Cargando…

Absence of clinical disease and contact transmission of HPAI H5NX clade 2.3.4.4 from North America in experimentally infected pigs

BACKGROUND: In the fall of 2014, highly pathogenic avian influenza (HPAI) subtype H5N8 clade 2.3.4.4 was introduced into North America by migrating waterfowl from Asia where, through reassortment, novel HPAI H5N2 and H5N1 viruses emerged. OBJECTIVES: Assess the susceptibility of pigs to HPAI H5N1, H...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaplan, Bryan S., Torchetti, Mia K., Lager, Kelly M., Webby, Richard J., Vincent, Amy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596520/
https://www.ncbi.nlm.nih.gov/pubmed/28688206
http://dx.doi.org/10.1111/irv.12463
_version_ 1783263547629764608
author Kaplan, Bryan S.
Torchetti, Mia K.
Lager, Kelly M.
Webby, Richard J.
Vincent, Amy L.
author_facet Kaplan, Bryan S.
Torchetti, Mia K.
Lager, Kelly M.
Webby, Richard J.
Vincent, Amy L.
author_sort Kaplan, Bryan S.
collection PubMed
description BACKGROUND: In the fall of 2014, highly pathogenic avian influenza (HPAI) subtype H5N8 clade 2.3.4.4 was introduced into North America by migrating waterfowl from Asia where, through reassortment, novel HPAI H5N2 and H5N1 viruses emerged. OBJECTIVES: Assess the susceptibility of pigs to HPAI H5N1, H5N2, and H5N8 clade 2.3.3.3 from North America. METHODS: Pigs and trachea explants were inoculated with a representative panel of H5NX clade 2.3.4.4 HPAI viruses from North America. Nasal swabs, BALF, and sera were collected to assess replication and transmission in challenged and direct contact pigs by RRT‐PCR, virus isolation, hemagglutination inhibition, and ELISA. RESULTS: Limited virus replication was restricted to the lower respiratory tract of challenged pigs, though absent in the nasal passages and trachea cultures, as determined by RRT‐PCR in all samples. Seroconversion of inoculated pigs was detected by NP ELISA but was not reliably detected by antigen‐specific hemagglutination inhibition. Boost with adjuvanted virus was required for the production of neutralizing antibodies to assess cross‐reactivity between wild‐type avian strains. All RRT‐PCR and serology tests were negative for contact animals indicating a failure of transmission from primary inoculated pigs. CONCLUSIONS: H5NX clade 2.3.4.4 strains can replicate in the lower respiratory tract of swine upon high titer inoculation, though appear to be incapable of replication in swine nasal epithelium in vivo or ex vivo in trachea explants in culture. Infected pigs did not produce high levels of serum antibodies following infection. Collectively, our data show HPAI H5NX clade 2.3.4.4 viruses to be poorly adapted for replication and transmission in swine.
format Online
Article
Text
id pubmed-5596520
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-55965202017-09-15 Absence of clinical disease and contact transmission of HPAI H5NX clade 2.3.4.4 from North America in experimentally infected pigs Kaplan, Bryan S. Torchetti, Mia K. Lager, Kelly M. Webby, Richard J. Vincent, Amy L. Influenza Other Respir Viruses Original Articles BACKGROUND: In the fall of 2014, highly pathogenic avian influenza (HPAI) subtype H5N8 clade 2.3.4.4 was introduced into North America by migrating waterfowl from Asia where, through reassortment, novel HPAI H5N2 and H5N1 viruses emerged. OBJECTIVES: Assess the susceptibility of pigs to HPAI H5N1, H5N2, and H5N8 clade 2.3.3.3 from North America. METHODS: Pigs and trachea explants were inoculated with a representative panel of H5NX clade 2.3.4.4 HPAI viruses from North America. Nasal swabs, BALF, and sera were collected to assess replication and transmission in challenged and direct contact pigs by RRT‐PCR, virus isolation, hemagglutination inhibition, and ELISA. RESULTS: Limited virus replication was restricted to the lower respiratory tract of challenged pigs, though absent in the nasal passages and trachea cultures, as determined by RRT‐PCR in all samples. Seroconversion of inoculated pigs was detected by NP ELISA but was not reliably detected by antigen‐specific hemagglutination inhibition. Boost with adjuvanted virus was required for the production of neutralizing antibodies to assess cross‐reactivity between wild‐type avian strains. All RRT‐PCR and serology tests were negative for contact animals indicating a failure of transmission from primary inoculated pigs. CONCLUSIONS: H5NX clade 2.3.4.4 strains can replicate in the lower respiratory tract of swine upon high titer inoculation, though appear to be incapable of replication in swine nasal epithelium in vivo or ex vivo in trachea explants in culture. Infected pigs did not produce high levels of serum antibodies following infection. Collectively, our data show HPAI H5NX clade 2.3.4.4 viruses to be poorly adapted for replication and transmission in swine. John Wiley and Sons Inc. 2017-09-02 2017-09 /pmc/articles/PMC5596520/ /pubmed/28688206 http://dx.doi.org/10.1111/irv.12463 Text en © 2017 The Authors. Influenza and Other Respiratory Viruses Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Kaplan, Bryan S.
Torchetti, Mia K.
Lager, Kelly M.
Webby, Richard J.
Vincent, Amy L.
Absence of clinical disease and contact transmission of HPAI H5NX clade 2.3.4.4 from North America in experimentally infected pigs
title Absence of clinical disease and contact transmission of HPAI H5NX clade 2.3.4.4 from North America in experimentally infected pigs
title_full Absence of clinical disease and contact transmission of HPAI H5NX clade 2.3.4.4 from North America in experimentally infected pigs
title_fullStr Absence of clinical disease and contact transmission of HPAI H5NX clade 2.3.4.4 from North America in experimentally infected pigs
title_full_unstemmed Absence of clinical disease and contact transmission of HPAI H5NX clade 2.3.4.4 from North America in experimentally infected pigs
title_short Absence of clinical disease and contact transmission of HPAI H5NX clade 2.3.4.4 from North America in experimentally infected pigs
title_sort absence of clinical disease and contact transmission of hpai h5nx clade 2.3.4.4 from north america in experimentally infected pigs
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596520/
https://www.ncbi.nlm.nih.gov/pubmed/28688206
http://dx.doi.org/10.1111/irv.12463
work_keys_str_mv AT kaplanbryans absenceofclinicaldiseaseandcontacttransmissionofhpaih5nxclade2344fromnorthamericainexperimentallyinfectedpigs
AT torchettimiak absenceofclinicaldiseaseandcontacttransmissionofhpaih5nxclade2344fromnorthamericainexperimentallyinfectedpigs
AT lagerkellym absenceofclinicaldiseaseandcontacttransmissionofhpaih5nxclade2344fromnorthamericainexperimentallyinfectedpigs
AT webbyrichardj absenceofclinicaldiseaseandcontacttransmissionofhpaih5nxclade2344fromnorthamericainexperimentallyinfectedpigs
AT vincentamyl absenceofclinicaldiseaseandcontacttransmissionofhpaih5nxclade2344fromnorthamericainexperimentallyinfectedpigs