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本文引用的文献

1
Automated high-throughput genotyping for study of global epidemiology of Mycobacterium tuberculosis based on mycobacterial interspersed repetitive units.基于分枝杆菌散布重复单位的用于结核分枝杆菌全球流行病学研究的自动化高通量基因分型
J Clin Microbiol. 2001 Oct;39(10):3563-71. doi: 10.1128/JCM.39.10.3563-3571.2001.
2
Spacer oligonucleotide typing of bacteria of the Mycobacterium tuberculosis complex: recommendations for standardised nomenclature.结核分枝杆菌复合群细菌的间隔区寡核苷酸分型:标准化命名建议
Int J Tuberc Lung Dis. 2001 Mar;5(3):216-9.
3
High-resolution minisatellite-based typing as a portable approach to global analysis of Mycobacterium tuberculosis molecular epidemiology.基于高分辨率微卫星的分型作为一种用于结核分枝杆菌分子流行病学全球分析的便捷方法。
Proc Natl Acad Sci U S A. 2001 Feb 13;98(4):1901-6. doi: 10.1073/pnas.98.4.1901.
4
Molecular epidemiology of tuberculosis and other mycobacterial infections: main methodologies and achievements.结核病及其他分枝杆菌感染的分子流行病学:主要方法与成就
J Intern Med. 2001 Jan;249(1):1-26. doi: 10.1046/j.1365-2796.2001.00772.x.
5
Transmission dynamics and molecular characterization of Mycobacterium tuberculosis isolates with low copy numbers of IS6110.低拷贝数IS6110的结核分枝杆菌分离株的传播动力学及分子特征
J Clin Microbiol. 2001 Jan;39(1):217-21. doi: 10.1128/JCM.39.1.217-221.2001.
6
Spoligotyping and polymorphic GC-rich repetitive sequence fingerprinting of mycobacterium tuberculosis strains having few copies of IS6110.对IS6110拷贝数较少的结核分枝杆菌菌株进行寡核苷酸分型和富含GC的多态性重复序列指纹分析。
J Clin Microbiol. 2000 Oct;38(10):3572-6. doi: 10.1128/JCM.38.10.3572-3576.2000.
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Variable human minisatellite-like regions in the Mycobacterium tuberculosis genome.结核分枝杆菌基因组中可变的类人微卫星区域。
Mol Microbiol. 2000 May;36(3):762-71. doi: 10.1046/j.1365-2958.2000.01905.x.
8
Multiplex PCR assay to aid in the identification of the highly transmissible Mycobacterium tuberculosis strain CDC1551.多重聚合酶链反应检测法有助于鉴定高传播性结核分枝杆菌菌株CDC1551。
Tuber Lung Dis. 1999;79(5):273-8. doi: 10.1054/tuld.1999.0197.
9
Characterization of Mycobacterium tuberculosis isolates from patients in Houston, Texas, by spoligotyping.采用间隔寡核苷酸分型法对得克萨斯州休斯敦市患者的结核分枝杆菌分离株进行特征分析。
J Clin Microbiol. 2000 Feb;38(2):669-76. doi: 10.1128/JCM.38.2.669-676.2000.
10
Comparison of methods based on different molecular epidemiological markers for typing of Mycobacterium tuberculosis complex strains: interlaboratory study of discriminatory power and reproducibility.基于不同分子流行病学标志物的结核分枝杆菌复合群菌株分型方法比较:鉴别力和可重复性的实验室间研究
J Clin Microbiol. 1999 Aug;37(8):2607-18. doi: 10.1128/JCM.37.8.2607-2618.1999.

利用分枝杆菌散布重复单位对IS6110拷贝数低的结核分枝杆菌分离株进行可变数目串联重复序列分型

Variable-number tandem repeat typing of Mycobacterium tuberculosis isolates with low copy numbers of IS6110 by using mycobacterial interspersed repetitive units.

作者信息

Cowan Lauren Steinlein, Mosher Laura, Diem Lois, Massey Jeffrey P, Crawford Jack T

机构信息

Division of AIDS, STD, and TB Laboratory Research, National Center for Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333, USA.

出版信息

J Clin Microbiol. 2002 May;40(5):1592-602. doi: 10.1128/JCM.40.5.1592-1602.2002.

DOI:10.1128/JCM.40.5.1592-1602.2002
PMID:11980927
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC130938/
Abstract

A study set of 180 Mycobacterium tuberculosis and Mycobacterium bovis isolates having low copy numbers of IS6110 were genotyped using the recently introduced method based on the variable-number tandem repeats of mycobacterial interspersed repetitive units (MIRU-VNTR). The results were compared with results of the more commonly used methods, IS6110 restriction fragment length polymorphism (RFLP) and spoligotyping. The isolates were collected in Michigan from 1996 to 1999 as part of a project to genotype all isolates from new cases of tuberculosis in the state. Twelve MIRU loci were amplified, and the amplicons were analyzed by agarose gel electrophoresis to determine the copy number at each MIRU locus. MIRU-VNTR produced more distinct patterns (80 patterns) than did IS6110 RFLP (58 patterns), as would be expected in this study set. Spoligotyping identified 59 patterns. No single method defined all unique isolates, and the combination of all three typing methods generated 112 distinct patterns identifying 90 unique isolates and 90 isolates in 22 clusters. The results confirm the potential utility of MIRU-VNTR typing and show that typing with multiple methods is required to attain maximum specificity.

摘要

对180株插入序列6110(IS6110)拷贝数较低的结核分枝杆菌和牛分枝杆菌分离株,采用基于分枝杆菌散布重复单位可变数目串联重复序列(MIRU-VNTR)的最新方法进行基因分型。将结果与更常用的方法——IS6110限制性片段长度多态性分析(RFLP)和间隔寡核苷酸分型(spoligotyping)的结果进行比较。这些分离株于1996年至1999年在密歇根州收集,作为该州对所有新结核病例分离株进行基因分型项目的一部分。扩增了12个MIRU位点,并通过琼脂糖凝胶电泳分析扩增产物,以确定每个MIRU位点的拷贝数。正如本研究集所预期的那样,MIRU-VNTR产生的图谱(80种图谱)比IS6110 RFLP(58种图谱)更为独特。间隔寡核苷酸分型鉴定出59种图谱。没有单一方法能定义所有独特的分离株,三种分型方法联合使用产生了112种不同的图谱,识别出90株独特的分离株以及22个簇中的90株分离株。结果证实了MIRU-VNTR分型的潜在效用,并表明需要采用多种方法进行分型才能获得最大的特异性。