Evidence map›Paper›PMID 35893690›Full record

ArticleViruses2022

Identification of Critical Genes and Pathways for Influenza A Virus Infections via Bioinformatics Analysis.

Gao Chen, Haoyue Li, Mingzhao Hao, Xiaolei Li, Yizhi Dong, Yue Zhang, Xiping Liu, Cheng Lu, Jing Zhao

Abstract read
In one paragraph

Article in Viruses, 2022. 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. Review
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  7. 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

9 authors.

Gao ChenSchool of Life Science, Hubei University, Wuhan 430062, China.
Haoyue LiInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences (CACMS), Beijing 100700, China.
Mingzhao HaoInstitute of History of Medicine and Medical Literature, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Xiaolei LiInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences (CACMS), Beijing 100700, China.
Yizhi DongInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences (CACMS), Beijing 100700, China.ORCID 0000-0002-1592-5677
Yue ZhangInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences (CACMS), Beijing 100700, China.
Xiping LiuInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences (CACMS), Beijing 100700, China.
Cheng LuInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences (CACMS), Beijing 100700, China.ORCID 0000-0002-6474-9198
Jing ZhaoInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences (CACMS), Beijing 100700, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Influenza A virus (IAV) requires the host cellular machinery for many aspects of its life cycle. Knowledge of these host cell requirements not only reveals molecular pathways exploited by the virus or triggered by the immune system but also provides further targets for antiviral drug development. To uncover critical pathways and potential targets of influenza infection, we assembled a large amount of data from 8 RNA sequencing studies of IAV infection for integrative network analysis. Weighted gene co-expression network analysis (WGCNA) was performed to investigate modules and genes correlated with the time course of infection and/or multiplicity of infection (MOI). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses were performed to explore the biological functions and pathways of the genes in 5 significant modules. Top hub genes were identified using the cytoHubba plugin in the protein interaction network. The correlation between expression levels of 7 top hub genes and time course or MOI was displayed and validated, including BCL2L13, PLSCR1, ARID5A, LMO2, NDRG4, HAP1, and CARD10. Dysregulated expression of these genes potently impacted the development of IAV infection through modulating IAV-related biological processes and pathways. This study provides further insights into the underlying molecular mechanisms and potential targets in IAV infection.

Indexed as

Influenza A virusInfluenza, HumanComputational BiologyGene Expression ProfilingGene OntologyGene Regulatory NetworksHumansProtein Interaction Mapsbioinformaticshub geneinfluenza A virusprotein interactionweighted gene co-expression network analysis

Identifiers

PMID35893690
PMCPMC9332270

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Registered trials

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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.