Latent herpes simplex virus 1 infection does not induce apoptosis in human trigeminal Ganglia

J Virol. 2015 May;89(10):5747-50. doi: 10.1128/JVI.03481-14. Epub 2015 Mar 11.

Abstract

Herpes simplex virus 1 (HSV-1) can establish lifelong latency in human trigeminal ganglia. Latently infected ganglia contain CD8(+) T cells, which secrete granzyme B and are thus capable of inducing neuronal apoptosis. Using immunohistochemistry and single-cell reverse transcription-quantitative PCR (RT-qPCR), higher frequency and transcript levels of caspase-3 were found in HSV-1-negative compared to HSV-1-positive ganglia and neurons, respectively. No terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assay-positive neurons were detected. The infiltrating T cells do not induce apoptosis in latently infected neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • CD8-Positive T-Lymphocytes / pathology
  • Caspase 3 / metabolism
  • Herpes Simplex / enzymology
  • Herpes Simplex / pathology*
  • Herpes Simplex / virology*
  • Herpesvirus 1, Human / genetics
  • Herpesvirus 1, Human / pathogenicity*
  • Herpesvirus 1, Human / physiology*
  • Host-Pathogen Interactions
  • Humans
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Neurons / enzymology
  • Neurons / pathology
  • Neurons / virology
  • Trigeminal Ganglion / virology*
  • Virus Latency

Substances

  • MicroRNAs
  • latency associated transcript, herpes simplex virus-1
  • CASP3 protein, human
  • Caspase 3