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Published on: June 28, 2024
A mutant bacteriophage evolved to infect resistant bacteria gained a broader host range
Michal Habusha1, Elhanan Tzipilevich1, Osher Fiyaksel1
1Department of Microbiology and Molecular Genetics, Institute for Medical Research Israel-Canada (IMRIC), The Hebrew University-Hadassah Medical School, The Hebrew University of Jerusalem, Jerusalem, Israel.
Bacteriophages (phages) evolved to infect new Bacillus species by altering host attachment mechanisms. This adaptation allowed phages to bypass specific bacterial surface receptors, demonstrating phage host-jumping capabilities.
Area of Science:
- Microbiology
- Virology
- Evolutionary Biology
Background:
- Bacteriophages (phages) are ubiquitous and play crucial roles in microbial ecosystems.
- Understanding phage host range expansion is vital for microbial ecology and phage therapy.
- The coevolution of Bacillus subtilis and phage SPO1 provides a model for studying host-phage interactions.
Purpose of the Study:
- To investigate the mechanisms by which bacteriophages acquire new hosts.
- To analyze the coevolutionary dynamics between Bacillus subtilis and phage SPO1.
- To understand how phage mutations enable the expansion of host range.
Main Methods:
- Co-cultivation of Bacillus subtilis and phage SPO1 to observe evolution.
- Isolation and characterization of phage-resistant bacterial mutants.
- Genomic analysis of evolved phages to identify mutations.
- Functional assays to determine phage-host binding and infection capabilities.
Main Results:
- Phage-resistant Bacillus subtilis mutants were defective in glycosylated wall teichoic acid (WTA) production.
- An evolved SPO1 phage mutant acquired the ability to infect resistant bacteria.
- Mutations in phage genes encoding baseplate and fibers were identified.
- The evolved phage demonstrated an expanded host range, infecting non-host Bacillus species by adhering to the conserved WTA backbone.
Conclusions:
- Phage evolution can lead to host range expansion by altering surface attachment proteins.
- Loss of dependency on specific glycosylation patterns facilitates crossing species barriers.
- The study provides insights into the molecular basis of phage adaptation and host jumping.
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