{"title":"Interplay between Bile Acids and Intestinal Microbiota: Regulatory Mechanisms and Therapeutic Potential for Infections.","authors":"Wenweiran Li, Hui Chen, Jianguo Tang","doi":"10.3390/pathogens13080702","DOIUrl":null,"url":null,"abstract":"<p><p>Bile acids (BAs) play a crucial role in the human body's defense against infections caused by bacteria, fungi, and viruses. BAs counteract infections not only through interactions with intestinal bacteria exhibiting bile salt hydrolase (BSH) activity but they also directly combat infections. Building upon our research group's previous discoveries highlighting the role of BAs in combating infections, we have initiated an in-depth investigation into the interactions between BAs and intestinal microbiota. Leveraging the existing literature, we offer a comprehensive analysis of the relationships between BAs and 16 key microbiota. This investigation encompasses bacteria (e.g., <i>Clostridioides difficile</i> (<i>C. difficile</i>), <i>Staphylococcus aureus</i> (<i>S. aureus</i>), <i>Escherichia coli</i>, <i>Enterococcus</i>, <i>Pseudomonas aeruginosa</i>, <i>Mycobacterium tuberculosis</i> (<i>M. tuberculosis</i>), <i>Bacteroides</i>, <i>Clostridium scindens</i> (<i>C. scindens</i>), <i>Streptococcus thermophilus</i>, <i>Clostridium butyricum</i> (<i>C. butyricum</i>), and lactic acid bacteria), fungi (e.g., <i>Candida albicans</i> (<i>C. albicans</i>) and <i>Saccharomyces boulardii</i>), and viruses (e.g., coronavirus SARS-CoV-2, influenza virus, and norovirus). Our research found that <i>Bacteroides</i>, <i>C. scindens</i>, <i>Streptococcus thermophilus</i>, <i>Saccharomyces boulardii</i>, <i>C. butyricum</i>, and lactic acid bacteria can regulate the metabolism and function of BSHs and 7α-dehydroxylase. BSHs and 7α-dehydroxylase play crucial roles in the conversion of primary bile acid (PBA) to secondary bile acid (SBA). It is important to note that PBAs generally promote infections, while SBAs often exhibit distinct anti-infection roles. In the antimicrobial action of BAs, SBAs demonstrate antagonistic properties against a wide range of microbiota, with the exception of norovirus. Given the intricate interplay between BAs and intestinal microbiota, and their regulatory effects on infections, we assert that BAs hold significant potential as a novel approach for preventing and treating microbial infections.</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2024-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11356816/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pathogens","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/pathogens13080702","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Bile acids (BAs) play a crucial role in the human body's defense against infections caused by bacteria, fungi, and viruses. BAs counteract infections not only through interactions with intestinal bacteria exhibiting bile salt hydrolase (BSH) activity but they also directly combat infections. Building upon our research group's previous discoveries highlighting the role of BAs in combating infections, we have initiated an in-depth investigation into the interactions between BAs and intestinal microbiota. Leveraging the existing literature, we offer a comprehensive analysis of the relationships between BAs and 16 key microbiota. This investigation encompasses bacteria (e.g., Clostridioides difficile (C. difficile), Staphylococcus aureus (S. aureus), Escherichia coli, Enterococcus, Pseudomonas aeruginosa, Mycobacterium tuberculosis (M. tuberculosis), Bacteroides, Clostridium scindens (C. scindens), Streptococcus thermophilus, Clostridium butyricum (C. butyricum), and lactic acid bacteria), fungi (e.g., Candida albicans (C. albicans) and Saccharomyces boulardii), and viruses (e.g., coronavirus SARS-CoV-2, influenza virus, and norovirus). Our research found that Bacteroides, C. scindens, Streptococcus thermophilus, Saccharomyces boulardii, C. butyricum, and lactic acid bacteria can regulate the metabolism and function of BSHs and 7α-dehydroxylase. BSHs and 7α-dehydroxylase play crucial roles in the conversion of primary bile acid (PBA) to secondary bile acid (SBA). It is important to note that PBAs generally promote infections, while SBAs often exhibit distinct anti-infection roles. In the antimicrobial action of BAs, SBAs demonstrate antagonistic properties against a wide range of microbiota, with the exception of norovirus. Given the intricate interplay between BAs and intestinal microbiota, and their regulatory effects on infections, we assert that BAs hold significant potential as a novel approach for preventing and treating microbial infections.
胆汁酸(BA)在人体抵御细菌、真菌和病毒感染的过程中发挥着至关重要的作用。胆汁酸不仅通过与具有胆盐水解酶(BSH)活性的肠道细菌相互作用来对抗感染,而且还能直接对抗感染。我们的研究小组之前的发现强调了 BAs 在抗感染中的作用,在此基础上,我们开始深入研究 BAs 与肠道微生物群之间的相互作用。利用现有文献,我们对 BAs 与 16 个关键微生物群之间的关系进行了全面分析。这项研究包括细菌(例如艰难梭菌(C. difficile)、金黄色葡萄球菌(S. aureus)、大肠杆菌、肠球菌、铜绿假单胞菌、结核分枝杆菌(M.嗜热链球菌、丁酸梭菌(C. butyricum)和乳酸菌)、真菌(如白色念珠菌(C、白念珠菌(C. albicans)和布拉氏酵母菌(Saccharomyces boulardii))以及病毒(如冠状病毒 SARS-CoV-2、流感病毒和诺罗病毒)。我们的研究发现,Bacteroides、C. scindens、嗜热链球菌、布拉氏酵母菌、丁酸杆菌和乳酸菌可以调节 BSHs 和 7α-dehydroxylase 的代谢和功能。BSHs和7α-脱羟化酶在初级胆汁酸(PBA)转化为次级胆汁酸(SBA)的过程中发挥着至关重要的作用。值得注意的是,初级胆汁酸通常会促进感染,而次级胆汁酸通常具有独特的抗感染作用。在 BA 的抗菌作用中,SBA 对多种微生物群具有拮抗作用,但诺如病毒除外。鉴于 BAs 与肠道微生物群之间错综复杂的相互作用及其对感染的调节作用,我们认为 BAs 作为一种预防和治疗微生物感染的新方法具有巨大的潜力。
期刊介绍:
Pathogens (ISSN 2076-0817) publishes reviews, regular research papers and short notes on all aspects of pathogens and pathogen-host interactions. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodical details must be provided for research articles.