Cargando…
A reversible mutation in a genomic hotspot saves bacterial swarms from extinction
Microbial adaptation to changing environmental conditions is frequently mediated by hypermutable sequences. Here we demonstrate that such a hypermutable hotspot within a gene encoding a flagellar unit of Paenibacillus glucanolyticus generated spontaneous non-swarming mutants with increased stress re...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941203/ https://www.ncbi.nlm.nih.gov/pubmed/36824284 http://dx.doi.org/10.1016/j.isci.2023.106043 |
_version_ | 1784891237340282880 |
---|---|
author | Hefetz, Idan Israeli, Ofir Bilinsky, Gal Plaschkes, Inbar Hazkani-Covo, Einat Hayouka, Zvi Lampert, Adam Helman, Yael |
author_facet | Hefetz, Idan Israeli, Ofir Bilinsky, Gal Plaschkes, Inbar Hazkani-Covo, Einat Hayouka, Zvi Lampert, Adam Helman, Yael |
author_sort | Hefetz, Idan |
collection | PubMed |
description | Microbial adaptation to changing environmental conditions is frequently mediated by hypermutable sequences. Here we demonstrate that such a hypermutable hotspot within a gene encoding a flagellar unit of Paenibacillus glucanolyticus generated spontaneous non-swarming mutants with increased stress resistance. These mutants, which survived conditions that eliminated wild-type cultures, could be carried by their swarming siblings when the colony spread, consequently increasing their numbers at the spreading edge. Of interest, the hypermutable nature of the aforementioned sequence enabled the non-swarming mutants to serve as “seeds” for a new generation of wild-type cells through reversion of the mutation. Using a mathematical model, we examined the survival dynamics of P. glucanolyticus colonies under fluctuating environments. Our experimental and theoretical results suggest that the non-swarming, stress-resistant mutants can save the colony from extinction. Notably, we identified this hypermutable sequence in flagellar genes of additional Paenibacillus species, suggesting that this phenomenon could be wide-spread and ecologically important. |
format | Online Article Text |
id | pubmed-9941203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99412032023-02-22 A reversible mutation in a genomic hotspot saves bacterial swarms from extinction Hefetz, Idan Israeli, Ofir Bilinsky, Gal Plaschkes, Inbar Hazkani-Covo, Einat Hayouka, Zvi Lampert, Adam Helman, Yael iScience Article Microbial adaptation to changing environmental conditions is frequently mediated by hypermutable sequences. Here we demonstrate that such a hypermutable hotspot within a gene encoding a flagellar unit of Paenibacillus glucanolyticus generated spontaneous non-swarming mutants with increased stress resistance. These mutants, which survived conditions that eliminated wild-type cultures, could be carried by their swarming siblings when the colony spread, consequently increasing their numbers at the spreading edge. Of interest, the hypermutable nature of the aforementioned sequence enabled the non-swarming mutants to serve as “seeds” for a new generation of wild-type cells through reversion of the mutation. Using a mathematical model, we examined the survival dynamics of P. glucanolyticus colonies under fluctuating environments. Our experimental and theoretical results suggest that the non-swarming, stress-resistant mutants can save the colony from extinction. Notably, we identified this hypermutable sequence in flagellar genes of additional Paenibacillus species, suggesting that this phenomenon could be wide-spread and ecologically important. Elsevier 2023-01-25 /pmc/articles/PMC9941203/ /pubmed/36824284 http://dx.doi.org/10.1016/j.isci.2023.106043 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Hefetz, Idan Israeli, Ofir Bilinsky, Gal Plaschkes, Inbar Hazkani-Covo, Einat Hayouka, Zvi Lampert, Adam Helman, Yael A reversible mutation in a genomic hotspot saves bacterial swarms from extinction |
title | A reversible mutation in a genomic hotspot saves bacterial swarms from extinction |
title_full | A reversible mutation in a genomic hotspot saves bacterial swarms from extinction |
title_fullStr | A reversible mutation in a genomic hotspot saves bacterial swarms from extinction |
title_full_unstemmed | A reversible mutation in a genomic hotspot saves bacterial swarms from extinction |
title_short | A reversible mutation in a genomic hotspot saves bacterial swarms from extinction |
title_sort | reversible mutation in a genomic hotspot saves bacterial swarms from extinction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941203/ https://www.ncbi.nlm.nih.gov/pubmed/36824284 http://dx.doi.org/10.1016/j.isci.2023.106043 |
work_keys_str_mv | AT hefetzidan areversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT israeliofir areversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT bilinskygal areversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT plaschkesinbar areversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT hazkanicovoeinat areversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT hayoukazvi areversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT lampertadam areversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT helmanyael areversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT hefetzidan reversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT israeliofir reversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT bilinskygal reversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT plaschkesinbar reversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT hazkanicovoeinat reversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT hayoukazvi reversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT lampertadam reversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction AT helmanyael reversiblemutationinagenomichotspotsavesbacterialswarmsfromextinction |