| Literature DB >> 32101705 |
Justin E Silpe1, Andrew A Bridges2, Xiuliang Huang2, Daniela R Coronado1, Olivia P Duddy1, Bonnie L Bassler3.
Abstract
Quorum sensing is a process of chemical communication that bacteria use to track cell density and coordinate gene expression across a population. Bacteria-infecting viruses, called phages, can encode quorum-sensing components that enable them to integrate host cell density information into the lysis-lysogeny decision. Vibriophage VP882 is one such phage, and activation of its quorum-sensing pathway leads to the production of an antirepressor called Qtip. Qtip interferes with the prophage repressor (cIVP882), leading to host-cell lysis. Here, we show that Qtip interacts with the N terminus of cIVP882, inhibiting both cIVP882 DNA binding and cIVP882 autoproteolysis. Qtip also sequesters cIVP882, localizing it to the poles. Qtip can localize to the poles independently of cIVP882. Alanine-scanning mutagenesis of Qtip shows that its localization and interference with cIVP882 activities are separable. Comparison of Qtip to a canonical phage antirepressor reveals that despite both proteins interacting with their partner repressors, only Qtip drives polar localization.Entities:
Keywords: Qtip; antirepressor; cI repressor; lysis-lysogeny; phage; quorum sensing
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Year: 2020 PMID: 32101705 PMCID: PMC7148176 DOI: 10.1016/j.chom.2020.01.024
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023