European Respiratory Journal · 2020 · 108 citations · 35 references
Public HealthMolecular BiologyDiagnostic MicrobiologyGenomicsTuberculosis ControlAntibiotic ResistanceMycobacterial DiagnosticsTuberculosis DiagnosisTuberculosis Diagnostic TestingAmplicon SequencingDrug Resistance TestingIsoniazid Resistance TestingMolecular Drug Susceptibility TestingPhenotypic Drug Susceptibility TestingTargeted Amplicon SequencingTuberculosis Drug ResistanceTuberculosis Molecular Testing
Conventional molecular tests for detecting Mycobacterium tuberculosis complex (MTBC) drug resistance on clinical samples cover a limited set of mutations. Whole-genome sequencing (WGS) typically requires culture. Here, we evaluated the Deeplex Myc-TB targeted deep-sequencing assay for prediction of resistance to 13 anti-tuberculous drugs/drug classes, directly applicable on sputum. With MTBC DNA tests, the limit of detection was 100–1000 genome copies for fixed resistance mutations. Deeplex Myc-TB captured in silico 97.1–99.3% of resistance phenotypes correctly predicted by WGS from 3651 MTBC genomes. On 429 isolates, the assay predicted 92.2% of 2369 first- and second-line phenotypes, with a sensitivity of 95.3% and a specificity of 95.0% (95.4% and 97.1%, respectively, when excluding ethionamide). 83 out of 102 (81.4%) residual discrepancies with phenotypic results involved pyrazinamide, ethambutol and ethionamide, and low-level rifampicin or isoniazid resistance mutations, all notoriously prone to phenotypic testing variability. Only two out of 96 (2.1%) resistance phenotypes undetected by Deeplex Myc-TB had known resistance-associated mutations by WGS analysis outside Deeplex Myc-TB targets. Phenotype predictions from Deeplex Myc-TB analysis directly on 109 sputa from a Djibouti survey matched those of MTBSeq/PhyResSE/Mykrobe, fed with WGS data from subsequent cultures, with a sensitivity of 93.5/98.5/93.1% and a specificity of 98.5/97.2/95.3%, respectively. Most residual discordances involved gene deletions/indels and 3–12% heteroresistant calls undetected by WGS analysis or natural pyrazinamide resistance of globally rare “ Mycobacterium canettii ” strains then unreported by Deeplex Myc-TB. On 1494 arduous sputa from a Democratic Republic of the Congo survey, 14 902 out of 19 422 (76.7%) possible susceptible or resistance phenotypes could be predicted culture-free. Deeplex Myc-TB may enable fast, tailored tuberculosis treatment.
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Thomas A. Kohl, Shaheed Vally Omar, Jessica Hedge et al. · The Lancet Infectious Diseases · 2015 · 693 citations · Full text
The Competitive Cost of Antibiotic Resistance in <i>Mycobacterium tuberculosis</i>
Sébastien Gagneux, Clara Davis Long, Peter M. Small et al. · Science · 2006 · 632 citations