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Journal of Clinical Microbiology, 10 1997, 2568-2572, Vol 35, No. 10
D Linton, AJ Lawson, RJ Owen and J Stanley
Three sets of primers were designed for PCR detection and differentiation
of Campylobacter jejuni and Campylobacter coli. The first PCR assay was
designed to coidentify C. jejuni and C. coli based on their 16S rRNA gene
sequences. The second PCR assay, based on the hippuricase gene sequence,
identified all tested reference strains of C. jejuni and also strains of
that species which lack detectable hippuricase activity. The third PCR
assay, based on the sequence of a cloned (putative) aspartokinase gene and
the downstream open reading frame, identified all tested reference strains
of C. coli. The assays will find immediate application in the rapid
identification to species level of isolates. The assays combine with a
protocol for purification of total DNA from fecal samples to allow
reproducible PCR identification of campylobacters directly from stools. Of
20 clinical samples from which campylobacters had been cultured, we
detected C. jejuni in 17, C. coli in 2, and coinfection of C. jejuni and
Campylobacter hyointestinalis in 1. These results were concordant with
culture and phenotypic identification to species level. Strain typing by
PCR-restriction fragment length polymorphism of the flagellin (flaA) gene
detected identical flaA types in fecal DNA and the corresponding
campylobacter isolate. Twenty-five Campylobacter-negative stool samples
gave no reaction with the PCR assays. These PCR assays can rapidly define
the occurrence, species incidence, and flaA genotypes of enteropathogenic
campylobacters.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
PCR detection, identification to species level, and fingerprinting of Campylobacter jejuni and Campylobacter coli direct from diarrheic samples
Virus Reference Division, Central Public Health Laboratory, London, United Kingdom.
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