Cargando…
Comparison of chitin‐induced natural transformation in pandemic Vibrio cholerae O1 El Tor strains
The human pathogen Vibrio cholerae serves as a model organism for many important processes ranging from pathogenesis to natural transformation, which has been extensively studied in this bacterium. Previous work has deciphered important regulatory circuits involved in natural competence induction as...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693049/ https://www.ncbi.nlm.nih.gov/pubmed/32860313 http://dx.doi.org/10.1111/1462-2920.15214 |
_version_ | 1783614654568726528 |
---|---|
author | Stutzmann, Sandrine Blokesch, Melanie |
author_facet | Stutzmann, Sandrine Blokesch, Melanie |
author_sort | Stutzmann, Sandrine |
collection | PubMed |
description | The human pathogen Vibrio cholerae serves as a model organism for many important processes ranging from pathogenesis to natural transformation, which has been extensively studied in this bacterium. Previous work has deciphered important regulatory circuits involved in natural competence induction as well as mechanistic details related to its DNA acquisition and uptake potential. However, since competence was first reported for V. cholerae in 2005, many researchers have struggled with reproducibility in certain strains. In this study, we therefore compare prominent seventh pandemic V. cholerae isolates, namely strains A1552, N16961, C6706, C6709, E7946, P27459, and the close relative MO10, for their natural transformability and decipher underlying defects that mask the high degree of competence conservation. Through a combination of experimental approaches and comparative genomics based on new whole‐genome sequences and de novo assemblies, we identify several strain‐specific defects, mostly in genes that encode key players in quorum sensing. Moreover, we provide evidence that most of these deficiencies might have recently occurred through laboratory domestication events or through the acquisition of mobile genetic elements. Lastly, we highlight that differing experimental approaches between research groups might explain more of the variations than strain‐specific alterations. |
format | Online Article Text |
id | pubmed-7693049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76930492020-12-08 Comparison of chitin‐induced natural transformation in pandemic Vibrio cholerae O1 El Tor strains Stutzmann, Sandrine Blokesch, Melanie Environ Microbiol Research Articles The human pathogen Vibrio cholerae serves as a model organism for many important processes ranging from pathogenesis to natural transformation, which has been extensively studied in this bacterium. Previous work has deciphered important regulatory circuits involved in natural competence induction as well as mechanistic details related to its DNA acquisition and uptake potential. However, since competence was first reported for V. cholerae in 2005, many researchers have struggled with reproducibility in certain strains. In this study, we therefore compare prominent seventh pandemic V. cholerae isolates, namely strains A1552, N16961, C6706, C6709, E7946, P27459, and the close relative MO10, for their natural transformability and decipher underlying defects that mask the high degree of competence conservation. Through a combination of experimental approaches and comparative genomics based on new whole‐genome sequences and de novo assemblies, we identify several strain‐specific defects, mostly in genes that encode key players in quorum sensing. Moreover, we provide evidence that most of these deficiencies might have recently occurred through laboratory domestication events or through the acquisition of mobile genetic elements. Lastly, we highlight that differing experimental approaches between research groups might explain more of the variations than strain‐specific alterations. John Wiley & Sons, Inc. 2020-09-09 2020-10 /pmc/articles/PMC7693049/ /pubmed/32860313 http://dx.doi.org/10.1111/1462-2920.15214 Text en © 2020 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Stutzmann, Sandrine Blokesch, Melanie Comparison of chitin‐induced natural transformation in pandemic Vibrio cholerae O1 El Tor strains |
title | Comparison of chitin‐induced natural transformation in pandemic Vibrio cholerae
O1 El Tor strains |
title_full | Comparison of chitin‐induced natural transformation in pandemic Vibrio cholerae
O1 El Tor strains |
title_fullStr | Comparison of chitin‐induced natural transformation in pandemic Vibrio cholerae
O1 El Tor strains |
title_full_unstemmed | Comparison of chitin‐induced natural transformation in pandemic Vibrio cholerae
O1 El Tor strains |
title_short | Comparison of chitin‐induced natural transformation in pandemic Vibrio cholerae
O1 El Tor strains |
title_sort | comparison of chitin‐induced natural transformation in pandemic vibrio cholerae
o1 el tor strains |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693049/ https://www.ncbi.nlm.nih.gov/pubmed/32860313 http://dx.doi.org/10.1111/1462-2920.15214 |
work_keys_str_mv | AT stutzmannsandrine comparisonofchitininducednaturaltransformationinpandemicvibriocholeraeo1eltorstrains AT blokeschmelanie comparisonofchitininducednaturaltransformationinpandemicvibriocholeraeo1eltorstrains |