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Updated: Jan 19, 2026

Precise Phage Mutagenesis with NgTET-Assisted CRISPR-Cas Systems
Published on: October 14, 2025
Phage-mediated delivery of CRISPR payloads
John Beckley1, Rodolphe Barrangou1
1Department of Food, Bioprocessing and Nutrition Sciences, North Carolina State University, Raleigh, NC 27606, USA.
None:
Over the past decade, improvements in sequencing technologies and computational tools have advanced our understanding of the composition and function of microbial communities in various environments. Now, in order to manipulate and engineer these communities, we need technologies that enable broadly applicable and specific alterations to establish and modulate the molecular basis for their functional roles. Recent advances in bacteriophage engineering strategies, synthetic biology techniques, and in silico approaches have greatly expanded our ability to perform in situ perturbations. Clustered regularly interspaced short palindromic repeats-Cas systems in particular can provide an efficient means of engineering phages, and can also be delivered as a recombinant payload to perform precision genome editing directly in the host environment. Modified Cas effectors have been developed that allow for increasingly diverse edits with applications in the fields of medicine, food, and agriculture. In this review, we discuss recent advances in using bacteriophages to deliver various clustered regularly interspaced short palindromic repeats-Cas effectors. While challenges remain regarding the phylogenetic breadth of deployment, recombinant phages generally present a unique and effective means to rationally engineering microbial community function and composition.
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