首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Genetic Variability within Borrelia burgdorferi Sensu Lato Genospecies Established by PCR-Single-Strand Conformation Polymorphism Analysis of the rrfA-rrlB Intergenic Spacer in Ixodes ricinus Ticks from the Czech Republic
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Genetic Variability within Borrelia burgdorferi Sensu Lato Genospecies Established by PCR-Single-Strand Conformation Polymorphism Analysis of the rrfA-rrlB Intergenic Spacer in Ixodes ricinus Ticks from the Czech Republic

机译:通过PCR-单链构象多态性分析建立的博氏疏螺旋体Sersu Lato基因组内的遗传变异在捷克共和国I蓟马Ti中的rrfA-rrlB基因间隔子

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摘要

In Europe the Borrelia burgdorferi sensu lato complex is represented by five distinct genospecies: Borrelia burgdorferi sensu stricto, Borrelia afzelii, Borrelia garinii, Borrelia valaisiana, and Borrelia lusitaniae. These taxonomic entities are known to differ in their specific associations with vertebrate hosts and to provoke distinct clinical manifestations in human patients. However, exceptions to these rules have often been observed, indicating that strains belonging to a single genospecies may be more heterogeneous than expected. It is, therefore, important to develop alternative identification tools which are able to distinguish Borrelia strains not only at the specific level but also at the intraspecific level. DNA from a sample of 370 Ixodes ricinus ticks collected in the Czech Republic was analyzed by PCR for the presence of a ∼230-bp fragment of the rrfA-rrlB intergenic spacer of Borrelia spp. A total of 20.5% of the ticks were found to be positive. The infecting genospecies were identified by analyzing the amplified products by the restriction fragment length polymorphism (RFLP) method with restriction enzyme MseI and by single-strand conformation polymorphism (SSCP) analysis. The two methods were compared, and PCR-SSCP analysis appeared to be a valuable tool for rapid identification of spirochetes at the intraspecific level, particularly when large samples are examined. Furthermore, by using PCR-SSCP analysis we identified a previously unknown Borrelia genotype, genotype I-77, which would have gone unnoticed if RFLP analysis alone had been used.
机译:在欧洲,伯氏疏螺旋体以五种不同的基因种为代表:伯氏疏螺旋体,严格疏螺旋体,非洲疏螺旋体,加里氏疏螺旋体,缬草疏螺旋体和卢氏疏螺旋体。已知这些分类实体与脊椎动物宿主的特异性关联不同,并且在人类患者中引起明显的临床表现。但是,经常会观察到这些规则的例外情况,这表明属于单一基因种的菌株可能比预期的更加异质。因此,重要的是开发替代的鉴定工具,该鉴定工具不仅能够在特定水平上而且能够在种内水平上区分疏螺旋体菌株。通过PCR分析了捷克共和国收集的370个蓖麻(Ixodes ricinus)tick的样本中的DNA,通过PCR分析了鲍氏疏螺旋体rrfA-rrlB基因间隔区的〜230 bp片段。总共有20.5%的刻度显示为阳性。通过用限制性酶MseI进行限制性片段长度多态性(RFLP)方法和单链构象多态性(SSCP)分析来分析扩增产物,从而鉴定出感染的基因型。比较了这两种方法,PCR-SSCP分析似乎是在种内水平快速鉴定螺旋体的有价值的工具,尤其是在检查大样本时。此外,通过使用PCR-SSCP分析,我们确定了以前未知的Borrelia基因型,即基因型I-77,如果仅使用RFLP分析,该基因型将不会被注意到。

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