Evidence map›Paper›PMID 41157656›Full record

ReviewViruses2025

Metabolic Hostile Takeover: How Influenza Virus Reprograms Cellular Metabolism for Replication.

Xianfeng Hui, Xiaowei Tian, Shihuan Ding, Ge Gao, Xin Zhao, Jiyan Cui, Yiru Hou, Tiesuo Zhao, Hui Wang

Abstract readReview
In one paragraph

Review in Viruses, 2025. 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. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. 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

9 authors.

Xianfeng HuiDepartment of Immunology, School of Basic Medical Sciences, Henan Medical University, Xinxiang 453003, China.
Xiaowei TianDepartment of Pathogenic Biology, School of Basic Medical Sciences, Henan Medical University, Xinxiang 453003, China.
Shihuan DingDepartment of Immunology, School of Basic Medical Sciences, Henan Medical University, Xinxiang 453003, China.
Ge GaoHenan Collaborative Innovation Center of Molecular Diagnosis and Laboratory Medicine, School of Medical Technology, Henan Medical University, Xinxiang 453003, China.
Xin ZhaoDepartment of Immunology, School of Basic Medical Sciences, Henan Medical University, Xinxiang 453003, China.
Jiyan CuiDepartment of Immunology, School of Basic Medical Sciences, Henan Medical University, Xinxiang 453003, China.
Yiru HouDepartment of Immunology, School of Basic Medical Sciences, Henan Medical University, Xinxiang 453003, China.
Tiesuo ZhaoDepartment of Immunology, School of Basic Medical Sciences, Henan Medical University, Xinxiang 453003, China.
Hui WangHenan Collaborative Innovation Center of Molecular Diagnosis and Laboratory Medicine, School of Medical Technology, Henan Medical University, Xinxiang 453003, China.ORCID 0000-0002-2454-3814

Funding

111 Project D20036Key Scientific Research Project of Higher Education of Henan Province 25A310013National Natural Science Foundation of China 32300120
6 · The paper itself

Abstract

Influenza viruses are adept at hijacking host cellular machinery to facilitate their replication and propagation. A critical aspect of this hijacking involves the reprogramming of host cell metabolism. This review summarizes current findings on how influenza virus infection alters major metabolic pathways, including enhanced glycolysis, suppression of oxidative phosphorylation, diversion of TCA cycle intermediates for biosynthesis, and upregulation of lipid and amino acid metabolism. Key nutrients like glucose, glutamine, and serine are redirected to support viral RNA synthesis, protein production, and membrane formation. Moreover, these metabolic changes also modulate host immune responses, potentially aiding in immune evasion. We highlight the role of transcription factors such as SREBPs in lipid synthesis and the impact of one-carbon metabolism on epigenetic regulation. Finally, we discuss how targeting virus-induced metabolic shifts, using agents like 2-deoxyglucose or fatty acid synthesis inhibitors, offers promising avenues for antiviral intervention, while emphasizing the need for selective approaches to minimize harm to normal cells.

Indexed as

Host-Pathogen InteractionsInfluenza, HumanOrthomyxoviridaeVirus ReplicationAnimalsCitric Acid CycleGlycolysisHumansLipid MetabolismMetabolic Networks and PathwaysOxidative Phosphorylationamino acid metabolismantiviral strategiescellular metabolismglycolysisinfluenza viruslipid biosynthesis

Identifiers

PMID41157656
PMCPMC12567686

What OpenQuestion holds

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LicenceCC BY
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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.