Affiliation:
1. Institute of Molecular Biology, Biochemistry and Microbiology
2. Institute of Hygiene, Karl-Franzens University
3. Department of Veterinary Administration in Styria, Graz, Austria
Abstract
ABSTRACT
Species-specific identification of campylobacters is problematic, primarily due to the absence of suitable biochemical assays and the existence of atypical strains. 16S rRNA gene (16S rDNA)-based identification of bacteria offers a possible alternative when phenotypic tests fail. Therefore, we evaluated the reliability of 16S rDNA sequencing for the species-specific identification of campylobacters. Sequence analyses were performed by using almost 94% of the complete 16S rRNA genes of 135 phenotypically characterized
Campylobacter
strains, including all known taxa of this genus. It was shown that 16S rDNA analysis enables specific identification of most
Campylobacter
species. The exception was a lack of discrimination among the taxa
Campylobacter jejuni
and
C. coli
and atypical
C. lari
strains, which shared identical or nearly identical 16S rDNA sequences. Subsequently, it was investigated whether partial 16S rDNA sequences are sufficient to determine species identity. Sequence alignments led to the identification of four 16S rDNA regions with high degrees of interspecies variation but with highly conserved sequence patterns within the respective species. A simple protocol based on the analysis of these sequence patterns was developed, which enabled the unambiguous identification of the majority of
Campylobacter
species. We recommend 16S rDNA sequence analysis as an effective, rapid procedure for the specific identification of campylobacters.
Publisher
American Society for Microbiology
Cited by
83 articles.
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