Abstract

BackgroundPlasmodium vivax is transmitted by members of the Anopheles Hyrcanus Group that includes six species in the Republic of Korea: Anopheles sinensis sensu stricto (s.s.), Anopheles pullus, Anopheles kleini, Anopheles belenrae, Anopheles lesteri, and Anopheles sineroides. Individual Anopheles species within the Hyrcanus Group demonstrate differences in their geographical distributions, vector competence and insecticide resistance, making it crucial for accurate species identification. Conventional species identification conducted using individual genotyping (or barcoding) based on species-specific molecular markers requires extensive time commitment and financial resources.ResultsA population-based quantitative sequencing (QS) protocol developed in this study provided a rapid estimate of species composition ratios among pooled mosquitoes as a cost-effective alternative to individual genotyping. This can be accomplished by using species- or group-specific nucleotide sequences of the mitochondrial cytochrome C oxidase subunit I (COI) and the ribosomal RNA internal transcribed spacer 2 (ITS2) region as species identification alleles in a two-step prediction protocol. Standard genomic DNA fragments of COI and ITS2 genes were amplified from each Anopheles species using group-specific universal primer sets. Following sequencing of the COI or ITS2 amplicons generated from sets of standard DNA mixtures, equations were generated via linear regression to predict species-specific nucleotide sequence frequencies at different positions. Species composition ratios between An. sineroides, An. pullus and An. lesteri were estimated from QS of the COI amplicons based on the mC.260A, mC.122C and mC.525C alleles at the first step, followed by the prediction of species composition ratios between An. sinensis, An. kleini and An. belenrae based on QS of the ITS2 amplicons using the rI.370G and rI.389T alleles. The COI copy number was not significantly different between species, suggesting the reliability of COI-based prediction. In contrast, ITS2 showed a slightly but significantly higher copy number in An. belenrae, requiring an adjustment of its predicted composition ratio. A blind test proved that predicted species composition ratios either from pooled DNA specimens or pooled mosquito specimens were not statistically different from the actual values, demonstrating that the QS-based prediction is accurate and reliable.ConclusionsThis two-step prediction protocol will facilitate rapid estimation of the species composition ratios in field-collected Anopheles Hyrcanus Group populations and is particularly useful for studying the vector ecology of Anopheles population and epidemiology of malaria.

Highlights

  • Plasmodium vivax is transmitted by members of the Anopheles Hyrcanus Group that includes six spe‐ cies in the Republic of Korea: Anopheles sinensis sensu stricto (s.s.), Anopheles pullus, Anopheles kleini, Anopheles belenrae, Anopheles lesteri, and Anopheles sineroides

  • Phylogenetic tree of collected specimens Based on the C oxidase subunit I (COI) phylogenetic tree, An. sineroides, An. pullus, and An. lesteri were clearly divided into separate clusters, whereas An. sinensis, An. kleini, and An. belenrae were clustered into a large monophyletic cluster (Additional file 4)

  • Search for species‐specific loci in COI and internal transcribed spacer 2 (ITS2) The results of COI and ITS2 sequence alignment were organized with different color codes for each species (Additional files 6, 7)

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Summary

Introduction

Plasmodium vivax is transmitted by members of the Anopheles Hyrcanus Group that includes six spe‐ cies in the Republic of Korea: Anopheles sinensis sensu stricto (s.s.), Anopheles pullus, Anopheles kleini, Anopheles belenrae, Anopheles lesteri, and Anopheles sineroides. Individual Anopheles species within the Hyrcanus Group demonstrate dif‐ ferences in their geographical distributions, vector competence and insecticide resistance, making it crucial for accu‐ rate species identification. Species identification is important because individual species within the Hyrcanus Group overlap geographically and demonstrate differences in their seasonal distributions, vector competence, and insecticide resistance [3,4,5]. An. kleini, and An. lesteri are primary vectors of Plasmodium vivax in the ROK, whereas An. pullus, An. belenrae, and An. sinensis are poor vectors [3,4,5]. Information on the abundance of Hyrcanus Group member species in areas of likely malaria transmission is crucial for understanding the population dynamics of vector populations and epidemiology of malaria for the development and implementation of an efficient vector management strategies

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