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Avian infectious bronchitis virus (IBV) is the causing agent of a highly contagious disease with a major economic impact on the poultry industry. It is characterised clinically by respiratory, renal and reproductive manifestations. Despite various vaccination protocols, IBV still plays a role in poultry flocks, mostly because of the appearance of new variant strains which are not neutralized by antibodies induced by available vaccines. Viral entry into host cells is mediated by binding of the viral glycoprotein S to a receptor on the cell surface. Alpha 2,3 linked sialic acid has been reported to play an important role as a receptor determinant for IBV. Here, a comparative study of current field strains, 4/91, Italy 02 and QX has been carried out to investigate their dependence of sialic acid for infection in different primary cell culture systems. To reflect the main target organs of an IBV infection in chicken, the following tissue cultures were used in this study: a) primary chicken embryo kidney cells, b) chicken tracheal organ cell cultures (TOCs), c) chicken precision-cut lung slices (PCLS) and d) chicken oviduct explants (COE).
This study investigates the role of sialic acid in the infection of primary avian cells by Avian infectious bronchitis virus (IBV). IBV causes a highly contagious disease with significant economic impact on the poultry industry, manifesting in respiratory, renal, and reproductive systems. Despite vaccination efforts, new variant strains continue to emerge, posing ongoing challenges. This research specifically examines the dependence of field strains (4/91, Italy 02, and QX) on sialic acid for infection across various primary cell culture systems, including kidney cells, tracheal organ cultures, lung slices, and oviduct explants, to mirror the virus's primary target organs in chickens.
This research paper details a comparative study on the role of sialic acid in IBV infection across various primary cell cultures. The methodology focuses on key target organs in chickens, utilizing kidney cells, tracheal organ cultures, lung slices, and oviduct explants. The findings are presented within the context of ongoing challenges posed by new IBV variant strains and the limitations of current vaccination protocols. The work contributes to understanding viral entry mechanisms and receptor determinants.
Page Count:
96
Publication Date:
2012-01-01
Publisher:
LAP Lambert Academic Publishing
ISBN-10:
3659234176
ISBN-13:
9783659234170
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