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Two enhancer binding proteins activate σ(54)-dependent transcription of a quorum regulatory RNA in a bacterial symbiont

To colonize a host, bacteria depend on an ensemble of signaling systems to convert information about the various environments encountered within the host into specific cellular activities. How these signaling systems coordinate transitions between cellular states in vivo remains poorly understood. T...

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Autores principales: Surrett, Ericka D, Guckes, Kirsten R, Cousins, Shyan, Ruskoski, Terry B, Cecere, Andrew G, Ludvik, Denise A, Okafor, C Denise, Mandel, Mark J, Miyashiro, Tim I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162802/
https://www.ncbi.nlm.nih.gov/pubmed/37145113
http://dx.doi.org/10.7554/eLife.78544
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author Surrett, Ericka D
Guckes, Kirsten R
Cousins, Shyan
Ruskoski, Terry B
Cecere, Andrew G
Ludvik, Denise A
Okafor, C Denise
Mandel, Mark J
Miyashiro, Tim I
author_facet Surrett, Ericka D
Guckes, Kirsten R
Cousins, Shyan
Ruskoski, Terry B
Cecere, Andrew G
Ludvik, Denise A
Okafor, C Denise
Mandel, Mark J
Miyashiro, Tim I
author_sort Surrett, Ericka D
collection PubMed
description To colonize a host, bacteria depend on an ensemble of signaling systems to convert information about the various environments encountered within the host into specific cellular activities. How these signaling systems coordinate transitions between cellular states in vivo remains poorly understood. To address this knowledge gap, we investigated how the bacterial symbiont Vibrio fischeri initially colonizes the light organ of the Hawaiian bobtail squid Euprymna scolopes. Previous work has shown that the small RNA Qrr1, which is a regulatory component of the quorum-sensing system in V. fischeri, promotes host colonization. Here, we report that transcriptional activation of Qrr1 is inhibited by the sensor kinase BinK, which suppresses cellular aggregation by V. fischeri prior to light organ entry. We show that Qrr1 expression depends on the alternative sigma factor σ(54) and the transcription factors LuxO and SypG, which function similar to an OR logic gate, thereby ensuring Qrr1 is expressed during colonization. Finally, we provide evidence that this regulatory mechanism is widespread throughout the Vibrionaceae family. Together, our work reveals how coordination between the signaling pathways underlying aggregation and quorum-sensing promotes host colonization, which provides insight into how integration among signaling systems facilitates complex processes in bacteria.
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spelling pubmed-101628022023-05-06 Two enhancer binding proteins activate σ(54)-dependent transcription of a quorum regulatory RNA in a bacterial symbiont Surrett, Ericka D Guckes, Kirsten R Cousins, Shyan Ruskoski, Terry B Cecere, Andrew G Ludvik, Denise A Okafor, C Denise Mandel, Mark J Miyashiro, Tim I eLife Microbiology and Infectious Disease To colonize a host, bacteria depend on an ensemble of signaling systems to convert information about the various environments encountered within the host into specific cellular activities. How these signaling systems coordinate transitions between cellular states in vivo remains poorly understood. To address this knowledge gap, we investigated how the bacterial symbiont Vibrio fischeri initially colonizes the light organ of the Hawaiian bobtail squid Euprymna scolopes. Previous work has shown that the small RNA Qrr1, which is a regulatory component of the quorum-sensing system in V. fischeri, promotes host colonization. Here, we report that transcriptional activation of Qrr1 is inhibited by the sensor kinase BinK, which suppresses cellular aggregation by V. fischeri prior to light organ entry. We show that Qrr1 expression depends on the alternative sigma factor σ(54) and the transcription factors LuxO and SypG, which function similar to an OR logic gate, thereby ensuring Qrr1 is expressed during colonization. Finally, we provide evidence that this regulatory mechanism is widespread throughout the Vibrionaceae family. Together, our work reveals how coordination between the signaling pathways underlying aggregation and quorum-sensing promotes host colonization, which provides insight into how integration among signaling systems facilitates complex processes in bacteria. eLife Sciences Publications, Ltd 2023-05-05 /pmc/articles/PMC10162802/ /pubmed/37145113 http://dx.doi.org/10.7554/eLife.78544 Text en © 2023, Surrett et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Microbiology and Infectious Disease
Surrett, Ericka D
Guckes, Kirsten R
Cousins, Shyan
Ruskoski, Terry B
Cecere, Andrew G
Ludvik, Denise A
Okafor, C Denise
Mandel, Mark J
Miyashiro, Tim I
Two enhancer binding proteins activate σ(54)-dependent transcription of a quorum regulatory RNA in a bacterial symbiont
title Two enhancer binding proteins activate σ(54)-dependent transcription of a quorum regulatory RNA in a bacterial symbiont
title_full Two enhancer binding proteins activate σ(54)-dependent transcription of a quorum regulatory RNA in a bacterial symbiont
title_fullStr Two enhancer binding proteins activate σ(54)-dependent transcription of a quorum regulatory RNA in a bacterial symbiont
title_full_unstemmed Two enhancer binding proteins activate σ(54)-dependent transcription of a quorum regulatory RNA in a bacterial symbiont
title_short Two enhancer binding proteins activate σ(54)-dependent transcription of a quorum regulatory RNA in a bacterial symbiont
title_sort two enhancer binding proteins activate σ(54)-dependent transcription of a quorum regulatory rna in a bacterial symbiont
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162802/
https://www.ncbi.nlm.nih.gov/pubmed/37145113
http://dx.doi.org/10.7554/eLife.78544
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