Abstract

BackgroundThe reservoir of Plasmodium infection in humans has traditionally been defined by blood slide positivity. This study was designed to characterize the local reservoir of infection in relation to the diverse var genes that encode the major surface antigen of Plasmodium falciparum blood stages and underlie the parasite's ability to establish chronic infection and transmit from human to mosquito.Methodology/Principal FindingsWe investigated the molecular epidemiology of the var multigene family at local sites in Gabon, Senegal and Kenya which differ in parasite prevalence and transmission intensity. 1839 distinct var gene types were defined by sequencing DBLα domains in the three sites. Only 76 (4.1%) var types were found in more than one population indicating spatial heterogeneity in var types across the African continent. The majority of var types appeared only once in the population sample. Non-parametric statistical estimators predict in each population at minimum five to seven thousand distinct var types. Similar diversity of var types was seen in sites with different parasite prevalences.Conclusions/Significance Var population genomics provides new insights into the epidemiology of P. falciparum in Africa where malaria has never been conquered. In particular, we have described the extensive reservoir of infection in local African sites and discovered a unique var population structure that can facilitate superinfection through minimal overlap in var repertoires among parasite genomes. Our findings show that var typing as a molecular surveillance system defines the extent of genetic complexity in the reservoir of infection to complement measures of malaria prevalence. The observed small scale spatial diversity of var genes suggests that var genetics could greatly inform current malaria mapping approaches and predict complex malaria population dynamics due to the import of var types to areas where no widespread pre-existing immunity in the population exists.

Highlights

  • Hundreds of millions of Plasmodium falciparum infections persist for many months in the human population to sustain malaria transmission where anopheline mosquito vectors are only seasonally available

  • We measured depth of var gene sampling in each population with a cumulative diversity curve [17] depicting the rate at which new var types were identified with the collection of unique sequences from each isolate

  • Success towards elimination would be monitored by measuring reductions in malaria transmission intensity using both entomological inoculation rate (EIR) [7] and antigenspecific serological methods [39]

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Summary

Introduction

Hundreds of millions of Plasmodium falciparum infections persist for many months in the human population to sustain malaria transmission where anopheline mosquito vectors are only seasonally available. These chronic, largely undetected, infections constitute the reservoir of infection and serve to fuel continued malaria transmission. Density-dependent regulation of parasitemia has been shown to occur among Plasmodium spp and genotypes in coinfected semi-immune children [3] Considering these infection dynamics, the parasite rate (prevalence) as defined by blood slide positivity does not accurately describe the complexity of the reservoir of infection and yet remains the mainstay for monitoring and evaluating malaria control [7]. This study was designed to characterize the local reservoir of infection in relation to the diverse var genes that encode the major surface antigen of Plasmodium falciparum blood stages and underlie the parasite’s ability to establish chronic infection and transmit from human to mosquito

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