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Structural Glycoprotein E2 of Classical Swine Fever Virus Interacts with Host Protein Dynactin Subunit 6 (DCTN6) during the Virus Infectious Cycle
Author(s) -
Manuel V. Borca,
Elizabeth A. Vuono,
Elizabeth Ramírez-Medina,
Paul A. Azzinaro,
Keith A. Berggren,
Michael Singer,
A. Rai,
Sarah Pruitt,
E B Silva,
Lauro Velázquez-Salinas,
C. Carrillo,
Douglas P. Gladue
Publication year - 2019
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.01642-19
Subject(s) - biology , virology , virus , classical swine fever , viral replication , vp40 , virulence , pestivirus , protein subunit , glycoprotein , viral protein , microbiology and biotechnology , flaviviridae , genetics , hepatitis c virus , gene
Structural glycoprotein E2 is an important component of CSFV due to its involvement in many virus activities, particularly virus-host interactions. Here, we present the description and characterization of the protein-protein interaction between E2 and the swine host protein DCTN6 during virus infection. The E2 amino acid residues mediating the interaction with DCTN6 were also identified. A recombinant CSFV harboring mutations disrupting the E2-DCTN6 interaction was created. The effect of disrupting the E2-DCTN6 protein-protein interaction was studied using reverse genetics. It was shown that the same amino acid substitutions that abrogated the E2-DCTN6 interactionin vitro constituted a critical factor in viral virulence in the natural host, domestic swine. This highlights the potential importance of the E2-DCTN6 protein-protein interaction in CSFV virulence and provides possible mechanisms of virus attenuation for the development of improved CSF vaccines.

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