Evidence map›Paper›PMID 42288136›Full record

ArticleVirologica Sinica2026

Degradation of ACSL3 by influenza A virus shifts unfolded protein response from antiviral defense to viral evasion.

Shuoxuan Zhao, Yichao Chen, Tianxin Zhang, Yaoyao Gao, Jing Wu, Fangji Yang, Yongxiang Liu, Xuesong Liu, Nan Qi

Abstract read
In one paragraph

Article in Virologica Sinica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Shuoxuan ZhaoState Key Laboratory of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou 510120, China.
Yichao ChenState Key Laboratory of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou 510120, China; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou 510005, China.
Tianxin ZhangGuangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou 510005, China.
Yaoyao GaoGuangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou 510005, China.
Jing WuState Key Laboratory of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou 510120, China.
Fangji YangState Key Laboratory of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou 510120, China.
Yongxiang LiuState Key Laboratory of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou 510120, China; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou 510005, China. Electronic address: liu_yongxiang@gzlab.ac.cn.
Xuesong LiuState Key Laboratory of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou 510120, China. Electronic address: liuxuesong1000@sina.com.
Nan QiState Key Laboratory of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou 510120, China; Guangzhou National Laboratory, Guangzhou International Bio-Island, Guangzhou 510005, China. Electronic address: qi_nan@gzlab.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Host restriction factors and viral evasion strategies involved in the virus-host arms races remain to be discovered. Through an initial membrane protein-targeted CRISPR-Cas9 screening, we identified Acyl-CoA synthetase long-chain family member 3 (ACSL3) as a restriction factor against influenza A virus (IAV). Clinical transcriptomic analysis shows that ACSL3 is upregulated in peripheral blood mononuclear cells from mildly ill patients with influenza. Ectopic expression and loss-of-function validation demonstrate the physiological role of ACSL3 in restricting viral proliferation of diverse IAV subtypes (H1N1, H3N2, H3N8) in vitro and in vivo. Mechanistically, ACSL3 potentiates the antiviral unfolded protein response (UPR) by engaging the endoplasmic reticulum (ER) stress sensors IRE1α and PERK, thereby enhancing the IRE1α-XBP1-s driven inflammation and inhibiting the PERK-ATF4-CHOP mediated apoptosis. Conversely, IAV triggers the lysosomal degradation of ACSL3 and thus reprograms UPR to promote an immunologically silent apoptosis for viral egress and dissemination. Our findings establish ACSL3 as a molecular switch balancing the UPR-mediated antiviral response, and reveal a targeted viral evasion strategy in the virus-host interplay.

Indexed as

Coenzyme A LigasesImmune EvasionInfluenza A virusInfluenza, HumanUnfolded Protein ResponseAnimalsApoptosisEndoplasmic Reticulum StressEndoribonucleasesHost-Pathogen InteractionsHumansInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeLong-Chain-Fatty-Acid-CoA LigaseMiceProtein Serine-Threonine KinasesCoenzyme A LigasesEndoribonucleasesERN1 protein, humanLong-Chain-Fatty-Acid-CoA LigaseProtein Serine-Threonine KinasesACSL3ApoptosisEndoplasmic reticulum stress (ER stress)Influenza A virus (IAV)Unfolded protein response (UPR)

Identifiers

PMID42288136
PMCPMC13469312

What Socratic 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 Socratic graph.