| Literature DB >> 27102817 |
Abdou Nagy1, Jinhwa Lee2, Ignacio Mena3, Jamie Henningson2, Yuhao Li2, Jingjiao Ma2, Michael Duff2, Yonghai Li2, Yuekun Lang2, Jianmei Yang4, Fatma Abdallah5, Juergen Richt2, Ahmed Ali5, Adolfo García-Sastre6, Wenjun Ma7.
Abstract
In order to produce an efficient poultry H9 avian influenza vaccine that provides cross-protection against multiple H9 lineages, two Newcastle disease virus (NDV) LaSota vaccine strain recombinant viruses were generated using reverse genetics. The recombinant NDV-H9Con virus expresses a consensus-H9 hemagglutinin (HA) that is designed based on available H9N2 sequences from Chinese and Middle Eastern isolates. The recombinant NDV-H9Chi virus expresses a chimeric-H9 HA in which the H9 ectodomain of A/Guinea Fowl/Hong Kong/WF10/99 was fused with the cytoplasmic and transmembrane domain of the fusion protein (F) of NDV. Both recombinant viruses expressed the inserted HA stably and grew to high titers. An efficacy study in chickens showed that both recombinant viruses were able to provide protection against challenge with a heterologous H9N2 virus. In contrast to the NDV-H9Chi virus, the NDV-H9Con virus induced a higher hemagglutination inhibition titer against both NDV and H9 viruses in immunized birds, and efficiently inhibited virus shedding through the respiratory route. Moreover, sera collected from birds immunized with either NDV-H9Con or NDV-H9Chi were able to cross-neutralize two different lineages of H9N2 viruses, indicating that NDV-H9Con and NDV-H9Chi are promising vaccine candidates that could provide cross-protection among different H9N2 lineage viruses.Entities:
Keywords: Cross-protection; H9N2; Influenza; Recombinant NDV LaSota viruses
Mesh:
Substances:
Year: 2016 PMID: 27102817 PMCID: PMC5556941 DOI: 10.1016/j.vaccine.2016.04.022
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641