Revised Interpretation of the Hain Lifescience GenoType MTBC To Differentiate Mycobacterium canettii and Members of the Mycobacterium tuberculosis Complex
Author(s) -
Chloé Loiseau,
Daniela Brites,
Irmgard Moser,
Francesc Coll,
Christine Pourcel,
Suelee RobbeAusterman,
Vincent Escuyer,
Kimberlee A. Musser,
Sharon J. Peacock,
Silke Feuerriegel,
Thomas A. Kohl,
Stefan Niemann,
Sébastien Gagneux,
Claudio U. Köser
Publication year - 2019
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.00159-19
Subject(s) - mycobacterium tuberculosis complex , mycobacterium tuberculosis , mycobacterium bovis , biology , mycobacterium , genotype , microbiology and biotechnology , tuberculosis , virology , genetics , gene , medicine , bacteria , pathology
Using 894 phylogenetically diverse genomes of theMycobacterium tuberculosis complex (MTBC), we simulatedin silico the ability of the Hain Lifescience GenoType MTBC assay to differentiate the causative agents of tuberculosis. Here, we propose a revised interpretation of this assay to reflect its strengths (e.g., it can distinguish some strains ofMycobacterium canettii and variants ofMycobacterium bovis that are not intrinsically resistant to pyrazinamide) and limitations (e.g.,Mycobacterium orygis cannot be differentiated fromMycobacterium africanum ).
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom