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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...

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Autores principales: Joffret, Marie-Line, Polston, Patsy M., Razafindratsimandresy, Richter, Bessaud, Maël, Heraud, Jean-Michel, Delpeyroux, Francis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
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.
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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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