Fachbereich Veterinärmedizin



    Benefits and Limits of Egg Yolk vs. Serum Samples for Avian Influenza Virus Serosurveillance (2016)

    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Abdelwhab, E M
    Grund, Christian
    Aly, Mona M
    Beer, Martin
    Harder, Timm C
    Hafez, Hafez M (WE 15)
    Avian diseases; 60(2) — S. 496–499
    ISSN: 0005-2086
    DOI: 10.1637/11207-060115-ResNote
    Pubmed: 27309294
    Institut für Geflügelkrankheiten

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    Abstract / Zusammenfassung

    Serologic tests are a valuable tool for retrospective surveillance of avian influenza viruses (AIV) and monitoring of postvaccination host immune response. Yet collection of serum samples, particularly in adult breeder chickens, is laborious, intrusive to birds, and may pose a serious risk to the biosecurity of a flock. In this study we compared the level of AIV-specific antibody titers in eggs and serum samples obtained from broiler breeder chickens vaccinated at 6, 12, and 18 wk of age with H5N2-inactivated vaccine. Nucleocapsid protein-specific ELISA and hemagglutination inhibition test (HI) against homologous as well as heterologous antigens were used. The eggs and sera were collected at 22, 30, 45, and 50 wk of age (i.e., 4, 12, 27, and 32 wk after the third and final immunization, respectively). Using ELISA, the number of positive egg yolk samples decreased over time after vaccination, from 97% to 47%, while the seropositivity rate of serum samples was 97%-100% during the whole investigation period. No antibody titers were detected in egg white. By HI, antibody titers in serum samples were higher than in egg yolk samples. Compared to the homologous H5N2 antigen, significantly lower HI titers were obtained by using a heterologous H5N1 virus of clade In addition, no HI titers were detected in egg yolk and/or serum samples tested against the antigen of an Egyptian H5N1 antigenic drift variant of clade This study indicates that egg yolk may be used to monitor the postvaccination immune status of broiler breeder chickens and retrospective serosurveillance-by HI when a matching antigen is available as well as by ELISA-particularly for up to 12 wk postvaccination.