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一种新型且普遍存在的海洋甲基噬菌体为病毒-宿主协同进化提供了新见解,并可能使海洋异养菌的宿主范围扩大。

A Novel and Ubiquitous Marine Methylophage Provides Insights into Viral-Host Coevolution and Possible Host-Range Expansion in Streamlined Marine Heterotrophic Bacteria.

机构信息

University of Exeter, School of Biosciences, Exeter, UK.

Plymouth Marine Laboratory, Plymouth, UK.

出版信息

Appl Environ Microbiol. 2022 Apr 12;88(7):e0025522. doi: 10.1128/aem.00255-22. Epub 2022 Mar 21.

DOI:10.1128/aem.00255-22
PMID:35311512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9004378/
Abstract

The methylotrophic OM43 clade are that comprise some of the smallest free-living cells known and have highly streamlined genomes. OM43 represents an important microbial link between marine primary production and remineralization of carbon back to the atmosphere. Bacteriophages shape microbial communities and are major drivers of mortality and global marine biogeochemistry. Recent cultivation efforts have brought the first viruses infecting members of the OM43 clade into culture. Here, we characterize a novel myophage infecting OM43 called Melnitz. Melnitz was isolated independently from water samples from a subtropical ocean gyre (Sargasso Sea) and temperate coastal (Western English Channel) systems. Metagenomic recruitment from global ocean viromes confirmed that Melnitz is globally ubiquitous, congruent with patterns of host abundance. Bacteria with streamlined genomes such as OM43 and the globally dominant SAR11 clade use riboswitches as an efficient method to regulate metabolism. Melnitz encodes a two-piece tmRNA (), controlled by a glutamine riboswitch, providing evidence that riboswitch use also occurs for regulation during phage infection of streamlined heterotrophs. Virally encoded tRNAs and found in Melnitz were phylogenetically more closely related to those found within the alphaproteobacterial SAR11 clade and their associated myophages than those within their gammaproteobacterial hosts. This suggests the possibility of an ancestral host transition event between SAR11 and OM43. Melnitz and a related myophage that infects SAR11 were unable to infect hosts of the SAR11 and OM43, respectively, suggesting host transition rather than a broadening of host range. Isolation and cultivation of viruses are the foundations on which the mechanistic understanding of virus-host interactions and parameterization of bioinformatic tools for viral ecology are based. This study isolated and characterized the first myophage known to infect the OM43 clade, expanding our knowledge of this understudied group of microbes. The nearly identical genomes of four strains of Melnitz isolated from different marine provinces and the global abundance estimations from metagenomic data suggest that this viral population is globally ubiquitous. Genome analysis revealed several unusual features in Melnitz and related genomes recovered from viromes, such as a curli operon and virally encoded tmRNA controlled by a glutamine riboswitch, neither of which are found in the host. Further phylogenetic analysis of shared genes indicates that this group of viruses infecting the gammaproteobacterial OM43 shares a recent common ancestor with viruses infecting the abundant alphaproteobacterial SAR11 clade. Host ranges are affected by compatible cell surface receptors, successful circumvention of superinfection exclusion systems, and the presence of required accessory proteins, which typically limits phages to singular narrow groups of closely related bacterial hosts. This study provides intriguing evidence that for streamlined heterotrophic bacteria, virus-host transitioning may not be necessarily restricted to phylogenetically related hosts but is a function of shared physical and biochemical properties of the cell.

摘要

嗜甲基 OM43 分支是由一些已知的最小的自由生活细胞组成,具有高度精简的基因组。OM43 代表了海洋初级生产和碳回大气再矿化之间的重要微生物联系。噬菌体塑造微生物群落,是死亡率和全球海洋生物地球化学的主要驱动因素。最近的培养工作将感染 OM43 分支成员的第一批病毒带入了培养。在这里,我们描述了一种感染 OM43 的新型噬藻体,称为 Melnitz。Melnitz 是从亚热带环流(马尾藻海)和温带沿海(西英吉利海峡)系统的水样中独立分离出来的。从全球海洋病毒组中进行的宏基因组招募证实,Melnitz 是全球性的普遍存在的,与宿主丰度的模式一致。具有精简基因组的细菌,如 OM43 和全球占主导地位的 SAR11 分支,使用核糖体开关作为一种有效的方法来调节代谢。Melnitz 编码了一个两片式 tmRNA (),受谷氨酰胺核糖体开关控制,这为核糖体开关在噬菌体感染精简异养生物时用于调节提供了证据。Melnitz 中发现的病毒编码 tRNA 和 与 alpha-proteobacterial SAR11 分支及其相关噬藻体中的那些在系统发育上更为密切相关,而不是与其 gamma-proteobacterial 宿主中的那些。这表明 SAR11 和 OM43 之间可能发生了祖先宿主的转变事件。Melnitz 和一种感染 SAR11 的相关噬藻体分别不能感染 SAR11 和 OM43 的宿主,这表明是宿主的转变而不是宿主范围的扩大。病毒的分离和培养是理解病毒-宿主相互作用的机制和为病毒生态学的生物信息学工具进行参数化的基础。本研究分离并鉴定了已知感染 OM43 分支的第一个噬藻体,扩展了我们对这组研究较少的微生物的了解。从不同海洋省份分离出的四个 Melnitz 菌株的几乎相同的基因组和宏基因组数据的全球丰度估计表明,这种病毒群体在全球范围内普遍存在。基因组分析揭示了 Melnitz 及其从病毒组中回收的相关基因组中的几个不寻常特征,例如卷曲菌操纵子和受谷氨酰胺核糖体开关控制的病毒编码 tmRNA,这些在宿主中都没有发现。共享基因的进一步系统发育分析表明,感染 gammaproteobacterial OM43 的这群病毒与感染丰富的 alpha-proteobacterial SAR11 分支的病毒具有最近的共同祖先。宿主范围受相容的细胞表面受体、成功规避超感染排除系统以及所需辅助蛋白的存在影响,这些通常将噬菌体限制在单一的密切相关的细菌宿主的狭窄群体中。本研究提供了有趣的证据,表明对于精简的异养细菌,病毒-宿主的转变不一定仅限于系统发育相关的宿主,而是与细胞的物理和生化特性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8eb/9004378/91fc922ab23d/aem.00255-22-f006.jpg
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