Key result
Recombinant duck adenovirus rDAdV3-VP1-188 provides complete DAdV3 protection and ~80% DHAV1 protection in ducks.
Why the study?
Duck hepatitis A virus type 1 and duck adenovirus type 3 cause significant economic losses in the Chinese duck industry, motivating development of effective vector vaccines.
The recombinant duck adenovirus rDAdV3-VP1-188 provides effective protection against both DAdV3 and DHAV1, demonstrating the potential of DAdV3 as a viral vector for avian vaccines.
Does not support field use in ducks; leaves open recombinant vector potential pending validation trials.
Adenovirus serves as an excellent viral vector and is employed in vector vaccine research. Duck hepatitis A virus type 1 (DHAV1) and duck adenovirus type 3 (DAdV3) cause significant economic losses in the Chinese duck industry. In this study, we found an excellent exogenous gene insertion site in DAdV3 genome of CH-GD-12-2014 strain, within 3 intergenic regions (IGR). Subsequently, we generated a recombinant duck adenovirus named rDAdV3-VP1-188, which exhibits excellent replication characteristics and immunogenicity of DAdV3 and DHAV1. Animal experiments showed that rDAdV3-VP1-188 can provide 100% protection against the DAdV3 and 80% protection against DHAV1. These results showed that rDAdV3-VP1-188 could induce protection against DAdV3 and DHAV1 in ducks, thus indicating the feasibility of DAdV3 as a vector for the development of avian vector vaccines. These insights contribute to the further development of DAdV3 vectors and other adenovirus vectors.
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Wen et al. (2023) studied Duck hepatitis A virus type 1 (DHAV1) and duck adenovirus type 3 (DAdV3) infection. rDAdV3-VP1-188 was evaluated on Protection against DAdV3 and DHAV1. The recombinant duck adenovirus rDAdV3-VP1-188 provided 100% protection against DAdV3 and 80% protection against DHAV1 in ducks.
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