Two amino acid pairs in the Gc glycoprotein of severe fever with thrombocytopenia syndrome virus responsible for the enhanced virulence

Severe fever with thrombocytopenia syndrome (SFTS) is a significant public health concern, with a high fatality rate in humans and cats. In this study, we explored the genetic determinants that contribute to the different virulence of SFTS virus (SFTSV) based on Tk-F123 and Ng-F264 strains isolated from cats. Tk-F123 was 100% lethal in type I interferon receptor-knockout mice, whereas Ng-F264 exhibited no fatality. We identified a pair of amino acid residues in the Gc protein, glycine and serine, at residues 581 and 934, respectively, derived from Tk-F123, leading to a fatal infection. Those in Ng-F264 were arginine and asparagine. These results suggest that this pair of residues affects the Gc protein function and regulates SFTSV virulence. Our findings provide useful clues for the elucidation of viral pathogenicity and the development of effective live-attenuated vaccines and antiviral strategies.

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Publication Details

Journal
Virology
Published
2024-11-06
DOI
https://doi.org/10.1016/j.virol.2024.110294
Citations
4
Primary Topic
Viral Infections and Vectors
Type
article
Field-Weighted Citation Impact
1.56
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article

Two amino acid pairs in the Gc glycoprotein of severe fever with thrombocytopenia syndrome virus responsible for the enhanced virulence

Sithumini M. W. Lokupathirage, Shelly Wulandari, Samuel Nyampong, Hiroshi Shimoda et al.
4 citations
Virology
Viral Infections and Vectors
1.56
article

Two amino acid pairs in the Gc glycoprotein of severe fever with thrombocytopenia syndrome virus responsible for the enhanced virulence

Sithumini M. W. Lokupathirage, Shelly Wulandari, Samuel Nyampong, Hiroshi Shimoda, Daisuke Hayasaka, Michaela Beránková, Kumiko Yoshimatsu
article en
4 citations

Abstract

Severe fever with thrombocytopenia syndrome (SFTS) is a significant public health concern, with a high fatality rate in humans and cats. In this study, we explored the genetic determinants that contribute to the different virulence of SFTS virus (SFTSV) based on Tk-F123 and Ng-F264 strains isolated from cats. Tk-F123 was 100% lethal in type I interferon receptor-knockout mice, whereas Ng-F264 exhibited no fatality. We identified a pair of amino acid residues in the Gc protein, glycine and serine, at residues 581 and 934, respectively, derived from Tk-F123, leading to a fatal infection. Those in Ng-F264 were arginine and asparagine. These results suggest that this pair of residues affects the Gc protein function and regulates SFTSV virulence. Our findings provide useful clues for the elucidation of viral pathogenicity and the development of effective live-attenuated vaccines and antiviral strategies.

VirologyVol. 601
Yamaguchi University (JP), Czech Academy of Sciences (CZ), Universitas Airlangga (ID), Hokkaido University (JP), Institute of Parasitology of the Slovak Academy of Sciences (SK)
Good health and well-being
Openalex Percentile: Top 16%
Viral Infections and Vectors
1.56
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Two amino acid pairs in the Gc glycoprotein of severe fever with thrombocytopenia syndrome virus responsible for the enhanced virulence — Sithumini M. W. Lokupathirage, Shelly Wulandari, et al. · Virology (2024) | TGRS Research Map | TGRS