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Journal of Clinical Microbiology, December 2003, p. 5492-5499, Vol. 41, No. 12
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.12.5492-5499.2003

Development of a Multitarget Real-Time TaqMan PCR Assay for Enhanced Detection of Francisella tularensis in Complex Specimens

Jessica L. Versage,{dagger} Darlena D. M. Severin,{ddagger} May C. Chu, and Jeannine M. Petersen*

Bacterial Zoonoses Branch, Division of Vector-Borne Infectious Diseases, National Center for Infectious Disease, Centers for Disease Control and Prevention, Ft. Collins, Colorado 80522

Received 4 June 2003/ Returned for modification 4 August 2003/ Accepted 26 August 2003

Tularemia is the zoonotic disease caused by the gram-negative coccobacillus Francisella tularensis. Its wide distribution in the environment poses a challenge for understanding the transmission, ecology, and epidemiology of the disease. F. tularensis is also considered a potential biological weapon due to its extreme infectivity. We have developed a multitarget real-time TaqMan PCR assay capable of rapidly and accurately detecting F. tularensis in complex specimens. Targeted regions included the ISFtu2 element and the 23kDa, fopA, and tul4 genes. Analysis of the four TaqMan assays demonstrated that three (ISFtu2, 23kDa, and tul4) performed within our established criterion of a detection limit of one organism. The combined use of the three assays was highly specific, displaying no cross-reactivity with the non-Francisella bacteria tested and capable of differentially diagnosing both F. tularensis and Francisella philomiragia. When the multitarget TaqMan assay (ISFtu2, 23kDa, and tul4) was compared to culturing, using environmentally contaminated specimens, the TaqMan PCR assay was significantly more sensitive than culturing (P <= 0.05). The sensitive and specific nature of this rapid multitarget TaqMan assay provides a valuable new tool that with future evaluations can be used for analyzing clinical specimens, field samples during bioterrorism threat assessment, and samples from outbreaks and for improving our understanding of the ecology and environmental prevalence of F. tularensis.

* Corresponding author. Mailing address: Centers for Disease Control and Prevention, Division of Vector-Borne Infectious Diseases, Foothills Campus, P.O. Box 2087, Ft. Collins, CO 80522. Phone: (970) 266-3524. Fax: (970) 221-6476. E-mail: nzp0{at}cdc.gov.

{dagger} Present address: College of Medicine, University of Florida, Gainesville, FL 32611.

{ddagger} Present address: Epidemiology and Biostatistics, School of Public Health, Loma Linda University, Loma Linda, CA 92350.

Journal of Clinical Microbiology, December 2003, p. 5492-5499, Vol. 41, No. 12
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.12.5492-5499.2003




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