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Estimation of Plasmodium falciparum Transmission Intensity in Lilongwe, Malawi, by Microscopy, Rapid Diagnostic Testing, and Nucleic Acid Detection
Author(s) -
Jonathan B. Parr,
Connor Belson,
Jaymin C. Patel,
Irving Hoffman,
Portia Kamthunzi,
Francis Martinson,
Gerald Tegha,
Isaac Thengolose,
Chris Drakeley,
Steven R. Meshnick,
Veronica Escamillia,
Michael Emch,
Jonathan J. Juliano
Publication year - 2016
Publication title -
american journal of tropical medicine and hygiene
Language(s) - English
Resource type - Journals
eISSN - 1476-1645
pISSN - 0002-9637
DOI - 10.4269/ajtmh.16-0156
Subject(s) - parasitemia , plasmodium falciparum , dipstick , biology , virology , malaria , polymerase chain reaction , nucleic acid , parasite hosting , protozoa , immunology , gene , genetics , biochemistry , world wide web , urine , computer science
Estimates of malaria transmission intensity (MTI) typically rely upon microscopy or rapid diagnostic testing (RDT). However, these methods are less sensitive than nucleic acid amplification techniques and may underestimate parasite prevalence. We compared microscopy, RDT, and polymerase chain reaction (PCR) for the diagnosis of Plasmodium falciparum parasitemia as part of an MTI study of 800 children and adults conducted in Lilongwe, Malawi. PCR detected more cases of parasitemia than microscopy or RDT. Age less than 5 years predicted parasitemia detected by PCR alone (adjusted odds ratio = 1.61, 95% confidence interval = 1.09-2.38, Wald P = 0.02). In addition, we identified one P. falciparum parasite with a false-negative RDT result due to a suspected deletion of the histidine-rich protein 2 (hrp2) gene and used a novel, ultrasensitive PCR assay to detect low-level parasitemia missed by traditional PCR. Molecular methods should be considered for use in future transmission studies as a supplement to RDT or microscopy.

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