Study of the host specificity of PB1-F2-associated virulence

Influenza A viruses cause important diseases in both human and animal. The PB1-F2 protein is a virulence factor expressed by some influenza viruses. Its deleterious action for the infected host is mostly described in mammals, while the available information is scarce in avian hosts. In this work, we...

Full description

Bibliographic Details
Main Authors: Joëlle Mettier, Daniel Marc, Laura Sedano, Bruno Da Costa, Christophe Chevalier, Ronan Le Goffic
Format: Article
Language:English
Published: Taylor & Francis Group 2021-12-01
Series:Virulence
Subjects:
Online Access:http://dx.doi.org/10.1080/21505594.2021.1933848
_version_ 1798014833484890112
author Joëlle Mettier
Daniel Marc
Laura Sedano
Bruno Da Costa
Christophe Chevalier
Ronan Le Goffic
author_facet Joëlle Mettier
Daniel Marc
Laura Sedano
Bruno Da Costa
Christophe Chevalier
Ronan Le Goffic
author_sort Joëlle Mettier
collection DOAJ
description Influenza A viruses cause important diseases in both human and animal. The PB1-F2 protein is a virulence factor expressed by some influenza viruses. Its deleterious action for the infected host is mostly described in mammals, while the available information is scarce in avian hosts. In this work, we compared the effects of PB1-F2 in avian and mammalian hosts by taking advantage of the zoonotic capabilities of an avian H7N1 virus. In vitro, the H7N1 virus did not behave differently when PB1-F2 was deficient while a H3N2 virus devoid of PB1-F2 was clearly less inflammatory. Likewise, when performing in vivo challenges of either chickens or embryonated eggs, with the wild-type or the PB1-F2 deficient virus, no difference could be observed in terms of mortality, host response or tropism. PB1-F2 therefore does not appear to play a major role as a virulence factor in the avian host. However, when infecting NF-κB-luciferase reporter mice with the H7N1 viruses, a massive PB1-F2-dependent inflammation was quantified, highlighting the host specificity of PB1-F2 virulence. Surprisingly, a chimeric 7:1 H3N2 virus harboring an H7N1-origin segment 2 (i.e. expressing the avian PB1-F2) induced a milder inflammatory response than its PB1-F2-deficient counterpart. This result shows that the pro-inflammatory activity of PB1-F2 is governed by complex mechanisms involving components from both the virus and its infected host. Thus, a mere exchange of segment 2 between strains is not sufficient to transmit the deleterious character of PB1-F2.
first_indexed 2024-04-11T15:24:41Z
format Article
id doaj.art-5e695070b82f4788b25faf81a691e381
institution Directory Open Access Journal
issn 2150-5594
2150-5608
language English
last_indexed 2024-04-11T15:24:41Z
publishDate 2021-12-01
publisher Taylor & Francis Group
record_format Article
series Virulence
spelling doaj.art-5e695070b82f4788b25faf81a691e3812022-12-22T04:16:18ZengTaylor & Francis GroupVirulence2150-55942150-56082021-12-011211647166010.1080/21505594.2021.19338481933848Study of the host specificity of PB1-F2-associated virulenceJoëlle Mettier0Daniel Marc1Laura Sedano2Bruno Da Costa3Christophe Chevalier4Ronan Le Goffic5Université Paris-Saclay, INRAE, UVSQ, UMR892 VIMUMR1282 Infectiologie Et Santé Publique, INRAEUniversité Paris-Saclay, INRAE, UVSQ, UMR892 VIMUniversité Paris-Saclay, INRAE, UVSQ, UMR892 VIMUniversité Paris-Saclay, INRAE, UVSQ, UMR892 VIMUniversité Paris-Saclay, INRAE, UVSQ, UMR892 VIMInfluenza A viruses cause important diseases in both human and animal. The PB1-F2 protein is a virulence factor expressed by some influenza viruses. Its deleterious action for the infected host is mostly described in mammals, while the available information is scarce in avian hosts. In this work, we compared the effects of PB1-F2 in avian and mammalian hosts by taking advantage of the zoonotic capabilities of an avian H7N1 virus. In vitro, the H7N1 virus did not behave differently when PB1-F2 was deficient while a H3N2 virus devoid of PB1-F2 was clearly less inflammatory. Likewise, when performing in vivo challenges of either chickens or embryonated eggs, with the wild-type or the PB1-F2 deficient virus, no difference could be observed in terms of mortality, host response or tropism. PB1-F2 therefore does not appear to play a major role as a virulence factor in the avian host. However, when infecting NF-κB-luciferase reporter mice with the H7N1 viruses, a massive PB1-F2-dependent inflammation was quantified, highlighting the host specificity of PB1-F2 virulence. Surprisingly, a chimeric 7:1 H3N2 virus harboring an H7N1-origin segment 2 (i.e. expressing the avian PB1-F2) induced a milder inflammatory response than its PB1-F2-deficient counterpart. This result shows that the pro-inflammatory activity of PB1-F2 is governed by complex mechanisms involving components from both the virus and its infected host. Thus, a mere exchange of segment 2 between strains is not sufficient to transmit the deleterious character of PB1-F2.http://dx.doi.org/10.1080/21505594.2021.1933848influenza viruspb1-f2species barrierzoonotic virusesreassortmenth7n1h3n2mouse modelintravital imagingchicken infection
spellingShingle Joëlle Mettier
Daniel Marc
Laura Sedano
Bruno Da Costa
Christophe Chevalier
Ronan Le Goffic
Study of the host specificity of PB1-F2-associated virulence
Virulence
influenza virus
pb1-f2
species barrier
zoonotic viruses
reassortment
h7n1
h3n2
mouse model
intravital imaging
chicken infection
title Study of the host specificity of PB1-F2-associated virulence
title_full Study of the host specificity of PB1-F2-associated virulence
title_fullStr Study of the host specificity of PB1-F2-associated virulence
title_full_unstemmed Study of the host specificity of PB1-F2-associated virulence
title_short Study of the host specificity of PB1-F2-associated virulence
title_sort study of the host specificity of pb1 f2 associated virulence
topic influenza virus
pb1-f2
species barrier
zoonotic viruses
reassortment
h7n1
h3n2
mouse model
intravital imaging
chicken infection
url http://dx.doi.org/10.1080/21505594.2021.1933848
work_keys_str_mv AT joellemettier studyofthehostspecificityofpb1f2associatedvirulence
AT danielmarc studyofthehostspecificityofpb1f2associatedvirulence
AT laurasedano studyofthehostspecificityofpb1f2associatedvirulence
AT brunodacosta studyofthehostspecificityofpb1f2associatedvirulence
AT christophechevalier studyofthehostspecificityofpb1f2associatedvirulence
AT ronanlegoffic studyofthehostspecificityofpb1f2associatedvirulence