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High-efficiency delivery of CRISPR-Cas9 by engineered probiotics enables precise microbiome editing.

Kevin NeilNancy AllardPatricia RoyFrédéric GrenierAlfredo MenendezVincent BurrusSébastien Rodrigue
Published in: Molecular systems biology (2022)
Antibiotic resistance threatens our ability to treat infectious diseases, spurring interest in alternative antimicrobial technologies. The use of bacterial conjugation to deliver CRISPR-cas systems programmed to precisely eliminate antibiotic-resistant bacteria represents a promising approach but requires high in situ DNA transfer rates. We have optimized the transfer efficiency of conjugative plasmid TP114 using accelerated laboratory evolution. We hence generated a potent conjugative delivery vehicle for CRISPR-cas9 that can eliminate > 99.9% of targeted antibiotic-resistant Escherichia coli in the mouse gut microbiota using a single dose. We then applied this system to a Citrobacter rodentium infection model, achieving full clearance within four consecutive days of treatment.
Keyphrases
  • crispr cas
  • genome editing
  • high efficiency
  • infectious diseases
  • escherichia coli
  • staphylococcus aureus
  • cell free
  • drug delivery
  • cystic fibrosis
  • pseudomonas aeruginosa
  • nucleic acid
  • biofilm formation