Identification of Escherichia coli Host Genes That Influence the Bacteriophage Lambda (λ) T4rII Exclusion (Rex) Phenotype
Autor: | Hibah Alattas, Shirley Wong, Roderick A. Slavcev |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
viruses
membrane proteins Sigma Factor Biology Investigations Viral Nonstructural Proteins medicine.disease_cause Bacteriophage 03 medical and health sciences Viral Proteins Lysogen Cellular Genetics Genetics medicine Escherichia coli bacteriophage T4rII Prophage 030304 developmental biology sigma factors 0303 health sciences 030306 microbiology Escherichia coli Proteins Cell Membrane biochemical phenomena metabolism and nutrition biology.organism_classification Phenotype Bacteriophage lambda Regulon Membrane protein Host-Pathogen Interactions bacteria Rex rpoS Bacterial Outer Membrane Proteins |
Zdroj: | Genetics |
ISSN: | 1943-2631 0016-6731 |
Popis: | Despite its historic role in evolving our understanding of modern molecular genetics, the mechanism governing the bacteriophage T4rII exclusion (Rex) phenotype has remained a mystery for over six decades. The Rex system is thought..... The T4rII exclusion (Rex) phenotype is the inability of T4rII mutant bacteriophage to propagate in hosts (Escherichia coli) lysogenized by bacteriophage lambda (λ). The Rex phenotype, triggered by T4rII infection of a rex+ λ lysogen, results in rapid membrane depolarization imposing a harsh cellular environment that resembles stationary phase. Rex “activation” has been proposed as an altruistic cell death system to protect the λ prophage and its host from T4rII superinfection. Although well studied for over 60 years, the mechanism behind Rex still remains unclear. We have identified key nonessential genes involved in this enigmatic exclusion system by examining T4rII infection across a collection of rex+ single-gene knockouts. We further developed a system for rapid, one-step isolation of host mutations that could attenuate/abrogate the Rex phenotype. For the first time, we identified host mutations that influence Rex activity and rex+ host sensitivity to T4rII infection. Among others, notable genes include tolA, ompA, ompF, ompW, ompX, ompT, lpp, mglC, and rpoS. They are critical players in cellular osmotic balance and are part of the stationary phase and/or membrane distress regulons. Based on these findings, we propose a new model that connects Rex to the σS, σE regulons and key membrane proteins. |
Databáze: | OpenAIRE |
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