Azithromycin Inhibits the Formation of Flagellar Filaments without Suppressing Flagellin Synthesis in Salmonella enterica Serovar Typhimurium

Author:

Matsui Hidenori12,Eguchi Masahiro12,Ohsumi Katsufumi2,Nakamura Akio3,Isshiki Yasunori2,Sekiya Kachiko4,Kikuchi Yuji12,Nagamitsu Tohru4,Masuma Rokuro12,Sunazuka Toshiaki12,Omura Satoshi142

Affiliation:

1. Kitasato Institute for Life Sciences

2. Center for Basic Research, The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8642

3. Department of Microbial Chemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan

4. School of Pharmaceutical Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641

Abstract

ABSTRACT The present study shows that a sub-MIC of the macrolide antibiotic azithromycin (AZM) diminishes the virulence function of Salmonella enterica serovar Typhimurium. We first constructed an AZM-resistant strain (MS248) by introducing ermBC , an erythromycin ribosome methylase gene, into serovar Typhimurium. The MIC of AZM for MS248 exceeded 100 μg/ml. Second, we managed to determine the efficacy with which a sub-MIC of AZM reduced the virulence of MS248 in vitro. On the one hand, AZM (10 μg/ml) in the culture medium was unable to inhibit the total protein synthesis, growth rate, or survival within macrophages of MS248. On the other hand, AZM (10 μg/ml) reduced MS248's swarming and swimming motilities in addition to its invasive activity in Henle-407 cells. Electron micrographs revealed no flagellar filaments on the surface of MS248 after overnight growth in L broth supplemented with AZM (10 μg/ml). However, immunoblotting analysis showed that flagellin (FliC) was fully synthesized within the bacterial cells in the presence of AZM (10 μg/ml). In contrast, the same concentration of AZM reduced the export of FliC to the culture medium. These results indicate that a sub-MIC of AZM was able to affect the formation of flagellar filaments, specifically by reducing the amount of flagellin exported from bacterial cells, but it was not involved in suppressing the synthesis of flagellin. Unfortunately, AZM treatment was ineffective against murine salmonellosis caused by MS248.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference56 articles.

1. Ahmer, B. M. 2004. Cell-to-cell signaling in Escherichia coli and Salmonella enterica. Mol. Microbiol.52:933-945.

2. Berg, H. C. 2003. The rotary motor of bacterial flagella. Annu. Rev. Biochem.72:19-54.

3. Evidence for natural gene transfer from gram-positive cocci to Escherichia coli

4. Brumell, J. H., and B. B. Finlay. 1999. Bacterial adherence, colonization, and invasion of mucosal surfaces, p. 3-17. In K. A. Brogden, J. A. Roth, T. B. Stanton, C. A. Bolin, F. C. Minion, and M. J. Wannemuehler (ed.), Virulence mechanisms of bacterial pathogenesis. American Society for Microbiology, Washington, D.C.

5. Butler, T. 2001. Effect of increased inoculum of Salmonella typhi on MIC of azithromycin and resultant growth characteristics. J. Antimicrob. Chemother.48:903-906.

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