1. Academic Validation
  2. Critical role for bone marrow stromal antigen 2 in acute Chikungunya virus infection

Critical role for bone marrow stromal antigen 2 in acute Chikungunya virus infection

  • J Gen Virol. 2014 Nov;95(Pt 11):2450-2461. doi: 10.1099/vir.0.068643-0.
Wadie D Mahauad-Fernandez 1 2 Philip H Jones 2 Chioma M Okeoma 1 2
Affiliations

Affiliations

  • 1 Interdisciplinary Graduate Program in Molecular and Cellular Biology (MCB), University of Iowa, Iowa City, IA, USA.
  • 2 Department of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
Abstract

Bone marrow stromal antigen 2 (BST-2; also known as tetherin or CD317) is an IFN-inducible gene that functions to block the release of a range of nascent enveloped virions from infected host cells. However, the role of BST-2 in viral pathogenesis remains poorly understood. BST-2 plays a multifaceted role in innate immunity, as it hinders retroviral Infection and possibly promotes Infection with some rhabdo- and orthomyxoviruses. This paradoxical role has probably hindered exploration of BST-2 Antiviral function in vivo. We reported previously that BST-2 tethers Chikungunya virus (CHIKV)-like particles on the cell plasma membrane. To explore the role of BST-2 in CHIKV replication and host protection, we utilized CHIKV strain 181/25 to examine early events during CHIKV Infection in a BST-2(-/-) mouse model. We observed an interesting dichotomy between WT and BST-2(-/-) mice. BST-2 deficiency increased inoculation site viral load, culminating in higher systemic viraemia and increased lymphoid tissues tropism. A suppressed inflammatory innate response demonstrated by impaired expression of IFN-α, IFN-γ and CD40 ligand was observed in BST-2(-/-) mice compared with the WT controls. These findings suggested that, in part, BST-2 protects lymphoid tissues from CHIKV Infection and regulates CHIKV-induced inflammatory response by the host.

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