Transcriptome analysis of jejunal mucosal tissue in breeder hens exposed to acute heat stress.

IF 3.8 1区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE Poultry Science Pub Date : 2024-11-08 DOI:10.1016/j.psj.2024.104532
Yongcai Zhu, Satoshi Kubota, Phocharapon Pasri, Sitthipong Rakngam, Supattra Okrathok, Chayanan Pukkung, Shenglin Yang, Sutisa Khempaka
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Abstract

Heat stress (HS) severely compromises intestinal barrier function in poultry, resulting in significant production losses. This study aimed to explore the molecular response of the small intestine to acute HS in breeder hens. Fifty 28-week-old breeder hens were raised individually in a cage and randomly assigned to control and heat-treated groups (25 hens each). Control group hens were maintained at thermoneutral conditions (23°C) and heat-treated group hens were subjected to acute HS (36°C for a 6-h). The heart rate and cloacal temperature were measured in all hens. The jejunal mucosa tissues were collected from 12 randomly selected hens per group for transcriptomic analysis. The acute HS induced significant physiological alterations, with a marked increase in the heart rate and cloacal temperature in hens (P = 0.001). Transcriptome analysis revealed 138 genes with altered expression patterns under acute HS conditions. Of these, 75 genes including heat shock proteins (HSPs) showed upregulated expression, while 63 genes including a key bile acid transport molecule (SLC10A2) exhibited downregulated expression. Functional analysis through gene ontology classification, pathway mapping via the Kyoto encyclopedia of genes and genomes, and protein interaction networks identified several important regulatory genes in thermal response (HSPA8 and HSPA2), energy homeostasis and fat metabolism (PDK4, PPARA, and CD36), glucose transport (SLC2A5), and cholesterol synthesis pathway (SQLE, CYP51A1, and HSD17B7). The findings suggest that acute HS might affect energy utilization, fat metabolism, and glucose transport mechanisms in the jejunal mucosa of breeder hens. The upregulation of HSPs appears to serve as a protective mechanism, potentially preserving intestinal nutrient processing capacity under acute HS. These findings provide foundational knowledge for further investigation into the molecular mechanisms governing HS responses in avian intestinal function and may inform strategies for maintaining gut health in commercial poultry operations exposed to environmental challenges.

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暴露于急性热应激的种鸡空肠粘膜组织的转录组分析。
热应激(HS)会严重损害家禽的肠道屏障功能,从而导致重大的生产损失。本研究旨在探讨种鸡小肠对急性热应激的分子反应。将 50 只 28 周龄的种母鸡单独饲养在笼中,并随机分配到对照组和热处理组(各 25 只)。对照组母鸡在中温条件下饲养(23°C),热处理组母鸡接受急性 HS(36°C,6 小时)。测量所有母鸡的心率和泄殖腔温度。每组随机抽取 12 只母鸡的空肠粘膜组织进行转录组学分析。急性 HS 引起了明显的生理变化,母鸡的心率和泄殖腔温度明显升高(P = 0.001)。转录组分析显示,在急性 HS 条件下,138 个基因的表达模式发生了改变。其中,包括热休克蛋白(HSPs)在内的 75 个基因表达上调,而包括关键胆汁酸转运分子(SLC10A2)在内的 63 个基因表达下调。通过基因本体分类、京都基因和基因组百科全书的通路映射以及蛋白质相互作用网络进行功能分析,发现了热反应(HSPA8 和 HSPA2)、能量平衡和脂肪代谢(PDK4、PPARA 和 CD36)、葡萄糖转运(SLC2A5)以及胆固醇合成通路(SQLE、CYP51A1 和 HSD17B7)中的几个重要调控基因。研究结果表明,急性 HS 可能会影响种鸡空肠粘膜的能量利用、脂肪代谢和葡萄糖转运机制。HSPs 的上调似乎是一种保护机制,有可能在急性 HS 的情况下保护肠道的营养处理能力。这些发现为进一步研究HS对禽类肠道功能影响的分子机制提供了基础知识,并可为暴露于环境挑战下的商业家禽饲养中维持肠道健康的策略提供参考。
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来源期刊
Poultry Science
Poultry Science 农林科学-奶制品与动物科学
CiteScore
7.60
自引率
15.90%
发文量
0
审稿时长
94 days
期刊介绍: First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers. An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.
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