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Transcriptional pathways across colony biofilm models in the symbiont Vibrio fischeri

Beneficial microbial symbionts that are horizontally acquired by their animal hosts undergo a lifestyle transition from free-living in the environment to associated with host tissues. In the model symbiosis between the Hawaiian bobtail squid and its microbial symbiont Vibrio fischeri, one mechanism...

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Autores principales: Griend, Jacob A. Vander, Isenberg, Ruth Y., Kotla, Ketan R., Mandel, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441365/
https://www.ncbi.nlm.nih.gov/pubmed/37609283
http://dx.doi.org/10.1101/2023.08.07.552283
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author Griend, Jacob A. Vander
Isenberg, Ruth Y.
Kotla, Ketan R.
Mandel, Mark J.
author_facet Griend, Jacob A. Vander
Isenberg, Ruth Y.
Kotla, Ketan R.
Mandel, Mark J.
author_sort Griend, Jacob A. Vander
collection PubMed
description Beneficial microbial symbionts that are horizontally acquired by their animal hosts undergo a lifestyle transition from free-living in the environment to associated with host tissues. In the model symbiosis between the Hawaiian bobtail squid and its microbial symbiont Vibrio fischeri, one mechanism used to make this transition during host colonization is the formation of biofilm-like aggregates in host mucosa. Previous work identified factors that are sufficient to induce V. fischeri biofilm formation, yet much remains unknown regarding the breadth of target genes induced by these factors. Here, we probed two widely-used in vitro models of biofilm formation to identify novel regulatory pathways in the squid symbiont V. fischeri ES114. We discovered a shared set of 232 genes that demonstrated similar patterns in expression in both models. These genes comprise multiple exopolysaccharide loci that are upregulated and flagellar motility genes that are downregulated, with a consistent decrease in measured swimming motility. Furthermore, we identified genes regulated downstream of the key sensor kinase RscS that are induced independent of the response regulator SypG. Our data suggest that putative response regulator VpsR plays a strong role in expression of at least a subset of these genes. Overall, this study adds to our understanding of the genes involved in V. fischeri biofilm regulation, while revealing new regulatory pathways branching from previously characterized signaling networks.
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spelling pubmed-104413652023-08-22 Transcriptional pathways across colony biofilm models in the symbiont Vibrio fischeri Griend, Jacob A. Vander Isenberg, Ruth Y. Kotla, Ketan R. Mandel, Mark J. bioRxiv Article Beneficial microbial symbionts that are horizontally acquired by their animal hosts undergo a lifestyle transition from free-living in the environment to associated with host tissues. In the model symbiosis between the Hawaiian bobtail squid and its microbial symbiont Vibrio fischeri, one mechanism used to make this transition during host colonization is the formation of biofilm-like aggregates in host mucosa. Previous work identified factors that are sufficient to induce V. fischeri biofilm formation, yet much remains unknown regarding the breadth of target genes induced by these factors. Here, we probed two widely-used in vitro models of biofilm formation to identify novel regulatory pathways in the squid symbiont V. fischeri ES114. We discovered a shared set of 232 genes that demonstrated similar patterns in expression in both models. These genes comprise multiple exopolysaccharide loci that are upregulated and flagellar motility genes that are downregulated, with a consistent decrease in measured swimming motility. Furthermore, we identified genes regulated downstream of the key sensor kinase RscS that are induced independent of the response regulator SypG. Our data suggest that putative response regulator VpsR plays a strong role in expression of at least a subset of these genes. Overall, this study adds to our understanding of the genes involved in V. fischeri biofilm regulation, while revealing new regulatory pathways branching from previously characterized signaling networks. Cold Spring Harbor Laboratory 2023-08-07 /pmc/articles/PMC10441365/ /pubmed/37609283 http://dx.doi.org/10.1101/2023.08.07.552283 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Griend, Jacob A. Vander
Isenberg, Ruth Y.
Kotla, Ketan R.
Mandel, Mark J.
Transcriptional pathways across colony biofilm models in the symbiont Vibrio fischeri
title Transcriptional pathways across colony biofilm models in the symbiont Vibrio fischeri
title_full Transcriptional pathways across colony biofilm models in the symbiont Vibrio fischeri
title_fullStr Transcriptional pathways across colony biofilm models in the symbiont Vibrio fischeri
title_full_unstemmed Transcriptional pathways across colony biofilm models in the symbiont Vibrio fischeri
title_short Transcriptional pathways across colony biofilm models in the symbiont Vibrio fischeri
title_sort transcriptional pathways across colony biofilm models in the symbiont vibrio fischeri
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441365/
https://www.ncbi.nlm.nih.gov/pubmed/37609283
http://dx.doi.org/10.1101/2023.08.07.552283
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