Excellent activity of FK037, a novel parenteral broad-spectrum cephalosporin, against methicillin-resistant staphylococci

• Published in: Journal of antibiotics Vol. 46; no. 1; pp. 99 - 119
• Main Authors: MINE, Y, WATANABE, Y, SAKAMOTO, H, HATANO, K, KUNO, K, KAMIMURA, T, TAWARA, S, MATSUMOTO, Y, MATSUMOTO, F, KUWAHARA, S
• Format: Journal Article
• Language: English
• Published: Tokyo Japan Antibiotics Research Association 1993
• Subjects: Abscess - drug therapy; Animals; Anti-Bacterial Agents - pharmacokinetics; Anti-Bacterial Agents - therapeutic use; Antibacterial agents; Antibiotics. Antiinfectious agents. Antiparasitic agents; Bacterial Proteins; Biological and medical sciences; Carrier Proteins - metabolism; Ceftizoxime - analogs & derivatives; Ceftizoxime - pharmacokinetics; Ceftizoxime - therapeutic use; Cell Membrane Permeability - drug effects; Drug Synergism; Endocarditis, Bacterial - drug therapy; Female; Granuloma - drug therapy; Hexosyltransferases; Male; Medical sciences; Methicillin Resistance; Mice; Mice, Inbred ICR; Microbial Sensitivity Tests; Muramoylpentapeptide Carboxypeptidase - metabolism; Penicillin-Binding Proteins; Peptidyl Transferases; Pharmacology. Drug treatments; Pneumonia - drug therapy; Staphylococcal Infections - drug therapy; Staphylococcus aureus - drug effects; Uterine Diseases - drug therapy; Staphylococcus aureus; In vivo; Antibiotic; Cephalosporin derivatives; Sensitivity resistance; Parenteral form; Multiple resistance; Bacteria; Micrococcales; Micrococcaceae; Antibacterial agent; In vitro; Staphylococcus aureus
• ISSN: 0021-8820; 1881-1469
• DOI: 10.7164/antibiotics.46.99

FK037 exhibits potent in vitro and in vivo antibacterial activity against methicillin-resistant staphylococci. In in vitro studies, FK037 was the most active of the cephalosporins and imipenem tested against the highly methicillin-resistant staphylococci (MIC > 100 micrograms/ml). Only 2 of 57 strains of highly methicillin-resistant Staphylococcus aureus (H-MRSA) had a FK037 MIC value of 50 micrograms/ml. On the other hand, 55, 40 and 19 strains had MICs of 50 or > or = 100 micrograms/ml to cefpirome, flomoxef and imipenem, respectively. Against 13 strains of highly methicillin-resistant coagulase-negative staphylococci (H-MRCNS), FK037 inhibited all the strains at < or = 50 micrograms/ml, but there were many strains highly resistant to the reference drugs with MICs of > or = 100 micrograms/ml. The influence of culture conditions such as low temperature, high inoculum and supplementation with 4% NaCl on the anti-MRSA activity of FK037 was less than those with cefpirome, flomoxef and imipenem. The in vitro frequency of spontaneous mutant cells highly resistant to FK037 in MRSA was lower than that to cefpirome and flomoxef. These findings were supported by lack of colonies inside the inhibition zone demarcated by FK037 in a disk sensitivity test, although many colonies proliferated inside the inhibition zone demarcated by flomoxef and imipenem. The increase in MIC of FK037 against a MRSA strain during subculture in the presence of the drug was smaller than that noted with the reference drugs. FK037 had higher affinity and faster binding for the PBP 2a of MRSA than that of the reference drugs. Moreover, the capacity to induce PBP 2a was lower for FK037 than that of cefpirome but higher than that of flomoxef. In an in vitro pharmacokinetic model simulating human plasma concentrations, FK037 showed potent bactericidal activity against H-MRSA in the plasma concentrations after intravenous infusion dosing with 1.0 g. FK037 was synergistically active against H-MRSA in combination with either imipenem of fosfomycin. The in vitro post-antibiotic effect (PAE) of FK037 against H-MRSA ranged from 1.2 to 1.7 hours at one to four times the MIC. FK037 had potent therapeutic effects against lethal systemic infections and experimental local infections in mice such as pneumonia, endocarditis, subcutaneous abscess, intrauterine infection and granuloma pouch infection due to MRSA or methicillin-resistant Staphylococcus epidermidis (MRSE). FK037 was about 4, 8 and 1.5 times more effective than cefpirome, flomoxef and imipenem, respectively, against lethal systemic infections with H-MRSA.