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精细定位确定与猪炎症和坏死综合征相关的候选基因。

Fine Mapping Identifies Candidate Genes Associated with Swine Inflammation and Necrosis Syndrome.

作者信息

Gerhards Katharina, Becker Sabrina, Kühling Josef, Mickan Joel, Lechner Mirjam, Willems Hermann, Reiner Gerald

机构信息

Clinic for Swine-Herd Health Management and Molecular Diagnostics, Justus-Liebig-University Giessen, Frankfurter Strasse 112, 35392 Giessen, Germany.

UEG Hohenlohe, Am Wasen 20, 91567 Herrieden, Germany.

出版信息

Vet Sci. 2025 May 21;12(5):508. doi: 10.3390/vetsci12050508.

DOI:10.3390/vetsci12050508
PMID:40431601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12115691/
Abstract

Swine inflammation and necrosis syndrome (SINS) is a widespread disease in pigs, causing pain, suffering, and damage. Inflammation is documented at different levels based on clinical signs, histopathology, clinical chemistry, metabolomics and transcriptomics. The influence of sow and boar, as well as a heritability of around 0.3, suggest a genetic component to the disease. The aim of the present study was to identify functional single nucleotide polymorphisms (SNPs) in the vicinity of gene markers previously mapped using GWAS. DNA samples were available from 234 already phenotyped piglets. These animals were re-sequenced with additional prior enrichment. The nine selected chromosomal regions cover a total length of 22 Mbp. The genome-wide association study (GWAS) revealed two series with a total of 15 significant missense polymorphisms on chromosomes 11, 14, and 15. The homozygous genotypes of the most discriminating SNPs in series 1 resulted in SINS scores of 3.5 and 17.9, respectively. Despite the partial linkage of the SNPs, interesting candidate genes were defined. The results allow a significant narrowing of the possible candidate genes for understanding the pathogenesis of SINS and for future use in selection breeding to overcome the syndrome. Further studies should be carried out on larger animal populations.

摘要

猪炎症与坏死综合征(SINS)是猪群中一种广泛传播的疾病,会导致疼痛、痛苦和损害。基于临床症状、组织病理学、临床化学、代谢组学和转录组学,炎症在不同层面都有记录。母猪和公猪的影响以及约0.3的遗传力表明该疾病存在遗传因素。本研究的目的是在先前通过全基因组关联研究(GWAS)定位的基因标记附近鉴定功能性单核苷酸多态性(SNP)。从234头已进行表型分析的仔猪获取了DNA样本。这些动物在进行额外的预先富集后重新测序。所选的9个染色体区域总长22兆碱基对。全基因组关联研究(GWAS)在11号、14号和15号染色体上发现了两个系列,共15个显著的错义多态性。系列1中最具区分性的SNP的纯合基因型分别导致SINS评分为3.5和17.9。尽管SNP存在部分连锁,但仍确定了有趣的候选基因。这些结果有助于大幅缩小可能的候选基因范围,以了解SINS的发病机制,并为未来用于选育以克服该综合征提供帮助。应在更大的动物群体上开展进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6db2/12115691/6ce341bd7b46/vetsci-12-00508-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6db2/12115691/97c8c0f01b1f/vetsci-12-00508-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6db2/12115691/c01c30a98f1e/vetsci-12-00508-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6db2/12115691/6ce341bd7b46/vetsci-12-00508-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6db2/12115691/97c8c0f01b1f/vetsci-12-00508-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6db2/12115691/c01c30a98f1e/vetsci-12-00508-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6db2/12115691/6ce341bd7b46/vetsci-12-00508-g003.jpg

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