Potent Bacteriolytic Activity of Ritipenem Associated with a Characteristic Profile of Affinities for Penicillin-Binding Proteins of Haemophilus influenzae
Author(s) -
Takashi Inui,
Tadahiro Oshida,
Toshio Endo,
Tadahiro Matsushita
Publication year - 1999
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.43.10.2534
Subject(s) - penicillin binding proteins , lysis , aztreonam , cefsulodin , haemophilus influenzae , microbiology and biotechnology , cefdinir , affinities , biology , cefotaxime , haemophilus , penicillin , cephalosporin , chemistry , antibiotics , biochemistry , bacteria , ceftazidime , pseudomonas aeruginosa , genetics , antibiotic resistance , imipenem
Ritipenem is highly bacteriolytic againstHaemophilus influenzae . Bacterial lysis was shown after treatments with ritipenem and cefsulodin at their MICs and after treatments with fropenem and cefdinir at four times their MICs, indicated by decreases in the culture turbidities and by morphological changes of the destroyed cells. These β-lactams were preferentially bound to penicillin-binding protein (PBP) 1b. Ritipenem, fropenem, and cefsulodin exhibited poor affinities to PBPs 3a and 3b, but cefdinir showed high affinities to these PBPs. Microscopic examinations revealed that selective PBP 3 inhibitors, such as aztreonam and cefotaxime, inhibited lysis induced by ritipenem. These results suggest that the preferential inactivation of PBP 1b could be essential to induce the lysis ofH. influenzae cells and that binding to PBPs 3a and 3b may interfere with lysis.
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