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Prediction of species composition ratios in pooled specimens of the Anopheles Hyrcanus group using quantitative sequencing

DC Field Value Language
dc.contributor.authorLee, Do Eun-
dc.contributor.authorKim, Heung-Chul-
dc.contributor.authorChong, Sung-Tae-
dc.contributor.authorKlein, Terry A.-
dc.contributor.authorKim, Ju Hyeon-
dc.contributor.authorLee, Si Hyeok-
dc.date.accessioned2021-08-25T01:55:02Z-
dc.date.available2021-08-25T10:59:06Z-
dc.date.issued2021-08-06-
dc.identifier.citationMalaria Journal. 2021 Aug 06;20(1):338ko_KR
dc.identifier.issn1475-2875-
dc.identifier.urihttps://hdl.handle.net/10371/174835-
dc.description.abstractBackground

Plasmodium 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.

Results
A 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.

Conclusions
This 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.
ko_KR
dc.description.sponsorshipThis research was supported by the Government-wide R&D Fund project for infectious disease research (GFID), Republic of Korea (Grant Number: HG18C0046) and the Armed Forces Health Surveillance Branch, Global Emerg‑ing Infections Surveillance and Response System (AFHSB-GEIS), Silver Spring, MD (ProMIS ID #P0131-20-ME-03). DE Lee was supported in part by Brain
Korea 21 Plus Program.
ko_KR
dc.language.isoenko_KR
dc.publisherBMCko_KR
dc.subjectAnopheles Hyrcanus Group-
dc.subjectSpecies composition-
dc.subjectCOI-
dc.subjectITS2-
dc.subjectQuantitative sequencing-
dc.titlePrediction of species composition ratios in pooled specimens of the Anopheles Hyrcanus group using quantitative sequencingko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor이도은-
dc.contributor.AlternativeAuthor김흥철-
dc.contributor.AlternativeAuthor김주현-
dc.contributor.AlternativeAuthor이시혁-
dc.identifier.doi10.1186/s12936-021-03868-y-
dc.citation.journaltitleMalaria Journalko_KR
dc.language.rfc3066en-
dc.rights.holderThe Author(s)-
dc.date.updated2021-08-08T03:29:43Z-
dc.citation.number1ko_KR
dc.citation.startpage338ko_KR
dc.citation.volume20ko_KR
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