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肠道拟杆菌目的适应性变化有助于与它们的裂解性噬菌体稳定共存。

Adaptations in gut Bacteroidales facilitate stable co-existence with their lytic bacteriophages.

作者信息

Cortés-Martín Adrián, Buttimer Colin, Maier Jessie L, Tobin Ciara A, Draper Lorraine A, Ross R Paul, Kleiner Manuel, Hill Colin, Shkoporov Andrey N

机构信息

APC Microbiome Ireland & School of Microbiology, University College Cork, Cork, Ireland.

Department of Plant and Microbial Biology, North Carolina State University, Raleigh, North Carolina, USA.

出版信息

Gut Microbes. 2025 Dec;17(1):2507775. doi: 10.1080/19490976.2025.2507775. Epub 2025 May 23.

Abstract

Bacteriophages (phages) and bacteria within the gut microbiome persist in long-term stable coexistence. These interactions are driven by eco-evolutionary dynamics, where bacteria employ a variety of mechanisms to evade phage infection, while phages rely on counterstrategies to overcome these defenses. Among the most abundant phages in the gut are the crAss-like phages that infect members of the order Bacteroidales, in particular, genus . In this study, we explored some of the mechanisms enabling the co-existence of four phage-Bacteroidales host pairs using a multi-omics approach (transcriptomics, proteomics and metabolomics). These included three species paired with three crAss-like phages ( and фcrAss001, and фcrAss002, and an acapsular mutant of with DAC15), and paired with the siphovirus фPDS1. We show that phase variation of individual capsular polysaccharides (CPSs) is the primary mechanism promoting phage co-existence in Bacteroidales, but this is not the only strategy. Alternative resistance mechanisms, while potentially less efficient than CPS phase variation, can be activated to support bacterial survival by regulating gene expression and resulting in metabolic adaptations, particularly in amino acid degradation pathways. These mechanisms, also likely regulated by phase variation, enable bacterial populations to persist in the presence of phages, and . An acapsular variant of demonstrated broader transcriptomic, proteomic, and metabolomic changes, supporting the involvement of additional resistance mechanisms beyond CPS variation. This study advances our understanding of long-term phage-host interaction, offering insights into the long-term persistence of crAss-like phages and extending these observations to other phages, such as фPDS1. Knowledge of the complexities of phage-bacteria interactions is essential for designing effective phage therapies and improving human health through targeted microbiome interventions.

摘要

肠道微生物群中的噬菌体和细菌长期稳定共存。这些相互作用是由生态进化动力学驱动的,细菌采用多种机制来逃避噬菌体感染,而噬菌体则依靠应对策略来克服这些防御机制。肠道中最丰富的噬菌体之一是类crAss噬菌体,它们感染拟杆菌目成员,特别是 属。在本研究中,我们采用多组学方法(转录组学、蛋白质组学和代谢组学)探索了四种噬菌体-拟杆菌宿主对共存的一些机制。其中包括三种 物种分别与三种类crAss噬菌体( 和фcrAss001、 和фcrAss002,以及 与DAC15的无荚膜突变体)配对,以及 与肌尾噬菌体фPDS1配对。我们表明,单个荚膜多糖(CPS)的相变是促进拟杆菌中噬菌体共存的主要机制,但这不是唯一的策略。替代抗性机制虽然可能比CPS相变效率低,但可以通过调节基因表达并导致代谢适应,特别是在氨基酸降解途径中被激活,以支持细菌存活。这些机制也可能受相变调节,使细菌群体能够在噬菌体存在的情况下持续存在。 的无荚膜变体表现出更广泛的转录组学、蛋白质组学和代谢组学变化,支持了除CPS变异之外还有其他抗性机制的参与。这项研究增进了我们对长期噬菌体-宿主相互作用的理解,为类crAss噬菌体的长期持久性提供了见解,并将这些观察结果扩展到其他噬菌体,如фPDS1。了解噬菌体-细菌相互作用的复杂性对于设计有效的噬菌体疗法和通过有针对性的微生物群干预改善人类健康至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe99/12118408/f13c29bb6c4b/KGMI_A_2507775_F0001_OC.jpg

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