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A mutant fitness assay identifies bacterial interactions in a model ocean hot spot

Bacteria that assemble in phycospheres surrounding living phytoplankton cells metabolize a substantial proportion of ocean primary productivity. Yet the type and extent of interactions occurring among species that colonize these micron-scale “hot spot” environments are challenging to study. We ident...

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Autores principales: Schreier, Jeremy E., Smith, Christa B., Ioerger, Thomas R., Moran, Mary Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041152/
https://www.ncbi.nlm.nih.gov/pubmed/36920927
http://dx.doi.org/10.1073/pnas.2217200120
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author Schreier, Jeremy E.
Smith, Christa B.
Ioerger, Thomas R.
Moran, Mary Ann
author_facet Schreier, Jeremy E.
Smith, Christa B.
Ioerger, Thomas R.
Moran, Mary Ann
author_sort Schreier, Jeremy E.
collection PubMed
description Bacteria that assemble in phycospheres surrounding living phytoplankton cells metabolize a substantial proportion of ocean primary productivity. Yet the type and extent of interactions occurring among species that colonize these micron-scale “hot spot” environments are challenging to study. We identified genes that mediate bacterial interactions in phycosphere communities by culturing a transposon mutant library of copiotrophic bacterium Ruegeria pomeroyi DSS-3 with the diatom Thalassiosira pseudonana CCMP1335 as the sole source of organic matter in the presence or absence of other heterotrophic bacterial species. The function of genes having significant effects on R. pomeroyi fitness indicated explicit cell–cell interactions initiated in the multibacterial phycospheres. We found that R. pomeroyi simultaneously competed for shared substrates while increasing reliance on substrates that did not support the other species’ growth. Fitness outcomes also indicated that the bacterium competed for nitrogen in the forms of ammonium and amino acids; obtained purines, pyrimidines, and cofactors via crossfeeding; both initiated and defended antagonistic interactions; and sensed an environment with altered oxygen and superoxide levels. The large genomes characteristic of copiotrophic marine bacteria are hypothesized to enable responses to dynamic ecological challenges occurring at the scale of microns. Here, we discover >200 nonessential genes implicated in the management of fitness costs and benefits of membership in a globally significant bacterial community.
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spelling pubmed-100411522023-03-28 A mutant fitness assay identifies bacterial interactions in a model ocean hot spot Schreier, Jeremy E. Smith, Christa B. Ioerger, Thomas R. Moran, Mary Ann Proc Natl Acad Sci U S A Biological Sciences Bacteria that assemble in phycospheres surrounding living phytoplankton cells metabolize a substantial proportion of ocean primary productivity. Yet the type and extent of interactions occurring among species that colonize these micron-scale “hot spot” environments are challenging to study. We identified genes that mediate bacterial interactions in phycosphere communities by culturing a transposon mutant library of copiotrophic bacterium Ruegeria pomeroyi DSS-3 with the diatom Thalassiosira pseudonana CCMP1335 as the sole source of organic matter in the presence or absence of other heterotrophic bacterial species. The function of genes having significant effects on R. pomeroyi fitness indicated explicit cell–cell interactions initiated in the multibacterial phycospheres. We found that R. pomeroyi simultaneously competed for shared substrates while increasing reliance on substrates that did not support the other species’ growth. Fitness outcomes also indicated that the bacterium competed for nitrogen in the forms of ammonium and amino acids; obtained purines, pyrimidines, and cofactors via crossfeeding; both initiated and defended antagonistic interactions; and sensed an environment with altered oxygen and superoxide levels. The large genomes characteristic of copiotrophic marine bacteria are hypothesized to enable responses to dynamic ecological challenges occurring at the scale of microns. Here, we discover >200 nonessential genes implicated in the management of fitness costs and benefits of membership in a globally significant bacterial community. National Academy of Sciences 2023-03-15 2023-03-21 /pmc/articles/PMC10041152/ /pubmed/36920927 http://dx.doi.org/10.1073/pnas.2217200120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Schreier, Jeremy E.
Smith, Christa B.
Ioerger, Thomas R.
Moran, Mary Ann
A mutant fitness assay identifies bacterial interactions in a model ocean hot spot
title A mutant fitness assay identifies bacterial interactions in a model ocean hot spot
title_full A mutant fitness assay identifies bacterial interactions in a model ocean hot spot
title_fullStr A mutant fitness assay identifies bacterial interactions in a model ocean hot spot
title_full_unstemmed A mutant fitness assay identifies bacterial interactions in a model ocean hot spot
title_short A mutant fitness assay identifies bacterial interactions in a model ocean hot spot
title_sort mutant fitness assay identifies bacterial interactions in a model ocean hot spot
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041152/
https://www.ncbi.nlm.nih.gov/pubmed/36920927
http://dx.doi.org/10.1073/pnas.2217200120
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