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 Miyamae, S.
Right arrow Articles by Nikaido, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Miyamae, S.
Right arrow Articles by Nikaido, H.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, December 2001, p. 3341-3346, Vol. 45, No. 12
0066-4804/01/$04.00+0   DOI: 10.1128/AAC.45.12.3341-3346.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

A MATE Family Multidrug Efflux Transporter Pumps out Fluoroquinolones in Bacteroides thetaiotaomicron

Shin Miyamae,1,2,3 Ohmi Ueda,2 Fuminobu Yoshimura,1,2 Jaiweon Hwang,1,dagger Yoshinobu Tanaka,3 and Hiroshi Nikaido1,*

Department of Molecular and Cell Biology, University of California, Berkeley, California,1 and Department of Microbiology2 and the First Department of Prosthodontics,3 School of Dentistry, Aichi-Gakuin University, Nagoya, Japan

Received 10 May 2001/Returned for modification 9 June 2001/Accepted 31 July 2001

We cloned a gene, bexA, that codes for a multidrug efflux transporter from the chromosomal DNA of Bacteroides thetaiotaomicron ATCC 29741 by using an Escherichia coli Delta acrAB Delta acrEF mutant as a host. Although the initial recombinant construct contained other open reading frames, the presence of bexA alone was sufficient to confer to the E. coli host elevated levels of resistance to norfloxacin, ciprofloxacin, and ethidium bromide. Disruption of bexA in B. thetaiotaomicron made the strain more susceptible to norfloxacin, ciprofloxacin, and ethidium bromide, showing that this gene is expressed in this organism and functions as a multidrug efflux pump. The deduced BexA protein sequence was homologous to the protein sequence of Vibrio parahaemolyticus NorM, a multidrug efflux transporter, and thus, BexA belongs to the multidrug and toxic compound extrusion (MATE) family.


* Corresponding author. Mailing address: Department of Molecular and Cell Biology, Room 229, Stanley Hall, University of California, Berkeley, CA 94720-3206. Phone: (510) 642-2027. Fax: (510) 643-9290. E-mail: nhiroshi{at}uclink4.berkeley.edu.

dagger Present address: Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94735.


Antimicrobial Agents and Chemotherapy, December 2001, p. 3341-3346, Vol. 45, No. 12
0066-4804/01/$04.00+0   DOI: 10.1128/AAC.45.12.3341-3346.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Rosner, J. L., Martin, R. G. (2009). An Excretory Function for the Escherichia coli Outer Membrane Pore TolC: Upregulation of marA and soxS Transcription and Rob Activity Due to Metabolites Accumulated in tolC Mutants. J. Bacteriol. 191: 5283-5292 [Abstract] [Full Text]  
  • Ge, Q., Yamada, Y., Zgurskaya, H. (2009). The C-Terminal Domain of AcrA Is Essential for the Assembly and Function of the Multidrug Efflux Pump AcrAB-TolC. J. Bacteriol. 191: 4365-4371 [Abstract] [Full Text]  
  • Ohta, K.-y., Imamura, Y., Okudaira, N., Atsumi, R., Inoue, K., Yuasa, H. (2009). Functional Characterization of Multidrug and Toxin Extrusion Protein 1 as a Facilitative Transporter for Fluoroquinolones. J. Pharmacol. Exp. Ther. 328: 628-634 [Abstract] [Full Text]  
  • Long, F., Rouquette-Loughlin, C., Shafer, W. M., Yu, E. W. (2008). Functional Cloning and Characterization of the Multidrug Efflux Pumps NorM from Neisseria gonorrhoeae and YdhE from Escherichia coli. Antimicrob. Agents Chemother. 52: 3052-3060 [Abstract] [Full Text]  
  • Papaparaskevas, J., Pantazatou, A., Katsandri, A., Houhoula, D. P., Legakis, N. J., Tsakris, A., Avlamis, A. (2008). Moxifloxacin resistance is prevalent among Bacteroides and Prevotella species in Greece. J Antimicrob Chemother 62: 137-141 [Abstract] [Full Text]  
  • Wexler, H. M. (2007). Bacteroides: the Good, the Bad, and the Nitty-Gritty. Clin. Microbiol. Rev. 20: 593-621 [Abstract] [Full Text]  
  • Dastidar, V., Mao, W., Lomovskaya, O., Zgurskaya, H. I. (2007). Drug-Induced Conformational Changes in Multidrug Efflux Transporter AcrB from Haemophilus influenzae. J. Bacteriol. 189: 5550-5558 [Abstract] [Full Text]  
  • Singh, A. K., Haldar, R., Mandal, D., Kundu, M. (2006). Analysis of the Topology of Vibrio cholerae NorM and Identification of Amino Acid Residues Involved in Norfloxacin Resistance. Antimicrob. Agents Chemother. 50: 3717-3723 [Abstract] [Full Text]  
  • Pumbwe, L., Chang, A., Smith, R. L., Wexler, H. M. (2006). Clinical significance of overexpression of multiple RND-family efflux pumps in Bacteroides fragilis isolates. J Antimicrob Chemother 58: 543-548 [Abstract] [Full Text]  
  • Pumbwe, L., Ueda, O., Yoshimura, F., Chang, A., Smith, R. L., Wexler, H. M. (2006). Bacteroides fragilis BmeABC efflux systems additively confer intrinsic antimicrobial resistance. J Antimicrob Chemother 58: 37-46 [Abstract] [Full Text]  
  • Piddock, L. J. V. (2006). Clinically Relevant Chromosomally Encoded Multidrug Resistance Efflux Pumps in Bacteria. Clin. Microbiol. Rev. 19: 382-402 [Abstract] [Full Text]  
  • Lau, S. Y., Zgurskaya, H. I. (2005). Cell Division Defects in Escherichia coli Deficient in the Multidrug Efflux Transporter AcrEF-TolC. J. Bacteriol. 187: 7815-7825 [Abstract] [Full Text]  
  • Ueda, O., Wexler, H. M., Hirai, K., Shibata, Y., Yoshimura, F., Fujimura, S. (2005). Sixteen Homologs of the Mex-Type Multidrug Resistance Efflux Pump in Bacteroides fragilis. Antimicrob. Agents Chemother. 49: 2807-2815 [Abstract] [Full Text]  
  • Poole, K. (2005). Efflux-mediated antimicrobial resistance. J Antimicrob Chemother 56: 20-51 [Abstract] [Full Text]  
  • Kaatz, G. W., McAleese, F., Seo, S. M. (2005). Multidrug Resistance in Staphylococcus aureus Due to Overexpression of a Novel Multidrug and Toxin Extrusion (MATE) Transport Protein. Antimicrob. Agents Chemother. 49: 1857-1864 [Abstract] [Full Text]  
  • Otsuka, M., Yasuda, M., Morita, Y., Otsuka, C., Tsuchiya, T., Omote, H., Moriyama, Y. (2005). Identification of Essential Amino Acid Residues of the NorM Na+/Multidrug Antiporter in Vibrio parahaemolyticus. J. Bacteriol. 187: 1552-1558 [Abstract] [Full Text]  
  • Rafii, F., Park, M., Novak, J. S. (2005). Alterations in DNA Gyrase and Topoisomerase IV in Resistant Mutants of Clostridium perfringens Found after In Vitro Treatment with Fluoroquinolones. Antimicrob. Agents Chemother. 49: 488-492 [Abstract] [Full Text]  
  • Franco, A. A. (2004). The Bacteroides fragilis Pathogenicity Island Is Contained in a Putative Novel Conjugative Transposon. J. Bacteriol. 186: 6077-6092 [Abstract] [Full Text]  
  • Tikhonova, E. B., Zgurskaya, H. I. (2004). AcrA, AcrB, and TolC of Escherichia coli Form a Stable Intermembrane Multidrug Efflux Complex. J. Biol. Chem. 279: 32116-32124 [Abstract] [Full Text]  
  • Ricci, V., Peterson, M. L., Rotschafer, J. C., Wexler, H., Piddock, L. J. V. (2004). Role of Topoisomerase Mutations and Efflux in Fluoroquinolone Resistance of Bacteroides fragilis Clinical Isolates and Laboratory Mutants. Antimicrob. Agents Chemother. 48: 1344-1346 [Abstract] [Full Text]  
  • Ricci, V., Piddock, L. (2003). Accumulation of garenoxacin by Bacteroides fragilis compared with that of five fluoroquinolones. J Antimicrob Chemother 52: 605-609 [Abstract] [Full Text]  
  • Golan, Y., McDermott, L. A., Jacobus, N. V., Goldstein, E. J. C., Finegold, S., Harrell, L. J., Hecht, D. W., Jenkins, S. G., Pierson, C., Venezia, R., Rihs, J., Iannini, P., Gorbach, S. L., Snydman, D. R. (2003). Emergence of fluoroquinolone resistance among Bacteroides species. J Antimicrob Chemother 52: 208-213 [Abstract] [Full Text]  
  • Rouquette-Loughlin, C., Dunham, S. A., Kuhn, M., Balthazar, J. T., Shafer, W. M. (2003). The NorM Efflux Pump of Neisseria gonorrhoeae and Neisseria meningitidis Recognizes Antimicrobial Cationic Compounds. J. Bacteriol. 185: 1101-1106 [Abstract] [Full Text]  
  • Li, X.-Z., Poole, K., Nikaido, H. (2003). Contributions of MexAB-OprM and an EmrE Homolog to Intrinsic Resistance of Pseudomonas aeruginosa to Aminoglycosides and Dyes. Antimicrob. Agents Chemother. 47: 27-33 [Abstract] [Full Text]  
  • Tikhonova, E. B., Wang, Q., Zgurskaya, H. I. (2002). Chimeric Analysis of the Multicomponent Multidrug Efflux Transporters from Gram-Negative Bacteria. J. Bacteriol. 184: 6499-6507 [Abstract] [Full Text]  
  • Braibant, M., Guilloteau, L., Zygmunt, M. S. (2002). Functional Characterization of Brucella melitensis NorMI, an Efflux Pump Belonging to the Multidrug and Toxic Compound Extrusion Family. Antimicrob. Agents Chemother. 46: 3050-3053 [Abstract] [Full Text]