感染植物促生长根杆菌克雷伯氏菌M5al的24个噬菌体的分离与鉴定。

IF 2.6 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2025-02-21 eCollection Date: 2025-01-01 DOI:10.1371/journal.pone.0313947
Marissa R Gittrich, Courtney M Sanderson, James M Wainaina, Cara M Noel, Jonathan E Leopold, Erica Babusci, Sumeyra C Selbes, Olivia R Farinas, Jack Caine, Joshua Davis Ii, Vivek K Mutalik, Paul Hyman, Matthew B Sullivan
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引用次数: 0

摘要

噬菌体主要通过裂解、基因转移和代谢重编程影响细菌群落,因此越来越多的人认为噬菌体改变了地球许多生态系统的营养和能量循环。然而,很少有模型系统来机械和定量地研究噬菌体-细菌的相互作用,特别是在土壤系统中。在这里,我们分离、测序并对24种感染克雷伯氏菌(Klebsiella sp. M5al)的新型噬菌体进行了基因组表征,克雷伯氏菌是一种促进植物生长的、非包被的根际相关细菌,并将它们的许多特征与所有565个测序的、dsDNA的克雷伯氏菌噬菌体基因组进行了比较。分类分析表明,这些克雷伯菌噬菌体属于3个已知的噬菌体科(Autographiviridae、Drexlerviridae和Straboviridae)和2个新发现的噬菌体科(Candidatus Mavericviridae和Ca. Rivulusviridae)。在噬菌体家族水平上,我们发现核心基因往往是噬菌体中心蛋白,如噬菌体头尾结构蛋白和DNA包装蛋白。相比之下,参与转录、翻译或假设蛋白质的基因通常不是共享的或灵活的基因。生态学上,我们评估了噬菌体在最近大规模宏基因组数据集中的普遍性,这表明它们并不普遍,以及通过筛选噬菌体编码的辅助代谢基因(AMGs)在感染期间重编程特定代谢中的可能直接作用。尽管AMGs在环境文献中很常见,但我们的噬菌体家族中只有Straboviridae一种含有AMGs,并且AMGs的类型在属水平上是相关的。宿主范围表型分析显示噬菌体具有广泛的传染性,可感染22株细菌中的1-14株,包括致病性克雷伯氏菌和拉乌尔氏菌。这表明并非所有的非囊性克雷伯菌噬菌体都有广泛的宿主范围。这些分离物连同相应的基因组、AMG和宿主范围分析,有助于建立克雷伯菌模型系统,用于研究根际相关细菌的噬菌体-宿主相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation and characterization of 24 phages infecting the plant growth-promoting rhizobacterium Klebsiella sp. M5al.

Bacteriophages largely impact bacterial communities via lysis, gene transfer, and metabolic reprogramming and thus are increasingly thought to alter nutrient and energy cycling across many of Earth's ecosystems. However, there are few model systems to mechanistically and quantitatively study phage-bacteria interactions, especially in soil systems. Here, we isolated, sequenced, and genomically characterized 24 novel phages infecting Klebsiella sp. M5al, a plant growth-promoting, nonencapsulated rhizosphere-associated bacterium, and compared many of their features against all 565 sequenced, dsDNA Klebsiella phage genomes. Taxonomic analyses revealed that these Klebsiella phages belong to three known phage families (Autographiviridae, Drexlerviridae, and Straboviridae) and two newly proposed phage families (Candidatus Mavericviridae and Ca. Rivulusviridae). At the phage family level, we found that core genes were often phage-centric proteins, such as structural proteins for the phage head and tail and DNA packaging proteins. In contrast, genes involved in transcription, translation, or hypothetical proteins were commonly not shared or flexible genes. Ecologically, we assessed the phages' ubiquity in recent large-scale metagenomic datasets, which revealed they were not widespread, as well as a possible direct role in reprogramming specific metabolisms during infection by screening their genomes for phage-encoded auxiliary metabolic genes (AMGs). Even though AMGs are common in the environmental literature, only one of our phage families, Straboviridae, contained AMGs, and the types of AMGs were correlated at the genus level. Host range phenotyping revealed the phages had a wide range of infectivity, infecting between 1-14 of our 22 bacterial strain panel that included pathogenic Klebsiella and Raoultella strains. This indicates that not all capsule-independent Klebsiella phages have broad host ranges. Together, these isolates, with corresponding genome, AMG, and host range analyses, help build the Klebsiella model system for studying phage-host interactions of rhizosphere-associated bacteria.

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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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