## Abstract The nested polymerase chain reaction was used to detect varicella zoster virus (VZV) DNA in 67 samples of peripheral blood mononuclear cells (PBMC) from 39 otherwise healthy children with varicella. Eleven were during the incubation period and 56 were after appearance of rash. VZV DNA w
Detection of varicella-zoster virus DNA in throat swabs of patients with herpes zoster and on air purifier filters
β Scribed by Kayoko Suzuki; Tetsushi Yoshikawa; Akiko Tomitaka; Kyoko Suzuki; Kayoko Matsunaga; Yoshizo Asano
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 57 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0146-6615
- DOI
- 10.1002/jmv.2182
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Zoster patients are considered to be less contagious than those with varicella because their infectious lesions are localized. However, it is not known when the spread of varicellaβzoster virus (VZV) from zoster patients begins, how long it continues, and how far the virus spreads from the zoster patients. Twelve cases of hospitalized zoster patients were studied. The polymerase chain reaction (PCR) was used to detect VZV DNA in samples taken from the surface of their eruptions, throats, and the air purifier filters in their rooms. In all patients, VZV DNA was detected in the samples from eruptions. VZV DNA was detected in 8 of 12 patients from the throats. VZV DNA was detected for 9 of 12 patients from the filter samples. This study shows the possibility of a wide distribution of VZV DNA to the environment from infected patients. VZV may be excreted from cutaneous eruptions or from the throats of patients. J. Med. Virol. 66:567β570, 2002. Β© 2002 WileyβLiss, Inc.
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