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dc.contributor.author | Chuquiyauri, Raul | |
dc.contributor.author | Peñataro, Pablo | |
dc.contributor.author | Brouwer, Kimberly C. | |
dc.contributor.author | Fasabi, Manuel | |
dc.contributor.author | Calderón Sánchez, Maritza Mercedes | |
dc.contributor.author | Torres, Sonia | |
dc.contributor.author | Gilman, Robert Hugh | |
dc.contributor.author | Kosek, Margaret | |
dc.contributor.author | Vinetz, Joseph Michael | |
dc.date.accessioned | 2022-01-04T20:33:21Z | |
dc.date.available | 2022-01-04T20:33:21Z | |
dc.date.issued | 2013 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12866/10768 | |
dc.description.abstract | To determine the magnitude of Plasmodium vivax relapsing malaria in rural Amazonia, we carried out a study in four sites in northeastern Peru. Polymerase chain reaction-restriction fragment length polymorphism of PvMSP-3α and tandem repeat (TR) markers were compared for their ability to distinguish relapse versus reinfection. Of 1,507 subjects with P. vivax malaria, 354 developed > 1 episode during the study; 97 of 354 (27.5%) were defined as relapse using Pvmsp-3α alone. The addition of TR polymorphism analysis significantly reduced the number of definitively defined relapses to 26 of 354 (7.4%) (P < 0.05). Multivariate logistic regression modeling showed that the probability of having > 1 infection was associated with the following: subjects in Mazan (odds ratio [OR] = 2.56; 95% confidence interval [CI] 1.87, 3.51), 15–44 years of age (OR = 1.49; 95% CI 1.03, 2.15), traveling for job purposes (OR = 1.45; 95%CI 1.03, 2.06), and travel within past month (OR = 1.46; 95% CI 1.0, 2.14). The high discriminatory capacity of the molecular tools shown here is useful for understanding the micro-geography of malaria transmission. | en_US |
dc.language.iso | eng | |
dc.publisher | American Society of Tropical Medicine and Hygiene | |
dc.relation.ispartofseries | American Journal of Tropical Medicine and Hygiene | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.subject | Geographical variation (species) | en_US |
dc.subject | major clinical study | en_US |
dc.subject | Peru | en_US |
dc.subject | polymerase chain reaction | en_US |
dc.subject | disease association | en_US |
dc.subject | Time Factors | en_US |
dc.subject | DNA, Protozoan | en_US |
dc.subject | disease transmission | en_US |
dc.subject | Plasmodium vivax | en_US |
dc.subject | Plasmodium vivax malaria | en_US |
dc.subject | Polymerase Chain Reaction | en_US |
dc.subject | Genetic Markers | en_US |
dc.subject | Genotype | en_US |
dc.subject | Molecular Epidemiology | en_US |
dc.subject | probability | en_US |
dc.subject | Recurrence | en_US |
dc.subject | Polymorphism, Genetic | en_US |
dc.subject | Protozoan Proteins | en_US |
dc.subject | chloroquine plus primaquine | en_US |
dc.subject | travel | en_US |
dc.subject | reinfection | en_US |
dc.subject | Polymorphism, Restriction Fragment Length | en_US |
dc.subject | restriction fragment length polymorphism | en_US |
dc.subject | tandem repeat | en_US |
dc.title | Microgeographical differences of Plasmodium vivax relapse and re-infection in the Peruvian Amazon | en_US |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | https://doi.org/10.4269/ajtmh.13-0060 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.03.06 | |
dc.relation.issn | 1476-1645 |
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