Abstract
The flagellin subunit of the flagellar filament in Campylobacter jejuni is encoded by two highly homologous tandem genes, flaA and flaB. The flaA gene was sequenced in 18 strains of C. jejuni, including isolates from three outbreak groups. Sequences obtained were compared with flaA sequences available in the GenBank database, and all were analyzed for mosaic gene structure by using recently described statistical tests for detecting gene conversion among aligned sets of sequences. Strong evidence was found supporting recombination between flaA genes of different strains (i.e., intergenomic recombination). Intragenomic recombination between the flaA and flaB genes of C. jejuni TGH9011 was also demonstrated. Both mechanisms of recombination may act as a potential means by which pathogenic strains can generate increased antigenic diversity, so allowing them to escape the immunological responses of the host. Furthermore, demonstration of recombination within and between flagellin loci of natural strains suggests that flagellin gene typing (restriction fragment length polymorphism analysis of PCR-amplified flagellin genes) cannot be considered a stable method for long-term monitoring of pathogenic Campylobacter populations.
MeSH Terms
Base Sequence
Campylobacter Infections/epidemiology,microbiology
Campylobacter jejuni/classification,genetics
Chromosome Mapping
DNA Primers/genetics
DNA, Bacterial/analysis,genetics
Flagellin/genetics
Genetic Variation
Humans
Molecular Epidemiology
Molecular Sequence Data
Mosaicism
Polymerase Chain Reaction
Polymorphism, Restriction Fragment Length
Recombination, Genetic
Sequence Alignment
Sequence Analysis, DNA
Chemicals
DNA Primers
DNA, Bacterial
Flagellin
flaA protein, bacteria
flaB flagellin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Harrington C S
Department of Medical Microbiology, University of Aberdeen, Scotland, United Kingdom.
[email protected]
Thomson-Carter F M
Carter P E
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