Mokrousov Igor, Narvskaya Olga, Limeschenko Elena, Vyazovaya Anna
Laboratory of Molecular Microbiology, St. Petersburg Pasteur Institute, 14, Mira St., St. Petersburg 197101, Russia.
J Clin Microbiol. 2005 Apr;43(4):1662-8. doi: 10.1128/JCM.43.4.1662-1668.2005.
A large diphtheria epidemic in the 1990s in Russia and neighboring countries was caused by a clonal group of closely related Corynebacterium diphtheriae strains (ribotypes Sankt-Peterburg and Rossija). In the recently published complete genome sequence of C. diphtheriae strain NCTC13129, representative of the epidemic clone (A. M. Cerdeno-Tarraga et al., Nucleic Acids Res. 31:6516-6523, 2003), we identified in silico two direct repeat (DR) loci 39 kb downstream and 180 kb upstream of the oriC region, consisting of minisatellite (27- to 36-bp) alternating DRs and variable spacers. We designated these loci DRA and DRB, respectively. A reverse-hybridization macroarray-based method has been developed to study polymorphism (the presence or absence of 21 different spacers) in the larger DRB locus. We name it spoligotyping (spacer oligonucleotide typing), analogously to a similar method of Mycobacterium tuberculosis genotyping. The method was evaluated with 154 clinical strains of the C. diphtheriae epidemic clone from the St. Petersburg area in Russia from 1997 to 2002. By comparison with the international ribotype database (Institut Pasteur, Paris, France), these strains were previously identified as belonging to ribotypes Sankt-Peterburg (n = 79) and Rossija (n = 75). The 154 strains were subdivided into 34 spoligotypes: 14 unique strains and 20 types shared by 2 to 46 strains; the Hunter Gaston discriminatory index (HGDI) was 0.85. DRB locus-based spoligotyping allows fast and efficient discrimination within the C. diphtheriae epidemic clonal group and is applicable to both epidemiological investigations and phylogenetic reconstruction. The results are easy to interpret and can be presented and stored in a user-friendly digital database (Excel file), allowing rapid type determination of new strains.
20世纪90年代在俄罗斯及周边国家爆发的大规模白喉疫情是由一组密切相关的白喉棒状杆菌菌株(圣彼得堡核糖型和俄罗斯核糖型)的克隆群引起的。在最近发表的白喉棒状杆菌菌株NCTC13129的全基因组序列中(该菌株代表疫情克隆群,A. M. 塞尔德诺 - 塔拉加等人,《核酸研究》31:6516 - 6523,2003年),我们通过计算机分析在oriC区域下游39 kb和上游180 kb处鉴定出两个直接重复(DR)位点,它们由微卫星(27至36 bp)交替DR和可变间隔区组成。我们分别将这些位点命名为DRA和DRB。已开发出一种基于反向杂交宏阵列的方法来研究较大的DRB位点中的多态性(21种不同间隔区的存在与否)。我们将其命名为间隔区寡核苷酸分型(spoligotyping),类似于结核分枝杆菌基因分型的类似方法。该方法用1997年至2002年从俄罗斯圣彼得堡地区采集的154株白喉棒状杆菌疫情克隆群的临床菌株进行了评估。通过与国际核糖型数据库(法国巴黎巴斯德研究所)比较,这些菌株先前被鉴定为属于圣彼得堡核糖型(n = 79)和俄罗斯核糖型(n = 75)。这154株菌株被细分为34种间隔区寡核苷酸分型:14种独特菌株和20种由2至46株菌株共享的类型;亨特 - 加斯顿鉴别指数(HGDI)为0.85。基于DRB位点的间隔区寡核苷酸分型能够在白喉棒状杆菌疫情克隆群内进行快速有效的鉴别,适用于流行病学调查和系统发育重建。结果易于解释,并且可以以用户友好的数字数据库(Excel文件)形式呈现和存储,从而能够快速确定新菌株的类型。