Publication: Evaluation of a real-time polymerase chain reaction assay for the diagnosis of malaria in patients from Thailand
Issued Date
2005-11-01
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ISSN
00029637
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2-s2.0-28044461080
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Mahidol University
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SCOPUS
Bibliographic Citation
American Journal of Tropical Medicine and Hygiene. Vol.73, No.5 (2005), 850-854
Suggested Citation
Heather Swan, Lynne Sloan, Anthony Muyombwe, Porntip Chavalitshewinkoon-Petmitr, Srivicha Krudsood, Wattana Leowattana, Polrat Wilairatana, Sornchai Looareesuwan, Jon Rosenblatt Evaluation of a real-time polymerase chain reaction assay for the diagnosis of malaria in patients from Thailand. American Journal of Tropical Medicine and Hygiene. Vol.73, No.5 (2005), 850-854. Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/16543
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Title
Evaluation of a real-time polymerase chain reaction assay for the diagnosis of malaria in patients from Thailand
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Abstract
We compared the diagnosis of malaria in 297 patients from Thailand by a real-time polymerase chain reaction (PCR) assay using the LightCycler with conventional microscopy using Giemsa-stained thick and thin blood films. The PCR assay can be completed in one hour and has the potential to detect and identify four species of Plasmodium in a single reaction by use of melting temperature curve analysis (however, we did not detect Plasmodium ovale in this study). Blood was collected, stored, and transported on IsoCode STIX, which provide a stable matrix for the archiving and rapid simple extraction of DNA. A genus-specific primer set corresponding to the 18S ribosomal RNA was used to amplify the target sequence. Fluorescence resonance energy technology hybridization probes were designed for P. falciparum over a region containing basepair mismatches, which allowed differentiation of the other Plasmodium species. The PCR results correlated with the microscopic results in 282 (95%) of 297 patient specimens. Most of these were single-species infections caused by P. vivax (150) and P. falciparum (120), along with 5 P. malariae, 2 mixed infections (P. falciparum and P. vivax), and 5 negative specimens. No negative microscopy specimens were positive by PCR (100% specificity for detection of any Plasmodium). The 15 discrepant results could not be resolved, but given the subjective nature of microscopy and the analytical objectivity of the PCR, the PCR results may be correct. The ability of the PCR method to detect mixed infections or to detect P. ovale could not be determined in this study. Within the limitations of initial equipment costs, this real-time PCR assay is a rapid, accurate, and efficient method for the specific diagnosis of malaria. It may have application in clinical laboratories, as well as in epidemiologic studies and antimalarial efficacy trials. Copyright © 2005 by The American Society of Tropical Medicine and Hygiene.