Intranasal NS1-truncated live attenuated canine influenza vaccine confers superior protection compared to inactivated vaccine in beagles

Canine influenza virus (CIV) H3N2 continues to circulate among companion animals, posing a zoonotic risk due to its potential for cross-species transmission. However, currently available inactivated vaccines offer limited mucosal immunity and suboptimal protection. Here, we developed a novel intranasal live attenuated CIV H3N2 vaccine carrying a truncated nonstructural protein 1 (NS1) gene and evaluated its safety, immunogenicity, and protective efficacy in beagle dogs. The NS1-truncated LAIV was well-tolerated and induced robust mucosal and systemic immune responses, including high titers of virus-specific secretory IgA. Following challenge with virulent CIV H3N2 at 120 days post-vaccination, LAIV-immunized dogs exhibited complete clinical protection and minimal viral shedding, whereas dogs receiving the inactivated vaccine showed moderate disease signs. These findings demonstrate that the NS1-truncated LAIV confers superior protection compared to conventional vaccines and represents a promising next-generation platform for canine influenza control within a One Health framework.

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Publication Details

Journal
Veterinary Research
Published
2025-09-25
DOI
https://doi.org/10.1186/s13567-025-01624-7
Citations
1
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
1.35

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article

Intranasal NS1-truncated live attenuated canine influenza vaccine confers superior protection compared to inactivated vaccine in beagles

Sun‐Woo Yoon, Dae Gwin Jeong, Jung‐Ah Kang, Hye Kwon Kim et al.
1 citations
Veterinary Research
Influenza Virus Research Studies
1.35
article

Intranasal NS1-truncated live attenuated canine influenza vaccine confers superior protection compared to inactivated vaccine in beagles

Sun‐Woo Yoon, Dae Gwin Jeong, Jung‐Ah Kang, Hye Kwon Kim, Woonsung Na, Suyun Moon, Eulhae Ga, Donghui Yu, Daesub Song, Jongwoo Lim, Eunseo Bae, Hwan‐Jung Yun, Minjoo Yeom, Jaehyun Hwang, Xing Xie, Jaeseok Choi
article en
1 citations

Abstract

Canine influenza virus (CIV) H3N2 continues to circulate among companion animals, posing a zoonotic risk due to its potential for cross-species transmission. However, currently available inactivated vaccines offer limited mucosal immunity and suboptimal protection. Here, we developed a novel intranasal live attenuated CIV H3N2 vaccine carrying a truncated nonstructural protein 1 (NS1) gene and evaluated its safety, immunogenicity, and protective efficacy in beagle dogs. The NS1-truncated LAIV was well-tolerated and induced robust mucosal and systemic immune responses, including high titers of virus-specific secretory IgA. Following challenge with virulent CIV H3N2 at 120 days post-vaccination, LAIV-immunized dogs exhibited complete clinical protection and minimal viral shedding, whereas dogs receiving the inactivated vaccine showed moderate disease signs. These findings demonstrate that the NS1-truncated LAIV confers superior protection compared to conventional vaccines and represents a promising next-generation platform for canine influenza control within a One Health framework.

Veterinary ResearchVol. 56(1)
Chonnam National University (KR), Gyeongguk National University (KR), Seoul National University (KR), Chungbuk National University (KR), Jiangsu Academy of Agricultural Sciences (CN), National University College (PR), Ministry of Agriculture and Rural Affairs (CN), Seoul National University Dental Hospital (KR), Korea Research Institute of Bioscience and Biotechnology (KR)
Seoul National University, Ministry of Food and Drug Safety
Openalex Percentile: Top 15%
Influenza Virus Research Studies
1.35
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