1 s from all 10 footbaths at the salon yielded
M. fortuitum.
2 r the most isolated NTM (71.0%), followed by
M. fortuitum (
9.5%) and M. nonchromogenicum (2.9%).
3 guidelines are presented for the testing of
M. fortuitum against clarithromycin; M. abscessus and M.
4 ositive for rapidly growing mycobacteria (32
M. fortuitum and 2 unidentified).
5 st- and slow-growing mycobacteria, including
M. fortuitum and M. avium.
6 M. fortuitum and Mycobacterium abscessus isolates harbor
7 PA positive for Mycobacterium spp. (six were
M. fortuitum,
and one was M. szulgai).
8 M. smegmatis oriC functioned only in
M. fortuitum,
but not in any of the slowly growing mycob
9 e M. chelonae-M. abscessus group (MCAG), the
M. fortuitum group (MFG), and M. mucogenicum.
10 One
M. fortuitum isolate and one of five M. kansasii isolate
11 The
M. fortuitum isolates from three footbaths and 14 patien
12 In contrast,
M. fortuitum isolates were able to grow in 100 microg of
13 Selected
M. fortuitum isolates, cultured from patients and the sa
14 that assay suspensions containing M. avium,
M. fortuitum,
M. gordonae, or M. marinum incubated with
15 M. fortuitum,
M. marinum, M. scrofulaceum, M. avium, and
16 . avium sub0:36 PMavium, as well as DNA from
M. fortuitum,
M. scofulaceum, M. phlei, M. smegmatis, an
17 -DNA homology with human isolates within the
M. fortuitum third biovariant complex.
18 ar identity between clinical isolates of the
M. fortuitum third biovariant D-sorbitol-negative group
19 inical and two environmental isolates of the
M. fortuitum third biovariant sorbitol-negative group, o
20 The activity of the compounds against
M. fortuitum was used as a barometer of M. tuberculosis
21 The MIC90 values for 20 isolates of
M. fortuitum were 2 mug/ml for tedizolid and 4 mug/ml fo
22 R-BI and SR-BII uniquely mediating uptake of
M. fortuitum,
which suggests a conserved role for class