4.5 Article

Temporal Changes in the Genetic Diversity of Plasmodium vivax Merozoite Surface Protein-1 in Myanmar

Journal

PATHOGENS
Volume 10, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/pathogens10080916

Keywords

Plasmodium vivax; merozoite surface protein-1; Myanmar; genetic diversity

Categories

Funding

  1. National Research Foundation of Korea (NRF) - Korean Government [2019K1A3A9A01000005]
  2. NRF - Korean government (MSIT) [2018M3A9H5055614]
  3. National Research Foundation of Korea [2019K1A3A9A01000005, 2018M3A9H5055614] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Despite a significant decline in malaria incidence in Myanmar, malaria remains a major public health concern. Recent years have seen an increase in genetic diversity of Plasmodium vivax population, attributed to accumulated mutations and recombination. Continuous molecular surveillance of genetic variation in Myanmar's P. vivax is necessary to monitor the ongoing genetic expansion.
Despite a significant decline in the incidence of malaria in Myanmar recently, malaria is still an important public health concern in the country. Although Plasmodium falciparum is associated with the highest incidence of malaria in Myanmar, the proportion of P. vivax cases has shown a gradual increase in recent years. The genetic diversity of P. vivax merozoite surface protein-1 block 5-6 (pvmsp-1 ICB 5-6) in the P. vivax population of Myanmar was analyzed to obtain a comprehensive insight into its genetic heterogeneity and evolutionary history. High levels of genetic diversity of pvmsp-1 ICB 5-6 were identified in the P. vivax isolates collected from Myanmar between 2013 and 2015. Thirty-nine distinct haplotypes of pvmsp-1 ICB 5-6 (13 for Sal I type, 20 for recombinant type, and 6 for Belem type) were found at the amino acid level. Comparative analyses of the genetic diversity of pvmsp-1 ICB 5-6 sequences in the recent (2013-2015) and the past (2004) P. vivax populations in Myanmar revealed genetic expansion of the pvmsp-1 ICB 5-6 in recent years, albeit with a declined incidence. The recent increase in the genetic heterogeneity of Myanmar pvmsp-1 ICB 5-6 is attributed to a combination of factors, including accumulated mutations and recombination. These results suggest that the size of the P. vivax population in Myanmar is sufficient to enable the generation and maintenance of genetic diversity, warranting continuous molecular surveillance of genetic variation in Myanmar P. vivax.

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