Evidence map›Paper›PMID 40016697›Full record

ArticleMalaria journal2025

Genetic polymorphisms of Plasmodium vivax transmission-blocking vaccine candidates Pvs48/45 and Pvs47 in Thailand.

Jiraporn Kuesap, Nutnicha Suphakhonchuwong, Benyapa Eksonthi, Saranchana Huaihongthong

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Article in Malaria journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Jiraporn KuesapFaculty of Allied Health Sciences, Thammasat University, 99 Moo 18 Khlong Nueng, Khlong Luang, Pathumthani, 12120, Thailand. jirajira28@yahoo.com.
Nutnicha SuphakhonchuwongFaculty of Allied Health Sciences, Thammasat University, 99 Moo 18 Khlong Nueng, Khlong Luang, Pathumthani, 12120, Thailand.
Benyapa EksonthiFaculty of Allied Health Sciences, Thammasat University, 99 Moo 18 Khlong Nueng, Khlong Luang, Pathumthani, 12120, Thailand.
Saranchana HuaihongthongFaculty of Allied Health Sciences, Thammasat University, 99 Moo 18 Khlong Nueng, Khlong Luang, Pathumthani, 12120, Thailand.

Funding

Thailand Science Research and Innovation Fundamental Fund fiscal year 2023 TUFF75/2566
6 · The paper itself

Abstract

backgroundThe genetic diversity of malaria parasites varies between regions in the world. The genetic polymorphisms of the genes Pvs48/45 and Pvs47 which encode gametocyte/gamete proteins of Plasmodium vivax, were studied because of their potential as transmission-blocking vaccine (TBV) targets. The aim of the present study was to investigate the genetic diversity of Pvs48/45 and Pvs47 in clinical isolates from endemic areas of Thailand.

methodsPlasmodium vivax samples collected from four provinces neighbouring either Myanmar or Malaysia were analysed using polymerase chain reaction and nucleotide sequencing.  

resultsFifteen and 18 amino acid substitutions were observed in 36 Pvs48/45 and 62 Pvs47 deduced amino acid sequences, respectively. Eleven haplotypes were identified in Pvs48/45 and 26 in Pvs47. Overall, low nucleotide diversities were observed for Pvs48/45 (π = 0.00104) and Pvs47 (π = 0.00321). Tajima's D, and Fu and Li's D* and F* values were negative for both genes, Pvs48/45 and Pvs47 while a significant difference was found in Pvs48/45 (P < 0.05).

conclusionThe limited polymorphism of the two investigated TBV candidate antigens observed in this study is consistent with findings in worldwide isolates. The collected genetic diversity data could be helpful for developing effective TBVs in malaria-endemic areas.

Indexed as

Antigens, ProtozoanMalaria VaccinesMalaria, VivaxPlasmodium vivaxPolymorphism, GeneticProtozoan ProteinsAmino Acid SubstitutionHumansSequence Analysis, DNAThailandAntigens, ProtozoanMalaria VaccinesProtozoan ProteinsGenetic polymorphismPlasmodium vivaxPvs47Pvs48/45Transmission-blocking vaccine

Identifiers

PMID40016697
PMCPMC11866859

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