Evaluation of different inactivation methods for high and low pathogenic avian influenza viruses in egg-fluids for antigen preparation

•0.1% beta-propiolactone (BPL), 0.1% formalin inactivated AI viruses used in the study.•Ether inactivated all tested low pathogenic AI viruses.•Ether with 0.2% and 0.5% Tween-20 inactivated high pathogenic AI viruses.•Treatment with BPL, formalin retained, while ether treatment increased virus titer...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of virological methods 2015-09, Vol.222, p.28-33
Hauptverfasser: Pawar, Shailesh D., Murtadak, Vinay B., Kale, Sandeep D., Shinde, Prashant V., Parkhi, Saurabh S.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•0.1% beta-propiolactone (BPL), 0.1% formalin inactivated AI viruses used in the study.•Ether inactivated all tested low pathogenic AI viruses.•Ether with 0.2% and 0.5% Tween-20 inactivated high pathogenic AI viruses.•Treatment with BPL, formalin retained, while ether treatment increased virus titers.•Inactivated viruses retained immunogenicity.•This data might be useful for preparation of AI virus antigens and inactivated vaccines. In view of the emerging avian influenza (AI) viruses, it is important to study the susceptibility of AI viruses to inactivating agents for preparation of antigens and inactivated vaccines. The available information on susceptibility of both the high and low pathogenic AI viruses to different inactivating agents is inadequate and ambiguous. It has been shown that different subtypes of influenza viruses require different physical and chemical conditions for inactivation of infectivity. The present study was undertaken to evaluate the use of beta-propiolactone (BPL), formalin and ether for inactivation and its impact on antigenicity of AI viruses. A total of nine high and low pathogenic AI viruses belonging to four influenza A subtypes were included in the study. The H5N1 viruses were from the clades 2.2, 2.3.2.1 and 2.3.4. The H9N2 virus included in the study was of the G1 genotype, while the H11N1 and H4N6 viruses were from the Eurasian lineage. The viruses were treated with BPL, formalin and with ether. The confirmation of virus inactivation was performed by two serial passages of inactivated viruses in embryonated chicken eggs. The infectivity of all tested AI viruses was eliminated using 0.1% BPL and 0.1% formalin. Ether eliminated infectivity of all tested low pathogenic AI viruses; however, ether with 0.2% or 0.5% Tween-20 was required for inactivation of the highly pathogenic AI H5N1 viruses. Treatment with BPL, ether and formalin retained virus hemagglutination (HA) titers. Interestingly ether treatment resulted in significant rise in HA titers (P
ISSN:0166-0934
1879-0984
DOI:10.1016/j.jviromet.2015.05.004