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Genetic variation and recurrent parasitaemia in Peruvian Plasmodium vivax populations

BACKGROUND: Plasmodium vivax is a predominant species of malaria in parts of South America and there is increasing resistance to drugs to treat infections by P. vivax. The existence of latent hypnozoites further complicates the ability to classify recurrent infections as treatment failures due to re...

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Autores principales: McCollum, Andrea M, Soberon, Valeria, Salas, Carola J, Santolalla, Meddly L, Udhayakumar, Venkatachalam, Escalante, Ananias A, Graf, Paul CF, Durand, Salomon, Cabezas, Cesar, Bacon, David J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941685/
https://www.ncbi.nlm.nih.gov/pubmed/24568141
http://dx.doi.org/10.1186/1475-2875-13-67
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author McCollum, Andrea M
Soberon, Valeria
Salas, Carola J
Santolalla, Meddly L
Udhayakumar, Venkatachalam
Escalante, Ananias A
Graf, Paul CF
Durand, Salomon
Cabezas, Cesar
Bacon, David J
author_facet McCollum, Andrea M
Soberon, Valeria
Salas, Carola J
Santolalla, Meddly L
Udhayakumar, Venkatachalam
Escalante, Ananias A
Graf, Paul CF
Durand, Salomon
Cabezas, Cesar
Bacon, David J
author_sort McCollum, Andrea M
collection PubMed
description BACKGROUND: Plasmodium vivax is a predominant species of malaria in parts of South America and there is increasing resistance to drugs to treat infections by P. vivax. The existence of latent hypnozoites further complicates the ability to classify recurrent infections as treatment failures due to relapse, recrudescence of hyponozoites or re-infections. Antigen loci are putatively under natural selection and may not be an optimal molecular marker to define parasite haplotypes in paired samples. Putatively neutral microsatellite loci, however, offer an assessment of neutral haplotypes. The objective here was to assess the utility of neutral microsatellite loci to reconcile cases of recurrent parasitaemia in Amazonian P. vivax populations in Peru. METHODS: Patient blood samples were collected from three locations in or around Iquitos in the Peruvian Amazon. Five putatively neutral microsatellite loci were characterized from 445 samples to ascertain the within and amongst population variation. A total of 30 day 0 and day of recurrent parasitaemia samples were characterized at microsatellite loci and five polymorphic antigen loci for haplotype classification. RESULTS: The genetic diversity at microsatellite loci was consistent with neutral levels of variation measured in other South American P. vivax populations. Results between antigen and microsatellite loci for the 30 day 0 and day of recurrent parasitaemia samples were the same for 80% of the pairs. The majority of non-concordant results were the result of differing alleles at microsatellite loci. This analysis estimates that 90% of the paired samples with the same microsatellite haplotype are unlikely to be due to a new infection. CONCLUSIONS: A population-level approach was used to yield a better estimate of the probability of a new infection versus relapse or recrudescence of homologous hypnozoites; hypnozoite activation was common for this cohort. Population studies are critical with the evaluation of genetic markers to assess P. vivax biology and epidemiology. The additional demonstration of microsatellite loci as neutral markers capable of distinguishing the origin of the recurrent parasites (new infection or originating from the patient) lends support to their use in assessment of treatment outcomes.
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spelling pubmed-39416852014-03-05 Genetic variation and recurrent parasitaemia in Peruvian Plasmodium vivax populations McCollum, Andrea M Soberon, Valeria Salas, Carola J Santolalla, Meddly L Udhayakumar, Venkatachalam Escalante, Ananias A Graf, Paul CF Durand, Salomon Cabezas, Cesar Bacon, David J Malar J Research BACKGROUND: Plasmodium vivax is a predominant species of malaria in parts of South America and there is increasing resistance to drugs to treat infections by P. vivax. The existence of latent hypnozoites further complicates the ability to classify recurrent infections as treatment failures due to relapse, recrudescence of hyponozoites or re-infections. Antigen loci are putatively under natural selection and may not be an optimal molecular marker to define parasite haplotypes in paired samples. Putatively neutral microsatellite loci, however, offer an assessment of neutral haplotypes. The objective here was to assess the utility of neutral microsatellite loci to reconcile cases of recurrent parasitaemia in Amazonian P. vivax populations in Peru. METHODS: Patient blood samples were collected from three locations in or around Iquitos in the Peruvian Amazon. Five putatively neutral microsatellite loci were characterized from 445 samples to ascertain the within and amongst population variation. A total of 30 day 0 and day of recurrent parasitaemia samples were characterized at microsatellite loci and five polymorphic antigen loci for haplotype classification. RESULTS: The genetic diversity at microsatellite loci was consistent with neutral levels of variation measured in other South American P. vivax populations. Results between antigen and microsatellite loci for the 30 day 0 and day of recurrent parasitaemia samples were the same for 80% of the pairs. The majority of non-concordant results were the result of differing alleles at microsatellite loci. This analysis estimates that 90% of the paired samples with the same microsatellite haplotype are unlikely to be due to a new infection. CONCLUSIONS: A population-level approach was used to yield a better estimate of the probability of a new infection versus relapse or recrudescence of homologous hypnozoites; hypnozoite activation was common for this cohort. Population studies are critical with the evaluation of genetic markers to assess P. vivax biology and epidemiology. The additional demonstration of microsatellite loci as neutral markers capable of distinguishing the origin of the recurrent parasites (new infection or originating from the patient) lends support to their use in assessment of treatment outcomes. BioMed Central 2014-02-24 /pmc/articles/PMC3941685/ /pubmed/24568141 http://dx.doi.org/10.1186/1475-2875-13-67 Text en Copyright © 2014 McCollum et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
McCollum, Andrea M
Soberon, Valeria
Salas, Carola J
Santolalla, Meddly L
Udhayakumar, Venkatachalam
Escalante, Ananias A
Graf, Paul CF
Durand, Salomon
Cabezas, Cesar
Bacon, David J
Genetic variation and recurrent parasitaemia in Peruvian Plasmodium vivax populations
title Genetic variation and recurrent parasitaemia in Peruvian Plasmodium vivax populations
title_full Genetic variation and recurrent parasitaemia in Peruvian Plasmodium vivax populations
title_fullStr Genetic variation and recurrent parasitaemia in Peruvian Plasmodium vivax populations
title_full_unstemmed Genetic variation and recurrent parasitaemia in Peruvian Plasmodium vivax populations
title_short Genetic variation and recurrent parasitaemia in Peruvian Plasmodium vivax populations
title_sort genetic variation and recurrent parasitaemia in peruvian plasmodium vivax populations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941685/
https://www.ncbi.nlm.nih.gov/pubmed/24568141
http://dx.doi.org/10.1186/1475-2875-13-67
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