Center for Inflammation, Immunity and Infection, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, USA.
Department of Microbiome Science, Max Planck Institute for Biology, Tübingen, Germany.
Gut Microbes. 2024 Jan-Dec;16(1):2392872. doi: 10.1080/19490976.2024.2392872. Epub 2024 Aug 27.
We sought to better understand how intestinal microbiota confer protection against () infection (CDI). We utilized gnotobiotic altered Schaedler flora (ASF) mice, which lack the abnormalities of germfree (GF) mice as well as the complexity and heterogeneity of antibiotic-treated mice. Like GF mice, ASF mice were highly prone to rapid lethal CDI, without antibiotics, while very low infectious doses resulted in chronic CDI. Administering such chronic CDI mice an undefined preparation of Clostridia lowered levels by several logs. Importantly, such resolution of CDI was associated with colonization of Lachnospiraceae. Fractionation of the Clostridia population to enrich for Lachnospiraceae led to the appreciation that its CDI-impeding property strongly associated with a specific Lachnospiraceae strain, namely uncultured bacteria and archaea (UBA) 3401. UBA3401 was recalcitrant to being propagated as a pure culture but could be maintained in ASF mice, wherein it comprised up to about 50% of the intestinal microbiota, which was sufficient to generate a high-quality genomic sequence of this bacterium. Sequence analysis and study of UBA3401 indicated that it had the ability to secrete substance(s) that directly impeded growth. Moreover, administration of UBA3401/ASF feces provided strong protection to challenge. Thus, UBA3401 may contribute to and/or provide a means to study microbiota-mediated CDI resistance.
我们试图更好地了解肠道微生物群如何赋予机体免受艰难梭菌感染(CDI)的保护作用。我们利用无菌改变的 Schaedler 菌群(ASF)小鼠,这些小鼠缺乏无菌(GF)小鼠的异常,也缺乏抗生素处理小鼠的复杂性和异质性。与 GF 小鼠一样,ASF 小鼠在没有抗生素的情况下极易迅速发生致命性 CDI,而非常低的感染剂量会导致慢性 CDI。给这些慢性 CDI 小鼠施用一种未定义的拟杆菌制剂可使水平降低几个对数级。重要的是,这种 CDI 的缓解与lachnospiraceae 的定植有关。对梭菌种群进行分级以富集lachnospiraceae 导致人们认识到,其 CDI 抑制特性与一种特定的lachnospiraceae 菌株(即未培养细菌和古菌(UBA)3401)强烈相关。UBA3401 难以作为纯培养物进行繁殖,但可在 ASF 小鼠中维持,其中其占肠道微生物群的约 50%,足以生成该细菌的高质量基因组序列。序列分析和 UBA3401 的研究表明,它具有分泌直接抑制生长的物质的能力。此外,UBA3401/ASF 粪便的给药为 提供了强大的保护作用。因此,UBA3401 可能有助于和/或提供一种研究微生物群介导的 CDI 抵抗的方法。