An avian influenza H5N1 virus vaccine candidate based on the extracellular domain produced in yeast system as subviral particles protects chickens from lethal challenge

Highly pathogenic avian influenza is an on-going problem in poultry and a potential human pandemic threat. Pandemics occur suddenly and vaccine production must be fast and effective to be of value in controlling the spread of the virus. In this study we evaluated the potential of a recombinant prote...

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Veröffentlicht in:Antiviral research 2016-09, Vol.133, p.242-249
Hauptverfasser: Pietrzak, Maria, Macioła, Agnieszka, Zdanowski, Konrad, Protas-Klukowska, Anna Maria, Olszewska, Monika, Śmietanka, Krzysztof, Minta, Zenon, Szewczyk, Bogusław, Kopera, Edyta
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Sprache:eng
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Zusammenfassung:Highly pathogenic avian influenza is an on-going problem in poultry and a potential human pandemic threat. Pandemics occur suddenly and vaccine production must be fast and effective to be of value in controlling the spread of the virus. In this study we evaluated the potential of a recombinant protein from the extracellular domain of an H5 hemagglutinin protein produced in a yeast expression system to act as an effective vaccine. Protein production was efficient, with up to 200 mg purified from 1 L of culture medium. We showed that the deletion of the multibasic cleavage site from the protein improves oligomerization and, consequentially, its immunogenicity. We also showed that immunization with this deleted protein protected chickens from challenge with a highly pathogenic avian influenza H5N1 virus. Our results suggest that this recombinant protein produced in yeast may be an effective vaccine against H5N1 virus in poultry. •Recombinant H5 antigen based on the extracellular domain is able to induce strong immunological response.•Deletion of the multibasic cleavage site in the H5 antigen improves protein oligomerization and its immunogenicity.•Transmission electron microscopy visualized H5 subviral particles.•This new antigen provides clinical protection following the challenge with HP H5N1 strain.
ISSN:0166-3542
1872-9096
DOI:10.1016/j.antiviral.2016.08.001