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Published on: October 14, 2011
Campylobacter jejuni motility is required for infection of the flagellotropic bacteriophage F341
Signe Berg Baldvinsson1, Martine C Holst Sørensen1, Christina S Vegge1
1Department of Veterinary Disease Biology, University of Copenhagen, Frederiksberg, Denmark.
Abstract:
Previous studies have identified a specific modification of the capsular polysaccharide as receptor for phages that infect Campylobacter jejuni. Using acapsular kpsM mutants of C. jejuni strains NCTC11168 and NCTC12658, we found that bacteriophage F341 infects C. jejuni independently of the capsule. In contrast, phage F341 does not infect C. jejuni NCTC11168 mutants that either lack the flagellar filaments (ΔflaAB) or that have paralyzed, i.e., nonrotating, flagella (ΔmotA and ΔflgP). Complementing flgP confirmed that phage F341 requires rotating flagella for successful infection. Furthermore, adsorption assays demonstrated that phage F341 does not adsorb to these nonmotile C. jejuni NCTC11168 mutants. Taken together, we propose that phage F341 uses the flagellum as a receptor. Phage-host interactions were investigated using fluorescence confocal and transmission electron microscopy. These data demonstrate that F341 binds to the flagellum by perpendicular attachment with visible phage tail fibers interacting directly with the flagellum. Our data are consistent with the movement of the C. jejuni flagellum being required for F341 to travel along the filament to reach the basal body of the bacterium. The initial binding to the flagellum may cause a conformational change of the phage tail that enables DNA injection after binding to a secondary receptor.
Insights
Bacteriophage F341 infects Campylobacter jejuni using its flagellum, not capsule, as a receptor. Flagellar rotation is essential for phage infection and adsorption, suggesting a novel mechanism for phage entry.
Area of Science:
- Microbiology
- Virology
- Bacteriology
Background:
- Campylobacter jejuni infections are a major cause of bacterial gastroenteritis.
- Bacteriophages are viruses that infect bacteria and are potential therapeutic agents.
- Previous research identified capsular polysaccharides as receptors for some C. jejuni phages.
Purpose of the Study:
- To investigate the receptor and infection mechanism of bacteriophage F341 in Campylobacter jejuni.
- To determine if the capsule or flagellum of C. jejuni serves as the receptor for phage F341.
Main Methods:
- Utilized acapsular mutants (kpsM) and flagellar mutants (ΔflaAB, ΔmotA, ΔflgP) of C. jejuni.
- Performed phage infection assays and adsorption experiments.
- Employed fluorescence confocal and transmission electron microscopy to visualize phage-host interactions.
Main Results:
- Phage F341 infected C. jejuni independently of the capsule.
- Phage F341 failed to infect C. jejuni mutants lacking flagella or with non-rotating flagella.
- Adsorption assays confirmed phage F341 requires rotating flagella for binding.
- Microscopy showed phage F341 binding to the flagellum via tail fibers, with movement along the filament.
Conclusions:
- The flagellum, not the capsule, serves as the primary receptor for bacteriophage F341.
- Flagellar rotation is crucial for phage F341 adsorption and infection.
- Phage F341 likely uses flagellar movement to reach the basal body, potentially initiating DNA injection via tail conformational changes and a secondary receptor.
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