Review
Bacterial multidrug efflux pumps: Mechanisms, physiology and pharmacological exploitations

https://doi.org/10.1016/j.bbrc.2014.05.090Get rights and content
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Highlights

  • Bacterial multidrug efflux pumps constitute an important class of resistance determinant.

  • The RND efflux pumps utilize a three-step, functional rotating mechanism to expel drugs.

  • Bacterial efflux pumps have broad physiological functions.

  • Expression of efflux genes is subject to regulation by local, global, and the two component systems.

  • Efflux pump inhibitors present as a promising intervention to treat bacterial infections.

Abstract

Multidrug resistance (MDR) refers to the capability of bacterial pathogens to withstand lethal doses of structurally diverse drugs which are capable of eradicating non-resistant strains. MDR has been identified as a major threat to the public health of human being by the World Health Organization (WHO). Among the four general mechanisms that cause antibiotic resistance including target alteration, drug inactivation, decreased permeability and increased efflux, drug extrusion by the multidrug efflux pumps serves as an important mechanism of MDR. Efflux pumps not only can expel a broad range of antibiotics owing to their poly-substrate specificity, but also drive the acquisition of additional resistance mechanisms by lowering intracellular antibiotic concentration and promoting mutation accumulation. Over-expression of multidrug efflux pumps have been increasingly found to be associated with clinically relevant drug resistance. On the other hand, accumulating evidence has suggested that efflux pumps also have physiological functions in bacteria and their expression is subject tight regulation in response to various of environmental and physiological signals. A comprehensive understanding of the mechanisms of drug extrusion, and regulation and physiological functions of efflux pumps is essential for the development of anti-resistance interventions. In this review, we summarize the development of these research areas in the recent decades and present the pharmacological exploitation of efflux pump inhibitors as a promising anti-drug resistance intervention.

Abbreviations

3OC6-HSL
3-oxohexanoyl homoserine lactone
3OC12-HSL
N-(3-oxododecanoyl)-l-homoserine lactone
ABC
the ATP (adenosine triphosphate)-binding cassette superfamily
ABI-PP
AcrAB/MexAB-specific inhibitor of pyridopyrimidine derivative
AHL
N-acylhomoserine lactones
BRC
BmrR C terminus
C4-HSL
N-butyryl homoserine lactone
CCCP
carbonylcyanide-3-chlorophenylhydrazone
CTD
C-terminal domain
DARPin
designed ankyrin repeat protein
DBD
DNA binding domain
DDM
n-dodecyl-d-maltoside
DMT
drug/metabolite transporter superfamily
DNP
2,4-dinitrophenol
EPI
efflux pump inhibitor
Eb
ethidium bromide
EMSA
electrophoretic mobility shift assay
Et
ethidium
MATE
the multidrug and toxic compound extrusion family
MDCK
Madin–Darby canine kidney
MDR
multidrug resistance
MFS
the major facilitator superfamily
MIC
minimum inhibitory concentration
NMP
naphthylpiperazines
NP
nature product
Pf
proflavin
PAβN
phenyl-arginine beta-naphthylamide
PQS
2-heptyl-3-hydroxy-4-quinolone
QS
quorum sensing
RND
the resistance-nodulation-division family
SMR
the small multidrug resistance family
TCS
two component system
TPP
tetraphenylphosphonium

Keywords

Antibiotics
Multidrug resistance
Multidrug efflux pumps
Regulation
Physiology
Efflux pump inhibitors

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1

These authors contribute equally.