A Bivalent Live Attenuated Influenza Virus Vaccine Protects against Drifted H1N2 and H3N2 Clinical Isolates in Swine

Influenza A viruses (IAVs) can cause a highly contagious respiratory disease for many mammalian species. In pigs, IAVs cause high morbidity and low mortality disease in susceptible populations that can have significant financial and production impacts. They can also present opportunities for mutatio...

Full description

Bibliographic Details
Main Authors: Lauren Aubrey, Ulises Barron-Castillo, Susan Detmer, Yan Zhou
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/15/1/46
_version_ 1797436481678082048
author Lauren Aubrey
Ulises Barron-Castillo
Susan Detmer
Yan Zhou
author_facet Lauren Aubrey
Ulises Barron-Castillo
Susan Detmer
Yan Zhou
author_sort Lauren Aubrey
collection DOAJ
description Influenza A viruses (IAVs) can cause a highly contagious respiratory disease for many mammalian species. In pigs, IAVs cause high morbidity and low mortality disease in susceptible populations that can have significant financial and production impacts. They can also present opportunities for mutations and gene reassortment, producing influenza strains with pandemic potential. Therefore, it is very important to prevent and control influenza infection in pigs, and the chief way to do so is through vaccination. The subtypes of IAV most prevalent in swine across the world are H1N1, H1N2, and H3N2; however, genetic diversity of these viruses can vary greatly by region. We previously developed an elastase-dependent bivalent live attenuated vaccine using two Canadian swine influenza A virus (swIAV) isolates, A/Swine/Alberta/SD0191/2016 (H1N2) [SD191] and A/Swine/Saskatchewan/SD0069/2015 (H3N2) [SD69], which provided protection against homologous strains. In this study, we demonstrate that this vaccine extends protection in pigs to more current, drifted non-homologous H1N2 and H3N2 strains, A/Swine/MB/SD0467/2019 (H1N2) [SD467] and A/Swine/AB/SD0435/2019 (H3N2) [SD435]. The vaccine elicited a robust immune response in the serum and the lung and reduced viral replication as well as lung pathology associated with these strains. Therefore, this bivalent vaccine remains a strong candidate that would be beneficial to the swine influenza vaccine market in North America.
first_indexed 2024-03-09T11:03:19Z
format Article
id doaj.art-72f8647acc384e09b3e82e68de8a575d
institution Directory Open Access Journal
issn 1999-4915
language English
last_indexed 2024-03-09T11:03:19Z
publishDate 2022-12-01
publisher MDPI AG
record_format Article
series Viruses
spelling doaj.art-72f8647acc384e09b3e82e68de8a575d2023-12-01T01:07:09ZengMDPI AGViruses1999-49152022-12-011514610.3390/v15010046A Bivalent Live Attenuated Influenza Virus Vaccine Protects against Drifted H1N2 and H3N2 Clinical Isolates in SwineLauren Aubrey0Ulises Barron-Castillo1Susan Detmer2Yan Zhou3Vaccine and Infectious Disease Organization (VIDO), University of Saskatchewan, Saskatoon, SK S7N 5E3, CanadaVaccine and Infectious Disease Organization (VIDO), University of Saskatchewan, Saskatoon, SK S7N 5E3, CanadaDepartment of Veterinary Pathology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK S7N 5B4, CanadaVaccine and Infectious Disease Organization (VIDO), University of Saskatchewan, Saskatoon, SK S7N 5E3, CanadaInfluenza A viruses (IAVs) can cause a highly contagious respiratory disease for many mammalian species. In pigs, IAVs cause high morbidity and low mortality disease in susceptible populations that can have significant financial and production impacts. They can also present opportunities for mutations and gene reassortment, producing influenza strains with pandemic potential. Therefore, it is very important to prevent and control influenza infection in pigs, and the chief way to do so is through vaccination. The subtypes of IAV most prevalent in swine across the world are H1N1, H1N2, and H3N2; however, genetic diversity of these viruses can vary greatly by region. We previously developed an elastase-dependent bivalent live attenuated vaccine using two Canadian swine influenza A virus (swIAV) isolates, A/Swine/Alberta/SD0191/2016 (H1N2) [SD191] and A/Swine/Saskatchewan/SD0069/2015 (H3N2) [SD69], which provided protection against homologous strains. In this study, we demonstrate that this vaccine extends protection in pigs to more current, drifted non-homologous H1N2 and H3N2 strains, A/Swine/MB/SD0467/2019 (H1N2) [SD467] and A/Swine/AB/SD0435/2019 (H3N2) [SD435]. The vaccine elicited a robust immune response in the serum and the lung and reduced viral replication as well as lung pathology associated with these strains. Therefore, this bivalent vaccine remains a strong candidate that would be beneficial to the swine influenza vaccine market in North America.https://www.mdpi.com/1999-4915/15/1/46influenzavaccineswine
spellingShingle Lauren Aubrey
Ulises Barron-Castillo
Susan Detmer
Yan Zhou
A Bivalent Live Attenuated Influenza Virus Vaccine Protects against Drifted H1N2 and H3N2 Clinical Isolates in Swine
Viruses
influenza
vaccine
swine
title A Bivalent Live Attenuated Influenza Virus Vaccine Protects against Drifted H1N2 and H3N2 Clinical Isolates in Swine
title_full A Bivalent Live Attenuated Influenza Virus Vaccine Protects against Drifted H1N2 and H3N2 Clinical Isolates in Swine
title_fullStr A Bivalent Live Attenuated Influenza Virus Vaccine Protects against Drifted H1N2 and H3N2 Clinical Isolates in Swine
title_full_unstemmed A Bivalent Live Attenuated Influenza Virus Vaccine Protects against Drifted H1N2 and H3N2 Clinical Isolates in Swine
title_short A Bivalent Live Attenuated Influenza Virus Vaccine Protects against Drifted H1N2 and H3N2 Clinical Isolates in Swine
title_sort bivalent live attenuated influenza virus vaccine protects against drifted h1n2 and h3n2 clinical isolates in swine
topic influenza
vaccine
swine
url https://www.mdpi.com/1999-4915/15/1/46
work_keys_str_mv AT laurenaubrey abivalentliveattenuatedinfluenzavirusvaccineprotectsagainstdriftedh1n2andh3n2clinicalisolatesinswine
AT ulisesbarroncastillo abivalentliveattenuatedinfluenzavirusvaccineprotectsagainstdriftedh1n2andh3n2clinicalisolatesinswine
AT susandetmer abivalentliveattenuatedinfluenzavirusvaccineprotectsagainstdriftedh1n2andh3n2clinicalisolatesinswine
AT yanzhou abivalentliveattenuatedinfluenzavirusvaccineprotectsagainstdriftedh1n2andh3n2clinicalisolatesinswine
AT laurenaubrey bivalentliveattenuatedinfluenzavirusvaccineprotectsagainstdriftedh1n2andh3n2clinicalisolatesinswine
AT ulisesbarroncastillo bivalentliveattenuatedinfluenzavirusvaccineprotectsagainstdriftedh1n2andh3n2clinicalisolatesinswine
AT susandetmer bivalentliveattenuatedinfluenzavirusvaccineprotectsagainstdriftedh1n2andh3n2clinicalisolatesinswine
AT yanzhou bivalentliveattenuatedinfluenzavirusvaccineprotectsagainstdriftedh1n2andh3n2clinicalisolatesinswine