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Antigenic variation of Campylobacter flagella
L A Harris1, S M Logan, P Guerry
1Department of Biochemistry and Microbiology, University of Victoria, British Columbia.
Journal of Bacteriology
|November 1, 1987
Summary
Campylobacter coli and Campylobacter jejuni can produce two types of flagellin subunits, leading to bidirectional antigenic variation. This variation allows the bacteria to evade immune detection through changes in flagellar structure.
Area of Science:
- Microbiology
- Immunology
- Bacterial Genetics
Background:
- Campylobacter species are significant human pathogens.
- Flagella play a crucial role in bacterial motility and host-pathogen interactions.
- Antigenic variation in bacterial surface structures is a key immune evasion strategy.
Purpose of the Study:
- To investigate the flagellar heterogeneity in Campylobacter coli and Campylobacter jejuni serogroup LIO 8.
- To characterize the flagellin subunits and their antigenic specificities.
- To elucidate the mechanism and rate of antigenic variation in Campylobacter.
Main Methods:
- Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) to analyze flagellin molecular weights.
- Immunoelectron microscopy to visualize flagellar filaments and their antigenic properties.
- Western blotting (immunoblotting) and immunoprecipitation to identify flagellin-antibody interactions.
- Rate determination of phase 1-to-phase 2 and phase 2-to-phase 1 transitions.
Main Results:
- Two flagellin subunits with different molecular weights (59,500 and 61,500 Da) were identified in Campylobacter strains of serogroup LIO 8.
- Two flagellum filaments with distinct antigenic specificities were observed.
- Flagella composed of Mr 61,500 flagellin did not carry the serological determinants for LIO 8 serogroup.
- Bidirectional antigenic variation between the two flagellum types was demonstrated in Campylobacter coli VC167.
- Phase 1-to-phase 2 transition rate was approximately 2.0 x 10(-5) per cell per generation.
- Phase 2-to-phase 1 transition rate was approximately 1.2 x 10(-6) per cell per generation.
Conclusions:
- Campylobacter strains can exhibit flagellar antigenic variation through the production of distinct flagellin subunits.
- This variation contributes to the serological diversity within Campylobacter serogroups.
- The observed rates suggest a significant capacity for immune evasion in Campylobacter infections.