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Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability
Extracellular pH has been assumed to play little if any role in how bacteria respond to antibiotics and antibiotic resistance development. Here, we show that the intracellular pH of Escherichia coli equilibrates to the environmental pH following treatment with the DNA damaging antibiotic nalidixic a...
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/PMC7655802/ https://www.ncbi.nlm.nih.gov/pubmed/33173044 http://dx.doi.org/10.1038/s41598-020-76426-2 |
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author | Booth, James Alexander Špírek, Mário Lobie, Tekle Airgecho Skarstad, Kirsten Krejci, Lumir Bjørås, Magnar |
author_facet | Booth, James Alexander Špírek, Mário Lobie, Tekle Airgecho Skarstad, Kirsten Krejci, Lumir Bjørås, Magnar |
author_sort | Booth, James Alexander |
collection | PubMed |
description | Extracellular pH has been assumed to play little if any role in how bacteria respond to antibiotics and antibiotic resistance development. Here, we show that the intracellular pH of Escherichia coli equilibrates to the environmental pH following treatment with the DNA damaging antibiotic nalidixic acid. We demonstrate that this allows the environmental pH to influence the transcription of various DNA damage response genes and physiological processes such as filamentation. Using purified RecA and a known pH-sensitive mutant variant RecA K250R we show how pH can affect the biochemical activity of a protein central to control of the bacterial DNA damage response system. Finally, two different mutagenesis assays indicate that environmental pH affects antibiotic resistance development. Specifically, at environmental pH’s greater than six we find that mutagenesis plays a significant role in producing antibiotic resistant mutants. At pH’s less than or equal to 6 the genome appears more stable but extensive filamentation is observed, a phenomenon that has previously been linked to increased survival in the presence of macrophages. |
format | Online Article Text |
id | pubmed-7655802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76558022020-11-12 Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability Booth, James Alexander Špírek, Mário Lobie, Tekle Airgecho Skarstad, Kirsten Krejci, Lumir Bjørås, Magnar Sci Rep Article Extracellular pH has been assumed to play little if any role in how bacteria respond to antibiotics and antibiotic resistance development. Here, we show that the intracellular pH of Escherichia coli equilibrates to the environmental pH following treatment with the DNA damaging antibiotic nalidixic acid. We demonstrate that this allows the environmental pH to influence the transcription of various DNA damage response genes and physiological processes such as filamentation. Using purified RecA and a known pH-sensitive mutant variant RecA K250R we show how pH can affect the biochemical activity of a protein central to control of the bacterial DNA damage response system. Finally, two different mutagenesis assays indicate that environmental pH affects antibiotic resistance development. Specifically, at environmental pH’s greater than six we find that mutagenesis plays a significant role in producing antibiotic resistant mutants. At pH’s less than or equal to 6 the genome appears more stable but extensive filamentation is observed, a phenomenon that has previously been linked to increased survival in the presence of macrophages. Nature Publishing Group UK 2020-11-10 /pmc/articles/PMC7655802/ /pubmed/33173044 http://dx.doi.org/10.1038/s41598-020-76426-2 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 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/. |
spellingShingle | Article Booth, James Alexander Špírek, Mário Lobie, Tekle Airgecho Skarstad, Kirsten Krejci, Lumir Bjørås, Magnar Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability |
title | Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability |
title_full | Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability |
title_fullStr | Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability |
title_full_unstemmed | Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability |
title_short | Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability |
title_sort | antibiotic-induced dna damage results in a controlled loss of ph homeostasis and genome instability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655802/ https://www.ncbi.nlm.nih.gov/pubmed/33173044 http://dx.doi.org/10.1038/s41598-020-76426-2 |
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