Evidence map›Paper›PMID 38962129›Full record

ArticleFrontiers in microbiology2024

A dicoumarol-graphene oxide quantum dot polymer inhibits porcine reproductive and respiratory syndrome virus through the JAK-STAT signaling pathway.

Zhuowei Li, Junjun Wang, Siyu Wang, Wei Zhao, Xiaolin Hou, Jianfang Wang, Hong Dong, Shuanghai Zhou, Yuan Gao, Wei Yao and 2 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2024. 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

12 authors.

Zhuowei Li *College of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.
Junjun Wang *College of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.
Siyu WangCollege of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.
Wei ZhaoCollege of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.
Xiaolin HouCollege of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.
Jianfang WangCollege of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.
Hong DongCollege of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.
Shuanghai ZhouCollege of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.
Yuan GaoLiaoning Agricultural Development Service Center Province, Shenyang, China.
Wei YaoLiaoning Agricultural Development Service Center Province, Shenyang, China.
Huanrong LiCollege of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.
Xuewei LiuCollege of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Porcine reproductive and respiratory syndrome virus (PRRSV) causes substantial economic losses in the global swine industry. The current vaccine options offer limited protection against PRRSV transmission, and there are no effective commercial antivirals available. Therefore, there is an urgent need to develop new antiviral strategies that slow global PRRSV transmission. Methods: In this study, we synthesized a dicoumarol-graphene oxide quantum dot (DIC-GQD) polymer with excellent biocompatibility. This polymer was synthesized via an electrostatic adsorption method using the natural drug DIC and GQDs as raw materials. Results: Our findings demonstrated that DIC exhibits high anti-PRRSV activity by inhibiting the PRRSV replication stage. The transcriptome sequencing analysis revealed that DIC treatment stimulates genes associated with the Janus kinase/signal transducer and activator of transcription (JAK/STAT) signalling pathway. In porcine alveolar macrophages (PAMs), DIC-GQDs induce TYK2, JAK1, STAT1, and STAT2 phosphorylation, leading to the upregulation of JAK1, STAT1, STAT2, interferon-β (IFN-β) and interferon-stimulated genes (ISGs). Animal challenge experiments further confirmed that DIC-GQDs effectively alleviated clinical symptoms and pathological reactions in the lungs, spleen, and lymph nodes of PRRSV-infected pigs. Discussion: These findings suggest that DIC-GQDs significantly inhibits PRRSV proliferation by activating the JAK/STAT signalling pathway. Therefore, DIC-GQDs hold promise as an alternative treatment for PRRSV infection.

Indexed as

antiviraldicoumarolgraphene oxide quantum dot polymerJAK/STAT signaling pathwayPRRSV

Identifiers

PMID38962129
PMCPMC11221364

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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.