This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ASM journals
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Champney, W. S.
Right arrow Articles by Burdine, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Champney, W. S.
Right arrow Articles by Burdine, R.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, Sep 1995, 2141-2144, Vol 39, No. 9
Copyright © 1995 by the American Society for Microbiology. All rights reserved.

Macrolide antibiotics inhibit 50S ribosomal subunit assembly in Bacillus subtilis and Staphylococcus aureus

WS Champney and R Burdine
Department of Biochemistry, J. H. Quillen College of Medicine, East Tennessee State University, Johnson City 37614, USA.

Macrolide antibiotics are clinically important antibiotics which are effective inhibitors of protein biosynthesis in bacterial cells. We have recently shown that some of these compounds also inhibit 50S ribosomal subunit formation in Escherichia coli. Now we show that certain macrolides have the same effect in two gram-positive organisms, Bacillus subtilis and Staphylococcus aureus. Assembly in B. subtilis was prevented by erythromycin, clarithromycin, and azithromycin but not by oleandomycin. 50S subunit formation in S. aureus was prevented by each of seven structurally related 14-membered macrolides but not by lincomycin or two streptogramin antibiotics. Erythromycin treatment did not stimulate the breakdown of performed 50S subunits in either organism. The formation of the 30S ribosomal subunit was also unaffected by these compounds. Assembly was also inhibited in a B. subtilis strain carrying a plasmid with the ermC gene that confers macrolide resistance by rRNA methylation. These results suggest that ribosomes contain an additional site for the inhibitory functions of macrolide antibiotics.


This article has been cited by other articles:

  • Siibak, T., Peil, L., Xiong, L., Mankin, A., Remme, J., Tenson, T. (2009). Erythromycin- and Chloramphenicol-Induced Ribosomal Assembly Defects Are Secondary Effects of Protein Synthesis Inhibition. Antimicrob. Agents Chemother. 53: 563-571 [Abstract] [Full Text]  
  • McGaha, S. M., Champney, W. S. (2007). Hygromycin B Inhibition of Protein Synthesis and Ribosome Biogenesis in Escherichia coli. Antimicrob. Agents Chemother. 51: 591-596 [Abstract] [Full Text]  
  • Champney, W. S., Tober, C. L. (2000). Evernimicin (SCH27899) Inhibits both Translation and 50S Ribosomal Subunit Formation in Staphylococcus aureus Cells. Antimicrob. Agents Chemother. 44: 1413-1417 [Abstract] [Full Text]  
  • Champney, W. S., Tober, C. L. (1999). Molecular Investigation of the Postantibiotic Effects of Clarithromycin and Erythromycin on Staphylococcus aureus Cells. Antimicrob. Agents Chemother. 43: 1324-1328 [Abstract] [Full Text]