<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rigouts L</submitter><funding>University of Antwerp</funding><funding>European Research Council</funding><funding>Damien Foundation Belgium</funding><funding>Dehousse</funding><funding>European Research Council Starting</funding><pagination>314-23</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4710215</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>71(2)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Mutations in the gyrase genes cause fluoroquinolone resistance in Mycobacterium tuberculosis. However, the predictive value of these markers for clinical outcomes in patients with MDR-TB is unknown to date. The objective of this study was to determine molecular markers and breakpoints predicting second-line treatment outcomes in M. tuberculosis patients treated with fourth-generation fluoroquinolones.&lt;h4>Methods&lt;/h4>We analysed treatment outcome data in relation to the gyrA and gyrB sequences and MICs of ofloxacin, gatifloxacin and moxifloxacin for pretreatment M. tuberculosis isolates from 181 MDR-TB patients in Bangladesh whose isolates were susceptible to injectable drugs.&lt;h4>Results&lt;/h4>The gyrA 90Val, 94Gly and 94Ala mutations were most frequent, with the highest re</pubmed_abstract><journal>The Journal of antimicrobial chemotherapy</journal><pubmed_title>Specific gyrA gene mutations predict poor treatment outcome in MDR-TB.</pubmed_title><pmcid>PMC4710215</pmcid><funding_grant_id>311725</funding_grant_id><pubmed_authors>Hossain MA</pubmed_authors><pubmed_authors>Fissette K</pubmed_authors><pubmed_authors>Rieder HL</pubmed_authors><pubmed_authors>Coeck N</pubmed_authors><pubmed_authors>Rigouts L</pubmed_authors><pubmed_authors>Van Deun A</pubmed_authors><pubmed_authors>Aung KJ</pubmed_authors><pubmed_authors>de Rijk WB</pubmed_authors><pubmed_authors>Meehan CJ</pubmed_authors><pubmed_authors>Gumusboga M</pubmed_authors><pubmed_authors>de Jong BC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Specific gyrA gene mutations predict poor treatment outcome in MDR-TB.</name><description>&lt;h4>Objectives&lt;/h4>Mutations in the gyrase genes cause fluoroquinolone resistance in Mycobacterium tuberculosis. However, the predictive value of these markers for clinical outcomes in patients with MDR-TB is unknown to date. The objective of this study was to determine molecular markers and breakpoints predicting second-line treatment outcomes in M. tuberculosis patients treated with fourth-generation fluoroquinolones.&lt;h4>Methods&lt;/h4>We analysed treatment outcome data in relation to the gyrA and gyrB sequences and MICs of ofloxacin, gatifloxacin and moxifloxacin for pretreatment M. tuberculosis isolates from 181 MDR-TB patients in Bangladesh whose isolates were susceptible to injectable drugs.&lt;h4>Results&lt;/h4>The gyrA 90Val, 94Gly and 94Ala mutations were most frequent, with the highest re</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Feb</publication><modification>2025-04-19T01:55:15.486Z</modification><creation>2019-03-27T02:06:45Z</creation></dates><accession>S-EPMC4710215</accession><cross_references><pubmed>26604243</pubmed><doi>10.1093/jac/dkv360</doi></cross_references></HashMap>