断奶仔猪细菌感染通过诱导NLRP3炎性体-焦亡途径促进腹泻。

IF 9.5 2区 生物学 Q1 BIOLOGY
Science China Life Sciences Pub Date : 2025-10-01 Epub Date: 2025-07-04 DOI:10.1007/s11427-024-2728-2
Jie Fu, Zipeng Jiang, Chaoyue Wen, Weifa Su, Mingzhi Yang, Huan He, Yalin Liu, Tao Gong, Shouchuan Jiang, Fengqin Wang, Zeqing Lu, Mingliang Jin, Yizhen Wang
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引用次数: 0

摘要

细菌感染是断奶仔猪腹泻甚至死亡的主要原因。然而,断奶仔猪细菌感染导致腹泻的机制尚不清楚。NLRP3炎性体和焦亡被认为是粘膜免疫损伤的关键因素。因此,我们的目的是研究断奶仔猪细菌感染是否通过NLRP3炎性体-焦亡途径促进腹泻。我们的研究结果表明,与断奶仔猪相比,断奶仔猪腹泻表现出NLRP3炎性体的激活和焦亡。腹泻断奶仔猪肠道菌群多样性降低,β-多样性差异显著,厚壁菌门与拟杆菌门比例显著升高,大肠杆菌和产气荚膜梭菌等致病菌丰度显著增加。产肠毒素大肠杆菌(ETEC) K88和产气荚膜原C.在断奶仔猪上的进一步感染实验表明,这些病原体破坏肠道完整性,促进腹泻发生率,升高血清IL-1β和IL-18水平,激活NLRP3炎症小体-焦亡途径。NLRP3基因敲除小鼠的机制研究显示,血清IL-1β和IL-18水平升高,肠道炎症细胞浸润,肠道屏障蛋白基因表达下调,ETEC K88和产气荚膜原杆菌感染引起的腹泻发生率降低。最后,我们研究了母猪母乳免疫球蛋白在激活NLRP3炎性体-焦亡通路和断奶仔猪腹泻发生率中的作用。由此可见,母猪母乳免疫球蛋白有利于保护断奶仔猪免受致病菌感染诱导的NLRP3炎性体激活和腹泻的发生。总之,我们的研究阐明了断奶后母猪母乳中免疫球蛋白水平降低导致仔猪腹泻的炎症机制,从而促进病原菌感染介导的NLRP3炎症小体-焦亡途径的激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bacterial infection in weaned piglets promotes diarrhea by inducing the NLRP3 inflammasome-pyroptosis pathway.

Bacterial infections in weaned piglets are a major cause of diarrhea and even death. However, the mechanism by which bacterial infections in weaned piglets lead to diarrhea remains unclear. The NLRP3 inflammasome and pyroptosis are considered key factors in mucosal immune damage. Therefore, we aimed to investigate whether bacterial infections in weaned piglets promote diarrhea through the NLRP3 inflammasome-pyroptosis pathway. Our research findings indicate that compared with weaned healthy piglets, those with weaning diarrhea exhibit activation of the NLRP3 inflammasome and pyroptosis. Weaned piglets with diarrhea had reduced microbiota diversity in the gut, significant differences in β-diversity, a notable increase in the ratio of Firmicutes to Bacteroidetes, and a significant increase in the abundance of pathogens, such as Escherichia coli and Clostridium perfringens. Further infection experiments with enterotoxigenic Escherichia coli (ETEC) K88 and C. perfringen in weaned piglets revealed that these pathogens disrupt intestinal integrity, promote diarrhea incidence, increase serum IL-1β and IL-18 levels, and activate the NLRP3 inflammasome-pyroptosis pathway. Mechanistic studies using NLRP3 knockout mice showed significant alleviation of elevated serum IL-1β and IL-18 levels, intestinal inflammatory cell infiltration, downregulation of intestinal barrier protein gene expression, and reduction in diarrhea incidence caused by ETEC K88 and C. perfringen infection. Finally, we investigated the role of sow's breast-milk immunoglobulins in activating the NLRP3 inflammasome-pyroptosis pathway and the incidence of diarrhea in weaned piglets. The results demonstrate that sow's breast milk immunoglobulins are beneficial for protecting weaned piglets from pathogenic bacterial infection-induced NLRP3 inflammasome activation and diarrhea occurrence. In conclusion, our study elucidates the inflammatory mechanisms underlying diarrhea occurrence in piglets due to reduced levels of immunoglobulins from sow's breast milk after weaning, thereby promoting NLRP3 inflammasome-pyroptosis pathway activation mediated by pathogenic bacterial infection.

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来源期刊
CiteScore
15.10
自引率
8.80%
发文量
2907
审稿时长
3.2 months
期刊介绍: Science China Life Sciences is a scholarly journal co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China, and it is published by Science China Press. The journal is dedicated to publishing high-quality, original research findings in both basic and applied life science research.
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