Changes in pathogenicity of gut microbiota during fasting-induced molting in laying hens and their impact on spleen immune function.

IF 4.2 1区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Poultry Science Pub Date : 2025-10-01 Epub Date: 2025-07-22 DOI:10.1016/j.psj.2025.105526
Hao Zhang, Chenxu Wang, Yujie Gong, Yidan Zhu, Mengyan Zhang, Donghua Li, Yadong Tian, Ruili Han, Yujie Guo, Yanhua Zhang, Xiangtao Kang, Ruirui Jiang
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引用次数: 0

Abstract

Fasting-induced molting (FIM) leverages the natural molting mechanism of aging laying hens to enhance their egg production and egg quality. However, fasting may also increase the risk of pathogen infection and activate immune regulation in the spleen. Understanding the specific types of pathogen infections triggered during FIM and their impacts on the spleen's immune regulation mechanisms is crucial for enhancing the immunological resilience of poultry. A total of 90, aged 60 weeks, late-laying hens were randomly assigned to undergo FIM. During FIM, hens kept regular feed and 16 hours light initially. A 3-day fast with 8 hours light followed. Then, they gradually resumed water and feed, increasing from 30 g to 120 g daily, with light returning to 16 hours. This study investigates the effects of FIM on the gut microbiota and metabolites through metagenomic sequencing and metabolomics. Additionally, blood routine tests and ELISA assays were conducted to measure serum Ig concentrations. Real-time quantitative PCR and ELISA were used to detect the expression of inflammatory factors and immune cell markers in the spleen. The study also analyzed gene expression levels in the PI3K/AKT pathway, systematically exploring fasting's regulatory impact on gut-spleen immunity. Results showed that during FIM, the abundance of pathogens utilizing non-carbohydrates as an energy source initially increased and then decreased, while the abundance of pathogens relying on carbohydrates as an energy source declined. Correspondingly, with beneficial metabolites initially decreased before increasing, while harmful metabolites exhibited the opposite trend. During fasting, the concentration of eosinophilic leukocytes in serum significantly increased (P < 0.05), while the concentration of IgA significantly decreased (P < 0.05). In the spleen, significant increase in the expression of immune-related metabolites, including NF-κB, IFN-β, iNOS, IL-1β, and IFN-α, were observed, along with significant increases in the secretion of TNF-α, TGF-β, IL-1, and IL-8, suggesting a significant activation of the immune response. After refeeding, these factors in serum and spleen returned to pre-fasting levels. Notably, the PI3K/AKT signaling pathway was significantly activated during fasting, indicating that fasting exerts broad effects on the immune system via the PI3K/AKT pathway. This study holds significant theoretical and practical value for enhancing the immunity of molting laying hens, reducing pathogenic bacterial infections, and optimizing production performance.

蛋鸡空腹换羽过程中肠道菌群致病性的变化及其对脾脏免疫功能的影响
禁食诱导蜕皮(FIM)是利用老龄蛋鸡的自然蜕皮机制来提高蛋鸡产蛋量和蛋品质。然而,禁食也可能增加病原体感染的风险,并激活脾脏的免疫调节。了解FIM过程中触发的特定病原体感染类型及其对脾脏免疫调节机制的影响,对于增强家禽免疫恢复力至关重要。随机选取90只60周龄的晚蛋鸡进行FIM试验。在试验期间,母鸡进行常规饲养和16小时光照。接下来是3天的禁食和8小时的光照。然后逐渐恢复饮水和摄食,从每天30 g增加到120 g,光照恢复到16 h。本研究通过宏基因组测序和代谢组学研究了FIM对肠道微生物群和代谢物的影响。此外,血常规检查和ELISA测定血清Ig浓度。采用实时荧光定量PCR和酶联免疫吸附法检测脾脏中炎症因子和免疫细胞标志物的表达。本研究还分析了PI3K/AKT通路的基因表达水平,系统地探讨了禁食对肠脾免疫的调节作用。结果表明,在FIM过程中,以非碳水化合物为能量来源的病原体丰度先增加后减少,而以碳水化合物为能量来源的病原体丰度则下降。相应的,有益代谢物先减少后增加,有害代谢物则呈现相反的趋势。禁食期间,血清嗜酸性白细胞浓度显著升高(P < 0.05), IgA浓度显著降低(P < 0.05)。脾脏中免疫相关代谢物NF-κB、IFN-β、iNOS、IL-1β、IFN-α表达显著升高,TNF-α、TGF-β、IL-1、IL-8分泌显著升高,提示免疫应答明显激活。复食后,血清和脾脏中的这些因子恢复到空腹前水平。值得注意的是,禁食期间PI3K/AKT信号通路被显著激活,表明禁食通过PI3K/AKT通路对免疫系统产生广泛影响。本研究对提高换羽蛋鸡免疫力,减少病原菌感染,优化生产性能具有重要的理论和实用价值。
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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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