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Updated: Sep 7, 2025

A High Resolution Method to Monitor Phosphorylation-dependent Activation of IRF3
Published on: January 24, 2016
Sandfly Fever Viruses Attenuate the Type I Interferon Response by Targeting the Phosphorylation of JAK-STAT
Yarden Moalem1, Yehonathan Malis2, Konstantin Voloshin1
1Department of Clinical Microbiology and Immunology, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Abstract:
Sandfly fever viruses are emerging Phleboviruses typically causing mild febrile illness. Some strains, however, can cause severe and occasionally fatal neuro-invasive disease. Like most viruses, Phleboviruses have devised various strategies to inhibit the type I interferon (IFN) response to support a productive infection. Still, most of the strategies identified so far focus on inhibiting the sensing arm of the IFN response. In contrast, the effect of sandfly virus infection on signaling from the IFN receptor is less characterized. Therefore, we tested the effect of sandfly fever virus Naples (SFNV) and Sicily (SFSV) infection on IFN signaling. We found that infection with either of these viruses inhibits signaling from the IFN receptor by inhibiting STAT1 phosphorylation and nuclear localization. We show that the viral nonstructural protein NSs mediates these effects, but only NSs from SFNV was found to interact with STAT1 directly. Thus, we tested the upstream IFN signaling components and found that Janus kinase 1 (Jak1) phosphorylation is also impaired by infection. Furthermore, the NSs proteins from both viruses directly interacted with Jak1. Last, we show that IFN inhibition by SFNV and SFSV is most likely downstream of the IFN receptor at the Jak1 level. Overall, our results reveal the multiple strategies used by these related viruses to overcome host defenses.
Insights
Sandfly fever viruses, like SFNV and SFSV, inhibit the host interferon response by blocking STAT1 and Jak1 signaling. This viral strategy helps these emerging Phleboviruses cause infection.
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- Sandfly fever viruses (Phleboviruses) can cause severe neuro-invasive disease.
- Viruses inhibit the type I interferon (IFN) response for productive infection.
- Mechanisms of IFN inhibition by these viruses, particularly downstream signaling, are not fully understood.
Purpose of the Study:
- To investigate the impact of sandfly fever virus Naples (SFNV) and Sicily (SFSV) infection on IFN signaling.
- To identify the viral components responsible for inhibiting IFN signaling.
Main Methods:
- Infection of cells with SFNV and SFSV.
- Analysis of STAT1 phosphorylation and nuclear localization.
- Investigation of Janus kinase 1 (Jak1) phosphorylation.
- Interaction studies of viral NSs protein with STAT1 and Jak1.
Main Results:
- SFNV and SFSV infection inhibit IFN receptor signaling by impairing STAT1 phosphorylation and nuclear localization.
- The viral nonstructural protein NSs mediates this inhibition.
- NSs proteins from both viruses directly interact with Jak1, and SFNV NSs interacts with STAT1.
- IFN inhibition occurs downstream of the IFN receptor, at the Jak1 level.
Conclusions:
- SFNV and SFSV employ multiple strategies to inhibit host IFN responses.
- Viral NSs proteins are key mediators of IFN inhibition by targeting Jak1 and STAT1 signaling pathways.
- Understanding these mechanisms is crucial for combating emerging Phlebovirus infections.
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