1 s from all 10 footbaths at the salon yielded M. fortuitum.

2  guidelines are presented for the testing of M. fortuitum against clarithromycin; M. abscessus and M.

3 ositive for rapidly growing mycobacteria (32 M. fortuitum and 2 unidentified).

4 st- and slow-growing mycobacteria, including M. fortuitum and M. avium.

5 PA positive for Mycobacterium spp. (six were M. fortuitum, and one was M. szulgai).

6         M. smegmatis oriC functioned only in M. fortuitum, but not in any of the slowly growing mycob

7 e M. chelonae-M. abscessus group (MCAG), the M. fortuitum group (MFG), and M. mucogenicum.

8                                          One M. fortuitum isolate and one of five M. kansasii isolate

9                                          The M. fortuitum isolates from three footbaths and 14 patien

10                                 In contrast, M. fortuitum isolates were able to grow in 100 microg of

11                                     Selected M. fortuitum isolates, cultured from patients and the sa

12  that assay suspensions containing M. avium, M. fortuitum, M. gordonae, or M. marinum incubated with

13                                              M. fortuitum, M. marinum, M. scrofulaceum, M. avium, and

14 . avium sub0:36 PMavium, as well as DNA from M. fortuitum, M. scofulaceum, M. phlei, M. smegmatis, an

15 -DNA homology with human isolates within the M. fortuitum third biovariant complex.

16 ar identity between clinical isolates of the M. fortuitum third biovariant D-sorbitol-negative group

17 inical and two environmental isolates of the M. fortuitum third biovariant sorbitol-negative group, o

18        The activity of the compounds against M. fortuitum was used as a barometer of M. tuberculosis

19          The MIC90 values for 20 isolates of M. fortuitum were 2 mug/ml for tedizolid and 4 mug/ml fo

20 R-BI and SR-BII uniquely mediating uptake of M. fortuitum, which suggests a conserved role for class