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Published on: July 29, 2014
ssRNA phage penetration triggers detachment of the F-pilus
Laith Harb1,2, Karthik Chamakura1,2, Pratick Khara3
1Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843.
Abstract:
Although the F-specific ssRNA phage MS2 has long had paradigm status, little is known about penetration of the genomic RNA (gRNA) into the cell. The phage initially binds to the F-pilus using its maturation protein (Mat), and then the Mat-bound gRNA is released from the viral capsid and somehow crosses the bacterial envelope into the cytoplasm. To address the mechanics of this process, we fluorescently labeled the ssRNA phage MS2 to track F-pilus dynamics during infection. We discovered that ssRNA phage infection triggers the release of F-pili from host cells, and that higher multiplicity of infection (MOI) correlates with detachment of longer F-pili. We also report that entry of gRNA into the host cytoplasm requires the F-plasmid-encoded coupling protein, TraD, which is located at the cytoplasmic entrance of the F-encoded type IV secretion system (T4SS). However, TraD is not essential for pilus detachment, indicating that detachment is triggered by an early step of MS2 engagement with the F-pilus or T4SS. We propose a multistep model in which the ssRNA phage binds to the F-pilus and through pilus retraction engages with the distal end of the T4SS channel at the cell surface. Continued pilus retraction pulls the Mat-gRNA complex out of the virion into the T4SS channel, causing a torsional stress that breaks the mature F-pilus at the cell surface. We propose that phage-induced disruptions of F-pilus dynamics provides a selective advantage for infecting phages and thus may be prevalent among the phages specific for retractile pili.
Insights
The F-specific ssRNA phage MS2 infection releases F-pili from host cells, with higher infection levels causing longer F-pili detachment. Genomic RNA entry requires the TraD protein, part of the type IV secretion system.
Area of Science:
- Microbiology
- Molecular Biology
- Virology
Background:
- The F-specific ssRNA phage MS2 is a model organism, but its genomic RNA (gRNA) cell penetration mechanism remains unclear.
- MS2 phage binds to the F-pilus via its maturation protein (Mat), releasing gRNA from the capsid to cross the bacterial envelope.
Purpose of the Study:
- To investigate the mechanics of F-specific ssRNA phage MS2 genomic RNA (gRNA) cell penetration.
- To elucidate the role of F-pili and the type IV secretion system (T4SS) in MS2 phage infection.
Main Methods:
- Fluorescently labeling ssRNA phage MS2 to track F-pilus dynamics during infection.
- Analyzing the correlation between multiplicity of infection (MOI) and F-pilus detachment.
- Investigating the requirement of the F-plasmid-encoded coupling protein TraD for gRNA entry.
Main Results:
- MS2 phage infection triggers F-pilus release from host cells.
- Higher MOI correlates with the detachment of longer F-pili.
- Genomic RNA entry into the host cytoplasm necessitates the F-plasmid-encoded coupling protein TraD, located at the T4SS entrance.
Conclusions:
- F-pilus detachment is an early event in MS2 infection, not dependent on TraD.
- A model is proposed where pilus retraction pulls the Mat-gRNA complex into the T4SS, leading to F-pilus breakage.
- Phage-induced disruption of F-pilus dynamics may offer a selective advantage for infecting phages.
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