Assessing the contribution of interferon antagonism to the virulence of West African Ebola viruses.

Eric C Dunham, Logan Banadyga, Allison Groseth, Abhilash I Chiramel, Sonja M Best, Hideki Ebihara, Heinz Feldmann, Thomas Hoenen
Author Information
  1. Eric C Dunham: Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 South 4th Street, Hamilton, Montana 59840, USA.
  2. Logan Banadyga: Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 South 4th Street, Hamilton, Montana 59840, USA.
  3. Allison Groseth: Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 South 4th Street, Hamilton, Montana 59840, USA.
  4. Abhilash I Chiramel: Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 South 4th Street, Hamilton, Montana 59840, USA.
  5. Sonja M Best: Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 South 4th Street, Hamilton, Montana 59840, USA.
  6. Hideki Ebihara: Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 South 4th Street, Hamilton, Montana 59840, USA.
  7. Heinz Feldmann: Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 South 4th Street, Hamilton, Montana 59840, USA.
  8. Thomas Hoenen: Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 South 4th Street, Hamilton, Montana 59840, USA.

Abstract

The current Ebola virus (EBOV) outbreak in West Africa is unprecedented in terms of both its size and duration, and there has been speculation and concern regarding the potential for EBOV to increase in virulence as a result of its prolonged circulation in humans. Here we investigate the relative potency of the interferon (IFN) inhibitors encoded by EBOVs from West Africa, since an important EBOV virulence factor is inhibition of the antiviral IFN response. Based on this work we show that, in terms of IFN antagonism, the West African viruses display no discernible differences from the prototype Mayinga isolate, which corroborates epidemiological data suggesting these viruses show no increased virulence compared with those from previous outbreaks. This finding has important implications for public health decisions, since it does not provide experimental support for theoretical claims that EBOV might gain increased virulence due to the extensive human-to-human transmission in the on-going outbreak.

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Grants

  1. Z99 AI999999/Intramural NIH HHS

MeSH Term

Africa, Western
Cloning, Molecular
Ebolavirus
HEK293 Cells
Humans
Interferon-beta
Viral Proteins
Viral Regulatory and Accessory Proteins

Chemicals

VP24 protein, Ebola virus
VP35 protein, filovirus
Viral Proteins
Viral Regulatory and Accessory Proteins
Interferon-beta

Word Cloud

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