Nature CommunicationsGenomicsPeer-reviewed journal article
Quantitative measurement of antibiotic resistance in Mycobacterium tuberculosis reveals genetic determinants of resistance and susceptibility in a target gene approach
Ivan BarilariD, Simone BattagliaiD, Emanuele BorroniiD, Angela Pires BrandãoiD, Alice E. BrankiniD, Andrea Maurizio CabibbeiD, Joshua J. CarteriD, Darren Chetty, Daniela María CirilloiD, Pauline Claxton, David A. CliftoniD, Ted CoheniD, Jorge CoroneliD, Derrick W. CrookiD, Viola DreyeriD, Sarah G. EarleiD, Vincent E. EscuyeriD, Lucilaine FerrazoliiD, Philip William FowleriD, George F. GaoiD, Jennifer L. GardyiD, Saheer E. GharbiaiD, Kelen Teixeira Ghisi, Arash GhodousiiD, Ana Lúıza Gibertoni CruziD, , Guy Edward ThwaitesiD
Abstract
The World Health Organization goal of universal drug susceptibility testing for patients with tuberculosis is most likely to be achieved through molecular diagnostics; however, to date these have focused largely on first-line drugs, and always on predicting binary susceptibilities. Here, we used whole genome sequencing and a quantitative microtiter plate assay to relate genomic mutations to minimum inhibitory concentration in 15,211 Mycobacterium tuberculosis patient isolates from 27 countries across five continents. This work identifies 449 unique MIC-elevating genetic determinants across thirteen drugs, as well as 91 mutations resulting in hypersensitivity for eleven drugs. Our results provide a guide for further implementation of personalized medicine for the treatment of tuberculosis using genetics-based diagnostics and can serve as a training set for novel approaches to predict drug resistance.
- organism: human
- assay: whole-genome sequencing
- research focus: variant calling
- approach: statistical model
- Citations
- 56
- FWCI
- 17.54
- Field percentile
- top 1%
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