Sensitive and inexpensive molecular test for falciparum malaria: detecting Plasmodium falciparum DNA directly from heat-treated blood by loop-mediated isothermal amplification

dc.contributor.authorPoon, L.en_US
dc.contributor.authorWong, B.W.en_US
dc.contributor.authorMa, E.H.en_US
dc.contributor.authorChan, K.H.en_US
dc.contributor.authorChow, L.M.en_US
dc.contributor.authorAbeyewickreme, W.en_US
dc.contributor.authorTangpukdee, N.en_US
dc.contributor.authorYuen, K.Y.en_US
dc.contributor.authorGuan, Y.en_US
dc.contributor.authorLooareesuwan, S.en_US
dc.contributor.authorPeiris, J.S.en_US
dc.creator.corporateauthorAmerican Association of Clinical Chemistsen_US
dc.creator.corporateauthorAmerican Association for Clinical Chemistryen_US
dc.date.accessioned2014-10-29T09:24:33Z
dc.date.available2014-10-29T09:24:33Z
dc.date.issued2006en_US
dc.descriptionIndexed in MEDLINE
dc.description.abstractBACKGROUND: Malaria is one of the most important parasitic infections in humans. A sensitive diagnostic test for malaria that could be applied at the community level could be useful in programs to control the disease. The aim of the present work was to develop a simple, inexpensive moleculartest for Plasmodium falciparum. METHODS: Blood was collected from controls (n = 100) and from patients diagnosed with falciparum malaria infection (n = 102), who were recruited to the study. Heat-treated blood samples were tested by a loop-mediated isothermal amplification (LAMP) assay for P. falciparum. Results were interpreted by a turbidity meter in real time or visually at the end of the assay. To evaluate the assay, DNA from these samples was purified and tested by PCR. Results from the LAMP and PCR assays were compared. RESULTS: The LAMP assay detected P. falciparum directly from heat-treated blood. The quantitative data from the assay correlated to the parasite counts obtained by blood-film microscopic analyses. When we used the PCR assay as the comparison method, the sensitivity and specificity of the LAMP assay were 95% and 99%, respectively. CONCLUSIONS: Unlike PCR, the LAMP assay does not require purified DNA for efficient DNA amplification, thereby reducing the cost and turnaround time for P. falciparum diagnosis. The assay requires only basic instruments, and assay positivity can be verified by visual inspection
dc.identifier.citationClinical Chemistry. 2006; 52(2): pp.303-306en_US
dc.identifier.departmentParasitologyen_US
dc.identifier.issn0009-9147 (Print)en_US
dc.identifier.issn1530-8561 (Electronic)en_US
dc.identifier.urihttp://repository.kln.ac.lk/handle/123456789/1746
dc.publisherAmerican Association For Clinical Chemistryen_US
dc.subjectMalaria, Falciparum
dc.subjectMalaria, Falciparum-blood
dc.subjectMalaria, Falciparum-diagnosis
dc.subjectMalaria, falciparum-genetics
dc.subjectPlasmodium falciparum-isolation and purification
dc.subjectPolymerase Chain Reaction
dc.subjectSensitivity and Specificity
dc.subjectSpecimen Handling-methods
dc.subjectDNA, Protozoan
dc.titleSensitive and inexpensive molecular test for falciparum malaria: detecting Plasmodium falciparum DNA directly from heat-treated blood by loop-mediated isothermal amplificationen_US
dc.typeArticleen_US

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