Loop Mediated Isothermal Amplification (LAMP) Accurately Detects Malaria DNA from Filter Paper Blood Samples of Low Density Parasitaemias

• Published in: PloS one Vol. 9; no. 8; p. e103905
• Main Authors: Aydin-Schmidt, Berit, Xu, Weiping, González, Iveth J., Polley, Spencer D., Bell, David, Shakely, Delér, Msellem, Mwinyi I., Björkman, Anders, Mårtensson, Andreas
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 08.08.2014; Public Library of Science (PLoS)
• Subjects: Accuracy; Biology and Life Sciences; Blood; Councils; Density; Deoxyribonucleic acid; Diagnostic systems; Diagnostic tests; DNA; DNA Primers - genetics; DNA, Protozoan - blood; DNA, Protozoan - isolation & purification; Fever; Filter paper; Humans; Infections; Infectious diseases; Laboratories; Limit of Detection; Malaria; Malaria - blood; Malaria - diagnosis; Malaria - genetics; Medicine and Health Sciences; Nucleic Acid Amplification Techniques - methods; Parasites; Parasitology; Patients; Plasmodium; Plasmodium falciparum; Polymerase chain reaction; Real time; Real-Time Polymerase Chain Reaction - methods; Research and Analysis Methods; Sampling methods; Sensitivity; Tanzania; Tropical diseases; Vector-borne diseases; Tanzania; United Kingdom > UK; Sweden; Zanzibar
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0103905

Loop mediated isothermal amplification (LAMP) provides an opportunity for improved, field-friendly detection of malaria infections in endemic areas. However data on the diagnostic accuracy of LAMP for active case detection, particularly low-density parasitaemias, are lacking. We therefore evaluated the performance of a new LAMP kit compared with PCR using DNA from filter paper blood spots. Samples from 865 fever patients and 465 asymptomatic individuals collected in Zanzibar were analysed for Pan (all species) and Pf (P. falciparum) DNA with the Loopamp MALARIA Pan/Pf kit. Samples were amplified at 65°C for 40 minutes in a real-time turbidimeter and results were compared with nested PCR. Samples with discordant results between LAMP and nested PCR were analysed with real-time PCR. The real-time PCR corrected nested PCR result was defined as gold standard. Among the 117 (13.5%) PCR detected P. falciparum infections from fever patients (mean parasite density 7491/µL, range 6-782,400) 115, 115 and 111 were positive by Pan-LAMP, Pf-LAMP and nested PCR, respectively. The sensitivities were 98.3% (95%CI 94-99.8) for both Pan and Pf-LAMP. Among the 54 (11.6%) PCR positive samples from asymptomatic individuals (mean parasite density 10/µL, range 0-4972) Pf-LAMP had a sensitivity of 92.7% (95%CI 80.1-98.5) for detection of the 41 P. falciparum infections. Pan-LAMP had sensitivities of 97% (95%CI 84.2-99.9) and 76.9% (95%CI 46.2-95) for detection of P. falciparum and P. malariae, respectively. The specificities for both Pan and Pf-LAMP were 100% (95%CI 99.1-100) in both study groups. Both components of the Loopamp MALARIA Pan/Pf detection kit revealed high diagnostic accuracy for parasite detection among fever patients and importantly also among asymptomatic individuals of low parasite densities from minute blood volumes preserved on filter paper. These data support LAMPs potential role for improved detection of low-density malaria infections in pre-elimination settings.