Simple jQuery Dropdowns
Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/43779
Title: Plasmodium vivax genetic diversity and heterozygosity in blood samples and resulting oocysts at the Thai–Myanmar border
Authors: Ingfar Soontarawirat
Andolina, Chiara
Paul, Richard
Day, Nicholas P. J.
Nosten, Francois
Woodrow, Charles J.
Mallika Imwong
Mahidol University. Faculty of Tropical Medicine. Department of Clinical Tropical Medicine
Mahidol University. Faculty of Tropical Medicine. Shoklo Malaria Research Unit
Mahidol University. Faculty of Tropical Medicine. Mahidol Oxford Research Unit
Mahidol University. Faculty of Tropical Medicine. Department of Molecular Tropical Medicine and Genetics
Keywords: Relapse;Plasmodium vivax;Oocyst;Meiosis;Genetic diversity
Issue Date: 2017
Citation: Malaria Journal. vol.16, No. 1 (2017), 355
Abstract: Background: Polyclonal blood-stage infections of Plasmodium vivax are frequent even in low transmission settings, allowing meiotic recombination between heterologous parasites. Empirical data on meiotic products are however lacking. This study examined microsatellites in oocysts derived by membrane feeding of mosquitoes from bloodstage P. vivax infections at the Thai–Myanmar border. Methods: Blood samples from patients presenting with vivax malaria were fed to Anopheles cracens by membrane feeding and individual oocysts from midguts were obtained by dissection after 7 days. DNA was extracted from oocysts and parental blood samples and tested by microsatellite analysis. Results: A focused study of eight microsatellite markers was undertaken for nine blood stage infections from 2013, for which derived oocysts were studied in six cases. One or more alleles were successfully amplifed for 131 oocysts, revealing high levels of allelic diversity in both blood and oocyst stages. Based on standard criteria for defning minor alleles, there was evidence of clear deviation from random mating (inbreeding) with relatively few heterozygous oocysts compared to variance across the entire oocyst population (FIT = 0.89). The main explanation appeared to be natural compartmentalisation at mosquito (FSC = 0.27) and human stages (FCT = 0.68). One single human case produced a total of 431 successfully amplifed loci (across 70 oocysts) that were homozygous and identical to parental alleles at all markers, indicating clonal infection and transmission. Heterozygous oocyst alleles were found at 15/176 (8.5%) successfully amplifed loci in the other fve cases. There was apparently reduced oocyst heterozygosity in individual oocysts compared to diversity within individual mosquitoes (FIS = 0.55), but this may simply refect the diffculty of detecting minor alleles in oocysts, given the high rate of amplifcation failure. Inclusion of minor allele peaks (irrespective of height) when matching peaks were found in related blood or oocyst samples, added 11 minor alleles for 9 oocysts, increasing the number of heterozygous loci to 26/176 (14.8%; p = 0.096). Conclusion: There was an apparently low level of heterozygous oocysts but this can be explained by a combination of factors: relatively low complexity of parental infection, natural compartmentalisation in humans and mosquitoes, and the methodological challenge of detecting minor alleles.
URI: http://repository.li.mahidol.ac.th/dspace/handle/123456789/43779
metadata.dc.identifier.url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584506/pdf/12936_2017_Article_2002.pdf
Appears in Collections:TM-Article

Files in This Item:
File Description SizeFormat 
tm-ar-mallika-2017-1.pdf1.55 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.