dc.date.accessioned2022-01-18T19:34:38Z
dc.date.available2022-01-18T19:34:38Z
dc.date.created2022-01-18T19:34:38Z
dc.date.issued2011
dc.identifierhttps://hdl.handle.net/20.500.12866/11084
dc.identifierhttps://doi.org/10.1371/journal.pone.0016257
dc.description.abstractBackground: There is an increasing body of literature reporting treatment failure of the currently recommended radical treatment of Plasmodium vivax infections. As P. vivax is the main malaria species outside the African continent, emerging tolerance to its radical treatment regime could have major consequences in countries like Peru, where 80% of malaria cases are due to P. vivax. Here we describe the results of a 1-year longitudinal follow up of 51 confirmed P. vivax patients living around Iquitos, Peruvian Amazon, and treated according to the Peruvian national guidelines. Methodology: Each month a blood sample for microscopy and later genotyping was systematically collected. Recent exposure to infection was estimated by detecting antibodies against the P. vivax circumsporozoite protein (CSP) and all PCR confirmed P. vivax infections were genotyped with 16 polymorphic microsatellites. Results: During a 1-year period, 84 recurrent infections, 22 positive also by microscopy, were identified, with a median survival time to first recurrent infection of 203 days. Most of them (71%) were asymptomatic; in 13 patients the infection persisted undetected by microscopy for several consecutive months. The genotype of mostly recurrent infections differed from that at day 0 while fewer differences were seen between the recurrent infections. The average expected heterozygosity was 0.56. There was strong linkage disequilibrium (IAs = 0.29, p<1.1024) that remained also when analyzing only the unique haplotypes, suggesting common inbreeding. Conclusion: In Peru, the P. vivax recurrent infections were common and displayed a high turnover of parasite genotypes compared to day 0. Plasmodium vivax patients, even when treated according to the national guidelines, may still represent an important parasite reservoir that can maintain transmission. Any elimination effort should consider such a hidden reservoir.
dc.languageeng
dc.publisherPublic Library of Science
dc.relationPLoS ONE
dc.relation1932-6203
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectPeru
dc.subjectcohort analysis
dc.subjectCohort Studies
dc.subjectcontrolled study
dc.subjectmajor clinical study
dc.subjectgenetics
dc.subjectGenotype
dc.subjectpolymerase chain reaction
dc.subjectdisease transmission
dc.subjectmicrosatellite marker
dc.subjectparasite transmission
dc.subjectPlasmodium vivax
dc.subjectchloroquine
dc.subjectblood
dc.subjectPolymerase Chain Reaction
dc.subjecthaplotype
dc.subjectgene frequency
dc.subjectgenetic association
dc.subjectheterozygosity
dc.subjectLongitudinal Studies
dc.subjectProspective Studies
dc.subjectMalaria, Vivax
dc.subjectPlasmodium vivax malaria
dc.subjectprimaquine
dc.subjectRecurrence
dc.subjectAntibodies, Protozoan
dc.subjectantibody titer
dc.subjectrecurrent disease
dc.subjectcircumsporozoite protein
dc.subjectgene linkage disequilibrium
dc.subjectgenetic variability
dc.subjectprotozoon antibody
dc.subjectsurvival time
dc.titlePlasmodium vivax sub-patent infections after radical treatment are common in peruvian patients: Results of a 1-year prospective cohort study
dc.typeinfo:eu-repo/semantics/article


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