The Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, AZ 86011-4073, USA; The Pathogen Genomics Division, The Translational Genomics Research Institute, 3051 W. Shamrell Blvd, Suite 106, Flagstaff, AZ 86001 USA.
The Robert Koch Institute, Berlin, Germany.
EBioMedicine. 2015 Oct 6;2(11):1613-8. doi: 10.1016/j.ebiom.2015.10.004. eCollection 2015 Nov.
Anthrax is a rare disease in humans but elicits great public fear because of its past use as an agent of bioterrorism. Injectional anthrax has been occurring sporadically for more than ten years in heroin consumers across multiple European countries and this outbreak has been difficult to trace back to a source.
We took a molecular epidemiological approach in understanding this disease outbreak, including whole genome sequencing of Bacillus anthracis isolates from the anthrax victims. We also screened two large strain repositories for closely related strains to provide context to the outbreak.
Analyzing 60 Bacillus anthracis isolates associated with injectional anthrax cases and closely related reference strains, we identified 1071 Single Nucleotide Polymorphisms (SNPs). The synapomorphic SNPs (350) were used to reconstruct phylogenetic relationships, infer likely epidemiological sources and explore the dynamics of evolving pathogen populations. Injectional anthrax genomes separated into two tight clusters: one group was exclusively associated with the 2009-10 outbreak and located primarily in Scotland, whereas the second comprised more recent (2012-13) cases but also a single Norwegian case from 2000.
Genome-based differentiation of injectional anthrax isolates argues for at least two separate disease events spanning > 12 years. The genomic similarity of the two clusters makes it likely that they are caused by separate contamination events originating from the same geographic region and perhaps the same site of drug manufacturing or processing. Pathogen diversity within single patients challenges assumptions concerning population dynamics of infecting B. anthracis and host defensive barriers for injectional anthrax.
This work was supported by the United States Department of Homeland Security grant no. HSHQDC-10-C-00,139 and via a binational cooperative agreement between the United States Government and the Government of Germany. This work was supported by funds from the German Ministry of Defense (Sonderforschungsprojekt 25Z1-S-431,214). Support for sequencing was also obtained from Illumina, Inc. These sources had no role in the data generation or interpretation, and had not role in the manuscript preparation.
PANEL 1 RESEARCH IN CONTEXT SYSTEMATIC REVIEW: We searched PubMed for any article published before Jun. 17, 2015, with the terms "Bacillus anthracis" and "heroin", or "injectional anthrax". Other than our previously published work (Price et al., 2012), we found no other relevant studies on elucidating the global phylogenetic relationships of B. anthracis strains associated with injectional anthrax caused by recreational heroin consumption of spore-contaminated drug. There were, however, publically available genome sequences of two strains involved (Price et al., 2012, Grunow et al., 2013) and the draft genome sequence of Bacillus anthracis UR-1, isolated from a German heroin user (Ruckert et al., 2012) with only limited information on the genotyping of closely related strains (Price et al., 2012, Grunow et al., 2013).
Injectional anthrax has been plaguing heroin drug users across Europe for more than 10 years. In order to better understand this outbreak, we assessed genomic relationships of all available injectional anthrax strains from four countries spanning a > 12 year period. Very few differences were identified using genome-based analysis, but these differentiated the isolates into two distinct clusters. This strongly supports a hypothesis of at least two separate anthrax spore contamination events perhaps during the drug production processes. Identification of two events would not have been possible from standard epidemiological analysis. These comprehensive data will be invaluable for classifying future injectional anthrax isolates and for future geographic attribution.
炭疽是一种罕见的人类疾病,但由于其过去被用作生物恐怖主义的制剂,因此引起了公众的极大恐惧。在多个欧洲国家,已有十多年来零星发生过注射性炭疽病,而且这种疫情很难追溯到源头。
我们采用分子流行病学方法来了解这种疾病的爆发,包括对炭疽受害者的炭疽杆菌分离株进行全基因组测序。我们还筛选了两个大型菌株库,以提供与疫情相关的密切相关菌株的背景信息。
分析了与注射性炭疽病例相关的 60 株炭疽杆菌分离株和密切相关的参考菌株,我们鉴定出了 1071 个单核苷酸多态性(SNP)。同形 SNP(350 个)用于重建系统发育关系,推断可能的流行病学来源,并探讨病原体种群的进化动态。注射性炭疽基因组分为两个紧密的簇:一组仅与 2009-10 年的疫情有关,主要位于苏格兰,而第二组包括最近(2012-13 年)的病例,但也包括来自 2000 年挪威的一个单独病例。
基于基因组的注射性炭疽分离株的分化表明,至少有两个单独的疾病事件跨越了 > 12 年。两个簇的基因组相似性表明,它们很可能是由来自同一地理区域且可能来自同一药物制造或加工地点的单独污染事件引起的。单个患者体内的病原体多样性挑战了关于感染炭疽杆菌的种群动态和注射性炭疽的宿主防御屏障的假设。
这项工作得到了美国国土安全部的资助(HSHQDC-10-C-00,139),并通过美国政府和德国政府之间的双边合作协议。这项工作得到了德国国防部的资助(特殊研究项目 25Z1-S-431,214)。测序工作还得到了 Illumina, Inc. 的支持。这些来源在数据生成或解释方面没有任何作用,也没有参与手稿的准备。
面板 1 研究背景系统评价:我们在 2015 年 6 月 17 日之前在 PubMed 上搜索了任何发表的文章,使用的术语是“炭疽杆菌”和“海洛因”或“注射性炭疽”。除了我们之前发表的工作(Price 等人,2012)之外,我们没有发现任何其他关于阐明与娱乐性海洛因消费污染的炭疽芽孢杆菌菌株相关的注射性炭疽的全球系统发育关系的相关研究。然而,有两个相关的菌株的公共基因组序列(Price 等人,2012,Grunow 等人,2013)和从德国海洛因使用者中分离的 Bacillus anthracis UR-1 的草案基因组序列(Ruckert 等人,2012),但只有关于密切相关菌株的有限基因分型信息(Price 等人,2012,Grunow 等人,2013)。
注射性炭疽病已经困扰欧洲的海洛因吸毒者 10 多年了。为了更好地了解这次疫情,我们评估了来自四个国家的所有可用的注射性炭疽菌株的基因组关系,跨越了 > 12 年的时间。使用基于基因组的分析只发现了很少的差异,但这些差异将分离株分为两个不同的簇。这强烈支持了至少有两个单独的炭疽芽孢污染事件的假设,也许是在药物生产过程中发生的。从标准的流行病学分析中不可能识别出两个事件。这些全面的数据将对分类未来的注射性炭疽分离株和未来的地理归因非常有价值。