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A multiplex real-time PCR assay for detection of oseltamivir-resistant strains of influenza virus
Influenza is a contagious disease of humans and animals caused by viruses belonging to the Orthomyxoviridae family. The influenza A virus genome consists of negative sense, single-stranded, segmented RNA. Influenza viruses are classified into subtypes based on two surface antigens known as hemagglut...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Versita
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088769/ https://www.ncbi.nlm.nih.gov/pubmed/32215120 http://dx.doi.org/10.2478/s11535-014-0296-z |
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author | Nidzworski, Dawid Dobkowska, Joanna Hołysz, Marcin Gromadzka, Beata Szewczyk, Bogusław |
author_facet | Nidzworski, Dawid Dobkowska, Joanna Hołysz, Marcin Gromadzka, Beata Szewczyk, Bogusław |
author_sort | Nidzworski, Dawid |
collection | PubMed |
description | Influenza is a contagious disease of humans and animals caused by viruses belonging to the Orthomyxoviridae family. The influenza A virus genome consists of negative sense, single-stranded, segmented RNA. Influenza viruses are classified into subtypes based on two surface antigens known as hemagglutinin (H) and neuraminidase (N). The main problem with influenza A viruses infecting humans is drug resistance, which is caused by antigenic changes. A few antiviral drugs are available, but the most popular is the neuraminidase inhibitor — oseltamivir. The resistance against this drug has probably developed through antigenic drift by a point mutation in one amino acid at position 275 (H275Y). In order to prevent a possible influenza pandemic it is necessary to develop fast diagnostic tests. The aim of this project was to develop a new test for detection of influenza A virus and determination of oseltamivir resistance/sensitivity in humans. Detection and differentiation of oseltamivir resistance/sensitivity of influenza A virus was based on real-time PCR. This test contains two TaqMan probes, which work at different wavelengths. Application of techniques like multiplex real-time PCR has greatly enhanced the capability for surveillance and characterization of influenza viruses. After its potential validation, this test can be used for diagnosis before treatment. |
format | Online Article Text |
id | pubmed-7088769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Versita |
record_format | MEDLINE/PubMed |
spelling | pubmed-70887692020-03-23 A multiplex real-time PCR assay for detection of oseltamivir-resistant strains of influenza virus Nidzworski, Dawid Dobkowska, Joanna Hołysz, Marcin Gromadzka, Beata Szewczyk, Bogusław Cent Eur J Biol Research Article Influenza is a contagious disease of humans and animals caused by viruses belonging to the Orthomyxoviridae family. The influenza A virus genome consists of negative sense, single-stranded, segmented RNA. Influenza viruses are classified into subtypes based on two surface antigens known as hemagglutinin (H) and neuraminidase (N). The main problem with influenza A viruses infecting humans is drug resistance, which is caused by antigenic changes. A few antiviral drugs are available, but the most popular is the neuraminidase inhibitor — oseltamivir. The resistance against this drug has probably developed through antigenic drift by a point mutation in one amino acid at position 275 (H275Y). In order to prevent a possible influenza pandemic it is necessary to develop fast diagnostic tests. The aim of this project was to develop a new test for detection of influenza A virus and determination of oseltamivir resistance/sensitivity in humans. Detection and differentiation of oseltamivir resistance/sensitivity of influenza A virus was based on real-time PCR. This test contains two TaqMan probes, which work at different wavelengths. Application of techniques like multiplex real-time PCR has greatly enhanced the capability for surveillance and characterization of influenza viruses. After its potential validation, this test can be used for diagnosis before treatment. Versita 2014-03-20 2014 /pmc/articles/PMC7088769/ /pubmed/32215120 http://dx.doi.org/10.2478/s11535-014-0296-z Text en © Versita Warsaw and Springer-Verlag Wien 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Research Article Nidzworski, Dawid Dobkowska, Joanna Hołysz, Marcin Gromadzka, Beata Szewczyk, Bogusław A multiplex real-time PCR assay for detection of oseltamivir-resistant strains of influenza virus |
title | A multiplex real-time PCR assay for detection of oseltamivir-resistant strains of influenza virus |
title_full | A multiplex real-time PCR assay for detection of oseltamivir-resistant strains of influenza virus |
title_fullStr | A multiplex real-time PCR assay for detection of oseltamivir-resistant strains of influenza virus |
title_full_unstemmed | A multiplex real-time PCR assay for detection of oseltamivir-resistant strains of influenza virus |
title_short | A multiplex real-time PCR assay for detection of oseltamivir-resistant strains of influenza virus |
title_sort | multiplex real-time pcr assay for detection of oseltamivir-resistant strains of influenza virus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088769/ https://www.ncbi.nlm.nih.gov/pubmed/32215120 http://dx.doi.org/10.2478/s11535-014-0296-z |
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