Mobile genes coding for efflux-mediated antimicrobial resistance in Gram-positive and Gram-negative bacteria

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

87 Scopus Citations
View graph of relations

Author(s)

Detail(s)

Original languageEnglish
Pages (from-to)205-210
Journal / PublicationInternational Journal of Antimicrobial Agents
Volume22
Issue number3
Publication statusPublished - 1 Sept 2003
Externally publishedYes

Abstract

Efflux mechanisms that account for resistance to a variety of antimicrobial agents are commonly found in a wide range of bacteria. Two major groups of efflux systems are known, specific exporters and transporters conferring multidrug resistance (MDR). The MDR systems are able to remove antimicrobials of different classes from the bacterial cell and occasionally play a role in the intrinsic resistance of some bacteria to certain antimicrobials. Their genes are commonly located on the bacterial chromosome. In contrast, the genes coding for specific efflux systems are often associated with mobile genetic elements which can easily be interchanged between bacteria. Specific efflux systems have mainly been identified with resistances to macrolides, lincosamides and/or streptogramins, tetracyclines, as well as chloramphenicol/florfenicol in Gram-positive and Gram-negative bacteria. In this review, we focus on the molecular biology of antimicrobial resistance mediated by specific efflux systems and highlight the association of the respective resistance genes with mobile genetic elements and their distribution across species and genus borders. © 2003 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.

Research Area(s)

  • Antibiotic resistance, Efflux systems, Multidrug transporters, Plasmids, Transposons

Bibliographic Note

Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected]