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[鼠疫耶尔森菌和假结核耶尔森菌基因组中IS285和IS100的流行情况]

[Prevalence of IS285 and IS100 in Yersinia pestis and Yersinia pseudotuberculosis genomes].

作者信息

Bobrov A G, Filippov A A

出版信息

Mol Gen Mikrobiol Virusol. 1997(2):36-40.

PMID:9213772
Abstract

Cell DNAs of various species of Enterobacteriaceae were hybridized with the probes based on IS285 and IS100, mobile genetic elements of Yersinia pestis. These IS elements are found only in the genomes of all tested Y. pestis strains and a number of strains of a related bacterium Y. pseudotuberculosis. Phylogenetic relations between the tested strains and correlation of fingerprints with the geographical origin of the strains were revealed by analysis of the hybridization profiles of Y. pestis and Y. pseudotuberculosis chromosomal DNAs with IS probes. Comparison of the chromosomal IS100 profiles of Y. pestis wild strain and its nonpigmented mutant helped us determine the minimal extension of the genetic rearrangement and detect at least three copies of the IS element in the mutant region.

摘要

将基于鼠疫耶尔森氏菌的移动遗传元件IS285和IS100的探针与各种肠杆菌科细菌的细胞DNA进行杂交。这些IS元件仅在所有测试的鼠疫耶尔森氏菌菌株以及一些相关细菌假结核耶尔森氏菌菌株的基因组中发现。通过分析鼠疫耶尔森氏菌和假结核耶尔森氏菌染色体DNA与IS探针的杂交图谱,揭示了测试菌株之间的系统发育关系以及指纹图谱与菌株地理来源的相关性。比较鼠疫耶尔森氏菌野生菌株及其无色素突变体的染色体IS100图谱,有助于我们确定基因重排的最小延伸范围,并在突变区域检测到至少三个IS元件拷贝。

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Efficient tracing of global isolates of Yersinia pestis by restriction fragment length polymorphism analysis using three insertion sequences as probes.使用三个插入序列作为探针,通过限制性片段长度多态性分析对鼠疫耶尔森菌全球分离株进行高效追踪。
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Evaluation of ribotyping as a tool for molecular typing of Yersinia pseudotuberculosis strains of worldwide origin.
评估核糖体分型作为对全球来源的假结核耶尔森氏菌菌株进行分子分型的工具。
J Clin Microbiol. 2005 Dec;43(12):6155-60. doi: 10.1128/JCM.43.12.6155-6160.2005.
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Intraspecific diversity of Yersinia pestis.鼠疫耶尔森氏菌的种内多样性。
Clin Microbiol Rev. 2004 Apr;17(2):434-64. doi: 10.1128/CMR.17.2.434-464.2004.
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