4.6 Review

Intracellular Events and Cell Fate in Filovirus Infection

Journal

VIRUSES-BASEL
Volume 3, Issue 8, Pages 1501-1531

Publisher

MDPI
DOI: 10.3390/v3081501

Keywords

Ebola Virus; Marburg Virus; filoviruses; viral replication cycle; target cells; animal models; ultrastructural analysis; virus-cell interaction; bystander apoptosis; cell death

Categories

Funding

  1. National Institutes of Health (NIH) [U01-AI082954, AI057159]
  2. New England Regional Center of Excellence-Kasper [149047-0743]
  3. Boston University

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Marburg and Ebola viruses cause a severe hemorrhagic disease in humans with high fatality rates. Early target cells of filoviruses are monocytes, macrophages, and dendritic cells. The infection spreads to the liver, spleen and later other organs by blood and lymph flow. A hallmark of filovirus infection is the depletion of non-infected lymphocytes; however, the molecular mechanisms leading to the observed bystander lymphocyte apoptosis are poorly understood. Also, there is limited knowledge about the fate of infected cells in filovirus disease. In this review we will explore what is known about the intracellular events leading to virus amplification and cell damage in filovirus infection. Furthermore, we will discuss how cellular dysfunction and cell death may correlate with disease pathogenesis.

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