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Updated: Jan 7, 2026

Phage-Mediated Genetic Manipulation of the Lyme Disease Spirochete Borrelia burgdorferi
Published on: September 28, 2022
A prophage-expressed type IV pilus component provides anti-phage defense
Kristina M Sztanko1, Taylor J Ellison2, Jill Greenlaw3
1Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada.
Abstract:
Phage genomes integrated within bacterial genomes, known as prophages, frequently encode proteins that provide defense against further phage infection. These proteins often function by altering the cell surface and preventing phages from attaching to their host receptor. Here, we describe prophage-encoded proteins that resemble FimU, a component of the Pseudomonas aeruginosa type IV pilus. These phage FimU proteins are incorporated into the pilus without altering its function, yet they mediate robust protection against infection by phages that bind to the tip of the pilus, where FimU is located. The phage FimU proteins and the phage tail proteins that likely interact with FimU are highly diverse, suggesting that evolution in this system is driven by phage versus phage competition. These phage FimU proteins represent an example of anti-phage defense mediated by the replacement of a bacterial cell surface component with a phage-encoded protein.
Insights
Prophages can protect bacteria from infection by encoding proteins that mimic cell surface structures. These phage-derived proteins, like FimU, prevent further phage attacks by altering bacterial pili, showcasing a novel anti-phage defense strategy.
Area of Science:
- Microbiology
- Bacteriology
- Virology
Background:
- Prophages, integrated phage genomes, often provide bacterial defense mechanisms.
- These defenses commonly involve altering bacterial cell surface receptors to block phage attachment.
Purpose of the Study:
- To describe novel prophage-encoded proteins resembling FimU.
- To investigate their role in anti-phage defense within Pseudomonas aeruginosa.
Main Methods:
- Analysis of prophage genomes for FimU-like proteins.
- Investigating the incorporation of these proteins into type IV pili.
- Assessing the protective effect against specific phage infections.
Main Results:
- Identified prophage-encoded proteins similar to FimU.
- These proteins integrate into type IV pili without functional impairment.
- Demonstrated robust protection against phages targeting the pilus tip.
Conclusions:
- Prophage FimU-like proteins offer a new mechanism of anti-phage defense.
- This defense involves replacing bacterial components with phage-encoded proteins.
- Evolutionary pressure from phage-phage competition likely drives this system's diversity.
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