Severe fever with thrombocytopenia syndrome virus (SFTSV) listed in the World Health Organization 9 most dangerous pathogens is an emerging Phlebovirus in the Phenuiviridae family. Due to the lack of therapy and vaccine against SFTSV infection, there is a pressing need to understand the pathogenesis of SFTSV to develop effective antiviral agents. Designated as Biosafety level 3 agent, SFTSV contains a genome comprised of three segments of negative or ambisense RNA designated as large, medium, and small. The S segment encodes a nucleoprotein and a nonstructural protein (NSs) via an ambisense coding strategy.
(Aim 1) We have discovered that NSs targets the Vps15-Vps34 lipid kinase complex to form virus-induced autophagosome-like inclusion bodies (IB), subsequently sequestrating IFN signaling effectors (RIG-I, TRIM25, and TBK1) to the IB and thereby suppressing IFN production.
(Aim 2) We have also found that SFTSV NSs plays an essential role in viral immunopathogenesis by targeting the TPL2-ABIN2-p105 kinase complex to robustly induce expression of immune suppressive genes, specifically IL-10 cytokine.
(Aim 3) We combined viral reverse genetics, a TPL2 kinase inhibitor, Tpl2-/- and il10-/- mouse models to show that the NSs-mediated activation of TPL2 signaling pathway robustly induced IL-10 production that was essential for viral pathogenesis. For the first time, we developed an age- dependent ferret model: young adult ferrets (<2 years old) did not show any clinical symptoms and mortality; however, SFTSV-infected aged ferrets (>4 years old) demonstrated severe thrombocytopenia, reduced white blood cells, and high fever with ~90% mortality rate, fully recapitulating human clinical manifestation. With well-established in vitro experimental conditions and novel in vivo animal models, the proposed study not only demonstrates the critical role of SFTSV NSs in viral immune evasion and pathogenesis, but also identifies potential therapeutic approaches to treat SFTSV-infected patients.

Public Health Relevance

SFTSV is listed in the WHO?s nine most dangerous pathogens. The proposed study not only demonstrates the critical role of SFTSV NSs in viral immune evasion and pathogenesis, but also identifies animal models for SFTSV pathogenesis and therapeutics to treat SFTSV-infected patients.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI140705-02
Application #
9735111
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Alarcon, Rodolfo M
Project Start
2018-07-01
Project End
2023-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Southern California
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
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