role of the efflux pumps in antimicrobial resistance in e....
TRANSCRIPT
-
Role of the Efflux Pumps in Antimicrobial Resistance in E. coli
Patrick PlésiatBacteriology Department
Teaching HospitalBesançon, France
-
ANTIBIOTIC
TARGET
-
Bacterial targets for antibiotics
Chromosome
Cell wall
Cytoplasmic membrane
Ribosomes
-
Main resistance mechanisms to drugs
ANTIBIOTIC
TARGET
Protection
Reduced affinity- mutations- recombinaisons- enzymatic modification
InactivationModification
EffluxImpermeability
SubstitutionAmplification
-
Gram-negative species with known efflux systems
♦Escherichia coli♦Salmonella Typhimurium♦Shigella dysenteriae♦Klebsiella pneumoniae♦Enterobacter aerogenes♦Serratia marcescens♦Proteus vulgaris♦Citrobacter freundii...
♦Pseudomonas aeruginosa♦Pseudomonas putida♦Burkholderia cepacia♦Burkholderia pseudomallei♦Stenotrophomonas maltophilia♦Alcaligenes eutrophus...
♦Haemophilus influenzae♦Campylobacter jejuni♦Helicobacter pylori♦Vibrio parahaemolyticus♦Vibrio cholerae♦Neisseria gonorrhoeae... ♦Bacteroides fragilis...
-
Efflux mechanisms: practical implications
Do efflux systems produce clinically relevant levels of resistance ?
Does the expression of drug transporters somewhat impair the virulence of bacterial pathogens ?
What is the prevalence of efflux systems relative to other resistance mechanisms among the clinical isolates ?
How to recognize efflux mutants in laboratory practice ?
What recommendations can be made to the physician for the treatment of patients infected with mdr strains ?
-
Drug accumulation experiments
TimeTime
Intra
cellu
lar a
ccum
ulat
ion
CCCP
ATPglucose
S
R
-
Structure of bacterial efflux systems
One component systems
– Mostly in Gram positive species (except Tet...)
– A single transporter protein in the cytoplasmic membrane
– Determines the substrate specificity and resistance
Three component (tripartite) systems
– Exclusively in Gram negative species (GNB)
♦♦ A A transportertransporter proteinprotein
♦♦ A periplasmic A periplasmic adaptoradaptor lipoproteinlipoprotein
♦♦ A outer membrane A outer membrane channelchannel proteinprotein
-
Energy sources
Antiporters
– PMF transporters (proton motive force)
– Na+-antibiotic antiporters
ABC transporters
– ATP binding cassette pumps
– Hydrolysis of ATP into ADP + Pi
– Mostly in Gram positive species
-
PMF transporters
Major Facilitator Superfamily (MFS)– Drug efflux
♦ 12 TMS transporters♦ 14 TMS transporters
– Active uptake/export♦ sugars...♦ amino acids, secondary metabolites...
Small Multidrug Resistance Family (SMR)♦ 4 TMS transporters
Resistance/Nodulation Cell Division Family (RND)♦ 12 TMS transporters
Multi Antimicrobial Extrusion Family (MATE)♦ 12 TMS transporters
-
Structure of drug efflux systems
H+
ATP ADP
antibiotic
MFS, SMR MATE ABC RND, MFS, ABC
Na+
antibiotic
H+
-
Fernandez-Recio J. et al. FEBS 2004, 578: 5-9
-
Murakami S. et al. Nature 2002, 419: 587
-
Murakami S. et al. Curr Opinion Struct. Biol. 2003, 13: 443
-
Murakami S. et al. Curr Opinion Struct. Biol. 2003, 13: 443
-
Efflux systems in E. coli
Chromosomally encoded pumps– 37 putative drug transporters: 19 MFS, 3 SMR, 7 RND, 7 ABC, 1
MATE
– 20 pumps are able to transport toxic/antibiotic molecules
– 15-17 pumps may provide with some resistance to antibiotics when overproduced from plasmid genes (Nishino K et al. J. Bacteriol. 2001)
– Upregulation of a single pump results in increased drug efflux
Acquisition of exogenous pump encoding genes– Genes carried by mobile elements (plasmids, transposons,
integrons)
-
Efflux pumps coded by mobile genetic elements
Species System Family Substrates
E. coli TetA/B/E MFS Tc, MinE. coli CmlA MFS CmpE. coli Flo MFS Cmp, FloE. coli OqxAB RND Olaquindox
Tc: tetracycline; Min: minocycline; Cmp: chloramphenicol; Flo: florfenicol
-
Efflux pumps of MFS, MATE, SMR, or ABC family
Species System Family Substrates Genes
E. coli EmrAB-TolC MFS Nal CE. coli Bcr MFS Tc, Km, Fos CE. coli MdfA MFS Tc, Rif, Cmp, Ery, Neo, Fq... CE. coli MdtG MFS Fos CE. coli MdtH MFS Fq CE. coli MdtL MFS Cmp CE. coli MdtM MFS Cmp, Fq CE. coli NorE MATE Cmp, Fq, Fos, Tmp CE. coli EmrE SMR Tc CE. coli MdtJK SMR Nal, Fos CE. coli MacAB-TolC ABC Ery C
Nal: nalidixic acid; Tc: tetracycline; Km: kanamycin; Fos: fosfomycin; Rif: rifampicin; Cmp: chloramphenicol; Ery: erythromycin; Neo: neomycin; Fq: fluoroquinolones; Tmp: trimethoprim
-
Efflux pumps of the RND family
Bacteria System Substrates
E. coli AcrAB-TolC1 Fq, ß-lactams3, Tc, Cmp, Nov, Ery, Fus, Rif…E. coli AcrEF-TolC2 Fq, ß-lactams3, Tc, Cmp, Nov, Ery, Fus, Rif…E. coli AcrD2-AcrA-TolC AGs, Ery, PolyBE. coli CusAB-?2 FosE. coli MdtABC-TolC2 FqE. coli MdtEF-TolC2 EryP. aeruginosa MexAB-OprM1 Fq, ß-lactams1, Tc, Cmp, Nov, Ery, Fus, Tm...P. aeruginosa MexCD-OprJ2 Fq, 3rd GC, Tc, Cmp, Ery, TmpP. aeruginosa MexEF-OprN2 Fq, Cmp, TmpP. aeruginosa MexXY2-OprM Fq, AGs, 3rdGC, Ery, TcN. gonorrhoeae MtrCDE1 Tc, Cmp, ß-lactams1, Ery, Fus, Rif...Fq: (fluoro)quinolones; Tc: tetracycline; Cmp: chloramphenicol; Nov: novobiocin; Ery: erythromycin; Fus: fusidic acid; Rif: rifampicin; AGs: aminoglycosides; PolyB: polymyxin B; Tmp: trimethoprim; Sulf: sulfamethoxazole; 3rdGC: cefepime, cefpirome. 1 expressed constitutively in wild type cells, 2 inducible expression, 3 except imipenem.
-
Induction of acrAB-tolC expression
tetracyclinechloramphenicol
salicylate-acetylsalicylatebenzoate
stress...
tetracyclinerchloramphenicolrquinolonesrerythromycinrsolvants, pine oil...
MarRABRob bile salts
SoxSR oxidative stress
∆∆ AcrABAcrAB∆ EmrAB
∇∇ Porin OmpFPorin OmpF∆∆ TolCTolC
∆∇Other proteins
Mar regulon
-
Overexpression of acrAB and mtrCDE operons
mtrDmtrDmtrCmtrC mtrEmtrEmtrRmtrR
acrRacrRacrBacrBacrAacrA
--
mutations mdrmutations mdr
MtrAMtrA
++
++
MarAMarA
--
MarRMarR__ (MppA)
SoxSSoxS SoxRSoxR__
-
Webber M. et al. Antimicrob. Agents Chemother. 2001, 45: 1550
-
Systems MtrCDE and FarAB in N. gonorrhoeae
Antibiotics wild type CDE++ CDE- FarAB-
Penicillin G 0.008 0.032 0.008 nd
Erythromycin 0.25 1 - 2 0.06 0.25
Tetracycline 0.25 0.5 nd nd
Rifampicin 0.06 0.25 0.015 nd
Linoleic acid 1600 nd 25 - 50 50
Palmitic acid 100 nd 12.5 12.5
-
System AcrAB-TolC in E. coli
Antibiotics wild type AcrAB++ AcrAB-
Nalidixic acid 4 - 6 8.5 - 32 0.6Norfloxacin 0.025 - 0.1 0.3 - 1.25 ndOfloxacin 0.06 - 0.07 0.25 - 0.3 ndCiprofloxacin 0.02 0.15 nd
Ampicillin 2 - 4 5 - 6 0.6 - 2Erythromycin 128 - 256 > 512 < 2 - 8Tetracycline 1.25 - 3 5 - 16 0.25 - 0.3Chloramphenicol 4 - 7.5 10 - 28 0.6
-
System MexAB-OprM in P. aeruginosa
Antibiotics wild type MexAB++ MexAB-
Norfloxacin 0.25 - 1 2 - 4 0.05 - 0.25Ofloxacin 0.4 - 1 1.6 - 8 0.025 - 0.05Ciprofloxacin 0.03 - 0.25 0.4 - 1.6 0.012 - 0.03
Carbenicillin 12.5 - 64 50 - 256 0.4 - 1Aztreonam 1.6 - 4 12.5 - 32 0.1 - 0.2Ceftazidime 0.4 - 2 1.6 - 8 0.2 - 0.4Cefepime 0.8 - 2 3 - 4 0.1 - 0.5Meropenem 0.2 - 0.5 0.8 - 2 0.1 - 0.2
Tetracycline 6.25 - 16 25 - 64 0.2 - 1.2Chloramphenicol 12.5 - 32 100 - 512 0.8 - 2
-
Active efflux
Outer membranepermeability
Other mechanisms
Interplays between resistance mechanisms in GNB
-
Efflux/target double mutants of E. coli
Genotype/Phenotype Oflo Cipro
wild type AG100 0.03 ≤0.015
AcrAB++ 0.125 0.06
gyrA (Asp87->Gly) 0.25 0.25
gyrA (Asp87->Gly; Ser83->Leu) 4 2
gyrA (Asp87->Gly), AcrAB++ 8 4
gyrA (Asp87->Gly), AcrAB-0.06 0.03
Oethinger et al. Antimicrob. Agents Chemother. 2000, 44: 10-13
-
Therapeutic implications of efflux systems
Resistance levels conferred by intrinsic pumps– Low to moderate drug resistance (MIC x 2 - 16)
– Clinical significance♦ Lack of clinical data !♦ Poor response to treatment when the concentrations of
antibiotics are low at the infection site (insufficient dosage, inappropriate drug, abcess...)
♦ Increased emergence of target mutants ?
Emergence of gain of efflux mutants under treatment– Cross resistance to structurally unrelated molecules
– Role of fluoroquinolones
-
PK/PD Monte Carlo
Treatment MIC (mg/L) Target Attainment Rate (%)Drug total daily dosage
(mg)unitary dose interval
(hours)Cmax/MIC > 10 AUC/MIC > 125
Ciproflox. 1200 8 0.12 66 87
0.25 6 7
1600 6 0.12 66 90
0.25 5 12
2400 8 0.12 98 100
0.25 60 85
0.5 4.2 3.7
Levoflox. 500 24 0.5 70 40
1 4 3
1000 12 0.5 72 72
1 4 5
Dupont P. et al. J. Antimicrob. Chemother. 2005
-
Efflux mutants, are they virulent ?
Clinical experience– Many examples of mdr isolates recovered from clinical specimens
(blood, urine, sputums…)
Other considerations– marA disruption mutants of S. Typhimurium remain fully virulent
in a murine BALB/c infection model (Sulavik, J. Bacteriol. 1997, 179: 1857)
– First step fluoroquinolone resistant mutants with mutations in gyrA, gyrB or marOR do not display significant loss of fitness (in vitro competition experiments, experimental urinary tract infection in mouse) (Komp Lindgren P., AAC 2005, 49: 2343)
– Role of secondary mutations ?
-
How to characterize efflux mechanismsPlasmid or transposon encoded efflux systems– Multiresistance phenotype
– Detection of efflux gene(s): PCR, nucleic probes
Upregulation of intrinsic efflux systems– Protein levels
♦ Western blotting of membrane extracts with specific antibodies
– mRNA levels♦ Northern blot, MacroArray, MicroArray♦ Real Time RT-PCR (Light Cycler, Taq Man, I Cycler…)
– Intracellular accumulation of antibiotics♦ [3H] ou [14C] radiolabeled or fluorescent compounds (BET,
acriflavine…)
– Sequencing of regulatory genes
-
Efflux inhibitors
Phenyl-Arginyl ß N-naphtylamide