Evidence map›Paper›PMID 39512588›Full record

ArticleFrontiers in cellular and infection microbiology2024

Virome analysis provides new insights into the pathogenesis mechanism and treatment of SLE disease.

Yifan Wu, Zhiyuan Zhang, Xinglian Wang, Xun Liu, Ye Qiu, Xingyi Ge, Zhichao Miao, Xiangxian Meng, Yousong Peng

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Article
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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.

Yifan WuHunan Provincial Key Laboratory of Medical Virology, College of Biology, Hunan University, Changsha, China.
Zhiyuan ZhangHunan Provincial Key Laboratory of Medical Virology, College of Biology, Hunan University, Changsha, China.
Xinglian WangHunan Provincial Key Laboratory of Medical Virology, College of Biology, Hunan University, Changsha, China.
Xun LiuHunan Provincial Key Laboratory of Medical Virology, College of Biology, Hunan University, Changsha, China.
Ye QiuHunan Provincial Key Laboratory of Medical Virology, College of Biology, Hunan University, Changsha, China.
Xingyi GeHunan Provincial Key Laboratory of Medical Virology, College of Biology, Hunan University, Changsha, China.
Zhichao MiaoGMU-GIBH Joint School of Life Sciences, The Guangdong-Hong Kong-Macau Joint Laboratory for Cell Fate Regulation and Diseases, Guangzhou National Laboratory, Guangzhou Medical University, Guangzhou, China.
Xiangxian MengHunan Provincial Key Laboratory of Medical Virology, College of Biology, Hunan University, Changsha, China.
Yousong PengHunan Provincial Key Laboratory of Medical Virology, College of Biology, Hunan University, Changsha, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: This study aimed to investigate the virome diversity of the SLE disease and the association between viral infections and the disease. Methods: SLE-related RNA-Seq data were retrieved from public databases. A rigorous computational workflow was employed to identify the human viruses. Differential expression analysis and functional enrichment analysis were conducted in R. Results: We identified ten human virus species from 826 RNA-Seq samples of human blood, comprising 688 SLE patients and 138 healthy controls. Eight of the ten virus species exhibited higher positive rates in SLE patients compared to healthy controls, with Human betaherpesvirus 5 (HHV5) having the highest positive rate (4.1%) and being exclusively detected in SLE samples. The virus abundances were low and comparable in both SLE patients and healthy controls. Analysis of the antiviral interferon-stimulated genes (ISGs) in samples showed higher ISG expression levels in HHV4 and HHV5-positive samples compared to virus-negative samples. Several genes that were up-regulated in SLE patients were further up-regulated after HHV5 infection, and they were mainly enriched in immune response-related biological processes. Additionally, the expression levels of several marker genes of SLE severity were compared between HHV5-positive and virus-negative SLE patients, suggesting that HHV5 infection may be associated with aggravated SLE disease. Discussion: We found that SLE patients are more susceptible to viral infections than healthy individuals. Viral infections, such as HHV5, may be associated with aggravated SLE disease. This study deepens our understanding of the association between viruses and SLE and provides new insights into prevention and control of the disease.

Indexed as

Lupus Erythematosus, SystemicViromeAdultCase-Control StudiesComputational BiologyFemaleHumansMaleRNA-SeqVirus DiseasesVirusesbioinformaticssystemic lupus erythematosusviromevirus-disease interactionvirus infection

Identifiers

PMID39512588
PMCPMC11540821

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