2001
DOI: 10.1128/jcm.39.5.2037-2038.2001
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Discordant Carbapenem Susceptibility in Methylobacterium Species and Its Application as a Method for Phenotypic Identification

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Cited by 13 publications
(13 citation statements)
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“…Discordant carbapenem susceptibilities, with high sensitivity to imipenem (MIC ϭ 0.25 to 1 mg/liter) and resistance to meropenem (MIC Ͼ 32 mg/liter), seem to be a distinctive feature of Methylobacterium spp. (13).…”
Section: Microbiology Laboratory Identification and Antibiotic Suscmentioning
confidence: 99%
“…Discordant carbapenem susceptibilities, with high sensitivity to imipenem (MIC ϭ 0.25 to 1 mg/liter) and resistance to meropenem (MIC Ͼ 32 mg/liter), seem to be a distinctive feature of Methylobacterium spp. (13).…”
Section: Microbiology Laboratory Identification and Antibiotic Suscmentioning
confidence: 99%
“…It might be possible for clinical microbiology laboratories to be able to infer the species identity of a Methylobacterium isolate from antibiotic sensitivity and thereby recommend an optimal regime of antibiotic treatment. Differential sensitivity has also been suggested as a means of phenotypic identification at the genus level of clinical isolates as Methylobacterium (Zaharatos et al 2001). This conjecture was based on differential sensitivity of four clinical isolates and ATCC cultures of Mtb extorquens, Mtb organophilum, and Mtb mesophilicum to imipenem (extreme susceptibility) and meropenem (high resistance).…”
Section: Methylobacterium and Animalsmentioning
confidence: 98%
“…In one example, intervention with five antibiotics was needed to cure the infection (Hornei et al 1999). Aminoglycoside antibiotics (imipenem, ticarcillin-clavulanic acid, sulfamethoxazole, and trimethoprim), tetracycline, rifamycin, and gentamycin have been reported to be effective against Methylobacterium, but a number of studies have shown resistance of some strains to antibiotics, including cephalosporins, ampicillin, piperacillin, carbenicillin, spectinomycin, puromycin, cefuroxime, erythromycin, vancomycin, chloramphenicol, fosfomycin, piperacillin, cefazolin, cefotetan, cerfuroxime, ceftazidime, ceftriaxone, ciprofloxacin, meropenem, nalidixic acid, teicoplanin, gentamycin, amikacin, nitrofurantoin, and p-fluorophenylalanine (Borsali et al 2011;Brown et al 1992;Furuhata et al 2006;Goodwin et al 1988;Korvick et al 1989;Lee et al 2004;Zaharatos et al 2001). Brown et al (1992) showed the majority of 15 clinical isolates of Methylobacterium were resistant to b-lactam drugs, with the exceptions of ceftriaxone and ceftizoxime, and that six of these were b-lactamase-negative with a minimum inhibitory concentration for ampicillin of 4 mg ml À1 , whereas nine b-lactamase-positive isolates were resistant to 8-32 mg ml À1 (or more).…”
Section: Methylobacterium and Animalsmentioning
confidence: 99%
“…However, most isolates demonstrate high MICs for beta-lactam drugs, with the exception of imipenem, for which an MIC 90 of 1 g/ml has been reported (2,4). Interestingly, the reported Methylobacterium MIC 90 for meropenem is Ͼ32 g/ml, a feature that may aid in the differentiation of Methylobacterium from Roseomonas, as both species have low MICs for both carbapenems (5).…”
Section: T He Organism Was Identified As Methylobacterium Fujisawaensementioning
confidence: 99%