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Journal of Clinical Microbiology, July 2006, p. 2367-2377, Vol. 44, No. 7
0095-1137/06/$08.00+0     doi:10.1128/JCM.00154-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Bacillus anthracis Virulent Plasmid pX02 Genes Found in Large Plasmids of Two Other Bacillus Species

Vicki A. Luna,1*,{dagger} Debra S. King,1,{dagger} K. Kealy Peak,1 Frank Reeves,2 Lea Heberlein-Larson,2 William Veguilla,1 L. Heller,1 Kathleen E. Duncan,3 Andrew C. Cannons,1 Philip Amuso,1,2 and Jacqueline Cattani1

Center for Biological Defense, College of Public Health, University of South Florida, Tampa, Florida,1 Florida Department of Health, Bureau of Laboratories, Tampa, Florida,2 Department of Botany and Microbiology, University of Oklahoma, Norman, Oklahoma3

Received 24 January 2006/ Returned for modification 28 March 2006/ Accepted 4 May 2006

In order to cause the disease anthrax, Bacillus anthracis requires two plasmids, pX01 and pX02, which carry toxin and capsule genes, respectively, that are used as genetic targets in the laboratory detection of the bacterium. Clinical, forensic, and environmental samples that test positive by PCR protocols established by the Centers for Disease Control and Prevention for B. anthracis are considered to be potentially B. anthracis until confirmed by culture and a secondary battery of tests. We report the presence of 10 genes (acpA, capA, capB, capC, capR, capD, IS1627, ORF 48, ORF 61, and repA) and the sequence for the capsule promoter normally found on pX02 in Bacillus circulans and a Bacillus species closely related to Bacillus luciferensis. Tests revealed these sequences to be present on a large plasmid in each isolate. The 11 sequences consistently matched to B. anthracis plasmid pX02, GenBank accession numbers AF188935.1, AE011191.1, and AE017335.3. The percent nucleotide identities for capD and the capsule promoter were 99.9% and 99.7%, respectively, and for the remaining nine genes, the nucleotide identity was 100% for both isolates. The presence of these genes, which are usually associated with the pX02 plasmid, in two soil Bacillus species unrelated to B. anthracis alerts us to the necessity of identifying additional sequences that will signal the presence of B. anthracis in clinical, forensic, and environmental samples.


* Corresponding author. Mailing address: Center for Biological Defense, University of South Florida, 3602 Spectrum Blvd., Tampa, FL 33612. Phone: (813) 974-3873. Fax: (813) 974-1479. E-mail: vluna{at}bt.usf.edu.

{dagger} V.A.L. and D.S.K. contributed equally to this paper.


Journal of Clinical Microbiology, July 2006, p. 2367-2377, Vol. 44, No. 7
0095-1137/06/$08.00+0     doi:10.1128/JCM.00154-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




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