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Global phylogeny of Mycobacterium tuberculosis based on single nucleotide polymorphism (SNP) analysis: insights into tuberculosis evolution, phylogenetic accuracy of other DNA fingerprinting systems, and recommendations for a minimal standard SNP set.基于单核苷酸多态性(SNP)分析的结核分枝杆菌全球系统发育:对结核病进化的见解、其他DNA指纹识别系统的系统发育准确性以及最小标准SNP集的建议。
J Bacteriol. 2006 Jan;188(2):759-72. doi: 10.1128/JB.188.2.759-772.2006.
2
Single-nucleotide polymorphism-based population genetic analysis of Mycobacterium tuberculosis strains from 4 geographic sites.基于单核苷酸多态性的来自4个地理区域的结核分枝杆菌菌株群体遗传学分析。
J Infect Dis. 2006 Jan 1;193(1):121-8. doi: 10.1086/498574. Epub 2005 Nov 28.
3
Ancient origin and gene mosaicism of the progenitor of Mycobacterium tuberculosis.结核分枝杆菌祖细胞的古老起源与基因镶嵌性
PLoS Pathog. 2005 Sep;1(1):e5. doi: 10.1371/journal.ppat.0010005. Epub 2005 Aug 19.
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Molecular evolutionary history of tubercle bacilli assessed by study of the polymorphic nucleotide within the nitrate reductase (narGHJI) operon promoter.通过对硝酸还原酶(narGHJI)操纵子启动子内多态性核苷酸的研究评估结核杆菌的分子进化史。
J Clin Microbiol. 2005 Aug;43(8):4010-4. doi: 10.1128/JCM.43.8.4010-4014.2005.
6
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Emerg Infect Dis. 2004 Dec;10(12):2258-10. doi: 10.3201/eid1012.040094.
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Mycobacterium africanum genotyping using novel spacer oligonucleotides in the direct repeat locus.利用直接重复序列位点中的新型间隔寡核苷酸对非洲分枝杆菌进行基因分型。
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J Bacteriol. 2004 Sep;186(18):6332-4. doi: 10.1128/JB.186.18.6332-6334.2004.
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J Clin Microbiol. 2004 Aug;42(8):3594-9. doi: 10.1128/JCM.42.8.3594-3599.2004.
10
High genetic diversity revealed by variable-number tandem repeat genotyping and analysis of hsp65 gene polymorphism in a large collection of "Mycobacterium canettii" strains indicates that the M. tuberculosis complex is a recently emerged clone of "M. canettii".通过可变数目串联重复序列基因分型以及对大量“卡内蒂分枝杆菌”菌株的hsp65基因多态性分析所揭示的高遗传多样性表明,结核分枝杆菌复合群是“卡内蒂分枝杆菌”最近出现的一个克隆。
J Clin Microbiol. 2004 Jul;42(7):3248-55. doi: 10.1128/JCM.42.7.3248-3255.2004.

进一步描绘结核分枝杆菌复合群系统发育的新型基因多态性。

Novel genetic polymorphisms that further delineate the phylogeny of the Mycobacterium tuberculosis complex.

作者信息

Huard Richard C, Fabre Michel, de Haas Petra, Lazzarini Luiz Claudio Oliveira, van Soolingen Dick, Cousins Debby, Ho John L

机构信息

Division of International Medicine and Infectious Diseases, Department of Medicine, Joan and Sanford I. Weill Medical College, Cornell University, Room A-421, 525 East 68th St., New York, NY 10021, USA.

出版信息

J Bacteriol. 2006 Jun;188(12):4271-87. doi: 10.1128/JB.01783-05.

DOI:10.1128/JB.01783-05
PMID:16740934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1482959/
Abstract

In a previous report, we described a PCR protocol for the differentiation of the various species of the Mycobacterium tuberculosis complex (MTC) on the basis of genomic deletions (R. C. Huard, L. C. de Oliveira Lazzarini, W. R. Butler, D. van Soolingen, and J. L. Ho, J. Clin. Microbiol. 41:1637-1650, 2003). That report also provided a broad cross-comparison of several previously identified, phylogenetically relevant, long-sequence and single-nucleotide polymorphisms (LSPs and SNPs, respectively). In the present companion report, we expand upon the previous work (i) by continuing the evaluation of known MTC phylogenetic markers in a larger collection of tubercle bacilli (n = 125), (ii) by evaluating additional recently reported MTC species-specific and interspecific polymorphisms, and (iii) by describing the identification and distribution of a number of novel LSPs and SNPs. Notably, new genomic deletions were found in various Mycobacterium tuberculosis strains, new species-specific SNPs were identified for "Mycobacterium canettii," Mycobacterium microti, and Mycobacterium pinnipedii, and, for the first time, intraspecific single-nucleotide DNA differences were discovered for the dassie bacillus, the oryx bacillus, and the two Mycobacterium africanum subtype I variants. Surprisingly, coincident polymorphisms linked one M. africanum subtype I genotype with the dassie bacillus and M. microti with M. pinnipedii, thereby suggesting closer evolutionary ties within each pair of species than had been previously thought. Overall, the presented data add to the genetic definitions of several MTC organisms as well as fine-tune current models for the evolutionary history of the MTC.

摘要

在之前的一份报告中,我们描述了一种基于基因组缺失来区分结核分枝杆菌复合群(MTC)各菌种的PCR方案(R. C. Huard、L. C. de Oliveira Lazzarini、W. R. Butler、D. van Soolingen和J. L. Ho,《临床微生物学杂志》41:1637 - 1650,2003年)。该报告还对几个先前鉴定的、系统发育相关的长序列和单核苷酸多态性(分别为LSPs和SNPs)进行了广泛的交叉比较。在本配套报告中,我们扩展了先前的工作:(i)通过在更大的结核杆菌集合(n = 125)中继续评估已知的MTC系统发育标记;(ii)通过评估其他最近报道的MTC菌种特异性和种间多态性;(iii)通过描述一些新的LSPs和SNPs的鉴定及分布。值得注意的是,在各种结核分枝杆菌菌株中发现了新的基因组缺失,为“卡内蒂分枝杆菌”、田鼠分枝杆菌和海豹分枝杆菌鉴定了新的菌种特异性SNPs,并且首次发现了南非山兔分枝杆菌、羚羊分枝杆菌以及两种非洲分枝杆菌I型变种的种内单核苷酸DNA差异。令人惊讶的是,重合的多态性将一种非洲分枝杆菌I型基因型与南非山兔分枝杆菌联系起来,将田鼠分枝杆菌与海豹分枝杆菌联系起来,从而表明每对物种之间的进化关系比之前认为的更为密切。总体而言,所呈现的数据增加了几种MTC生物体的遗传定义,并对当前MTC进化历史模型进行了微调。