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Chorioallantoic membranes of embryonated chicken eggs as an alternative system for isolation of equine influenza virus

BACKGROUND: Influenza virus isolation in embryonated chicken eggs (ECEs) is not applicable for rapid diagnosis, however it allows the recovery and propagation of the viable virus. A low number of infectious virus particles in the swabs, poor quality of samples or individual strain properties can lea...

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Autores principales: Gora, Ilona Marcelina, Kwasnik, Malgorzata, Zmudzinski, Jan Franciszek, Rozek, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480115/
https://www.ncbi.nlm.nih.gov/pubmed/28637468
http://dx.doi.org/10.1186/s12985-017-0788-3
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author Gora, Ilona Marcelina
Kwasnik, Malgorzata
Zmudzinski, Jan Franciszek
Rozek, Wojciech
author_facet Gora, Ilona Marcelina
Kwasnik, Malgorzata
Zmudzinski, Jan Franciszek
Rozek, Wojciech
author_sort Gora, Ilona Marcelina
collection PubMed
description BACKGROUND: Influenza virus isolation in embryonated chicken eggs (ECEs) is not applicable for rapid diagnosis, however it allows the recovery and propagation of the viable virus. A low number of infectious virus particles in the swabs, poor quality of samples or individual strain properties can lead to difficulties during the virus isolation process. We propose to utilize chorioallantoic membranes (CAM) of ECEs with the assistance of real-time RT PCR to facilitate equine influenza virus isolation. METHODS: Real-time RT PCR was used to detect influenza virus genetic material in amniotic/allantoic fluids (AF) and CAM of ECEs. Haemagglutination assay was used for AF. We used highly diluted virus as a substitute of clinical specimen for ECEs inoculation. RESULTS: Our study demonstrated that real-time RT PCR testing of CAM homogenates was more useful than testing of AF for EIV detection in ECEs. Positive results from CAM allowed to select the embryos from those with haemagglutination assay (HA) - and real-time RT PCR-negative AF for further passages. Using homogenates of CAM for subsequent passages, we finally obtained HA-positive AF, which confirmed virus replication. CONCLUSION: We postulate that real-time RT PCR testing of CAM homogenates and their subsequent passages may facilitate the isolation of equine influenza viruses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12985-017-0788-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-54801152017-06-23 Chorioallantoic membranes of embryonated chicken eggs as an alternative system for isolation of equine influenza virus Gora, Ilona Marcelina Kwasnik, Malgorzata Zmudzinski, Jan Franciszek Rozek, Wojciech Virol J Short Report BACKGROUND: Influenza virus isolation in embryonated chicken eggs (ECEs) is not applicable for rapid diagnosis, however it allows the recovery and propagation of the viable virus. A low number of infectious virus particles in the swabs, poor quality of samples or individual strain properties can lead to difficulties during the virus isolation process. We propose to utilize chorioallantoic membranes (CAM) of ECEs with the assistance of real-time RT PCR to facilitate equine influenza virus isolation. METHODS: Real-time RT PCR was used to detect influenza virus genetic material in amniotic/allantoic fluids (AF) and CAM of ECEs. Haemagglutination assay was used for AF. We used highly diluted virus as a substitute of clinical specimen for ECEs inoculation. RESULTS: Our study demonstrated that real-time RT PCR testing of CAM homogenates was more useful than testing of AF for EIV detection in ECEs. Positive results from CAM allowed to select the embryos from those with haemagglutination assay (HA) - and real-time RT PCR-negative AF for further passages. Using homogenates of CAM for subsequent passages, we finally obtained HA-positive AF, which confirmed virus replication. CONCLUSION: We postulate that real-time RT PCR testing of CAM homogenates and their subsequent passages may facilitate the isolation of equine influenza viruses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12985-017-0788-3) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-21 /pmc/articles/PMC5480115/ /pubmed/28637468 http://dx.doi.org/10.1186/s12985-017-0788-3 Text en © The Author(s). 2017 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 Short Report
Gora, Ilona Marcelina
Kwasnik, Malgorzata
Zmudzinski, Jan Franciszek
Rozek, Wojciech
Chorioallantoic membranes of embryonated chicken eggs as an alternative system for isolation of equine influenza virus
title Chorioallantoic membranes of embryonated chicken eggs as an alternative system for isolation of equine influenza virus
title_full Chorioallantoic membranes of embryonated chicken eggs as an alternative system for isolation of equine influenza virus
title_fullStr Chorioallantoic membranes of embryonated chicken eggs as an alternative system for isolation of equine influenza virus
title_full_unstemmed Chorioallantoic membranes of embryonated chicken eggs as an alternative system for isolation of equine influenza virus
title_short Chorioallantoic membranes of embryonated chicken eggs as an alternative system for isolation of equine influenza virus
title_sort chorioallantoic membranes of embryonated chicken eggs as an alternative system for isolation of equine influenza virus
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480115/
https://www.ncbi.nlm.nih.gov/pubmed/28637468
http://dx.doi.org/10.1186/s12985-017-0788-3
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