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• W2888310513 abstract "Tuberculosis patients taking second line drugs such as ethionamide (ETH) have often experienced previous treatment failure and usually have a complex history of disease and treatment that can span decades. Mutations in the ETH activating enzyme, EthA, confer resistance through undescribed mechanisms. To explore the impact of EthA mutations on ETH resistance, data from a total of 160 ETHR isolates was analysed. The most frequently mutated positions are within regions that display sequence conservation with the active site of OTEMO, another FAD-containing NADH-binding Baeyer-Villiger monooxygenase (BVMO), or with the sugar binding site of galectin-4N. Additionally, to look at a possible role of EthR on ETH resistance we purified an EthR mutant identified in a clinical isolate, F110L, and found it to bind the ethA-ethR intergenic region with higher affinity than the wild type regulator in gel shift assays. The ability of cyclic di-GMP to enhance DNA binding is maintained in the EthR mutant. To our knowledge, this is the first ETH resistance study that combines sequence and resistance data of clinical isolates with functional and structural information." @default.
• W2888310513 created "2018-08-31" @default.
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• W2888310513 date "2018-12-01" @default.
• W2888310513 modified "2023-09-23" @default.
• W2888310513 title "Integrated analysis of ethionamide resistance loci in Mycobacterium tuberculosis clinical isolates" @default.
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• W2888310513 doi "https://doi.org/10.1016/j.tube.2018.08.010" @default.
• W2888310513 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30514498" @default.
• W2888310513 hasPublicationYear "2018" @default.
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