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In vitro activity of tedizolid against Staphylococcus aureus and Streptococcus pneumoniae collected in 2013 and 2014 from sites in Latin American countries, Australia, New Zealand, and China
Tedizolid is an oxazolidinone with an antimicrobial in vitro potency advantage against Gram-positive bacterial pathogens compared to other currently marketed drugs in this class, including linezolid. Tedizolid was compared to linezolid when tested against Staphylococcus aureus and Streptococcus pneu...
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Published in: | European journal of clinical microbiology & infectious diseases 2016-12, Vol.35 (12), p.1933-1939 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Tedizolid is an oxazolidinone with an antimicrobial in vitro potency advantage against Gram-positive bacterial pathogens compared to other currently marketed drugs in this class, including linezolid. Tedizolid was compared to linezolid when tested against
Staphylococcus aureus
and
Streptococcus pneumoniae
isolates collected from countries in Latin America and the Asia-Pacific. Isolates were tested by broth microdilution susceptibility methods against tedizolid, linezolid, and non-class comparators in accordance with the Clinical and Laboratory Standards Institute (CLSI) guidelines. The activity of tedizolid against
S. aureus
was potent and consistent in Latin America (MIC
90
, 0.5 mg/L), Australia and New Zealand (MIC
90
, 0.25 mg/L), and China (MIC
90
, 0.5 mg/L). Based on MIC
90
results, tedizolid was four- to eight-fold more active than linezolid against
S. aureus
, including both methicillin-susceptible and -resistant isolates. Only two tedizolid non-susceptible strains were observed; both had intermediate minimum inhibitory concentration (MIC) values of 1 mg/L, for which the MICs of linezolid was higher (≥2 mg/L). Tedizolid (MIC
90
, 0.25 mg/L) was four-fold more potent than linezolid (MIC
90
, 1 mg/L) against
S. pneumoniae
in all countries that provided isolates. The findings from this study support the global clinical development of tedizolid for Gram-positive infections. |
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ISSN: | 0934-9723 1435-4373 |
DOI: | 10.1007/s10096-016-2744-3 |