First identification of canine adenovirus 1 in mink and bioinformatics analysis of its 100 K protein

• Published in: Frontiers in Microbiology
• Main Authors: Hou, Jinyu, Xu, Jinfeng, Wang, Ben, Zhang, Hongling, Yin, Baishuang, Li, Goujiang, Lei, Fashou, Cai, Xiaoming, Zhu, Yanzhu, Wang, Longtao
• Other Authors: Department of Science and Technology of Jilin Province
• Format: Article in Journal/Newspaper
• Language: unknown
• Published: Frontiers Media SA 2023
• Subjects: Arctic Fox
• Online Access: http://dx.doi.org/10.3389/fmicb.2023.1245581; https://www.frontiersin.org/articles/10.3389/fmicb.2023.1245581/full

Introduction Animal trade favors the spreading of emerging canine adenovirus 1 (CAdV-1) in mink. Because the 100K protein is not exposed to the viral surface at any stage, it can be used to differentiate the vaccine from wild virus infection. However, no related research has been conducted. This study aimed to find evidence of CAdV-1 in mink and predict the character of the 100K protein in the current circulating CAdV-1 strain of mink. Method In this experiment, the identification of CAdV-1, the phylogenetic tree, homology, and bioinformatics analysis of 100K were conducted. Results The results showed that the CAdV-1 was identified in the mink and that its Fiber was located in a separate branch. It was closely related to strains isolated from Norwegian Arctic fox and Red fox. 100K was located in a separate branch, which had the closest genetic relationship with skunks, porcupines, raccoons, and hedgehogs and a far genetic relationship with the strains in dogs. 100K protein is an unstable and hydrophobic protein. It had evidence of selective pressure and recombination, 1 glycosylation site, 48 phosphorylation sites, 60 dominant B cell epitopes, and 9 peptides of MHC-I and MHC-II. Its subcellular localization was mainly in the endoplasmic reticulum and mitochondria. The binding sites of 100K proteins were DBP proteins and 33K proteins. Discussion The stains in the mink were different from fox. The exploration of its genomic characteristics will provide us with a deeper understanding of the prevention of canine adenovirus.