PMID- 25530314 OWN - NLM STAT- MEDLINE DCOM- 20150507 LR - 20150224 IS - 1528-1167 (Electronic) IS - 0013-9580 (Linking) VI - 56 IP - 2 DP - 2015 Feb TI - Large-scale analysis of viral nucleic acid spectrum in temporal lobe epilepsy biopsies. PG - 234-43 LID - 10.1111/epi.12890 [doi] AB - OBJECTIVE: 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. CI - Wiley Periodicals, Inc. (c) 2014 International League Against Epilepsy. FAU - Esposito, Laura AU - Esposito L AD - Department of Neuropathology, University of Bonn Medical Center, Bonn, Germany. FAU - Drexler, Jan F AU - Drexler JF FAU - Braganza, Oliver AU - Braganza O FAU - Doberentz, Elke AU - Doberentz E FAU - Grote, Alexander AU - Grote A FAU - Widman, Guido AU - Widman G FAU - Drosten, Christian AU - Drosten C FAU - Eis-Hubinger, Anna M AU - Eis-Hubinger AM FAU - Schoch, Susanne AU - Schoch S FAU - Elger, Christian E AU - Elger CE FAU - Becker, Albert J AU - Becker AJ FAU - Niehusmann, Pitt AU - Niehusmann P LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20141220 PL - United States TA - Epilepsia JT - Epilepsia JID - 2983306R RN - 0 (DNA, Viral) SB - IM MH - Adolescent MH - Adult MH - Aged MH - Biopsy MH - DNA, Viral/*analysis MH - Epilepsy, Temporal Lobe/*pathology/virology MH - Female MH - Herpesvirus 6, Human/*genetics MH - Humans MH - Male MH - Middle Aged MH - Polymerase Chain Reaction/methods MH - Young Adult OTO - NOTNLM OT - Encephalitis OT - Epileptogenesis OT - Febrile seizures OT - HHV-6 OT - Inflammation EDAT- 2014/12/23 06:00 MHDA- 2015/05/08 06:00 CRDT- 2014/12/23 06:00 PHST- 2014/11/10 00:00 [accepted] PHST- 2014/12/23 06:00 [entrez] PHST- 2014/12/23 06:00 [pubmed] PHST- 2015/05/08 06:00 [medline] AID - 10.1111/epi.12890 [doi] PST - ppublish SO - Epilepsia. 2015 Feb;56(2):234-43. doi: 10.1111/epi.12890. Epub 2014 Dec 20.