Genome replication dynamics of a bacteriophage and its satellite reveal strategies for parasitism and viral restriction. Issue 1 (31st October 2019)

• Record Type: Journal Article
• Authors: Barth, Zachary K; Silvas, Tania V; Angermeyer, Angus; Seed, Kimberley D
• Is Part Of: Nucleic acids research. Volume 48:Issue 1(2020)
• Page Start: 249
• Page End: 263
• Publication Date: 2019-10-31
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gkz1005
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: Phage-inducible chromosomal island-like elements (PLEs) are bacteriophage satellites found in Vibrio cholerae . PLEs parasitize the lytic phage ICP1, excising from the bacterial chromosome, replicating, and mobilizing to new host cells following cell lysis. PLEs protect their host cell populations by completely restricting the production of ICP1 progeny. Previously, it was found that ICP1 replication was reduced during PLE(+) infection. Despite robust replication of the PLE genome, relatively few transducing units are produced. We investigated if PLE DNA replication itself is antagonistic to ICP1 replication. Here we identify key constituents of PLE replication and assess their role in interference of ICP1. PLE encodes a RepA_N initiation factor that is sufficient to drive replication from the PLE origin of replication during ICP1 infection. In contrast to previously characterized bacteriophage satellites, expression of the PLE initiation factor was not sufficient for PLE replication in the absence of phage. Replication of PLE was necessary for interference of ICP1 DNA replication, but replication of a minimalized PLE replicon was not sufficient for ICP1 DNA replication interference. Despite restoration of ICP1 DNA replication, non-replicating PLE remained broadly inhibitory against ICP1. These results suggest that PLE DNA replication is one of multiple mechanisms contributing to ICP1 restriction.