In vitro Activities of Oral Cephem and Telithromycin Against Clinical Isolates of Major Respiratory Pathogens in Japan.
10.3346/jkms.2007.22.1.20
- Author:
Atsuyuki SHIMIZU
1
;
Kazunori MAEBASHI
;
Masashi NIIDA
;
Takeshi MIKUNIYA
;
Muneo HIKIDA
;
Kimiko UBUKATA
Author Information
1. Pharmaceutical Research Center, Meiji Seika Kaisha, Kanagawa, Japan. atsuyuki_shimizu@meiji.co.jp
- Publication Type:Original Article
- Keywords:
cefditoren;
telithromycin;
Microbial Sensitivity Tests;
Minimum Inhibitory Concentration;
beta-Lactams
- MeSH:
Streptococcus pyogenes/*drug effects;
Streptococcus pneumoniae/*drug effects;
Staphylococcus aureus/*drug effects;
Microbial Sensitivity Tests;
Methicillin Resistance;
Ketolides/*pharmacology;
Humans;
Haemophilus influenzae/*drug effects;
Cephalosporins/*pharmacology;
Administration, Oral
- From:Journal of Korean Medical Science
2007;22(1):20-25
- CountryRepublic of Korea
- Language:English
-
Abstract:
The in vitro antibacterial activities of oral cephem antibiotics and ketolide telithromycin against major respiratory pathogens possessing beta-lactam-resistant mutations (within the pbp gene) and/or macrolide-resistant genes (erm and mef) were examined in clinical isolates collected at 66 institutes in all over the Japan between 2002 and 2003. Telithromycin showed the strongest antibacterial activity against methicillinsusceptible Staphylococcus aureus strains with and without macrolide-resistant genes, such as ermA or ermC gene. All the cephem antibiotics showed potent antibacterial activity against Streptococcus pyogenes, with minimum inhibitory concentrations (MICs) of 0.015 mg/L or lower. Cefdinir had a much higher MIC90 against genotypic penicillin-resistant Streptococcus pneumoniae (gPRSP) than cefditoren and cefcapene (8 mg/L cefdinir vs. 1 mg/L cefditoren and cefcapene). The majority of gPRSP harbored either ermB or mefA, and the antibacterial activity of telithromycin against these strains was decreased however some susceptibility was still sustained. Cefditoren exerted the strongest antibacterial activity against beta-lactamase-negative ampicillin-resistant Haemophilus influenzae, with an MIC90 of 0.5 mg/L. These results underline the importance of checking the susceptibility and selecting an appropriate antibiotic against target pathogens.
