Evidence map›Paper›PMID 35732914›Full record

ArticleCellular & molecular immunology2022

SARS-CoV-2 virus NSP14 Impairs NRF2/HMOX1 activation by targeting Sirtuin 1.

Shilei Zhang, Jingfeng Wang, Lulan Wang, Saba Aliyari, Genhong Cheng

Open access · hybridAbstract read
In one paragraph

Article in Cellular & molecular immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
17.0field-weighted citation impact, top 1% 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

50 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Expression of angiotensin-converting enzyme 2, transmembrane serine protease 2, and sirtuin 1 proteins in lungs of different age groups.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2026
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

5 authors at 1 institution in 1 country.

Shilei ZhangDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, 90095, CA, USA.ORCID http://orcid.org/0000-0002-1171-9470
Jingfeng WangDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, 90095, CA, USA.
Lulan WangDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, 90095, CA, USA.
Saba AliyariDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, 90095, CA, USA.
Genhong ChengDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, 90095, CA, USA. gcheng@mednet.ucla.edu.
University of California, Los Angeles · US

Funding

Viral Mediated Type I Interferon InductionR01AI069120 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHENG, GENHONG · 2006 to 2021
$6.0M
Develop broad-spectrum antiviral agents against COVID-19 based on innate immune response to SARS-CoV-2 infectionR01AI158154 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JUNG, MICHAEL E · 2020 to 2025
$1.9M
NIAID NIH HHS R01 AI069120NIAID NIH HHS R01 AI158154
6 · The paper itself

Abstract

Most deaths from the COVID-19 pandemic are due to acute respiratory distress syndrome (ARDS)-related respiratory failure. Cytokine storms and oxidative stress are the major players in ARDS development during respiratory virus infections. However, it is still unknown how oxidative stress is regulated by viral and host factors in response to SARS-CoV-2 infection. Here, we found that activation of NRF2/HMOX1 significantly suppressed SARS-CoV-2 replication in multiple cell types by producing the metabolite biliverdin, whereas SARS-CoV-2 impaired the NRF2/HMOX1 axis through the action of the nonstructural viral protein NSP14. Mechanistically, NSP14 interacts with the catalytic domain of the NAD-dependent deacetylase Sirtuin 1 (SIRT1) and inhibits its ability to activate the NRF2/HMOX1 pathway. Furthermore, both genetic and pharmaceutical evidence corroborated the novel antiviral activity of SIRT1 against SARS-CoV-2. Therefore, our findings reveal a novel mechanism by which SARS-CoV-2 dysregulates the host antioxidant defense system and emphasize the vital role played by the SIRT1/NRF2 axis in host defense against SARS-CoV-2.

Indexed as

COVID-19Respiratory Distress SyndromeAntiviral AgentsExoribonucleasesHeme Oxygenase-1HumansNF-E2-Related Factor 2PandemicsSARS-CoV-2Sirtuin 1Viral Nonstructural ProteinsVirus ReplicationAntiviral AgentsExoribonucleasesHeme Oxygenase-1HMOX1 protein, humanNF-E2-Related Factor 2Sirtuin 1Viral Nonstructural ProteinsHMOX1NRF2NSP14Oxidative stressSARS-CoV-2SIRT1

Identifiers

PMID35732914
PMCPMC9217730
OpenAlexW4283320458

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.