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Antimicrob Agents Chemother. 2004 Sep; 48(9): 3298–3304.
PMCID: PMC514774

Expression of the RND-Type Efflux Pump AdeABC in Acinetobacter baumannii Is Regulated by the AdeRS Two-Component System


The AdeABC pump of Acinetobacter baumannii BM4454, which confers resistance to various antibiotic classes including aminoglycosides, is composed of the AdeA, AdeB, and AdeC proteins; AdeB is a member of the RND superfamily. The adeA, adeB, and adeC genes are contiguous and adjacent to adeS and adeR, which are transcribed in the opposite direction and which specify proteins homologous to sensors and regulators of two-component systems, respectively (S. Magnet, P. Courvalin, and T. Lambert, Antimicrob. Agents Chemother. 45:3375-3380, 2001). Analysis by Northern hybridization indicated that the three genes were cotranscribed, although mRNAs corresponding to adeAB and adeC were also present. Cotranscription of the two regulatory genes was demonstrated by reverse transcription-PCR. Inactivation of adeS led to aminoglycoside susceptibility. Transcripts corresponding to adeAB were not detected in susceptible A. baumannii CIP 70-10 but were present in spontaneous gentamicin-resistant mutants obtained in vitro. Analysis of these mutants revealed the substitutions Thr153→Met in AdeS downstream from the putative His-149 site of autophosphorylation, which is presumably responsible for the loss of phosphorylase activity by the sensor, and Pro116→Leu in AdeR at the first residue of the α5 helix of the receiver domain, which is involved in interactions that control the output domain of response regulators. These mutations led to constitutive expression of the pump and, thus, to antibiotic resistance. These data indicate that the AdeABC pump is cryptic in wild A. baumannii due to stringent control by the AdeRS two-component system.

Acinetobacter baumannii is a ubiquitous nonfermentative gram-negative bacterial species able to colonize patients in intensive care units. During the last 20 years this microorganism has become an important opportunistic nosocomial pathogen responsible for pneumonia, urinary tract infections, septicemia, and meningitis (9). Epidemic strains of A. baumannii are often multidrug resistant due to their capacity to acquire and accumulate resistance determinants. However, we recently reported that resistance to aminoglycosides, β-lactams, chloramphenicol, erythromycin, tetracyclines, and the dye ethidium bromide in clinical isolate BM4454 was due to overexpression of the AdeABC pump (22). The chromosomally encoded pump is a tripartite efflux machinery that belongs to the RND-type family (28). The AdeB protein contains 12 transmembrane segments and exhibits a high degree of identity (approximately 50%) with several RND proteins (27, 28). AdeA is homologous to membrane fusion proteins, whereas AdeC is most similar to the outer membrane protein OprM from Pseudomonas aeruginosa. The structural genes adeA, adeB, and adeC are contiguous and directly oriented, suggesting that they constitute an operon. They are preceded by two adjacent open reading frames, AdeR and AdeS, that are transcribed in the opposite direction and whose deduced products are closely related to proteins of two-component regulatory systems. Two-component systems are signal transduction pathways in bacteria that respond to environmental conditions (16). They consist of a sensor kinase and its cognate response regulator. Signal transduction by the histidine protein kinase domain of the sensor and the response regulator domain of the transcriptional activator involves the reversible phosphorylation of each domain and the transfer of phosphoryl groups between these domains. The sensor monitors certain environmental conditions and, accordingly, modulates the active state of the response regulator, which controls gene expression. Two-component systems mediate adaptive responses to a broad range of environmental stimuli (16). However, they are an uncommon mode of regulation of drug efflux transporters, although these systems have recently been associated with RND-type multidrug exporters, such as MdtABC and YhiUV of Escherichia coli (7, 25, 26), RagCD of Bradyrhizobium japonicum (18), and SmeABC of Stenotrophomonas maltophilia (20). The aim of this work was to study the role of AdeRS in the regulation of expression of the AdeABC efflux pump of A. baumannii BM4454.


Strains, plasmids, and growth conditions.

The bacterial strains and plasmids used in this study are listed in Table Table1.1. Cells were grown at 37°C in brain heart infusion (BHI) broth and agar (Difco Laboratories, Detroit, Mich.). Antibiotic susceptibility was tested by disk diffusion on Mueller-Hinton agar (Bio-Rad, Marnes-la-Coquette, France), and MICs were determined by the Etest procedure (AB Biodisk, Solna, Sweden).

Bacterial strains and plasmids used in this study

DNA manipulations.

Plasmid DNA was prepared by the alkaline lysis method (29) or with a Wizard minipreps DNA kit (Promega, Madison, Wis.). A. baumannii genomic DNA was extracted as described previously (5). Digestion of DNA by restriction endonucleases, ligation, transformation, and agarose gel electrophoresis were performed as described previously (29). DNA fragments were extracted from agarose gels with a QIAquick gel extraction kit (Qiagen, Inc., Chatsworth, Calif.). PCR was performed in a GeneAmp PCR system 2400 (Perkin-Elmer Cetus, Norwalk, Conn.) with Pfu DNA polymerase (Stratagene, La Jolla, Calif.), according to the recommendations of the manufacturers. PCR products were purified with a QIAQuick PCR purification kit (Qiagen). Nucleotide sequencing was carried out with a CEQ 2000 DNA analysis system automatic sequencer (Beckman Instruments, Inc., Palo Alto, Calif.), according to the recommendations of the manufacturer.

Search for a promoter for adeC gene.

The 228- and 809-bp fragments located upstream from the initiation codon of adeC were amplified with primer pairs AdeCpless1-AdeCpless3r and AdeCpless2-AdeCpless3r, respectively (Table (Table2).2). The PCR products were cloned at the BamHI site of pKK232-8 (Amersham Pharmacia Biotech, Uppsala, Sweden), leading to plasmids pAT804 and pAT805 (Table (Table1),1), respectively. The orientations of the inserts were determined by sequencing. Escherichia coli Top10 harboring plasmid pKK232-8, pAT804, or pAT805 was grown in BHI broth containing ampicillin (100 μg/ml) to an optical density at 600 nm of 0.7. The cells were washed, treated with lysozyme, and sonicated. After centrifugation at 100,000 × g for 45 min, the supernatant was used to determine chloramphenicol acetyltransferase activity. Formation of 5-thio-2-nitrobenzoate was measured at 37°C in the presence and absence of chloramphenicol, as described previously (4).

Oligonucleotides used in this study

Insertion-inactivation of ade genes.

Insertion-inactivation of the adeC, adeR, and adeS genes was performed as described previously (22). Briefly, a fragment internal to the adeC, adeR, or adeS gene was amplified with specific primer pairs C-am and C-av, R-am and R-av, and S-am and S-av, respectively (Table (Table2).2). The PCR products were cloned into SmaI-linearized pUC18 DNA and transformed into E. coli. The cloned fragments were sequenced, and the recombinant plasmids were introduced into strain BM4454 by electrotransformation. Since pUC18 is a suicide vector in A. baumannii, the transformants stably resistant to ticarcillin should be the result of a homologous recombination event. Total DNA from these clones was screened for insertion by PCR with the M13 reverse and M13 (−20) forward primers and two primers complementary to the regions flanking the inserts in the BM4454 chromosome. The resulting derivatives with an inactivated adeB, adeC, adeR, or adeS gene were designated BM4542 (22), BM4543, BM4544, and BM4545, respectively (Table (Table11).

Computer analysis of sequence data.

Nucleotide sequence data were analyzed with the Clustal W program (31). Amino acid sequences were analyzed at the websites of the National Center for Biotechnology Information (www.ncbi.nlm.nih.gov/BLAST) and the European Molecular Biology Laboratory (www.smart.embl-heidelberg.de/). The GenBank and protein databases were screened for sequence similarity.

RNA isolation and Northern analysis.

The A. baumannii strains were grown to an optical density at 600 nm of 0.6, and total RNA was extracted as described previously (37). The mRNA was depleted of rRNA by use of a MICROBExpress kit (Ambion, Austin, Tex.); and equal amounts (10 μg) were electrophoresed on a 1.2% agarose-formaldehyde gel, transferred onto a nylon membrane, and hybridized as described previously (37). To generate the probes, PCR products corresponding to the genes of interest (Fig. (Fig.1)1) were treated with the Megaprime DNA labeling system (Amersham Biosciences, Orsay, France).

FIG. 1.
Schematic representation of the ade gene cluster of BM4454 and recombinant plasmids. Open arrows represent coding sequences and indicate the direction of transcription. Closed arrowheads indicate the positions and orientations of the primers used to generate ...


Reverse transcription (RT)-PCR was performed as described previously (29). Briefly, RT was carried out for 45 min at 50°C with 0.5 μg of A. baumannii RNA as the template and 20 pmol of primer RS-av in a 20-μl reaction mixture. An aliquot of the cDNA (5 μl of the RT reaction mixture) was amplified by PCR with 20 pmol each of primers RS-av and RS-am. The PCR products (10 μl) were separated on an agarose gel and transferred onto a Hybond N+ membrane (Amersham Biosciences), followed by hybridization with probes specific for the adeR and adeS genes (Fig. (Fig.11).

Primer extension.

Primer extension was carried out as described previously (12). Briefly, the EA-adeA oligonucleotide was end labeled with [γ-33P]ATP and polynucleotide kinase, purified, and annealed to 25 μg of total RNA extracted from strain BM4454 for the extension reaction. The sample, together with the corresponding sequencing reaction, was run on a 6% polyacrylamide-urea sequencing gel.

Nucleotide sequence accession number.

The 2,824-bp sequence of A. baumannii CIP 70-10 has been deposited in the GenBank data library under accession number no. AY426969.


Transcriptional analysis of adeABC and adeRS genes.

To analyze the transcription of the adeABC gene cluster, total RNA extracted from BM4454 cells was analyzed by Northern hybridization with probes specific for regions internal to every gene of the cluster (Fig. (Fig.1).1). A transcript of approximately 6 kb, which cohybridized with probes adeA, adeB, and adeC, was detected, indicating that the three genes are cotranscribed (Fig. (Fig.2).2). However, a stronger signal of approximately 4.5 kb, detected with the adeA- and adeB-specific probes, showed that the main transcript corresponded to the adeAB genes (Fig. (Fig.2).2). A transcript of approximately 1.4 kb, which corresponds to the size of adeC, was also detected (Fig. (Fig.2).2). These data suggest the independent transcription of adeC, consistent with the presence of a hairpin structure (ΔG = −12.9 kJ) in the adeB-adeC intergenic region. Similarly, it has been established that the smeABC multidrug efflux operon of S. maltophilia generates a transcript that corresponds to the SmeC outer membrane protein (20). To test this hypothesis, a promoter for the adeC gene was searched for by cloning the 228- and 809-bp fragments upstream from the initiation codon of the adeC gene upstream from the promoterless cat reporter gene of plasmid pKK232-8 (11), generating pAT804 and pAT805, respectively (Table (Table1).1). Expression of the cat gene was tested for indirectly by determining the chloramphenicol MICs and was tested for directly by assaying enzymatic activity in E. coli Top10 harboring pKK232-8, pAT804, or pAT805. Chloramphenicol acetyltransferase activity could not be detected by either technique (data not shown). The presence of the adeC transcript could thus be accounted for by cleavage of the adeABC mRNA into two mRNAs, adeAB and adeC mRNAs, which displayed differences in their stabilities.

FIG. 2.
Transcription analysis of the adeA, adeB, and adeC genes by Northern hybridization. Total RNA depleted of 16S and 23S RNA from BM4454 (lane 1), CIP 70-10 (lane 2), BM4546 (CIP 70-10 AdeST153M) (lane 3), and BM4547 (CIP 70-10 AdeRP116L) (lane 4) was hybridized ...

On the basis of these results, primer extension was performed to determine the transcriptional start site for adeABC by using primer EA-adeA, whose sequence is complementary to the 5′ end of adeA (Table (Table2).2). The DNA fragment generated allowed the positioning of the transcriptional start site (Fig. (Fig.3)3) and suggested the presence of −35 TTATCA (positions 2999 to 3004; GenBank accession no. AF370885) and −10 CGTCA motifs, which were separated by 17 bp, as the promoter. The −10 sequence did not display homology with those recognized by the main σ factors but contained the CGwC consensus sequence recognized by Bacillus subtilis σx (15). This factor belongs to the family of extracytoplasmic function (ECF) σ factors that are cotranscribed with anti-σ factors located in the cytoplasmic membrane and are released upon interaction with an extracytoplasmic signal (15). Several ECF factors have been described in B. subtilis and P. aeruginosa (15), but they have not yet been described in A. baumannii. Moreover, promoters recognized by certain transcriptional activators, such as some belonging to the two-component system family, lack a clear −35 sequence.

FIG. 3.
Identification of the transcriptional start site for the adeABC operon in BM4454 by primer extension analysis. (Left panel) Lanes T, G, C, and A, results of sequencing reactions performed with primer EA-adeA; lane 1, control without RNA; lane 2, primer ...

Since Northern hybridization performed with the adeS- and adeR-specific probes was not sensitive enough to reveal an mRNA (data not shown), transcription of the adeR and adeS genes was analyzed by RT. Internal adeS-specific primer RS-av was used to produce a cDNA which was amplified with the same oligonucleotide and RS-am, whose sequence is specific for a region located in adeR (Table (Table2).2). A PCR product of the expected size of 650 bp was obtained, and the product cohybridized with the adeS- and adeR-specific probes (Fig. (Fig.4).4). Altogether, these results demonstrate that the structural genes for the AdeABC efflux pump and the two genes for the regulatory system, adeR and adeS, are located in two divergently transcribed operons.

FIG. 4.
Transcription analysis of adeR and adeS genes. (Left) Agarose gel electrophoresis of the product obtained by RT-PCR with primers RS-av and RS-am and corresponding Southern hybridizations with probes specific for adeS (center) and adeR (right). Lane 1, ...

Inactivation of adeA, adeB, and adeC genes in BM4454.

Disruption of the adeB gene in BM4454 is responsible for the loss of multiple-antibiotic resistance by the host (22). However, the insertion could have had a polar effect on the transcription of the downstream adeC gene. To study the contribution of this gene to resistance, we constructed strain BM4543 (BM4454 adeC::pAT798), in which adeC was inactivated by insertion. This derivative displayed resistance to the various substrates of the AdeABC pump similar to that of parental strain BM4454, indicating that adeC is not essential for resistance. Some efflux gene clusters, such as mexXY from P. aeruginosa and acrAB from E. coli, do not encode an outer membrane protein (2, 21, 24). To form a functional tripartite complex, MexXY recruits OprM, whereas AcrA associates with TolC (14), a multifunctional outer membrane channel (17, 30, 38). That AdeC is not required for resistance suggests that AdeAB can utilize another outer membrane constituent. The AdeK outer membrane protein associated with the AdeIJK RND efflux pump recently identified in BM4454 also (L. Damier-Piolle et al., unpublished data) could be a candidate. In contrast, the OprM outer membrane protein of P. aeruginosa plays a crucial role in the intrinsic multidrug resistance conferred by MexAB (19). The SmeC outer membrane protein is also necessary for the resistance conferred by the smeABC multidrug efflux operon in S. maltophilia (20).

Involvement of adeRS in expression of adeABC genes.

The predicted products of the adeR and adeS genes showed substantial similarity with transcriptional activators and sensor kinases, respectively, that work together to regulate target gene expression in response to stimuli. To assess the role of adeRS in the regulation of adeABC expression, the adeR and adeS genes of A. baumannii BM4454 were disrupted by insertion of a suicide plasmid following homologous recombination, and the resulting mutants were tested for their antimicrobial susceptibilities. In order for the insertion not to exert a polar effect on the adeABC operon, recombination was performed upstream from the transcriptional start site for adeABC. As expected, inactivation of adeR in BM4544 (BM4454 adeR::pAT799) and of the adeS gene in BM4545 (BM4454 adeS::pAT800) led to susceptibility to aminoglycosides (Table (Table3)3) and to other substrates for the pump, a result which confirmed the role of adeRS in the control of expression of the efflux genes.

MICs of gentamicin and kanamycin for strains expressing or not expressing the AdeABC pump

Thus, the adeS gene appears to be essential for expression of the adeABC operon in that strain. These experiments did not allow the determination of the role of AdeR alone, since inactivation of adeR in BM4544 could have a polar effect on adeS. In two-component regulatory systems it has been established that the sensor kinase autophosphorylates at an internal histidine (the H box) in response to a stimulus and that the phosphate group is then transferred to an aspartate residue of the response regulator. The phosphorylated regulator may also be dephosphorylated by the phosphatase activity of the sensor (8, 34). The histidine kinases are bifunctional, in that they phosphorylate and dephosphorylate their cognate response regulator (34), which leads to a switch between these two activities and directs the state of the regulators, thus governing expression of the genes on which they act. The observation that BM4545 (BM4454 adeS::pAT800) was susceptible to aminoglycoside could have resulted from the loss of AdeS kinase activity.

Analysis of adeABC gene expression in CIP 70-10 resistant mutants.

Since it is likely that expression of AdeABC in clinical isolate BM4454 is secondary to an alteration in AdeRS, we analyzed this regulatory system in A. baumannii CIP 70-10. This reference strain is susceptible to antibiotics and harbors the adeABC and adeRS genes, as evidenced by PCR (data not shown) and sequencing (GenBank accession no. AY426969). The AdeR regulator from CIP 70-10 shared 98% amino acid identity with that from BM4454, and the AdeS sensor shared 96.7% amino acid identity with that from BM4454, although the latter protein was shorter by 4 amino acids. The proteins contained the conserved motifs previously reported for histidine kinases and response regulators (32), and inside these motifs, no differences were detected between the sequences from the two strains. Spontaneous one-step mutants of CIP 70-10 exhibiting a multidrug resistance phenotype indistinguishable from that of BM4454 were selected on BHI agar containing 4 μg of gentamicin per ml. Nine mutants were obtained, and sequence analysis of their adeRS operons showed two mutations. The first one, Thr153→Met, which was detected in six mutants, was located in the kinase; and derivative BM4546 (CIP 70-10 AdeST153M) was selected for further studies. The second mutation, Pro116→Leu, which was detected in three strains, was located in the response regulator; and BM4547 (CIP 70-10 AdeRP116L) was studied further. Total RNA from CIP 70-10, BM4546 (CIP 70-10 AdeST153M), and BM4547 (CIP 70-10 AdeRP116L) cells was analyzed by Northern hybridization with probes specific for every gene of the adeABC operon (Fig. (Fig.1).1). The adeAB transcript was detected only in the two mutants (Fig. (Fig.2),2), whereas the adeC transcript was present in CIP 70-10 and its two derivatives (Fig. (Fig.2).2). These data indicate (i) that multidrug resistance in the mutants involves the AdeABC efflux system and (ii) that resistance is due to point mutations in the two-component system. As opposed to BM4454, the adeABC transcript was not detected in CIP 70-10 or its derivatives (Fig. (Fig.2).2). Although the aminoglycoside resistance levels of BM4546 (CIP 70-10 AdeST153M) and BM4547 (CIP 70-10 AdeRP116L) were similar (Table (Table3),3), the amount of adeAB mRNA was higher in BM4546 (Fig. (Fig.2).2). There was thus no obvious relationship between the level of resistance and the quantities of the adeA and adeB transcripts. In BM4546 (CIP 70-10 AdeST153M), the mutation was located in the H box of the sensor, the motif which contains the conserved histidine residue (His-149), which is the site of autophosphorylation. The Thr153→Met substitution, located 4 amino acids downstream, was associated with a constitutive resistance. Substitutions at the corresponding positions of EnvZ (T247→R), PhoR (T220→N), and VanSB (T237→K) result in a defect in phosphatase activity but not a defect in kinase activity (1, 6, 35). The constitutive phenotype associated with the AdeS Thr153→Met mutation may therefore also be due to a similar defect in AdeR dephosphorylation. In BM4547 (CIP 70-10 AdeRP116L), the mutation took place at the 3′ end of the CheY-homologous receiver region of the response regulator. Response regulators usually contain two domains separated by a flexible linker, and the N-terminal receiver domain modulates the activity of the C-terminal effector domain (3, 32, 33). It has been established in this family of proteins that phosphorylation of the aspartic acid involved in phosphate transfer of the N terminus induces rearrangements within the active site, leading to a larger-scale conformational change of the protein which most often enhances the affinity of its C terminus for specific DNA regions. The Pro116→Leu mutation in AdeR of BM4547 (CIP 70-10 AdeRP116L) corresponds to position 113 in the conventional numbering based on the CheY structure (32). This mutation occurs in the first amino acid of the α5 helix just downstream from the VIb turn involving the VKPF conserved residues at the end of β5 (32). In this motif, K109 (K112 in AdeR) is absolutely conserved in response regulators homologous to CheY. Moreover, it has been established for PhoB that the β55 loop and the α5 helix from the receiver domain are required to propagate the phosphorylation-triggered signal from the receiver domain to the output domain (3, 13). The C-terminal domain of PhoB belongs to the winged-helix-turn-helix family of transcription factors (23). Phosphorylation of PhoB relieves the inhibition of DNA binding of the C terminus, which is otherwise constitutively active for transcription. In the absence of phosphorylation, the α5 helix is responsible for inhibition of the PhoB effector. The Pro116→Leu substitution in the α5 helix of AdeR from BM4547 (CIP 70-10 AdeRP116L) led to constitutive transcription of adeABC by possibly affecting the ability of the α5 helix to silence the activity of the DNA-binding domain.

The nature of the signal and the mechanism of AdeRS activation in BM4454 remain unknown. Sequence alignment of AdeR and AdeS from clinical isolate BM4454 and drug-susceptible strains A. baumannii BM4548 and CIP 70-10 suggests that the G136V substitution in the output domain of the regulator could enhance the affinity of the effector for its specific DNA target. Unfortunately, the very low transformation efficiency of CIP 70-10 precludes the critical testing of this hypothesis by site-specific mutagenesis. As already mentioned, two-component systems have so far only rarely been shown to be involved in the modulation of expression of genes mediating resistance by efflux. It is therefore all the more interesting that multidrug-resistant derivatives could be one-step regulatory mutants.


We thank T. Msadek for helpful discussions.

This work was supported by an unrestricted grant from Pfizer Inc. to P.C.


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