4.7 Article

Reduced Chlorhexidine Susceptibility Is Associated with Tetracycline Resistance tet Genes in Clinical Isolates of Escherichia coli

期刊

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/aac.01972-21

关键词

chlorhexidine; Escherichia coli; GWAS; tetracyclines

资金

  1. Fondation pour la Recherche Medicale (Equipe FRM 2016) [DEQ20161136698]
  2. Poste d'accueil - Assistance Publique-Hopitaux de Paris (AP-HP)
  3. Commissariat a l'energie atomique et aux energies alternatives (CEA)
  4. University of Fribourg
  5. Swiss National Science Foundation [JPI-AMR FNS-31003A_163432, PNR72-40AR40_173686]
  6. INSERM, Paris, France

向作者/读者索取更多资源

Chlorhexidine is a widely used antiseptic, but there is a growing concern about decreased susceptibility to this compound in bacteria. This study investigated the resistance mechanisms of Escherichia coli to chlorhexidine through whole-genome sequence analysis. The results showed that two different evolutionary paths lead to chlorhexidine decreased susceptibility, one involving a retrograde phospholipid transport system and the other associated with efflux pump TetA.
Chlorhexidine is a widely used antiseptic in hospital and community health care. Decreased susceptibility to this compound has been recently described in Klebsiella pneumoniae and Pseudomonas aeruginosa, together with cross-resistance to colistin. Chlorhexidine is a widely used antiseptic in hospital and community health care. Decreased susceptibility to this compound has been recently described in Klebsiella pneumoniae and Pseudomonas aeruginosa, together with cross-resistance to colistin. Surprisingly, few data are available for Escherichia coli, the main species responsible for community and health care-associated infections. In order to decipher chlorhexidine resistance mechanisms in E. coli, we studied both in vitro derived and clinical isolates through whole-genome sequence analysis. Comparison of strains grown in vitro under chlorhexidine pressure identified mutations in the gene mlaA coding for a phospholipid transport system. Phenotypic analyses of single-gene mutants from the Keio collection confirmed the role of this mutation in the decreased susceptibility to chlorhexidine. However, mutations in mlaA were not found in isolates from large clinical collections. In contrast, genome wide association studies (GWAS) showed that, in clinical strains, chlorhexidine reduced susceptibility was associated with the presence of tetA genes of class B coding for efflux pumps and located in a Tn10 transposon. Construction of recombinant strains in E. coli K-12 confirmed the role of tetA determinant in acquired resistance to both chlorhexidine and tetracycline. Our results reveal that two different evolutionary paths lead to chlorhexidine decreased susceptibility: one restricted to in vitro evolution conditions and involving a retrograde phospholipid transport system; the other observed in clinical isolates associated with efflux pump TetA. None of these mechanisms provide cross-resistance to colistin. This work demonstrates the GWAS power to identify new resistance mechanisms in bacterial species.

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