Genome-wide Characterization of Diverse Bacteriophages Enabled by RNA-Binding CRISPRi

Author:

Adler Benjamin A.ORCID,Al-Shimary Muntathar J.ORCID,Patel Jaymin R.,Armbruster Emily,Colognori DavidORCID,Charles Emeric J.ORCID,Miller Kate V.,Lahiri ArushiORCID,Trinidad MarenaORCID,Boger RonORCID,Nomburg JasonORCID,Beurnier SebastienORCID,Cui Michael L.ORCID,Barrangou Rodolphe,Mutalik Vivek K.ORCID,Schoeniger Joseph S.ORCID,Pogliano Joseph A.ORCID,Savage David F.ORCID,Doudna Jennifer A.ORCID,Cress Brady F.ORCID

Abstract

AbstractBacteriophages constitute one of the largest sources of unknown gene content in the biosphere. Even for well-studied model phages, robust experimental approaches to identify and study their essential genes remain elusive. We uncover and exploit the conserved vulnerability of the phage transcriptome to facilitate genome-wide protein expression knockdown via programmable RNA-binding protein dRfxCas13d (CRISPRi-ART) across diverse phages and their host. Establishing the first broad-spectrum phage functional genomics platform, we predict over 90 essential genes across four phage genomes, a third of which have no known function. These results highlight hidden infection strategies encoded in the most abundant biological entities on earth and provide a facile platform to study them.

Publisher

Cold Spring Harbor Laboratory

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