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      The origins and relatedness structure of mixed infections vary with local prevalence of P. falciparum malaria

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          Abstract

          Individual malaria infections can carry multiple strains of Plasmodium falciparum with varying levels of relatedness. Yet, how local epidemiology affects the properties of such mixed infections remains unclear. Here, we develop an enhanced method for strain deconvolution from genome sequencing data, which estimates the number of strains, their proportions, identity-by-descent (IBD) profiles and individual haplotypes. Applying it to the Pf3k data set, we find that the rate of mixed infection varies from 29% to 63% across countries and that 51% of mixed infections involve more than two strains. Furthermore, we estimate that 47% of symptomatic dual infections contain sibling strains likely to have been co-transmitted from a single mosquito, and find evidence of mixed infections propagated over successive infection cycles. Finally, leveraging data from the Malaria Atlas Project, we find that prevalence correlates within Africa, but not Asia, with both the rate of mixed infection and the level of IBD.

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          Most cited references39

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          Analysis of Plasmodium falciparum diversity in natural infections by deep sequencing

          Malaria elimination strategies require surveillance of the parasite population for genetic changes that demand a public health response, such as new forms of drug resistance. 1,2 Here we describe methods for large-scale analysis of genetic variation in Plasmodium falciparum by deep sequencing of parasite DNA obtained from the blood of patients with malaria, either directly or after short term culture. Analysis of 86,158 exonic SNPs that passed genotyping quality control in 227 samples from Africa, Asia and Oceania provides genome-wide estimates of allele frequency distribution, population structure and linkage disequilibrium. By comparing the genetic diversity of individual infections with that of the local parasite population, we derive a metric of within-host diversity that is related to the level of inbreeding in the population. An open-access web application has been established for exploration of regional differences in allele frequency and of highly differentiated loci in the P. falciparum genome.
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            Multiple populations of artemisinin-resistant Plasmodium falciparum in Cambodia

            We describe an analysis of genome variation in 825 Plasmodium falciparum samples from Asia and Africa that reveals an unusual pattern of parasite population structure at the epicentre of artemisinin resistance in western Cambodia. Within this relatively small geographical area we have discovered several distinct but apparently sympatric parasite subpopulations with extremely high levels of genetic differentiation. Of particular interest are three subpopulations, all associated with clinical resistance to artemisinin, which have skewed allele frequency spectra and remarkably high levels of haplotype homozygosity, indicative of founder effects and recent population expansion. We provide a catalogue of SNPs that show high levels of differentiation in the artemisinin-resistant subpopulations, including codon variants in various transporter proteins and DNA mismatch repair proteins. These data provide a population genetic framework for investigating the biological origins of artemisinin resistance and for defining molecular markers to assist its elimination.
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              Is Open Access

              Global Epidemiology of Plasmodium vivax

              Plasmodium vivax is the most widespread human malaria, putting 2.5 billion people at risk of infection. Its unique biological and epidemiological characteristics pose challenges to control strategies that have been principally targeted against Plasmodium falciparum. Unlike P. falciparum, P. vivax infections have typically low blood-stage parasitemia with gametocytes emerging before illness manifests, and dormant liver stages causing relapses. These traits affect both its geographic distribution and transmission patterns. Asymptomatic infections, high-risk groups, and resulting case burdens are described in this review. Despite relatively low prevalence measurements and parasitemia levels, along with high proportions of asymptomatic cases, this parasite is not benign. Plasmodium vivax can be associated with severe and even fatal illness. Spreading resistance to chloroquine against the acute attack, and the operational inadequacy of primaquine against the multiple attacks of relapse, exacerbates the risk of poor outcomes among the tens of millions suffering from infection each year. Without strategies accounting for these P. vivax-specific characteristics, progress toward elimination of endemic malaria transmission will be substantially impeded.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Role: Senior Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                12 July 2019
                2019
                : 8
                : e40845
                Affiliations
                [1 ]deptBig Data Institute, Li Ka Shing Centre for Health Information and Discovery University of Oxford OxfordUnited Kingdom
                [2 ]deptWellcome Centre for Human Genetics University of Oxford OxfordUnited Kingdom
                [3 ]deptMedical Research Council Centre for Genomics and Global Health University of Oxford OxfordUnited Kingdom
                [4 ]Wellcome Sanger Institute HinxtonUnited Kingdom
                McGill University Canada
                McGill University Canada
                McGill University Canada
                Harvard School of Public Health United States
                University of California, San Francisco United States
                Broad Institute United States
                Author notes
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0001-7566-2787
                https://orcid.org/0000-0003-4164-3179
                https://orcid.org/0000-0002-0595-7333
                https://orcid.org/0000-0002-7386-3566
                https://orcid.org/0000-0002-5012-4162
                Article
                40845
                10.7554/eLife.40845
                6684230
                31298657
                6b92ef41-6d9e-40b4-bee5-4548991391a2
                © 2019, Zhu et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 09 August 2018
                : 10 July 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100004440, Wellcome;
                Award ID: 206194
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100004440, Wellcome;
                Award ID: 090770
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100004440, Wellcome;
                Award ID: 100956/Z/13/Z
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100007421, Li Ka Shing Foundation;
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100004440, Wellcome;
                Award ID: 204911
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000265, Medical Research Council;
                Award ID: G0600718
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000278, Department for International Development;
                Award ID: M006212
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Tools and Resources
                Epidemiology and Global Health
                Microbiology and Infectious Disease
                Custom metadata
                Variation in the rate of mixed infections by malaria parasites and the relatedness structure among infecting strains reveals diversity in local epidemiological processes.

                Life sciences
                malaria,genome,epidemiology,relatedness,p. falciparum
                Life sciences
                malaria, genome, epidemiology, relatedness, p. falciparum

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