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Applied and Environmental Microbiology, August 2001, p. 3759-3762, Vol. 67, No. 8
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.8.3759-3762.2001

Identification of Nucleotide Sequences for the Specific and Rapid Detection of Yersinia pestis

Lyndsay Radnedge,1 Silvia Gamez-Chin,1 Paula M. McCready,1 Patricia L. Worsham,2 and Gary L. Andersen1,*

Biology and Biotechnology Research Program, Lawrence Livermore National Laboratory, Livermore, California 94551,1 and United States Army Research Institute of Infectious Diseases, Fort Detrick, Maryland 217022

Received 1 March 2001/Accepted 7 May 2001

Suppression subtractive hybridization, a cost-effective approach for targeting unique DNA, was used to identify a 41.7-kb Yersinia pestis-specific region. One primer pair designed from this region amplified PCR products from natural isolates of Y. pestis and produced no false positives for near neighbors, an important criterion for unambiguous bacterial identification.


* Corresponding author. Mailing address: Biology and Biotechnology Research Program, L-441, 7000 East Avenue, Livermore, CA 94550. Phone: (925) 423-2525. Fax: (925) 422-2282. E-mail: Andersen2{at}LLNL.GOV.


Applied and Environmental Microbiology, August 2001, p. 3759-3762, Vol. 67, No. 8
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.8.3759-3762.2001



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