Hoffmaster Alex R, Ravel Jacques, Rasko David A, Chapman Gail D, Chute Michael D, Marston Chung K, De Barun K, Sacchi Claudio T, Fitzgerald Collette, Mayer Leonard W, Maiden Martin C J, Priest Fergus G, Barker Margaret, Jiang Lingxia, Cer Regina Z, Rilstone Jennifer, Peterson Scott N, Weyant Robbin S, Galloway Darrell R, Read Timothy D, Popovic Tanja, Fraser Claire M
Epidemiologic Investigations Laboratory, Meningitis and Special Pathogens Branch, Centers for Disease Control and Prevention, 1600 Clifton Road, MS G34, Atlanta, GA 30333, USA.
Proc Natl Acad Sci U S A. 2004 Jun 1;101(22):8449-54. doi: 10.1073/pnas.0402414101. Epub 2004 May 21.
Bacillus anthracis is the etiologic agent of anthrax, an acute fatal disease among mammals. It was thought to differ from Bacillus cereus, an opportunistic pathogen and cause of food poisoning, by the presence of plasmids pXO1 and pXO2, which encode the lethal toxin complex and the poly-gamma-d-glutamic acid capsule, respectively. This work describes a non-B. anthracis isolate that possesses the anthrax toxin genes and is capable of causing a severe inhalation anthrax-like illness. Although initial phenotypic and 16S rRNA analysis identified this isolate as B. cereus, the rapid generation and analysis of a high-coverage draft genome sequence revealed the presence of a circular plasmid, named pBCXO1, with 99.6% similarity with the B. anthracis toxin-encoding plasmid, pXO1. Although homologues of the pXO2 encoded capsule genes were not found, a polysaccharide capsule cluster is encoded on a second, previously unidentified plasmid, pBC218. A/J mice challenged with B. cereus G9241 confirmed the virulence of this strain. These findings represent an example of how genomics could rapidly assist public health experts responding not only to clearly identified select agents but also to novel agents with similar pathogenic potentials. In this study, we combined a public health approach with genome analysis to provide insight into the correlation of phenotypic characteristics and their genetic basis.
炭疽芽孢杆菌是炭疽病的病原体,炭疽病是一种在哺乳动物中具有急性致死性的疾病。人们认为它与蜡样芽孢杆菌不同,蜡样芽孢杆菌是一种机会致病菌且会导致食物中毒,炭疽芽孢杆菌因存在分别编码致死毒素复合物和聚γ-d-谷氨酸荚膜的质粒pXO1和pXO2而与之有别。本文描述了一种非炭疽芽孢杆菌分离株,它拥有炭疽毒素基因且能够引发严重的吸入性炭疽样疾病。尽管最初的表型和16S rRNA分析将该分离株鉴定为蜡样芽孢杆菌,但对高覆盖度基因组草图序列的快速生成和分析显示存在一个环状质粒,名为pBCXO1,它与炭疽芽孢杆菌的毒素编码质粒pXO1有99.6%的相似性。尽管未发现pXO2编码的荚膜基因的同源物,但在第二个此前未鉴定的质粒pBC218上编码了一个多糖荚膜簇。用蜡样芽孢杆菌G9241攻击A/J小鼠证实了该菌株的毒力。这些发现代表了一个例子,说明基因组学如何能够迅速协助公共卫生专家不仅应对明确识别的特定病原体,而且应对具有相似致病潜力的新型病原体。在本研究中,我们将公共卫生方法与基因组分析相结合,以深入了解表型特征与其遗传基础之间的相关性。