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• W4318215312 abstract "The lytic bacteriophages have potential application value in the treatment of bacterial infections. However, the narrow host spectrum of these phages limits their range of clinical application. Here, we demonstrate the use of scarless Cas9-assisted recombination (no-SCAR) gene-editing technology to regulate phage-host range. We used phage PHB20 as the scaffold to create agents targeting different multidrug-resistant Escherichia coli by replacing its phage tail fiber gene (ORF40). The engineered phages were polyvalent and capable of infecting both the original host bacteria and new targets. Phage-tail fiber genes can be amplified by PCR to construct a recombinant phage PHB20 library that can deal with multidrug-resistant bacteria in the future. Our results provide a better understanding of phage-host interactions, and we describe new anti-bacterial editing methods." @default.
• W4318215312 created "2023-01-27" @default.
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• W4318215312 date "2023-01-27" @default.
• W4318215312 modified "2023-10-18" @default.
• W4318215312 title "Phage Engineering for Targeted Multidrug-Resistant Escherichia coli" @default.
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• W4318215312 doi "https://doi.org/10.3390/ijms24032459" @default.
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