Abstract

Plasmodium falciparum isolates from China–Myanmar border (CMB) have experienced regional special selective pressures and adaptive evolution. However, the genomes of P. falciparum isolates from this region to date are poorly characterized. Herein, we performed whole-genome sequencing of 34 P. falciparum isolates from CMB and a series of genome-wide sequence analyses to reveal their genetic diversity, population structures, and comparisons with the isolates from other epidemic regions (Thai–Cambodia border, Thai–Myanmar border, and West Africa). Totally 59,720 high-quality single-nucleotide polymorphisms (SNPs) were identified in the P. falciparum isolates from CMB, with average nucleotide diversity (π = 4.59 × 10−4) and LD decay (132 bp). The Tajima’s D and Fu and Li’s D values of the CMB isolates were −0.8 (p < 0.05) and −0.84 (p < 0.05), respectively, suggesting a demographic history of recent population expansion or purifying selection. Moreover, 78 genes of the parasite were identified that could be under positive selection, including those genes conferring drug resistance such as pfubp1. In addition, 33 SNPs were identified for tracing the source of the parasites with a high accuracy by analysis of the most differential SNPs among the four epidemic regions. Collectively, our data demonstrated high diversity of the CMB isolates’ genomes forming a distinct population, and the identification of 33-SNP barcode provides a valuable surveillance of parasite migration among the regions.

Highlights

  • The global malaria burden caused by Plasmodium falciparum has been substantially reduced since the artemisinin-based combination therapies were recommended as first-line antimalarial drugs for treatment of falciparum malaria in all the endemic regions

  • We identified a total of 59,720 high-quality single-nucleotide polymorphisms (SNPs) from the China–Myanmar border (CMB) isolates, representing a density of one SNP every 390 bp

  • We investigated the genetic diversity among the P. falciparum isolates from different regions worldwide, including WAF (n = 40), Thai–Cambodia border (TCB) (n = 60), and TMB (n = 40) through obtaining their genome sequence data from European Nucleotide Archive (ENA)

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Summary

Introduction

The global malaria burden caused by Plasmodium falciparum has been substantially reduced since the artemisinin-based combination therapies were recommended as first-line antimalarial drugs for treatment of falciparum malaria in all the endemic regions. The number of imported malaria cases has been continuously increasing in China due to the increasing international exchange activities, especially in the border regions. In the malaria-free areas, tracing the origins of new malaria infections (local or imported) is pivotal to the maintenance of malaria-free zones and prompt responses to the individual cases, interrupting the parasites transmission cycle, and, to disease eradication. Analysis of genetic diversity and population structure of P. falciparum should provide a fundamental basis for developing tools to trace the origins of new malaria infections in malaria-free zones

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