A Systems Approach Reveals MAVS Signaling in Myeloid Cells as Critical for Resistance to Ebola Virus in Murine Models of Infection

Cell Rep. 2017 Jan 17;18(3):816-829. doi: 10.1016/j.celrep.2016.12.069.

Abstract

The unprecedented 2013-2016 outbreak of Ebola virus (EBOV) resulted in over 11,300 human deaths. Host resistance to RNA viruses requires RIG-I-like receptor (RLR) signaling through the adaptor protein, mitochondrial antiviral signaling protein (MAVS), but the role of RLR-MAVS in orchestrating anti-EBOV responses in vivo is not known. Here we apply a systems approach to MAVS-/- mice infected with either wild-type or mouse-adapted EBOV. MAVS controlled EBOV replication through the expression of IFNα, regulation of inflammatory responses in the spleen, and prevention of cell death in the liver, with macrophages implicated as a major cell type influencing host resistance. A dominant role for RLR signaling in macrophages was confirmed following conditional MAVS deletion in LysM+ myeloid cells. These findings reveal tissue-specific MAVS-dependent transcriptional pathways associated with resistance to EBOV, and they demonstrate that EBOV adaptation to cause disease in mice involves changes in two distinct events, RLR-MAVS antagonism and suppression of RLR-independent IFN-I responses.

Keywords: Ebola virus; MAVS; RLR; conditional; interferon; knockout; macrophages; mouse adapted.

MeSH terms

  • Adaptor Proteins, Signal Transducing / antagonists & inhibitors
  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • DEAD Box Protein 58 / antagonists & inhibitors
  • DEAD Box Protein 58 / metabolism
  • Disease Models, Animal
  • Ebolavirus / physiology*
  • Hemorrhagic Fever, Ebola / metabolism
  • Hemorrhagic Fever, Ebola / mortality
  • Hemorrhagic Fever, Ebola / pathology*
  • Humans
  • Interferon Type I / metabolism
  • Kaplan-Meier Estimate
  • Liver / metabolism
  • Liver / pathology
  • Liver / virology
  • Macrophages / cytology
  • Macrophages / immunology
  • Macrophages / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myeloid Cells / cytology
  • Myeloid Cells / metabolism
  • Myeloid Cells / virology
  • Signal Transduction
  • Spleen / metabolism
  • Spleen / pathology
  • Spleen / virology
  • Virus Replication

Substances

  • Adaptor Proteins, Signal Transducing
  • Interferon Type I
  • DEAD Box Protein 58