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RssAB Signaling Coordinates Early Development of Surface Multicellularity in Serratia marcescens
Bacteria can coordinate several multicellular behaviors in response to environmental changes. Among these, swarming and biofilm formation have attracted significant attention for their correlation with bacterial pathogenicity. However, little is known about when and where the signaling occurs to tri...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162612/ https://www.ncbi.nlm.nih.gov/pubmed/21887380 http://dx.doi.org/10.1371/journal.pone.0024154 |
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author | Tsai, Yu-Huan Wei, Jun-Rong Lin, Chuan-Sheng Chen, Po-Han Huang, Stella Lin, Yu-Ching Wei, Chia-Fong Lu, Chia-Chen Lai, Hsin-Chih |
author_facet | Tsai, Yu-Huan Wei, Jun-Rong Lin, Chuan-Sheng Chen, Po-Han Huang, Stella Lin, Yu-Ching Wei, Chia-Fong Lu, Chia-Chen Lai, Hsin-Chih |
author_sort | Tsai, Yu-Huan |
collection | PubMed |
description | Bacteria can coordinate several multicellular behaviors in response to environmental changes. Among these, swarming and biofilm formation have attracted significant attention for their correlation with bacterial pathogenicity. However, little is known about when and where the signaling occurs to trigger either swarming or biofilm formation. We have previously identified an RssAB two-component system involved in the regulation of swarming motility and biofilm formation in Serratia marcescens. Here we monitored the RssAB signaling status within single cells by tracing the location of the translational fusion protein EGFP-RssB following development of swarming or biofilm formation. RssAB signaling is specifically activated before surface migration in swarming development and during the early stage of biofilm formation. The activation results in the release of RssB from its cognate inner membrane sensor kinase, RssA, to the cytoplasm where the downstream gene promoters are located. Such dynamic localization of RssB requires phosphorylation of this regulator. By revealing the temporal activation of RssAB signaling following development of surface multicellular behavior, our findings contribute to an improved understanding of how bacteria coordinate their lifestyle on a surface. |
format | Online Article Text |
id | pubmed-3162612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31626122011-09-01 RssAB Signaling Coordinates Early Development of Surface Multicellularity in Serratia marcescens Tsai, Yu-Huan Wei, Jun-Rong Lin, Chuan-Sheng Chen, Po-Han Huang, Stella Lin, Yu-Ching Wei, Chia-Fong Lu, Chia-Chen Lai, Hsin-Chih PLoS One Research Article Bacteria can coordinate several multicellular behaviors in response to environmental changes. Among these, swarming and biofilm formation have attracted significant attention for their correlation with bacterial pathogenicity. However, little is known about when and where the signaling occurs to trigger either swarming or biofilm formation. We have previously identified an RssAB two-component system involved in the regulation of swarming motility and biofilm formation in Serratia marcescens. Here we monitored the RssAB signaling status within single cells by tracing the location of the translational fusion protein EGFP-RssB following development of swarming or biofilm formation. RssAB signaling is specifically activated before surface migration in swarming development and during the early stage of biofilm formation. The activation results in the release of RssB from its cognate inner membrane sensor kinase, RssA, to the cytoplasm where the downstream gene promoters are located. Such dynamic localization of RssB requires phosphorylation of this regulator. By revealing the temporal activation of RssAB signaling following development of surface multicellular behavior, our findings contribute to an improved understanding of how bacteria coordinate their lifestyle on a surface. Public Library of Science 2011-08-26 /pmc/articles/PMC3162612/ /pubmed/21887380 http://dx.doi.org/10.1371/journal.pone.0024154 Text en Tsai et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tsai, Yu-Huan Wei, Jun-Rong Lin, Chuan-Sheng Chen, Po-Han Huang, Stella Lin, Yu-Ching Wei, Chia-Fong Lu, Chia-Chen Lai, Hsin-Chih RssAB Signaling Coordinates Early Development of Surface Multicellularity in Serratia marcescens |
title | RssAB Signaling Coordinates Early Development of Surface Multicellularity in Serratia marcescens
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title_full | RssAB Signaling Coordinates Early Development of Surface Multicellularity in Serratia marcescens
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title_fullStr | RssAB Signaling Coordinates Early Development of Surface Multicellularity in Serratia marcescens
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title_full_unstemmed | RssAB Signaling Coordinates Early Development of Surface Multicellularity in Serratia marcescens
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title_short | RssAB Signaling Coordinates Early Development of Surface Multicellularity in Serratia marcescens
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title_sort | rssab signaling coordinates early development of surface multicellularity in serratia marcescens |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162612/ https://www.ncbi.nlm.nih.gov/pubmed/21887380 http://dx.doi.org/10.1371/journal.pone.0024154 |
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