Key result
Disrupting the E2-DCTN6 protein-protein interaction via amino acid substitutions abrogated the interaction in vitro and attenuated viral virulence in domestic swine.
Why the study?
Structural glycoprotein E2 is an important component of CSFV involved in virus-host interactions, but its interaction with host protein DCTN6 remained to be characterized.
Does disrupting the E2-DCTN6 interaction attenuate Classical Swine Fever Virus virulence in domestic swine?
Does disrupting the E2-DCTN6 interaction attenuate Classical Swine Fever Virus virulence in domestic swine?
Disrupting the interaction between CSFV glycoprotein E2 and host protein DCTN6 attenuates viral virulence, providing a potential mechanism for developing improved CSF vaccines.
Answers are grounded in this paper and cite their sources.
Provides mechanistic basis for CSFV vaccine attenuation in swine; leaves open field validation and regulatory translation.
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 interaction in 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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Borca et al. (2019) studied Classical Swine Fever Virus (CSFV) infection. Mutation disrupting E2-DCTN6 interaction was evaluated on Viral virulence in domestic swine. Disrupting the E2-DCTN6 protein-protein interaction via amino acid substitutions abrogated the interaction in vitro and attenuated viral virulence in domestic swine.
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