Cargando…

Analysis of Synchronous and Asynchronous In Vitro Infections with Homologous Murine Norovirus Strains Reveals Time-Dependent Viral Interference Effects

Viral recombination is a key mechanism in the evolution and diversity of noroviruses. In vivo, synchronous single-cell coinfection by multiple viruses, the ultimate prerequisite to viral recombination, is likely to be a rare event and delayed secondary infections are a more probable occurrence. Here...

Descripción completa

Detalles Bibliográficos
Autores principales: Ludwig-Begall, Louisa F., Di Felice, Elisabetta, Toffoli, Barbara, Ceci, Chiara, Di Martino, Barbara, Marsilio, Fulvio, Mauroy, Axel, Thiry, Etienne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147416/
https://www.ncbi.nlm.nih.gov/pubmed/34063220
http://dx.doi.org/10.3390/v13050823
_version_ 1783697625930792960
author Ludwig-Begall, Louisa F.
Di Felice, Elisabetta
Toffoli, Barbara
Ceci, Chiara
Di Martino, Barbara
Marsilio, Fulvio
Mauroy, Axel
Thiry, Etienne
author_facet Ludwig-Begall, Louisa F.
Di Felice, Elisabetta
Toffoli, Barbara
Ceci, Chiara
Di Martino, Barbara
Marsilio, Fulvio
Mauroy, Axel
Thiry, Etienne
author_sort Ludwig-Begall, Louisa F.
collection PubMed
description Viral recombination is a key mechanism in the evolution and diversity of noroviruses. In vivo, synchronous single-cell coinfection by multiple viruses, the ultimate prerequisite to viral recombination, is likely to be a rare event and delayed secondary infections are a more probable occurrence. Here, we determine the effect of a temporal separation of in vitro infections with the two homologous murine norovirus strains MNV-1 WU20 and CW1 on the composition of nascent viral populations. WU20 and CW1 were either synchronously inoculated onto murine macrophage cell monolayers (coinfection) or asynchronously applied (superinfection with varying titres of CW1 at half-hour to 24-h delays). Then, 24 h after initial co-or superinfection, quantification of genomic copy numbers and discriminative screening of plaque picked infectious progeny viruses demonstrated a time-dependent predominance of primary infecting WU20 in the majority of viral progenies. Our results indicate that a time interval from one to two hours onwards between two consecutive norovirus infections allows for the establishment of a barrier that reduces or prevents superinfection.
format Online
Article
Text
id pubmed-8147416
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-81474162021-05-26 Analysis of Synchronous and Asynchronous In Vitro Infections with Homologous Murine Norovirus Strains Reveals Time-Dependent Viral Interference Effects Ludwig-Begall, Louisa F. Di Felice, Elisabetta Toffoli, Barbara Ceci, Chiara Di Martino, Barbara Marsilio, Fulvio Mauroy, Axel Thiry, Etienne Viruses Communication Viral recombination is a key mechanism in the evolution and diversity of noroviruses. In vivo, synchronous single-cell coinfection by multiple viruses, the ultimate prerequisite to viral recombination, is likely to be a rare event and delayed secondary infections are a more probable occurrence. Here, we determine the effect of a temporal separation of in vitro infections with the two homologous murine norovirus strains MNV-1 WU20 and CW1 on the composition of nascent viral populations. WU20 and CW1 were either synchronously inoculated onto murine macrophage cell monolayers (coinfection) or asynchronously applied (superinfection with varying titres of CW1 at half-hour to 24-h delays). Then, 24 h after initial co-or superinfection, quantification of genomic copy numbers and discriminative screening of plaque picked infectious progeny viruses demonstrated a time-dependent predominance of primary infecting WU20 in the majority of viral progenies. Our results indicate that a time interval from one to two hours onwards between two consecutive norovirus infections allows for the establishment of a barrier that reduces or prevents superinfection. MDPI 2021-05-02 /pmc/articles/PMC8147416/ /pubmed/34063220 http://dx.doi.org/10.3390/v13050823 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Ludwig-Begall, Louisa F.
Di Felice, Elisabetta
Toffoli, Barbara
Ceci, Chiara
Di Martino, Barbara
Marsilio, Fulvio
Mauroy, Axel
Thiry, Etienne
Analysis of Synchronous and Asynchronous In Vitro Infections with Homologous Murine Norovirus Strains Reveals Time-Dependent Viral Interference Effects
title Analysis of Synchronous and Asynchronous In Vitro Infections with Homologous Murine Norovirus Strains Reveals Time-Dependent Viral Interference Effects
title_full Analysis of Synchronous and Asynchronous In Vitro Infections with Homologous Murine Norovirus Strains Reveals Time-Dependent Viral Interference Effects
title_fullStr Analysis of Synchronous and Asynchronous In Vitro Infections with Homologous Murine Norovirus Strains Reveals Time-Dependent Viral Interference Effects
title_full_unstemmed Analysis of Synchronous and Asynchronous In Vitro Infections with Homologous Murine Norovirus Strains Reveals Time-Dependent Viral Interference Effects
title_short Analysis of Synchronous and Asynchronous In Vitro Infections with Homologous Murine Norovirus Strains Reveals Time-Dependent Viral Interference Effects
title_sort analysis of synchronous and asynchronous in vitro infections with homologous murine norovirus strains reveals time-dependent viral interference effects
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147416/
https://www.ncbi.nlm.nih.gov/pubmed/34063220
http://dx.doi.org/10.3390/v13050823
work_keys_str_mv AT ludwigbegalllouisaf analysisofsynchronousandasynchronousinvitroinfectionswithhomologousmurinenorovirusstrainsrevealstimedependentviralinterferenceeffects
AT difeliceelisabetta analysisofsynchronousandasynchronousinvitroinfectionswithhomologousmurinenorovirusstrainsrevealstimedependentviralinterferenceeffects
AT toffolibarbara analysisofsynchronousandasynchronousinvitroinfectionswithhomologousmurinenorovirusstrainsrevealstimedependentviralinterferenceeffects
AT cecichiara analysisofsynchronousandasynchronousinvitroinfectionswithhomologousmurinenorovirusstrainsrevealstimedependentviralinterferenceeffects
AT dimartinobarbara analysisofsynchronousandasynchronousinvitroinfectionswithhomologousmurinenorovirusstrainsrevealstimedependentviralinterferenceeffects
AT marsiliofulvio analysisofsynchronousandasynchronousinvitroinfectionswithhomologousmurinenorovirusstrainsrevealstimedependentviralinterferenceeffects
AT mauroyaxel analysisofsynchronousandasynchronousinvitroinfectionswithhomologousmurinenorovirusstrainsrevealstimedependentviralinterferenceeffects
AT thiryetienne analysisofsynchronousandasynchronousinvitroinfectionswithhomologousmurinenorovirusstrainsrevealstimedependentviralinterferenceeffects