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J Virol Methods. 2013 Oct;193(1):128-30. doi: 10.1016/j.jviromet.2013.05.019. Epub 2013 Jun 5.

Rapid and sensitive detection of varicella zoster virus in saliva of patients with herpes zoster.

Author information

1
Enterprise Advisory Services, Inc, Houston, TX 77598, USA. satish.k.mehta@nasa.gov

Abstract

VZV reactivation produces zoster (shingles) which may be further complicated by meningoencephalitis, myelopathy, vasculopathy and multiple ocular disorders. Importantly, these neurological and ocular complications of VZV reactivation can occur without rash. In such instances, virological verification relies on detection of VZV DNA or anti-VZV IgG antibody in cerebrospinal fluid (CSF), or less often, the presence of VZV DNA in blood mononuclear cells or anti-VZV IgM antibody in serum or CSF. If VZV were readily detected in other tissue samples (e.g., saliva or tears) in patients with neurological disease in the absence of rash and shown to correlate with the standard tests listed above, more invasive tests such as lumbar puncture might be obviated. In patients with acute herpes zoster, the yield of cell DNA was greater in saliva collected by passive drool or synthetic swab than by cotton swab. The time to process saliva from collection to obtaining DNA was 1h. VZV DNA was present exclusively in the pelleted fraction of saliva and was found in 100% of patients before antiviral treatment. This rapid sensitive method can be applied readily to saliva from humans with neurologic and other disease that might be caused by VZV in the absence of rash.

KEYWORDS:

DNA; PCR; Saliva; Varicella zoster virus

PMID:
23747545
PMCID:
PMC3735804
DOI:
10.1016/j.jviromet.2013.05.019
[Indexed for MEDLINE]
Free PMC Article

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