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Utility of Plasmodium falciparum DNA from rapid diagnostic test kits for molecular analysis and whole genome amplification

BACKGROUND: Rapid diagnostic tests (RDTs) have become the most common diagnostic tool for detection of Plasmodium falciparum malaria, in particular in remote areas. RDT blood spots provide a source of parasite DNA for molecular analysis. In this study, the utility of RDTs for molecular analysis and...

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Autores principales: Srisutham, Suttipat, Suwannasin, Kanokon, Mathema, Vivek Bhakta, Sriprawat, Kanlaya, Smithuis, Frank M., Nosten, Francois, White, Nicholas J., Dondorp, Arjen M., Imwong, Mallika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251736/
https://www.ncbi.nlm.nih.gov/pubmed/32460780
http://dx.doi.org/10.1186/s12936-020-03259-9
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author Srisutham, Suttipat
Suwannasin, Kanokon
Mathema, Vivek Bhakta
Sriprawat, Kanlaya
Smithuis, Frank M.
Nosten, Francois
White, Nicholas J.
Dondorp, Arjen M.
Imwong, Mallika
author_facet Srisutham, Suttipat
Suwannasin, Kanokon
Mathema, Vivek Bhakta
Sriprawat, Kanlaya
Smithuis, Frank M.
Nosten, Francois
White, Nicholas J.
Dondorp, Arjen M.
Imwong, Mallika
author_sort Srisutham, Suttipat
collection PubMed
description BACKGROUND: Rapid diagnostic tests (RDTs) have become the most common diagnostic tool for detection of Plasmodium falciparum malaria, in particular in remote areas. RDT blood spots provide a source of parasite DNA for molecular analysis. In this study, the utility of RDTs for molecular analysis and the performance of different methods for whole genome amplification were investigated. METHODS: Positive P. falciparum RDTs were collected from Kayin, Myanmar from August 2014 to January 2016. The RDT samples were stored for 6 months, 9 months, 20 months, 21 months, and 32 months before DNA extraction and subsequent molecular analysis of P. falciparum kelch 13 (pfkelch13) mutations, P. falciparum multidrug resistance 1 (pfmdr1), and P. falciparum plasmepsin 2 (pfplasmepsin2) gene amplification. In addition, performance of four whole genome amplification (WGA) kits were compared, including REPLI-g(®), MALBAC(TM), PicoPLEX(®), and GenomePlex(®), for which DNA quantity and quality were compared between original DNA and post-WGA products. RESULTS: The proportion of successful amplification of the different molecular markers was similar between blood spots analysed from RDTs stored for 6, 9, 20, 21, or 32 months. Successful amplification was dependent on the molecular markers fragment length (p value < 0.05): 18% for a 1245 bp fragment of pfkelch13, 71% for 364 bp of pfkelch13, 81% for 87 bp of pfmdr1, 81% for 108 bp of pfplasmepsin2. Comparison of the four WGA assay kits showed that REPLI-g(®), MALBAC(TM), and PicoPLEX(®) increased the quantity of DNA 60 to 750-fold, whereas the ratio of parasite DNA amplification over human DNA was most favourable for MALBAC(®). Sequencing results of pfkelch13, P. falciparum chloroquine resistance transporter (pfcrt), P. falciparum dihydrofolate reductase (pfdhfr) and six microsatellite markers assessed from the post-WGA product was the same as from the original DNA. CONCLUSIONS: Blood spots from RDTs are a good source for molecular analysis of P. falciparum, even after storage up to 32 months. WGA of RDT-derived parasite DNA reliably increase DNA quantity with sufficient quality for molecular analysis of resistance markers.
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spelling pubmed-72517362020-06-04 Utility of Plasmodium falciparum DNA from rapid diagnostic test kits for molecular analysis and whole genome amplification Srisutham, Suttipat Suwannasin, Kanokon Mathema, Vivek Bhakta Sriprawat, Kanlaya Smithuis, Frank M. Nosten, Francois White, Nicholas J. Dondorp, Arjen M. Imwong, Mallika Malar J Methodology BACKGROUND: Rapid diagnostic tests (RDTs) have become the most common diagnostic tool for detection of Plasmodium falciparum malaria, in particular in remote areas. RDT blood spots provide a source of parasite DNA for molecular analysis. In this study, the utility of RDTs for molecular analysis and the performance of different methods for whole genome amplification were investigated. METHODS: Positive P. falciparum RDTs were collected from Kayin, Myanmar from August 2014 to January 2016. The RDT samples were stored for 6 months, 9 months, 20 months, 21 months, and 32 months before DNA extraction and subsequent molecular analysis of P. falciparum kelch 13 (pfkelch13) mutations, P. falciparum multidrug resistance 1 (pfmdr1), and P. falciparum plasmepsin 2 (pfplasmepsin2) gene amplification. In addition, performance of four whole genome amplification (WGA) kits were compared, including REPLI-g(®), MALBAC(TM), PicoPLEX(®), and GenomePlex(®), for which DNA quantity and quality were compared between original DNA and post-WGA products. RESULTS: The proportion of successful amplification of the different molecular markers was similar between blood spots analysed from RDTs stored for 6, 9, 20, 21, or 32 months. Successful amplification was dependent on the molecular markers fragment length (p value < 0.05): 18% for a 1245 bp fragment of pfkelch13, 71% for 364 bp of pfkelch13, 81% for 87 bp of pfmdr1, 81% for 108 bp of pfplasmepsin2. Comparison of the four WGA assay kits showed that REPLI-g(®), MALBAC(TM), and PicoPLEX(®) increased the quantity of DNA 60 to 750-fold, whereas the ratio of parasite DNA amplification over human DNA was most favourable for MALBAC(®). Sequencing results of pfkelch13, P. falciparum chloroquine resistance transporter (pfcrt), P. falciparum dihydrofolate reductase (pfdhfr) and six microsatellite markers assessed from the post-WGA product was the same as from the original DNA. CONCLUSIONS: Blood spots from RDTs are a good source for molecular analysis of P. falciparum, even after storage up to 32 months. WGA of RDT-derived parasite DNA reliably increase DNA quantity with sufficient quality for molecular analysis of resistance markers. BioMed Central 2020-05-27 /pmc/articles/PMC7251736/ /pubmed/32460780 http://dx.doi.org/10.1186/s12936-020-03259-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology
Srisutham, Suttipat
Suwannasin, Kanokon
Mathema, Vivek Bhakta
Sriprawat, Kanlaya
Smithuis, Frank M.
Nosten, Francois
White, Nicholas J.
Dondorp, Arjen M.
Imwong, Mallika
Utility of Plasmodium falciparum DNA from rapid diagnostic test kits for molecular analysis and whole genome amplification
title Utility of Plasmodium falciparum DNA from rapid diagnostic test kits for molecular analysis and whole genome amplification
title_full Utility of Plasmodium falciparum DNA from rapid diagnostic test kits for molecular analysis and whole genome amplification
title_fullStr Utility of Plasmodium falciparum DNA from rapid diagnostic test kits for molecular analysis and whole genome amplification
title_full_unstemmed Utility of Plasmodium falciparum DNA from rapid diagnostic test kits for molecular analysis and whole genome amplification
title_short Utility of Plasmodium falciparum DNA from rapid diagnostic test kits for molecular analysis and whole genome amplification
title_sort utility of plasmodium falciparum dna from rapid diagnostic test kits for molecular analysis and whole genome amplification
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7251736/
https://www.ncbi.nlm.nih.gov/pubmed/32460780
http://dx.doi.org/10.1186/s12936-020-03259-9
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