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Genome-wide association study identifies novel loci associated with resistance tobovine tuberculosis

机译:全基因组关联研究确定了与耐药相关的新基因座牛结核病

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摘要

Tuberculosis (TB) caused by Mycobacterium bovis is a re-emerging disease of livestock that is of major economic importance worldwide, as well as being a zoonotic risk. There is significant heritability for host resistance to bovine TB (bTB) in dairy cattle. To identify resistance loci for bTB, we undertook a genome-wide association study in female Holstein–Friesian cattle with 592 cases and 559 age-matched controls from case herds. Cases and controls were categorised into distinct phenotypes: skin test and lesion positive vs skin test negative on multiple occasions, respectively. These animals were genotyped with the Illumina BovineHD 700K BeadChip. Genome-wide rapid association using linear and logistic mixed models and regression (GRAMMAR), regional heritability mapping (RHM) and haplotype-sharing analysis identified two novel resistance loci that attained chromosome-wise significance, protein tyrosine phosphatase receptor T (PTPRT; P=4.8 × 10−7) and myosin IIIB (MYO3B; P=5.4 × 10−6). We estimated that 21% of the phenotypic variance in TB resistance could be explained by all of the informative single-nucleotide polymorphisms, of which the region encompassing the PTPRT gene accounted for 6.2% of the variance and a further 3.6% was associated with a putative copy number variant in MYO3B. The results fromthis study add to our understanding of variation in host control of infection and suggestthat genetic marker-based selection for resistance to bTB has the potential to make asignificant contribution to bTB control.
机译:牛分枝杆菌引起的结核病是一种重新出现的牲畜疾病,在世界范围内具有重要的经济意义,而且是人畜共患病风险。宿主对奶牛牛结核病(bTB)的抵抗力具有显着的遗传力。为了确定bTB的抗性位点,我们对雌性荷斯坦–弗里斯兰牛进行了全基因组关联研究,该研究有592例病例和559例年龄匹配的成群对照。将病例和对照分为不同的表型:分别在多种情况下皮肤测试和病变阳性与皮肤测试阴性。用Illumina BovineHD 700K BeadChip对这些动物进行基因分型。使用线性和逻辑混合模型和回归(GRAMMAR),区域遗传力作图(RHM)和单倍型共享分析进行全基因组范围的快速关联,确定了两个具有染色体意义的新型抗性位点,蛋白酪氨酸磷酸酶受体T(PTPRT; P = 4.8×10 −7 )和肌球蛋白IIIB(MYO3B; P = 5.4×10 −6 )。我们估计,结核病抗性的表型变异可通过所有信息性单核苷酸多态性解释,其中包含PTPRT基因的区域占变异的6.2%,另外3.6%与推定的相关MYO3B中的副本编号变体。结果来自这项研究加深了我们对感染宿主控制变异的理解,并建议基于遗传标记的bTB抗性选择有可能对bTB控制的重要贡献。

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