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Data from: The efficacy of inactivated vaccine against H5 clade 2.3.4.4b highly pathogenic avian influenza virus in turkeys

Published by Agricultural Research Service | Department of Agriculture | Metadata Last Checked: December 01, 2025 | Last Modified: 2025-11-21
The global outbreak of clade 2.3.4.4b H5N1 highly pathogenic avian influenza (HPAI) virus has caused tremendous losses in poultry. Although turkeys are a smaller sector in poultry production compared to chickens, they tend to be affected more severely by HPAI virus because they can usually be infected with a lower dose of influenza A virus than chickens (i.e., they are more susceptible). Exposure to non-replicating proteins may help control HPAI, however data with turkeys are somewhat limited regarding how well they work and approaches to modifying surveillance have not been developed. Here, an H5N9 non-replicating protein comprised of a clade 2.3.4.4b H5 hemagglutinin from A/turkey/Indiana/22-003707-003/2022 (TK/IN/22) and a North American wild bird lineage N9 was evaluated in commercial broad breasted white turkeys by challenge to live virus. Turkeys were divided into three groups, where each group was exposed to the non-replicating protein once at 3 (3wk), 7 (7wk), or 9 (9wk) weeks of age. All birds were challenged at 10 weeks of age with TK/IN/22 HPAIV. There was 100% survival in all groups except the sham exposure group which had 100% mortality. A significant decrease in viral shedding was observed in all exposed groups compared to the shams, although the 9wk group shed significantly higher quantities by the cloacal route at seven days post challenge (DPC) compared to the 3wk group. The neuraminidase inhibition-enzyme linked lectin assay (NI-ELLA) was used as a serological test that was able to detect antibody in birds that had been infected after exposure and challenge based on antibodies to the NA protein of the challenge virus (N1 NA) in serum collected 7, 10 and 14DPC. Between 50 and 90% of turkeys, depending on age at exposure, were positive by NI-ELLA at 7DPC and 100% were positive at 14DPC regardless of age at exposure.

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