z-logo
open-access-imgOpen Access
Activity of the oxazolidinones AZD2563 and linezolid against Corynebacterium jeikeium and other Corynebacterium spp.
Author(s) -
Alan P. Johnson
Publication year - 2003
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkg129
Subject(s) - linezolid , microbiology and biotechnology , corynebacterium , medicine , bacteria , biology , staphylococcus aureus , vancomycin , genetics
Correspondence Activity of the oxazolidinones AZD2563 and linezolid against Corynebacterium jeikeium and other Corynebacterium spp. Sir, Aerobic diphtheroids are commonly isolated from clinical specimens, but were long dismissed as contaminants. This view changed in the 1970s when several groups reported cases of sepsis caused by a previously undescribed Coryne-bacterium species resistant to multiple antibiotics. 1,2 In 1979, Riley et al. 3 reported that 95 such isolates submitted to the CDC over the previous 15 years comprised a homogeneous group, based on their cultural and biochemical characteristics. They designated these organisms 'group JK coryne-forms'. Subsequently, on the basis of DNA hybridization patterns and protein profiles, these organisms were assigned to a new species, Corynebacterium jeikeium. 4 C. jeikeium is now recognized as a cause of infections in hospitalized patients, particularly those who are immuno-compromised, have in-dwelling devices and have received broad-spectrum antibiotics. Reported infections include those of skin and soft tissue, septicaemia, native and prosthetic valve endocarditis, osteomyelitis, arthritis and ventricular cerebrospinal fluid shunts. Many infections are thought to be endogenous, as C. jeikeium is recoverable from the skin flora, although it can also be recovered from the hospital environment. C. jeikeium is resistant to a wide but variable range of antibiotics including β-lactams, aminoglycosides, macro-lides, tetracycline, rifampicin and quinolones. Resistance to glycopeptides and quinupristin/dalfopristin has not been described, but there is, nonetheless, a need for new agents, both to increase the range of treatment options and to minimize selective pressure for spread of vancomycin-resistant enterococci and staphylococci. In this study, we evaluated the activity of the oxazo-lidinones AZD2563 (AstraZeneca, Macclesfield, UK) and linezolid (Pharmacia, Milton Keynes, UK), against 72 isolates of C. jeikeium, 17 isolates of seven other Corynebacter-ium species and three isolates of Corynebacterium that could not be identified to species level (Table 1). Comparator agents included penicillin, erythromycin, gentamicin, vancomycin (all from Sigma, Poole, UK), levofloxacin and teicoplanin (Aventis, West Malling, UK). The isolates were selected from those referred to the Laboratory of Hospital Infection between 1999 and 2002, with the exception of four strains of C. jeikeium obtained from the National Collection of Type Cultures (Colindale, London, UK). They were identified by phenotypic tests using serum water sugars with plate tests, as described previously, 5 and the API CORYNE kit (bio-Mérieux, Basingstoke, UK). MICs were determined in air on Mueller–Hinton agar supplemented with 5% sheep blood. As there are no NCCLS or other recommended breakpoints for coryneforms, …

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom