5′ Nuclease PCR Assay To Detect Yersinia pestis
- 1 August 1998
- journal article
- research article
- Published by American Society for Microbiology in Journal of Clinical Microbiology
- Vol. 36 (8) , 2284-2288
- https://doi.org/10.1128/jcm.36.8.2284-2288.1998
Abstract
The 5′ nuclease PCR assay uses a fluorescently labeled oligonucleotide probe (TaqMan) to rapidly detect and quantitate DNA templates in clinical samples. We developed a 5′ nuclease PCR assay targeting the plasminogen activator gene ( pla ) of Yersinia pestis . The assay is species specific, with a detection threshold of 2.1 × 10 5 copies of the pla target or 1.6 pg of total cell DNA. The assay detected Y. pestis in experimentally infected Xenopsylla cheopis fleas and in experimentally infected monkey blood and oropharyngeal swabs. The TaqMan assay is simple to perform and rapid and shows promise as a future field-adaptable technique.Keywords
This publication has 27 references indexed in Scilit:
- The evaluation of a fluorogenic polymerase chain reaction assay for the detection of Salmonella species in food commoditiesInternational Journal of Food Microbiology, 1997
- The potential of 5′ nuclease PCR for detecting a single-base polymorphism inOrthopoxvirusMolecular and Cellular Probes, 1997
- Detection of Rift Valley fever virus in mosquitoes by RT-PCRMolecular and Cellular Probes, 1997
- Book Reviews The Horned Dinosaurs, review by K. Padian * Biochemistry of Smooth Muscle Contraction, M. Ikebe * Vignettes * Books ReceivedScience, 1996
- Detection and Identification of Yersinia pestis by Polymerase Chain Reaction (PCR) Using Multiplex PrimersMicrobiology and Immunology, 1996
- A novel method for real time quantitative RT-PCR.Genome Research, 1996
- Real time quantitative PCR.Genome Research, 1996
- Role of the Yersinia pestis Hemin Storage ( hms ) Locus in the Transmission of Plague by FleasScience, 1996
- Development of a diagnostic test for Yersinia pestis by the polymerase chain reactionJournal of Applied Bacteriology, 1994
- Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase.Proceedings of the National Academy of Sciences, 1991