Bovine Lymphocyte Intestinal Retention Deficiency - detection of causal mutation among Holstein-Friesian bulls using the PCR-RFLP technique.

IF 1
S Kamiński
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Abstract

The aim of this study was to develop a PCR-RFLP diagnostic test to detect the causal mutation for Bovine Lymphocyte Intestinal Retention Deficiency (BLIRD). A total of 217 bulls were tested, including 112 bulls being sons of a known BLIRD-carrier sire and 105 bulls used in insemination from 2020 - 2024 with no indication of BLIRD in their pedigree data. Genomic DNA was isolated from the commercial semen straw. The method developed for identifying the causative BLIRD mutation involved PCR amplification of a 412 base pair fragment of the ITGB7 gene and its digestion with the restriction enzyme Ssi I, which allowed for the clear and cost-effective genotyping of BLIRD. In the first group of 112 bulls, 60 BLIRD carriers and 2 BLIRD-affected bulls were identified. They were sons of internationally known top sires, Manfred (US2183007), Convincer (US2249055) and Justice (US22358313). In the second group of 105 bulls, 7 BLIRD carriers were found, giving a frequency of 6.67% among bulls born within the last five years. Further research should be conducted on a larger number of bulls, particularly those for which there is a risk of carrier status based on the bull's pedigree.

牛淋巴细胞肠潴留缺乏症——用PCR-RFLP技术检测荷斯坦-弗里马公牛的致病突变。
本研究的目的是建立一种PCR-RFLP诊断试验来检测牛淋巴细胞肠保留缺乏症(blrd)的致病突变。总共对217头公牛进行了测试,其中112头公牛是已知的blind携带者的儿子,105头公牛在2020年至2024年进行了授精,他们的血统数据中没有blind的迹象。从商品精液吸管中分离出基因组DNA。用于鉴定致病性突变的方法是对ITGB7基因的412个碱基对片段进行PCR扩增,并用限制性内切酶Ssi I进行酶切,从而实现了明确且经济的blad基因分型。在第一组112头公牛中,鉴定出60头携带盲犬和2头感染盲犬。他们是国际知名的顶级爵士的儿子,Manfred (US2183007), weller (US2249055)和Justice (US22358313)。在第二组105头公牛中,有7头被发现为盲症携带者,在最近5年内出生的公牛中,盲症携带者的频率为6.67%。应该对更多的公牛进行进一步的研究,特别是那些根据公牛的血统有携带风险的公牛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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