The Journal of Infectious Diseases · 2019 · 21 citations · 10 references
Life SciencesInfectious DiseasesMicrobiologyAntimicrobial ResistanceMedical MicrobiologyMicrobial PathogenesisAntibiotic ResistancePulmonary TuberculosisEfflux Pump MutationsEfflux Pump RegulationLoss-of-function VariantsMycobacterium Tuberculosis InfectionMycobacterium Tuberculosis PathogenesisResistance In Clinical IsolatesRifampicin TherapyTuberculosis Drug Resistance
The Mycobacterium tuberculosis lineage 4 strains CDC1551 and H37Rv develop tolerance to multiple antibiotics upon macrophage residence. To determine whether macrophage-induced tolerance is a general feature of clinical M. tuberculosis isolates, we assessed macrophage-induced drug tolerance in strains from lineages 1-3, representing the other predominant M. tuberculosis strains responsible for tuberculosis globally. All 3 lineages developed isoniazid tolerance. While lineage 1, 3, and 4 strains developed rifampin tolerance, lineage 2 Beijing strains did not. Their failure to develop tolerance may be explained by their harboring of a loss-of-function mutation in the Rv1258c efflux pump that is linked to macrophage-induced rifampicin tolerance.
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Drug Tolerance in Replicating Mycobacteria Mediated by a Macrophage-Induced Efflux Mechanism
Kristin N. Adams, Kevin K. Takaki, Lynn Connolly et al. · Cell · 2011 · 536 citations · Full text
Kristin N. Adams, John D. Szumowski, Lalita Ramakrishnan · The Journal of Infectious Diseases · 2014 · 137 citations · Full text