tetano
Editor, Senior Moderator
Viruses. 2020 Mar 31;12(4). pii: E383. doi: 10.3390/v12040383.
Next-Generation Sequencing Analysis of Cellular Response to Influenza B Virus Infection.
Sheng Z[SUP]1[/SUP], Huang C[SUP]2[/SUP], Liu R[SUP]2[/SUP], Guo Y[SUP]1[/SUP], Ran Z[SUP]2[/SUP], Li F[SUP]2[/SUP], Wang D[SUP]2[/SUP].
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Abstract
Influenza B virus (IBV) is a respiratory pathogen that infects humans and causes seasonal influenza epidemics. However, cellular response to IBV infection in humans and mechanisms of host-mediated restriction of IBV replication are not thoroughly understood. In this study, we used next-generation sequencing (NGS) to perform transcriptome profiling of IBV-infected human lung epithelial A549 cells at 0, 6, 12, and 24 h post infection (hpi) and characterized the cellular gene expression dynamics. We observed that more than 4000 host genes were differentially regulated during the study period, which included up regulation of genes encoding proteins, having a role in the innate antiviral immune responses, immune activation, cellular metabolism, autophagy, and apoptosis, as well as down regulation of genes involved in mitosis and cell proliferation. Further analysis of RNA-Seq data coupled with RT-qPCR validation collectively showed that double-strand RNA recognition pathways, including retinoic acid-inducible gene I (RIG-I) and Toll-like receptor 3 (TLR3), were substantially activated following IBV infection. Taken together, these results provide important initial insights into the intimate interaction between IBV and lung epithelial cells, which can be further explored towards elucidation of the cellular mechanisms in restriction or elimination of IBV infections in humans.
KEYWORDS:
Influenza B virus; RNA-Seq; infection; innate immune response
PMID:32244344DOI:10.3390/v12040383
Free full text
Next-Generation Sequencing Analysis of Cellular Response to Influenza B Virus Infection.
Sheng Z[SUP]1[/SUP], Huang C[SUP]2[/SUP], Liu R[SUP]2[/SUP], Guo Y[SUP]1[/SUP], Ran Z[SUP]2[/SUP], Li F[SUP]2[/SUP], Wang D[SUP]2[/SUP].
Author information
Abstract
Influenza B virus (IBV) is a respiratory pathogen that infects humans and causes seasonal influenza epidemics. However, cellular response to IBV infection in humans and mechanisms of host-mediated restriction of IBV replication are not thoroughly understood. In this study, we used next-generation sequencing (NGS) to perform transcriptome profiling of IBV-infected human lung epithelial A549 cells at 0, 6, 12, and 24 h post infection (hpi) and characterized the cellular gene expression dynamics. We observed that more than 4000 host genes were differentially regulated during the study period, which included up regulation of genes encoding proteins, having a role in the innate antiviral immune responses, immune activation, cellular metabolism, autophagy, and apoptosis, as well as down regulation of genes involved in mitosis and cell proliferation. Further analysis of RNA-Seq data coupled with RT-qPCR validation collectively showed that double-strand RNA recognition pathways, including retinoic acid-inducible gene I (RIG-I) and Toll-like receptor 3 (TLR3), were substantially activated following IBV infection. Taken together, these results provide important initial insights into the intimate interaction between IBV and lung epithelial cells, which can be further explored towards elucidation of the cellular mechanisms in restriction or elimination of IBV infections in humans.
KEYWORDS:
Influenza B virus; RNA-Seq; infection; innate immune response
PMID:32244344DOI:10.3390/v12040383
Free full text