Screening of possibly anthrax-contaminated burial sites in eastern and southern Ukraine

IF 0.4 Q4 AGRICULTURE, MULTIDISCIPLINARY Agricultural Science and Practice Pub Date : 2020-12-25 DOI:10.15407/AGRISP7.03.003
O. V. Biloivan, B. Stegniy, A. Gerilovych, V. Arefiev, R. Wölfel, J. Schwarz, C. Popp, G. Grass
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引用次数: 1

Abstract

Aim. The aim of this study was to screen soil samples of 17 anthrax burial sites in Eastern and Southern Ukraine for the presence of B. anthracis. Methods. Soil samples were collected from anthrax grave sites located in Kharkiv, Sumy and Mykolaiv regions (diseased animals dated from 1946 to 2003). Isolation of B. anthracis from collected soil samples was performed with the GABRI method. From single colonies without hemolysis, that were inactivated with peracetic acid- containing 2 % Terralin PAA solution, DNA was extracted and analyzed by qPCR for the presence of chromosomal marker dhp61, as well as the markers pagA and capC located on virulence plasmids pXO1 and pXO2, respectively. Results. Eleven fi eld trips were conducted from July, 2016 to October, 2018 in which 369 soil samples from 17 burial sites in Kharkiv, Sumy and Mykolaiv oblasts were collected from different depths of presumed anthrax carcass sites. In most cases (12 out of 17 cases), the current status of these burial sites was deteriorated and not prop- erly accounted for. It was possible to obrain viable B. anthracis isolate was obtained from 50 cm depth at the grave site near Koviagy village, Valky district, Kharkiv region (49.92373°N, 35.48951°E). This isolate was named KhR/ VD/Kov2-2-05-3 and deposited in the Collection of Animal Infectious Pathogens of the National Scientifi c Center “Institute of Experimental and Clinical Veterinary Medicine”, Kharkiv, Ukraine. The contamination level of soil at the isolation site reached about 10 4 CFU per g as determined by plate counting. qPCR analysis of this isolate identi- fi ed both the dhp61 B. anthracis chromosomal and the pagA virulence plasmid marker. However, the plasmid pXO2 marker, required for capsule-formation could not be detected. Conclusions. The anthrax burial sites were created between the 1920s and 1960s, however, only approximate locations could be found and demarcated. In most cases the status of the sites was unsuitable for sampling. Nevertheless, isolation of B. anthracis in one case in the Valky district shows that old anthrax burial sites (13.500 exist in Ukraine) still pose a risk as potential source of the infection and therefore require more attention and surveillance, for which a surveillance plan will be developed.
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对乌克兰东部和南部可能受炭疽污染的墓地进行筛查
目标这项研究的目的是筛选乌克兰东部和南部17个炭疽埋葬地点的土壤样本中是否存在炭疽杆菌。方法。从哈尔科夫、苏梅和米科拉伊夫地区的炭疽病墓地采集了土壤样本(1946年至2003年的患病动物)。采用GABRI法从采集的土壤样品中分离炭疽杆菌。从用含过乙酸的2%Terralin PAA溶液灭活的无溶血的单菌落中提取DNA,并通过qPCR分析染色体标记dhp61的存在,以及分别位于毒力质粒pXO1和pXO2上的标记pagA和capC的存在。后果从2016年7月到2018年10月,共进行了11次实地考察,从哈尔科夫州、苏梅州和米科莱夫州的17个埋葬地点的不同深度采集了369份土壤样本。在大多数情况下(17例中有12例),这些埋葬地点的现状恶化,没有得到充分解释。有可能在哈尔科夫地区瓦尔基区Koviagy村附近50厘米深的墓地(49.92373°N,35.48951°E)获得活的炭疽杆菌分离物。该分离物命名为KhR/VD/Kov2-2-05-3,存放在哈尔科夫国家科学中心“实验和临床兽医研究所”的动物传染病病原体保藏中心,乌克兰。通过平板计数测定,分离点土壤的污染水平达到每克10 4 CFU左右。该分离物的qPCR分析鉴定了dhp61炭疽杆菌染色体和pagA毒力质粒标记。然而,无法检测到形成胶囊所需的质粒pXO2marker。结论。炭疽病埋葬地点是在20世纪20年代到60年代之间创建的,然而,只能找到并划定大致的位置。在大多数情况下,现场的状态不适合取样。然而,瓦尔基区一例炭疽杆菌的分离表明,旧的炭疽埋葬地(乌克兰有13500个)仍然是潜在的感染源,因此需要更多的关注和监测,为此将制定监测计划。
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Agricultural Science and Practice
Agricultural Science and Practice AGRICULTURE, MULTIDISCIPLINARY-
自引率
25.00%
发文量
6
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