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Simultaneous detection of Legionella species and L. anisa, L. bozemanii, L. longbeachae and L. micdadei using conserved primers and multiple probes in a multiplex real-time PCR assay.

Authors :
Cross KE
Mercante JW
Benitez AJ
Brown EW
Diaz MH
Winchell JM
Source :
Diagnostic microbiology and infectious disease [Diagn Microbiol Infect Dis] 2016 Jul; Vol. 85 (3), pp. 295-301. Date of Electronic Publication: 2016 Apr 02.
Publication Year :
2016

Abstract

Legionnaires' disease is a severe respiratory disease that is estimated to cause between 8,000 and 18,000 hospitalizations each year, though the exact burden is unknown due to under-utilization of diagnostic testing. Although Legionella pneumophila is the most common species detected in clinical cases (80-90%), other species have also been reported to cause disease. However, little is known about Legionnaires' disease caused by these non-pneumophila species. We designed a multiplex real-time PCR assay for detection of all Legionella spp. and simultaneous specific identification of four clinically-relevant Legionella species, L. anisa, L. bozemanii, L. longbeachae, and L. micdadei, using 5'-hydrolysis probe real-time PCR. The analytical sensitivity for detection of nucleic acid from each target species was ≤50fg per reaction. We demonstrated the utility of this assay in spiked human sputum specimens. This assay could serve as a tool for understanding the scope and impact of non-pneumophila Legionella species in human disease.<br /> (Published by Elsevier Inc.)

Details

Language :
English
ISSN :
1879-0070
Volume :
85
Issue :
3
Database :
MEDLINE
Journal :
Diagnostic microbiology and infectious disease
Publication Type :
Academic Journal
Accession number :
27107536
Full Text :
https://doi.org/10.1016/j.diagmicrobio.2016.03.022