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Construction of a Transcriptome-Driven Network at the Early Stage of Infection with Influenza A H1N1 in Human Lung Alveolar Epithelial Cells
Article de En | WPRIM | ID: wpr-714737
Bibliothèque responsable: WPRO
ABSTRACT
We aimed to understand the molecular changes in host cells that accompany infection by the seasonal influenza A H1N1 virus because the initial response rapidly changes owing to the fact that the virus has a robust initial propagation phase. Human epithelial alveolar A549 cells were infected and total RNA was extracted at 30 min, 1 h, 2 h, 4 h, 8 h, 24 h, and 48 h post infection (h.p.i.). The differentially expressed host genes were clustered into two distinct sets of genes as the infection progressed over time. The patterns of expression were significantly different at the early stages of infection. One of the responses showed roles similar to those associated with the enrichment gene sets to known ‘gp120 pathway in HIV.’ This gene set contains genes known to play roles in preventing the progress of apoptosis, which infected cells undergo as a response to viral infection. The other gene set showed enrichment of ‘Drug Metabolism Enzymes (DMEs).’ The identification of two distinct gene sets indicates that the virus regulates the cell's mechanisms to create a favorable environment for its stable replication and protection of gene metabolites within 8 h.
Sujet(s)
Mots clés
Texte intégral: 1 Indice: WPRIM Sujet Principal: Saisons / ARN / Régulation de l'expression des gènes / Apoptose / Cellules épithéliales / Grippe humaine / Sous-type H1N1 du virus de la grippe A / Séquençage nucléotidique à haut débit / Poumon / Métabolisme Limites du sujet: Humans langue: En Texte intégral: Biomolecules & Therapeutics Année: 2018 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Saisons / ARN / Régulation de l'expression des gènes / Apoptose / Cellules épithéliales / Grippe humaine / Sous-type H1N1 du virus de la grippe A / Séquençage nucléotidique à haut débit / Poumon / Métabolisme Limites du sujet: Humans langue: En Texte intégral: Biomolecules & Therapeutics Année: 2018 Type: Article