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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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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. |
format | Online Article Text |
id | pubmed-10162802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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