Diagnostics of Neisseriaceae and Moraxellaceae by Ribosomal DNA Sequencing: Ribosomal Differentiation of Medical Microorganisms

Author:

Harmsen Dag1,Singer Christian1,Rothgänger Jörg2,Tønjum Tone3,Sybren de Hoog Gerrit4,Shah Haroun5,Albert Jürgen2,Frosch Matthias1

Affiliation:

1. Institute of Hygiene and Microbiology,1 and

2. Department of Computer Science II,2 University of Würzburg, Würzburg, Germany;

3. Institute of Medical Microbiology, Department of Molecular Biology, University of Oslo, National Hospital, Oslo, Norway3;

4. Centraalbureau voor Schimmelcultures, Utrecht, The Netherlands4; and

5. National Collections of Type Cultures, Central Public Health Laboratory, London, United Kingdom5

Abstract

ABSTRACT Fast and reliable identification of microbial isolates is a fundamental goal of clinical microbiology. However, in the case of some fastidious gram-negative bacterial species, classical phenotype identification based on either metabolic, enzymatic, or serological methods is difficult, time-consuming, and/or inadequate. 16S or 23S ribosomal DNA (rDNA) bacterial sequencing will most often result in accurate speciation of isolates. Therefore, the objective of this study was to find a hypervariable rDNA stretch, flanked by strongly conserved regions, which is suitable for molecular species identification of members of the Neisseriaceae and Moraxellaceae . The inter- and intrageneric relationships were investigated using comparative sequence analysis of PCR-amplified partial 16S and 23S rDNAs from a total of 94 strains. When compared to the type species of the genera Acinetobacter, Moraxella , and Neisseria , an average of 30 polymorphic positions was observed within the partial 16S rDNA investigated (corresponding to Escherichia coli positions 54 to 510) for each species and an average of 11 polymorphic positions was observed within the 202 nucleotides of the 23S rDNA gene (positions 1400 to 1600). Neisseria macacae and Neisseria mucosa subsp. mucosa (ATCC 19696) had identical 16S and 23S rDNA sequences. Species clusters were heterogeneous in both genes in the case of Acinetobacter lwoffii, Moraxella lacunata , and N. mucosa. Neisseria meningitidis isolates failed to cluster only in the 23S rDNA subset. Our data showed that the 16S rDNA region is more suitable than the partial 23S rDNA for the molecular diagnosis of Neisseriaceae and Moraxellaceae and that a reference database should include more than one strain of each species. All sequence chromatograms and taxonomic and disease-related information are available as part of our ribosomal differentiation of medical microorganisms (RIDOM) web-based service ( http://www.ridom.hygiene.uni-wuerzburg.de/ ). Users can submit a sequence and conduct a similarity search against the RIDOM reference database for microbial identification purposes.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference42 articles.

1. The 16s/23s ribosomal spacer region as a target for DNA probes to identify eubacteria;Barry T.;PCR Methods Appl.,1991

2. Proposal to divide the genus Moraxella Lwoff 1939 emend. Henriksen and Bøvre 1968 into two subgenera, subgenus Moraxella (Lwoff 1939) Bøvre 1979 and subgenus Branhamella (Catlin 1970) Bøvre 1979;Bøvre K.;Int. J. Syst. Bacteriol.,1979

3. Neisseriaceae Prevot 1933;Bøvre K.;Bergey's manual of systematic bacteriology,1984

4. Council for International Organizations of Medical Sciences International nomenclature of diseases. II. Infectious diseases 1985 Council for International Organizations of Medical Sciences Geneva Switzerland

5. Evaluation of amplified ribosomal DNA restriction analysis for identification of Acinetobacter genomic species;Dijkshoorn L.;Syst. Appl. Microbiol.,1998

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