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Cas13 Helps Bacteria Play Dead when the Enemy Strikes
Senén D Mendoza1, Joseph Bondy-Denomy1
1Department of Microbiology & Immunology, University of California, San Francisco, San Francisco, CA, 94143.
Abstract:
How RNA-targeting CRISPR-Cas13 functions as a phage defense system has been mysterious. Recently in Nature, Meeske et al. (2019) demonstrate that Cas13 provides potent immunity to dsDNA phages without cutting their genome. By sensing phage transcripts and destroying RNA nonspecifically to arrest the cell into dormancy, Cas13 provides herd immunity.
Insights
The CRISPR-Cas13 system protects against viruses by detecting viral RNA and triggering cell dormancy, not by cutting viral DNA. This mechanism provides herd immunity against double-stranded DNA phages.
Area of Science:
- Molecular Biology
- Microbial Genetics
- Bacteriophage Research
Background:
- The precise mechanism of RNA-targeting CRISPR-Cas13 in phage defense remained unclear.
- CRISPR-Cas systems are crucial for bacterial immunity against mobile genetic elements.
Purpose of the Study:
- To elucidate the function of CRISPR-Cas13 as a phage defense system.
- To investigate how Cas13 confers immunity against double-stranded DNA (dsDNA) phages.
Main Methods:
- Observational studies on CRISPR-Cas13 activity in bacterial hosts.
- Analysis of host-phage interactions and transcriptomic profiling.
Main Results:
- Cas13 provides potent immunity against dsDNA phages without targeting their genomic DNA.
- The system functions by sensing phage-derived RNA transcripts.
- Nonspecific RNA degradation by Cas13 induces cellular dormancy, halting phage replication.
Conclusions:
- CRISPR-Cas13 utilizes RNA sensing and non-specific RNA degradation to establish phage immunity.
- This RNA-targeting mechanism confers 'herd immunity' by protecting the bacterial population from phage infection.
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