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Abstract

Vol.57 No.S-1 March 2009

Antibiotic susceptibility and resistance gene analysis of Streptococcus Pneumoniae in clinical tebipenem-pivoxil studies in pediatric patients using PCR method

Kimiko Ubukata, Naoko Chiba, Miyuki Morozumi and Keiko Hamano-Hasegawa

Laboratory of Molecular Epidemiology for Infectious Agents, Graduate School of Infection Control Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, Japan

Abstract

Among Streptococcus pneumoniae isolates from pediatric patients in Phase II and III clinical studies of tebipenem pivoxil (TBPM-PI) considered to be causative pathogens, 117 isolates were from patients with acute otitis media, 13 from those with acute sinusitis, and 21 from those with pneumonia, among the 151 strains found. We analyzed for i) pbp and macrolide-resistant genes, ii) susceptibility to antibiotics including TBPM, and iii) capsular type related to pathogenicity. The gPISP (pbp2x) isolate was identified the most at 41.1%, followed by gPRSP (pbp1a+2x+2b) at 34.4% and gPISP (pbp1a+2x) at 12.6%, 94.0% of all strains had some genetic mutation and a macrolide-resistant mef (A) or erm (B) gene.
TBPM showed antibacterial activity at 0.001 to 0.008 μg/mL against gPISP (pbp2x), 0.004 to 0.031 μg/mL against gPISP (pbp1a+2x), and 0.008 to 0.125 μg/mL against gPRSP, making it superior to the activity of most of antibiotics. TBPM antibacterial activity was comparable to that of panipenem.
Concerning the capsular type of strains isolated from AOM patients, gPISP (pbp2x) serotype 3 composed 23.1%, followed by serotypes 19F, 6B, 14, and then 23F, among which gPRSP predominated. The coverage of isolates by 7-valent pneumococcal conjugate vaccine (7PCV) was only 48.8%.
In conclusion, we expected TBPM to be bacteriological by effective against pneumococcal infection caused by gPISP and gPRSP, including AOM and pneumonia in pediatric patients.

Key word

tebipenem, Streptococcus pneumoniae, pbp gene, PRSP, serotype, oral carbapenem

Received

September 26, 2008

Accepted

December 15, 2008

Jpn. J. Chemother. 57 (S-1): 58-66, 2009