| Literature DB >> 29073031 |
Ruchao Peng1,2, Shuijun Zhang1, Yingzi Cui1,2, Yi Shi1,2,3,4, George F Gao5,2,3,4,6, Jianxun Qi5,2.
Abstract
Thogotoviruses are emerging tick-borne zoonotic orthomyxoviruses infecting both humans and domestic animals with severe clinical consequences. These viruses utilize a single-envelope glycoprotein (Gp) to facilitate their entry into host cells. Here, we present the Gp structures of Thogoto and Dhori viruses, both of which are members of the Thogotovirus genus in the family Orthomyxoviridae These structures, determined in the postfusion conformation, identified them as class III viral fusion proteins. It is intriguing that the Gp structures are similar to the envelope protein of baculovirus, although sharing a low sequence identity of ∼28%. Detailed structural and phylogenic analyses demonstrated that these Gps originated from a common ancestor. Among the structures, domain I is the most conserved region, particularly the fusion loops. Domain II showed the highest variability among different viruses, which might be related to their distinct host tropism. These findings increase our understanding of the divergent evolution processes of various orthomyxoviruses and indicate potential targets for developing antiviral therapeutics by intercepting virus entry. Published under the PNAS license.Entities:
Keywords: Othomyxoviridae; Thogotovirus; crystal structure; evolution; fusion protein
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Year: 2017 PMID: 29073031 PMCID: PMC5651748 DOI: 10.1073/pnas.1706125114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205