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Risks Posed by Reston, the Forgotten Ebolavirus

Cantoni, D, Hamlet, A, Michaelis, Martin, Wass, Mark N., Rossman, Jeremy S. (2016) Risks Posed by Reston, the Forgotten Ebolavirus. mSphere, 1 (6). Article Number 32216. ISSN 2379-5042. E-ISSN 2379-5042. (doi:10.1128/mSphere.00322-16) (KAR id:59759)

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http://dx.doi.org/10.1128/mSphere.00322-16

Abstract

Out of the five members of the Ebolavirus family, four cause lifethreatening disease, whereas the fifth, Reston virus (RESTV), is nonpathogenic in humans. The reasons for this discrepancy remain unclear. In this review, we analyze the currently available information to provide a state-of-the-art summary of the factors that determine the human pathogenicity of Ebolaviruses. RESTV causes sporadic infections in cynomolgus monkeys and is found in domestic pigs throughout the Philippines and China. Phylogenetic analyses revealed that RESTV is most closely related to the Sudan virus, which causes a high mortality rate in humans. Amino acid sequence differences between RESTV and the other Ebolaviruses are found in all nine Ebolavirus proteins, though no one residue appears sufficient to confer pathogenicity. Changes in the glycoprotein contribute to differences in Ebolavirus pathogenicity but are not sufficient to confer pathogenicity on their own. Similarly, differences in VP24 and VP35 affect viral immune evasion and are associated with changes in human pathogenicity. A recent in silico analysis systematically determined the functional consequences of sequence variations between RESTV and human-pathogenic Ebolaviruses. Multiple positions in VP24 were differently conserved between RESTV and the other Ebolaviruses and may alter human pathogenicity. In conclusion, the factors that determine the pathogenicity of Ebolaviruses in humans remain insufficiently understood. An improved understanding of these pathogenicity-determining factors is of crucial importance for disease prevention and for the early detection of emergent and potentially human-pathogenic RESTVs.

Item Type: Article
DOI/Identification number: 10.1128/mSphere.00322-16
Uncontrolled keywords: Ebolavirus, pathogenicity, Reston
Subjects: Q Science > QR Microbiology
Divisions: Divisions > Division of Natural Sciences > School of Biosciences
Depositing User: Jeremy Rossman
Date Deposited: 29 Dec 2016 10:01 UTC
Last Modified: 16 Oct 2020 12:52 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/59759 (The current URI for this page, for reference purposes)
Michaelis, Martin: https://orcid.org/0000-0002-5710-5888
Wass, Mark N.: https://orcid.org/0000-0001-5428-6479
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