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In vitro synergy of clindamycin and aminoglycosides against Chlamydia trachomatis
Author(s) -
Mark D. Pearlman,
S Faro,
Gerald Riddle,
Guillermo Tortolero
Publication year - 1990
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.34.7.1399
Subject(s) - clindamycin , chlamydia trachomatis , tobramycin , gentamicin , aminoglycoside , pelvic inflammatory disease , doxycycline , microbiology and biotechnology , antibiotics , chlamydiaceae , medicine , chlamydia , antibacterial agent , biology , virology , immunology , surgery
The importance of Chlamydia trachomatis as an etiologic agent in the development of pelvic inflammatory disease (PID) is well documented. Although there are numerous antimicrobial agents that are effective against C. trachomatis, one of the most frequent combinations that is used to treat PID is clindamycin and gentamicin. The efficacy of clindamycin as the sole treatment for chlamydial infections has been questioned. In fact, the Centers for Disease Control (Atlanta, Ga.) has recommended the use of doxycycline following clindamycin and gentamicin treatment of PID confirmed or suspected to be caused by C. trachomatis. This study was designed to determine whether there is any synergistic in vitro activity between clindamycin and gentamicin or tobramycin on inhibition of C. trachomatis replication. In this experiment, the MIC of clindamycin decreased two- to threefold when an aminoglycoside was added. This occurred even though aminoglycosides by themselves had essentially no effect against C. trachomatis. The mechanism of this interaction is uncertain.

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