Peer-reviewed veterinary case report
Development and application of a novel ELISA for detecting antibodies against group I fowl adenoviruses.
- Journal:
- Applied microbiology and biotechnology
- Year:
- 2020
- Authors:
- Pan, Qing et al.
Plain-English summary
Since 2015, there have been serious outbreaks of a disease called hepatitis-hydropericardium syndrome (HPS) in chickens caused by a new type of fowl adenovirus known as FAdV-4. This has led to significant economic losses in China, and there is a need for a reliable test to detect different types of fowl adenoviruses. Researchers developed a new blood test called ELISA that can identify antibodies against 12 different types of these viruses without mixing up results. This test is more sensitive than previous versions and can accurately detect antibodies in chickens that have been vaccinated against various fowl adenoviruses. Overall, this new ELISA could be very useful for tracking these viruses and helping to create vaccines.
Abstract
Since 2015, outbreaks of hepatitis-hydropericardium syndrome (HPS) caused by a novel genotype of fowl adenovirus 4 (FAdV-4) infection have created serious economic losses in China. Given that other serotypes of hypervirulent FAdVs have also been reported in poultry around the world, a common ELISA for all serotypes within the group I fowl adenoviruses (FAdV-I) is urgently needed, especially for clinical epidemic serotypes. In this study, we used high purity and concentration virions of FAdV-4 and developed a common ELISA for detecting antibodies against 12 FAdV-I serotypes. The developed ELISA was able to distinguish between antibodies against FAdV-I, FAdV-III, and other heterologous viruses without any cross-reaction. Furthermore, the ELISA showed higher sensitivity than the FAdV-1-based ELISA to the novel FAdV-4 found in China. Moreover, since there are no commercial vaccines against FAdVs in China, the ELISA was applied to detect sera samples from specific pathogen-free chickens inoculated with inactivated FAdV-1, FAdV-4, and FAdV-8a. The assay showed high sensitivities for all three detected serotypes within FAdV-I. In conclusion, a novel, common ELISA for FAdV-I was developed in this study and could be a powerful tool for seroepidemiological investigations and FAdVs vaccine development.
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Search related cases →Original publication: https://pubmed.ncbi.nlm.nih.gov/31836910/