The effect of oxidative stress on the mutation rate of Mycobacterium tuberculosis with impaired catalase/peroxidase function
Objectives To determine the effect of oxidative stress on isoniazid-resistant Mycobacterium tuberculosis deficient in catalase/peroxidase activity to varying degrees through mutation in katG. Methods The mutation rate was determined for a set of isogenic strains with different katG alleles giving di...
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description | Objectives To determine the effect of oxidative stress on isoniazid-resistant Mycobacterium tuberculosis deficient in catalase/peroxidase activity to varying degrees through mutation in katG. Methods The mutation rate was determined for a set of isogenic strains with different katG alleles giving different catalase and/or peroxidase activities following exposure to the oxidizing agent, hydrogen peroxide. Mutants were selected on rifampicin, and the location and nature of the mutation were identified by sequencing the rpoB gene. Results No evidence was found to suggest that strains that had impaired catalase/peroxidase activity were hypermutable, and the presence of excess hydrogen peroxide had no effect on the mutation rate. An unusual pattern of mutations in rpoB was observed in catalase-deficient strains with only 3 of 66 having mutations within the rifampicin resistance-determining region. Conclusions The mutation rate of M. tuberculosis in response to oxidative stress is not increased in strains with significant deficits in catalase and peroxidase activity. Our data suggest that isoniazid-resistant strains compensate for their reduced ability to detoxify oxidative stress effectively. Interestingly, mutations were found in unusual locations at positions similar to those found in clinical isoniazid-resistant strains. |
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M. ; McHugh, T. D. ; Gillespie, S. H.</creator><creatorcontrib>O'Sullivan, D. M. ; McHugh, T. D. ; Gillespie, S. H.</creatorcontrib><description>Objectives To determine the effect of oxidative stress on isoniazid-resistant Mycobacterium tuberculosis deficient in catalase/peroxidase activity to varying degrees through mutation in katG. Methods The mutation rate was determined for a set of isogenic strains with different katG alleles giving different catalase and/or peroxidase activities following exposure to the oxidizing agent, hydrogen peroxide. Mutants were selected on rifampicin, and the location and nature of the mutation were identified by sequencing the rpoB gene. Results No evidence was found to suggest that strains that had impaired catalase/peroxidase activity were hypermutable, and the presence of excess hydrogen peroxide had no effect on the mutation rate. An unusual pattern of mutations in rpoB was observed in catalase-deficient strains with only 3 of 66 having mutations within the rifampicin resistance-determining region. Conclusions The mutation rate of M. tuberculosis in response to oxidative stress is not increased in strains with significant deficits in catalase and peroxidase activity. Our data suggest that isoniazid-resistant strains compensate for their reduced ability to detoxify oxidative stress effectively. Interestingly, mutations were found in unusual locations at positions similar to those found in clinical isoniazid-resistant strains.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkn259</identifier><identifier>PMID: 18577539</identifier><identifier>CODEN: JACHDX</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Anti-Bacterial Agents - pharmacology ; Antibacterial agents ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Bacteria ; Bacterial diseases ; Bacterial Proteins - genetics ; Biological and medical sciences ; Catalase - genetics ; DNA Mutational Analysis ; DNA, Bacterial - chemistry ; DNA, Bacterial - genetics ; DNA-Directed RNA Polymerases - genetics ; Drug Resistance, Bacterial ; Genotype ; Human bacterial diseases ; Hydrogen Peroxide - pharmacology ; Infectious diseases ; isoniazid ; M. tuberculosis ; Medical sciences ; Microbiology ; Mutation ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - drug effects ; Mycobacterium tuberculosis - enzymology ; Mycobacterium tuberculosis - genetics ; Oxidants - pharmacology ; Oxidation ; Oxidative Stress ; oxidative stress response ; Pharmacology. Drug treatments ; Rifampin - pharmacology ; Sequence Analysis, DNA ; Tuberculosis ; Tuberculosis and atypical mycobacterial infections</subject><ispartof>Journal of antimicrobial chemotherapy, 2008-10, Vol.62 (4), p.709-712</ispartof><rights>The Author 2008. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org 2008</rights><rights>2008 INIST-CNRS</rights><rights>The Author 2008. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-780b7f16e8d55e8c8427d512c13798404ea4b418184ffcddeb87d170080c34803</citedby><cites>FETCH-LOGICAL-c441t-780b7f16e8d55e8c8427d512c13798404ea4b418184ffcddeb87d170080c34803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20702855$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18577539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>O'Sullivan, D. M.</creatorcontrib><creatorcontrib>McHugh, T. D.</creatorcontrib><creatorcontrib>Gillespie, S. H.</creatorcontrib><title>The effect of oxidative stress on the mutation rate of Mycobacterium tuberculosis with impaired catalase/peroxidase function</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>Objectives To determine the effect of oxidative stress on isoniazid-resistant Mycobacterium tuberculosis deficient in catalase/peroxidase activity to varying degrees through mutation in katG. Methods The mutation rate was determined for a set of isogenic strains with different katG alleles giving different catalase and/or peroxidase activities following exposure to the oxidizing agent, hydrogen peroxide. Mutants were selected on rifampicin, and the location and nature of the mutation were identified by sequencing the rpoB gene. Results No evidence was found to suggest that strains that had impaired catalase/peroxidase activity were hypermutable, and the presence of excess hydrogen peroxide had no effect on the mutation rate. An unusual pattern of mutations in rpoB was observed in catalase-deficient strains with only 3 of 66 having mutations within the rifampicin resistance-determining region. Conclusions The mutation rate of M. tuberculosis in response to oxidative stress is not increased in strains with significant deficits in catalase and peroxidase activity. Our data suggest that isoniazid-resistant strains compensate for their reduced ability to detoxify oxidative stress effectively. Interestingly, mutations were found in unusual locations at positions similar to those found in clinical isoniazid-resistant strains.</description><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibacterial agents</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Bacteria</subject><subject>Bacterial diseases</subject><subject>Bacterial Proteins - genetics</subject><subject>Biological and medical sciences</subject><subject>Catalase - genetics</subject><subject>DNA Mutational Analysis</subject><subject>DNA, Bacterial - chemistry</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA-Directed RNA Polymerases - genetics</subject><subject>Drug Resistance, Bacterial</subject><subject>Genotype</subject><subject>Human bacterial diseases</subject><subject>Hydrogen Peroxide - pharmacology</subject><subject>Infectious diseases</subject><subject>isoniazid</subject><subject>M. tuberculosis</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Mutation</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - drug effects</subject><subject>Mycobacterium tuberculosis - enzymology</subject><subject>Mycobacterium tuberculosis - genetics</subject><subject>Oxidants - pharmacology</subject><subject>Oxidation</subject><subject>Oxidative Stress</subject><subject>oxidative stress response</subject><subject>Pharmacology. Drug treatments</subject><subject>Rifampin - pharmacology</subject><subject>Sequence Analysis, DNA</subject><subject>Tuberculosis</subject><subject>Tuberculosis and atypical mycobacterial infections</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90V1rFDEUBuAgil2rN_4ACYK9EMZNJskkc1nW6ootglYQb0Imc0KznZms-dAW_PHOuksLXngVTnh4z4EXoeeUvKGkZcuNscv-eqpF-wAtKG9IVZOWPkQLwoioJBfsCD1JaUMIaUSjHqMjqoSUgrUL9PvyCjA4Bzbj4HC48b3J_ifglCOkhMOE8yzGkufveYgmww5e3NrQGZsh-jLiXDqItgwh-YR_-XyF_bg1PkKPrclmMAmWW4h_0xNgVya7S3uKHjkzJHh2eI_R13dnl6t1df7p_YfV6XllOae5kop00tEGVC8EKKt4LXtBa0uZbBUnHAzvOFVUceds30OnZE8lIYpYxhVhx-hkn7uN4UeBlPXok4VhMBOEkjRtJRWtEjN8-Q_chBKn-TZdU9k0tRDtjF7vkY0hpQhOb6MfTbzVlOhdIXouRO8LmfGLQ2LpRujv6aGBGbw6AJOsGVw0k_XpztVEkloJce9C2f5_YbV3PmW4uZMmXutGMin0-tt3_faCffz8Zb3SK_YHdQqxUg</recordid><startdate>20081001</startdate><enddate>20081001</enddate><creator>O'Sullivan, D. M.</creator><creator>McHugh, T. D.</creator><creator>Gillespie, S. H.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20081001</creationdate><title>The effect of oxidative stress on the mutation rate of Mycobacterium tuberculosis with impaired catalase/peroxidase function</title><author>O'Sullivan, D. M. ; McHugh, T. D. ; Gillespie, S. H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-780b7f16e8d55e8c8427d512c13798404ea4b418184ffcddeb87d170080c34803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antibacterial agents</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Bacteria</topic><topic>Bacterial diseases</topic><topic>Bacterial Proteins - genetics</topic><topic>Biological and medical sciences</topic><topic>Catalase - genetics</topic><topic>DNA Mutational Analysis</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - genetics</topic><topic>DNA-Directed RNA Polymerases - genetics</topic><topic>Drug Resistance, Bacterial</topic><topic>Genotype</topic><topic>Human bacterial diseases</topic><topic>Hydrogen Peroxide - pharmacology</topic><topic>Infectious diseases</topic><topic>isoniazid</topic><topic>M. tuberculosis</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Mutation</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - drug effects</topic><topic>Mycobacterium tuberculosis - enzymology</topic><topic>Mycobacterium tuberculosis - genetics</topic><topic>Oxidants - pharmacology</topic><topic>Oxidation</topic><topic>Oxidative Stress</topic><topic>oxidative stress response</topic><topic>Pharmacology. Drug treatments</topic><topic>Rifampin - pharmacology</topic><topic>Sequence Analysis, DNA</topic><topic>Tuberculosis</topic><topic>Tuberculosis and atypical mycobacterial infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>O'Sullivan, D. M.</creatorcontrib><creatorcontrib>McHugh, T. D.</creatorcontrib><creatorcontrib>Gillespie, S. 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M.</au><au>McHugh, T. D.</au><au>Gillespie, S. H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of oxidative stress on the mutation rate of Mycobacterium tuberculosis with impaired catalase/peroxidase function</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>2008-10-01</date><risdate>2008</risdate><volume>62</volume><issue>4</issue><spage>709</spage><epage>712</epage><pages>709-712</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><coden>JACHDX</coden><abstract>Objectives To determine the effect of oxidative stress on isoniazid-resistant Mycobacterium tuberculosis deficient in catalase/peroxidase activity to varying degrees through mutation in katG. Methods The mutation rate was determined for a set of isogenic strains with different katG alleles giving different catalase and/or peroxidase activities following exposure to the oxidizing agent, hydrogen peroxide. Mutants were selected on rifampicin, and the location and nature of the mutation were identified by sequencing the rpoB gene. Results No evidence was found to suggest that strains that had impaired catalase/peroxidase activity were hypermutable, and the presence of excess hydrogen peroxide had no effect on the mutation rate. An unusual pattern of mutations in rpoB was observed in catalase-deficient strains with only 3 of 66 having mutations within the rifampicin resistance-determining region. Conclusions The mutation rate of M. tuberculosis in response to oxidative stress is not increased in strains with significant deficits in catalase and peroxidase activity. Our data suggest that isoniazid-resistant strains compensate for their reduced ability to detoxify oxidative stress effectively. Interestingly, mutations were found in unusual locations at positions similar to those found in clinical isoniazid-resistant strains.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>18577539</pmid><doi>10.1093/jac/dkn259</doi><tpages>4</tpages></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | Anti-Bacterial Agents - pharmacology Antibacterial agents Antibiotics. Antiinfectious agents. Antiparasitic agents Bacteria Bacterial diseases Bacterial Proteins - genetics Biological and medical sciences Catalase - genetics DNA Mutational Analysis DNA, Bacterial - chemistry DNA, Bacterial - genetics DNA-Directed RNA Polymerases - genetics Drug Resistance, Bacterial Genotype Human bacterial diseases Hydrogen Peroxide - pharmacology Infectious diseases isoniazid M. tuberculosis Medical sciences Microbiology Mutation Mycobacterium tuberculosis Mycobacterium tuberculosis - drug effects Mycobacterium tuberculosis - enzymology Mycobacterium tuberculosis - genetics Oxidants - pharmacology Oxidation Oxidative Stress oxidative stress response Pharmacology. Drug treatments Rifampin - pharmacology Sequence Analysis, DNA Tuberculosis Tuberculosis and atypical mycobacterial infections |
title | The effect of oxidative stress on the mutation rate of Mycobacterium tuberculosis with impaired catalase/peroxidase function |
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