4.7 Article

In vitro activity of tedizolid (TR-700) against linezolid-resistant staphylococci

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JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
卷 67, 期 1, 页码 167-169

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OXFORD UNIV PRESS
DOI: 10.1093/jac/dkr403

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oxazolidinones; resistance; Staphylococcus aureus; coagulase-negative staphylococci; torezolid

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Objectives: To compare the activity of tedizolid (formally known as torezolid and TR-700) with that of 15 agents against a collection of linezolid-resistant staphylococci (164 coagulase-negative staphylococci and 5 Staphylococcus aureus). Methods: Antimicrobial susceptibility tests were performed using the broth microdilution method following the recommendations of the CLSI. Results: All isolates were susceptible to vancomycin and tigecycline. Based on the MIC90 values, the potency of tedizolid against coagulase-negative staphylococci was >16-fold greater than that of linezolid. Tedizolid retained activity against most of the linezolid-resistant staphylococci tested, including multidrug-resistant isolates with elevated linezolid MICs (32 to >128 mg/L). Of the isolates, 79.2% and 31.4% were inhibited by tedizolid at <= 4 mg/L and <= 2 mg/L, respectively. Conclusions: The results of this study confirm the activity of tedizolid against linezolid-resistant staphylococci. This new oxazolidinone could have an important role as a potential therapeutic agent against multidrug-resistant staphylococci.

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