van den Berg Renate J, Schaap Inge, Templeton Kate E, Klaassen Corné H W, Kuijper Ed J
Department of Medical Microbiology, Center of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
J Clin Microbiol. 2007 Mar;45(3):1024-8. doi: 10.1128/JCM.02023-06. Epub 2006 Dec 13.
Using the genomic sequence of Clostridium difficile strain 630, we developed multiple-locus variable-number tandem-repeat analysis (MLVA) with automated fragment analysis and multicolored capillary electrophoresis as a typing method for C. difficile. All reference strains, representing 31 serogroups, 25 toxinotypes, and 7 known subtypes of PCR ribotype 001, could be discriminated from each other. Application of MLVA to 28 isolates from 7 outbreaks due to the emerging hypervirulent PCR ribotype 027-pulsed-field gel electrophoresis type NAP1 resulted in recognition of 13 clusters. Additionally, 29 toxin A-negative, toxin B-positive isolates belonging to PCR ribotype 017 from eight different countries revealed eight country-specific clusters. MLVA is a highly discriminatory genotyping method and a new tool for subtyping of newly emerging variants of C. difficile.
利用艰难梭菌630菌株的基因组序列,我们开发了多位点可变数目串联重复序列分析(MLVA),并采用自动片段分析和多色毛细管电泳作为艰难梭菌的分型方法。所有代表31个血清群、25个毒素型和PCR核糖体分型001的7个已知亚型的参考菌株都能相互区分。将MLVA应用于因新兴的高毒力PCR核糖体分型027(脉冲场凝胶电泳型NAP1)导致的7次暴发中的28株分离株,结果识别出13个簇。此外,来自8个不同国家的29株属于PCR核糖体分型017的毒素A阴性、毒素B阳性分离株显示出8个国家特异性簇。MLVA是一种高度鉴别性的基因分型方法,也是艰难梭菌新出现变异体亚型分型的新工具。