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本文引用的文献

1
Development of a new ligation-mediated PCR method for the differentiation of Mycobacterium tuberculosis strains.一种用于区分结核分枝杆菌菌株的新型连接介导PCR方法的开发。
Int J Tuberc Lung Dis. 2014 Mar;18(3):302-9. doi: 10.5588/ijtld.13.0538.
2
IS6110-based differentiation of Mycobacterium tuberculosis strains.基于 IS6110 的结核分枝杆菌菌株分化。
Pol J Microbiol. 2013;62(2):201-4.
3
The new LM-PCR/shifter method for the genotyping of microorganisms based on the use of a class IIS restriction enzyme and ligation mediated PCR.基于 II S 类限制酶和连接介导 PCR 的微生物基因分型新 LM-PCR/移位方法。
J Microbiol Biotechnol. 2011 Dec;21(12):1336-44. doi: 10.4014/jmb.1104.04019.
4
Epidemiological analysis of Mycobacterium tuberculosis strains isolated in Lodz, Poland.波兰罗兹分离的结核分枝杆菌菌株的流行病学分析。
Int J Tuberc Lung Dis. 2011 Sep;15(9):1252-8, i. doi: 10.5588/ijtld.10.0718.
5
Molecular epidemiology of tuberculosis: current insights.结核病的分子流行病学:当前见解
Clin Microbiol Rev. 2006 Oct;19(4):658-85. doi: 10.1128/CMR.00061-05.
6
Proposal for standardization of optimized mycobacterial interspersed repetitive unit-variable-number tandem repeat typing of Mycobacterium tuberculosis.结核分枝杆菌优化的分枝杆菌插入重复单位-可变数目串联重复序列分型标准化方案。
J Clin Microbiol. 2006 Dec;44(12):4498-510. doi: 10.1128/JCM.01392-06. Epub 2006 Sep 27.
7
Evaluation of a PCR melting profile technique for bacterial strain differentiation.用于细菌菌株鉴别的聚合酶链反应熔解曲线技术评估
J Clin Microbiol. 2006 Jul;44(7):2327-32. doi: 10.1128/JCM.00052-06.
8
Discriminatory power and reproducibility of novel DNA typing methods for Mycobacterium tuberculosis complex strains.结核分枝杆菌复合群菌株新型DNA分型方法的鉴别能力和可重复性。
J Clin Microbiol. 2005 Nov;43(11):5628-38. doi: 10.1128/JCM.43.11.5628-5638.2005.
9
Fast ligation-mediated PCR, a fast and reliable method for IS6110-based typing of Mycobacterium tuberculosis complex.快速连接介导的PCR,一种用于结核分枝杆菌复合群基于IS6110分型的快速且可靠的方法。
J Clin Microbiol. 2005 Nov;43(11):5622-7. doi: 10.1128/JCM.43.11.5622-5627.2005.
10
Evaluation of a two-step approach for large-scale, prospective genotyping of Mycobacterium tuberculosis isolates in the United States.美国结核分枝杆菌分离株大规模前瞻性基因分型两步法的评估
J Clin Microbiol. 2005 Feb;43(2):688-95. doi: 10.1128/JCM.43.2.688-695.2005.

结扎介导的聚合酶链反应方法在结核分枝杆菌菌株鉴别中的比较

Comparison of ligation-mediated PCR methods in differentiation of Mycobacterium tuberculosis strains.

作者信息

Zaczek Anna, Brzostek Anna, Wojtasik Arkadiusz, Sajduda Anna, Dziadek Jaroslaw

机构信息

Department of Biochemistry and Cell Biology, University of Rzeszow, 35-601 Rzeszow, Poland.

Institute of Medical Biology, Polish Academy of Science, 93-232 Lodz, Poland.

出版信息

Biomed Res Int. 2014;2014:782071. doi: 10.1155/2014/782071. Epub 2014 Feb 16.

DOI:10.1155/2014/782071
PMID:24696162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3947874/
Abstract

Fast and inexpensive identification of epidemiological links between limited number of Mycobacterium tuberculosis strains is required to initially evaluate hospital outbreaks, laboratory crosscontaminations, and family or small community transmissions. The ligation-mediated PCR methods (LM-PCR) appear sufficiently discriminative and reproducible to be considered as a good candidate for such initial, epidemiological analysis. Here, we compared the discriminative power of the recently developed in our laboratory fast ligation amplification polymorphism (FLAP) method with fast ligation-mediated PCR (FLiP). Verification of the results was based on analyzing a set of reference strains and RFLP-IS6110 typing. The HGDI value was very similar for both LM-PCR methods and RFLP-IS6110 typing. However, only 52% of strains were correspondingly grouped by both FLiP and FLAP methods. Differentiation by FLAP method demonstrated a limited similarity to IS6110-RFLP (37,7%). As much as 78,7% of strains were grouped identically when differentiated by FLiP and IS6110-RFLP methods. The analysis differentiated 31, 35, and 36 groups when using FLAP, FLiP, and RFLP-IS6110 methods, respectively.

摘要

为初步评估医院内的疫情爆发、实验室交叉污染以及家庭或小社区内的传播情况,需要快速且经济地鉴定有限数量的结核分枝杆菌菌株之间的流行病学联系。连接介导的PCR方法(LM-PCR)似乎具有足够的鉴别力和可重复性,可被视为进行此类初步流行病学分析的良好候选方法。在此,我们将实验室最近开发的快速连接扩增多态性(FLAP)方法与快速连接介导的PCR(FLiP)方法的鉴别力进行了比较。结果验证基于对一组参考菌株的分析以及RFLP-IS6110分型。两种LM-PCR方法和RFLP-IS6110分型的HGDI值非常相似。然而,只有52%的菌株通过FLiP和FLAP方法相应地分组。通过FLAP方法进行的区分与IS6110-RFLP的相似性有限(37.7%)。当通过FLiP和IS6110-RFLP方法进行区分时,多达78.7%的菌株分组相同。使用FLAP、FLiP和RFLP-IS6110方法进行分析时,分别区分出31、35和36个组。