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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of spoligotyping in a study of the transmission of Mycobacterium tuberculosis.
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Evaluation of spoligotyping in a study of the transmission of Mycobacterium tuberculosis.

机译:在结核分枝杆菌的传播研究中评估分型方法。

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Spoligotyping (for spacer oligotyping) is an easy, economical, and rapid way of typing Mycobacterium tuberculosis complex strains with the DR spacer markers (J. Kamerbeek et al., J. Clin. Microbiol. 35:907-914, 1997; D. van Soolingen et al., 33:3234-3248, 1995). The stability of the markers was demonstrated by showing that all the Mycobacterium bovis BCG strains tested gave the same spoligotyping pattern. None of the 42 atypical mycobacterial strains tested gave a spoligotyping signal, indicating the specificity of the technique for M. tuberculosis complex. The utility of the spoligotyping method was demonstrated by analyzing 106 isolates of M. tuberculosis obtained over 1 year in three Paris hospitals. The results obtained by this technique were compared to those obtained by Torrea et al. (G. Torrea et al., J. Clin. Microbiol. 34:1043-1049, 1996) by IS6110-based restriction fragment length polymorphism (RFLP) analysis. Strains from patients with epidemiological relationships that were in the same IS6110-RFLP cluster were also in the same spoligotyping group. Spoligotyping was more discriminative than RFLP analysis for strains with one or two copies of IS6110. RFLP analysis did not discriminate between the nine strains with one or two IS6110 bands with no known epidemiological relation, whereas spoligotyping distinguished between eight different types. IS6I10-RFLP analysis split some of the spoligotyping clusters, particularly when the IS6110 copy number was high. Therefore, we propose a strategy for typing M. tuberculosis strains in which both markers are used.
机译:寡核苷酸分型(用于间隔子寡核苷酸分型)是一种容易,经济且快速的用DR间隔子标记分型结核分枝杆菌复杂菌株的方法(J.Kamerbeek等,J.Clin.Microbiol.35:907-914,1997; D。 van Soolingen等,33:3234-3248,1995)。通过显示所有测试的牛分枝杆菌BCG菌株均具有相同的基因分型模式,证明了标记物的稳定性。测试的42种非典型分枝杆菌菌株均未给出血吸虫分型信号,表明该技术对结核分枝杆菌复合物的特异性。通过分析在巴黎的三家医院历时1年以上获得的106株结核分枝杆菌,证明了这种方法的实用性。将该技术获得的结果与Torrea等人获得的结果进行了比较。 (G.Torora等人,J.Clin.Microbiol.34:1043-1049,1996)通过基于IS6110的限制性片段长度多态性(RFLP)分析。来自同一IS6110-RFLP群体的具有流行病学关系的患者的菌株也属于同一基因分型组。对于一两个IS6110拷贝的菌株,Spoligotyping比RFLP分析更具判别力。 RFLP分析未区分9个带有1个或2个IS6110波段且没有已知流行病学关系的菌株,而血吸虫分型则区分了8种不同类型。 IS6I10-RFLP分析拆分了一些盗版聚类,特别是当IS6110拷贝数很高时。因此,我们提出了一种使用两种标记物对结核分枝杆菌菌株进行分型的策略。

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