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RespiCoV: Simultaneous identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and 46 respiratory tract viruses and bacteria by amplicon-based Oxford-Nanopore MinION sequencing

Since December 2019 the world has been facing the outbreak of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Identification of infected patients and discrimination from other respiratory infections have so far been accomplished by using highly specific real-time PCRs. Here we pres...

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Autores principales: Brinkmann, Annika, Uddin, Steven, Ulm, Sophie-Luisa, Pape, Katharina, Förster, Sophie, Enan, Khalid, Nourlil, Jalal, Krause, Eva, Schaade, Lars, Michel, Janine, Nitsche, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906600/
https://www.ncbi.nlm.nih.gov/pubmed/35263362
http://dx.doi.org/10.1371/journal.pone.0264855
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author Brinkmann, Annika
Uddin, Steven
Ulm, Sophie-Luisa
Pape, Katharina
Förster, Sophie
Enan, Khalid
Nourlil, Jalal
Krause, Eva
Schaade, Lars
Michel, Janine
Nitsche, Andreas
author_facet Brinkmann, Annika
Uddin, Steven
Ulm, Sophie-Luisa
Pape, Katharina
Förster, Sophie
Enan, Khalid
Nourlil, Jalal
Krause, Eva
Schaade, Lars
Michel, Janine
Nitsche, Andreas
author_sort Brinkmann, Annika
collection PubMed
description Since December 2019 the world has been facing the outbreak of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Identification of infected patients and discrimination from other respiratory infections have so far been accomplished by using highly specific real-time PCRs. Here we present a rapid multiplex approach (RespiCoV), combining highly multiplexed PCRs and MinION sequencing suitable for the simultaneous screening for 41 viral and five bacterial agents related to respiratory tract infections, including the human coronaviruses NL63, HKU1, OC43, 229E, Middle East respiratory syndrome coronavirus, SARS-CoV, and SARS-CoV-2. RespiCoV was applied to 150 patient samples with suspected SARS-CoV-2 infection and compared with specific real-time PCR. Additionally, several respiratory tract pathogens were identified in samples tested positive or negative for SARS-CoV-2. Finally, RespiCoV was experimentally compared to the commercial RespiFinder 2SMART multiplex screening assay (PathoFinder, The Netherlands).
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spelling pubmed-89066002022-03-10 RespiCoV: Simultaneous identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and 46 respiratory tract viruses and bacteria by amplicon-based Oxford-Nanopore MinION sequencing Brinkmann, Annika Uddin, Steven Ulm, Sophie-Luisa Pape, Katharina Förster, Sophie Enan, Khalid Nourlil, Jalal Krause, Eva Schaade, Lars Michel, Janine Nitsche, Andreas PLoS One Research Article Since December 2019 the world has been facing the outbreak of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Identification of infected patients and discrimination from other respiratory infections have so far been accomplished by using highly specific real-time PCRs. Here we present a rapid multiplex approach (RespiCoV), combining highly multiplexed PCRs and MinION sequencing suitable for the simultaneous screening for 41 viral and five bacterial agents related to respiratory tract infections, including the human coronaviruses NL63, HKU1, OC43, 229E, Middle East respiratory syndrome coronavirus, SARS-CoV, and SARS-CoV-2. RespiCoV was applied to 150 patient samples with suspected SARS-CoV-2 infection and compared with specific real-time PCR. Additionally, several respiratory tract pathogens were identified in samples tested positive or negative for SARS-CoV-2. Finally, RespiCoV was experimentally compared to the commercial RespiFinder 2SMART multiplex screening assay (PathoFinder, The Netherlands). Public Library of Science 2022-03-09 /pmc/articles/PMC8906600/ /pubmed/35263362 http://dx.doi.org/10.1371/journal.pone.0264855 Text en © 2022 Brinkmann et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Brinkmann, Annika
Uddin, Steven
Ulm, Sophie-Luisa
Pape, Katharina
Förster, Sophie
Enan, Khalid
Nourlil, Jalal
Krause, Eva
Schaade, Lars
Michel, Janine
Nitsche, Andreas
RespiCoV: Simultaneous identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and 46 respiratory tract viruses and bacteria by amplicon-based Oxford-Nanopore MinION sequencing
title RespiCoV: Simultaneous identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and 46 respiratory tract viruses and bacteria by amplicon-based Oxford-Nanopore MinION sequencing
title_full RespiCoV: Simultaneous identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and 46 respiratory tract viruses and bacteria by amplicon-based Oxford-Nanopore MinION sequencing
title_fullStr RespiCoV: Simultaneous identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and 46 respiratory tract viruses and bacteria by amplicon-based Oxford-Nanopore MinION sequencing
title_full_unstemmed RespiCoV: Simultaneous identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and 46 respiratory tract viruses and bacteria by amplicon-based Oxford-Nanopore MinION sequencing
title_short RespiCoV: Simultaneous identification of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and 46 respiratory tract viruses and bacteria by amplicon-based Oxford-Nanopore MinION sequencing
title_sort respicov: simultaneous identification of severe acute respiratory syndrome coronavirus 2 (sars-cov-2) and 46 respiratory tract viruses and bacteria by amplicon-based oxford-nanopore minion sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906600/
https://www.ncbi.nlm.nih.gov/pubmed/35263362
http://dx.doi.org/10.1371/journal.pone.0264855
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