Identification and Genotyping of Mycobacterium tuberculosis Complex Species by Use of a SNaPshot Minisequencing-Based Assay

被引:38
作者
Bouakaze, C. [1 ]
Keyser, C. [1 ]
de Martino, S. J. [2 ]
Sougakoff, W. [3 ,4 ,5 ]
Veziris, N. [4 ,5 ,6 ]
Dabernat, H. [7 ,8 ]
Ludes, B. [1 ]
机构
[1] Univ Strasbourg, Inst Med Legale, EA Physiopathol & Med Translat 4438, F-67085 Strasbourg, France
[2] Univ Strasbourg, Fac Med, Bacteriol Lab, F-67085 Strasbourg, France
[3] Univ Paris 06, UPMC, UMRS Site Pitie Salpetriere 872 12, Dept Bacteriol Hyg, Paris, France
[4] Hop La Pitie Salpetriere, AP HP, Lab Bacteriol Hyg, Paris, France
[5] Ctr Natl Reference Mycobacteries & Resistance Myc, Paris, France
[6] Univ Paris 06, UPMC, EA 1541, Lab Bacteriol Hyg, Paris, France
[7] Univ Toulouse 3, CNRS, FRE 2960, Lab Anthropol Mol & Imagerie Synth AMIS, F-31062 Toulouse, France
[8] Fac Med Purpan, Bacteriol Lab, Toulouse, France
关键词
SINGLE-NUCLEOTIDE POLYMORPHISMS; Y-CHROMOSOME SNPS; MULTIPLEX SNAPSHOT; PCR AMPLIFICATION; GENE POLYMORPHISM; RAPID METHOD; ANCIENT DNA; MTBC ASSAY; DIFFERENTIATION; MUTATIONS;
D O I
10.1128/JCM.02255-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The aim of the present study was to investigate the use of the SNaPshot minisequencing method for the identification of Mycobacterium tuberculosis complex (MTBC) isolates to the species level and for further genotyping of M. tuberculosis isolates. We developed an innovative strategy based on two multiplex allele-specific minisequencing assays that allowed detection of eight species-specific and eight lineage-specific single nucleotide polymorphisms (SNPs). Each assay consisted of an eightplex PCR amplification, followed by an eightplex minisequencing reaction with the SNaPshot multiplex kit (Applied Biosystems) and, finally, analysis of the extension products by capillary electrophoresis. The whole strategy was developed with a panel of 56 MTBC strains and 15 negative controls. All MTBC strains tested except one M. africanum clinical isolate were accurately identified to the species level, and all M. tuberculosis isolates were successfully further genotyped. This two-step strategy based on SNaPshot minisequencing allows the simultaneous differentiation of closely related members of the MTBC, the distinction between principal genetic groups, and the characterization of M. tuberculosis isolates into one of the seven prominent SNP cluster groups (SCGs) and could be a useful tool for diagnostic and epidemiological purposes.
引用
收藏
页码:1758 / 1766
页数:9
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