Abstract

BackgroundWild ducks play an important role in the evolution of avian influenza viruses (AIVs). Domestic ducks in China are known to carry and spread H9N2 AIVs that are thought to have contributed internal genes for the recent outbreak of zoonotic H7N9 virus. In order to protect animal and public health, an effective vaccine is urgently needed to block and prevent the spread of H9N2 virus in ducks. We developed an inactivated H9N2 vaccine (with adjuvant Montanide ISA 70VG) based on an endemic H9N2 AIV and evaluated this vaccine in ducks.FindingsThe results showed that the inactivated H9N2 vaccine was able to induce a strong and fast humoral immune response in vaccinated ducks. The hemagglutination inhibition titer in the sera increased fast, and reached its peak of 12.3 log2 at 5 weeks post-vaccination in immunized birds and remained at a high level for at least 37 weeks post-vaccination. Moreover, viral shedding was completely blocked in vaccinated ducks after challenge with a homologous H9N2 AIV at both 3 and 37 weeks post-vaccination.ConclusionsThe results of this study indicate that the inactivated H9N2 vaccine induces high and prolonged immune response in vaccinated ducks and are efficacious in protecting ducks from H9N2 infection.

Highlights

  • Wild ducks play an important role in the evolution of avian influenza viruses (AIVs)

  • The results of this study indicate that the inactivated H9N2 vaccine induces high and prolonged immune response in vaccinated ducks and are efficacious in protecting ducks from H9N2 infection

  • There is an increasing public health concern regarding the spread of H9N2 avian influenza viruses (AIVs) due to its potential for host-range extension, virulence enhancement, and providing internal genes, resulting in reassortment with other subtype influenza viruses through horizontal transmission [1,2,3,4,5,6]

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Summary

Introduction

Wild ducks play an important role in the evolution of avian influenza viruses (AIVs). Oropharyngeal and cloacal swabs were collected each day from 1 to 5 post-inoculation (dpi) for detecting virus shedding. The results showed that no virus was detected in any cloacal swabs collected from all ducks inoculated with each virus.

Results
Conclusion
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