4.7 Article

Role of Epistasis in Amikacin, Kanamycin, Bedaquiline, and Clofazimine Resistance in Mycobacterium tuberculosis Complex

期刊

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.01164-21

关键词

Mycobacterium tuberculosis; amikacin; antibiotic resistance; bedaquiline; clofazimine; drug susceptibility test; genomics; kanamycin

资金

  1. National Science Foundation Graduate Research Fellowship [DGE1745303]
  2. NIH NIAID [R01 AI55765]
  3. Research Computing Group at HarvardMedical School

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Antibiotic resistance among bacterial pathogens is a major global health threat, with Mycobacterium tuberculosis complex having the highest resistance rates globally. By analyzing over 31,000 MTBC genomes, it was demonstrated that certain mutations may not confer resistance independently and might require multiple mutations to act together. Understanding the association between specific mutations and resistance through genome analysis can help improve drug susceptibility testing.
Antibiotic resistance among bacterial pathogens poses a major global health threat. Mycobacterium tuberculosis complex (MTBC) is estimated to have the highest resistance rates of any pathogen globally. Given the low growth rate and the need for a biosafety level 3 laboratory, the only realistic avenue to scale up drug susceptibility testing (DST) for this pathogen is to rely on genotypic techniques. This raises the fundamental question of whether a mutation is a reliable surrogate for phenotypic resistance or whether the presence of a second mutation can completely counteract its effect, resulting in major diagnostic errors (i.e., systematic false resistance results). To date, such epistatic interactions have only been reported for streptomycin that is now rarely used. By analyzing more than 31,000 MTBC genomes, we demonstrated that the eis C-14T promoter mutation, which is interrogated by several genotypic DST assays endorsed by the World Health Organization, cannot confer resistance to amikacin and kanamycin if it coincides with loss-of-function (LoF) mutations in the coding region of eis. To our knowledge, this represents the first definitive example of antibiotic reversion in MTBC. Moreover, we raise the possibility that mmpR (Rv0678) mutations are not valid markers of resistance to bedaquiline and clofazimine if these coincide with an LoF mutation in the efflux pump encoded by mmpS5 (Rv0677c) and mmpL5 (Rv0676c).

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