Host stress drives tolerance and persistence: The bane of anti-microbial therapeutics

Cell Host Microbe. 2024 Jun 12;32(6):852-862. doi: 10.1016/j.chom.2024.04.019.

Abstract

Antibiotic resistance, typically associated with genetic changes within a bacterial population, is a frequent contributor to antibiotic treatment failures. Antibiotic persistence and tolerance, which we collectively term recalcitrance, represent transient phenotypic changes in the bacterial population that prolong survival in the presence of typically lethal concentrations of antibiotics. Antibiotic recalcitrance is challenging to detect and investigate-traditionally studied under in vitro conditions, our understanding during infection and its contribution to antibiotic failure is limited. Recently, significant progress has been made in the study of antibiotic-recalcitrant populations in pathogenic species, including Mycobacterium tuberculosis, Staphylococcus aureus, Salmonella enterica, and Yersiniae, in the context of the host environment. Despite the diversity of these pathogens and infection models, shared signals and responses promote recalcitrance, and common features and vulnerabilities of persisters and tolerant bacteria have emerged. These will be discussed here, along with progress toward developing therapeutic interventions to better treat recalcitrant pathogens.

Publication types

  • Review

MeSH terms

  • Animals
  • Anti-Bacterial Agents* / pharmacology
  • Anti-Bacterial Agents* / therapeutic use
  • Bacteria* / drug effects
  • Bacteria* / genetics
  • Bacterial Infections / drug therapy
  • Bacterial Infections / microbiology
  • Drug Resistance, Bacterial
  • Host-Pathogen Interactions / drug effects
  • Humans
  • Mycobacterium tuberculosis / drug effects
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / genetics
  • Stress, Physiological

Substances

  • Anti-Bacterial Agents