Evidence map›Paper›PMID 38466095›Full record

ArticleJournal of virology2024

SQSTM1 downregulates avian metapneumovirus subgroup C replication via mediating selective autophagic degradation of viral M2-2 protein.

Jinshuo Guo, Yongyan Shi, Genghong Jiang, Penghui Zeng, Zhi Wu, Dedong Wang, Yongqiu Cui, Xiaoyu Yang, Jianwei Zhou, Xufei Feng and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

12 authors at 1 institution in 1 country.

Jinshuo GuoCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Yongyan ShiCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Genghong JiangCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Penghui ZengCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Zhi WuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Dedong WangCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Yongqiu CuiCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Xiaoyu YangCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Jianwei ZhouCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Xufei FengCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Lei HouCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.ORCID 0009-0006-6301-5471
Jue LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, China.ORCID 0000-0001-7457-7492
Yangzhou University · CN

Funding

MOST | National Natural Science Foundation of China (NSFC) 31830095The 111 Project D18007The Priority Academic Program Development of Jiangsu Higher Education Institutions PAPD
6 · The paper itself

Abstract

Avian metapneumovirus subgroup C (aMPV/C), an important pathogen causing acute respiratory infection in chickens and turkeys, contributes to substantial economic losses in the poultry industry worldwide. aMPV/C has been reported to induce autophagy, which is beneficial to virus replication. Sequestosome 1 (SQSTM1/P62), a selective autophagic receptor, plays a crucial role in viral replication by clearing ubiquitinated proteins. However, the relationship between SQSTM1-mediated selective autophagy and aMPV/C replication is unclear. In this study, we found that the expression of SQSTM1 negatively regulates aMPV/C replication by reducing viral protein expression and viral titers. Further studies revealed that the interaction between SQSTM1 and aMPV/C M2-2 protein is mediated via the Phox and Bem1 (PB1) domain of the former, which recognizes a ubiquitinated lysine at position 67 of the M2-2 protein, and finally degrades M2-2 via SQSTM1-mediated selective autophagy. Collectively, our results reveal that SQSTM1 degrades M2-2 via a process of selective autophagy to suppress aMPV/C replication, thereby providing novel insights for the prevention and control of aMPV/C infection.IMPORTANCEThe selective autophagy plays an important role in virus replication. As an emerging pathogen of avian respiratory virus, clarification of the effect of SQSTM1, a selective autophagic receptor, on aMPV/C replication in host cells enables us to better understand the viral pathogenesis. Previous study showed that aMPV/C infection reduced the SQSTM1 expression accompanied by virus proliferation, but the specific regulatory mechanism between them was still unclear. In this study, we demonstrated for the first time that SQSTM1 recognizes the 67th amino acid of M2-2 protein by the interaction between them, followed by M2-2 degradation via the SQSTM1-mediated selective autophagy, and finally inhibits aMPV/C replication. This information supplies the mechanism by which SQSTM1 negatively regulates viral replication, and provides new insights for preventing and controlling aMPV/C infection.

Indexed as

AutophagyBirdsMetapneumovirusProteolysisSequestosome-1 ProteinViral ProteinsVirus ReplicationAnimalsHEK293 CellsHumansParamyxoviridae InfectionsProtein BindingVero CellsSequestosome-1 ProteinViral ProteinsaMPV/CM2-2 proteinselective autophagySQSTM1viral replication

Identifiers

PMID38466095
PMCPMC11019959
OpenAlexW4392643981

What OpenQuestion holds

Textmetadata
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.