Tail-Engineered Phage P2 Enables Delivery of Antimicrobials into Multiple Gut Pathogens.
Jidapha Fa-ArunYang Wei HuanElise DarmonBaojun WangPublished in: ACS synthetic biology (2023)
Bacteriophages can be reprogrammed to deliver antimicrobials for therapeutic and biocontrol purposes and are a promising alternative treatment to antimicrobial-resistant bacteria. Here, we developed a bacteriophage P4 cosmid system for the delivery of a Cas9 antimicrobial into clinically relevant human gut pathogens Shigella flexneri and Escherichia coli O157:H7. Our P4 cosmid design produces a high titer of cosmid-transducing units without contamination by a helper phage. Further, we demonstrate that genetic engineering of the phage tail fiber improves the transduction efficiency of cosmid DNA in S. flexneri M90T as well as allows recognition of a nonnative host, E. coli O157:H7. We show that the transducing units with the chimeric tails enhanced the overall Cas9-mediated killing of both pathogens. This study demonstrates the potential of our P4 cas9 cosmid system as a DNA sequence-specific antimicrobial against clinically relevant gut pathogenic bacteria.
Keyphrases
- crispr cas
- genome editing
- escherichia coli
- staphylococcus aureus
- pseudomonas aeruginosa
- gram negative
- antimicrobial resistance
- endothelial cells
- multidrug resistant
- biofilm formation
- risk assessment
- human health
- cell therapy
- dendritic cells
- genome wide
- cystic fibrosis
- drinking water
- gene expression
- combination therapy
- copy number
- immune response
- klebsiella pneumoniae
- mesenchymal stem cells
- replacement therapy
- candida albicans
- climate change
- pluripotent stem cells