Cargando…

Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case study

BACKGROUND: Viral infection by dengue virus is a major public health problem in tropical countries. Early diagnosis and detection are increasingly based on quantitative reverse transcriptase real-time polymerase chain reaction (RT-qPCR) directed against genomic regions conserved between different is...

Descripción completa

Detalles Bibliográficos
Autores principales: Vanneste, Kevin, Garlant, Linda, Broeders, Sylvia, Van Gucht, Steven, Roosens, Nancy H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123964/
https://www.ncbi.nlm.nih.gov/pubmed/30180800
http://dx.doi.org/10.1186/s12859-018-2313-0
_version_ 1783352940129419264
author Vanneste, Kevin
Garlant, Linda
Broeders, Sylvia
Van Gucht, Steven
Roosens, Nancy H.
author_facet Vanneste, Kevin
Garlant, Linda
Broeders, Sylvia
Van Gucht, Steven
Roosens, Nancy H.
author_sort Vanneste, Kevin
collection PubMed
description BACKGROUND: Viral infection by dengue virus is a major public health problem in tropical countries. Early diagnosis and detection are increasingly based on quantitative reverse transcriptase real-time polymerase chain reaction (RT-qPCR) directed against genomic regions conserved between different isolates. Genetic variation can however result in mismatches of primers and probes with their targeted nucleic acid regions. Whole genome sequencing allows to characterize and track such changes, which in turn enables to evaluate, optimize, and (re-)design novel and existing RT-qPCR methods. The immense amount of available sequence data renders this however a labour-intensive and complex task. RESULTS: We present a bioinformatics approach that enables in silico evaluation of primers and probes intended for routinely employed RT-qPCR methods. This approach is based on analysing large amounts of publically available whole genome data, by first employing BLASTN to mine the genomic regions targeted by the RT-qPCR method(s), and afterwards using BLASTN-SHORT to evaluate whether primers and probes will anneal based on a set of simple in silico criteria. Using dengue virus as a case study, we evaluated 18 published RT-qPCR methods using more than 3000 publically available genomes in the NCBI Virus Variation Resource, and provide a systematic overview of method performance based on in silico sensitivity and specificity. CONCLUSIONS: We provide a comprehensive overview of dengue virus RT-qPCR method performance that will aid appropriate method selection allowing to take specific measures that aim to contain and prevent viral spread in afflicted regions. Notably, we find that primer-template mismatches at their 3′ end may represent a general issue for dengue virus RT-qPCR detection methods that merits more attention in their development process. Our approach is also available as a public tool, and demonstrates how utilizing genomic data can provide meaningful insights in an applied public health setting such as the detection of viral species in human diagnostics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2313-0) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6123964
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-61239642018-09-10 Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case study Vanneste, Kevin Garlant, Linda Broeders, Sylvia Van Gucht, Steven Roosens, Nancy H. BMC Bioinformatics Research Article BACKGROUND: Viral infection by dengue virus is a major public health problem in tropical countries. Early diagnosis and detection are increasingly based on quantitative reverse transcriptase real-time polymerase chain reaction (RT-qPCR) directed against genomic regions conserved between different isolates. Genetic variation can however result in mismatches of primers and probes with their targeted nucleic acid regions. Whole genome sequencing allows to characterize and track such changes, which in turn enables to evaluate, optimize, and (re-)design novel and existing RT-qPCR methods. The immense amount of available sequence data renders this however a labour-intensive and complex task. RESULTS: We present a bioinformatics approach that enables in silico evaluation of primers and probes intended for routinely employed RT-qPCR methods. This approach is based on analysing large amounts of publically available whole genome data, by first employing BLASTN to mine the genomic regions targeted by the RT-qPCR method(s), and afterwards using BLASTN-SHORT to evaluate whether primers and probes will anneal based on a set of simple in silico criteria. Using dengue virus as a case study, we evaluated 18 published RT-qPCR methods using more than 3000 publically available genomes in the NCBI Virus Variation Resource, and provide a systematic overview of method performance based on in silico sensitivity and specificity. CONCLUSIONS: We provide a comprehensive overview of dengue virus RT-qPCR method performance that will aid appropriate method selection allowing to take specific measures that aim to contain and prevent viral spread in afflicted regions. Notably, we find that primer-template mismatches at their 3′ end may represent a general issue for dengue virus RT-qPCR detection methods that merits more attention in their development process. Our approach is also available as a public tool, and demonstrates how utilizing genomic data can provide meaningful insights in an applied public health setting such as the detection of viral species in human diagnostics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2313-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-04 /pmc/articles/PMC6123964/ /pubmed/30180800 http://dx.doi.org/10.1186/s12859-018-2313-0 Text en © The Author(s). 2018 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 Article
Vanneste, Kevin
Garlant, Linda
Broeders, Sylvia
Van Gucht, Steven
Roosens, Nancy H.
Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case study
title Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case study
title_full Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case study
title_fullStr Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case study
title_full_unstemmed Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case study
title_short Application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by RT-qPCR using dengue virus as a case study
title_sort application of whole genome data for in silico evaluation of primers and probes routinely employed for the detection of viral species by rt-qpcr using dengue virus as a case study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123964/
https://www.ncbi.nlm.nih.gov/pubmed/30180800
http://dx.doi.org/10.1186/s12859-018-2313-0
work_keys_str_mv AT vannestekevin applicationofwholegenomedataforinsilicoevaluationofprimersandprobesroutinelyemployedforthedetectionofviralspeciesbyrtqpcrusingdenguevirusasacasestudy
AT garlantlinda applicationofwholegenomedataforinsilicoevaluationofprimersandprobesroutinelyemployedforthedetectionofviralspeciesbyrtqpcrusingdenguevirusasacasestudy
AT broederssylvia applicationofwholegenomedataforinsilicoevaluationofprimersandprobesroutinelyemployedforthedetectionofviralspeciesbyrtqpcrusingdenguevirusasacasestudy
AT vanguchtsteven applicationofwholegenomedataforinsilicoevaluationofprimersandprobesroutinelyemployedforthedetectionofviralspeciesbyrtqpcrusingdenguevirusasacasestudy
AT roosensnancyh applicationofwholegenomedataforinsilicoevaluationofprimersandprobesroutinelyemployedforthedetectionofviralspeciesbyrtqpcrusingdenguevirusasacasestudy