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. 2018 Feb 2;13(2):e0192291. doi: 10.1371/journal.pone.0192291

Table 1. Rates of correct identification of different mycobacterial species using the conventional Microchip MTB method compared to direct identification from positive MGIT broths using the MALDI-TOF MS Vitek MS system with a IVD database (v3.0) prepared without any washing step (Direct) and washed once with 0.1% SDS (SDS) protocol (N = 83).

Species No. of samples No. of samples identified:
First Repeat
Microchip MTB
n (%)
Direct
n (%)
SDS
n (%)
Direct
n (%)
SDS
n (%)
MAC* 40 39 (97.5) 30 (75.0) 32 (80.0) 37 (92.5) 40 (100.0)
M. abscessus 16 16(100.0) 16 (100.0) 16 (100.0) 16 (100.0) 16 (100.0)
M. kansasii 9 9 (100.0) 8 (88.9) 8 (88.9) 9 (100.0) 9 (100.0)
M. fortuitum 9 9 (100.0) 9 (100.0) 9(100.0) 9 (100.0) 9 (100.0)
M. chelonae 2 2 (100.0) 2 (100.0) 2 (100.0) 2 (100.0) 2 (100.0)
M. szulgai 1 1 (100.0) 1 (100.0) 1 (100.0) 1 (100.0) 1 (100.0)
M. gordonae 3 3 (100.0) 3 (100.0) 3 (100.0) 3 (100.0) 3 (100.0)
M. cosmeticum$ 1 0 1 (100.0) 1 (100.0) 1 (100.0) 1 (100.0)
M. simiae 1 1 (100.0) 1 (100.0) 1 (100.0) 1 (100.0) 1 (100.0)
M. mageritense 1 0 1 (100.0) 1 (100.0) 1 (100.0) 1 (100.0)
Total 83 80 (97.6) 72 (86.7) 74 (89.2) 80 (96.4) 81 (100*)

*MAC: M. avium-intracellulare complex

$Identified as M. neoneunm by Microchip MTB; M. cosmeticum by MS and PRA.