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Molecular Diagnosis of Malaria by Photo-Induced Electron Transfer Fluorogenic Primers: PET-PCR
Author(s) -
Naomi W. Lucchi,
N. Jothikumar,
Mara A. Karell,
Maniphet Xayavong,
Simon Kariuki,
Alexandre J. da Silva,
Vincent R. Hill,
Venkatachalam Udhayakumar
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0056677
Subject(s) - plasmodium falciparum , primer (cosmetics) , gold standard (test) , malaria , biology , virology , polymerase chain reaction , plasmodium ovale , diagnosis of malaria , nested polymerase chain reaction , plasmodium malariae , plasmodium vivax , parasitemia , microbiology and biotechnology , medicine , genetics , chemistry , immunology , organic chemistry , gene
There is a critical need for developing new malaria diagnostic tools that are sensitive, cost effective and capable of performing large scale diagnosis. The real-time PCR methods are particularly robust for large scale screening and they can be used in malaria control and elimination programs. We have designed novel self-quenching photo-induced electron transfer (PET) fluorogenic primers for the detection of P. falciparum and the Plasmodium genus by real-time PCR. A total of 119 samples consisting of different malaria species and mixed infections were used to test the utility of the novel PET-PCR primers in the diagnosis of clinical samples. The sensitivity and specificity were calculated using a nested PCR as the gold standard and the novel primer sets demonstrated 100% sensitivity and specificity. The limits of detection for P. falciparum was shown to be 3.2 parasites/µl using both Plasmodium genus and P. falciparum- specific primers and 5.8 parasites/µl for P. ovale , 3.5 parasites/µl for P. malariae and 5 parasites/µl for P. vivax using the genus specific primer set. Moreover, the reaction can be duplexed to detect both Plasmodium spp. and P. falciparum in a single reaction. The PET-PCR assay does not require internal probes or intercalating dyes which makes it convenient to use and less expensive than other real-time PCR diagnostic formats. Further validation of this technique in the field will help to assess its utility for large scale screening in malaria control and elimination programs.

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