Isolate-anchored comparisons reveal evolutionary and functional differentiation across SAR86 marine bacteria

Oscar Ramfelt, Kelle C Freel, Sarah J Tucker, Olivia D Nigro, Michael S Rappé
{"title":"Isolate-anchored comparisons reveal evolutionary and functional differentiation across SAR86 marine bacteria","authors":"Oscar Ramfelt, Kelle C Freel, Sarah J Tucker, Olivia D Nigro, Michael S Rappé","doi":"10.1093/ismejo/wrae227","DOIUrl":null,"url":null,"abstract":"SAR86 is one of the most abundant groups of bacteria in the global surface ocean. However, since its discovery over 30 years ago, it has remained recalcitrant to isolation and many details regarding this group are still unknown. Here we report the cellular characteristics from the first SAR86 isolate brought into culture, Magnimaribacter mokuoloeensis strain HIMB1674, and use its closed genome in concert with over 700 environmental genomes to assess the phylogenomic and functional characteristics of this order-level lineage of marine Gammaproteobacteria. The SAR86 order Magnimaribacterales invest significant genomic resources into the capacity for $\\beta$-oxidation, which is present in most genomes in high gene copy numbers. This cyclical set of reactions appears to be fed by components of cell membranes that include lipids such as phosphatidylcholine, phosphatidylethanolamine, glycolipids, and sulfolipids. In addition to the widespread capacity to degrade the side chain of steroidal compounds via $\\beta$-oxidation, several SAR86 sublineages also appear able to fully degrade the steroid polycyclic ring structure as well as other aromatic, polycyclic, and heterocyclic molecules. Read recruitment from publicly available metagenomes reveals that the Magnimaribacterales compose up to 6% of the global surface ocean microbial community. Only a subset of genera drive these high relative abundances, with some more globally dominant and others restricted to specific oceanic regions. This study provides an unprecedented foundation through which to understand this highly abundant yet poorly understood lineage of marine bacteria, and charts a path to bring more representatives of this order into laboratory culture.","PeriodicalId":516554,"journal":{"name":"The ISME Journal","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The ISME Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/ismejo/wrae227","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

SAR86 is one of the most abundant groups of bacteria in the global surface ocean. However, since its discovery over 30 years ago, it has remained recalcitrant to isolation and many details regarding this group are still unknown. Here we report the cellular characteristics from the first SAR86 isolate brought into culture, Magnimaribacter mokuoloeensis strain HIMB1674, and use its closed genome in concert with over 700 environmental genomes to assess the phylogenomic and functional characteristics of this order-level lineage of marine Gammaproteobacteria. The SAR86 order Magnimaribacterales invest significant genomic resources into the capacity for $\beta$-oxidation, which is present in most genomes in high gene copy numbers. This cyclical set of reactions appears to be fed by components of cell membranes that include lipids such as phosphatidylcholine, phosphatidylethanolamine, glycolipids, and sulfolipids. In addition to the widespread capacity to degrade the side chain of steroidal compounds via $\beta$-oxidation, several SAR86 sublineages also appear able to fully degrade the steroid polycyclic ring structure as well as other aromatic, polycyclic, and heterocyclic molecules. Read recruitment from publicly available metagenomes reveals that the Magnimaribacterales compose up to 6% of the global surface ocean microbial community. Only a subset of genera drive these high relative abundances, with some more globally dominant and others restricted to specific oceanic regions. This study provides an unprecedented foundation through which to understand this highly abundant yet poorly understood lineage of marine bacteria, and charts a path to bring more representatives of this order into laboratory culture.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
隔离锚定比较揭示了 SAR86 海洋细菌的进化和功能分化
SAR86 是全球表层海洋中数量最多的细菌群之一。然而,自 30 多年前发现以来,它一直难以分离,有关该菌群的许多细节仍然未知。在此,我们报告了第一个分离培养的 SAR86 菌株 Magnimaribacter mokuoloeensis 菌株 HIMB1674 的细胞特征,并将其封闭基因组与 700 多个环境基因组结合使用,以评估这一海洋伽马蛋白杆菌纲的系统发生组和功能特征。SAR86 目 Magnimaribacterales 对 $\beta$-oxidation 的能力投入了大量基因组资源,这种能力以高基因拷贝数存在于大多数基因组中。这一系列循环反应似乎是由细胞膜成分提供的,其中包括磷脂酰胆碱、磷脂酰乙醇胺、糖脂和硫脂等脂质。除了通过(beta)氧化作用降解类固醇化合物侧链的广泛能力外,一些 SAR86 亚系似乎还能完全降解类固醇多环环结构以及其他芳香族、多环和杂环分子。从公开的元基因组中进行的读取显示,木兰杆菌属(Magnimaribacterales)占全球表层海洋微生物群落的 6%。只有一小部分菌属驱动了这些高相对丰度,其中一些菌属在全球占主导地位,另一些则局限于特定的海洋区域。这项研究提供了一个前所未有的基础,通过这个基础,我们可以了解这一数量巨大但却鲜为人知的海洋细菌谱系,并为将更多的该谱系代表引入实验室培养指明了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Coastal bacteria and protists assimilate viral carbon and nitrogen Pathobiont and symbiont contribute to microbiota homeostasis through Malpighian tubules-gut countercurrent flow in Bactrocera dorsalis Urea assimilation and oxidation support activity of phylogenetically diverse microbial communities of the dark ocean Aminolipids in bacterial membranes and the natural environment Isolate-anchored comparisons reveal evolutionary and functional differentiation across SAR86 marine bacteria
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1