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

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dc.contributor.author Poon, L. en_US
dc.contributor.author Wong, B.W. en_US
dc.contributor.author Ma, E.H. en_US
dc.contributor.author Chan, K.H. en_US
dc.contributor.author Chow, L.M. en_US
dc.contributor.author Abeyewickreme, W. en_US
dc.contributor.author Tangpukdee, N. en_US
dc.contributor.author Yuen, K.Y. en_US
dc.contributor.author Guan, Y. en_US
dc.contributor.author Looareesuwan, S. en_US
dc.contributor.author Peiris, J.S. en_US
dc.date.accessioned 2014-10-29T09:24:33Z
dc.date.available 2014-10-29T09:24:33Z
dc.date.issued 2006 en_US
dc.identifier.citation Clinical Chemistry. 2006; 52(2): pp.303-306 en_US
dc.identifier.issn 0009-9147 (Print) en_US
dc.identifier.issn 1530-8561 (Electronic) en_US
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/1746
dc.description Indexed in MEDLINE
dc.description.abstract BACKGROUND: 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.publisher American Association For Clinical Chemistry en_US
dc.subject Malaria, Falciparum
dc.subject Malaria, Falciparum-blood
dc.subject Malaria, Falciparum-diagnosis
dc.subject Malaria, falciparum-genetics
dc.subject Plasmodium falciparum-isolation and purification
dc.subject Polymerase Chain Reaction
dc.subject Sensitivity and Specificity
dc.subject Specimen Handling-methods
dc.subject DNA, Protozoan
dc.title Sensitive and inexpensive molecular test for falciparum malaria: detecting Plasmodium falciparum DNA directly from heat-treated blood by loop-mediated isothermal amplification en_US
dc.type Article en_US
dc.identifier.department Parasitology en_US
dc.creator.corporateauthor American Association of Clinical Chemists en_US
dc.creator.corporateauthor American Association for Clinical Chemistry en_US


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