Effect of eleutheroside B1 on non‑coding RNAs and protein profiles of influenza A virus‑infected A549 cells.
A549 Cells
Blotting, Western
Carrier Proteins
/ genetics
Eleutherococcus
Humans
Influenza A Virus, H1N1 Subtype
/ pathogenicity
Influenza A virus
/ pathogenicity
Plant Extracts
/ pharmacology
RNA, Long Noncoding
/ genetics
RNA, Untranslated
/ genetics
Reverse Transcriptase Polymerase Chain Reaction
Sequence Analysis, RNA
/ methods
Journal
International journal of molecular medicine
ISSN: 1791-244X
Titre abrégé: Int J Mol Med
Pays: Greece
ID NLM: 9810955
Informations de publication
Date de publication:
Mar 2020
Mar 2020
Historique:
received:
13
06
2019
accepted:
09
12
2019
pubmed:
28
1
2020
medline:
3
11
2020
entrez:
28
1
2020
Statut:
ppublish
Résumé
Influenza viruses often pose a serious threat to animals and human health. In an attempt to explore the potential of herbal medicine as a treatment for influenza virus infection, eleutheroside B1, a coumarin compound extracted from herba sarcandrae, was identified, which exhibited antiviral and anti‑inflammatory activities against influenza A virus. In this study, high‑throughput RNA sequencing and isobaric tags for relative and absolute quantification (iTRAQ) assays were performed to determine alterations in the non‑coding RNA (ncRNA) transcriptome and proteomics. Bioinformatics and target prediction analyses were used to decipher the potential roles of altered ncRNAs in the function of eleutheroside B1. Furthermore, long ncRNA (lncRNA) and mRNA co‑expressing networks were constructed to analyze the biological functions by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses. The analysis of RNA sequencing data revealed that 5 differentially expressed ncRNAs were upregulated and 3 ncRNAs were downregulated in the A549 cells infected with A/PR8/34/H1N1, with or without eleutheroside B1 treatment (PR8+eleu and PR8, respectively). Nuclear paraspeckle assembly transcript 1 (NEAT1) was differentially expressed between the PR8 and A549 cell groups. GO and KEGG pathway analyses indicated that eleutheroside B1 took advantage of the host cell biological processes and molecular function for its antiviral and anti‑inflammatory activities, as well as for regulating cytokine‑cytokine receptor interaction in the immune system, consistent with previous findings. The results of the iTRAQ assays indicated that L antigen family member 3 (LAGE3) protein, essential for tRNA processing, tRNA metabolic processes and ncRNA processing, was downregulated in the PR8+eleu compared with the PR8 group. In the present study, these comprehensive, large‑scale data analysis enhanced the understanding of multiple aspects of the transcriptome and proteomics that are involved in the antiviral and anti‑inflammatory activities of eleutheroside B1. These findings demonstrate the potential of eleutheroside B1 for use in the prevention and treatment of influenza A virus‑mediated infections.
Identifiants
pubmed: 31985023
doi: 10.3892/ijmm.2020.4468
pmc: PMC7015140
doi:
Substances chimiques
Carrier Proteins
0
LAGE3 protein, human
0
NEAT1 long non-coding RNA, human
0
Plant Extracts
0
RNA, Long Noncoding
0
RNA, Untranslated
0
eleutherosides
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
753-768Références
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