Evidence map›Paper›PMID 40511919›Full record

ArticleJournal of virology2025

MARCH6 suppresses Tembusu virus replication by targeting viral NS5 protein for TOLLIP-mediated selective autophagic degradation.

Peng Zhou, Wanrong Wu, Jiani Wei, Yueshan Yang, Anan Jongkaewwattana, Yuncai Xiao, Hui Jin, Hongbo Zhou, Rui Luo

Abstract read
In one paragraph

Article in Journal of virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Multidimensional mechanisms of SFTSV-host interactions: viral protein functions, mFrontiers in cellular and infection microbiology · 2026
    Review
  6. Article
  7. Article
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

9 authors.

Peng ZhouState Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agriculture University, Wuhan, China.ORCID 0009-0000-3325-008X
Wanrong WuState Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agriculture University, Wuhan, China.
Jiani WeiState Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agriculture University, Wuhan, China.
Yueshan YangState Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agriculture University, Wuhan, China.
Anan JongkaewwattanaVirology and Cell Technology Research Team, National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency (NSTDA), Pathum Thani, Thailand.
Yuncai XiaoState Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agriculture University, Wuhan, China.
Hui JinState Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agriculture University, Wuhan, China.ORCID 0000-0001-8004-2662
Hongbo ZhouState Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agriculture University, Wuhan, China.ORCID 0000-0002-3954-3972
Rui LuoState Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agriculture University, Wuhan, China.ORCID 0000-0002-1966-251X

Funding

China Postdoctoral Science Foundation 2024M761078China Postdoctoral Science Foundation GZC20230912Earmarked Fund for China Agriculture Research System CARS-41Fundamental Research Funds for the Central Universities 2662023PY005National Natural Science Foundation of China 32272989National Natural Science Foundation of China 32402865Natural Science Foundation of Hubei Province 2024AFB125Natural Science Foundation of Hubei Province 2025AFB600Postdoctoral Science Foundation of Hubei Province 2024HBBHCXA047
6 · The paper itself

Abstract

The E3 ligase membrane-associated RING finger 6 (MARCH6) plays a pivotal role in various cellular processes; however, its role in viral defense remains largely unexplored. In this study, we have elucidated a novel antiviral mechanism of avian MARCH6 against duck Tembusu virus (TMUV), revealing a previously uncharacterized host defense strategy. Notably, MARCH6 expression was significantly upregulated during TMUV infection in several duck cell lines, suggesting a conserved cellular response. Functional analyses revealed that overexpression of MARCH6 effectively suppressed TMUV replication, whereas its knockdown markedly enhanced viral replication. Mechanistically, MARCH6 directly interacts with the viral non-structural protein 5 (NS5), mediating its targeted degradation through an unprecedented E3 ligase activity-independent mechanism. Moreover, MARCH6 recruits the autophagic cargo receptor TOLLIP, which facilitates the NS5-TOLLIP interaction independent of ubiquitin signaling and subsequently directs NS5 to phagophores for degradation. These findings reveal a novel antiviral mechanism that focuses on the MARCH6-NS5-TOLLIP axis and represents a critical host defense strategy against viral infections. This study not only provides insights into the antiviral functions of MARCH6 but also emphasizes the importance of selective autophagy as a fundamental mechanism to control viral infection.IMPORTANCETMUV, an emerging pathogenic flavivirus, has rapidly spread across major duck farming regions in Asia since 2010, causing substantial economic losses in the duck industry. More recently, TMUV has expanded its host range, raising concerns about its potential threat to mammals. Understanding TMUV-host interactions is essential for developing effective treatments and vaccines. Here, we uncover a previously uncharacterized role of avian MARCH6 in antiviral defense against TMUV. We demonstrate that MARCH6 restricts TMUV replication through an E3 ligase activity-independent mechanism by targeting the viral NS5 protein for degradation. Notably, MARCH6 promotes NS5 degradation via selective autophagy by recruiting the cargo receptor TOLLIP, bypassing conventional ubiquitin signaling. These findings reveal a novel host antiviral strategy centered on the MARCH6-NS5-TOLLIP axis, broadening our understanding of selective autophagy in antiviral defense.

Indexed as

AutophagyFlavivirusFlavivirus InfectionsIntracellular Signaling Peptides and ProteinsUbiquitin-Protein LigasesViral Nonstructural ProteinsVirus ReplicationAnimalsCell LineDucksHEK293 CellsHost-Pathogen InteractionsHumansProteolysisIntracellular Signaling Peptides and ProteinsNS5 protein, flavivirusUbiquitin-Protein LigasesViral Nonstructural Proteinsautophagic degradationMARCH6NS5TMUV replicationTOLLIP

Identifiers

PMID40511919
PMCPMC12282148

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.