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- W4311887675 abstract "The widespread use of antibiotics has placed bacterial pathogens under intense pressure to evolve new survival mechanisms. Genomic analysis of 51,229 Mycobacterium tuberculosis ( Mtb ) clinical isolates has identified an essential transcriptional regulator, Rv1830 , herein called resR for resilience regulator, as a frequent target of positive (adaptive) selection. resR mutants do not show canonical drug resistance or drug tolerance but instead shorten the post-antibiotic effect, meaning that they enable Mtb to resume growth after drug exposure substantially faster than wild-type strains. We refer to this phenotype as antibiotic resilience. ResR acts in a regulatory cascade with other transcription factors controlling cell growth and division, which are also under positive selection in clinical isolates of Mtb . Mutations of these genes are associated with treatment failure and the acquisition of canonical drug resistance." @default.
- W4311887675 created "2023-01-02" @default.
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- W4311887675 date "2022-12-09" @default.
- W4311887675 modified "2023-10-17" @default.
- W4311887675 title "Tuberculosis treatment failure associated with evolution of antibiotic resilience" @default.
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- W4311887675 doi "https://doi.org/10.1126/science.abq2787" @default.
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