Skip to main page content

• HOME
• Current Issue
• Archive
• Alerts
• About ASM
• Contact us
• Tech Support
• Journals.ASM.org

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Mani, N. Articles by Grossman, T. H. Search for Related Content PubMed PubMed Citation Articles by Mani, N. Articles by Grossman, T. H.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, April 2006, p. 1228-1237, Vol. 50, No. 4
0066-4804/06/$08.00+0     doi:10.1128/AAC.50.4.1228-1237.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

In Vitro Characterization of the Antibacterial Spectrum of Novel Bacterial Type II Topoisomerase Inhibitors of the Aminobenzimidazole Class

Nagraj Mani, Christian H. Gross, Jonathan D. Parsons, Brian Hanzelka, Ute Müh, Steve Mullin, Yusheng Liao, Anne-Laure Grillot, Dean Stamos, Paul S. Charifson, and Trudy H. Grossman^*

Vertex Pharmaceuticals Incorporated, Cambridge, Massachusetts 02139

Received 9 October 2005/ Returned for modification 5 December 2005/ Accepted 18 January 2006

Top Abstract Introduction Materials and Methods Results and Discussion References

 
Antibiotics with novel mechanisms of action are becoming increasingly important in the battle against bacterial resistance to all currently used classes of antibiotics. Bacterial DNA gyrase and topoisomerase IV (topoIV) are the familiar targets of fluoroquinolone and coumarin antibiotics. Here we present the characterization of two members of a new class of synthetic bacterial topoII ATPase inhibitors: VRT-125853 and VRT-752586. These aminobenzimidazole compounds were potent inhibitors of both DNA gyrase and topoIV and had excellent antibacterial activities against a wide spectrum of problematic pathogens responsible for both nosocomial and community-acquired infections, including staphylococci, streptococci, enterococci, and mycobacteria. Consistent with the novelty of their structures and mechanisms of action, antibacterial potency was unaffected by commonly encountered resistance phenotypes, including fluoroquinolone resistance. In time-kill assays, VRT-125853 and VRT-752586 were bactericidal against Staphylococcus aureus, Streptococcus pneumoniae, Enterococcus faecalis, and Haemophilus influenzae, causing 3-log reductions in viable cells within 24 h. Finally, similar to the fluoroquinolones, relatively low frequencies of spontaneous resistance to VRT-125853 and VRT-752586 were found, a property consistent with their in vitro dual-targeting activities.

Top Abstract Introduction Materials and Methods Results and Discussion References

 
Antibiotic resistance in both hospital and community settings is steadily increasing, severely limiting the effectiveness of all currently used classes of antibiotics (4, 12, 17). Approximately 50% of Staphylococcus aureus hospital isolates are methicillin resistant, while 30% of enterococci are reported to be vancomycin resistant (4). The frequency of intermediate and high-level penicillin resistance in the community pathogen Streptococcus pneumoniae is approaching 50% (1, 12, 26). In addition, bacteria that are simultaneously resistant to more than one drug class are becoming increasingly prevalent (2). A significant problem with the majority of currently marketed antibiotics is that they are derived from structural classes that have been in widespread use for many years. For instance, resistance mechanisms acting on older ß-lactams, fluoroquinolones, and macrolides often impact newer generations of these commonly used classes of antibiotics. As a result, an actively pursued strategy of the antibiotic industry to thwart current drug resistance mechanisms is to create structurally novel class of antibiotics with new mechanisms of action. During the last 3 decades, only two truly novel classes of antibacterials with unique mechanisms of action, linezolid and daptomycin, have been developed to combat the problem of antibiotic resistance. Interestingly, there are already reports of linezolid resistance arising in the clinic (22), which underscores the need for new antibiotics with novel mechanisms of action.

Because of their essentiality and evolutionary conservation, DNA topoisomerases have become important antibiotic targets (11, 19). Both DNA gyrase and topoisomerase IV (topoIV) are highly homologous functional A₂B₂ heterotetramers (5). DNA gyrase is uniquely responsible for introducing negative supercoils into DNA, while the primary function of topoIV appears to be decatenation of replicated chromosomes and relaxation of DNA (6, 15, 31). The catalytic functions of both enzymes involve the breakage and rejoining of double-stranded DNA, with the intermediate passage of a second double strand of DNA through the break. Consistent with their high degree of structural and functional relatedness, both DNA gyrase and topoIV have been identified as the primary and secondary targets of the fluoroquinolone class of antibiotics which stabilize the enzyme-DNA complex in the double-strand break stage formed by gyrase and topoIV in bacteria (9). DNA gyrase and topoIV are also inhibited by members of the coumarin class of antibiotics, such as novobiocin and coumermycin, which target the ATP-binding sites of the corresponding B subunits (19), thereby inhibiting the energy source necessary for strand passage. At present, most coumarin resistance mutations in several organisms have mapped within the region of gyrB, encoding the ATP-binding site (10, 21, 29). However, recent in vitro studies have shown that novobiocin can also inhibit the ATPase activity of topoIV at higher concentrations than are necessary for inhibition of the gyrase enzyme (3). Therefore, the potential for "dual targeting" of both gyrase and topoIV exists at multiple steps during the catalytic pathway.

Antibiotics that inhibit multiple targets, such as some fluoroquinolones, tend to exhibit lower spontaneous-resistance frequencies, and their antibacterial activity is less affected by individual, target-based mutations (7). This potentially delays the emergence of high-level resistance during use, a major cause of treatment failure. In order to exploit the dual-targeting potential of the GyrB and ParE ATP-binding sites, a series of compounds belonging to the aminobenzimidazole class were optimized by using structure-guided drug design. In this report, we describe the characterization of two representative compounds of this class, VRT-125853 and VRT-752586 (Fig. 1), with respect to their abilities to inhibit the essential ATPase activities of Escherichia coli and S. aureus gyrase and topoIV, their antibacterial potencies and spectrum of activity against clinically prevalent resistant isolates, their bactericidal effectiveness in time-kill assays, and the frequency of the emergence of resistance in vitro.

View larger version (12K): [in this window] [in a new window]

FIG. 1. Chemical structures of dual-targeting aminobenzimidazoles VRT-125853 and VRT-752586.

Top Abstract Introduction Materials and Methods Results and Discussion References

 
Compounds. VRT-125853 and VRT-752586 (Fig. 1) were synthesized at Vertex Pharmaceuticals Incorporated, and dry powder was dissolved in 100% dimethyl sulfoxide (DMSO) at a concentration of 25.6 mg/ml. Aliquots of DMSO stock solutions were stored at –20°C prior to use. Novobiocin (Sigma, St. Louis, MO), linezolid, (Zyvox, resuspended oral suspension; Pfizer, New York, NY), and ciprofloxacin (US Biological, Swampscott, MA) stocks were prepared and stored as described above. All of the other antibiotics used in this study were from standard commercial sources.

Enzyme assays and K_i determinations. (i) DNA gyrase and topoIV ATPase assays. Enzymes were recombinantly expressed and purified as previously described for the E. coli enzymes (3, 10). Enzymatic hydrolysis of ATP to ADP was coupled to the conversion of NADH to NAD⁺. The decrease in NADH absorbance was monitored at 340 nm for 20 min with a Molecular Devices plate reader. The rate of enzymatic hydrolysis was plotted against a serial dilution of inhibitor to determine potency, and the data were fitted to the Morrison equation for tight-binding inhibition (20). Standard coupled enzyme reactions were carried out at 30°C in a final volume of 100 µl. E. coli gyrase A₂B₂ assay reaction mixtures contained 100 mM Tris-HCl (pH 7.5), 1.5 mM MgCl₂, 150 mM KCl, 2.5 mM phosphoenolpyruvate (PEP), 0.2 mM NADH, 1 mM dithiothreitol (DTT), 0.03 mg of pyruvate kinase per ml, 0.01 mg of lactate dehydrogenase per ml, 4% DMSO, 0.9 mM ATP (equal to the K_m), and 40 nM (active enzyme) E. coli gyrase A₂B₂. E. coli topoIV C₂E₂ assay reaction mixtures contained 100 mM Tris-HCl (pH 7.5), 6 mM MgCl₂, 20 mM KCl, 2.5 mM PEP, 0.2 mM NADH, 10 mM DTT, 0.03 mg of pyruvate kinase per ml, 0.01 mg of lactate dehydrogenase per ml, 4% DMSO, 0.05 mg of bovine serum albumin per ml, 5 µg of HindIII-linearized pBR322 plasmid DNA per ml, 0.7 mM ATP (equal to the K_m), and 20 nM E. coli topoIV C₂E₂ (active enzyme). S. aureus gyrase A₂B₂ assay reaction mixtures contained 100 mM Tris-HCl (pH 7.5), 1.5 mM MgCl₂, 150 mM KCl, 2.5 mM PEP, 0.2 mM NADH, 1 mM DTT, 0.03 mg of pyruvate kinase per ml, 0.01 mg of lactate dehydrogenase per ml, 4% DMSO, 0.55 mM ATP (equal to the K_m), and 60 nM S. aureus gyrase A₂B₂ (active enzyme). For S. aureus topoIV C₂E₂ (encoded by the grlA [C subunit] and grlB [E subunit] genes) assay, reaction mixtures contained 100 mM Tris-HCl (pH 7.5), 2 mM MgCl₂, 200 mM potassium glutamate, 2.5 mM PEP, 0.2 mM NADH, 1 mM DTT, 0.03 mg of pyruvate kinase per ml, 0.01 mg of lactate dehydrogenase per ml, 4% DMSO, 0.05 mg of bovine serum albumin per ml, 5 µg of HindIII-linearized pBR322 plasmid DNA per ml, 0.24 mM ATP (equal to the K_m), and 21 nM S. aureus topoIV C₂E₂ (active enzyme).

(ii) Human topoII DNA decatenation assay. Human topoII was assayed for its enzymatic activity, the ability to convert catenated kinetoplast DNA to decatenated DNA, by using a kit and the human topoII enzyme, which were both obtained from TopoGEN (Columbus, OH). After 20 min, the reaction was stopped with 5 µl of quench buffer (250 mM EDTA, 50% glycerol, 25 µg of bromophenol blue per ml). The DNA was separated and visualized on a 1% agarose gel stained with ethidium bromide. Standard reactions were carried out at 37°C (reaction mixture volume, 25 µl) with the following components: 100 mM Tris-HCl (pH 7.5), 10 mM MgCl₂, 120 mM KCl, 1 mM DTT, 20 µg of kinetoplast DNA per ml, 4% DMSO, 1.5 mM ATP, and 0.08 U of human topoII activity per µl. The EC₅₀ is the compound concentration where approximately 50% inhibition of decatenation activity was observed, as determined by densitometric quantitation.

Bacterial strains. All bacteria, as indicated, were either from our laboratory stocks, the proprietary clinical isolate collection of Focus Technologies (Herndon, VA), the American Type Culture Collection (ATCC; Manassas, VA), or the E. coli Genetic Stock Center (Yale University, New Haven, CT). Haemophilus influenzae strain Rd 0894 acrA::kan was a generous gift from H. Nikaido (27). S. aureus strains SA-1199, SA-1199B (NorA overproducer, GrlA A116E mutant), SA-8325-4, and SA-K2068 (MepA overproducer) were generous gifts from G. Kaatz (13, 14).

Susceptibility testing. Susceptibility testing was performed at either Vertex Pharmaceuticals Incorporated or Focus Technologies (Herndon, VA). For aerobic organisms, MIC determinations were performed in liquid medium in 96-well microtiter plates as described by the Clinical and Laboratory Standards Institute (CLSI [formerly the National Committee for Clinical and Laboratory Standards]; 23). Liquid medium was supplemented as appropriate for optimal growth (23). Serial twofold dilution series of 200x-concentrated compound stocks were prepared in 100% DMSO, and 0.5 µl of each compound dilution was added to 50 µl of liquid medium in 96-well microtiter assay plates. An additional 50 µl of liquid medium containing the appropriate bacterial cells was then added to the assay plate. The final DMSO concentration in the assay was 0.5%. Compounds and cells were mixed, and plates were incubated at 35°C for at least 18 h prior to reading the susceptibility result. A twofold variation in the MIC was the standard error of the assay and hence considered insignificant. To measure the relative effects of serum on compound susceptibility, human serum (US Biological, Swampscott, MA) was added to liquid medium to a final concentration of 50% in assays performed with S. aureus ATCC 29213. For determining the MICs of anaerobic organisms, the agar proportion method was used according to CLSI recommendations (24). Susceptibility testing of Mycoplasma pneumoniae was performed by a reference broth microdilution method established by Waites et al. (30). MICs for Legionella pneumophila were determined by the standardized CLSI method (23). Mycobacterium tuberculosis susceptibility testing was performed with the BACTEC 460 TB System manufactured by Becton Dickinson, Cockeysville, MD. MICs for the Mycobacterium avium complex (MAC) were determined by the agar proportion method recommended for testing slow-growing mycobacterium species (25). All of the test methods used met acceptable standards based on recommended quality control ranges for all comparator antibiotics and the appropriate ATCC strain.

Determination of spontaneous-resistance frequencies. The microtiter MIC of a given compound stock was verified prior to determination of spontaneous-resistance frequencies. Resistance frequencies were minimally determined in duplicate with two independently inoculated cultures. Fresh overnight cultures or glycerol seed stocks of mid-log-phase cultures were diluted 100-fold into appropriate fresh medium and grown at 37°C with a floor shaker rotating at 300 rpm, until late-log phase (approximately 10⁸ to 10⁹ CFU/ml). The inoculum was serially diluted and plated to confirm the starting number of CFU. Selection plates were prepared by adding an appropriate dilution of compound in 100% DMSO to 50 ml of molten agar at 55°C (ß-NAD and hemin for HTM [23] was added at this time for H. influenzae, fresh 5% defibrinated sheep blood [Bioreclamation, Inc., Hicksville, NY] was added to brain heart infusion agar for S. pneumoniae, and 5% laked horse blood [Quad Five, Ryegate, MT] was added to Mueller-Hinton broth agar for Enterococcus faecalis and Enterococcus faecium) and poured into sterile polystyrene petri plates (150 by 15 mm). The final concentration of compound was a multiple of the liquid MIC (2x, 4x, or 8x), and the final concentration of DMSO per plate was <0.1%. Plates were dried in a sterile hood for approximately 30 min prior to plating of bacteria. The late-log-phase inoculum was concentrated 10-fold by low-speed centrifugation, and approximately 10¹⁰ CFU were spread onto the surface of compound-containing agar plates. Plates were incubated at 35°C for a minimum of 3 days prior to counting of colonies. The resistance frequency was calculated as the number of compound-resistant colonies divided by the total number of CFU plated.

Bactericidal (time-kill) assays. Five milliliters of appropriate growth medium was inoculated with approximately 10⁶ log-phase cells, and cultures were grown in 15-ml sterile polypropylene conical tubes containing various dilutions of VRT-125853, VRT-752586, or control antibiotics. The final concentration of DMSO per culture was <0.5%. A sample of the inoculum was also serially diluted and plated to determine the starting number of CFU. Cultures were grown horizontally on a wheel (S. aureus ATCC 29213, S. pneumoniae ATCC BAA-255 [strain R6], and E. faecalis ATCC 29212) rotating rapidly (approximately 70 rpm) at 37°C or by shaking (H. influenzae ATCC 51907) in a tilted position in a floor shaker at 300 rpm. Samples (0.1 ml) were removed from cultures at timed intervals, serially diluted, and plated for CFU determinations on agar plates. Bactericidal activity was defined as a 3-log drop in the starting number of CFU in the culture within 24 h. Novobiocin, ciprofloxacin, and linezolid were run as controls.

Top Abstract Introduction Materials and Methods Results and Discussion References

 
Dual targeting of DNA gyrase and topoIV enzymes by VRT-125853 and VRT-752586. VRT-125853 and VRT-752586 were shown to be inhibitors of both the DNA gyrase and topoIV enzymes derived from E. coli and S. aureus (Table 1). For the E. coli enzymes, both compounds were significantly more potent against DNA gyrase than against topoIV. The lower K_is of both VRT-125853 and VRT-752586 against E. coli DNA gyrase versus topoIV suggested that DNA gyrase would be the primary target for both compounds in this organism in the absence of a cellular permeability barrier (see next section). In contrast to what was observed with the E. coli enzymes, the activities of VRT-125853 and VRT-752586 were more similar against both of the S. aureus enzymes, with topoIV/DNA gyrase K_i ratios of 5 and <0.4, respectively. The potent inhibition of both the gyrase and topoIV enzymes of E. coli and S. aureus demonstrated the in vitro dual-targeting properties of VRT-125853 and VRT-752586; however, the topoIV/DNA gyrase K_i ratios appeared to be both compound and organism specific. In contrast, novobiocin was found to be a more potent inhibitor of DNA gyrase than of topoIV in both sets of enzymes, consistent with findings in the literature that DNA gyrase is the major target of novobiocin in both E. coli and S. aureus (10, 21, 29). In a decatenation assay, neither aminobenzimidazole significantly inhibited human topoII (EC₅₀, >25 µM; Table 1), a homologue with strong sequence similarity to both bacterial enzymes (5), indicating that the compounds are selective for the bacterial topoisomerases.

View this table: [in this window] [in a new window]

TABLE 1. Dual inhibition of bacterial gyrase and topoIV by VRT-125853 and VRT-752586

Spectrum of activity of VRT-125853 and VRT-752586. The antibacterial activities of VRT-125853 and VRT-752586 were determined against panels composed of recent drug-resistant and -susceptible aerobic, facultatively anaerobic, anaerobic, and atypical clinical isolates (Tables 2 and 3). Susceptibility results in Table 2 show that VRT-125853 and VRT-752586 had excellent activities against S. aureus, S. epidermidis, S. pneumoniae, S. pyogenes, E. faecalis, and E. faecium, suggesting their potential for use in a variety of hospital- and community-acquired infections. Although VRT-125853 and VRT-752586 were not active (MIC, >64 µg/ml) against Acinetobacter spp., E. coli, Salmonella enterica serovar Typhimurium, Klebsiella pneumoniae, Proteus mirabilis, Providencia spp., Pseudomonas aeruginosa, and Stenotrophomonas maltophilia (not shown), both compounds had significant activity against aerobic gram-negative respiratory pathogens H. influenzae and Moraxella catarrhalis (Table 2).

View this table: [in this window] [in a new window]

TABLE 2. Activities of VRT-125853 and VRT-752586 against aerobic and facultatively anaerobic bacteria

View this table: [in this window] [in a new window]

TABLE 3. Activities of VRT-125853 and VRT-752586 against anaerobic and atypical bacteria

Confirmation of a gyrase-mediated mechanism of action of both compounds in bacteria was demonstrated by an upward shift in the MIC with an S. aureus strain containing a GyrB T173I mutation compared to wild-type parental strain ATCC 29213. Mutations in threonine 173 in S. aureus GyrB have been previously implicated in conferring novobiocin resistance (29); the MIC of novobiocin (0.063 µg/ml) was increased by eightfold for the GyrB T173I mutant strain; however, the MICs of other antibiotics (ciprofloxacin, vancomycin, and linezolid) were unaffected (data not shown). The GyrB T173I mutation increased the MICs of VRT-125853 (2 µg/ml) and VRT-752586 (0.032 µg/ml) by 8-fold and 16-fold, respectively, indicating that the MICs of these compounds for wild-type S. aureus are dependent on an interaction with GyrB and that their site of interaction with GyrB overlaps the binding site of novobiocin.

Increased susceptibilities of E. coli mutant strains with either improved permeability (impA mutant) or decreased efflux (tolC mutant), and an H. influenzae mutant with decreased efflux (acrA::kan), suggested that permeability and efflux reduce the antibacterial potency of both compounds in these, and perhaps other, gram-negative organisms (Table 4). The improved potency of VRT-752586 versus VRT-125853 against gram-positive bacteria such as staphylococci, enterococci, and streptococci (Table 2) could be attributed, at least in part, to the superior enzymatic potency and dual-targeting properties of VRT-752586 (Table 1). It is also possible that VRT-752586 is better able to permeate or is less prone to efflux in gram-positive bacteria. Susceptibility testing against an S. aureus NorA-overproducing strain, SA-1199B, and a MepA-overproducing strain, SA-K2068, indicated that these particular efflux pumps, implicated in fluoroquinolone resistance (13, 14), do not appreciably recognize VRT-125853 and VRT-752586; the susceptibility of both efflux pump mutant strains was similar to that of the corresponding wild-type parental strains (data not shown). These results do not rule out the possibility that other gram-positive efflux systems are involved in the efflux of our aminobenzimidazole compounds to different degrees. Interestingly, we found that the naturally novobiocin-resistant organism Staphylococcus saprophyticus was susceptible to both VRT-125853 and VRT-752586 (MICs equal to 2 and <0.008 µg/ml, respectively), comparable to what was observed with the other staphylococci tested. The novobiocin MIC for the S. saprophyticus isolate tested was >8 µg/ml. This result indicated that the mechanism of novobiocin resistance in this organism has no effect on its susceptibility to aminobenzimidazole inhibitors.

View this table: [in this window] [in a new window]

TABLE 4. Activities of VRT-125853 and VRT-752586 against gram-negative bacteria

Improved activity of VRT-752586 versus VRT-125853 was also observed for most of the anaerobic and atypical organisms tested (Table 3). Presumably, this finding is also due to the greater enzymatic potency and dual-targeting properties of VRT-752586. Additionally, neither compound had any measurable effect on the growth of Candida albicans up to 64 µg/ml (highest tested concentration), which was used as a convenient indicator of nonspecific eukaryotic toxicity (data not shown).

Activity of aminobenzimidazole compounds against drug-resistant pathogens. Consistent with the novel mechanism of action of VRT-125853 and VRT-752586, susceptibility was unaffected by commonly encountered resistance phenotypes (Tables 2 and 3). Oxacillin-, levofloxacin-, telithromycin-, and vancomycin-resistant S. aureus strains were as susceptible to both compounds as were nonresistant isolates. Amoxicillin, ceftriaxone, azithromycin, and levofloxacin resistance similarly had no effect on the susceptibility of S. pneumoniae. Levofloxacin, linezolid, and vancomycin resistance had no effect on the susceptibility of E. faecalis and E. faecium to VRT-125853 and VRT-752586. In H. influenzae, where for 13 out of 36 isolates the MIC of VRT-752586 was >2 µg/ml, no correlation of ß-lactam resistance with reduced aminobenzimidazole susceptibility was observed. Unlike the multigenerational members of the ß-lactam, macrolide, glycopeptide, and fluoroquinolone antibiotic families, it is anticipated that this new class of aminobenzimidazole antibiotics would not be vulnerable to most of the resistance mechanisms present in current clinical isolates. The finding that the antibacterial activities of VRT-125853 and VRT-752586 were unaffected by fluoroquinolone resistance (Table 2) suggests that fluoroquinolone resistance mutations in GyrA and ParC are far enough removed in the heterotetramer and do not impact the ATP-binding site in GyrB and ParE.

Antimycobacterial activities of VRT-125853 and VRT-752586. VRT-125853 and VRT-752586 were active in vitro against multiple strains of drug-susceptible and -resistant M. tuberculosis (Table 5), suggesting that, similar to fluoroquinolones (8), these aminobenzimidazoles would be effective against current and emerging multidrug-resistant strains. VRT-752586 exhibited limited activity against MAC isolates; VRT-125853 was inactive against all of the MAC isolates tested (Table 5). Similar to other observed antibacterial activities, VRT-752586 had greater potency against M. tuberculosis than did VRT-125853. That the activities of both compounds against M. tuberculosis and MAC isolates (VRT-752586 only) are mediated through inhibition of gyrase remains to be confirmed. Mycobacterial DNA gyrase has been shown to possess both efficient negative supercoiling and decatenase activities in vitro under physiological conditions (18). Given that M. tuberculosis has no distinct topoIV enzyme (18), the improved potency of VRT-752586 cannot be attributed to dual targeting and may result from an ability to permeate, reduced recognition by efflux pumps, or potent inhibition of the bifunctional enzyme in this organism.

View this table: [in this window] [in a new window]

TABLE 5. Activities of VRT-125853 and VRT-752586 against M. tuberculosis and the MAC

Effects of human serum on aminobenzimidazole activity. As an indicator of relative serum-binding potential, compounds were tested in an MIC assay with S. aureus ATCC 29213 in the presence and absence of 50% human serum, similar to the actual serum content of blood. Compound activity in the presence of serum provides an estimation of the amount of unbound compound available to inhibit bacterial growth in human blood. A twofold shift in the VRT-125853 MIC and a 16-fold shift in the VRT-752586 MIC suggested that the latter compound was relatively more highly protein bound by human serum. Regardless of the greater degree of serum binding, the serum-shifted MIC of VRT-752586 still remained below 1 µg/ml. Consistent with reports in the literature (16, 28), in this assay the MIC of novobiocin was shifted greater than 60-fold, confirming previous results showing that novobiocin is highly protein bound in human serum. The clinical relevance of these serum-binding results for VRT-125853 and VRT-752586 remains to be explored by animal efficacy studies.

Spontaneous-resistance frequencies and mutant prevention concentrations (MPCs) of VRT-125853 and VRT-752586. It has been estimated that the bacterial population at a given infection site can reach on the order of 10¹⁰ cells (7). If spontaneous antibiotic-resistant mutants arise during the expansion of an infection, then antibiotic treatment will likely fail to eradicate the infection. To estimate the probability that resistant mutants would arise in a naive population of approximately 10¹⁰ cells, the in vitro frequencies of spontaneous resistance of several relevant pathogens to VRT-125853, VRT-752586, and comparators were measured (Table 6). In general, across the organism panel, the spontaneous-resistance frequencies observed for VRT-125853 and VRT-752586 were comparable to, or in some cases better than, those obtained with novobiocin, ciprofloxacin, and linezolid at similar multiples of their respective MICs (Table 6).

View this table: [in this window] [in a new window]

TABLE 6. Frequencies of spontaneous resistance to VRT-125853 and VRT-752586a

The MPC has recently been suggested as a way to rank antibiotics with regard to the ability to suppress the emergence of resistance during infection (7). The MPC reflects the ability of an antibiotic to block the growth of first-step mutants without regard for whether the mutations cause alterations in the molecular target, drug efflux, drug inactivation, or drug exclusion. Theoretically, if the MPC for an infecting organism is maintained at the infection site, the growth of resistant mutants will be suppressed. In most cases, except for H. influenzae (VRT-125853 and VRT-752586) and S. pneumoniae (VRT-125853 only), the spontaneous-resistance frequencies were approximately <10^–10 at concentrations within eight times the MIC, illustrating favorable MPCs of these compounds for each organism (Table 6). Lower spontaneous-resistance frequencies are consistent with the inhibition of more than one essential target at a given compound concentration. The spontaneous-resistance frequencies of E. faecalis (both compounds) and E. faecium (VRT-752586 only) were below the level of detection at two times the MIC, suggesting the inhibition of more than one target in these organisms. For other organisms, complete suppression of spontaneous emergence of resistance was achieved at higher multiples of the MIC (Table 6). Additional experiments with animal models of infection are necessary to determine whether the MPC for each compound with regard to each organism is achieved at a given site of infection.

Bactericidal activities of VRT-125853 and VRT-752586. All antibiotics are bacteriostatic (i.e., they stop bacterial cell growth); however, some antibiotics also kill bacteria (i.e., they are bactericidal). Bacteriostatic antibiotics require the host's natural defense mechanisms to play a role in completely eradicating the infection, while bactericidal antibiotics are able to clear infections independently of the host's defenses. In the case of immunocompromised host defenses, antibiotics with bactericidal activity are therefore preferred.

The in vitro bactericidal activities of VRT-125853 and VRT-752586 against S. aureus, E. faecalis, S. pneumoniae, and H. influenzae were evaluated in standard time-kill assays. Representative time-kill curves are shown in Fig. 2. Both VRT-125853 and VRT-752586 were found to be bactericidal against all of the strains tested, as defined by a 3-log reduction in the starting inoculum by 24 h (Fig. 2). Interestingly, the rate of killing was fastest for H. influenzae, where a 3-log reduction was observed in 3 to 5 h. While the explanation for this finding is unclear, the rapid bactericidal action against H. influenzae seems to be a property of the aminobenzimidazole class since a similar phenomenon has been observed with other members of the class as well (data not shown). Because the mechanism of action of VRT-125853 and VRT-752586 is inhibition of the ATPase activity of DNA gyrase and topoIV, the rate of killing was not as rapid as that seen with ciprofloxacin (data not shown), a drug which promotes DNA breakage, triggering a rapid cascade of lethal events in the cell (9). Linezolid, as expected, was bacteriostatic against all bacteria except H. influenzae in this assay (data not shown). Consistent with the related mechanism of action, the rate of killing for both VRT-125853 and VRT-752586 was similar to, or slightly faster than, the rate of killing by novobiocin for all of the organisms tested (data not shown).

View larger version (22K): [in this window] [in a new window]

FIG. 2. Bactericidal activities of VRT-125853 and VRT-752586. Cells were cultured as described in Materials and Methods. Cells were grown in the presence of the indicated compound concentrations: , no drug; , 4 times the MIC; x, 8 times the MIC; , 10 times the MIC. MICs (µg/ml) for VRT-125853 and VRT-752586, respectively, were as follows: S. aureus ATCC 29213, 2 and 0.032; S. pneumoniae ATCC BAA255, 0.13 and 0.004; E. faecalis ATCC 29212, 0.5 and 0.016; H. influenzae ATCC 51907, 4 and 1.

Summary. VRT-125853 and VRT-752586 are representatives of a novel aminobenzimidazole class of bacterial topoisomerase inhibitors. Their potent activity against resistant and susceptible staphylococci, enterococci, streptococci, and respiratory gram-negative bacteria (H. influenzae and M. catarrhalis) suggests their potential utility against a variety of both nosocomial and community infections. VRT-125853 and VRT-752586 also showed favorable pharmacokinetic properties in animals and demonstrated efficacy in animal models of infection, supporting their use for skin and skin structure infections, as well as respiratory infections caused by drug-susceptible and -resistant pathogens (unpublished data), thereby making them a promising new class of antibacterials for combating the problem of drug resistance.

 
We thank John Thomson, Eric Olson, Ann Kwong, and Michael Briggs for support and helpful suggestions. We are grateful to Focus Technologies for help in designing and performing the MIC₉₀ studies.

 
* Corresponding author. Mailing address: Vertex Pharmaceuticals, 130 Waverly Street, Cambridge MA 02139. Phone: (617) 444-6252. Fax: (617) 444-6210. E-mail: trudy_grossman{at}vrtx.com.

Present address: Novartis Institutes for BioMedical Research, Inc., Cambridge, Massachusetts.

Top Abstract Introduction Materials and Methods Results and Discussion References

 

1
1. Aspa, J., O. Rajas, F. Rodriguez de Castro, J. Blanquer, R. Zalacain, A. Fenoll, R. de Celes, A. Vargas, F. R. Salvanes, P. P. Espana, J. Rello, and A. Torres. 2004. Drug-resistant pneumococcal pneumonia: clinical relevance and related factors. Clin. Infect. Dis. 38:787-798.[CrossRef][Medline]
2
2. Barrett, C. T., and J. F. Barrett. 2003. Antibacterials: are the new entries enough to deal with the emerging resistance problems? Curr. Opin. Biotech. 14:621-626.[CrossRef][Medline]
3
3. Bellon, S., J. D. Parsons, Y. Wei, K. Haykawa, L. L. Swenson, P. S. Charifson, J. A. Lippke, R. Aldape, and C. H. Gross. 2004. Crystal structures of Escherichia coli topoisomerase IV ParE subunit (24 and 43 kilodaltons): a single residue dictates differences in novobiocin potency against topoisomerase IV and DNA gyrase. Antimicrob. Agents Chemother. 48:1856-1864.[Abstract/Free Full Text]
4
4. Centers for Disease Control and Prevention. 2004. National Nosocomial Infections Surveillance (NNIS) System report, data summary from January 1992 through June 2004, issued October 2004. www.cdc.gov/ncidod/hip/NNIS/2004NNISreport.pdf.
5
5. Champoux, J. J. 2001. DNA topoisomerases: structure, function and mechanism. Annu. Rev. Biochem. 70:369-413.[CrossRef][Medline]
6
6. Deibler, R. W., S. Rahmati, and E. L. Zechiedrich. 2001. Topoisomerase IV, alone, unknots DNA in E. coli. Genes Dev. 15:748-761.[Abstract/Free Full Text]
7
7. Drlica, K. 2001. A strategy for fighting antibiotic resistance. ASM News 67:27-33.
8
8. Ginsburg, A. S., J. H. Grosset, and W. R. Bishai. 2003. Fluoroquinolones, tuberculosis, and resistance. Lancet 3:432-442.
9
9. Gootz, T. D., and K. E. Brighty. 1998. Chemistry and mechanism of action of the quinolone antibacterials, p. 29-80. In V. T. Andriole (ed.), The quinolones, second edition. Academic Press, Inc., New York, N.Y.
10
10. Gross, C. H., J. D. Parsons, T. H. Grossman, P. S. Charifson, S. Bellon, J. Jernee, M. Dwyer, S. P. Chambers, W. Markland, M. Botfield, and S. A. Raybuck. 2003. Active-site residues of Escherichia coli DNA gyrase required in coupling ATP hydrolysis to DNA supercoiling and amino acid substitutions leading to novobiocin resistance. Antimicrob. Agents Chemother. 47:1037-1046.[Abstract/Free Full Text]
11
11. Heisig, P. 2001. Inhibitors of bacterial topoisomerases: mechanisms of action and resistance and clinical aspects. Planta Med. 67:3-12.[CrossRef][Medline]
12
12. Jacobs, M. R. 2003. Worldwide trends in antimicrobial resistance among common respiratory tract pathogens. Pediatr. Infect. Dis. J. 22:S109-S119.[CrossRef][Medline]
13
13. Kaatz, G. W., V. V. Moudgal, S. M. Seo, and J. E. Kristiansen. 2003. Phenothiazines and thioxanthenes inhibit multidrug efflux pump activity in Staphylococcus aureus. Antimicrob. Agents Chemother. 47:719-726.[Abstract/Free Full Text]
14
14. Kaatz, G. W., F. McAleese, and S. M. Seo. 2005. Multidrug resistance in Staphylococcus aureus due to overexpression of a novel multidrug and toxin extrusion (MATE) transport protein. Antimicrob. Agents Chemother. 49:1857-1864.[Abstract/Free Full Text]
15
15. Kato, J.-I., Y. Nishimura, R. Imamura, H. Niki, S. Hiraga, and H. Susuki. 1990. New topoisomerase essential for chromosome segregation in E. coli. Cell 63:393-404.[CrossRef][Medline]
16
16. Kucers, A., S. M. Crowe, M. L. Grayson, and J. F. Hoy (ed.). 1997. The use of antibiotics, 5th edition, p. 663-666. Butterworth-Heinemann, Linacre House, Jordan Hill, Oxford, United Kingdom.
17
17. Livermore, D. M. 2004. The need for new antibiotics. Clin. Microbiol. Infect. 10(Suppl. 4):1-9.
18
18. Manjunatha, U. H., M. Dalal, M. Chatterji, D. R. Radha, S. S. Visweswariah, and V. Nagaraja. 2002. Functional characterization of mycobacterial DNA gyrase: an efficient decatenase. Nucleic Acids Res. 30:2144-2153.[Abstract/Free Full Text]
19
19. Maxwell, A., and D. M. Lawson. 2003. The ATP-binding site of type II topoisomerases as a target for antibacterial drugs. Curr. Top. Med. Chem. 3:283-303.[CrossRef][Medline]
20
20. Morrison, J. F. 1982. The slow-binding, tight-binding inhibition of enzyme catalyzed reactions. Trends Biochem. Sci. 7:102-105.
21
21. Munoz, R., M. Bustamante, and A. G. de la Campa. 1995. Ser-127-Leu substitution in the DNA gyrase B subunit of Streptococcus pneumoniae is implicated in novobiocin resistance. J. Bacteriol. 177:4166-4170.[Abstract/Free Full Text]
22
22. Mutnick, A. H., V. Enne, and R. N. Jones. 2003. Linezolid resistance since 2001: SENTRY Antimicrobial Surveillance Program. Ann. Pharmacother. 37:769-774.[Abstract/Free Full Text]
23
23. National Committee for Clinical Laboratory Standards. 2003. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically, 6th edition, volume 23, number 2. Approved standard M7-A6. National Committee for Clinical Laboratory Standards, Wayne, Pa.
24
24. National Committee for Clinical Laboratory Standards. 2004. Methods for antimicrobial susceptibility testing of anaerobic bacteria, 6th edition, volume 24, number 2. Approved standard M11-A6. National Committee for Clinical Laboratory Standards, Wayne, Pa.
25
25. National Committee for Clinical Laboratory Standards. 2003. Susceptibility testing of mycobacteria, nocardiae, and other aerobic actinomycetes, volume 23, number 18. Approved standard M24-A. National Committee for Clinical Laboratory Standards, Wayne, Pa.
26
26. Pottumarthy, S., T. R. Fritsche, and R. N. Jones. 2005. Comparative activity of oral and parenteral cephalosporins tested against multidrug-resistant Streptococcus pneumoniae: report from the SENTRY Antimicrobial Surveillance Program (1997-2003). Diagn. Microbiol. Infect. Dis. 51:147-150.[CrossRef][Medline]
27
27. Sanchez, L., W. Pan, M. Vinas, and H. Nikaido. 1997. The acrAB homolog of Haemophilus influenzae codes for a functional multidrug efflux pump. J. Bacteriol. 179:6855-6857.[Abstract/Free Full Text]
28
28. Schio, L., F. Chatreaux, V. Loyau, M. Murer, A. Ferreira, P. Mauvais, A. Bonnefoy, and M. Klich. 2001. Fine tuning of physico-chemical parameters to optimise a new series of novobiocin analogues. Bioorg. Med. Chem. Lett. 11:1461-1464.[CrossRef][Medline]
29
29. Stieger, M., P. Angehrn, B. Wohlgensinger, and H. Gmunder. 1996. GyrB mutations in Staphylococcus aureus strains resistant to cyclothialidine, coumermycin, and novobiocin. Antimicrob. Agents Chemother. 40:1060-1062.[Abstract]
30
30. Waites, K. B., L. B. Duffy, T. Schmid, D. Crabb, M. S. Pate, and G. H. Cassell. 1991. In vitro susceptibilities of Mycoplasma pneumoniae, Mycoplasma hominis, and Ureaplasma urealyticum to sparfloxacin and PD127391. Antimicrob. Agents Chemother. 35:1181-1185.[Abstract/Free Full Text]
31
31. Zechiedrich, E. L., A. B. Khodrusky, S. Bachellier, R. Schneider, D. Chen, D. M. J. Lilley, and N. R. Cozzarelli. 2000. Roles of topoisomerases in maintaining steady-state DNA supercoiling in Escherichia coli. J. Biol. Chem. 11:8103-8113.

---

Antimicrobial Agents and Chemotherapy, April 2006, p. 1228-1237, Vol. 50, No. 4
0066-4804/06/$08.00+0     doi:10.1128/AAC.50.4.1228-1237.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

This article has been cited by other articles:

• Ostrov, D. A., Hernandez Prada, J. A., Corsino, P. E., Finton, K. A., Le, N., Rowe, T. C. (2007). Discovery of Novel DNA Gyrase Inhibitors by High-Throughput Virtual Screening. Antimicrob. Agents Chemother. 51: 3688-3698 [Abstract] [Full Text]  
• Grossman, T. H., Bartels, D. J., Mullin, S., Gross, C. H., Parsons, J. D., Liao, Y., Grillot, A.-L., Stamos, D., Olson, E. R., Charifson, P. S., Mani, N. (2007). Dual Targeting of GyrB and ParE by a Novel Aminobenzimidazole Class of Antibacterial Compounds. Antimicrob. Agents Chemother. 51: 657-666 [Abstract] [Full Text]  

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Mani, N. Articles by Grossman, T. H. Search for Related Content PubMed PubMed Citation Articles by Mani, N. Articles by Grossman, T. H.