Host genome regulation of the porcine gut microbiota and its impact on feed conversion efficiency.

IF 4.5 Q1 MICROBIOLOGY
Qitian Wu, Xiaoqing Wang, Qiming Mu, Jingjing Tian, Hailing Wang, Jiayi Yang, Zhen Peng, Lili Gao, Pengfei Gao, Fuping Zhao
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Abstract

This study aims to elucidate the regulatory mechanisms of host genetics on the porcine gut microbiota and their subsequent impact on the feed conversion ratio (FCR). While initial genome-wide association studies (GWAS) did not identify significant SNPs directly associated with FCR, we investigated the gut microbiota as a potential intermediate phenotype influencing feed efficiency. Nonmetric multidimensional scaling (NMDS) based on Bray–Curtis distances demonstrated a distinct separation in microbial community structure between the high-feed conversion ratio (HFCR) and low-feed conversion ratio (LFCR) groups (stress = 0.19), suggesting a link between FCR and gut microbial composition. Furthermore, a significant, albeit weak, negative correlation was observed between the genomic relatedness matrices and microbial Bray‒Curtis dissimilarity (r = −0.0143, p = 0.0031), indicating host genetic control over the microbiome. Microbiome genome-wide association study (mGWAS) identified 117 significant SNPs associated with 28 microbial taxa. Functional annotation highlighted eight candidate genes (DCY8, PATJ, PTPN2, FTO, SLC13A1, ADAM28, MGST1, and PTGS2) involved in the regulation of taxa, including Campylobacter, Faecalibacterium, Streptococcus, Succinivibrio, Treponema, Turicibacter, uncultured Erysipelotrichales, and uncultured Peptococcaceae 2. Collectively, these findings establish that the gut microbiota is a heritable trait influenced by the host genome, providing novel targets for breeding strategies designed to optimize microbial composition for improved feed efficiency.

猪肠道菌群宿主基因组调控及其对饲料转化率的影响
本研究旨在阐明宿主遗传对猪肠道菌群的调控机制及其对饲料系数的影响。虽然最初的全基因组关联研究(GWAS)没有发现与饲料效率直接相关的显著snp,但我们研究了肠道微生物群作为影响饲料效率的潜在中间表型。基于Bray-Curtis距离的非度量多维标度(NMDS)结果显示,高饲料系数(HFCR)组和低饲料系数(LFCR)组(应激值= 0.19)之间的微生物群落结构存在明显差异,提示FCR与肠道微生物组成之间存在关联。此外,基因组亲缘关系矩阵与微生物Bray-Curtis dissimilarity之间存在显著的负相关(r = - 0.0143, p = 0.0031),表明宿主对微生物组具有遗传控制作用。微生物组全基因组关联研究(mGWAS)鉴定出与28个微生物类群相关的117个显著snp。功能注释突出了8个参与类群调控的候选基因(DCY8、PATJ、PTPN2、FTO、SLC13A1、ADAM28、MGST1和PTGS2),包括Campylobacter、Faecalibacterium、Streptococcus、Succinivibrio、Treponema、Turicibacter、未培养的Erysipelotrichales和未培养的Peptococcaceae 2。总之,这些发现表明肠道微生物群是受宿主基因组影响的一种可遗传性状,为优化微生物组成以提高饲料效率的育种策略提供了新的靶点。
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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来源期刊
CiteScore
7.20
自引率
0.00%
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0
审稿时长
13 weeks
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