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This review uncovers genetic mechanisms that contribute to antibiotic heterogeneity in bacteria, suggesting implications for treatment strategies.
Antibiotic response phenotypes have traditionally been classified as either sensitive or resistant. However, accumulating evidence indicates that bacterial responses to antibiotics are far more heterogeneous than previously appreciated. A growing set of new descriptors-including antibiotic persistence, tolerance, heteroresistance, resilience, and perseverance-has been introduced to capture noncanonical antibiotic phenotypes, which are widespread in bacteria and recognized as a cause of treatment failure. Although defined by different criteria, these phenotypes all converge on the heterogeneous nature of bacterial antibiotic responses. In this review, we focus on the heterogeneity-causing mechanisms embedded in genome maintenance, transcription, and translation; discuss how within-host evolved mutations can modulate regulatory stochasticity and shift population dynamics in ways that favor bacterial propagation; and highlight key future directions.
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Liu et al. (2026) studied this question.
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