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Journal of Clinical Microbiology, August 2003, p. 3835-3839, Vol. 41, No. 8
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.8.3835-3839.2003

Real-Time PCR Assay To Detect Smallpox Virus

M. Sofi Ibrahim,1* David A. Kulesh,1 Sharron S. Saleh,1 Inger K. Damon,2 Joseph J. Esposito,2 Alan L. Schmaljohn,1 and Peter B. Jahrling1

The United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland 21702,1 Centers for Disease Control and Prevention, Atlanta, Georgia2

Received 27 November 2002/ Returned for modification 18 March 2003/ Accepted 11 April 2003

We developed a highly sensitive and specific assay for the rapid detection of smallpox virus DNA on both the Smart Cycler and LightCycler platforms. The assay is based on TaqMan chemistry with the orthopoxvirus hemagglutinin gene used as the target sequence. With genomic DNA purified from variola virus Bangladesh 1975, the limit of detection was estimated to be approximately 25 copies on both machines. The assay was evaluated in a blinded study with 322 coded samples that included genomic DNA from 48 different isolates of variola virus; 25 different strains and isolates of camelpox, cowpox, ectromelia, gerbilpox, herpes, monkeypox, myxoma, rabbitpox, raccoonpox, skunkpox, vaccinia, and varicella-zoster viruses; and two rickettsial species at concentrations mostly ranging from 100 fg/µl to 1 ng/µl. Contained within those 322 samples were variola virus DNA, obtained from purified viral preparations, at concentrations of 1 fg/µl to 1 ng/µl. On the Smart Cycler platform, 2 samples with false-positive results were detected among the 116 samples not containing variola virus tested; i.e., the overall specificity of the assay was 98.3%. On the LightCycler platform, five samples with false-positive results were detected (overall specificity, 95.7%). Of the 206 samples that contained variola virus DNA ranging in concentrations from 100 fg/µl to 1 ng/µl, 8 samples were considered negative on the Smart Cycler platform and 1 sample was considered negative on the LightCycler platform. Thus, the clinical sensitivities were 96.1% for the Smart Cycler instrument and 99.5% for the LightCycler instrument. The vast majority of these samples were derived from virus-infected cell cultures and variola virus-infected tissues; thus, the DNA material contained both viral DNA and cellular DNA. Of the 43 samples that contained purified variola virus DNA ranging in concentration from 1 fg/µl to 1 ng/µl, the assay correctly detected the virus in all 43 samples on both the Smart Cycler and the LightCycler platforms. The assay may be useful for the early detection of smallpox virus infections should such infections occur as a result of a deliberate or an accidental recurrence.

* Corresponding author. Mailing address: Virology Division, USAMRIID, 1425 Porter St., Fort Detrick, MD 21702-5011. Phone: (301) 619-6294. Fax: (301) 619-2290. E-mail: Sofi.Ibrahim{at}det.amedd.army.mil.

Journal of Clinical Microbiology, August 2003, p. 3835-3839, Vol. 41, No. 8
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.8.3835-3839.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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