Proteomic screening of variola virus reveals a unique NF-kappaB inhibitor that is highly conserved among pathogenic orthopoxviruses

天花病毒的蛋白质组学筛选揭示了一种独特的 NF-κB 抑制剂,该抑制剂在致病性正痘病毒中高度保守

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作者:Mohamed R Mohamed, Masmudur M Rahman, Jerry S Lanchbury, Donna Shattuck, Chris Neff, Max Dufford, Nick van Buuren, Katharine Fagan, Michele Barry, Scott Smith, Inger Damon, Grant McFadden

Abstract

Identification of the binary interactions between viral and host proteins has become a valuable tool for investigating viral tropism and pathogenesis. Here, we present the first systematic protein interaction screening of the unique variola virus proteome by using yeast 2-hybrid screening against a variety of human cDNA libraries. Several protein-protein interactions were identified, including an interaction between variola G1R, an ankryin/F-box containing protein, and human nuclear factor kappa-B1 (NF-kappaB1)/p105. This represents the first direct interaction between a pathogen-encoded protein and NF-kappaB1/p105. Orthologs of G1R are present in a variety of pathogenic orthopoxviruses, but not in vaccinia virus, and expression of any one of these viral proteins blocks NF-kappaB signaling in human cells. Thus, proteomic screening of variola virus has the potential to uncover modulators of the human innate antiviral responses.

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