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Assessment of a multiplex PCR and Nanopore-based method for dengue virus sequencing in Indonesia

BACKGROUND: Dengue virus (DENV) infects hundreds of thousands of people annually in Indonesia. However, DENV sequence data from the country are limited, as samples from outbreaks must be shipped across long-distances to suitably equipped laboratories to be sequenced. This approach is time-consuming,...

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Autores principales: Stubbs, Samuel C. B., Blacklaws, Barbara A., Yohan, Benediktus, Yudhaputri, Frilasita A., Hayati, Rahma F., Schwem, Brian, Salvaña, Edsel M., Destura, Raul V., Lester, James S., Myint, Khin S., Sasmono, R. Tedjo, Frost, Simon D. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020346/
https://www.ncbi.nlm.nih.gov/pubmed/32054488
http://dx.doi.org/10.1186/s12985-020-1294-6
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author Stubbs, Samuel C. B.
Blacklaws, Barbara A.
Yohan, Benediktus
Yudhaputri, Frilasita A.
Hayati, Rahma F.
Schwem, Brian
Salvaña, Edsel M.
Destura, Raul V.
Lester, James S.
Myint, Khin S.
Sasmono, R. Tedjo
Frost, Simon D. W.
author_facet Stubbs, Samuel C. B.
Blacklaws, Barbara A.
Yohan, Benediktus
Yudhaputri, Frilasita A.
Hayati, Rahma F.
Schwem, Brian
Salvaña, Edsel M.
Destura, Raul V.
Lester, James S.
Myint, Khin S.
Sasmono, R. Tedjo
Frost, Simon D. W.
author_sort Stubbs, Samuel C. B.
collection PubMed
description BACKGROUND: Dengue virus (DENV) infects hundreds of thousands of people annually in Indonesia. However, DENV sequence data from the country are limited, as samples from outbreaks must be shipped across long-distances to suitably equipped laboratories to be sequenced. This approach is time-consuming, expensive, and frequently results in failure due to low viral load or degradation of the RNA genome. METHODS: We evaluated a method designed to address this challenge, using the ‘Primal Scheme’ multiplex PCR tiling approach to rapidly generate short, overlapping amplicons covering the complete DENV coding-region, and sequencing the amplicons on the portable Nanopore MinION device. The resulting sequence data was assessed in terms of genome coverage, consensus sequence accuracy and by phylogenetic analysis. RESULTS: The multiplex approach proved capable of producing near complete coding-region coverage from all samples tested ([Formula: see text] = 99.96%, n = 18), 61% of which could not be fully amplified using the current, long-amplicon PCR, approach. Nanopore-generated consensus sequences were found to be between 99.17–99.92% identical to those produced by high-coverage Illumina sequencing. Consensus accuracy could be improved by masking regions below 20X coverage depth (99.69–99.92%). However, coding-region coverage was reduced at this depth ([Formula: see text] = 93.48%). Nanopore and Illumina consensus sequences generated from the same samples formed monophyletic clades on phylogenetic analysis, and Indonesian consensus sequences accurately clustered by geographical origin. CONCLUSION: The multiplex, short-amplicon approach proved superior for amplifying DENV genomes from clinical samples, particularly when the virus was present at low concentrations. The accuracy of Nanopore-generated consensus sequences from these amplicons was sufficient for identifying the geographic origin of the samples, demonstrating that the approach can be a useful tool for identifying and monitoring DENV clades circulating in low-resource settings across Indonesia. However, the inaccuracies in Nanopore-generated consensus sequences mean that the approach may not be appropriate for higher resolution transmission studies, particularly when more accurate sequencing technologies are available.
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spelling pubmed-70203462020-02-20 Assessment of a multiplex PCR and Nanopore-based method for dengue virus sequencing in Indonesia Stubbs, Samuel C. B. Blacklaws, Barbara A. Yohan, Benediktus Yudhaputri, Frilasita A. Hayati, Rahma F. Schwem, Brian Salvaña, Edsel M. Destura, Raul V. Lester, James S. Myint, Khin S. Sasmono, R. Tedjo Frost, Simon D. W. Virol J Research BACKGROUND: Dengue virus (DENV) infects hundreds of thousands of people annually in Indonesia. However, DENV sequence data from the country are limited, as samples from outbreaks must be shipped across long-distances to suitably equipped laboratories to be sequenced. This approach is time-consuming, expensive, and frequently results in failure due to low viral load or degradation of the RNA genome. METHODS: We evaluated a method designed to address this challenge, using the ‘Primal Scheme’ multiplex PCR tiling approach to rapidly generate short, overlapping amplicons covering the complete DENV coding-region, and sequencing the amplicons on the portable Nanopore MinION device. The resulting sequence data was assessed in terms of genome coverage, consensus sequence accuracy and by phylogenetic analysis. RESULTS: The multiplex approach proved capable of producing near complete coding-region coverage from all samples tested ([Formula: see text] = 99.96%, n = 18), 61% of which could not be fully amplified using the current, long-amplicon PCR, approach. Nanopore-generated consensus sequences were found to be between 99.17–99.92% identical to those produced by high-coverage Illumina sequencing. Consensus accuracy could be improved by masking regions below 20X coverage depth (99.69–99.92%). However, coding-region coverage was reduced at this depth ([Formula: see text] = 93.48%). Nanopore and Illumina consensus sequences generated from the same samples formed monophyletic clades on phylogenetic analysis, and Indonesian consensus sequences accurately clustered by geographical origin. CONCLUSION: The multiplex, short-amplicon approach proved superior for amplifying DENV genomes from clinical samples, particularly when the virus was present at low concentrations. The accuracy of Nanopore-generated consensus sequences from these amplicons was sufficient for identifying the geographic origin of the samples, demonstrating that the approach can be a useful tool for identifying and monitoring DENV clades circulating in low-resource settings across Indonesia. However, the inaccuracies in Nanopore-generated consensus sequences mean that the approach may not be appropriate for higher resolution transmission studies, particularly when more accurate sequencing technologies are available. BioMed Central 2020-02-13 /pmc/articles/PMC7020346/ /pubmed/32054488 http://dx.doi.org/10.1186/s12985-020-1294-6 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Stubbs, Samuel C. B.
Blacklaws, Barbara A.
Yohan, Benediktus
Yudhaputri, Frilasita A.
Hayati, Rahma F.
Schwem, Brian
Salvaña, Edsel M.
Destura, Raul V.
Lester, James S.
Myint, Khin S.
Sasmono, R. Tedjo
Frost, Simon D. W.
Assessment of a multiplex PCR and Nanopore-based method for dengue virus sequencing in Indonesia
title Assessment of a multiplex PCR and Nanopore-based method for dengue virus sequencing in Indonesia
title_full Assessment of a multiplex PCR and Nanopore-based method for dengue virus sequencing in Indonesia
title_fullStr Assessment of a multiplex PCR and Nanopore-based method for dengue virus sequencing in Indonesia
title_full_unstemmed Assessment of a multiplex PCR and Nanopore-based method for dengue virus sequencing in Indonesia
title_short Assessment of a multiplex PCR and Nanopore-based method for dengue virus sequencing in Indonesia
title_sort assessment of a multiplex pcr and nanopore-based method for dengue virus sequencing in indonesia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020346/
https://www.ncbi.nlm.nih.gov/pubmed/32054488
http://dx.doi.org/10.1186/s12985-020-1294-6
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