This Article
Right arrow Full Text
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 Similar articles in this journal
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 Hu, Z.-Q.
Right arrow Articles by Shimamura, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hu, Z.-Q.
Right arrow Articles by Shimamura, T.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, February 2002, p. 558-560, Vol. 46, No. 2
0066-4804/01/$04.00+0     DOI: 10.1128/AAC.46.2.558-560.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Epigallocatechin Gallate Synergistically Enhances the Activity of Carbapenems against Methicillin-Resistant Staphylococcus aureus

Zhi-Qing Hu,1* Wei-Hua Zhao,1 Nozomi Asano,1 Yoshiyuki Yoda,1 Yukihiko Hara,2 and Tadakatsu Shimamura1

Department of Microbiology and Immunology, Showa University School of Medicine,1 Tokyo Food Techno Co. Ltd., Tokyo, Japan2

Received 13 April 2001/ Returned for modification 22 August 2001/ Accepted 25 October 2001

Combinations of carbapenems and epigallocatechin gallate (EGCg; a main constituent of tea catechins) showed potent synergy against 24 clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA). MICs of imipenem in the presence of EGCg at 3.125, 6.25, 12.5, and 25 µg/ml, were restored to the susceptible breakpoint (<=4 µg/ml) for 8, 38, 46, and 75% of the MRSA isolates, respectively. Similar results were also observed for combinations of panipenem or meropenem and EGCg. Therefore, the combinations may be worthy of further evaluation in vivo against MRSA infection.


* Corresponding author. Mailing address: Department of Microbiology and Immunology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan. Phone: 81-3-3784-8131. Fax: 81-3-3784-3069. E-mail: zqhu{at}med.showa-u.ac.jp.


Antimicrobial Agents and Chemotherapy, February 2002, p. 558-560, Vol. 46, No. 2
0066-4804/01/$04.00+0     DOI: 10.1128/AAC.46.2.558-560.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Ishida, I., Kohda, C., Yanagawa, Y., Miyaoka, H., Shimamura, T. (2007). Epigallocatechin gallate suppresses expression of receptor activator of NF-{kappa}B ligand (RANKL) in Staphylococcus aureus infection in osteoblast-like NRG cells. J Med Microbiol 56: 1042-1046 [Abstract] [Full Text]  
  • Navarro-Martinez, M. D., Navarro-Peran, E., Cabezas-Herrera, J., Ruiz-Gomez, J., Garcia-Canovas, F., Rodriguez-Lopez, J. N. (2005). Antifolate Activity of Epigallocatechin Gallate against Stenotrophomonas maltophilia. Antimicrob. Agents Chemother. 49: 2914-2920 [Abstract] [Full Text]  
  • Shibata, H., Kondo, K., Katsuyama, R., Kawazoe, K., Sato, Y., Murakami, K., Takaishi, Y., Arakaki, N., Higuti, T. (2005). Alkyl Gallates, Intensifiers of {beta}-Lactam Susceptibility in Methicillin-Resistant Staphylococcus aureus. Antimicrob. Agents Chemother. 49: 549-555 [Abstract] [Full Text]  
  • Hu, Z.-Q., Zhao, W.-H., Yoda, Y., Asano, N., Hara, Y., Shimamura, T. (2002). Additive, indifferent and antagonistic effects in combinations of epigallocatechin gallate with 12 non-{beta}-lactam antibiotics against methicillin-resistant Staphylococcus aureus. J Antimicrob Chemother 50: 1051-1054 [Abstract] [Full Text]  
  • Zhao, W.-H., Hu, Z.-Q., Hara, Y., Shimamura, T. (2002). Inhibition of Penicillinase by Epigallocatechin Gallate Resulting in Restoration of Antibacterial Activity of Penicillin against Penicillinase-Producing Staphylococcus aureus. Antimicrob. Agents Chemother. 46: 2266-2268 [Abstract] [Full Text]