Abstract

Plasmodium ovale curtisi and Plasmodium ovale wallikeri are two sympatric human malaria species prevalent in Africa, Asia and Oceania. The reported prevalence of both P. ovale spp. was relatively low compared to other malaria species, but more sensitive molecular detection techniques have shown that asymptomatic low-density infections are more common than previously thought. Whole genome sequencing of both P. ovale spp. revealed genetic dissociation between P. ovale curtisi and P. ovale wallikeri suggesting a species barrier. In this study we further evaluate such a barrier by assessing polymorphisms in the genes of three vaccine candidate surface protein: circumsporozoite protein/ thrombospondin-related anonymous-related protein (ctrp), circumsporozoite surface protein (csp) and merozoite surface protein 1 (msp1). The complete coding sequence of ctrp and csp, and a partial fragment of msp1 were isolated from 25 P. ovale isolates and compared to previously reported reference sequences. A low level of nucleotide diversity (Pi = 0.02–0.10) was observed in all three genes. Various sizes of tandem repeats were observed in all ctrp, csp and msp1 genes. Both tandem repeat unit and nucleotide polymorphism in all three genes exhibited clear dimorphism between P. ovale curtisi and P. ovale wallikeri, supporting evidence of non-recombination between these two species.

Highlights

  • A semi-nested PCR of potra gene was performed with a primer specific to both P. ovale spp. (PoTRA-F/PoTRA rev3) in the primary reaction and with specific P. ovale curtisi (PoTRA-F/ PocTRA-R) and P. ovale wallikeri (PoTRA-F/PowTRA-R) primers in the secondary reaction [23]

  • The complete coding sequence of poctrp gene was obtained from 11 P. ovale curtisi and 14 P. ovale wallikeri isolates

  • Sequence alignment of these 25 poctrp sequences, together with another two poctrp sequences available in the NCBI database, and other ctrp sequences from the other Plasmodium spp. that infect humans, showed that poctrp is composed of a signal peptide, six vWA domains, seven TSP1 domains, transmembrane domain, and a cytoplasmic region (Fig 1)

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Summary

Introduction

Plasmodium ovale curtisi and Plasmodium ovale walllikeri are two sympatric species of malaria parasites found across many malaria endemic countries in Africa, Asia and Oceania [1,2,3]. Genetic dissociation of Plasmodium ovale curtisi and Plasmodium ovale wallikeri study design, data collection and analysis, decision to publish, or preparation of the manuscript

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