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

被引:80
|
作者
Bermingham, M. L. [1 ,2 ]
Bishop, S. C. [1 ,2 ]
Woolliams, J. A. [1 ,2 ]
Pong-Wong, R. [1 ,2 ]
Allen, A. R. [3 ]
McBride, S. H. [3 ]
Ryder, J. J. [4 ]
Wright, D. M. [4 ]
Skuce, R. A. [3 ,4 ]
McDowell, S. W. J. [3 ]
Glass, E. J. [1 ,2 ]
机构
[1] Univ Edinburgh, Roslin Inst, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Univ Edinburgh, Royal Dick Sch Vet Studies, Edinburgh EH9 1QH, Midlothian, Scotland
[3] Agrifood & Biosci Inst Stormont, Belfast, Antrim, North Ireland
[4] Queens Univ Belfast, Ctr Med Biol, Sch Biol Sci, Belfast BT9 7BL, Antrim, North Ireland
基金
英国生物技术与生命科学研究理事会;
关键词
genome-wide association study; bovine tuberculosis; novel resistance loci; MYCOBACTERIUM-BOVIS; GENES; IRELAND; CATTLE; SUSCEPTIBILITY; SURVEILLANCE; INFECTION; TRAITS;
D O I
10.1038/hdy.2013.137
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
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 x 10(-7)) and myosin IIIB (MYO3B; P = 5.4 x 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 from this study add to our understanding of variation in host control of infection and suggest that genetic marker-based selection for resistance to bTB has the potential to make a significant contribution to bTB control.
引用
收藏
页码:543 / 551
页数:9
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