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Comparison of methods available for identification of Mycobacterium chimaera
E. Lecorche, S. Haenn, F. Mougari, S. Kumanski, N. Veziris, H. Benmansour, L. Raskine, L. Moulin, E. Cambau A. Aubry, F. Brossier, A. Chauffour, J. Jaffre, V. Jarlier, J. Robert, W. Sougakoff E. Lecorche, S. Haenn, F. Mougari, S. Kumanski, N. Veziris, H. Benmansour, L. Raskine, L. Moulin, E. Cambau A. Aubry, F. Brossier, A. Chauffour, J. Jaffre, V. Jarlier, J. Robert, W. Sougakoff Clinical Microbiology and Infection Volume 24, Issue 4, Pages (April 2018) DOI: /j.cmi Copyright © 2017 European Society of Clinical Microbiology and Infectious Diseases Terms and Conditions
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Fig. 1 Identification pattern of Mycobacterium avium (MA), M. chimaera (MC) and M. intracellulare (MI) using three commercial line probe assays tested: GenoType Mycobacterium CM 1.0, INNO-LiPA Mycobacteria 2 and GenoType NTM-DR 1.0. CC, Conjugate Control probe (to check binding of conjugate on strip and chromogenic reaction); GC, genus control probe (detects mycobacteria belonging to Mycobacterium genus); UC, Universal Control probe (to detect mycobacteria and members of group of Gram-positive bacteria with high G+C content). Clinical Microbiology and Infection , DOI: ( /j.cmi ) Copyright © 2017 European Society of Clinical Microbiology and Infectious Diseases Terms and Conditions
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Fig. 2 Score-oriented dendrogram based on matrix-assisted desorption ionization–time of flight mass spectrometry identification. Distance is displayed in relative units. Spectra of reference strains included in Bruker 3 database (Mycobacterium chelonae DSM 43485, M. avium DSM 44158) were considered for dendrogram. Clinical Microbiology and Infection , DOI: ( /j.cmi ) Copyright © 2017 European Society of Clinical Microbiology and Infectious Diseases Terms and Conditions
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