Culture-supported ecophysiology of the SAR116 clade demonstrates metabolic and spatial niche partitioning.

IF 10 1区 环境科学与生态学 Q1 ECOLOGY
Jordan T Coelho, Lauren Teubner, Michael W Henson, V Celeste Lanclos, Conner Y Kojima, J Cameron Thrash
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引用次数: 0

Abstract

Marine SAR116 bacterioplankton are ubiquitous in surface waters across global oceans and form their own order, Puniceispirillales, within the Alphaproteobacteria. To date no comparative physiology among diverse SAR116 isolates has been performed to capture the functional diversity within the clade, and further, diversity through the lens of metabolic potential and environmental preferences via clade-wide pangenomics continues to evolve with the addition of new genomes. Using high-throughput dilution-to-extinction cultivation, we isolated and genome sequenced five new and diverse SAR116 isolates from the northern Gulf of Mexico. Here we present a comparative physiological analysis of these SAR116 isolates, along with a pangenomic investigation of the SAR116 clade using a combination of metagenome-assembled genomes (MAGs, n = 258), single-amplified genomes (n = 84), previously existing (n = 2), and new isolate genomes (n = 5), totaling 349 SAR116 genomes. Phylogenomic investigation supported the division of SAR116 into three distinct subclades, each with additional structure totaling 15 monophyletic groups. Our SAR116 isolates belonged to three groups within subclade I representing distinct genera with different morphologies and varied phenotypic responses to salinity and temperature. Overall, SAR116 genomes encoded differences in vitamin and amino acid synthesis, trace metal transport, and osmolyte synthesis and transport. They also had genetic potential for diverse sulfur oxidation metabolisms, placing SAR116 at the confluence of the organic and inorganic sulfur pools. SAR116 subclades showed distinct patterns in habitat preferences across open ocean, coastal, and estuarine environments, and three of our isolates represented the most abundant coastal and estuarine subclade. This investigation provides the most comprehensive exploration of SAR116 to date anchored by new culture genomes and physiology.

培养支持的SAR116进化枝的生态生理学证明了代谢和空间生态位划分。
海洋SAR116浮游细菌普遍存在于全球海洋的地表水中,并在阿尔法变形菌门中形成了自己的目——Puniceispirillales。到目前为止,还没有在不同的SAR116分离株之间进行比较生理学来捕捉分支内的功能多样性,而且,通过全分支全基因组学的代谢潜力和环境偏好的多样性随着新基因组的加入而继续进化。利用高通量稀释灭绝培养,我们从墨西哥湾北部分离出5个新的多样化SAR116分离株并对其进行了基因组测序。在此,我们对这些SAR116分离株进行了比较生理学分析,并对SAR116分支进行了全基因组学研究,使用宏基因组组装基因组(258个)、单扩增基因组(84个)、先前存在的基因组(2个)和新分离基因组(5个),共计349个SAR116基因组。系统基因组学研究支持SAR116分为三个不同的亚支系,每个亚支系都有额外的结构,总计15个单系群。我们的SAR116分离株属于亚枝I中的三个类群,代表不同的属,具有不同的形态和对盐度和温度的不同表型反应。总的来说,SAR116基因组编码了维生素和氨基酸合成、微量金属运输和渗透液合成和运输的差异。它们还具有多种硫氧化代谢的遗传潜力,将SAR116置于有机和无机硫池的交汇处。SAR116亚支系在开阔海洋、沿海和河口环境中表现出不同的生境偏好模式,其中3个分离株代表了最丰富的沿海和河口亚支系。这项研究为SAR116提供了迄今为止最全面的探索,以新的培养基因组和生理学为基础。
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来源期刊
ISME Journal
ISME Journal 环境科学-生态学
CiteScore
22.10
自引率
2.70%
发文量
171
审稿时长
2.6 months
期刊介绍: The ISME Journal covers the diverse and integrated areas of microbial ecology. We encourage contributions that represent major advances for the study of microbial ecosystems, communities, and interactions of microorganisms in the environment. Articles in The ISME Journal describe pioneering discoveries of wide appeal that enhance our understanding of functional and mechanistic relationships among microorganisms, their communities, and their habitats.
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