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Interferons Inhibit Ebola Virus Infection of Human Keratinocytes
Jonah Elliff1,2, Hanora Van Ert1,2, Kristina Sevcik1
1Department of Microbiology and Immunology, University of Iowa, Iowa City, IA 52242, USA.
Zaire Ebola virus (EBOV) infects human skin keratinocytes. Interferon pre-treatment of these cells inhibited EBOV infection, suggesting interferon-stimulated genes could be EBOV therapeutics.
Area of Science:
- Virology
- Immunology
- Dermatology
Background:
- Zaire Ebola virus (EBOV) causes severe hemorrhagic disease in humans.
- While macrophages are early targets, other cells like keratinocytes are infected later.
- Infectious EBOV on skin surfaces may transmit the virus between individuals.
Purpose of the Study:
- To investigate EBOV infection in human skin keratinocytes.
- To determine the effect of interferons (IFNs) on EBOV infection in keratinocytes.
- To identify host genes modulated by IFNs in keratinocytes during EBOV infection.
Main Methods:
- EBOV and modified EBOV (EBOVΔVP30) infection of normal human skin keratinocytes (NHSK-1).
- Pre-treatment of NHSK-1 cells with type I, II, and III interferons (IFNs).
- Transcriptome analysis of IFN-treated keratinocytes to identify interferon-stimulated genes (ISGs).
Main Results:
- EBOV infects NHSK-1 cells.
- IFN pre-treatment inhibited EBOVΔVP30 and rVSV/EBOV GP infection in a dose-dependent manner.
- IFN treatment upregulated a subset of ISGs in keratinocytes, common across all three IFN types.
Conclusions:
- Interferon-stimulated genes induced in keratinocytes can reduce EBOV infection.
- ISGs represent potential therapeutic targets for EBOV infection.
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