Suppr超能文献

探索人类肠道噬菌体组的“暗物质”:培养辅助宏基因组学助力新型噬菌体的快速发现与宿主关联

Probing the "Dark Matter" of the Human Gut Phageome: Culture Assisted Metagenomics Enables Rapid Discovery and Host-Linking for Novel Bacteriophages.

作者信息

Fitzgerald C Brian, Shkoporov Andrey N, Upadrasta Aditya, Khokhlova Ekaterina V, Ross R Paul, Hill Colin

机构信息

APC Microbiome Ireland, University College Cork, Cork, Ireland.

出版信息

Front Cell Infect Microbiol. 2021 Mar 15;11:616918. doi: 10.3389/fcimb.2021.616918. eCollection 2021.

Abstract

Recent years have been marked by the growing interest towards virulent and temperate bacteriophage populations inhabiting the human lower gastrointestinal tract - the gut phageome. A number of studies demonstrated high levels of specificity and temporal stability of individual gut phageomes, as well as their specific alterations in disease cohorts, in parallel with changes in the bacteriome. It has been speculated that phages might have an active role in shaping the taxonomic composition and functional properties of the human gut bacteriome. An overwhelming majority of gut bacteriophages, however, remain uncultured, unclassified, and their specific hosts and infection strategies are still unknown. They are often referred to as "the viral dark matter". A possible breakthrough in understanding of the phageome can only become possible when a significant proportion of the "the viral dark matter" is identified and linked to bacterial hosts. Here, we describe a method that enables rapid discovery and host-linking of novel bacteriophages in the gut a combination of serial enrichment cultures and shotgun metagenomics of viral DNA. Using this approach dozens of novel and previously known bacteriophages were detected, including the ones infecting difficult-to-culture anaerobic bacteria. The majority of phages failed to produce lysis and propagate on host cultures in traditional assays. The newly identified phages include representatives of , , , and crAss-like viruses, infecting diverse bacterial taxa of Bacteroidetes, Firmicutes, Actinobacteria, Verrucomicrobia and Proteobacteria phyla. The proposed new method has a potential for high-throughput screening applications for mass discovery of new phages in different environments.

摘要

近年来,人们对居住在人类下消化道的烈性和温和噬菌体群体——肠道噬菌体组越来越感兴趣。多项研究表明,个体肠道噬菌体组具有高度的特异性和时间稳定性,以及在疾病队列中的特定改变,同时伴随着细菌群落的变化。据推测,噬菌体可能在塑造人类肠道细菌群落的分类组成和功能特性方面发挥积极作用。然而,绝大多数肠道噬菌体仍未培养、未分类,其特定宿主和感染策略仍不清楚。它们常被称为“病毒暗物质”。只有当相当一部分“病毒暗物质”被识别并与细菌宿主联系起来时,才有可能在噬菌体组的理解上取得突破。在这里,我们描述了一种方法,该方法能够在肠道中快速发现新型噬菌体并将其与宿主联系起来——这是一种连续富集培养和病毒DNA鸟枪法宏基因组学的组合。使用这种方法检测到了数十种新型和先前已知的噬菌体,包括感染难以培养的厌氧菌的噬菌体。在传统检测中,大多数噬菌体未能产生裂解并在宿主培养物上繁殖。新鉴定的噬菌体包括、、和类crAss病毒的代表,它们感染拟杆菌门、厚壁菌门、放线菌门、疣微菌门和变形菌门的不同细菌类群。所提出的新方法具有高通量筛选应用的潜力,可用于在不同环境中大规模发现新噬菌体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a1/8005731/de0995e32197/fcimb-11-616918-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验