Field deployment of loop-mediated isothermal amplification for centralized mass-screening of asymptomatic malaria in Zanzibar: a pre-elimination setting

被引:34
|
作者
Morris, Ulrika [1 ]
Khamis, Mwinyi [2 ]
Aydin-Schmidt, Berit [1 ]
Abass, Ali K. [2 ]
Msellem, Mwinyi I. [2 ]
Nassor, Majda H. [2 ]
Gonzalez, Iveth J. [3 ]
Martensson, Andreas [1 ,4 ,5 ]
Ali, Abdullah S. [2 ]
Bjorkman, Anders [1 ]
Cook, Jackie [1 ,6 ]
机构
[1] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Malaria Res, S-17177 Stockholm, Sweden
[2] Minist Hlth, Zanzibar Malaria Eliminat Programme ZAMEP, Zanzibar, Tanzania
[3] Fdn Innovat New Diagnost, Geneva, Switzerland
[4] Karolinska Inst, Dept Publ Hlth Sci, S-17177 Stockholm, Sweden
[5] Uppsala Univ, Ctr Clin Res Sormland, Uppsala, Sweden
[6] London Sch Hyg & Trop Med, London WC1, England
来源
MALARIA JOURNAL | 2015年 / 14卷
基金
英国医学研究理事会;
关键词
Plasmodium; Malaria; Low-density; Asymptomatic; Loop-mediated isothermal amplification; Mass screening; DNA contamination; DIAGNOSIS; LAMP; POINT; INFECTIONS; KIT; PCR;
D O I
10.1186/s12936-015-0731-2
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Molecular tools for detection of low-density asymptomatic Plasmodium infections are needed in malaria elimination efforts. This study reports results from the hitherto largest implementation of loop-mediated isothermal amplification (LAMP) for centralized mass screening of asymptomatic malaria in Zanzibar. Methods: Healthy individuals present and willing to participate in randomly selected households in 60 villages throughout Zanzibar were screened for malaria by rapid diagnostic tests (RDT). In 50% of the study households, participants were asked to provide 60 mu L of finger-prick blood for additional LAMP screening. LAMP was conducted in two centralized laboratories in Zanzibar, by trained technicians with limited or no previous experience of molecular methods. The LAMP assay was performed with Loopamp(TM) MALARIA Pan/Pf Detection Kit (Eiken Chemical Company, Japan). Samples positive for Plasmodium genus (Pan)-LAMP were re-tested using Plasmodium falciparum-specific LAMP kits. Results: Paired RDT and LAMP samples were available from 3983 individuals. The prevalence of asymptomatic malaria was 0.5% (CI 95% 0.1-0.8) and 1.6% (CI 95% 1.1-2.2) by RDT and Pan-LAMP, respectively. LAMP detected 3.4 (CI 95% 2.2-5.2) times more Plasmodium positive samples than RDT. DNA contamination was experienced, but solved by repetitive decontamination of all equipment and reagents. Conclusions: LAMP is a simple and sensitive molecular tool, and has potential in active surveillance and mass-screening programmes for detection of low-density asymptomatic malaria in pre-elimination settings. However, in order to deploy LAMP more effectively in field settings, protocols may need to be adapted for processing larger numbers of samples. A higher throughput, affordable closed system would be ideal to avoid contamination.
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收藏
页数:6
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