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Causes and Consequences of a Variant Strain of Phaeobacter inhibens With Reduced Competition

Phaeobacter inhibens 2.10 is an effective biofilm former and colonizer of marine surfaces and has the ability to outcompete other microbiota. During biofilm dispersal P. inhibens 2.10 produces heritable phenotypic variants, including those that have a reduced ability to inhibit the co-occurring bact...

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Autores principales: Majzoub, Marwan E., McElroy, Kerensa, Maczka, Michael, Thomas, Torsten, Egan, Suhelen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224355/
https://www.ncbi.nlm.nih.gov/pubmed/30450086
http://dx.doi.org/10.3389/fmicb.2018.02601
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author Majzoub, Marwan E.
McElroy, Kerensa
Maczka, Michael
Thomas, Torsten
Egan, Suhelen
author_facet Majzoub, Marwan E.
McElroy, Kerensa
Maczka, Michael
Thomas, Torsten
Egan, Suhelen
author_sort Majzoub, Marwan E.
collection PubMed
description Phaeobacter inhibens 2.10 is an effective biofilm former and colonizer of marine surfaces and has the ability to outcompete other microbiota. During biofilm dispersal P. inhibens 2.10 produces heritable phenotypic variants, including those that have a reduced ability to inhibit the co-occurring bacterium Pseudoalteromonas tunicata. However, the genetic changes that underpin the phenotypic variation and what the ecological consequences are for variants within the population are unclear. To answer these questions we sequenced the genomes of strain NCV12a1, a biofilm variant of P. inhibens 2.10 with reduced inhibitory activity and the P. inhibens 2.10 WT parental strain. Genome wide analysis revealed point mutations in genes involved in synthesis of the antibacterial compound tropodithietic acid (TDA) and indirectly in extracellular polymeric substances (EPS) production. However, confocal laser scanning microscopy analyses found little differences in biofilm growth between P. inhibens 2.10 WT (parental) and NCV12a1. P. inhibens NCV12a1 was also not outcompeted in co-cultured biofilms with P. tunicata, despite its reduced inhibitory activity, rather these biofilms were thicker than those produced when the WT strain was co-cultured with P. tunicata. Notably, dispersal populations from biofilms of P. inhibens NCV12a1 had a higher proportion of WT-like morphotypes when co-cultured with P. tunicata. These observations may explain why the otherwise non-inhibiting variant persists in the presence of a natural competitor, adding to our understanding of the relative importance of genetic diversification in microbial biofilms.
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spelling pubmed-62243552018-11-16 Causes and Consequences of a Variant Strain of Phaeobacter inhibens With Reduced Competition Majzoub, Marwan E. McElroy, Kerensa Maczka, Michael Thomas, Torsten Egan, Suhelen Front Microbiol Microbiology Phaeobacter inhibens 2.10 is an effective biofilm former and colonizer of marine surfaces and has the ability to outcompete other microbiota. During biofilm dispersal P. inhibens 2.10 produces heritable phenotypic variants, including those that have a reduced ability to inhibit the co-occurring bacterium Pseudoalteromonas tunicata. However, the genetic changes that underpin the phenotypic variation and what the ecological consequences are for variants within the population are unclear. To answer these questions we sequenced the genomes of strain NCV12a1, a biofilm variant of P. inhibens 2.10 with reduced inhibitory activity and the P. inhibens 2.10 WT parental strain. Genome wide analysis revealed point mutations in genes involved in synthesis of the antibacterial compound tropodithietic acid (TDA) and indirectly in extracellular polymeric substances (EPS) production. However, confocal laser scanning microscopy analyses found little differences in biofilm growth between P. inhibens 2.10 WT (parental) and NCV12a1. P. inhibens NCV12a1 was also not outcompeted in co-cultured biofilms with P. tunicata, despite its reduced inhibitory activity, rather these biofilms were thicker than those produced when the WT strain was co-cultured with P. tunicata. Notably, dispersal populations from biofilms of P. inhibens NCV12a1 had a higher proportion of WT-like morphotypes when co-cultured with P. tunicata. These observations may explain why the otherwise non-inhibiting variant persists in the presence of a natural competitor, adding to our understanding of the relative importance of genetic diversification in microbial biofilms. Frontiers Media S.A. 2018-11-02 /pmc/articles/PMC6224355/ /pubmed/30450086 http://dx.doi.org/10.3389/fmicb.2018.02601 Text en Copyright © 2018 Majzoub, McElroy, Maczka, Thomas and Egan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Majzoub, Marwan E.
McElroy, Kerensa
Maczka, Michael
Thomas, Torsten
Egan, Suhelen
Causes and Consequences of a Variant Strain of Phaeobacter inhibens With Reduced Competition
title Causes and Consequences of a Variant Strain of Phaeobacter inhibens With Reduced Competition
title_full Causes and Consequences of a Variant Strain of Phaeobacter inhibens With Reduced Competition
title_fullStr Causes and Consequences of a Variant Strain of Phaeobacter inhibens With Reduced Competition
title_full_unstemmed Causes and Consequences of a Variant Strain of Phaeobacter inhibens With Reduced Competition
title_short Causes and Consequences of a Variant Strain of Phaeobacter inhibens With Reduced Competition
title_sort causes and consequences of a variant strain of phaeobacter inhibens with reduced competition
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224355/
https://www.ncbi.nlm.nih.gov/pubmed/30450086
http://dx.doi.org/10.3389/fmicb.2018.02601
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