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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 en En | WPRIM | ID: wpr-714737
Biblioteca 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.
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Texto completo: 1 Base de datos: WPRIM Asunto principal: Estaciones del Año / ARN / Regulación de la Expresión Génica / Apoptosis / Células Epiteliales / Gripe Humana / Subtipo H1N1 del Virus de la Influenza A / Secuenciación de Nucleótidos de Alto Rendimiento / Pulmón / Metabolismo Límite: Humans Idioma: En Revista: Biomolecules & Therapeutics Año: 2018 Tipo del documento: Article
Texto completo: 1 Base de datos: WPRIM Asunto principal: Estaciones del Año / ARN / Regulación de la Expresión Génica / Apoptosis / Células Epiteliales / Gripe Humana / Subtipo H1N1 del Virus de la Influenza A / Secuenciación de Nucleótidos de Alto Rendimiento / Pulmón / Metabolismo Límite: Humans Idioma: En Revista: Biomolecules & Therapeutics Año: 2018 Tipo del documento: Article