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Specific Real-Time PCR for Simultaneous Detection and Identification of Legionella pneumophila Serogroup 1 in Water and Clinical Samples

Authors :
Sophie Jarraud
Jerome Etienne
Carmen Buchrieser
Laura Gomez-Valero
Christophe Rusniok
Nathalie Merault
M. Marin
Christine Lawrence
Jean-Louis Gaillard
Jean-Louis Herrmann
Etienne Brachet
Christel Cazalet
Philippe Aegerter
Source :
Applied and Environmental Microbiology. 77:1708-1717
Publication Year :
2011
Publisher :
American Society for Microbiology, 2011.

Abstract

Legionella pneumophila , a bacterium that replicates within aquatic amoebae and persists in the environment as a free-living microbe, is the causative agent of Legionnaires' disease. Among the many Legionella species described, L. pneumophila is associated with 90% of human disease, and within the 15 serogroups (Sg), L. pneumophila Sg1 causes more than 84% of Legionnaires' disease worldwide. Thus, rapid and specific identification of L. pneumophila Sg1 is of the utmost importance for evaluation of the contamination of collective water systems and the risk posed. Previously we had shown that about 20 kb of the 33-kb locus carrying the genes coding for the proteins involved in lipopolysaccharide biosynthesis (LPS gene cluster) by L. pneumophila was highly specific for Sg1 strains and that three genes ( lpp0831 , wzm , and wzt ) may serve as genetic markers. Here we report the sequencing and comparative analyses of this specific region of the LPS gene cluster in L. pneumophila Sg6, -10, -12, -13, and -14. Indeed, the wzm and wzt genes were present only in the Sg1 LPS gene cluster, which showed a very specific gene content with respect to the other five serogroups investigated. Based on this observation, we designed primers and developed a classical and a real-time PCR method for the detection and simultaneous identification of L. pneumophila Sg1 in clinical and environmental isolates. Evaluation of the selected primers with 454 Legionella and 38 non- Legionella strains demonstrated 100% specificity. Sensitivity, specificity, and predictive values were further evaluated with 209 DNA extracts from water samples of hospital water supply systems and with 96 respiratory specimens. The results showed that the newly developed quantitative Sg1-specific PCR method is a highly specific and efficient tool for the surveillance and rapid detection of high-risk L. pneumophila Sg1 in water and clinical samples.

Details

ISSN :
10985336 and 00992240
Volume :
77
Database :
OpenAIRE
Journal :
Applied and Environmental Microbiology
Accession number :
edsair.doi.dedup.....483a40f5151140f1b4e432aabe1b9315
Full Text :
https://doi.org/10.1128/aem.02261-10