Abstract

In the southern Pacific coast of Chiapas, Mexico (SM), the two most abundant vector species, Nyssorhynchus albimanus and Anopheles pseudopunctipennis, were susceptible to different Plasmodium vivax Pvs25/28 haplotypes. To broaden our understanding of the existing P. vivax in the area, genes encoding proteins relevant for ookinete development and the 18S rRNA were studied. P. vivax infectivity (percentage of infected mosquitoes and oocyst numbers) was evaluated by simultaneously feeding infected blood samples from patients to Ny. albimanus and An. pseudopunctipennis female mosquitoes. Three infectivity patterns were identified: one group of parasites were more infective to An. pseudopunctipennis than to Ny. albimanus, another group was more infective to Ny. albimanus, while a third group infected both vectors similarly. In 29 parasite isolates, the molecular variations of ookinete-specific genes and the 18S rRNA-type S were analyzed. Using concatenated sequences, phylogenetic trees, and Structure analysis, parasite clustering within SM isolates and between these and those from other geographical origins were investigated. A ML phylogenetic tree resolved two parasite lineages: PvSM-A and PvSM-B. They were associated to a different 18S rRNA variant. PvSM-A parasites had 18S rRNA variant rV2 and correspond to parasites causing high oocyst infection in Ny. albimanus. A new ML tree and Structure analysis, both comprising global sequences, showed PvSM-A clustered with Latin American parasites. Meanwhile, all isolates of PvSM-B had 18S rRNA variant rV1 and remained as unique genetic cluster comprising two subgroups: PvSM-Ba, producing high infection in An. pseudopunctipennis, and PvSM-Bb, causing similar oocyst infection in both vector species. PvSM-A parasites were genetically similar to parasites from South America. Meanwhile, PvSM-B were exclusive to southern Mexico and share ancestry with Asian parasites. The results suggest that these lineages evolved separately, likely by geographic and vector restriction.

Highlights

  • Plasmodium vivax causes more than 70% of malaria cases in America [Pan American Health Organization (PAHO), 2016]

  • Our results showed a polymorphism at Circumsporozoite and Thrombospondin-Related Adhesive Protein (CTRP) and Secreted Ookinete Adhesive Protein (SOAP), and an association of the 18S 18S small subunit ribosomal RNA type S (rRNA) variants to Pvs25 and Pvs28 variants, and to the PvSM-A and PvSM-B parasite lineages

  • Based on genes located at different chromosomes that code for surface and microneme proteins from the ookinete stage along with ribosomal rRNA variants, our findings highlight the presence of two P. vivax lineages in southern Mexico

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Summary

Introduction

Plasmodium vivax causes more than 70% of malaria cases in America [Pan American Health Organization (PAHO), 2016]. At least 10 species of the family Culicidae transmit malaria in this continent. For P. vivax, two 18S rRNA variants have been detected at different geographical sites (Prajapati et al, 2011); variant rV2, present in the Sal I reference strain, occurs in Central America. These parasites are highly infective to local Ny. albimanus; while Asian parasites expressing a different variant (rV1) produced low infections in this vector (Li et al, 2001)

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