Tolcapone Potently Inhibits Seminal Amyloid Fibrils Formation and Blocks Entry of Ebola Pseudoviruses

Ebola virus (EBOV), the causative pathogen of the deadly EBOV disease (EVD), can be transmitted sexual transmission. Seminal amyloid fibrils have been found enhancers of EBOV infection. Currently, limited preventive vaccine or therapeutic is available to block EBOV infection through sexual intercour...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in microbiology Vol. 11; p. 504
Main Authors Qiu, Mengjie, Li, Zhaofeng, Chen, Yuliu, Guo, Jiayin, Xu, Wei, Qi, Tao, Qiu, Yurong, Pang, Jianxin, Li, Lin, Liu, Shuwen, Tan, Suiyi
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 30.04.2020
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Ebola virus (EBOV), the causative pathogen of the deadly EBOV disease (EVD), can be transmitted sexual transmission. Seminal amyloid fibrils have been found enhancers of EBOV infection. Currently, limited preventive vaccine or therapeutic is available to block EBOV infection through sexual intercourse. In this study, we repurpose tolcapone, a US Food and Drug Administration (FDA)-approved agent for Parkinson's disease, as a potent inhibitor of seminal amyloid fibrils, among which semen-derived enhancer of viral infection (SEVI) is the best-characterized. Tolcapone binds to the amyloidogenic region of the SEVI precursor peptide (PAP248-286) and inhibits PAP248-286 aggregation by disrupting PAP248-286 oligomerization. In addition, tolcapone interacts with preformed SEVI fibrils and influences the activity of SEVI in promoting infection of pseudovirus (PsV) carrying the envelope glycoprotein (GP) of the EBOV Zaire or Sudan species (Zaire PsV and Sudan PsV, respectively). Tolcapone significantly antagonizes SEVI-mediated enhancement of both Zaire PsV and Sudan PsV binding to and subsequent internalization in HeLa cells. Of note, tolcapone is also effective in inhibiting the entry of both Zaire PsV and Sudan PsV. Tolcapone inhibits viral entry possibly through binding with critical residues in EBOV GP. Moreover, the combination of tolcapone with two small-molecule entry inhibitors, including bepridil and sertraline, exhibited synergistic anti-EBOV effects in semen. Collectively, as a bifunctional agent targeting the viral infection-enhancing amyloid and the virus itself during sexual intercourse, tolcapone can act as either a prophylactic topical agent to prevent the sexual transmission of EBOV or a therapeutic to treat EBOV infection.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Edited by: Christopher C. Broder, Uniformed Services University of the Health Sciences, United States
This article was submitted to Virology, a section of the journal Frontiers in Microbiology
Reviewed by: Asuka Nanbo, Nagasaki University, Japan; Masfique Mehedi, University of North Dakota, United States
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2020.00504