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Whole Genome Sequencing of Enteroviruses Species A to D by High-Throughput Sequencing: Application for Viral Mixtures
Human enteroviruses (EV) consist of more than 100 serotypes classified within four species for enteroviruses (EV-A to -D) and three species for rhinoviruses, which have been implicated in a variety of human illnesses. Being able to simultaneously amplify the whole genome and identify enteroviruses i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172331/ https://www.ncbi.nlm.nih.gov/pubmed/30323802 http://dx.doi.org/10.3389/fmicb.2018.02339 |
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author | Joffret, Marie-Line Polston, Patsy M. Razafindratsimandresy, Richter Bessaud, Maël Heraud, Jean-Michel Delpeyroux, Francis |
author_facet | Joffret, Marie-Line Polston, Patsy M. Razafindratsimandresy, Richter Bessaud, Maël Heraud, Jean-Michel Delpeyroux, Francis |
author_sort | Joffret, Marie-Line |
collection | PubMed |
description | Human enteroviruses (EV) consist of more than 100 serotypes classified within four species for enteroviruses (EV-A to -D) and three species for rhinoviruses, which have been implicated in a variety of human illnesses. Being able to simultaneously amplify the whole genome and identify enteroviruses in samples is important for studying the viral diversity in different geographical regions and populations. It also provides knowledge about the evolution of these viruses. Therefore, we developed a rapid, sensitive method to detect and genetically classify all human enteroviruses in mixtures. Strains of EV-A (15), EV-B (40), EV-C (20), and EV-D (2) viruses were used in addition to 20 supernatants from RD cells infected with stool extracts or sewage concentrates. Two overlapping fragments were produced using a newly designed degenerated primer targeting the conserved CRE region for enteroviruses A-D and one degenerated primer set designed to specifically target the conserved region for each enterovirus species (EV-A to -D). This method was capable of sequencing the full genome for all viruses except two, for which nearly 90% of the genome was sequenced. This method also demonstrated the ability to discriminate, in both spiked and unspiked mixtures, the different enterovirus types present. |
format | Online Article Text |
id | pubmed-6172331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61723312018-10-15 Whole Genome Sequencing of Enteroviruses Species A to D by High-Throughput Sequencing: Application for Viral Mixtures Joffret, Marie-Line Polston, Patsy M. Razafindratsimandresy, Richter Bessaud, Maël Heraud, Jean-Michel Delpeyroux, Francis Front Microbiol Microbiology Human enteroviruses (EV) consist of more than 100 serotypes classified within four species for enteroviruses (EV-A to -D) and three species for rhinoviruses, which have been implicated in a variety of human illnesses. Being able to simultaneously amplify the whole genome and identify enteroviruses in samples is important for studying the viral diversity in different geographical regions and populations. It also provides knowledge about the evolution of these viruses. Therefore, we developed a rapid, sensitive method to detect and genetically classify all human enteroviruses in mixtures. Strains of EV-A (15), EV-B (40), EV-C (20), and EV-D (2) viruses were used in addition to 20 supernatants from RD cells infected with stool extracts or sewage concentrates. Two overlapping fragments were produced using a newly designed degenerated primer targeting the conserved CRE region for enteroviruses A-D and one degenerated primer set designed to specifically target the conserved region for each enterovirus species (EV-A to -D). This method was capable of sequencing the full genome for all viruses except two, for which nearly 90% of the genome was sequenced. This method also demonstrated the ability to discriminate, in both spiked and unspiked mixtures, the different enterovirus types present. Frontiers Media S.A. 2018-09-28 /pmc/articles/PMC6172331/ /pubmed/30323802 http://dx.doi.org/10.3389/fmicb.2018.02339 Text en Copyright © 2018 Joffret, Polston, Razafindratsimandresy, Bessaud, Heraud and Delpeyroux. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Joffret, Marie-Line Polston, Patsy M. Razafindratsimandresy, Richter Bessaud, Maël Heraud, Jean-Michel Delpeyroux, Francis Whole Genome Sequencing of Enteroviruses Species A to D by High-Throughput Sequencing: Application for Viral Mixtures |
title | Whole Genome Sequencing of Enteroviruses Species A to D by High-Throughput Sequencing: Application for Viral Mixtures |
title_full | Whole Genome Sequencing of Enteroviruses Species A to D by High-Throughput Sequencing: Application for Viral Mixtures |
title_fullStr | Whole Genome Sequencing of Enteroviruses Species A to D by High-Throughput Sequencing: Application for Viral Mixtures |
title_full_unstemmed | Whole Genome Sequencing of Enteroviruses Species A to D by High-Throughput Sequencing: Application for Viral Mixtures |
title_short | Whole Genome Sequencing of Enteroviruses Species A to D by High-Throughput Sequencing: Application for Viral Mixtures |
title_sort | whole genome sequencing of enteroviruses species a to d by high-throughput sequencing: application for viral mixtures |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6172331/ https://www.ncbi.nlm.nih.gov/pubmed/30323802 http://dx.doi.org/10.3389/fmicb.2018.02339 |
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