Tackling antibiotic resistance by inducing transient and robust collateral sensitivity

Sara Hernando-Amado (), Pablo Laborda and José Luis Martínez ()
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Sara Hernando-Amado: Centro Nacional de Biotecnología, CSIC
Pablo Laborda: Centro Nacional de Biotecnología, CSIC
José Luis Martínez: Centro Nacional de Biotecnología, CSIC

Nature Communications, 2023, vol. 14, issue 1, 1-12

Abstract: Abstract Collateral sensitivity (CS) is an evolutionary trade-off traditionally linked to the mutational acquisition of antibiotic resistance (AR). However, AR can be temporally induced, and the possibility that this causes transient, non-inherited CS, has not been addressed. Mutational acquisition of ciprofloxacin resistance leads to robust CS to tobramycin in pre-existing antibiotic-resistant mutants of Pseudomonas aeruginosa. Further, the strength of this phenotype is higher when nfxB mutants, over-producing the efflux pump MexCD-OprJ, are selected. Here, we induce transient nfxB-mediated ciprofloxacin resistance by using the antiseptic dequalinium chloride. Notably, non-inherited induction of AR renders transient tobramycin CS in the analyzed antibiotic-resistant mutants and clinical isolates, including tobramycin-resistant isolates. Further, by combining tobramycin with dequalinium chloride we drive these strains to extinction. Our results support that transient CS could allow the design of new evolutionary strategies to tackle antibiotic-resistant infections, avoiding the acquisition of AR mutations on which inherited CS depends.

Date: 2023
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DOI: 10.1038/s41467-023-37357-4

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