Evidence map›Paper›PMID 37759218›Full record

SynthesisJournal of neuroinflammation2023

Glycolytic shift during West Nile virus infection provides new therapeutic opportunities.

Patricia Mingo-Casas, Ana-Belén Blázquez, Marta Gómez de Cedrón, Ana San-Félix, Susana Molina, Estela Escribano-Romero, Eva Calvo-Pinilla, Nereida Jiménez de Oya, Ana Ramírez de Molina, Juan-Carlos Saiz and 2 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Journal of neuroinflammation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
8.4field-weighted citation impact, top 2% of its field
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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
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  5. Article
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  8. Metabolic Programming Drives Protective and Inflammatory Monocyte Fates in Viral Encephalitis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. West Nile virus unmasked: from gene variability to future challenges.Frontiers in cellular and infection microbiology · 2025
    Review
  14. Article
  15. 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 at 5 institutions in 1 country.

Patricia Mingo-Casas *Department of Biotechnology, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Consejo Superior de Investigaciones Científicas (INIA-CSIC), 28040, Madrid, Spain.
Ana-Belén Blázquez *Department of Biotechnology, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Consejo Superior de Investigaciones Científicas (INIA-CSIC), 28040, Madrid, Spain.
Marta Gómez de CedrónMolecular Oncology Group, IMDEA Food Institute, CEI UAM + CSIC, 28049, Madrid, Spain.
Ana San-FélixInstituto de Quimica Medica (IQM), CSIC, 28006, Madrid, Spain.
Susana MolinaMolecular Oncology Group, IMDEA Food Institute, CEI UAM + CSIC, 28049, Madrid, Spain.
Estela Escribano-RomeroDepartment of Biotechnology, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Consejo Superior de Investigaciones Científicas (INIA-CSIC), 28040, Madrid, Spain.
Eva Calvo-PinillaDepartment of Biotechnology, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Consejo Superior de Investigaciones Científicas (INIA-CSIC), 28040, Madrid, Spain.
Nereida Jiménez de OyaDepartment of Biotechnology, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Consejo Superior de Investigaciones Científicas (INIA-CSIC), 28040, Madrid, Spain.
Ana Ramírez de MolinaMolecular Oncology Group, IMDEA Food Institute, CEI UAM + CSIC, 28049, Madrid, Spain.
Juan-Carlos SaizDepartment of Biotechnology, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Consejo Superior de Investigaciones Científicas (INIA-CSIC), 28040, Madrid, Spain.
María-Jesús Pérez-PérezInstituto de Quimica Medica (IQM), CSIC, 28006, Madrid, Spain.
Miguel A Martín-AcebesDepartment of Biotechnology, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Consejo Superior de Investigaciones Científicas (INIA-CSIC), 28040, Madrid, Spain. martin.mangel@inia.csic.es.
Consejo Superior de Investigaciones Científicas · ESInstituto de Química Médica · ESInstituto Nacional de Investigación y Tecnología Agraria y Alimentaria · ESUniversidad Autónoma de Madrid · ESIMDEA Food · ES

Funding

Agencia Estatal de Investigación PID2019-105117RR-C21Agencia Estatal de Investigación PID2019-105117RR-C22Agencia Estatal de Investigación PID2020-119195RJ-I00Agencia Estatal de Investigación PRE2020-093374Comunidad de Madrid NUTRISION-CM/Y2020/BIO-6350European Commission NextGenerationEU through CSIC's Global Health Platform (PTI Salud Global)
6 · The paper itself

Abstract

backgroundViral rewiring of host bioenergetics and immunometabolism may provide novel targets for therapeutic interventions against viral infections. Here, we have explored the effect on bioenergetics during the infection with the mosquito-borne flavivirus West Nile virus (WNV), a medically relevant neurotropic pathogen causing outbreaks of meningitis and encephalitis worldwide.

resultsA systematic literature search and meta-analysis pointed to a misbalance of glucose homeostasis in the central nervous system of WNV patients. Real-time bioenergetic analyses confirmed upregulation of aerobic glycolysis and a reduction of mitochondrial oxidative phosphorylation during viral replication in cultured cells. Transcriptomics analyses in neural tissues from experimentally infected mice unveiled a glycolytic shift including the upregulation of hexokinases 2 and 3 (Hk2 and Hk3) and pyruvate dehydrogenase kinase 4 (Pdk4). Treatment of infected mice with the Hk inhibitor, 2-deoxy-D-glucose, or the Pdk4 inhibitor, dichloroacetate, alleviated WNV-induced neuroinflammation.

conclusionsThese results highlight the importance of host energetic metabolism and specifically glycolysis in WNV infection in vivo. This study provides proof of concept for the druggability of the glycolytic pathway for the future development of therapies to combat WNV pathology.

Indexed as

West Nile FeverAnimalsCentral Nervous SystemDisease OutbreaksGene Expression ProfilingGlycolysisHumansMiceGlycolysisImmunometabolismNeuroinflammationWest Nile virus

Identifiers

PMID37759218
PMCPMC10537838
OpenAlexW4387097030

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.