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Presence of herpesvirus DNA in cerebrospinal fluid of patients with tick‐borne encephalitis and enteroviral meningoencephalitis
Author(s) -
Labská Klára,
Roubalová Kateřina,
Pícha Dušan,
Marešová Vilma
Publication year - 2015
Publication title -
journal of medical virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 121
eISSN - 1096-9071
pISSN - 0146-6615
DOI - 10.1002/jmv.24172
Subject(s) - meningoencephalitis , cerebrospinal fluid , encephalitis , medicine , human herpesvirus 6 , rash , tick borne encephalitis , virology , immunology , meningitis , herpesviridae , virus , viral disease , pediatrics
Reactivation of HHVs in the CNS due to inflammation has not been well described yet. The primary aim of this study was to investigate the frequency of HHV DNA detection in the cerebrospinal fluid (CSF) of immunocompetent patients with meningoencephalitis of other than HHV origin. The secondary aim of this study was to evaluate the impact of herpesvirus co‐infection on the clinical course and patient outcome. Ninety‐six patients with clinically and laboratory proven tick‐borne encephalitis (TBE) and 77 patients with a confirmed diagnosis of enteroviral meningitis (EVM), along with a control group of 107 patients without evidence of inflammation in the CSF were retrospectively tested by nested PCR for the presence of DNA of the neurotropic herpesviruses HSV1, HSV2, VZV, and HHV6 in the CSF. The clinical course, laboratory tests, antiviral treatment, and neurological complications in a 6‐month follow‐up were compared between the groups positive or negative for HHV DNA in the CSF. HHV DNA was found in the CSF of 12 (6.9%) patients (6.3% and 7.8% in the TBE and EVM groups, respectively) and in 1 (0.9%) control patient. None of the patients had recent blisters or rash. The clinical course was comparably mild in all patients. No permanent neurological sequelae were observed. Only the CSF total protein level was significantly higher in HHV DNA‐positive than in HHV‐negative patients. J. Med. Virol. 87:1235–1240, 2015 . © 2015 Wiley Periodicals, Inc.

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