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The Histidine Kinase BinK Is a Negative Regulator of Biofilm Formation and Squid Colonization

Bacterial colonization of animal epithelial tissue is a dynamic process that relies on precise molecular communication. Colonization of Euprymna scolopes bobtail squid by Vibrio fischeri bacteria requires bacterial aggregation in host mucus as the symbiont transitions from a planktonic lifestyle in...

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Autores principales: Brooks, John F., Mandel, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019070/
https://www.ncbi.nlm.nih.gov/pubmed/26977108
http://dx.doi.org/10.1128/JB.00037-16
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author Brooks, John F.
Mandel, Mark J.
author_facet Brooks, John F.
Mandel, Mark J.
author_sort Brooks, John F.
collection PubMed
description Bacterial colonization of animal epithelial tissue is a dynamic process that relies on precise molecular communication. Colonization of Euprymna scolopes bobtail squid by Vibrio fischeri bacteria requires bacterial aggregation in host mucus as the symbiont transitions from a planktonic lifestyle in seawater to a biofilm-associated state in the host. We have identified a gene, binK (biofilm inhibitor kinase; VF_A0360), which encodes an orphan hybrid histidine kinase that negatively regulates the V. fischeri symbiotic biofilm (Syp) in vivo and in vitro. We identified binK mutants as exhibiting a colonization advantage in a global genetic screen, a phenotype that we confirmed in controlled competition experiments. Bacterial biofilm aggregates in the host are larger in strains lacking BinK, whereas overexpression of BinK suppresses biofilm formation and squid colonization. Signaling through BinK is required for temperature modulation of biofilm formation at 28°C. Furthermore, we present evidence that BinK acts upstream of SypG, the σ(54)-dependent transcriptional regulator of the syp biofilm locus. The BinK effects are dependent on intact signaling in the RscS-Syp biofilm pathway. Therefore, we propose that BinK antagonizes the signal from RscS and serves as an integral component in V. fischeri biofilm regulation. IMPORTANCE Bacterial lifestyle transitions underlie the colonization of animal hosts from environmental reservoirs. Formation of matrix-enclosed, surface-associated aggregates (biofilms) is common in beneficial and pathogenic associations, but investigating the genetic basis of biofilm development in live animal hosts remains a significant challenge. Using the bobtail squid light organ as a model, we analyzed putative colonization factors and identified a histidine kinase that negatively regulates biofilm formation at the host interface. This work reveals a novel in vivo biofilm regulator that influences the transition of bacteria from their planktonic state in seawater to tight aggregates of cells in the host. The study enriches our understanding of biofilm regulation and beneficial colonization by an animal's microbiome.
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spelling pubmed-50190702016-09-23 The Histidine Kinase BinK Is a Negative Regulator of Biofilm Formation and Squid Colonization Brooks, John F. Mandel, Mark J. J Bacteriol Meeting Presentations Bacterial colonization of animal epithelial tissue is a dynamic process that relies on precise molecular communication. Colonization of Euprymna scolopes bobtail squid by Vibrio fischeri bacteria requires bacterial aggregation in host mucus as the symbiont transitions from a planktonic lifestyle in seawater to a biofilm-associated state in the host. We have identified a gene, binK (biofilm inhibitor kinase; VF_A0360), which encodes an orphan hybrid histidine kinase that negatively regulates the V. fischeri symbiotic biofilm (Syp) in vivo and in vitro. We identified binK mutants as exhibiting a colonization advantage in a global genetic screen, a phenotype that we confirmed in controlled competition experiments. Bacterial biofilm aggregates in the host are larger in strains lacking BinK, whereas overexpression of BinK suppresses biofilm formation and squid colonization. Signaling through BinK is required for temperature modulation of biofilm formation at 28°C. Furthermore, we present evidence that BinK acts upstream of SypG, the σ(54)-dependent transcriptional regulator of the syp biofilm locus. The BinK effects are dependent on intact signaling in the RscS-Syp biofilm pathway. Therefore, we propose that BinK antagonizes the signal from RscS and serves as an integral component in V. fischeri biofilm regulation. IMPORTANCE Bacterial lifestyle transitions underlie the colonization of animal hosts from environmental reservoirs. Formation of matrix-enclosed, surface-associated aggregates (biofilms) is common in beneficial and pathogenic associations, but investigating the genetic basis of biofilm development in live animal hosts remains a significant challenge. Using the bobtail squid light organ as a model, we analyzed putative colonization factors and identified a histidine kinase that negatively regulates biofilm formation at the host interface. This work reveals a novel in vivo biofilm regulator that influences the transition of bacteria from their planktonic state in seawater to tight aggregates of cells in the host. The study enriches our understanding of biofilm regulation and beneficial colonization by an animal's microbiome. American Society for Microbiology 2016-09-09 /pmc/articles/PMC5019070/ /pubmed/26977108 http://dx.doi.org/10.1128/JB.00037-16 Text en Copyright © 2016 Brooks and Mandel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Meeting Presentations
Brooks, John F.
Mandel, Mark J.
The Histidine Kinase BinK Is a Negative Regulator of Biofilm Formation and Squid Colonization
title The Histidine Kinase BinK Is a Negative Regulator of Biofilm Formation and Squid Colonization
title_full The Histidine Kinase BinK Is a Negative Regulator of Biofilm Formation and Squid Colonization
title_fullStr The Histidine Kinase BinK Is a Negative Regulator of Biofilm Formation and Squid Colonization
title_full_unstemmed The Histidine Kinase BinK Is a Negative Regulator of Biofilm Formation and Squid Colonization
title_short The Histidine Kinase BinK Is a Negative Regulator of Biofilm Formation and Squid Colonization
title_sort histidine kinase bink is a negative regulator of biofilm formation and squid colonization
topic Meeting Presentations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019070/
https://www.ncbi.nlm.nih.gov/pubmed/26977108
http://dx.doi.org/10.1128/JB.00037-16
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