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1000 Titel
  • Identification of COVID-19 and Dengue Host Factor Interaction Networks Based on Integrative Bioinformatics Analyses
1000 Autor/in
  1. Zheng, Wenjiang |
  2. Wu, Hui |
  3. Liu, Chengxin |
  4. Yan, Qian |
  5. Wang, Ting |
  6. Wu, Peng |
  7. Liu, Xiaohong |
  8. Jiang, Yong |
  9. Zhan, Shaofeng |
1000 Verlag
  • Frontiers Media S.A.
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-07-28
1000 Erschienen in
1000 Quellenangabe
  • 12:707287
1000 Copyrightjahr
  • 2021
1000 Embargo
  • 2022-01-30
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.3389/fimmu.2021.707287 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8356054/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Abstract/Summary
  • <jats:sec><jats:title>Background</jats:title><jats:p>The outbreak of Coronavirus disease 2019 (COVID-19) has become an international public health crisis, and the number of cases with dengue co-infection has raised concerns. Unfortunately, treatment options are currently limited or even unavailable. Thus, the aim of our study was to explore the underlying mechanisms and identify potential therapeutic targets for co-infection.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>To further understand the mechanisms underlying co-infection, we used a series of bioinformatics analyses to build host factor interaction networks and elucidate biological process and molecular function categories, pathway activity, tissue-specific enrichment, and potential therapeutic agents.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>We explored the pathologic mechanisms of COVID-19 and dengue co-infection, including predisposing genes, significant pathways, biological functions, and possible drugs for intervention. In total, 460 shared host factors were collected; among them, CCL4 and AhR targets were important. To further analyze biological functions, we created a protein-protein interaction (PPI) network and performed Molecular Complex Detection (MCODE) analysis. In addition, common signaling pathways were acquired, and the toll-like receptor and NOD-like receptor signaling pathways exerted a significant effect on the interaction. Upregulated genes were identified based on the activity score of dysregulated genes, such as IL-1, Hippo, and TNF-α. We also conducted tissue-specific enrichment analysis and found ICAM-1 and CCL2 to be highly expressed in the lung. Finally, candidate drugs were screened, including resveratrol, genistein, and dexamethasone.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>This study probes host factor interaction networks for COVID-19 and dengue and provides potential drugs for clinical practice. Although the findings need to be verified, they contribute to the treatment of co-infection and the management of respiratory disease.</jats:p></jats:sec>
1000 Sacherschließung
gnd 1206347392 COVID-19
lokal dengue
lokal SARS-CoV-2/drug effects [MeSH]
lokal host factor interaction networks
lokal Chemokine CCL2/metabolism [MeSH]
lokal Lung/metabolism [MeSH]
lokal Genistein/therapeutic use [MeSH]
lokal COVID-19/pathology [MeSH]
lokal Intercellular Adhesion Molecule-1/metabolism [MeSH]
lokal Gene Expression Regulation/genetics [MeSH]
lokal co-infection
lokal Dengue/pathology [MeSH]
lokal Dengue Virus/drug effects [MeSH]
lokal Resveratrol/therapeutic use [MeSH]
lokal Dexamethasone/therapeutic use [MeSH]
lokal Dengue/drug therapy [MeSH]
lokal Immunology
lokal Coinfection [MeSH]
lokal COVID-19/drug therapy [MeSH]
lokal Humans [MeSH]
lokal COVID-19
lokal Protein Interaction Maps/physiology [MeSH]
lokal Signal Transduction [MeSH]
lokal Antiviral Agents/therapeutic use [MeSH]
lokal Computational Biology/methods [MeSH]
lokal bioinformatics analyses
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/WmhlbmcsIFdlbmppYW5n|https://frl.publisso.de/adhoc/uri/V3UsIEh1aQ==|https://frl.publisso.de/adhoc/uri/TGl1LCBDaGVuZ3hpbg==|https://frl.publisso.de/adhoc/uri/WWFuLCBRaWFu|https://frl.publisso.de/adhoc/uri/V2FuZywgVGluZw==|https://frl.publisso.de/adhoc/uri/V3UsIFBlbmc=|https://frl.publisso.de/adhoc/uri/TGl1LCBYaWFvaG9uZw==|https://frl.publisso.de/adhoc/uri/SmlhbmcsIFlvbmc=|https://frl.publisso.de/adhoc/uri/WmhhbiwgU2hhb2Zlbmc=
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