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A novel phase variant of the cholera pathogen shows stress-adaptive cryptic transcriptomic signatures
BACKGROUND: In a process known as phase variation, the marine bacterium and cholera pathogen Vibrio cholerae alternately expresses smooth or rugose colonial phenotypes, the latter being associated with advanced biofilm architecture and greater resistance to ecological stress. To define phase variati...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109742/ https://www.ncbi.nlm.nih.gov/pubmed/27842489 http://dx.doi.org/10.1186/s12864-016-3233-x |
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author | Lambert, Bliss Dassanayake, Maheshi Oh, Dong-Ha Garrett, Shana B. Lee, Sang-Yeol Pettis, Gregg S. |
author_facet | Lambert, Bliss Dassanayake, Maheshi Oh, Dong-Ha Garrett, Shana B. Lee, Sang-Yeol Pettis, Gregg S. |
author_sort | Lambert, Bliss |
collection | PubMed |
description | BACKGROUND: In a process known as phase variation, the marine bacterium and cholera pathogen Vibrio cholerae alternately expresses smooth or rugose colonial phenotypes, the latter being associated with advanced biofilm architecture and greater resistance to ecological stress. To define phase variation at the transcriptomic level in pandemic V. cholerae O1 El Tor strain N16961, we compared the RNA-seq-derived transcriptomes among the smooth parent N16961, its rugose derivative (N16961R) and a smooth form obtained directly from the rugose at high frequencies consistent with phase variation (N16961SD). RESULTS: Differentially regulated genes which clustered into co-expression groups were identified for specific cellular functions, including acetate metabolism, gluconeogenesis, and anaerobic respiration, suggesting an important link between these processes and biofilm formation in this species. Principal component analysis separated the transcriptome of N16961SD from the other phase variants. Although N16961SD was defective in biofilm formation, transcription of its biofilm-related vps and rbm gene clusters was nevertheless elevated as judged by both RNA-seq and RT-qPCR analyses. This transcriptome signature was shared with N16961R, as were others involving two-component signal transduction, chemotaxis, and c-di-GMP synthesis functions. CONCLUSIONS: Precise turnarounds in gene expression did not accompany reversible phase transitions (i.e., smooth to rugose to smooth) in the cholera pathogen. Transcriptomic signatures consisting of up-regulated genes involved in biofilm formation, environmental sensing and persistence, chemotaxis, and signal transduction, which were shared by N16961R and N16961SD variants, may implicate a stress adaptation in the pathogen that facilitates transition of the N16961SD smooth form back to rugosity should environmental conditions dictate. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3233-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5109742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51097422016-11-28 A novel phase variant of the cholera pathogen shows stress-adaptive cryptic transcriptomic signatures Lambert, Bliss Dassanayake, Maheshi Oh, Dong-Ha Garrett, Shana B. Lee, Sang-Yeol Pettis, Gregg S. BMC Genomics Research Article BACKGROUND: In a process known as phase variation, the marine bacterium and cholera pathogen Vibrio cholerae alternately expresses smooth or rugose colonial phenotypes, the latter being associated with advanced biofilm architecture and greater resistance to ecological stress. To define phase variation at the transcriptomic level in pandemic V. cholerae O1 El Tor strain N16961, we compared the RNA-seq-derived transcriptomes among the smooth parent N16961, its rugose derivative (N16961R) and a smooth form obtained directly from the rugose at high frequencies consistent with phase variation (N16961SD). RESULTS: Differentially regulated genes which clustered into co-expression groups were identified for specific cellular functions, including acetate metabolism, gluconeogenesis, and anaerobic respiration, suggesting an important link between these processes and biofilm formation in this species. Principal component analysis separated the transcriptome of N16961SD from the other phase variants. Although N16961SD was defective in biofilm formation, transcription of its biofilm-related vps and rbm gene clusters was nevertheless elevated as judged by both RNA-seq and RT-qPCR analyses. This transcriptome signature was shared with N16961R, as were others involving two-component signal transduction, chemotaxis, and c-di-GMP synthesis functions. CONCLUSIONS: Precise turnarounds in gene expression did not accompany reversible phase transitions (i.e., smooth to rugose to smooth) in the cholera pathogen. Transcriptomic signatures consisting of up-regulated genes involved in biofilm formation, environmental sensing and persistence, chemotaxis, and signal transduction, which were shared by N16961R and N16961SD variants, may implicate a stress adaptation in the pathogen that facilitates transition of the N16961SD smooth form back to rugosity should environmental conditions dictate. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3233-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-14 /pmc/articles/PMC5109742/ /pubmed/27842489 http://dx.doi.org/10.1186/s12864-016-3233-x Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Lambert, Bliss Dassanayake, Maheshi Oh, Dong-Ha Garrett, Shana B. Lee, Sang-Yeol Pettis, Gregg S. A novel phase variant of the cholera pathogen shows stress-adaptive cryptic transcriptomic signatures |
title | A novel phase variant of the cholera pathogen shows stress-adaptive cryptic transcriptomic signatures |
title_full | A novel phase variant of the cholera pathogen shows stress-adaptive cryptic transcriptomic signatures |
title_fullStr | A novel phase variant of the cholera pathogen shows stress-adaptive cryptic transcriptomic signatures |
title_full_unstemmed | A novel phase variant of the cholera pathogen shows stress-adaptive cryptic transcriptomic signatures |
title_short | A novel phase variant of the cholera pathogen shows stress-adaptive cryptic transcriptomic signatures |
title_sort | novel phase variant of the cholera pathogen shows stress-adaptive cryptic transcriptomic signatures |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109742/ https://www.ncbi.nlm.nih.gov/pubmed/27842489 http://dx.doi.org/10.1186/s12864-016-3233-x |
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