Luna Vicki A, King Debra S, Peak K Kealy, Reeves Frank, Heberlein-Larson Lea, Veguilla William, Heller L, Duncan Kathleen E, Cannons Andrew C, Amuso Philip, Cattani Jacqueline
Center for Biological Defense, College of Public Health, University of South Florida, 3602 Spectrum Blvd., Tampa, FL 33612, USA.
J Clin Microbiol. 2006 Jul;44(7):2367-77. doi: 10.1128/JCM.00154-06.
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.
为了引发炭疽病,炭疽芽孢杆菌需要两个质粒,即pX01和pX02,它们分别携带毒素基因和荚膜基因,这些基因在该细菌的实验室检测中用作基因靶点。按照美国疾病控制与预防中心建立的针对炭疽芽孢杆菌的PCR检测方法,临床、法医和环境样本检测呈阳性的,在通过培养和第二轮检测确认之前,都被视为可能感染了炭疽芽孢杆菌。我们报告了在环状芽孢杆菌和一种与发光芽孢杆菌密切相关的芽孢杆菌中存在10个基因(acpA、capA、capB、capC、capR、capD、IS1627、ORF 48、ORF 61和repA)以及通常在pX02上发现的荚膜启动子序列。检测发现这些序列存在于每个分离株的一个大质粒上。这11个序列与炭疽芽孢杆菌质粒pX02(GenBank登录号AF188935.1、AE011191.1和AE017335.3)一致匹配。capD和荚膜启动子的核苷酸同一性百分比分别为99.9%和99.7%,对于其余9个基因,两个分离株的核苷酸同一性均为100%。在与炭疽芽孢杆菌无关的两种土壤芽孢杆菌中存在这些通常与pX02质粒相关的基因,这提醒我们有必要识别其他序列,以便在临床、法医和环境样本中指示炭疽芽孢杆菌的存在。