New insights into the combined effects of aflatoxin B1 and Eimeria ovinoidalis on uterine function by disrupting the gut-blood-reproductive axis in sheep.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Shu-Cheng Huang, Kai-Li Liu, Pan Chen, Bo-Wen Xu, Wen-Li Ding, Tao-Jing Yue, Ya-Nan Lu, Sen-Yang Li, Jia-Kui Li, Fu-Chun Jian
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Abstract

Background: Sheep coccidiosis is an infectious parasitic disease that primarily causes diarrhea and growth retardation in young animals, significantly hindering the development of the sheep breeding industry. Cereal grains and animal feeds are frequently contaminated with mycotoxins worldwide, with aflatoxin B1 (AFB1) being the most common form. AFB1 poses a serious threat to gastrointestinal health upon ingestion and affects the function of parenteral organs, thus endangering livestock health. However, the impact of the combined effects of coccidia and AFB1 on the reproductive system of sheep has not been reported. Therefore, this study utilized sheep as an animal model to investigate the mechanisms underlying the reproductive toxicity induced by the individual or combined effects of AFB1 and Eimeria ovinoidalis (E. ovinoidalis) on the gut-blood-reproductive axis.

Results: The results showed that AFB1 and coccidia adversely affect the reproductive system defense of sheep by altering uterine histopathology and hormone levels and triggering inflammation, which is associated with changes in the gut microbiota and metabolites. Moreover, co-exposure to AFB1 and coccidia disrupted the intestinal structure of the colon, resulting in reduced crypt depth. The impaired barrier function of the colon manifests primarily through the suppression of barrier protein expression, changes in the gut microbiome composition, and disruptions in gut metabolism. Importantly, the levels of blood inflammatory factors (IL-6, IL-10, TNF-α, and LPS) increased, suggesting that exposure to AFB1 and coccidia compromises the function of uterine organs in sheep by perturbing the gut-blood-reproductive axis. Blood metabolomics analysis further revealed that the differential metabolites predominantly concentrate in the amino acid pathway, particularly N-acetyl-L-phenylalanine. This metabolite is significantly correlated with IL-6, TNF-α, LPS, ERα, and ERβ, and it influences hormone levels while inducing uterine damage through the regulation of the downstream genes PI3K, AKT, and eNOS in the relaxin signaling pathway, as demonstrated by RNA sequencing.

Conclusions: These findings reveal for the first time that the combined effects of AFB1 and E. ovinoidalis on sheep uterine function operate at the level of the gut-blood-reproductive axis. This suggests that regulating gut microbiota and its metabolites may represent a potential therapeutic strategy for addressing mycotoxins and coccidia-co-induced female reproductive toxicity.

黄曲霉毒素B1和卵形艾美球虫通过破坏羊肠-血-生殖轴对子宫功能联合影响的新认识。
背景:绵羊球虫病是一种主要导致幼龄动物腹泻和生长迟缓的传染性寄生虫病,严重阻碍了绵羊养殖业的发展。世界各地的谷物和动物饲料经常受到真菌毒素的污染,黄曲霉毒素B1 (AFB1)是最常见的形式。AFB1误食后对胃肠道健康构成严重威胁,影响肠外器官功能,危害牲畜健康。然而,球虫和AFB1联合作用对绵羊生殖系统的影响尚未见报道。因此,本研究以绵羊为动物模型,探讨AFB1和卵形艾美耳虫(E. ovinoidalis)单独或联合作用对肠-血-生殖轴的生殖毒性机制。结果:结果表明,AFB1和球虫通过改变子宫组织病理学和激素水平,引发炎症,从而对绵羊生殖系统防御产生不利影响,而炎症与肠道菌群和代谢物的变化有关。此外,AFB1和球虫的共同暴露破坏了结肠的肠道结构,导致隐窝深度减少。结肠屏障功能受损主要表现为屏障蛋白表达的抑制、肠道微生物组组成的改变和肠道代谢的中断。重要的是,血液炎症因子(IL-6、IL-10、TNF-α和LPS)水平升高,表明暴露于AFB1和球虫通过扰乱肠道-血液-生殖轴损害绵羊子宫器官的功能。血液代谢组学分析进一步表明,差异代谢物主要集中在氨基酸途径,特别是n -乙酰- l-苯丙氨酸。经RNA测序证实,该代谢物与IL-6、TNF-α、LPS、ERα和ERβ显著相关,通过调控松弛素信号通路下游基因PI3K、AKT和eNOS影响激素水平,同时诱导子宫损伤。结论:本研究首次揭示了AFB1和卵黄杆菌对绵羊子宫功能的联合作用是在肠-血-生殖轴水平上起作用的。这表明调节肠道微生物群及其代谢物可能是解决真菌毒素和球虫共同诱导的雌性生殖毒性的潜在治疗策略。
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
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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