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Engineered toxin–intein antimicrobials can selectively target and kill antibiotic-resistant bacteria in mixed populations

Authors :
Universidad de Sevilla. Departamento de Bioquímica Vegetal y Biología Molecular
Universidad de Sevilla. Departamento de Genética
Centre national de la recherche scientifique (CNRS). France
French Government Investissement d'Avenir. France
Agencia Estatal de Investigación. España
Comunidad Autónoma de Madrid
Fondation pour la Recherche Médicale. France
López Igual, Rocío
Bernal Bayard, Joaquín
Rodríguez Patón, Alfonso
Ghigo, Jean Marc
Mazel, Didier
Universidad de Sevilla. Departamento de Bioquímica Vegetal y Biología Molecular
Universidad de Sevilla. Departamento de Genética
Centre national de la recherche scientifique (CNRS). France
French Government Investissement d'Avenir. France
Agencia Estatal de Investigación. España
Comunidad Autónoma de Madrid
Fondation pour la Recherche Médicale. France
López Igual, Rocío
Bernal Bayard, Joaquín
Rodríguez Patón, Alfonso
Ghigo, Jean Marc
Mazel, Didier
Publication Year :
2019

Abstract

Targeted killing of pathogenic bacteria without harming beneficial members of host microbiota holds promise as a strategy to cure disease and limit both antimicrobial-related dysbiosis and development of antimicrobial resistance. We engineer toxins that are split by inteins and deliver them by conjugation into a mixed population of bacteria. Our toxin–intein antimicrobial is only activated in bacteria that harbor specific transcription factors. We apply our antimicrobial to specifically target and kill antibiotic-resistant Vibrio cholerae present in mixed populations. We find that 100% of antibiotic-resistant V. cholerae receiving the plasmid are killed. Escape mutants were extremely rare (10−6–10−8). We show that conjugation and specific killing of targeted bacteria occurs in the microbiota of zebrafish and crustacean larvae, which are natural hosts for Vibrio spp. Toxins split with inteins could form the basis of precision antimicrobials to target pathogens that are antibiotic resistant.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1423389467
Document Type :
Electronic Resource