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Spontaneous quorum-sensing hierarchy reprogramming in Pseudomonas aeruginosa laboratory strain PAO1

Pseudomonas aeruginosa strain PAO1 has been commonly used in the laboratory, with frequent genome variations reported. Quorum sensing (QS), a cell–cell communication system, plays important role in controlling a variety of virulence factors. However, the evolution and adaptability of QS in those lab...

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Autores principales: Cheng, Xiaoyan, Lu, Mingqi, Qiu, Huifang, Li, Yuanhao, Huang, Linfeng, Dai, Weijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8792115/
https://www.ncbi.nlm.nih.gov/pubmed/35083573
http://dx.doi.org/10.1186/s13568-022-01344-7
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author Cheng, Xiaoyan
Lu, Mingqi
Qiu, Huifang
Li, Yuanhao
Huang, Linfeng
Dai, Weijun
author_facet Cheng, Xiaoyan
Lu, Mingqi
Qiu, Huifang
Li, Yuanhao
Huang, Linfeng
Dai, Weijun
author_sort Cheng, Xiaoyan
collection PubMed
description Pseudomonas aeruginosa strain PAO1 has been commonly used in the laboratory, with frequent genome variations reported. Quorum sensing (QS), a cell–cell communication system, plays important role in controlling a variety of virulence factors. However, the evolution and adaptability of QS in those laboratory strains are still poorly understood. Here we used the QS reporter and whole-genome sequencing (WGS) to systematically investigate the QS phenotypes and corresponding genetic basis in collected laboratory PAO1 strains. We found that the PAO1-z strain has an inactive LasR protein, while bearing an active Rhl QS system and exhibiting QS-controlled protease-positive activity. Our study revealed that an 18-bp insertion in mexT gene gave rise to the active QS system in the PAO1-z strain. This MexT inactivation restored the QS activity caused by the inactive LasR, showing elevated production of pyocyanin, cyanide and elastase. Our results implied the evolutionary trajectory for the PAO1-z strain, with the evulutionary order from the first Las QS inactivation to the final Rhl QS activation. Our findings point out that QS homeostasis occurs in the laboratory P. aeruginosa strain, offering a potential platform for the QS study in clinical isolates. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13568-022-01344-7.
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spelling pubmed-87921152022-02-02 Spontaneous quorum-sensing hierarchy reprogramming in Pseudomonas aeruginosa laboratory strain PAO1 Cheng, Xiaoyan Lu, Mingqi Qiu, Huifang Li, Yuanhao Huang, Linfeng Dai, Weijun AMB Express Original Article Pseudomonas aeruginosa strain PAO1 has been commonly used in the laboratory, with frequent genome variations reported. Quorum sensing (QS), a cell–cell communication system, plays important role in controlling a variety of virulence factors. However, the evolution and adaptability of QS in those laboratory strains are still poorly understood. Here we used the QS reporter and whole-genome sequencing (WGS) to systematically investigate the QS phenotypes and corresponding genetic basis in collected laboratory PAO1 strains. We found that the PAO1-z strain has an inactive LasR protein, while bearing an active Rhl QS system and exhibiting QS-controlled protease-positive activity. Our study revealed that an 18-bp insertion in mexT gene gave rise to the active QS system in the PAO1-z strain. This MexT inactivation restored the QS activity caused by the inactive LasR, showing elevated production of pyocyanin, cyanide and elastase. Our results implied the evolutionary trajectory for the PAO1-z strain, with the evulutionary order from the first Las QS inactivation to the final Rhl QS activation. Our findings point out that QS homeostasis occurs in the laboratory P. aeruginosa strain, offering a potential platform for the QS study in clinical isolates. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13568-022-01344-7. Springer Berlin Heidelberg 2022-01-26 /pmc/articles/PMC8792115/ /pubmed/35083573 http://dx.doi.org/10.1186/s13568-022-01344-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Cheng, Xiaoyan
Lu, Mingqi
Qiu, Huifang
Li, Yuanhao
Huang, Linfeng
Dai, Weijun
Spontaneous quorum-sensing hierarchy reprogramming in Pseudomonas aeruginosa laboratory strain PAO1
title Spontaneous quorum-sensing hierarchy reprogramming in Pseudomonas aeruginosa laboratory strain PAO1
title_full Spontaneous quorum-sensing hierarchy reprogramming in Pseudomonas aeruginosa laboratory strain PAO1
title_fullStr Spontaneous quorum-sensing hierarchy reprogramming in Pseudomonas aeruginosa laboratory strain PAO1
title_full_unstemmed Spontaneous quorum-sensing hierarchy reprogramming in Pseudomonas aeruginosa laboratory strain PAO1
title_short Spontaneous quorum-sensing hierarchy reprogramming in Pseudomonas aeruginosa laboratory strain PAO1
title_sort spontaneous quorum-sensing hierarchy reprogramming in pseudomonas aeruginosa laboratory strain pao1
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8792115/
https://www.ncbi.nlm.nih.gov/pubmed/35083573
http://dx.doi.org/10.1186/s13568-022-01344-7
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