Model Communities Hint at Promiscuous Metabolic Linkages between Ubiquitous Free-Living Freshwater Bacteria
ABSTRACT Genome streamlining is frequently observed in free-living aquatic microorganisms and results in physiological dependencies between microorganisms. However, we know little about the specificity of these microbial associations. In order to examine the specificity and extent of these associati...
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American Society for Microbiology
2018
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oai:doaj.org-article:1e2fbb9c187948739d55214f99017b022021-11-15T15:24:22ZModel Communities Hint at Promiscuous Metabolic Linkages between Ubiquitous Free-Living Freshwater Bacteria10.1128/mSphere.00202-182379-5042https://doaj.org/article/1e2fbb9c187948739d55214f99017b022018-06-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00202-18https://doaj.org/toc/2379-5042ABSTRACT Genome streamlining is frequently observed in free-living aquatic microorganisms and results in physiological dependencies between microorganisms. However, we know little about the specificity of these microbial associations. In order to examine the specificity and extent of these associations, we established mixed cultures from three different freshwater environments and analyzed the cooccurrence of organisms using a metagenomic time series. Free-living microorganisms with streamlined genomes lacking multiple biosynthetic pathways showed no clear recurring pattern in their interaction partners. Free-living freshwater bacteria form promiscuous cooperative associations. This notion contrasts with the well-documented high specificities of interaction partners in host-associated bacteria. Considering all data together, we suggest that highly abundant free-living bacterial lineages are functionally versatile in their interactions despite their distinct streamlining tendencies at the single-cell level. This metabolic versatility facilitates interactions with a variable set of community members.Sarahi L. GarciaMoritz BuckJoshua J. HamiltonChristian WurzbacherHans-Peter GrossartKatherine D. McMahonAlexander EilerAmerican Society for Microbiologyarticlecommunityinteractionsmetagenomicsmicrobial ecologymixed culturespromiscuousMicrobiologyQR1-502ENmSphere, Vol 3, Iss 3 (2018) |
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community interactions metagenomics microbial ecology mixed cultures promiscuous Microbiology QR1-502 |
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community interactions metagenomics microbial ecology mixed cultures promiscuous Microbiology QR1-502 Sarahi L. Garcia Moritz Buck Joshua J. Hamilton Christian Wurzbacher Hans-Peter Grossart Katherine D. McMahon Alexander Eiler Model Communities Hint at Promiscuous Metabolic Linkages between Ubiquitous Free-Living Freshwater Bacteria |
description |
ABSTRACT Genome streamlining is frequently observed in free-living aquatic microorganisms and results in physiological dependencies between microorganisms. However, we know little about the specificity of these microbial associations. In order to examine the specificity and extent of these associations, we established mixed cultures from three different freshwater environments and analyzed the cooccurrence of organisms using a metagenomic time series. Free-living microorganisms with streamlined genomes lacking multiple biosynthetic pathways showed no clear recurring pattern in their interaction partners. Free-living freshwater bacteria form promiscuous cooperative associations. This notion contrasts with the well-documented high specificities of interaction partners in host-associated bacteria. Considering all data together, we suggest that highly abundant free-living bacterial lineages are functionally versatile in their interactions despite their distinct streamlining tendencies at the single-cell level. This metabolic versatility facilitates interactions with a variable set of community members. |
format |
article |
author |
Sarahi L. Garcia Moritz Buck Joshua J. Hamilton Christian Wurzbacher Hans-Peter Grossart Katherine D. McMahon Alexander Eiler |
author_facet |
Sarahi L. Garcia Moritz Buck Joshua J. Hamilton Christian Wurzbacher Hans-Peter Grossart Katherine D. McMahon Alexander Eiler |
author_sort |
Sarahi L. Garcia |
title |
Model Communities Hint at Promiscuous Metabolic Linkages between Ubiquitous Free-Living Freshwater Bacteria |
title_short |
Model Communities Hint at Promiscuous Metabolic Linkages between Ubiquitous Free-Living Freshwater Bacteria |
title_full |
Model Communities Hint at Promiscuous Metabolic Linkages between Ubiquitous Free-Living Freshwater Bacteria |
title_fullStr |
Model Communities Hint at Promiscuous Metabolic Linkages between Ubiquitous Free-Living Freshwater Bacteria |
title_full_unstemmed |
Model Communities Hint at Promiscuous Metabolic Linkages between Ubiquitous Free-Living Freshwater Bacteria |
title_sort |
model communities hint at promiscuous metabolic linkages between ubiquitous free-living freshwater bacteria |
publisher |
American Society for Microbiology |
publishDate |
2018 |
url |
https://doaj.org/article/1e2fbb9c187948739d55214f99017b02 |
work_keys_str_mv |
AT sarahilgarcia modelcommunitieshintatpromiscuousmetaboliclinkagesbetweenubiquitousfreelivingfreshwaterbacteria AT moritzbuck modelcommunitieshintatpromiscuousmetaboliclinkagesbetweenubiquitousfreelivingfreshwaterbacteria AT joshuajhamilton modelcommunitieshintatpromiscuousmetaboliclinkagesbetweenubiquitousfreelivingfreshwaterbacteria AT christianwurzbacher modelcommunitieshintatpromiscuousmetaboliclinkagesbetweenubiquitousfreelivingfreshwaterbacteria AT hanspetergrossart modelcommunitieshintatpromiscuousmetaboliclinkagesbetweenubiquitousfreelivingfreshwaterbacteria AT katherinedmcmahon modelcommunitieshintatpromiscuousmetaboliclinkagesbetweenubiquitousfreelivingfreshwaterbacteria AT alexandereiler modelcommunitieshintatpromiscuousmetaboliclinkagesbetweenubiquitousfreelivingfreshwaterbacteria |
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