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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Veröffentlicht in:Journal of antimicrobial chemotherapy 2008-10, Vol.62 (4), p.709-712
Hauptverfasser: O'Sullivan, D. M., McHugh, T. D., Gillespie, S. H.
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creator O'Sullivan, D. M.
McHugh, T. D.
Gillespie, S. H.
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.
doi_str_mv 10.1093/jac/dkn259
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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. 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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. 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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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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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