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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.
- 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.)
- Subjects :
- Humans
Legionella genetics
Sensitivity and Specificity
DNA Primers genetics
Legionella classification
Legionella isolation & purification
Legionnaires' Disease microbiology
Multiplex Polymerase Chain Reaction methods
Oligonucleotide Probes genetics
Real-Time Polymerase Chain Reaction methods
Subjects
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