Flagellin gene sequences from 64 clinical isolates of the opportunisti
c pathogen Pseudomonas aeruginosa were amplified by PCR and subjected
to RFLP analysis by using seven restriction enzymes to digest the ampl
ified products. Using this approach the isolates were assigned to one
of 13 groups. The method was rapid, reproducible and applicable to all
isolates. In contrast, serotyping failed to satisfactorily resolve 49
% of the strains tested. The vast majority of clinical isolates genera
ted amplified products of 1.02 kb (type a) or 1.25 kb (type b). Electr
on microscopical analysis revealed evidence for some flagellar structu
ral variation between P. aeruginosa strains. This study provides furth
er evidence that the flagellin gene is a widely applicable and useful
genetic marker for studying genetic variation within populations of cl
osely related bacteria.