Non-replicative phage particles delivering CRISPR-Cas9 to target major bla.sub.CTX-M variants

Cluster regularly interspaced short palindromic repeats and CRISPR associated protein 9 (CRISPR-Cas9) is a promising tool for antimicrobial re-sensitization by inactivating antimicrobial resistance (AMR) genes of bacteria. Here, we programmed CRISPR-Cas9 with common spacers to target predominant bla.sub.CTX-M variants in group 1 and group 9 and their promoter in an Escherichia coli model. The CRISPR-Cas9 was delivered by non-replicative phagemid particles from a two-step process, including insertion of spacer in CRISPR and construction of phagemid vector. Spacers targeting bla.sub.CTX-M promoters and internal sequences of bla.sub.CTX-M group 1 (bla.sub.CTX-M-15 and -55) and group 9 (bla.sub.CTX-M-14, -27, -65, and -90) were cloned into pCRISPR and phagemid pRC319 for spacer evaluation and phagemid particle production. Re-sensitization and plasmid clearance were mediated by the spacers targeting internal sequences of each group, resulting in 3 log.sub.10 to 4 log.sub.10 reduction of the ratio of resistant cells, but not by those targeting the promoters. The CRISPR-Cas9 delivered by modified [PHI]RC319 particles were capable of re-sensitizing E. coli K-12 carrying either bla.sub.CTX-M group 1 or group 9 in a dose-dependent manner from 0.1 to 100 multiplicity of infection (MOI). In conclusion, CRISPR-Cas9 system programmed with well-designed spacers targeting multiple variants of AMR gene along with a phage-based delivery system could eliminate the widespread bla.sub.CTX-M genes for efficacy restoration of available third-generation cephalosporins by reversal of resistance in bacteria.