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利用本地祖先信息识别布基纳法索包勒牛与瘤牛杂交牛对锥虫感染的选择反应

Local Ancestry to Identify Selection in Response to Trypanosome Infection in Baoulé x Zebu Crossbred Cattle in Burkina Faso.

作者信息

Yougbaré Bernadette, Ouédraogo Dominique, Tapsoba Arnaud S R, Soudré Albert, Zoma Bienvenue L, Orozco-terWengel Pablo, Moumouni Sanou, Ouédraogo-Koné Salifou, Wurzinger Maria, Tamboura Hamidou H, Traoré Amadou, Mwai Okeyo Ally, Sölkner Johann, Khayatzadeh Negar, Mészáros Gábor, Burger Pamela A

机构信息

Department of Sustainable Agricultural Systems, University of Natural Resources and Life Sciences Vienna (BOKU), Vienna, Austria.

Institut de l'Environnement et de Recherches Agricoles (INERA), Ouagadougou, Burkina Faso.

出版信息

Front Genet. 2021 Sep 27;12:670390. doi: 10.3389/fgene.2021.670390. eCollection 2021.

DOI:10.3389/fgene.2021.670390
PMID:34646296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8504455/
Abstract

The genomes of crossbred (admixed) individuals are a mosaic of ancestral haplotypes formed by recombination in each generation. The proportion of these ancestral haplotypes in certain genomic regions can be responsible for either susceptibility or tolerance against pathogens, and for performances in production traits. Using a medium-density genomic marker panel from the Illumina Bovine SNP50 BeadChip, we estimated individual admixture proportions for Baoulé x Zebu crossbred cattle in Burkina Faso, which were tested for trypanosome infection by direct ELISA from blood samples. Furthermore, we calculated local ancestry deviation from average for each SNP across 29 autosomes to identify potential regions under selection in the trypanotolerant Baoulé cattle and their crossbreds. We identified significant deviation from the local average ancestry (above 5 and 10% genome-wide thresholds) on chromosomes 8 and 19 in the positive animals, while the negative ones showed higher deviation on chromosomes 6, 19, 21, and 22. Some candidate genes on chromosome 6 () and chromosome 19 () have been found associated to trypanotolerance in West African taurines. Screening for outliers in trypanosome positive/negative animals we detected seven variants putatively under selection. Finally, we identified a minimum set of highly ancestry informative markers for routine admixture testing. The results of this study contribute to a better understanding of the genetic basis of trypanotolerance in Baoulé cattle and their crossbreeds. Furthermore, we provide a small informative marker set to monitor admixture in this valuable indigenous breed. As such, our results are important for conserving the genetic uniqueness and trypanotolerance of Baoulé cattle, as well as for the improvement of Baoulé and Zebu crossbreds in specific community-based breeding programs.

摘要

杂交(混合)个体的基因组是由每一代重组形成的祖先单倍型的镶嵌体。这些祖先单倍型在某些基因组区域的比例可能决定对病原体的易感性或耐受性,以及生产性状的表现。我们使用来自Illumina牛SNP50芯片的中密度基因组标记面板,估计了布基纳法索鲍勒牛×瘤牛杂交牛的个体混合比例,并通过对血样进行直接ELISA检测锥虫感染情况。此外,我们计算了29条常染色体上每个单核苷酸多态性(SNP)相对于平均值的局部祖先偏差,以确定耐锥虫的鲍勒牛及其杂交后代中可能受到选择的区域。我们在阳性动物的8号和19号染色体上发现了与全基因组平均祖先有显著偏差(超过5%和10%的全基因组阈值),而阴性动物在6号、19号、21号和22号染色体上有更高的偏差。在西非黄牛中,已发现6号染色体()和19号染色体()上的一些候选基因与耐锥虫性有关。通过筛选锥虫阳性/阴性动物中的异常值,我们检测到7个可能受到选择的变异。最后,我们确定了一组用于常规混合检测的高度祖先信息性标记的最小集合。本研究结果有助于更好地理解鲍勒牛及其杂交后代耐锥虫性的遗传基础。此外,我们提供了一个小型信息性标记集,以监测这一珍贵本土品种的混合情况。因此,我们的结果对于保护鲍勒牛的遗传独特性和耐锥虫性,以及在特定的社区育种计划中改良鲍勒牛和瘤牛杂交后代具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/d7b693f4d8a6/fgene-12-670390-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/88b55c6f1c0f/fgene-12-670390-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/da70da52b66b/fgene-12-670390-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/b565d68f3854/fgene-12-670390-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/eab92f0746b6/fgene-12-670390-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/1f83eda128a1/fgene-12-670390-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/97a25a879e0f/fgene-12-670390-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/cf35fb840f4e/fgene-12-670390-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/d7b693f4d8a6/fgene-12-670390-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/88b55c6f1c0f/fgene-12-670390-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/da70da52b66b/fgene-12-670390-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/b565d68f3854/fgene-12-670390-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/eab92f0746b6/fgene-12-670390-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/1f83eda128a1/fgene-12-670390-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/97a25a879e0f/fgene-12-670390-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/cf35fb840f4e/fgene-12-670390-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415b/8504455/d7b693f4d8a6/fgene-12-670390-g008.jpg

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