Activities of Linezolid against Rapidly Growing Mycobacteria
Open Access
- 1 March 2001
- journal article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 45 (3) , 764-767
- https://doi.org/10.1128/aac.45.3.764-767.2001
Abstract
Linezolid is an oxazolidinone available as an oral drug which has activity against most gram-positive bacteria. However, few species of the genusMycobacteriumhave been studied. We tested 249 clinical isolates and 10 reference strains of rapidly growing mycobacteria for susceptibility to linezolid by broth microdilution. Clinical species included theMycobacterium fortuitumgroup (n= 74),M. abscessus(n= 98),M. chelonae(n= 50),M. mucogenicum(n= 10), andM. fortuitumthird biovariant complex (10). The modal MIC forM. mucogenicumwas 1.0 μg/ml, and the MIC at which 90% of the isolates tested are inhibited (MIC90) was 4 μg/ml; the modal MIC for theM. fortuitumgroup was 4 μg/ml, and the MIC90was 16 μg/ml; the modal MIC for theM. fortuitumthird biovariant complex was 4 μg/ml, and the MIC90was 8 μg/ml; the modal MIC forM. chelonaewas 8 μg/ml, and the MIC90was 16 μg/ml; and the modal MIC forM. abscessuswas 32 μg/ml, and the MIC90was 64 μg/ml. Based on peak levels of linezolid in serum of 15 to 20 μg/ml, we propose the following broth MIC breakpoints for these species: susceptible, ≤ 8 μg/ml; moderately susceptible, 16 μg/ml; and resistant, ≥32 μg/ml). These studies demonstrate the excellent potential of linezolid for therapy of rapidly growing mycobacteria.Keywords
This publication has 29 references indexed in Scilit:
- Mycobacterium immunogenum sp. nov., a novel species related to Mycobacterium abscessus and associated with clinical disease, pseudo-outbreaks and contaminated metalworking fluids: an international cooperative study on mycobacterial taxonomy.International Journal of Systematic and Evolutionary Microbiology, 2001
- Use of Linezolid, an Oxazolidinone, in the Treatment of Multidrug-Resistant Gram-Positive Bacterial InfectionsClinical Infectious Diseases, 2000
- A Single 16S Ribosomal RNA Substitution Is Responsible for Resistance to Amikacin and Other 2‐Deoxystreptamine Aminoglycosides inMycobacterium abscessusandMycobacterium chelonaeThe Journal of Infectious Diseases, 1998
- Rapid Development of Resistance to Clarithromycin Following Monotherapy for Disseminated Mycobacterium chelonae Infection in a Heart Transplant PatientClinical Infectious Diseases, 1995
- Restriction fragment length polymorphisms of 16S rRNA genes in the differentiation of fast-growing mycobacterial speciesFEMS Microbiology Letters, 1994
- Taxonomy of Rapidly Growing MycobacteriaClinical Infectious Diseases, 1994
- Skin, Soft Tissue, and Bone Infections Due to Mycobacterium chelonae chelonae: Importance of Prior Corticosteroid Therapy, Frequency of Disseminated Infections, and Resistance to Oral Antimicrobials Other than ClarithromycinThe Journal of Infectious Diseases, 1992
- Clinical Disease, Drug Susceptibility, and Biochemical Patterns of the Unnamed Third Biovariant Complex of Mycobacterium fortuitumThe Journal of Infectious Diseases, 1991
- Mycobacteria possess a surprisingly small number of ribosomal RNA genes in relation to the size of their genomeBiochemical and Biophysical Research Communications, 1986
- Spectrum of Disease Due to Rapidly Growing MycobacteriaClinical Infectious Diseases, 1983