Varicella-zoster virus (VZV) reactivation causes facial nerve palsy in Ramsay Hunt syndrome (RHS) and zoster sine herpete (ZSH) with and without zoster rash, respectively. In the present study, we analyzed the VZV DNA copy number in saliva samples from 25 patients with RHS and 31 patients with ZSH using a TaqMan PCR assay to determine differences in the viral load between the two diseases. VZV copy number in saliva peaked near the day of the appearance of zoster in patients with RHS. Consequently, VZV DNA was less frequently detected in patients with RHS who exhibited facial palsy several days after the appearance of zoster. These findings suggest that the VZV load in saliva samples reflects the kinetics of viral reactivation in patients with RHS. In addition, VZV DNA was equally detected in saliva from patients with RHS and ZSH, and there was no significant difference in the highest viral copy number between patients with RHS and those with ZSH. The VZV load does not appear to reflect a major difference between RHS and ZSH.Ramsay Hunt syndrome (RHS) is a varicella-zoster virus (VZV)-associated neurological disease, characterized by zoster around the ears or in the oropharynx and by acute peripheral facial palsy. In addition, RHS is frequently complicated by a disorder of the eighth cranial nerve. Facial palsy and zoster do not always appear simultaneously, and some patients with RHS exhibit facial palsy several days before or after the onset of zoster. VZV also causes acute peripheral facial palsy with the absence of skin lesions; such cases are termed zoster sine herpete (ZSH) and are usually diagnosed using serological assays (11) or PCR (3, 12, 13). Although VZV reactivation causes facial nerve disorder in both RHS and ZSH, no study has analyzed the difference in virological background between these two diseases. One hypothesis to explain the presence or absence of mucocutaneous lesions (zoster) is that the VZV load is higher in RHS than in ZSH.Only a few studies have investigated the VZV load in patients with varicella and zoster. Studies using a TaqMan-based PCR assay have reported that the viral copy number of peripheral blood mononuclear cells (PBMCs) in patients with varicella was higher than that in patients with zoster (6, 10). However, in these studies, VZV DNA was detected in PBMCs from only 20% of patients with zoster. In addition, it has been demonstrated that VZV DNA was not detected in PBMCs from patients with ZSH (3). Judging from these reports, an analysis of PBMCs does not provide a useful measure of the VZV load in facial palsy patients.Since it has been reported that VZV DNA is detectable in saliva samples from 58 to 59% of patients with RHS and ZSH (4), we employed a TaqMan PCR assay of DNAs from saliva samples for quantitation of VZV DNA and initially analyzed whether the viral copy number in saliva reflects the kinetics of VZV reactivation. We then compared the viral load between RHS and ZSH.
MATERIALS AND METHODSPatient samples. Twenty-five patients with RHS and 31 patients with ZSH wer...