Loading…

Application of multilocus sequence analysis (MLSA) for rapid identification of Enterococcus species based on rpoA and pheS genes

1 Laboratory of Microbiology, Ghent University, K. L. Ledeganckstraat 35, Ghent 9000, Belgium 2 BCCM/LMG Bacteria Collection, Ghent University, K. L. Ledeganckstraat 35, Ghent 9000, Belgium 3 Bioinformatics and Evolutionary Genomics, Ghent University/VIB, Technologiepark 927, Ghent 9052, Belgium Cor...

Full description

Saved in:
Bibliographic Details
Published in:Microbiology (Society for General Microbiology) 2005-07, Vol.151 (7), p.2141-2150
Main Authors: Naser, Sabri M, Thompson, Fabiano L, Hoste, Bart, Gevers, Dirk, Dawyndt, Peter, Vancanneyt, Marc, Swings, Jean
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:1 Laboratory of Microbiology, Ghent University, K. L. Ledeganckstraat 35, Ghent 9000, Belgium 2 BCCM/LMG Bacteria Collection, Ghent University, K. L. Ledeganckstraat 35, Ghent 9000, Belgium 3 Bioinformatics and Evolutionary Genomics, Ghent University/VIB, Technologiepark 927, Ghent 9052, Belgium Correspondence Sabri M. Naser Sabri.Naser{at}Ugent.be The aim of this study was to evaluate the use of RNA polymerase subunit ( rpoA ) and phenylalanyl-tRNA synthase ( pheS ) gene sequences as species identification tools for enterococci. Ninety-six representative strains comprising all currently recognized Enterococcus species were examined. rpoA gene sequences generated a robust classification into species groups similar to the one based on 16S rRNA gene sequence analysis. On the other hand, the pheS gene is a fast-evolving clock even better suited for species delineation than the rpoA gene, but not for recognition of species groups within Enterococcus as determined by both rpoA and 16S rRNA genes. All enterococcal species were clearly differentiated on the basis of their rpoA and pheS sequences. Evaluation of intraspecies variation showed that both rpoA and pheS genes have a high degree of homogeneity among strains of the same species. Strains of the same enterococcal species have at least 99 % rpoA and 97 % pheS gene sequence similarity, whereas, different enterococcal species have at maximum 97 % rpoA and 86 % pheS gene sequence similarity. It was concluded that both genes can be used as reliable tools for identification of clinical and environmental species of Enterococcus and are efficient screening methods for the detection of novel species. The sequence data obtained in this study were compared to the available atpA and 16S rRNA gene sequences. The MLSA approach to Enterococcus taxonomy provides portable, highly reproducible data with lower costs for rapid identification of all enterococcal species. Abbreviations: MLSA, multilocus sequence analysis The GenBank/EMBL/DDBJ accession numbers for the sequences reported in this paper are AJ843476–AJ843515, AJ843517–AJ843523, AJ843525–AJ843534, AJ843537–AJ843553, AJ843555–AJ843556 and AJ843558–AJ843560 ( rpoA partial gene sequences), and AJ843373–AJ843387, AJ843389–AJ843402, AJ843404–AJ843410, AJ843412–AJ843435, AJ843438–AJ843444 and AJ843446–AJ843474 ( pheS partial gene sequences). A presentation of the polymorphic sites present in the RpoA and PheS dataset is available as supplementary data with the online vers
ISSN:1350-0872
1465-2080
DOI:10.1099/mic.0.27840-0