Modulation of autophagy and mTOR signaling pathway genes in respiratory epithelium by respiratory syncytial virus (RSV) in children suffering from acute lower respiratory tract infections.


Journal

Journal of medical virology
ISSN: 1096-9071
Titre abrégé: J Med Virol
Pays: United States
ID NLM: 7705876

Informations de publication

Date de publication:
03 2023
Historique:
revised: 01 03 2023
received: 18 08 2022
accepted: 09 03 2023
medline: 30 3 2023
pubmed: 14 3 2023
entrez: 13 3 2023
Statut: ppublish

Résumé

The study was planned to carry out the molecular characterization of the respiratory syncytial virus (RSV) circulating strains and to elucidate the gene expression of autophagy and mammalian target of rapamycin (mTOR) signaling pathways in children with acute lower respiratory tract infection (ALRTI). Nasopharyngeal aspirate (NPA) samples (n = 145) from children suffering from ALRTI were subjected to the detection of RSV. Of them, 31 RSV positive strains were subjected for sequencing. Semi-quantitative gene expression analysis for mTOR signaling and autophagy pathway genes was performed in respiratory tract epithelial cells using 25 RSV positive cases, and 10 age and sex matched healthy control subjects. Five representative genes were selected for each pathway and subjected to SYBR green real-time polymerase chain reaction. RSV was positive in 69 (47.6%) samples and the representative (n = 31) RSV strains belonged to RSV-A. Thirty-one strains of RSV-A on phylogenetic analysis clustered with the novel ON1 genotype having 72 bp nucleotide duplicationby targeting the ecto-domain portion of the G gene. Further, the stains belonged to lineage 1 (51.6%), followed by lineage 3 (29%) and lineage 2 (19.4%). Autophagy gene expression analysis revealed significant upregulation in NPC1 and ATG3 autophagy genes. mTOR, AKT1, and TSC1 genes of the mTOR pathway were significantly downregulated in RSV positive patients. Thus, RSV infection inducing autophagy pathway genes (NPC1 and ATG3) and suppressing mTOR signaling pathway genes (AKT1, mTOR, and TSC1) to possibly evade the host immune system through dysregulating these pathways for its way of survival within the host.

Identifiants

pubmed: 36912368
doi: 10.1002/jmv.28666
doi:

Substances chimiques

TOR Serine-Threonine Kinases EC 2.7.11.1
MTOR protein, human EC 2.7.1.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e28666

Informations de copyright

© 2023 Wiley Periodicals LLC.

Références

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Auteurs

Sarjana Shuchi (S)

Department of Virology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Radha Kanta Ratho (RK)

Department of Virology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Gursimran Kaur Mohi (GK)

Department of Virology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Suresh Kumar Angurana (S)

Department of Paediatrics, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Subhabrata Sarkar (S)

Department of Virology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Isheeta Jangra (I)

Department of Virology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

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Classifications MeSH