Innate immune response in astrocytes infected with herpes simplex virus 1.
Yashvant D BansodeDebprasad ChattopadhyayBhaskar SahaPublished in: Archives of virology (2019)
Herpes simplex virus 1 (HSV-1), a double-stranded DNA virus, infects epithelial surfaces and establishes latency in the central nervous system, where astrocytes are a major immune cell type. Here, we report changes that occur in the expression of pathogen recognition receptors, such as Toll-like receptors, DNA and RNA sensors, interferons, and interferon-stimulated genes, when astrocytes are infected with HSV-1 strain F. We observed upregulation of Toll-like receptors 2, 6 and 9, MDA5, and DAI along with an increase in the expression of type I interferons and interferon-stimulated genes such as IFIT1, IFIT3 and RNase L. These genes encode proteins that mediate the antiviral immune response.
Keyphrases
- herpes simplex virus
- poor prognosis
- genome wide
- immune response
- innate immune
- dendritic cells
- binding protein
- circulating tumor
- bioinformatics analysis
- nucleic acid
- genome wide identification
- single molecule
- cell free
- long non coding rna
- cell proliferation
- genome wide analysis
- candida albicans
- dna methylation
- biofilm formation
- escherichia coli
- cerebrospinal fluid
- pseudomonas aeruginosa
- cell cycle arrest