Bacillus paralicheniformis, an acetate-producing probiotic, alleviates ulcerative colitis via protecting the intestinal barrier and regulating the NLRP3 inflammasome

IF 6.1 1区 生物学 Q1 MICROBIOLOGY Microbiological research Pub Date : 2024-07-23 DOI:10.1016/j.micres.2024.127856
Nini Dai , Xinting Yang , Peilong Pan , Guanghui Zhang , Kangliang Sheng , Jingmin Wang , Xiao Liang , Yongzhong Wang
{"title":"Bacillus paralicheniformis, an acetate-producing probiotic, alleviates ulcerative colitis via protecting the intestinal barrier and regulating the NLRP3 inflammasome","authors":"Nini Dai ,&nbsp;Xinting Yang ,&nbsp;Peilong Pan ,&nbsp;Guanghui Zhang ,&nbsp;Kangliang Sheng ,&nbsp;Jingmin Wang ,&nbsp;Xiao Liang ,&nbsp;Yongzhong Wang","doi":"10.1016/j.micres.2024.127856","DOIUrl":null,"url":null,"abstract":"<div><p>Ulcerative colitis (UC) presents a challenging scenario in digestive health, characterized by recurrent inflammation that is often hard to manage. Bacteria capable of producing short-chain fatty acids (SCFAs) play a pivotal role in mitigating UC symptoms, rendering them promising candidates for probiotic therapy. In this investigation, we assessed the impact of <em>Bacillus paralicheniformis</em> HMPM220325 on dextran sodium sulfate (DSS)-induced UC in mice. Genomic analysis of the strain revealed the presence of protease genes associated with acetate and butyrate synthesis, with acetic acid detected in its fermentation broth. Administration of <em>B. paralicheniformis</em> HMPM220325 to UC mice ameliorated pathological manifestations of the condition and restored intestinal barrier function. Furthermore, <em>B. paralicheniformis</em> HMPM220325 suppressed the activation of the NLRP3 inflammasome signaling pathway and modulated the composition of the intestinal microbiota. These findings shed significant light on the potential of <em>B. paralicheniformis</em> as a probiotic candidate, offering a novel avenue for the prevention and therapeutic intervention of colitis.</p></div>","PeriodicalId":18564,"journal":{"name":"Microbiological research","volume":"287 ","pages":"Article 127856"},"PeriodicalIF":6.1000,"publicationDate":"2024-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiological research","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S094450132400257X","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Ulcerative colitis (UC) presents a challenging scenario in digestive health, characterized by recurrent inflammation that is often hard to manage. Bacteria capable of producing short-chain fatty acids (SCFAs) play a pivotal role in mitigating UC symptoms, rendering them promising candidates for probiotic therapy. In this investigation, we assessed the impact of Bacillus paralicheniformis HMPM220325 on dextran sodium sulfate (DSS)-induced UC in mice. Genomic analysis of the strain revealed the presence of protease genes associated with acetate and butyrate synthesis, with acetic acid detected in its fermentation broth. Administration of B. paralicheniformis HMPM220325 to UC mice ameliorated pathological manifestations of the condition and restored intestinal barrier function. Furthermore, B. paralicheniformis HMPM220325 suppressed the activation of the NLRP3 inflammasome signaling pathway and modulated the composition of the intestinal microbiota. These findings shed significant light on the potential of B. paralicheniformis as a probiotic candidate, offering a novel avenue for the prevention and therapeutic intervention of colitis.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
副坏死性芽孢杆菌是一种能产生醋酸盐的益生菌,它能通过保护肠道屏障和调节 NLRP3 炎症小体来缓解溃疡性结肠炎
溃疡性结肠炎(UC)是消化系统健康的一大挑战,其特点是炎症反复发作,往往难以控制。能够产生短链脂肪酸(SCFAs)的细菌在减轻 UC 症状方面发挥着关键作用,因此很有希望成为益生菌疗法的候选菌。在这项研究中,我们评估了 HMPM220325 对右旋糖酐硫酸钠(DSS)诱导的小鼠 UC 的影响。对该菌株的基因组分析表明,它含有与乙酸盐和丁酸盐合成相关的蛋白酶基因,其发酵液中还检测到乙酸。给 UC 小鼠服用 HMPM220325 可改善病理表现,恢复肠道屏障功能。此外,HMPM220325 还能抑制 NLRP3 炎性体信号通路的激活,并调节肠道微生物群的组成。这些发现揭示了 HMPM220325 作为候选益生菌的潜力,为结肠炎的预防和治疗干预提供了一条新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Microbiological research
Microbiological research 生物-微生物学
CiteScore
10.90
自引率
6.00%
发文量
249
审稿时长
29 days
期刊介绍: Microbiological Research is devoted to publishing reports on prokaryotic and eukaryotic microorganisms such as yeasts, fungi, bacteria, archaea, and protozoa. Research on interactions between pathogenic microorganisms and their environment or hosts are also covered.
期刊最新文献
Adapted evolution towards flagellar loss in Pseudomonas syringae. Role of gut microbiota in rheumatoid arthritis: Potential cellular mechanisms regulated by prebiotic, probiotic, and pharmacological interventions Synergistic effect of Adathoda vasica plant-derived biostimulant and PGPR on Zea mays L. for drought stress management Coagulase-Negative Staphylococci phages panorama: Genomic diversity and in vitro studies for a therapeutic use The LysR-type transcriptional factor PacR controls heterocyst differentiation and C/N metabolism in the cyanobacterium Anabaena PCC 7120.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1