Abstract

Large-scale molecular epidemiologic studies of Plasmodium falciparum parasites have provided insights into parasite biology and transmission, can identify the spread of drug resistance, and are useful in assessing vaccine targets. The polyclonal nature infections in high transmission settings is problematic for traditional genotyping approaches. Next-generation sequencing (NGS) approaches to parasite genotyping allow sensitive detection of minority variants, disaggregation of complex parasite mixtures, and scalable processing of large samples sets. Therefore, we designed, validated, and applied to field parasites an approach that leverages sequencing of individually barcoded samples in a multiplex manner. We utilize variant barcodes, invariant linker sequences and modular template-specific primers to allow for the simultaneous generation of high-dimensional sequencing data of multiple gene targets. This modularity permits a cost-effective and reproducible way to query many genes at once. In mixtures of reference parasite genomes, we quantitatively detected unique haplotypes comprising as little as 2% of a polyclonal infection. We applied this genotyping approach to field-collected parasites collected in Western Kenya in order to simultaneously obtain parasites genotypes at three unlinked loci. In summary, we present a rapid, scalable, and flexible method for genotyping individual parasites that enables molecular epidemiologic studies of parasite evolution, population structure and transmission.

Highlights

  • T diversity at the same nucleotides in multiple parasites within individual patients[14,16]

  • next generation sequencing (NGS) approaches to parasite genotyping allow for the sensitive detection of minority variants, disaggregation of complex parasite mixtures, and scalable processing of large sample sets

  • We designed, validated, and applied an overlap extension barcoding and multiplexing NGS approach to parasite genotyping that leverages NGS of individually barcoded samples in a scalable, modular, and multiplex manner

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Summary

Introduction

T diversity at the same nucleotides in multiple parasites within individual patients[14,16]. We designed, validated, and applied an overlap extension barcoding and multiplexing protocol followed by NGS that permits the rapid and parallel sequencing of multiple polyclonal parasite gene targets in individual infections. Using this approach, we simultaneously genotype P. falciparum population genetic markers for population structure, drug resistance, and vaccine-resistance in both control and field-collected DNA samples from Western Kenya. We simultaneously genotype P. falciparum population genetic markers for population structure, drug resistance, and vaccine-resistance in both control and field-collected DNA samples from Western Kenya This modular, multiplex and quantitative approach to P. falciparum genotyping allows for estimation of allele frequencies and haplotypes in multiple gene targets within complex polyclonal P. falciparum parasitemias. Our approach has the potential to improve both routine surveillance and research studies

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