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Author Spotlight: Efficiently Eliminating Bacteriophages from Infected Salmonella Cultures Using Lipopolysaccharides
Published on: June 28, 2024
The arms race between bacteria CBASS and bacteriophages
Lan Wang1,2,3, Leiliang Zhang1,2,3
1Department of Clinical Laboratory Medicine, The First Affiliated Hospital of Shandong First Medical University and Shandong Provincial Qianfoshan Hospital, Jinan, Shandong, China.
Abstract:
The Bacterial Cyclic oligonucleotide-Based Anti-phage Signaling System (CBASS) is an innate immune system that induces cell suicide to defend against phage infections. This system relies on cGAS/DncV-like nucleotidyltransferases (CD-NTase) to synthesize cyclic oligonucleotides (cOs) and CD-NTase-associated proteins (Caps) to execute cell death through DNA cleavage, membrane damage, and NAD depletion, thereby inhibiting phage replication. Ancillary proteins expressed in CBASS, in combination with CD-NTase, ensure the normal synthesis of cOs and prepare CD-NTase for full activation by binding to phage genomes, proteins, or other unknown products. To counteract cell death induced by CBASS, phage genes encode immune evasion proteins that curb Cap recognition of cOs, allowing for phage replication, assembly, and propagation in bacterial cells. This review provides a comprehensive understanding of CBASS immunity, comparing it with different bacterial immune systems and highlighting the interplay between CBASS and phage. Additionally, it explores similar immune escape methods based on shared proteins and action mechanisms between prokaryotic and eukaryotic viruses.
Insights
Bacterial Cyclic oligonucleotide-Based Anti-phage Signaling System (CBASS) uses cell suicide to fight phages. Phages evolve evasion proteins to overcome this bacterial defense, creating an ongoing evolutionary arms race.
Area of Science:
- Microbiology
- Immunology
- Virology
Background:
- The Bacterial Cyclic oligonucleotide-Based Anti-phage Signaling System (CBASS) is a key bacterial innate immune system.
- CBASS utilizes cyclic oligonucleotides (cOs) synthesized by CD-NTase enzymes to trigger cell death, inhibiting phage replication.
- Phages have evolved sophisticated mechanisms to evade CBASS-mediated immunity.
Purpose of the Study:
- To provide a comprehensive review of the CBASS innate immune system.
- To elucidate the intricate interplay between CBASS and phage anti-immune strategies.
- To explore conserved viral immune evasion mechanisms across prokaryotic and eukaryotic systems.
Main Methods:
- Literature review and synthesis of existing research on CBASS and phage-bacteria interactions.
- Comparative analysis of bacterial immune systems and viral evasion tactics.
- Exploration of molecular mechanisms underlying CBASS activation and phage counter-defense.
Main Results:
- CBASS functions by synthesizing cOs and activating effector proteins (Caps) that induce DNA cleavage, membrane damage, and NAD depletion.
- Ancillary proteins are crucial for cO synthesis and priming CD-NTase for activation.
- Phages employ immune evasion proteins to disrupt Cap recognition of cOs, ensuring their own propagation.
Conclusions:
- CBASS represents a potent bacterial defense against phage infection, characterized by programmed cell death.
- The co-evolutionary battle between CBASS and phages drives the development of diverse immune evasion strategies.
- Understanding these interactions offers insights into broader viral-host dynamics and potential therapeutic targets.
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