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Large-scale analysis of viral nucleic acid spectrum in temporal lobe epilepsy biopsies.

AbstractOBJECTIVE:
Chronic inflammatory processes are important promotors of temporal lobe epilepsy (TLE) development. Based on human herpesvirus 6 (HHV-6) DNA detection in brain tissue from patients with TLE, an association of persistent viral infection with TLE has been discussed. Individual studies reported increased HHV-6 DNA in patients with clinical signs of previous inflammatory brain reaction, that is, febrile seizures or meningoencephalitis. However, detection rates vary considerably between different studies. Here we performed a large-scale analysis of viral DNA/RNA spectrum in high-quality TLE biopsies. In addition to all Herpesviridae, we addressed potentially relevant neurotropic RNA viruses.
METHODS:
DNA and RNA were extracted from 346 fresh-frozen tissue samples removed by epilepsy surgery. Real-time polymerase chain reaction (PCR) and nested PCR were performed for Herpesviridae and RNA viruses, respectively. Clinical data were analyzed for earlier signs of inflammatory brain reactions. Fresh-frozen hippocampal tissue samples from patients without chronic central nervous system (CNS) disease served as controls (n = 62). Seven previous PCR studies with overall 178 TLE patients were additionally analyzed regarding a correlation of clinical parameters and HHV-6 detection.
RESULTS:
PCR revealed HHV-6B DNA in 34 specimens (9.8%) from TLE patients. HHV-6B DNA was also present in eight control samples (12.9%; p > 0.05), but showed a lower virus concentration (p < 0.001). Other herpesviruses and RNA viruses were virtually absent. In patients with clinical signs of previous brain inflammation, HHV-6B DNA was observed in 15.0%, whereas only 6.3% of the samples from patients without febrile seizures or meningoencephalitis were positive for HHV-6B DNA (p < 0.05). A meta-analysis of the eight HHV-6 PCR studies revealed similar results.
SIGNIFICANCE:
This biopsy-based study shows no differences in frequency of HHV-6B DNA detection between TLE patients and controls. These results do not support the hypothesis of a persistent HHV-6B infection as a major pathogenetic factor in TLE. However, the higher virus load in TLE patients and the increased detection rate of HHV-6B DNA in patients with previous inflammatory brain reactions require further investigations.
AuthorsLaura Esposito, Jan F Drexler, Oliver Braganza, Elke Doberentz, Alexander Grote, Guido Widman, Christian Drosten, Anna M Eis-Hübinger, Susanne Schoch, Christian E Elger, Albert J Becker, Pitt Niehusmann
JournalEpilepsia (Epilepsia) Vol. 56 Issue 2 Pg. 234-43 (Feb 2015) ISSN: 1528-1167 [Electronic] United States
PMID25530314 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightWiley Periodicals, Inc. © 2014 International League Against Epilepsy.
Chemical References
  • DNA, Viral
Topics
  • Adolescent
  • Adult
  • Aged
  • Biopsy
  • DNA, Viral (analysis)
  • Epilepsy, Temporal Lobe (pathology, virology)
  • Female
  • Herpesvirus 6, Human (genetics)
  • Humans
  • Male
  • Middle Aged
  • Polymerase Chain Reaction (methods)
  • Young Adult

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