Evidence map›Paper›PMID 40511850›Full record

ArticleThe ISME journal2025

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

Jordan T Coelho, Lauren Teubner, Michael W Henson, V Celeste Lanclos, Conner Y Kojima, J Cameron Thrash

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Article in The ISME journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jordan T CoelhoDepartment of Biological Sciences, University of Southern California, Los Angeles, CA 90089, United States.
Lauren TeubnerDepartment of Biological Sciences, University of Southern California, Los Angeles, CA 90089, United States.
Michael W HensonDepartment of Biological Sciences, Northern Illinois University, DeKalb, IL 60115, United States.
V Celeste LanclosDepartment of Biological Sciences, University of Southern California, Los Angeles, CA 90089, United States.
Conner Y KojimaDepartment of Biological Sciences, University of Southern California, Los Angeles, CA 90089, United States.
J Cameron ThrashDepartment of Biological Sciences, University of Southern California, Los Angeles, CA 90089, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AlphaproteobacteriaSeawaterEcosystemGenome, BacterialGulf of AmericaMetagenomePhylogenyAlphaproteobacteriabacterioplanktonculturinggenomicsheterotrophsSAR116

Identifiers

PMID40511850
PMCPMC12262181

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.