dc.contributor.author |
Serra-Casas, Elisa |
|
dc.contributor.author |
Manrique Valverde, Paulo Cesar |
|
dc.contributor.author |
Ding, Xavier C. |
|
dc.contributor.author |
Carrasco Escobar, Gabriel |
|
dc.contributor.author |
Alava, Freddy |
|
dc.contributor.author |
Gave, Anthony |
|
dc.contributor.author |
Rodriguez, Hugo |
|
dc.contributor.author |
Contreras-Mancilla, Juan |
|
dc.contributor.author |
Rosas-Aguirre, Angel |
|
dc.contributor.author |
Speybroeck, Niko |
|
dc.contributor.author |
González, Iveth J. |
|
dc.contributor.author |
Rosanas-Urgell, Anna |
|
dc.contributor.author |
Gamboa Vilela, Dionicia Baziliza |
|
dc.date.accessioned |
2019-01-25T15:28:05Z |
|
dc.date.available |
2019-01-25T15:28:05Z |
|
dc.date.issued |
2017 |
|
dc.identifier.uri |
https://hdl.handle.net/20.500.12866/4694 |
|
dc.description.abstract |
BACKGROUND: Loop-mediated isothermal DNA amplification (LAMP) methodology offers an opportunity for point-of-care (POC) molecular detection of asymptomatic malaria infections. However, there is still little evidence on the feasibility of implementing this technique for population screenings in isolated field settings. METHODS: Overall, we recruited 1167 individuals from terrestrial ('road') and hydric ('riverine') communities of the Peruvian Amazon for a cross-sectional survey to detect asymptomatic malaria infections. The technical performance of LAMP was evaluated in a subgroup of 503 samples, using real-time Polymerase Chain Reaction (qPCR) as reference standard. The operational feasibility of introducing LAMP testing in the mobile screening campaigns was assessed based on field-suitability parameters, along with a pilot POC-LAMP assay in a riverine community without laboratory infrastructure. RESULTS: LAMP had a sensitivity of 91.8% (87.7-94.9) and specificity of 91.9% (87.8-95.0), and the overall accuracy was significantly better among samples collected during road screenings than riverine communities (p≤0.004). LAMP-based diagnostic strategy was successfully implemented within the field-team logistics and the POC-LAMP pilot in the riverine community allowed for a reduction in the turnaround time for case management, from 12-24 hours to less than 5 hours. Specimens with haemolytic appearance were regularly observed in riverine screenings and could help explaining the hindered performance/interpretation of the LAMP reaction in these communities. CONCLUSIONS: LAMP-based molecular malaria diagnosis can be deployed outside of reference laboratories, providing similar performance as qPCR. However, scale-up in remote field settings such as riverine communities needs to consider a number of logistical challenges (e.g. environmental conditions, labour-intensiveness in large population screenings) that can influence its optimal implementation. |
en_US |
dc.language.iso |
eng |
|
dc.publisher |
Public Library of Science |
|
dc.relation.ispartofseries |
PLoS ONE |
|
dc.rights |
info:eu-repo/semantics/restrictedAccess |
|
dc.rights.uri |
https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es |
|
dc.subject |
Adolescent |
en_US |
dc.subject |
Child |
en_US |
dc.subject |
Child, Preschool |
en_US |
dc.subject |
DNA, Protozoan/genetics |
en_US |
dc.subject |
Female |
en_US |
dc.subject |
Humans |
en_US |
dc.subject |
Malaria/diagnosis/epidemiology/parasitology |
en_US |
dc.subject |
Male |
en_US |
dc.subject |
Peru/epidemiology |
en_US |
dc.subject |
Pilot Projects |
en_US |
dc.subject |
Plasmodium/genetics |
en_US |
dc.subject |
Prevalence |
en_US |
dc.subject |
Real-Time Polymerase Chain Reaction |
en_US |
dc.title |
Loop-mediated isothermal DNA amplification for asymptomatic malaria detection in challenging field settings: Technical performance and pilot implementation in the Peruvian Amazon |
en_US |
dc.type |
info:eu-repo/semantics/article |
|
dc.identifier.doi |
https://doi.org/10.1371/journal.pone.0185742 |
|
dc.subject.ocde |
https://purl.org/pe-repo/ocde/ford#3.03.06 |
|
dc.subject.ocde |
https://purl.org/pe-repo/ocde/ford#3.03.08 |
|
dc.relation.issn |
1932-6203 |
|