Tetraspanin CD9 Is a Positive Regulator of Filovirus Egress

Filoviruses, including Ebola (EBOV) and Marburg (MARV) viruses, are zoonotic pathogens that cause severe hemorrhagic fever in humans, with mortality rates reaching up to 90%. Filovirus egress and spread are driven by the viral matrix protein VP40 and regulated both positively and negatively by a growing number of specific host interactors. Here, we identify tetraspanin protein CD9, a plasma membrane organizing and scaffolding protein, as playing a role in facilitating efficient egress of EBOV and MARV. Indeed, we observed a significant decrease in viral egress of VLPs and live filoviruses from CD9-KD cells as compared to that from WT cells. Moreover, exogenous expression of CD9 rescued egress of VP40 VLPs close to WT levels in the CD9-KD cells. These findings identify tetraspanin CD9 as a positive regulator of filovirus egress, and thus CD9 may represent a potential new target for antiviral therapies targeting the late stage of the filovirus lifecycle.

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Publication Details

Journal
Viruses
Published
2026-01-13
DOI
https://doi.org/10.3390/v18010104
Primary Topic
Viral Infections and Outbreaks Research
Type
article
Field-Weighted Citation Impact
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article

Tetraspanin CD9 Is a Positive Regulator of Filovirus Egress

Olena Shtanko, Marija A. Djurkovic, Ronald N. Harty, Loveleena K. Anand et al.
Viruses
Viral Infections and Outbreaks Research
article

Tetraspanin CD9 Is a Positive Regulator of Filovirus Egress

Olena Shtanko, Marija A. Djurkovic, Ronald N. Harty, Loveleena K. Anand, Ariel Shepley-McTaggart
article en

Abstract

Filoviruses, including Ebola (EBOV) and Marburg (MARV) viruses, are zoonotic pathogens that cause severe hemorrhagic fever in humans, with mortality rates reaching up to 90%. Filovirus egress and spread are driven by the viral matrix protein VP40 and regulated both positively and negatively by a growing number of specific host interactors. Here, we identify tetraspanin protein CD9, a plasma membrane organizing and scaffolding protein, as playing a role in facilitating efficient egress of EBOV and MARV. Indeed, we observed a significant decrease in viral egress of VLPs and live filoviruses from CD9-KD cells as compared to that from WT cells. Moreover, exogenous expression of CD9 rescued egress of VP40 VLPs close to WT levels in the CD9-KD cells. These findings identify tetraspanin CD9 as a positive regulator of filovirus egress, and thus CD9 may represent a potential new target for antiviral therapies targeting the late stage of the filovirus lifecycle.

VirusesVol. 18(1)
Texas Biomedical Research Institute (US), The University of Texas at San Antonio (US), University of Pennsylvania (US)
Good health and well-being
Openalex Percentile: Top 87%
Viral Infections and Outbreaks Research
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