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Temperate and lytic bacteriophages programmed to sensitize and kill antibiotic-resistant bacteria.

Ido YosefMiriam ManorRuth KiroQimron Udi
Published in: Proceedings of the National Academy of Sciences of the United States of America (2015)
The increasing threat of pathogen resistance to antibiotics requires the development of novel antimicrobial strategies. Here we present a proof of concept for a genetic strategy that aims to sensitize bacteria to antibiotics and selectively kill antibiotic-resistant bacteria. We use temperate phages to deliver a functional clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated (Cas) system into the genome of antibiotic-resistant bacteria. The delivered CRISPR-Cas system destroys both antibiotic resistance-conferring plasmids and genetically modified lytic phages. This linkage between antibiotic sensitization and protection from lytic phages is a key feature of the strategy. It allows programming of lytic phages to kill only antibiotic-resistant bacteria while protecting antibiotic-sensitized bacteria. Phages designed according to this strategy may be used on hospital surfaces and hand sanitizers to facilitate replacement of antibiotic-resistant pathogens with sensitive ones.
Keyphrases
  • crispr cas
  • genome editing
  • genome wide
  • escherichia coli
  • healthcare
  • machine learning
  • staphylococcus aureus
  • gene expression
  • pseudomonas aeruginosa
  • copy number
  • biofilm formation
  • hepatitis c virus
  • adverse drug