lunes, 6 de octubre de 2014

Sequence-specific antimicrobials using efficiently delivered RNA-guided nucleases : Nature Biotechnology : Nature Publishing Group

Sequence-specific antimicrobials using efficiently delivered RNA-guided nucleases : Nature Biotechnology : Nature Publishing Group




Figure 1RGN constructs delivered by bacteriophage particles (ΦRGN) exhibit efficient and specific antimicrobial effects against strains harboring plasmid or chromosomal target sequences.

RGN constructs delivered by bacteriophage particles ([Phi]RGN) exhibit efficient and specific antimicrobial effects against strains harboring plasmid or chromosomal target sequences.
(a) Bacteriophage-delivered RGN constructs differentially affect host cell physiology in a sequence-dependent manner. If the target sequence is: (i) absent, the RGN exerts no effect; (ii) chromosomal, RGN activity is cytotoxic; (iii) e…



Sequence-specific antimicrobials using efficiently delivered RNA-guided nucleases

Nature Biotechnology
 
 
doi:10.1038/nbt.3011
Received
 
Accepted
 
Published online
 
Current antibiotics tend to be broad spectrum, leading to indiscriminate killing of commensal bacteria and accelerated evolution of drug resistance. Here, we use CRISPR-Cas technology to create antimicrobials whose spectrum of activity is chosen by design. RNA-guided nucleases (RGNs) targeting specific DNA sequences are delivered efficiently to microbial populations using bacteriophage or bacteria carrying plasmids transmissible by conjugation. The DNA targets of RGNs can be undesirable genes or polymorphisms, including antibiotic resistance and virulence determinants in carbapenem-resistant Enterobacteriaceae and enterohemorrhagic Escherichia coli. Delivery of RGNs significantly improves survival in a Galleria mellonella infection model. We also show that RGNs enable modulation of complex bacterial populations by selective knockdown of targeted strains based on genetic signatures. RGNs constitute a class of highly discriminatory, customizable antimicrobials that enact selective pressure at the DNA level to reduce the prevalence of undesired genes, minimize off-target effects and enable programmable remodeling of microbiota.

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