Scientific Reports · 2022 · 14 citations · 47 references
Life SciencesMicrobiologyMolecular BiologyAntimicrobial ResistanceDna RepairMicrobial GeneticsAntibacterial ResistanceAntibiotic ResistanceAntibiotic Resistance EvolutionAntibiotic Resistance MechanismsBacterial SurvivalResistance GenesEpistatic InteractionsEpistatic Interactions In ResistanceFitness Cost EstimationMulti-drug ResistanceMutational Pathways Of ResistancePersister Cell EvolutionPersister Cell FormationPersister Cell Tolerance
In this study, we probe the role of secondary messenger c-di-AMP in drug tolerance, which includes both persister and resistant mutant characterization of Mycobacterium smegmatis. Specifically, with the use of c-di-AMP null and overproducing mutants, we showed how c-di-AMP plays a significant role in resistance mutagenesis against antibiotics with different mechanisms of action. We elucidated the specific molecular mechanism linking the elevated intracellular c-di-AMP level and high mutant generation and highlighted the significance of non-homology-based DNA repair. Further investigation enabled us to identify the unique mutational landscape of target and non-target mutation categories linked to intracellular c-di-AMP levels. Overall fitness cost of unique target mutations was estimated in different strain backgrounds, and then we showed the critical role of c-di-AMP in driving epistatic interactions between resistance genes, resulting in the evolution of multi-drug tolerance. Finally, we identified the role of c-di-AMP in persister cells regrowth and mutant enrichment upon cessation of antibiotic treatment.
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Cyclic GMP–AMP signalling protects bacteria against viral infection
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