Identification and Structural Characterization of Viroporins from Deadly Hemorrhagic Viruses

Crimean-Congo hemorrhagic fever virus (CCHF-V) and Ebola virus are lethal pathogens that cause widespread outbreaks of hemorrhagic fever. Both diseases can be transmitted through contact with the bodily fluids of infected individuals, but as an arbovirus, CCHF-V is primarily transmitted through tick bites. Both of these viruses are classified as Risk Group 4 due to the appreciable health threat they pose. To date, there are few effective treatments available to combat these deadly hemorrhagic fevers. Consequently, identifying and characterizing ion channels (viroporins) encoded in the viral genomes may lead to potential targeted drug development. Therefore, using bacteria-based genetic assays, two viroporin candidates from CCHF-V and Ebola have been examined, and their proposed structures have been modeled to aid in further drug discovery. The results indicate that CCHF-V-gp exhibits channel activity, which is indistinguishable from established viroporins found in other viruses. In contrast, our experimental approach was unable to uncover a viroporin candidate in the Ebola virus.

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Publication Details

Journal
Viruses
Published
2025-08-14
DOI
https://doi.org/10.3390/v17081120
Citations
1
Primary Topic
Viral Infections and Vectors
Type
article
Field-Weighted Citation Impact
1.40

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article

Identification and Structural Characterization of Viroporins from Deadly Hemorrhagic Viruses

Kingshuk Basu, Isaiah T. Arkin, Hiya Lahiri
1 citations
Viruses
Viral Infections and Vectors
1.40
article

Identification and Structural Characterization of Viroporins from Deadly Hemorrhagic Viruses

Kingshuk Basu, Isaiah T. Arkin, Hiya Lahiri
article en
1 citations

Abstract

Crimean-Congo hemorrhagic fever virus (CCHF-V) and Ebola virus are lethal pathogens that cause widespread outbreaks of hemorrhagic fever. Both diseases can be transmitted through contact with the bodily fluids of infected individuals, but as an arbovirus, CCHF-V is primarily transmitted through tick bites. Both of these viruses are classified as Risk Group 4 due to the appreciable health threat they pose. To date, there are few effective treatments available to combat these deadly hemorrhagic fevers. Consequently, identifying and characterizing ion channels (viroporins) encoded in the viral genomes may lead to potential targeted drug development. Therefore, using bacteria-based genetic assays, two viroporin candidates from CCHF-V and Ebola have been examined, and their proposed structures have been modeled to aid in further drug discovery. The results indicate that CCHF-V-gp exhibits channel activity, which is indistinguishable from established viroporins found in other viruses. In contrast, our experimental approach was unable to uncover a viroporin candidate in the Ebola virus.

VirusesVol. 17(8)
City University of Hong Kong (HK), Hebrew University of Jerusalem (IL)
United States - Israel Binational Agricultural Research and Development Fund, City University of Hong Kong, Israel Science Foundation, National Institutes of Health
Openalex Percentile: Top 17%
Viral Infections and Vectors
1.40
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