TY - JOUR
T1 - Sensitive and inexpensive molecular test for falciparum malaria: Defecting Plasmodium falciparum DNA directly from heat-treated blood by loop-mediated isothermal amplification
AU - Poon, Leo L.M.
AU - Wong, Bonnie W.Y.
AU - Ma, Edmund H.T.
AU - Chan, Kwok H.
AU - Chow, Ming Cheung
AU - Abeyewickreme, Wimal
AU - Tangpukdee, Noppadon
AU - Yuen, Kwok Y.
AU - Guan, Yi
AU - Looareesuwan, Sornchai
AU - Peiris, J. S.Malik
PY - 2006/2/1
Y1 - 2006/2/1
N2 - 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 molecular test 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.
AB - 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 molecular test 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.
UR - http://www.scopus.com/inward/record.url?scp=31844450172&partnerID=8YFLogxK
U2 - 10.1373/clinchem.2005.057901
DO - 10.1373/clinchem.2005.057901
M3 - Journal article
C2 - 16339303
SN - 0009-9147
VL - 52
SP - 303
EP - 306
JO - Clinical Chemistry
JF - Clinical Chemistry
IS - 2
ER -
