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胆汁酸影响微生物群、宿主和动态,为深入了解 FMT 和专注于微生物组的治疗方法的疗效机制提供了线索。

Bile acids impact the microbiota, host, and dynamics providing insight into mechanisms of efficacy of FMTs and microbiota-focused therapeutics.

机构信息

Genetics Program, Department of Biological Sciences, College of Science, North Carolina State University, Raleigh, NC, USA.

Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.

出版信息

Gut Microbes. 2024 Jan-Dec;16(1):2393766. doi: 10.1080/19490976.2024.2393766. Epub 2024 Sep 3.

DOI:10.1080/19490976.2024.2393766
PMID:39224076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11376424/
Abstract

is a major nosocomial pathogen, causing significant morbidity and mortality worldwide. Antibiotic usage, a major risk factor for infection (CDI), disrupts the gut microbiota, allowing to proliferate and cause infection, and can often lead to recurrent CDI (rCDI). Fecal microbiota transplantation (FMT) and live biotherapeutic products (LBPs) have emerged as effective treatments for rCDI and aim to restore colonization resistance provided by a healthy gut microbiota. However, much is still unknown about the mechanisms mediating their success. Bile acids, extensively modified by gut microbes, affect 's germination, growth, and toxin production while also shaping the gut microbiota and influencing host immune responses. Additionally, microbial interactions, such as nutrient competition and cross-feeding, contribute to colonization resistance against and may contribute to the success of microbiota-focused therapeutics. Bile acids as well as other microbial mediated interactions could have implications for other diseases being treated with microbiota-focused therapeutics. This review focuses on the intricate interplay between bile acid modifications, microbial ecology, and host responses with a focus on , hoping to shed light on how to move forward with the development of new microbiota mediated therapeutic strategies to combat rCDI and other intestinal diseases.

摘要

艰难梭菌是一种主要的医院获得性病原体,在全球范围内导致了大量的发病率和死亡率。抗生素的使用是艰难梭菌感染(CDI)的一个主要危险因素,它会破坏肠道微生物群,使艰难梭菌得以增殖并引起感染,而且常常导致复发性 CDI(rCDI)。粪便微生物群移植(FMT)和活体生物治疗产品(LBPs)已成为 rCDI 的有效治疗方法,旨在恢复健康肠道微生物群提供的定植抵抗力。然而,关于介导它们成功的机制,我们还有很多未知。胆汁酸经过肠道微生物的广泛修饰,影响艰难梭菌的发芽、生长和毒素产生,同时也塑造肠道微生物群并影响宿主免疫反应。此外,微生物相互作用,如营养竞争和交叉喂养,有助于抵抗艰难梭菌的定植,并可能有助于菌群为重点的治疗方法的成功。胆汁酸以及其他微生物介导的相互作用可能对其他使用菌群为重点的治疗方法治疗的疾病有影响。这篇综述重点关注胆汁酸修饰、微生物生态学和宿主反应之间的复杂相互作用,重点关注艰难梭菌,希望能为开发新的菌群介导的治疗策略以对抗 rCDI 和其他肠道疾病提供一些思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11376424/47f349528fed/KGMI_A_2393766_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11376424/47f349528fed/KGMI_A_2393766_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11376424/47f349528fed/KGMI_A_2393766_F0001_OC.jpg

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