Multi-omics integrated approach reveals host-microbiome interactions in the adaptive mechanisms of weaning piglets.

IF 3.2 3区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Journal of Animal Science and Technology Pub Date : 2026-03-01 Epub Date: 2026-03-31 DOI:10.5187/jast.2500436
Ji-Yeong Lee, Chiwoong Lim, Young-Jun Seo, Hyunjin Kyoung, Sanghoon Lee, Younghoon Kim, Minhye Shin, Minho Song, YounChul Ryu, Jun-Mo Kim
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引用次数: 0

Abstract

The weaning transition is a critical phase in piglet development, marked by physiological challenges that influence growth and health. Therefore, this study aims to investigate host-microbiome interactions during the weaning transition using a multi-omics integrated approach. Fecal samples were collected from piglets on the weaning day (W0), 7 days post-weaning (W7), and 14 days post-weaning (W14). Ileal microbiota, microbial-derived metabolites, and tissue samples (ileum, thymus, and mesenteric lymph nodes) were collected at W0 and W14. Fecal microbiota analysis revealed a more stable community at W14 than at W7, with increased presence of fiber-degrading bacteria, including Prevotella, Treponema, Muribaculaceae, and Lachnospiraceae. The ileal microbiota exhibited an adaptive pattern with increases in Lactobacillus, Clostridium_sensu stricto_1, and Enterobacteriaceae, optimized for solid feed digestion and gut stabilization. Morphological analysis of the ileum showed changes in villus architecture between W0 and W14, including increased crypt depth and villus area and decreased villus width, while villus height and goblet cell counts were numerically higher at W14. Transcriptomic profiling revealed the ileum as the primary site of molecular adaptation, with 506 differentially expressed genes (DEGs) involved in immune response pathways, including viral protein interactions with cytokine and cytokine receptor pathways and T cell receptor signaling. The thymus (158 DEGs) and mesenteric lymph nodes (30 DEGs) exhibited modulation of structural pathways linked to systemic immune development, indicating tissue-specific molecular adaptation. Integrated analysis of the host transcriptome and microbial-derived metabolites revealed upregulated glycerophospholipid and glutathione metabolic pathways in piglets 14 days post-weaning, consistent with modulation of membrane structure, barrier function, and antioxidant defense during gut adaptation. Overall, the multi-omics findings provide a comprehensive description of molecular changes associated with weaning adaptation and identify candidate targets for piglet health management during the weaning transition.

多组学综合方法揭示断奶仔猪宿主-微生物相互作用的适应机制。
断奶过渡是仔猪发育的关键阶段,其特征是影响生长和健康的生理挑战。因此,本研究旨在利用多组学综合方法研究断奶过渡期间宿主-微生物组的相互作用。分别于仔猪断奶日(W0)、断奶后7天(W7)和断奶后14天(W14)采集粪便样本。在W0和W14收集回肠微生物群、微生物衍生代谢物和组织样本(回肠、胸腺和肠系膜淋巴结)。粪便微生物群分析显示,W14比W7更稳定的群落,纤维降解细菌的存在增加,包括普雷沃氏菌,密螺旋体,Muribaculaceae和Lachnospiraceae。回肠菌群表现出一种适应模式,乳酸杆菌、梭菌和肠杆菌科的增加对固体饲料的消化和肠道的稳定最有利。形态学分析显示,回肠绒毛结构在W0和W14之间发生了变化,包括隐窝深度和绒毛面积增加,绒毛宽度减少,而绒毛高度和杯状细胞计数在W14时明显增加。转录组学分析显示回肠是分子适应的主要位点,其中506个差异表达基因(deg)参与免疫反应途径,包括病毒蛋白与细胞因子和细胞因子受体途径的相互作用以及T细胞受体信号传导。胸腺(158℃)和肠系膜淋巴结(30℃)表现出与全身免疫发育相关的结构通路的调节,表明组织特异性分子适应。综合分析宿主转录组和微生物衍生代谢物发现,断奶后14天仔猪甘油磷脂和谷胱甘肽代谢途径上调,与肠道适应过程中膜结构、屏障功能和抗氧化防御的调节一致。总体而言,多组学研究结果提供了与断奶适应相关的分子变化的全面描述,并确定了断奶过渡期间仔猪健康管理的候选靶点。
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
Journal of Animal Science and Technology
Journal of Animal Science and Technology Agricultural and Biological Sciences-Food Science
CiteScore
4.50
自引率
8.70%
发文量
96
审稿时长
7 weeks
期刊介绍: Journal of Animal Science and Technology (J. Anim. Sci. Technol. or JAST) is a peer-reviewed, open access journal publishing original research, review articles and notes in all fields of animal science. Topics covered by the journal include: genetics and breeding, physiology, nutrition of monogastric animals, nutrition of ruminants, animal products (milk, meat, eggs and their by-products) and their processing, grasslands and roughages, livestock environment, animal biotechnology, animal behavior and welfare. Articles generally report research involving beef cattle, dairy cattle, pigs, companion animals, goats, horses, and sheep. However, studies involving other farm animals, aquatic and wildlife species, and laboratory animal species that address fundamental questions related to livestock and companion animal biology will also be considered for publication. The Journal of Animal Science and Technology (J. Anim. Technol. or JAST) has been the official journal of The Korean Society of Animal Science and Technology (KSAST) since 2000, formerly known as The Korean Journal of Animal Sciences (launched in 1956).
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