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...
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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. |
doi_str_mv | 10.1038/s41598-020-76426-2 |
format | Article |
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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.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-020-76426-2</identifier><identifier>PMID: 33173044</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/326/1320 ; 631/337/1427/2566 ; Anti-Bacterial Agents - pharmacology ; Antibiotic resistance ; Antibiotics ; Deoxyribonucleic acid ; DNA ; DNA damage ; DNA Damage - drug effects ; DNA Damage - genetics ; DNA Damage - radiation effects ; Drug resistance ; E coli ; Electrophoretic Mobility Shift Assay ; Escherichia coli - drug effects ; Escherichia coli - genetics ; Escherichia coli - radiation effects ; Filamentation ; Flow Cytometry ; Genomes ; Genomic instability ; Genomic Instability - drug effects ; Genomic Instability - genetics ; Genomic Instability - radiation effects ; Homeostasis ; Humanities and Social Sciences ; Hydrogen-Ion Concentration ; Macrophages ; Microbial Viability - drug effects ; Microbial Viability - radiation effects ; multidisciplinary ; Mutagenesis ; Nalidixic acid ; Nalidixic Acid - pharmacology ; pH effects ; Propidium - pharmacology ; RecA protein ; Resistant mutant ; Rifampin - pharmacology ; Science ; Science (multidisciplinary) ; Transcription ; Ultraviolet Rays</subject><ispartof>Scientific reports, 2020-11, Vol.10 (1), p.19422, Article 19422</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>info:eu-repo/semantics/openAccess</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c535t-4e03eccb9393c09d82ecd6e057a799311a38937ecfa6f46dc4c718d386317b9d3</citedby><cites>FETCH-LOGICAL-c535t-4e03eccb9393c09d82ecd6e057a799311a38937ecfa6f46dc4c718d386317b9d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655802/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655802/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,26544,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33173044$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Booth, James Alexander</creatorcontrib><creatorcontrib>Špírek, Mário</creatorcontrib><creatorcontrib>Lobie, Tekle Airgecho</creatorcontrib><creatorcontrib>Skarstad, Kirsten</creatorcontrib><creatorcontrib>Krejci, Lumir</creatorcontrib><creatorcontrib>Bjørås, Magnar</creatorcontrib><title>Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><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.</description><subject>631/326/1320</subject><subject>631/337/1427/2566</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibiotic resistance</subject><subject>Antibiotics</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA damage</subject><subject>DNA Damage - drug effects</subject><subject>DNA Damage - genetics</subject><subject>DNA Damage - radiation effects</subject><subject>Drug resistance</subject><subject>E coli</subject><subject>Electrophoretic Mobility Shift Assay</subject><subject>Escherichia coli - drug effects</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - radiation effects</subject><subject>Filamentation</subject><subject>Flow Cytometry</subject><subject>Genomes</subject><subject>Genomic instability</subject><subject>Genomic Instability - 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radiation effects</topic><topic>multidisciplinary</topic><topic>Mutagenesis</topic><topic>Nalidixic acid</topic><topic>Nalidixic Acid - pharmacology</topic><topic>pH effects</topic><topic>Propidium - pharmacology</topic><topic>RecA protein</topic><topic>Resistant mutant</topic><topic>Rifampin - pharmacology</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Transcription</topic><topic>Ultraviolet Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Booth, James Alexander</creatorcontrib><creatorcontrib>Špírek, Mário</creatorcontrib><creatorcontrib>Lobie, Tekle Airgecho</creatorcontrib><creatorcontrib>Skarstad, Kirsten</creatorcontrib><creatorcontrib>Krejci, Lumir</creatorcontrib><creatorcontrib>Bjørås, Magnar</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>NORA - Norwegian Open Research Archives</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Booth, James Alexander</au><au>Špírek, Mário</au><au>Lobie, Tekle Airgecho</au><au>Skarstad, Kirsten</au><au>Krejci, Lumir</au><au>Bjørås, Magnar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2020-11-10</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>19422</spage><pages>19422-</pages><artnum>19422</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33173044</pmid><doi>10.1038/s41598-020-76426-2</doi><oa>free_for_read</oa></addata></record> |
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subjects | 631/326/1320 631/337/1427/2566 Anti-Bacterial Agents - pharmacology Antibiotic resistance Antibiotics Deoxyribonucleic acid DNA DNA damage DNA Damage - drug effects DNA Damage - genetics DNA Damage - radiation effects Drug resistance E coli Electrophoretic Mobility Shift Assay Escherichia coli - drug effects Escherichia coli - genetics Escherichia coli - radiation effects Filamentation Flow Cytometry Genomes Genomic instability Genomic Instability - drug effects Genomic Instability - genetics Genomic Instability - radiation effects Homeostasis Humanities and Social Sciences Hydrogen-Ion Concentration Macrophages Microbial Viability - drug effects Microbial Viability - radiation effects multidisciplinary Mutagenesis Nalidixic acid Nalidixic Acid - pharmacology pH effects Propidium - pharmacology RecA protein Resistant mutant Rifampin - pharmacology Science Science (multidisciplinary) Transcription Ultraviolet Rays |
title | Antibiotic-induced DNA damage results in a controlled loss of pH homeostasis and genome instability |
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