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Alterations in glucose metabolism in Vibrio cholerae serogroup O1 El Tor biotype strains
The 2 biotypes of Vibrio cholerae O1 serogroup strains—classical and El Tor—use glucose in distinct ways. Classical biotype strains perform organic acid-producing fermentation and eventually lose viability due to the self-induced creation of an acidic environment, whereas El Tor biotype strains use...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962216/ https://www.ncbi.nlm.nih.gov/pubmed/31941909 http://dx.doi.org/10.1038/s41598-019-57093-4 |
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author | Lee, Donghyun Kim, Eun Jin Baek, Yeongjun Lee, Jiwon Yoon, Youngbae Nair, G. B. Yoon, Sang Sun Kim, Dong Wook |
author_facet | Lee, Donghyun Kim, Eun Jin Baek, Yeongjun Lee, Jiwon Yoon, Youngbae Nair, G. B. Yoon, Sang Sun Kim, Dong Wook |
author_sort | Lee, Donghyun |
collection | PubMed |
description | The 2 biotypes of Vibrio cholerae O1 serogroup strains—classical and El Tor—use glucose in distinct ways. Classical biotype strains perform organic acid-producing fermentation and eventually lose viability due to the self-induced creation of an acidic environment, whereas El Tor biotype strains use an alternative neutral fermentation pathway, which confers them with survival advantages. However, we report that the neutral fermentation pathway has only been recruited in prototype Wave 1 El Tor biotype strains, which have not been isolated since the mid-1990s. Current Wave 2 and Wave 3 atypical El Tor strains contain a single-base deletion in a gene that directs bacteria toward neutral fermentation, resulting in the loss of neutral fermentation and an appearance that is similar to classical biotype strains. Moreover, when sufficient glucose was supplied, Wave 1 El Tor strains maintained their use of acid-producing fermentation, in parallel with neutral fermentation, and thus lost viability in the late stationary phase. The global replacement of Wave 1 El Tor strains by Wave 2 and 3 atypical El Tor strains implies that the acidic fermentation pathway may not be disadvantageous to V. cholerae. The characteristics that we have reported might improve oral rehydration in the treatment of cholera. |
format | Online Article Text |
id | pubmed-6962216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69622162020-01-23 Alterations in glucose metabolism in Vibrio cholerae serogroup O1 El Tor biotype strains Lee, Donghyun Kim, Eun Jin Baek, Yeongjun Lee, Jiwon Yoon, Youngbae Nair, G. B. Yoon, Sang Sun Kim, Dong Wook Sci Rep Article The 2 biotypes of Vibrio cholerae O1 serogroup strains—classical and El Tor—use glucose in distinct ways. Classical biotype strains perform organic acid-producing fermentation and eventually lose viability due to the self-induced creation of an acidic environment, whereas El Tor biotype strains use an alternative neutral fermentation pathway, which confers them with survival advantages. However, we report that the neutral fermentation pathway has only been recruited in prototype Wave 1 El Tor biotype strains, which have not been isolated since the mid-1990s. Current Wave 2 and Wave 3 atypical El Tor strains contain a single-base deletion in a gene that directs bacteria toward neutral fermentation, resulting in the loss of neutral fermentation and an appearance that is similar to classical biotype strains. Moreover, when sufficient glucose was supplied, Wave 1 El Tor strains maintained their use of acid-producing fermentation, in parallel with neutral fermentation, and thus lost viability in the late stationary phase. The global replacement of Wave 1 El Tor strains by Wave 2 and 3 atypical El Tor strains implies that the acidic fermentation pathway may not be disadvantageous to V. cholerae. The characteristics that we have reported might improve oral rehydration in the treatment of cholera. Nature Publishing Group UK 2020-01-15 /pmc/articles/PMC6962216/ /pubmed/31941909 http://dx.doi.org/10.1038/s41598-019-57093-4 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lee, Donghyun Kim, Eun Jin Baek, Yeongjun Lee, Jiwon Yoon, Youngbae Nair, G. B. Yoon, Sang Sun Kim, Dong Wook Alterations in glucose metabolism in Vibrio cholerae serogroup O1 El Tor biotype strains |
title | Alterations in glucose metabolism in Vibrio cholerae serogroup O1 El Tor biotype strains |
title_full | Alterations in glucose metabolism in Vibrio cholerae serogroup O1 El Tor biotype strains |
title_fullStr | Alterations in glucose metabolism in Vibrio cholerae serogroup O1 El Tor biotype strains |
title_full_unstemmed | Alterations in glucose metabolism in Vibrio cholerae serogroup O1 El Tor biotype strains |
title_short | Alterations in glucose metabolism in Vibrio cholerae serogroup O1 El Tor biotype strains |
title_sort | alterations in glucose metabolism in vibrio cholerae serogroup o1 el tor biotype strains |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962216/ https://www.ncbi.nlm.nih.gov/pubmed/31941909 http://dx.doi.org/10.1038/s41598-019-57093-4 |
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