Chlamydia pneumoniae Growth Inhibition in Cells by the Steroid Receptor Antagonist RU486 (Mifepristone)

Author:

Yamaguchi Hiroyuki123,Kamiya Shigeru1,Uruma Tomonori14,Osaki Takako1,Taguchi Haruhiko1,Hanawa Tomoko1,Fukuda Minoru5,Kawakami Hayato6,Goto Hajime4,Friedman Herman7,Yamamoto Yoshimasa72

Affiliation:

1. Division of Microbiology, Department of Infectious Disease

2. Division of Molecular Microbiology, Department of Basic Laboratory Sciences, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan

3. Department of Laboratory Sciences, College of Medical Technology, Hokkaido University, Nishi-5 Kita-12 Jo, Kita-ku, Sapporo, Hokkaido 060-0812, Japan

4. Department of 1st Internal Medicine

5. Laboratory of Electron Microscopy

6. Department of Anatomy, Kyorin University School of Medicine, Tokyo 181-8611, Japan

7. Department of Medical Microbiology and Immunology, University of South Florida College of Medicine, Tampa, Florida 33612

Abstract

ABSTRACT Since steroids are powerful anti-inflammatory agents and increase susceptibility to a variety of infections, including Chlamydia ( Chlamydophila ) pneumoniae respiratory tract infections, the effect of the steroid receptor antagonist RU486 (mifepristone) on C. pneumoniae growth in epithelial HEp-2 cells was examined. Treatment of HEp-2 cells with RU486 significantly inhibited the growth of C. pneumoniae in a dose-dependent manner. Electron microscopic studies also revealed that the treatment of infected cells with RU486 resulted in a marked destruction of infecting organisms. The addition of the host cell protein synthesis inhibitor cycloheximide to the infected cells did not alter the inhibition of C. pneumoniae growth by RU486. Pretreatment of C. pneumoniae organisms with RU486 before addition to culture also did not result in any modulation of bacterial growth in the cells. However, the binding of RU486 to C. pneumoniae organisms in cells at 24 h after infection was demonstrated by immune electron microscopy with anti-RU486 antibody. Incubation of cells with anti-RU486 antibody completely diminished the inhibition of C. pneumoniae growth by RU486. These results indicate that RU486 may directly bind to the bacteria within cells and cause the destruction of C. pneumoniae . This novel mode of regulation of C. pneumoniae growth in cells by RU486 might provide a new approach to understanding complicated aspects of C. pneumoniae infection.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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