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

Author:

Bouakaze C.1,Keyser C.1,de Martino S. J.2,Sougakoff W.34,Veziris N.45,Dabernat H.6,Ludes B.1

Affiliation:

1. EA4438 Physiopathologie et Médecine Translationnelle, Université de Strasbourg, Institut de Médecine Légale, Strasbourg, France

2. Laboratoire de Bactériologie, Faculté de Médecine, Université de Strasbourg, Strasbourg, France

3. UPMC Université Paris 06, UMRS872-12 Site Pitié-Salpêtrière, Département de Bactériologie-Hygiène, Paris, France

4. AP-HP, Hôpital Pitié-Salpêtrière, Laboratoire de Bactériologie-Hygiène, Paris, France, and Centre National de Référence des Mycobactéries et de la Résistance des Mycobactéries aux Antituberculeux, Paris, France

5. UPMC Université Paris 06, EA 1541, Laboratoire de Bactériologie-Hygiène, Paris, France

6. Laboratoire d'Anthropologie Moléculaire et Imagerie de Synthèse (AMIS), CNRS FRE 2960, Université Paul Sabatier, Toulouse, France, and Laboratoire de Bactériologie, Faculté de Médecine Purpan, Toulouse, France

Abstract

ABSTRACT 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.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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