In Vitro Susceptibility Testing of Tedizolid against Nontuberculous Mycobacteria
Tedizolid is a new oxazolidinone with improved and intracellular potency against , including multidrug-resistant strains, and some species of nontuberculous mycobacteria (NTM) compared with that of linezolid. Using the current Clinical and Laboratory Standards Institute (CLSI)-recommended method of...
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Veröffentlicht in: | Journal of clinical microbiology 2017-06, Vol.55 (6), p.1747-1754 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Tedizolid is a new oxazolidinone with improved
and intracellular potency against
, including multidrug-resistant strains, and some species of nontuberculous mycobacteria (NTM) compared with that of linezolid. Using the current Clinical and Laboratory Standards Institute (CLSI)-recommended method of broth microdilution, susceptibility testing of 170 isolates of rapidly growing mycobacteria showed equivalent or lower (1- to 8-fold) MIC
and/or MIC
values for tedizolid compared with that for linezolid. The tedizolid MIC
values for 81 isolates of
subsp.
and 12 isolates of
subsp.
were 8 μg/ml and 4 μg/ml, respectively, compared with linezolid MIC
values of 32 μg/ml for both. The MIC
values for 20 isolates of
were 2 μg/ml for tedizolid and 4 μg/ml for linezolid. Twenty-two isolates of
had tedizolid and linezolid MIC
s of 2 μg/ml and 16 μg/ml, respectively. One hundred forty-two slowly growing NTM, including 7/7
, 7/7
, and 7/11 of other less commonly isolated species, had tedizolid MICs of ≤1 μg/ml and linezolid MICs of ≤4 μg/ml. One hundred isolates of
complex and eight
isolates had tedizolid MIC
s of 8 μg/ml and linezolid MIC
s 32 and 64 μg/ml, respectively. Nine
isolates had MIC
s of 4 μg/ml and 16 μg/ml for tedizolid and linezolid, respectively. These findings demonstrate a greater
potency of tedizolid than linezolid against NTM and suggest that an evaluation of tedizolid as a potential treatment agent for infections caused by selected NTM is warranted. |
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ISSN: | 0095-1137 1098-660X |
DOI: | 10.1128/JCM.00274-17 |