Evidence map›Paper›PMID 42065594›Full record

ArticlemBio2026

Japanese encephalitis virus NS1 and NS4B synergistically target TLR3 signaling to promote viral replication.

Quan Zeng, Maozhou He, Mengyao Li, Dong Yang, Lei Wang, Chenlin Hao, Zhaoqing Wang, Minmin Zhou, Tianrenzheng Zhu, Xueshi Niu and 7 more

Abstract read
In one paragraph

Article in mBio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Quan Zeng *College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.
Maozhou He *School of Pharmaceutical Science and Technology, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou, China.
Mengyao Li *College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.
Dong Yang *Xianghu Laboratory, Hangzhou, Zhejiang, China.
Lei WangState Key Laboratory of Emerging Infectious Diseases, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, and Pandemic Research Alliance at The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
Chenlin HaoCollege of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.
Zhaoqing WangCollege of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.
Minmin ZhouState Key Laboratory of Emerging Infectious Diseases, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, and Pandemic Research Alliance at The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
Tianrenzheng ZhuState Key Laboratory of Emerging Infectious Diseases, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, and Pandemic Research Alliance at The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
Xueshi NiuCollege of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.
Zhihui ChenCollege of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.
Bingqian ZhangCollege of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.
Shaopo ZuCollege of Veterinary Medicine, Henan Agricultural University, Ministry of Education Key Laboratory for Animal Pathogens and Biosafety, Henan Province Key Laboratory of Animal Food Pathogens Surveillance, Zhengzhou, China.
Xueyan DingCollege of Veterinary Medicine, Henan Agricultural University, Ministry of Education Key Laboratory for Animal Pathogens and Biosafety, Henan Province Key Laboratory of Animal Food Pathogens Surveillance, Zhengzhou, China.
Zhanyong WeiCollege of Veterinary Medicine, Henan Agricultural University, Ministry of Education Key Laboratory for Animal Pathogens and Biosafety, Henan Province Key Laboratory of Animal Food Pathogens Surveillance, Zhengzhou, China.ORCID 0000-0001-8705-6426
Hin ChuState Key Laboratory of Emerging Infectious Diseases, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, and Pandemic Research Alliance at The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.ORCID 0000-0003-2855-9837
Honglei ZhangState Key Laboratory of Emerging Infectious Diseases, Department of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, and Pandemic Research Alliance at The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.ORCID 0000-0002-6540-5231

Funding

National Natural Science Foundation of China 32002297National Natural Science Foundation of China 32122001
6 · The paper itself

Abstract

To establish effective infection, viral pathogens employ diverse strategies through encoded proteins to interfere with host antiviral responses. While previous studies have predominantly focused on elucidating the mechanisms by which individual viral proteins regulate type I interferon (IFN) responses, this study presents the first demonstration that Japanese encephalitis virus (JEV)-encoded NS1 and NS4B proteins cooperatively target the TLR3 receptor signaling pathway to suppress IFN production. Here, we first discovered JEV-encoded multifunctional glycoprotein NS1, which inhibits TLR3-mediated IFN-β production by targeting TLR3 and TRIF. Mechanistically, NS1 interacts with these host factors and may induce their degradation via the autophagy pathway. Building on these findings, we further demonstrated that NS1 and NS4B act synergistically to suppress type I IFN production by enhancing TLR3 and TRIF degradation, thereby facilitating JEV replication. Structural simulation of the NS1-NS4B-TLR3 complex unveiled a dynamic mechanism that NS4B binding induces conformational changes in dimerized NS1, which leads to a tighter binding posture between NS1 and TLR3. Notably, NS4B binding expands the interface between NS1 and TLR3 by 1.5-fold that results in enhanced TLR3 degradation and downstream IFN-β suppression. Functional analysis confirmed that the C291/K293/R314 triple mutation in NS1 synergistically impairs TLR3 degradation. Collectively, using JEV as a model, this study reveals a novel mechanism by which two viral components can act synergistically to evade the host antiviral response. Given the common coexistence and functional interplay of viral-encoded proteins in naturally infected cells, this study establishes a framework for investigating cooperative interactions among multiple viral proteins. IMPORTANCE: Viruses evade host immunity through encoded viral proteins, while previous research has predominantly focused on single protein mechanisms. This study reveals a novel cooperative immune evasion strategy, demonstrating for the first time that Japanese encephalitis virus NS1 and NS4B proteins act synergistically to degrade the host's TLR3 and TRIF adaptor, thereby suppressing type I interferon production. Structural simulations show that NS4B induces conformational changes in NS1, enhancing its binding to TLR3 and accelerating its degradation. This work establishes a new paradigm for how multiple viral components can function cooperatively to subvert antiviral defenses. Given that viral proteins naturally coexist and interact, this study provides a crucial framework for investigating complex viral protein interplay, which is fundamental to understanding viral pathogenesis.

Indexed as

Encephalitis Virus, JapaneseSignal TransductionToll-Like Receptor 3Viral Nonstructural ProteinsVirus ReplicationAdaptor Proteins, Vesicular TransportAnimalsCell LineEncephalitis, JapaneseHEK293 CellsHost-Pathogen InteractionsHumansImmune EvasionInterferon-betaProtein BindingAdaptor Proteins, Vesicular TransportInterferon-betaNS1 protein, FlavivirusNS4B protein, flavivirusTICAM1 protein, humanTLR3 protein, humanToll-Like Receptor 3Viral Nonstructural Proteinsimmune escapeJapanese encephalitis virusNS1 and NS4Bsynergistic interactionTLR3 signaling pathwayviral replication

Identifiers

PMID42065594
PMCPMC13251397

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.