Abstract

BackgroundMexico advanced to the pre-elimination phase in 2009 due to a significant reduction in malaria cases, and since 2000, Plasmodium vivax is the only species transmitted. During the last two decades, malaria transmission has been mostly local and isolated to a few regions. It is important to gain further insights into the impact of control measures on the parasite population structure. Hence, the aim of the current study was to determine detailed changes in P. vivax genetic diversity and population structure based on analysing the gene that encodes the apical membrane antigen 1 (pvama1). This analysis covered from control to pre-elimination (1993–2011) in a hypo-endemic region in southern Mexico.ResultsThe 213 pvama1I-II sequences presently analysed were grouped into six periods of three years each. They showed low genetic diversity, with 15 haplotypes resolved. Among the DNA sequences, there was a gradual decrease in genetic diversity, the number of mixed genotype infections and the intensity of positive selection, in agreement with the parallel decline in malaria cases. At the same time, linkage disequilibrium (R2) increased. The three-dimensional haplotype network revealed that pvama1I-II haplotypes were separated by 1–11 mutational steps, and between one another by 0–3 unsampled haplotypes. In the temporal network, seven haplotypes were detected in at least two of the six-time layers, and only four distinct haplotypes were evidenced in the pre-elimination phase. Structure analysis indicated that three subpopulations fluctuated over time. Only 8.5% of the samples had mixed ancestry. In the pre-elimination phase, subpopulation P1 was drastically reduced, and the admixture was absent.ConclusionsThe results suggest that P. vivax in southern Mexico evolved based on local adaptation into three “pseudoclonal” subpopulations that diversified at the regional level and persisted over time, although with varying frequency. Control measures and climate events influenced the number of malaria cases and the genetic structure. The sharp decrease in parasite diversity and other related genetic parameters during the pre-elimination phase suggests that malaria elimination is possible in the near future. These results are useful for epidemiological surveillance.

Highlights

  • Mexico advanced to the pre-elimination phase in 2009 due to a significant reduction in malaria cases, and since 2000, Plasmodium vivax is the only species transmitted

  • Patients lived in Jurisdiction VII of the State of Chiapas in Mexico, which comprises an area of 4644.07 km2 of tropical and template regions, with the altitude ranging from sea level to foothills up to 4,000 m above sea level

  • Plasmodium vivax ama1I-II from southern Mexico, 1993–2011 Polymorphism and mixed genotype infections (MGI) One hundred and seventy-eight pvama1I-II sequences comprising a fragment of 702 bp were obtained from 176 parasite isolates; eighty-four percent (n = 89) of whole blood samples, and only

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Summary

Introduction

Mexico advanced to the pre-elimination phase in 2009 due to a significant reduction in malaria cases, and since 2000, Plasmodium vivax is the only species transmitted. The aim of the current study was to determine detailed changes in P. vivax genetic diversity and population structure based on analysing the gene that encodes the apical membrane antigen 1 (pvama). The aim of the current study was to determine detailed changes in P. vivax genetic diversity and population structure based on analysing the gene that encodes the apical membrane antigen 1 (pvama1) This analysis covered from control to pre-elimination (1993–2011) in a hypo-endemic region in southern Mexico. Plasmodium vivax is the most prevalent malaria species in Latin America, the Middle East, South and Southeast Asia, Oceania and The Horn of Africa [1] In these regions, more than 2.5 billion people are at risk [1], and approximately 13.8 million cases were reported in 2014 [2]. In the former case, along the Mexican side of the border is the State of Chiapas, and transmission occurs at the pacific side and in the Lacandon rainforest [3, 4]

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