AAC
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Abstract Freely available
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 Google Scholar
Google Scholar
Right arrow Articles by Struble, J. M.
Right arrow Articles by Gill, R. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Struble, J. M.
Right arrow Articles by Gill, R. T.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, July 2006, p. 2506-2515, Vol. 50, No. 7
0066-4804/06/$08.00+0     doi:10.1128/AAC.01640-05
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Reverse Engineering Antibiotic Sensitivity in a Multidrug-Resistant Pseudomonas aeruginosa Isolate

Julie M. Struble and Ryan T. Gill*

Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309

Received 27 December 2005/ Returned for modification 20 February 2006/ Accepted 7 April 2006


   ABSTRACT
Top
 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 References
 
Antibiotic resistance is a pervasive and growing clinical problem. We describe an evaluation of a reverse engineering approach for identifying cellular mechanisms and genes that could be manipulated to increase antibiotic sensitivity in a resistant Pseudomonas aeruginosa isolate. We began by chemically mutating a broadly resistant isolate of P. aeruginosa and screening for mutants with increased sensitivity to the aminoglycoside amikacin, followed by performing whole-genome transcriptional profiling of the mutant and wild-type strains to characterize the global changes occurring as a result of the mutations. We then performed a series of assays to characterize the mechanisms involved in the increased sensitivity of the mutant strains. We report four primary results: (i) mutations that increase sensitivity occur at a high frequency (10–2) relative to the frequency of those that increase resistance (10–5 to 10–10) and occur at a frequency 104 higher than the frequency of a single point mutation; (ii) transcriptional profiles were altered in sensitive mutants, resulting in overall expression patterns more similar to those of the sensitive laboratory strain PAO1 than those of the parental resistant strain; (iii) genes found from transcriptional profiling had the more dramatic changes in expression-encoded functions related to cellular membrane permeability and aminoglycoside modification, both of which are known aminoglycoside resistance mechanisms; and finally, (iv) even though we did not identify the specific sites of mutation, several different follow-up MIC assays suggested that the mutations responsible for increased sensitivity differed between sensitive mutants.


   INTRODUCTION
Top
 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 References
 
Antibiotic resistance develops rapidly after the introduction of a new antibiotic and now exists, to some extent, for all antibiotics. Resistance has even evolved for drugs specifically designed to prevent selection for resistance (10, 23, 27, 30, 43, 52, 74, 85, 86). These factors underline the importance of understanding the genetic and phenotypic bases underlying antibiotic resistance and developing new strategies to combat the proliferation of resistant organisms. One approach has been to combine new and conventional antibiotics to simultaneously increase the sensitivities of resistant organisms and target essential genes (40, 50, 51, 73). The success of such an approach is dependent upon the identification of genes and/or mechanisms that might be targeted to increase sensitivity. We report here on our efforts to evaluate a reverse engineering approach for identifying such genes and mechanisms. Specifically, we have identified aminoglycoside-sensitive mutants of a multiple-drug-resistant Pseudomonas aeruginosa isolate and characterized the global changes in gene expression associated with mutations that restored sensitivity in two of these mutants as well as the resistant parental strain and the sensitive laboratory strain PAO1.

We chose to study a clinical isolate, named B1, that showed high levels of resistance to five aminoglycosides tested: amikacin, gentamicin, kanamycin, streptomycin, and tobramycin. B1 was found to be of serotype O12, a serotype that has been associated with multiresistance to a number of antibiotic classes, including aminoglycosides and beta-lactams (4, 15, 46, 65, 66). B1 was chemically mutagenized and screened to identify mutants that exhibited increased levels of susceptibility to amikacin. Based on the fact that resistance can arise due to genetic mutation (2, 13, 14, 29), we expected that it would also be possible to restore sensitivity to an already resistant strain through mutation. We hypothesized that the frequency of finding mutations that increase sensitivity would be higher than the frequency of isolating mutants with increased resistance. This is based on the premise that, with only a limited number of point mutations providing a selective advantage in the presence of an antibiotic, a larger percentage of mutations may either have no impact or decrease the level of antibiotic tolerance. Although the frequency of finding sensitivity mutations is a key consideration in assessing the potential of combination therapies, the ability to identify sensitivity-restoring genes/mechanisms is the critical parameter in the design of such therapies.

We hypothesized that whole-genome transcriptional profiling with Affymetrix PAO1 GeneChips could be used for such a purpose. To test this hypothesis, we compared the expression patterns among strain B1, two of its susceptible mutants (named M5 and M31), and laboratory strain PAO1 (81). Moreover, we assessed the resistance mechanisms suggested by transcriptional profiling by MIC assays performed under a variety of conditions (in the presence of verapamil, carbonyl cyanide m-chlorophenylhydrazone [CCCP], and polymyxin B and with spheroplasts) as well as PCR-based gene identification approaches.


   MATERIALS AND METHODS
Top
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 References
 
Strains and culturing conditions. All isolates of P. aeruginosa were obtained from Mike Vasil at the University of Colorado Health Sciences Center, Denver. All strains were cultured in Luria-Bertani (LB) broth at 37°C with constant shaking at 225 rpm. Serotyping was performed by Adriana Vasil at the University of Colorado Health Sciences Center.

Disk susceptibility and MIC determination. Susceptibility to aminoglycosides (amikacin, gentamicin, kanamycin, streptomycin, tobramycin) was determined by methods similar to the disk diffusion method described previously (58) with LB agar plates. LB agar plates were inoculated by swabbing with a turbid culture. Immediately following inoculation, BBL Sensi-Discs (Fisher Scientific, Pittsburgh, PA) were placed with sterile forceps onto the plate. The plates were incubated overnight, and the diameters around the disks were measured.

MICs were determined by a standard broth dilution method in LB medium (1). The lowest concentration at which no growth was noted after 18 h was deemed the MIC. Cultures at an optical density at 600 nm of 0.6 were used for MIC studies For preparation of the medium to be used in studies of MICs determined in the presence of CCCP or verapamil, either CCCP was added to LB medium to achieve a 250 µM solution (87) or verapamil was added to LB medium to achieve a final concentration of 100 µg/ml. This medium was then used in the standard broth dilution MIC assay, with the appropriate levels of amikacin added.

For MIC assays performed with spheroplasts, spheroplasts of P. aeruginosa were formed by treating the cells with EDTA and lysozyme (77). Spheroplast formation was checked by osmotic shock (5, 59).

Random mutagenesis and sensitivity screening. Random mutagenesis with N-methyl-N'-nitro-N-nitrosoguanidine (MNNG; TCI America, Portland, OR) was carried out as described previously (53). Cells were exposed to MNNG at a concentration of 50 µg/ml for 8 min. This level of mutagenesis was sufficient to result in the survival of 50% of the exposed cells. The mutated cells were then plated onto LB agar plates. The contents of the master plates were then replica plated (44) onto LB agar plates containing increasing levels of amikacin. MIC studies were carried out with the colonies that grew on the master plate but not on the imprints to confirm sensitive phenotypes.

For studies conducted to examine the frequencies of sensitivity-restoring mutations, mutated cells were plated onto LB agar plates and incubated overnight. The cells were then patched into 384-well plates containing LB medium. These plates were then patched by using a 384-pin blot replicator into 384-well plates containing increasing amounts of amikacin. After 18 h of incubation, growth in the 384-well plates was confirmed by once again replica plating the cells from the amikacin-containing plates into plates containing LB medium with no amikacin. These plates were then incubated, and growth was determined visually after 18 h.

Detection of plasmids. Strain B1 was examined for the presence of plasmids. No plasmids were found from plasmid extractions with a QIAprep Spin Miniprep kit (QIAGEN, Valencia, CA) or the hot alkaline method of Kado and Liu (36) which has been shown to be effective for the isolation of plasmids in the size range of 2.6 to 350 MDa.

LPS gels. Lipopolysaccharide (LPS) was isolated by first lysing the cells and treating the lysate with proteinase K (26). LPS was run on 16.5% acrylamide Tris-Tricine gels (Bio-Rad, Hercules, CA) and silver stained (20).

Transcriptional profiling. Cultures were grown in medium containing amikacin at a concentration of 50% of the respective MIC and were incubated until logarithmic phase. Volumes of the culture (10 ml) were collected and immediately immersed in liquid nitrogen for 10 s. The samples were then centrifuged (5,000 x g, 10 min, 4°C) and the supernatant was removed. The cell pellets were then once again immersed in liquid nitrogen for 15 s and then stored at –80°C for later RNA extraction.

RNA was extracted from strain B1 and its mutants by using a TRIzol Max bacterial RNA isolation kit (Invitrogen Life Technologies, Carlsbad, CA), followed by further purification with an RNeasy Mini kit (QIAGEN), according to the manufacturer's specifications. RNA from strain PAO1 was extracted by using just the RNeasy Mini kit, but the samples were further purified by using an additional RNeasy mini spin column (63).

Microarray probes were prepared according to the Affymetrix (Santa Clara, CA) P. aeruginosa GeneChip expression analysis protocol, with the slight modification that 2x PCR Enhancer Solution (Invitrogen Life Technologies) was added during cDNA synthesis. Target hybridization, washing, staining, and scanning were performed by the University of Colorado DNA Microarray Facility, according to the manufacturer's specifications, by using a GeneChip hybridization oven, a GeneChip fluidics station, a GeneArray scanner, and GeneChip operating software (v1.1) (Affymetrix).

Microarray data analysis. Microarray data were analyzed with ArrayAssist (Stratagene, La Jolla, CA). The data were analyzed by first performing robust multichip averaging (6, 32, 33), followed by principal component analysis (72), hierarchical clustering (18), and t tests. Data for a third replicate of strain B1 were removed from the analysis due to the large discrepancies in the results of principal component analysis and hierarchical clustering between it and the two other replicates. Additionally, the third replicate of B1 was generated by using a microarray from a different batch of Affymetrix GeneChips. Log fold differences are of base 2.


   RESULTS
Top
 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 References
 
Screening of mutants for increased amikacin sensitivity. Our efforts here were directed at reverse engineering of sensitivity into a resistant isolate of P. aeruginosa and then determining the extent to which the transcriptional profiles could be used to elucidate sensitivity genes and/or mechanisms. First, we determined how much we could increase the sensitivity of a resistant isolate and how frequently we would identify mutants with increased sensitivity. To do so, multidrug-resistant isolate B1 was subjected to random chemical mutagenesis with MNNG and screened to identify mutants with increased levels of sensitivity to amikacin. We chose chemical mutagenesis over other forms of mutatgenesis, such as random or targeted insertion-based mutagenesis, because the B1 isolate studied was found to be resistant to many antibiotics for which there are available selective markers, including chloramphenicol, tetracycline, zeocin, blasticidin, carbenicillin, mercury, trimethoprim, and nalidixic acid, and because chemical mutagenesis can result in mutations that affect not only the expression of a gene but also the function of the encoded gene product.

Initially, 850 mutants were screened by using replica plating for increased susceptibility to amikacin. Of the 850 mutants, 4 were confirmed to have MICs lower than that of B1 (amikacin MIC, 25 µg/ml) (Table 1). Three mutants (M5, M50, and M52) had MICs at intermediate levels of 8, 10, and 8 µg/ml, respectively, while mutant M31 had an MIC equal to that of laboratory strain PAO1 (4 µg/ml). It is of note that we performed the MIC assays with changes in concentrations less than the standard twofold change, with significance determined by t tests.


View this table:
[in this window]
[in a new window]
  		TABLE 1. MICs of PAO1, B1, and the sensitive mutants characterized

 
Our initial round of reverse engineering suggested that the frequency of sensitivity-conferring mutations was surprisingly high (4/850). To more thoroughly investigate the frequency of sensitivity-conferring mutations, we screened an additional 1,500 mutants produced from a single round of random mutagenesis. The frequency of mutations leading to an 80% decrease in the MIC was found to be about 4.8 x 10–2 ± 0.01.

To gain an idea of the number of places on the genome that could be mutated to increase susceptibility to amikacin, we compared the frequencies for which we found sensitive mutants to the frequency of finding a mutant resistant to rifampin, which is known to be due to a single point mutation. The frequency of finding B1 mutants resistant to rifampin when they were subjected to the same level of exposure to MNNG was found to be 3.4 x 10–6, over 4 orders of magnitude less than the frequency of finding a sensitivity-increasing mutation.

Finally, we wanted to assess in greater detail whether or not sensitivity could be further increased through recursive mutagenesis. To do so, we subjected the most sensitive mutant resulting from a single round of mutagenesis, mutant M31, to a second round of random mutagenesis with MNNG. From this additional round, a total of close to 3,000 mutants were screened for increased susceptibility to amikacin. Interestingly, none were found to have further increased sensitivity relative to that of the M31 parental strain.

Transcriptional profiling. Transcriptional profiles were obtained for strain B1, the sensitive mutants M31 and M5, and strain PAO1 grown in the presence of half of their respective amikacin MICs. Amikacin was included in the medium so that the profiles of the strains would reflect the transcription of the strains under similar levels of antibiotic stress. In all cases, cells were cultured identically and samples were obtained in early exponential phase. To determine the extent to which sensitivity mutations altered the overall transcriptional profiles, we performed hierarchical clustering and principal component analysis with the gene expression data corresponding to each strain evaluated. Hierarchical clustering results (Fig. 1a) revealed that the sensitive mutants had expression patterns more similar to that of the laboratory strain PAO1 than to that of parental isolate B1. To further assess this unexpected result, we used principal component analysis (Fig. 1b) to reduce the large amount of data generated from the microarray experiments to a few key variables, called principal components, that account for much of the variation among samples (72). Again, the principal component analysis values corresponding to replicate microarrays of the sensitive mutants and PAO1 strain clustered tightly together, while those of strain B1 were separated from the other samples along the first and second principal components (which accounted for 54% and 23% of the overall variation, respectively). This indicated that, with respect to these principal components, PAO1 and the sensitive mutants were more similar to each other than to B1. The discrepancies observed between the B1 replicates could, in part, be explained by the difficulty of working with the mRNA of this isolate. This, however, does not detract from the finding that the sensitive mutants exhibited expression patterns more similar to that of PAO1 than to those of either of the B1 replicates. This result suggests that the major variation in the overall gene expression data is the result of differences between the B1 profiles and all other profiles.


Figure 1
View larger version (8K):
[in this window]
[in a new window]
  		FIG. 1. (a) Hierarchical clustering (b) and principal component analysis of transcriptional profiles of strain B1, strain PAO1, and sensitive mutants M5 and M31. Replicates are labeled 1 and 2.

 
Our results indicated that significant changes in gene expression had occurred among the resistant and the sensitive strains. We wanted to determine if the changes in gene expression associated with increased sensitivity were coordinated between the two different sensitive mutants, which, if this were the case, would suggest that both mutants had converged upon similar overall gene expression phenotypes, or if the mutants had altered expression of entirely different sets of gene. In order to assess this possibility, t tests were performed to identify the number of genes with significantly altered expression among each strain evaluated. Between mutant M5 and strain B1, the difference in the expression of 694 genes both was statistically significant (P ≤ 0.05) and showed at least a 1 log fold (base 2) difference. A twofold change in expression (equivalent to 1 log fold, base 2) has previously been found to be sufficient for the detection of nearly 95% of differentially expressed genes by the use of Affymetrix GeneChips (11). The number of genes differentially expressed between M31 and B1 was also high (350 genes). Of these sets of genes, only 101 genes were found to be differentially expressed in both mutants. It should be noted that the changes in gene expression not only might be due directly to a mutation in that gene or a regulator of that gene but also might be due to the response of the overall genetic regulatory network to such mutations.

Of the genes that were differentially expressed in mutant M5 or M31 compared with their expression in B1, a vast majority were genes that were grouped into three functional categories or that had no assigned function. The largest proportion of these genes were categorized as unclassified or as having only hypothetical functions (281 genes for M5 and 134 genes for M31). The largest functional category of genes (Fig. 2) comprised genes involved in cell permeability, LPS synthesis, efflux, and the transport of small molecules. There were changes in the expression levels in 113 of these genes for M5 and 71 for M31. The second and third categories contained genes involved in transcription or translation (88 for M5 and 32 for M31) and genes involved in metabolism, catabolism, and biosynthesis (92 for M5 and 40 for M31). Of particular interest, six genes encoding for aminoglycoside-modifying enzymes (AMEs) were found in both M5 and M31 to exhibit decreased expression relative to that in B1, suggesting that both strains would be similarly altered in aminoglycoside-modifying activity. Table 2 provides a detailed summary of the selected genes belonging to the AME or permeability functional class that had significant changes in expression.


Figure 2
View larger version (22K):
[in this window]
[in a new window]
  		FIG. 2. Differentially expressed genes (log fold difference [base 2] ≥ 1; P ≤ 0.05) between sensitive mutants and strain B1. The pie charts show the distribution of the functional categories of differentially expressed genes between (a) B1 and M5 and (b) B1 and M31. Following the name of each functional category are the number of genes in that category and the percentage of differentially expressed genes for which those genes account.

 

View this table:
[in this window]
[in a new window]
  		TABLE 2. Genes differentially expressed between B1 and sensitive mutants M5 and M31

 
PCR of AME genes. In effort to confirm the presence of a number of genes encoding AMEs, we used primers specific for particular AME genes and attempted to amplify these genes by PCR (80, 82, 84). PCR of aadB, ant(4')-IIa, and aac(3)-Ib based on this method gave no bands when they were run on agarose gels. PCR of aadA6, aac(3)-IIIb, and aac(3)-IIIc gave several bands when they were run on agarose gels; but none was of the appropriate size. These bands were not observed by using the same conditions with PAO1 genomic DNA. Finally, we were able to amplify by PCR an aac(6)-Ib gene from strain B1 as well as its sensitive mutants.

Assays and MIC studies to further characterize sensitive mutants. Several hypotheses were developed on the basis of our transcriptional profile studies. First, the observed increase in the sensitivity of M5 and M31 could be due to the decreased expression of several AME genes relative to their levels of expression in strain B1. Second, the sensitivities of M5 and M31 could be the result of mutations affecting amikacin permeability. To test these hypotheses, we assessed changes in the MICs for the mutants strains, B1, and PAO1 (i) to multiple aminoglycosides to assess AME contributions, (ii) to amikacin in the presence of compounds that effect afflux pump activity, (iii) to the polycationic antibiotic polymyxin B to assess altered LPS mechanisms, and, finally, (iv) with spheroplasts of each strain to delineate between the mechanisms present within the plasma membrane and those due to the outer membrane and LPS structures (Table 1).

To examine changes in mutants M5 and M31 that may have been due to AMEs, MIC studies with four additional aminoglycosides were carried out (49). Only the MIC of amikacin for M5 was affected. Since genes affecting the accumulation of amikacin within the cell are less likely to be amikacin specific, the increased sensitivity of M5 is likely due to the decreased activity of an AME that has the capacity to modify amikacin. In contrast, M31 had decreased resistance not only to amikacin but also to tobramycin, gentamicin, kanamycin, and streptomycin. This would indicate that M31 has mutations that confer either increased accumulation of amikacin or, possibly, decreased AME activity.

To further examine the possibility of altered amikacin accumulation, the MIC of amikacin was determined in the presence of CCCP and verapamil. CCCP is an uncoupling proton ionophore that can carry protons across the cytoplasmic membrane and that can thus inhibit efflux pumps and other transporters that are dependent upon the proton motive force as a source of energy (47, 48, 69, 87). Verapamil, a calcium channel blocker, has been noted to inhibit efflux pumps, including ATP-binding cassette (ABC) efflux pumps (12, 35, 45). CCCP (250 µM) and verapamil (100 µg/ml) had no impact upon the MIC of amikacin for PAO1, M5, M31, or B1, indicating that efflux pumps are not substantially contributing to the changes in resistance levels.

Since efflux did not appear to contribute to resistance, we next sought to determine if altered uptake was affected. Polymyxin B is a polycationic antibiotic that is thought to exhibit self-promoted uptake mechanisms for entry into the cell membrane similar to those of aminoglycosides by first interacting with LPS molecules (62). Cross-resistance to polymyxin B and aminoglycosides has been noted for a number of systems (55, 70), possibly due to overall changes in the charge of the outer membrane (83) or the presence of outer membrane proteins that may be blocking antibiotic binding to the membrane (60, 61). The MICs for B1, M5, and M31 were the same as that for PAO1, indicating that changes in sensitivity levels were likely not due to significant changes that would hinder polycationic antibiotic binding to the LPS.

Finally, to delineate between resistance conferred by the outer membrane and resistance mechanisms within the cytoplasmic membrane, spheroplasts of B1, M31, M5, and PAO1 were made; and the MIC of amikacin was then determined. Interestingly, the MICs for spheroplasts of B1, M5, and PAO1 all decreased, while the MIC for the spheroplast for M31 was the same as that for unaltered M31 (Fig. 3). It should be noted that slight changes in MICs may not be clinically relevant but may be biologically relevant. Based upon replicates of this experiment, our results have been shown to be repeatable and statistically significant. The MIC for B1 spheroplasts decreased significantly, but not to the level of those for the M5 and M31 spheroplasts. The M5 spheroplasts had the same MIC as M31 and the M31 spheroplasts. This suggests that the resistance of B1 is due in large part to altered outer membrane permeability and, to a lesser extent, internal mechanisms or mechanisms related to the cytoplasmic membrane. M5 has an increased level of amikacin resistance compared with that for M31, and this increase is likely due to a mutation in permeability. Once the permeability barrier has been removed, the MIC drops to that for M31. The unchanged MICs for M31 and the M31 spheroplasts indicate that the susceptibility of M31 is due to mutations that affect cell permeability. The fact that the MICs for M5 and M31 spheroplasts did not drop to the levels for the PAO1 spheroplasts indicates that there are still mechanisms aside from the permeability of the outer membrane that are contributing to resistance. Furthermore, the internal resistance mechanisms of M5 and M31 are attenuated compared with those of B1.


Figure 3
View larger version (10K):
[in this window]
[in a new window]
  		FIG. 3. Amikacin MICs for untreated cells and spheroplasts of strain PAO1, strain B1, and mutants M5 and M31. In all cases, the standard deviation was 0 (n = 4).

 

   DISCUSSION
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
References
 
From our screening for sensitive mutants of B1, we found that mutations leading to sensitivity occurred at a relatively high frequency, 4.8 x 10–2 ± 0.01, leading to an 80% decrease in the MIC, whereas the frequencies of mutations leading to increased resistance are reported to be 10–5 to 10–10 (16, 21, 28, 39, 42). The range of MICs found suggested that a number of different mutations or combination of mutations that led to increased sensitivity could have occurred. Since mutagenesis with MNNG has been shown to mutate hot spots, resulting in a number of mutations concentrated within a few minutes on the genome (24), particularly at the DNA replication fork (9), these results suggested that more than a single point mutation and likely more than one gene are responsible for the identified increased sensitivity phenotypes. Our inability to find mutants, created after a second round of mutagenesis, that had increased sensitivity levels compared with those of the parent mutant implies that there may be a lower limit to which sensitivity can be restored through chemical mutagenesis. This may be because P. aeruginosa has a large number of intrinsic resistance traits that would have to be altered in combination to further increase susceptibility to amikacin.

A notable detriment to the use of chemical mutagenesis is the lack of an efficient way to determine the mutations that occur. One of the promises of transcriptional profiling is an improved ability to decipher the genetic basis of relevant phenotypes through comparisons of gene expression profiles. Thus, we next sought to determine if transcriptional profiling could be used to identify relevant genetic alterations in two sensitive mutants of the B1 isolate. We reasoned that if only minor changes were required for the restoration of sensitivity, then the transcriptional profiles of sensitive mutants should strongly correlate with the profile of the parental resistant strain and not with the profile of the laboratory PAO1 strain. We hypothesized that the profiles of sensitive mutants would differ in the expression of a limited number of genes, which might allow prediction of the sensitivity-restoring mechanism or mechanisms.

From hierarchical clustering and principal component analysis of gene expression data obtained from strain B1, mutants M5 and M31, and strain PAO1, we found that the sensitive mutants had significant changes in gene expression and that their gene expression patterns were more similar to that of PAO1 than to that of their parent isolate, B1. Upon examination of the genes that were differentially expressed in the sensitive mutants compared with their expression in B1, we found that (i) a large number of genes had altered expression in both mutants and (ii) the overall changes in gene expression were similarly distributed among different functional categories for both M5 and M31.

According to GeneChip analysis, several AMEs exhibited decreased expression in both M5 and M31. Among them were the genes for aminoglycoside 3'-N-acetyltransferases [aac(3)-Ib, aac(3)-IIIb, and aac(3)-IIIc], aminoglycoside adenyltransferases from integron cassettes (aadA6 and aadB), as well as an aminoglycoside-4'-adenyltransferase (ant(4')-IIa). Amikacin is believed to be protected by steric hindrance or folding from modification by aminoglycoside 3'-N-acetyltransferases (54). The aadA6 gene has been shown to render resistance to streptomycin and spectinomycin (57, 79), while aadB has been linked to gentamicin, kanamycin, and tobramycin resistance (56, 79). The AME gene with the largest difference in expression between B1 and the sensitive mutants was ant(4')-IIa, which encodes for an AME that has been shown to confer resistance to both tobramycin and amikacin (79). However, the level of amikacin resistance displayed by B1 is an order of magnitude lower than the MICs previously reported for other P. aeruginosa strains expressing this gene (34, 75, 78). Aminoglycoside-resistant isolates of serotype O12 have been reported to react with probes for the genes ant(3') and aac(6')-I and -II (46).

When attempting to confirm the presence of genes encoding for AMEs by PCR with AME-specific primers, we were able to amplify by PCR an aac(6)-Ib gene from strain B1 and mutants M5 and M31. This gene has been associated with amikacin resistance, with the reported levels of amikacin resistance of strains carrying this gene being similar to the levels found in strain B1 and the sensitive mutants (22). It is feasible that a decrease in expression due to a mutation in a regulator of this gene could cause a decrease in tolerance to amikacin or that a mutation in this gene could also affect its specificity for amikacin (41). Probes for this gene are not available on the Affymetrix P. aeruginosa GeneChip, which explains its absence from our transcriptional profiling studies. Based on this analysis and the high level of resistance to several aminoglycosides displayed by B1, we suspect that B1 does contain a set of AMEs that is partially responsible for its increased overall aminoglycoside tolerance but that these enzymes are not effective at modifying amikacin or are poorly expressed.

Transcriptional profiling also suggested that genes related to the cellular membrane or transport of small molecules were of interest. Of particular note was the change in expression of genes involved in O-antigen synthesis and assembly. The Affymetrix PAO1 GeneChip has probes for O-antigen genes from serotypes O6 (3) and O11 (17), in addition to PAO1 serotype O5 (8). Although strain B1 and its sensitive mutants are of serotype O12, genes involved in O-antigen biosynthesis (wbp genes) and assembly (wzx and wzz) from the O5, O6, and O11 serogroups showed 2- to 4-log-fold decreases in expression levels in sensitive mutants M5 and M31 compared with that in B1. The changes noted in genes from several serotypes may be explained by the fact that hybridization occurs for sequences with greater than approximately 70% identity. Notably, genes related to the B-band O antigen had significant changes in expression, suggesting that altered B-band synthesis could be responsible for the increased sensitivities of the M5 and M31 mutants. There are mixed reports of the impact that the loss of O antigens has upon resistance. The loss of the B-band O antigen has been shown to result in an increase in resistance levels to aminoglycosides in P. aeruginosa (7, 38), possibly because the B band is highly anionic and may thus attract and attach to the highly cationic aminoglycosides. On the other hand, the loss of O-specific antigen, and possibly other parts of the core region, has also been shown to decrease resistance to gentamicin, with the explanation that negatively charged sites of the lipid A of LPS may be involved in aminoglycoside uptake (76). Despite the changes in gene expression noted, sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis of LPS showed that all strains had smooth LPS, with no detectable differences in the LPS of B1 and the sensitive mutants.

Other genes that were identified as having significant changes in expression included oprF, oprG, and oprI, which encode outer membrane protein or lipoprotein precursors. These genes were all shown to have higher levels of expression in mutants M5 and M31 than in strain B1. OprF is a major porin of P. aeruginosa (25), and a decrease in expression of this porin has been observed in antibiotic-resistant strains of P. aeruginosa (37, 68) (the strains were not tested for aminoglycoside resistance). Additionally, M5 and M31 also have decreased expression of probable ABC-type transporters. Certain ABC transporters have been found to serve as efflux pumps for antibiotics and have been shown to increase the levels of resistance to a number of antibiotics (19, 31, 64, 67). Recently, inactivation of the glmR gene, which is believed to be involved in amino sugar metabolism, has been shown to increase sensitivity to aminoglycosides (71). This gene was found to have no significant change in expression between B1, M5, and M31.

Transcriptional profiling results suggested that the increased sensitivity of M5 and M31 could be due in part to modified AME activity or changes in amikacin permeation. We found that M5 had a change in its MIC for amikacin but not for other aminoglycosides, while M31 had a decreased tolerance for other aminoglycosides, in addition to amikacin. Additionally, spheroplasts of M5 had decreased tolerance to amikacin, while spheroplasts of M31 had no changes in amikacin resistance. We rationalized that mutations affecting AMEs would likely be more specific for different aminoglycosides, while mutations affecting permeability would likely be less specific and would possibly be indicated by changes in MICs between untreated cells and spheroplasts of cells. Thus, our results imply that M5 has mutations that affected the ability of AMEs to modify amikacin and that M31 has mutations that affect amikacin permeability and possibly mutations that affect AME activity.

Conclusion. This work describes an assessment of a reverse engineering approach for the identification and characterization of sensitive mutants of a resistant P. aeruginosa isolate. Our results indicate that the frequency of identification of sensitive mutants was unexpectedly high and was several orders of magnitude higher than the reported frequencies of finding resistant mutants. From the frequencies of detection of mutations, along with the various levels of amikacin resistance among the mutants that were identified, it was shown that there are multiple ways in which sensitivity could be increased. This result was bolstered by the dramatic and different changes in gene expression observed for each sensitive mutant, as well as the findings of detailed MIC assays performed with the two mutants examined in greater detail.

A key issue in our evaluation was whether or not whole-genome transcriptional profiling could be used to gain insight into sensitivity-restoring genes/pathways, which is the critical information required for the development of new therapies. Unexpectedly, we found that the changes leading to sensitivity resulted in dramatic but only partially coordinated alterations in gene expression between the two sensitive mutants. Furthermore, the transcriptional profiles of the sensitive mutants more closely resembled that of sensitive laboratory strain PAO1 than that of the resistant parental isolate. Analysis of such transcriptional profiles indicated that changes in amikacin permeability and/or modification by AMEs was the most likely source of the increased sensitivity in mutants M5 and M31, which was later confirmed by several additional assays. Although the transcriptional profiling results provided interesting general insights into sensitivity-restoring mechanisms, the surprisingly large number of genes displaying significant changes in expression prohibited the identification of any single target gene or mutation. Furthermore, this study was hindered by the lack of an array containing probes for all of the genes found within the resistant isolate but not found within the PAO1 genome. Future applications might benefit from the use of a combination of this approach with the use of conventional genetic strategies involving screening of a knockout library to study the impact that gene disruption may have upon sensitivity or screening of an overexpression library in which the effects of increased copy numbers of genes could be examined.


   ACKNOWLEDGMENTS
 
This work was supported by NIH grants R21 AI055773-01 and K25AI064338, as well as a fellowship for J. M. Struble from the National Science Foundation Graduate Assistance in Areas of National Need grant to the University of Colorado Department of Chemical and Biological Engineering.

We thank Mike Vasil (Department of Microbiology, University of Colorado Health Sciences Center) for supplying strains evaluated in this study. We also thank Shelley Copley (Department of Molecular, Cellular, and Developmental Biology, CU—Boulder) and Mike Lynch for thoughtful suggestions throughout this work.


   FOOTNOTES
 
* Corresponding author. Mailing address: Department of Chemical and Biological Engineering, University of Colorado, 1111 Engineering Drive, Campus Box 424, Boulder, CO 80309. Phone: (303) 492-2627. Fax: (303) 492-4341. E-mail: rtg{at}colorado.edu. Back


   REFERENCES
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 References
 

  1. Balows, A., and W. J. Hausler (ed.). 1991. Manual of clinical microbiology, 5th ed. ASM Press, Washington D.C.
  2. Baughman, G. A., and S. R. Fahnestock. 1979. Chloramphenicol resistance mutation in Escherichia coli which maps in the major ribosomal protein gene cluster. J. Bacteriol. 137:1315-1323.[Abstract/Free Full Text]
  3. Belanger, M., L. L. Burrows, and J. S. Lam. 1999. Functional analysis of genes responsible for the synthesis of the B-band O antigen of Pseudomonas aeruginosa serotype O6 lipopolysaccharide. Microbiology 145(Pt 12):3505-3521.[Abstract/Free Full Text]
  4. Bert, F., and N. Lambert-Zechovsky. 1996. Comparative distribution of resistance patterns and serotypes in Pseudomonas aeruginosa isolates from intensive care units and other wards. J. Antimicrob. Chemother. 37:809-813.[Abstract/Free Full Text]
  5. Birdsell, D. C., and E. H. Cota-Robles. 1967. Production and ultrastructure of lysozyme and ethylenediaminetetraacetate-lysozyme spheroplasts of Escherichia coli. J. Bacteriol. 93:427-437.[Abstract/Free Full Text]
  6. Bolstad, B. M., R. A. Irizarry, M. Astrand, and T. P. Speed. 2003. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias. Bioinformatics 19:185-193.[Abstract/Free Full Text]
  7. Bryan, L. E., K. O'Hara, and S. Wong. 1984. Lipopolysaccharide changes in impermeability-type aminoglycoside resistance in Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 26:250-255.[Abstract/Free Full Text]
  8. Burrows, L. L., D. F. Charter, and J. S. Lam. 1996. Molecular characterization of the Pseudomonas aeruginosa serotype O5 (PAO1) B-band lipopolysaccharide gene cluster. Mol. Microbiol. 22:481-495.[CrossRef][Medline]
  9. Cerda-Olmedo, E., P. C. Hanawalt, and N. Guerola. 1968. Mutagenesis of the replication point by nitrosoguanidine: map and pattern of replication of the Escherichia coli chromosome. J. Mol. Biol. 33:705-719.[CrossRef][Medline]
  10. Cetinkaya, Y., P. Falk, and C. Mayhall. 2000. Vancomycin-resistant enterococci. Clin. Microbiol. Rev. 13:686-707.[Abstract/Free Full Text]
  11. Choe, S. E., M. Boutros, A. M. Michelson, G. M. Church, and M. S. Halfon. 2005. Preferred analysis methods for Affymetrix GeneChips revealed by a wholly defined control dataset. Genome Biol. 6:R16.[CrossRef][Medline]
  12. Choudhuri, B. S., S. Bhakta, R. Barik, J. Basu, M. Kundu, and P. Chakrabarti. 2002. Overexpression and functional characterization of an ABC (ATP-binding cassette) transporter encoded by the genes drrA and drrB of Mycobacterium tuberculosis. Biochem. J. 367:279-285.[CrossRef][Medline]
  13. Chu, C., L. H. Su, C. H. Chu, S. Baucheron, A. Cloeckaert, and C. H. Chiu. 2005. Resistance to fluoroquinolones linked to gyrA and parC mutations and overexpression of acrAB efflux pump in Salmonella enterica serotype Choleraesuis. Microb. Drug Resist. 11:248-253.[CrossRef][Medline]
  14. Cirz, R. T., J. K. Chin, D. R. Andes, V. de Crecy-Lagard, W. A. Craig, and F. E. Romesberg. 2005. Inhibition of mutation and combating the evolution of antibiotic resistance. PLoS Biol. 3:e176.[CrossRef][Medline]
  15. Crespo, M. P., N. Woodford, A. Sinclair, M. E. Kaufmann, J. Turton, J. Glover, J. D. Velez, C. R. Castaneda, M. Recalde, and D. M. Livermore. 2004. Outbreak of carbapenem-resistant Pseudomonas aeruginosa producing VIM-8, a novel metallo-ß-lactamase, in a tertiary care center in Cali, Colombia. J. Clin. Microbiol. 42:5094-5101.[Abstract/Free Full Text]
  16. Davies, E. A., and M. R. Adams. 1994. Resistance of Listeria monocytogenes to the bacteriocin nisin. Int. J. Food Microbiol. 21:341-347.[CrossRef][Medline]
  17. Dean, C. R., C. V. Franklund, J. D. Retief, M. J. Coyne, Jr., K. Hatano, D. J. Evans, G. B. Pier, and J. B. Goldberg. 1999. Characterization of the serogroup O11 O-antigen locus of Pseudomonas aeruginosa PA103. J. Bacteriol. 181:4275-4284.[Abstract/Free Full Text]
  18. Eisen, M. B., P. T. Spellman, P. O. Brown, and D. Botstein. 1998. Cluster analysis and display of genome-wide expression patterns. Proc. Natl. Acad. Sci. USA 95:14863-14868.[Abstract/Free Full Text]
  19. Fernandez-Moreno, M. A., L. Carbo, T. Cuesta, C. Vallin, and F. Malpartida. 1998. A silent ABC transporter isolated from Streptomyces rochei F20 induces multidrug resistance. J. Bacteriol. 180:4017-4023.[Abstract/Free Full Text]
  20. Fomsgaard, A., M. A. Freudenberg, and C. Galanos. 1990. Modification of the silver staining technique to detect lipopolysaccharide in polyacrylamide gels. J. Clin. Microbiol. 28:2627-2631.[Abstract/Free Full Text]
  21. Fung-Tomc, J., E. Huczko, M. Pearce, and R. E. Kessler. 1988. Frequency of in vitro resistance of Pseudomonas aeruginosa to cefepime, ceftazidime, and cefotaxime. Antimicrob. Agents Chemother. 32:1443-1445.[Abstract/Free Full Text]
  22. Galimand, M., T. Lambert, G. Gerbaud, and P. Courvalin. 1993. Characterization of the aac(6')-Ib gene encoding an aminoglycoside 6'-N-acetyltransferase in Pseudomonas aeruginosa BM2656. Antimicrob. Agents Chemother. 37:1456-1462.[Abstract/Free Full Text]
  23. Garza-Ramos, G., L. Xiong, P. Zhong, and A. Mankin. 2001. BInding site of macrolide antibiotics on the ribosome: new resistance mutation identifies a specific interaction of ketolides with rRNA. J. Bacteriol. 183:6898-6907.[Abstract/Free Full Text]
  24. Guerola, N., J. L. Ingraham, and E. Cerda-Olmedo. 1971. Induction of closely linked multiple mutations by nitrosoguanidine. Nat. New Biol. 230:122-125.[Medline]
  25. Hancock, R. E., and F. S. Brinkman. 2002. Function of Pseudomonas porins in uptake and efflux. Annu. Rev. Microbiol. 56:17-38.[CrossRef][Medline]
  26. Hitchcock, P. J., and T. M. Brown. 1983. Morphological heterogeneity among Salmonella lipopolysaccharide chemotypes in silver-stained polyacrylamide gels. J. Bacteriol. 154:269-277.[Abstract/Free Full Text]
  27. Ho, I., C. Chan, and A. Cheng. 2000. Aminoglycoside resistance in Mycobacterium kansasii, M. avium-M. intracellulare, and M. fortuitum: are aminoglycoside-modifying enzymes responsible? Antimicrob. Agents Chemother. 44:39-42.[Abstract/Free Full Text]
  28. Hooper, D. C. 2001. Emerging mechanisms of fluoroquinolone resistance. Emerg. Infect. Dis. 7:337-341.[Medline]
  29. Huang, T. S., C. M. Kunin, S. Shin-Jung Lee, Y. S. Chen, H. Z. Tu, and Y. C. Liu. 2005. Trends in fluoroquinolone resistance of Mycobacterium tuberculosis complex in a Taiwanese medical centre: 1995-2003. J. Antimicrob. Chemother.
  30. Hurley, J., G. Miller, and A. Smith. 1995. Mechanism of amikacin resistance in Pseudomonas aeruginosa isolates from patients with cystic fibrosis. Diagn. Microbiol. Infect. Dis. 22:331-336.[CrossRef][Medline]
  31. Ikeno, S., Y. Yamane, Y. Ohishi, N. Kinoshita, M. Hamada, K. S. Tsuchiya, and M. Hori. 2000. ABC transporter genes, kasKLM, responsible for self-resistance of a kasugamycin producer strain. J. Antibiot. (Tokyo) 53:373-384.[Medline]
  32. Irizarry, R. A., B. M. Bolstad, F. Collin, L. M. Cope, B. Hobbs, and T. P. Speed. 2003. Summaries of Affymetrix GeneChip probe level data. Nucleic Acids Res. 31:e15.[Abstract/Free Full Text]
  33. Irizarry, R. A., B. Hobbs, F. Collin, Y. D. Beazer-Barclay, K. J. Antonellis, U. Scherf, and T. P. Speed. 2003. Exploration, normalization, and summaries of high density oligonucleotide array probe level data. Biostatistics 4:249-264.[Abstract]
  34. Jacoby, G. A., M. J. Blaser, P. Santanam, H. Hachler, F. H. Kayser, R. S. Hare, and G. H. Miller. 1990. Appearance of amikacin and tobramycin resistance due to 4'-aminoglycoside nucleotidyltransferase [ANT(4')-II] in gram-negative pathogens. Antimicrob. Agents Chemother. 34:2381-2386.[Abstract/Free Full Text]
  35. Jonas, B. M., B. E. Murray, and G. M. Weinstock. 2001. Characterization of emeA, a norA homolog and multidrug resistance efflux pump, in Enterococcus faecalis. Antimicrob. Agents Chemother. 45:3574-3579.[Abstract/Free Full Text]
  36. Kado, C. I., and S. T. Liu. 1981. Rapid procedure for detection and isolation of large and small plasmids. J. Bacteriol. 145:1365-1373.[Abstract/Free Full Text]
  37. Kadry, A. A. 2003. Lack of efflux mechanism in a clinical isolate of Pseudomonas aeruginosa highly resistant to beta-lactams and imipenem. Folia Microbiol. (Praha) 48:529-533.
  38. Kadurugamuwa, J., J. Lam, and T. Beveridge. 1993. Interaction of gentamicin with the A band and B band lipopolysaccharides of Pseudomonas aeruginosa and its possible lethal effect. Antimicrob. Agents Chemother. 37:715-721.[Abstract/Free Full Text]
  39. Kohler, T., M. Michea-Hamzehpour, P. Plesiat, A. L. Kahr, and J. C. Pechere. 1997. Differential selection of multidrug efflux systems by quinolones in Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 41:2540-2543.[Abstract]
  40. Kozovska, Z., and J. Subik. 2003. Screening for effectors that modify multidrug resistance in yeast. Int. J. Antimicrob. Agents 22:284-290.[Medline]
  41. Lambert, T., M. C. Ploy, and P. Courvalin. 1994. A spontaneous point mutation in the aac(6')-Ib' gene results in altered substrate specificity of aminoglycoside 6'-N-acetyltransferase of a Pseudomonas fluorescens strain. FEMS Microbiol. Lett. 115:297-304.[Medline]
  42. LeClerc, J. E., B. Li, W. L. Payne, and T. A. Cebula. 1996. High mutation frequencies among Escherichia coli and Salmonella pathogens. Science 274:1208-1211.[Abstract/Free Full Text]
  43. Leclercq, R. 2001. Safeguarding future antimicrobial options: strategies to minimize resistance. Clin. Microbiol. Infect. 7:18-23.
  44. Lederberg, J., and E. M. Lederberg. 1952. Replica plating and indirect selection of bacterial mutants. J. Bacteriol. 63:399-406.[Free Full Text]
  45. Lee, E. W., M. N. Huda, T. Kuroda, T. Mizushima, and T. Tsuchiya. 2003. EfrAB, an ABC multidrug efflux pump in Enterococcus faecalis. Antimicrob. Agents Chemother. 47:3733-3738.[Abstract/Free Full Text]
  46. Legakis, N. J., M. Aliferopoulou, J. Papavassiliou, and M. Papapetropoulou. 1982. Serotypes of Pseudomonas aeruginosa in clinical specimens in relation to antibiotic susceptibility. J. Clin. Microbiol. 16:458-463.[Abstract/Free Full Text]
  47. Li, X. Z., L. Zhang, and K. Poole. 1998. Role of the multidrug efflux systems of Pseudomonas aeruginosa in organic solvent tolerance. J. Bacteriol. 180:2987-2991.[Abstract/Free Full Text]
  48. Li, Y., T. Mima, Y. Komori, Y. Morita, T. Kuroda, T. Mizushima, and T. Tsuchiya. 2003. A new member of the tripartite multidrug efflux pumps, MexVW-OprM, in Pseudomonas aeruginosa. J. Antimicrob. Chemother. 52:572-575.[Abstract/Free Full Text]
  49. Livermore, D. M., T. G. Winstanley, and K. P. Shannon. 2001. Interpretative reading: recognizing the unusual and inferring resistance mechanisms from resistance phenotypes. J. Antimicrob. Chemother. 48(Suppl. 1):87-102.[Abstract]
  50. Lomovskaya, O., A. Lee, K. Hoshino, H. Ishida, A. Mistry, M. Warren, E. Boyer, S. Chamberland, and V. Lee. 1999. Use of a genetic approach to evaluate the consequences of inhibition of efflux pumps in Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 43:1340-1346.[Abstract/Free Full Text]
  51. Lomovskaya, O., M. Warren, A. Lee, J. Galazzo, R. Fronko, M. Lee, J. Blais, D. Cho, S. Chamberland, T. Renau, R. Leger, S. Hecker, W. Watkins, K. Hoshino, H. Ishida, and V. Lee. 2001. Identification and characterization of inhibitors of multidrug resistance efflux pumps in Pseudomonas aeruginosa: novel agents for combination therapy. Antimicrob. Agents Chemother. 45:105-116.[Abstract/Free Full Text]
  52. Maloney, J., D. Rimland, D. Stephens, and A. Whitney. 1989. Analysis of amikacin-resistant Pseudomonas aeruginosa developing in patients receiving amikacin. Arch. Intern. Med. 149:630-640.[Abstract]
  53. Miller, J. H. 1972. Experiments in molecular genetics. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
  54. Mingeot-Leclercq, M. P., Y. Glupczynski, and P. M. Tulkens. 1999. Aminoglycosides: activity and resistance. Antimicrob. Agents Chemother. 43:727-737.[Free Full Text]
  55. Moore, R. A., and R. E. Hancock. 1986. Involvement of outer membrane of Pseudomonas cepacia in aminoglycoside and polymyxin resistance. Antimicrob. Agents Chemother. 30:923-926.[Abstract/Free Full Text]
  56. Naas, T., L. Poirel, A. Karim, and P. Nordmann. 1999. Molecular characterization of In50, a class 1 integron encoding the gene for the extended-spectrum beta-lactamase VEB-1 in Pseudomonas aeruginosa. FEMS Microbiol. Lett. 176:411-419.[Medline]
  57. Naas, T., L. Poirel, and P. Nordmann. 1999. Molecular characterisation of In51, a class 1 integron containing a novel aminoglycoside adenylyltransferase gene cassette, aadA6, in Pseudomonas aeruginosa. Biochim. Biophys. Acta 1489:445-451.[Medline]
  58. National Committee for Clinical Laboratory Standards. 1990. Performance standards for antimicrobial disk susceptibility tests. Approved standard M2-A4, 4th ed. National Committee for Clinical Laboratory Standards, Villanova, Pa.
  59. Neu, H. C., and L. A. Heppel. 1964. The release of ribonuclease into the medium when E. coli cells are converted to spheroplasts. Biochem. Biophys. Res. Commun. 14:109-112.[CrossRef][Medline]
  60. Nicas, T. I., and R. E. Hancock. 1983. Alteration of susceptibility to EDTA, polymyxin B and gentamicin in Pseudomonas aeruginosa by divalent cation regulation of outer membrane protein H1. J. Gen. Microbiol. 129:509-517.[Medline]
  61. Nicas, T. I., and R. E. Hancock. 1980. Outer membrane protein H1 of Pseudomonas aeruginosa: involvement in adaptive and mutational resistance to ethylenediaminetetraacetate, polymyxin B, and gentamicin. J. Bacteriol. 143:872-878.[Abstract/Free Full Text]
  62. Nikaido, H., and M. Vaara. 1985. Molecular basis of bacterial outer membrane permeability. Microbiol. Rev. 49:1-32.[Free Full Text]
  63. Ochsner, U. A., P. J. Wilderman, A. I. Vasil, and M. L. Vasil. 2002. GeneChip expression analysis of the iron starvation response in Pseudomonas aeruginosa: identification of novel pyoverdine biosynthesis genes. Mol. Microbiol. 45:1277-1287.[CrossRef][Medline]
  64. Otto, M., and F. Gotz. 2001. ABC transporters of staphylococci. Res. Microbiol. 152:351-356.[Medline]
  65. Patzer, J., and D. Dzierzanowska. 1991. The resistance patterns and serotypes of Pseudomonas aeruginosa strains isolated from children. J. Antimicrob. Chemother. 28:869-875.[Abstract/Free Full Text]
  66. Pitt, T. L., D. M. Livermore, G. Miller, A. Vatopoulos, and N. J. Legakis. 1990. Resistance mechanisms of multiresistant serotype O12 Pseudomonas aeruginosa isolated in Europe. J. Antimicrob. Chemother. 26:319-328.[Abstract/Free Full Text]
  67. Poelarends, G. J., P. Mazurkiewicz, M. Putman, R. H. Cool, H. W. Veen, and W. N. Konings. 2000. An ABC-type multidrug transporter of Lactococcus lactis possesses an exceptionally broad substrate specificity. Drug Resist. Update 3:330-334.[CrossRef][Medline]
  68. Pumbwe, L., M. J. Everett, R. E. Hancock, and L. J. Piddock. 1996. Role of gyrA mutation and loss of OprF in the multiple antibiotic resistance phenotype of Pseudomonas aeruginosa G49. FEMS Microbiol. Lett. 143:25-28.[CrossRef][Medline]
  69. Pumbwe, L., and L. J. Piddock. 2000. Two efflux systems expressed simultaneously in multidrug-resistant Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 44:2861-2864.[Abstract/Free Full Text]
  70. Rahaman, S. O., J. Mukherjee, A. Chakrabarti, and S. Pal. 1998. Decreased membrane permeability in a polymyxin B-resistant Escherichia coli mutant exhibiting multiple resistance to beta-lactams as well as aminoglycosides. FEMS Microbiol. Lett. 161:249-254.[Medline]
  71. Ramos-Aires, J., P. Plesiat, L. Kocjancic-Curty, and T. Kohler. 2004. Selection of an antibiotic-hypersusceptible mutant of Pseudomonas aeruginosa: identification of the GlmR transcriptional regulator. Antimicrob. Agents Chemother. 48:843-851.[Abstract/Free Full Text]
  72. Raychaudhuri, S., J. M. Stuart, and R. B. Altman. 2000. Principal components analysis to summarize microarray experiments: application to sporulation time series. Pac. Symp. Biocomput. 2000:455-466.
  73. Renau, T., R. Leger, E. Flamme, J. Sangalang, M. She, R. Yen, C. Ganno, D. Griffith, S. Chamberland, O. Lomovskaya, S. Hecker, V. Lee, T. Ohta, and K. Nakayama. 1999. Inhibitors of efflux pumps in Pseudomonas aeruginosa potentiate the activity of the fluoroquinolone antibacterial levofloxacin. J. Med. Chem. 42:4928-4931.[CrossRef][Medline]
  74. Saavedra, S., D. Vera, and C. Ramirez-Ronda. 1986. Susceptibility of aerobic gram-negative bacilli to aminoglycosides. Effects of 45 months of amikacin as first-line aminoglycoside therapy. Am. J. Med. 80:65-70.[Medline]
  75. Sabtcheva, S., M. Galimand, G. Gerbaud, P. Courvalin, and T. Lambert. 2003. Aminoglycoside resistance gene ant(4')-IIb of Pseudomonas aeruginosa BM4492, a clinical isolate from Bulgaria. Antimicrob. Agents Chemother. 47:1584-1588.[Abstract/Free Full Text]
  76. Saika, T., M. Hasegawa, I. Kobayashi, and M. Nishida. 1999. Ionic binding of 3H-gentamicin and short-time bactericidal activity of gentamicin against Pseudomonas aeruginosa isolates with different lipopolysaccharide structures. Chemotherapy 45:296-302.[Medline]
  77. Sambrook, J., E. F. Fritsch, and T. Maniatis. 1989. Molecular cloning: a laboratory manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
  78. Shaw, K. J., H. Munayyer, P. N. Rather, R. S. Hare, and G. H. Miller. 1993. Nucleotide sequence analysis and DNA hybridization studies of the ant(4')-IIa gene from Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 37:708-714.[Abstract/Free Full Text]
  79. Shaw, K. J., P. N. Rather, R. S. Hare, and G. H. Miller. 1993. Molecular genetics of aminoglycoside resistance genes and familial relationships of the aminoglycoside-modifying enzymes. Microbiol. Rev. 57:138-163.[Abstract/Free Full Text]
  80. Shervington, A., L. Abbasi, and S. Bdour. 2001. PCR detection of four genes encoding for aminoglycoside-modifying enzymes in bacteria of clinical isolates of Jordan University Hospital. World J. Microbiol. Biotechnol. 17:139-142.[CrossRef]
  81. Stover, C. K., X. Q. Pham, A. L. Erwin, S. D. Mizoguchi, P. Warrener, M. J. Hickey, F. S. Brinkman, W. O. Hufnagle, D. J. Kowalik, M. Lagrou, R. L. Garber, L. Goltry, E. Tolentino, S. Westbrock-Wadman, Y. Yuan, L. L. Brody, S. N. Coulter, K. R. Folger, A. Kas, K. Larbig, R. Lim, K. Smith, D. Spencer, G. K. Wong, Z. Wu, I. T. Paulsen, J. Reizer, M. H. Saier, R. E. Hancock, S. Lory, and M. V. Olson. 2000. Complete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogen. Nature 406:959-964.[CrossRef][Medline]
  82. Udo, E. E., and A. A. Dashti. 2000. Detection of genes encoding aminoglycoside-modifying enzymes in staphylococci by polymerase chain reaction and dot blot hybridization. Int. J. Antimicrob. Agents 13:273-279.[CrossRef][Medline]
  83. Vaara, M., T. Vaara, M. Jensen, I. Helander, M. Nurminen, E. T. Rietschel, and P. H. Makela. 1981. Characterization of the lipopolysaccharide from the polymyxin-resistant pmrA mutants of Salmonella typhimurium. FEBS Lett. 129:145-149.[CrossRef][Medline]
  84. Vanhoof, R., J. Content, E. Van Bossuyt, E. Nulens, P. Sonck, F. Depuydt, J. M. Hubrechts, P. Maes, and E. Hannecart-Pokorni. 1993. Use of the polymerase chain reaction (PCR) for the detection of aacA genes encoding aminoglycoside-6'-N-acetyltransferases in reference strains and gram-negative clinical isolates from two Belgium hospitals. J. Antimicrob. Chemother. 32:23-35.[Abstract/Free Full Text]
  85. White, R. 2002. Antibiotic resistance: where do ketolides fit? Pharmacotherapy 22:18S-29S.[CrossRef][Medline]
  86. Xiong, Y., J. Caillon, H. Drugeon, G. Potel, and D. Baron. 1996. Influence of pH on adaptive resistance of Pseudomonas aeruginosa to aminoglycosides and their postantiobiotic effects. Antimicrob. Agents Chemother. 40:35-39.[Abstract]
  87. Zhao, Q., X. Z. Li, A. Mistry, R. Srikumar, L. Zhang, O. Lomovskaya, and K. Poole. 1998. Influence of the TonB energy-coupling protein on efflux-mediated multidrug resistance in Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 42:2225-2231.[Abstract/Free Full Text]

Antimicrobial Agents and Chemotherapy, July 2006, p. 2506-2515, Vol. 50, No. 7
0066-4804/06/$08.00+0     doi:10.1128/AAC.01640-05
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




This Article
Right arrow Abstract Freely available
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 Google Scholar
Google Scholar
Right arrow Articles by Struble, J. M.
Right arrow Articles by Gill, R. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Struble, J. M.
Right arrow Articles by Gill, R. T.

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Clin. Vaccine Immunol. Clin. Microbiol. Rev.
J. Clin. Microbiol.