unknown, but sporadic cases may appear. As artificial insemination is widely used in dairy cattle breeding, carriers of BLAD, CVM and FXID are likely present within the population of breeding sires. It is recommended to screen breeding sires for these defective genes in order to avoid an unwanted spread within the population.
机译:背景牛白细胞粘附缺乏症(BLAD),尿苷一磷酸合酶缺乏症(DUMPS),复杂椎体畸形(CVM),牛瓜氨酸血症(BC)和XI缺乏症(FXID)是常染色体隐性遗传性疾病,它们对隐性遗传性疾病有重大影响世界范围内的奶牛繁殖。在这项研究中,对350只在土耳其饲养的荷斯坦奶牛进行了BLAD,DUMPS,CVM,BC和FXID基因型筛选,以表明这些缺陷在土耳其荷斯坦奶牛中的重要性。方法从血液中提取基因组DNA,并通过PCR获得BLAD,DUMPS,CVM,BC和FXID的扩增子。 PCR产物分别用TaqI,AvaI和AvaII限制性内切酶消化,用于BLAD,DUMPS和BC。通过溴化乙锭染色的琼脂糖凝胶电泳分析FXID的这些消化产物和PCR产物。通过DNA测序检测CVM基因型。另外,通过DNA测序确认所有基因型以确定是否存在突变等位基因。结果在检查的350头荷斯坦奶牛中,发现了14只BLAD,12个CVM和4个FXID携带者,而未检测到DUMPS和BC携带者。 BLAD,CVM和FXID的突变等位基因频率分别计算为0.02、0.017和0.006,相应的载体患病率分别为4.0%(BLAD),3.4%(CVM)和1.2%(FXID)。结论该研究表明,土耳其荷斯坦牛种群中存在BLAD,CVM和FXID的携带者,尽管频率较低。临床病例的实际数量是未知的,但可能会出现零星病例。由于人工授精广泛用于奶牛育种,因此育种公牛中可能存在BLAD,CVM和FXID的携带者。为避免这些缺陷基因,建议筛选种系,以免在种群中扩散。

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