Metagenomic selections reveal diverse antiphage defenses in human and environmental microbiomes.

Luis Rodriguez-Rodriguez, James Pfister, Liam Schuck, Arabella E Martin, Luis M Mercado-Santiago, Vincent S Tagliabracci, Kevin J Forsberg
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Abstract

To prevent phage infection, bacteria have developed an arsenal of antiphage defense systems. Using functional metagenomic selections, we identified new examples of these systems from human fecal, human oral, and grassland soil microbiomes. Our antiphage selections in Escherichia coli revealed over 200 putative defenses from 14 diverse bacterial phyla, highlighting the broad phylogenetic interoperability of these systems. Many defense systems were unrecognizable based on sequence or predicted structure, so could only be identified via functional assays. In mechanistic studies, we show that some defense systems encode nucleases that only degrade covalently modified phage DNA, but which accommodate diverse chemical modifications. We also identify outer membrane proteins that prevent phage adsorption and a set of previously unknown defense systems with diverse antiphage profiles and modalities. Most defenses acted against at least two phages, indicating that broadly acting systems are widely distributed among non-model bacteria.

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宏基因组选择揭示了人类和环境微生物组中不同的噬菌体防御。
为了防止噬菌体感染,细菌已经发展出一系列的抗噬菌体防御系统。利用功能宏基因组选择,我们从人类粪便、人类口腔和草地土壤微生物组中发现了这些系统的新例子。我们在大肠杆菌中选择的抗噬菌体揭示了来自14个不同细菌门的200多种推定防御,突出了这些系统广泛的系统发育互操作性。许多防御系统无法根据序列或预测结构来识别,因此只能通过功能分析来识别。在机制研究中,我们发现一些防御系统编码的核酸酶只能降解共价修饰的噬菌体DNA,但可以适应多种化学修饰。我们还鉴定了防止噬菌体吸附的外膜蛋白和一套以前未知的具有不同噬菌体谱和模式的防御系统。大多数防御至少对两种噬菌体起作用,这表明广泛作用的系统广泛分布于非模式细菌中。
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