Abstract
Ciprofloxacin (CIP), a fluoroquinolone antibacterial drug, is widely used in the treatment of serious infections in humans. Its degradation by basidiomycetous fungi was studied by monitoring 14CO2 production from [14C]CIP in liquid cultures. Sixteen species inhabiting wood, soil, humus, or animal dung produced up to 35% 14CO2 during 8 weeks of incubation. Despite some low rates of 14CO2 formation, all species tested had reduced the antibacterial activity of CIP in supernatants to between 0 and 33% after 13 weeks. Gloeophyllum striatum was used to identify the metabolites formed from CIP. After 8 weeks, mycelia had produced 17 and 10% 14CO2 from C-4 and the piperazinyl moiety, respectively, although more than half of CIP (applied at 10 ppm) had been transformed into metabolites already after 90 h. The structures of 11 metabolites were elucidated by high-performance liquid chromatography combined with electrospray ionization mass spectrometry and 1H nuclear magnetic resonance spectroscopy. They fell into four categories as follows: (i) monohydroxylated congeners, (ii) dihydroxylated congeners, (iii) an isatin-type compound, proving elimination of C-2, and (iv) metabolites indicating both elimination and degradation of the piperazinyl moiety. A metabolic scheme previously described for enrofloxacin degradation could be confirmed and extended. A new type of metabolite, 6-defluoro-6-hydroxy-deethylene-CIP, provided confirmatory evidence for the proposed network of congeners. This may result from sequential hydroxylation of CIP and its congeners by hydroxyl radicals. Our findings reveal for the first time the widespread potential for CIP degradation among basidiomycetes inhabiting various environments, including agricultural soils and animal dung.
Being active against many gram-negative and gram-positive pathogenic bacterial species, fluoroquinolones (FQs) have found wide application in human medicine. Ciprofloxacin (CIP [Fig. 1]) is used to treat infections of the urinary, respiratory, and gastrointestinal tracts (23). During its passage through the human body, CIP can be metabolized by sulfation and, to a limited extent, by oxidation of its piperazine moiety (4). Similar metabolites as well as glucuronidation, but not degradation of the heterocyclic core, have been observed in various animal species (4). A significant quantity of an FQ may be excreted unchanged and introduced into the environment through wastewater, predominantly from clinical settings (11). However, CIP and other FQs were shown to be tightly bound by human feces (6, 26) and soil (18, 22, 27), being no longer bioavailable and, hence, are unlikely to exert a significant selection pressure (14, 20, 26, 27). On the other hand, strong binding may delay biodegradation and could partly explain the supposed recalcitrance of FQs (12, 18, 21). Their fate in sewage sludge which, if not burned or deposited in landfills, may be further processed by composting, is unknown.
FIG. 1.
Molecular structure of ciprofloxacin and positions of the 14C label in [4-14C]CIP (∗) and [piperazine-2,3-14C]CIP (+).
Only a few fluorinated aliphatic compounds such as poisonous fluoroacetate occur in some species of plants and streptomycetes. Fluorinated aromatics, as exemplified by FQs, are not found among natural products (10). This raised concern about their biodegradability and environmental impact (21). Recently, we have shown in vitro degradation of the veterinary FQ enrofloxacin (EFL) by basidiomycetes, notably, the brown rot fungus Gloeophyllum striatum as well as three species of white rot fungi (19). G. striatum was most active, evolving up to 50% 14CO2 within 8 weeks from [4-14C]EFL bound to wheat straw. EFL, preadsorbed to agricultural soil, could also be mineralized, although at a much lower rate (19). Metabolites formed from [4-14C]EFL by G. striatum in liquid cultures included various mono- and dihydroxylated congeners as well as compounds indicating the cleavage of both its heterocyclic core and amine moiety (31).
White rot fungi are able to degrade the lignin of woody plant cell walls and, in addition, a broad spectrum of pollutants (2). These activities are attributed to extracellular ligninolytic enzymes such as lignin peroxidase, manganese-dependent peroxidase, and laccase. Such enzymes catalyze degradation via diffusible oxidizing agents, e.g., aryloxy radicals, Mn3+, or specific mediators (4a, 7, 9, 13). In contrast, brown rot fungi appear to preferentially degrade the cellulose and hemicellulose components of wood, while lignin is modified by hydroxylation and demethylation and, to a minor extent, by depolymerization (9). As G. striatum did not exhibit peroxidase or laccase activity, a hydroxyl radical-based degradation mechanism was postulated to be operative (31). The involvement of a Fenton-type reaction in wood degradation was first proposed by Koenigs (17). Hydroxyl radicals were thought to be generated through reduction of hydrogen peroxide by ferrous iron (1, 8, 9, 15, 17) as follows: Fe2+ + H2O2 → Fe3+ + HO· + HO−.
The aim of our study was (i) to assess inactivation and degradation of CIP by G. striatum, (ii) to identify metabolites formed from CIP, verifying and possibly extending the metabolic scheme described for EFL (31), and (iii) to test basidiomycetes inhabiting ecologically relevant sites such as agricultural soils and pastures for FQ degradation potential.
Preliminary results have already been reported ([29, 32]).
MATERIALS AND METHODS
Organisms.
G. striatum DSM 9592, isolated by M. Capelari in May 1992, in Assis, São Paulo, Brazil, served as the primary model organism, while G. striatum DSM 10335 was employed as a reference (19). Cultures of the other species listed in Table 1 were (i) obtained from the Deutsche Sammlung von Mikroorganismen und Zellkulturen, Braunschweig, Germany, (ii) isolated from fruiting bodies collected by M. Stadler (strain designation, WP), or (iii) provided by W. Fritsche, Jena, Germany (Agrocybe praecox P1). A taxonomic evaluation of the latter strains will be reported elsewhere (24).
TABLE 1.
Degradation of ciprofloxacin in various taxonomic groups of basidiomycota
Order | Family | Genus and species | Strain | Habitat | Cumulative 14CO2 production (%)c after indicated week from:
|
Residual antibacterial activity (%)a | |||||
---|---|---|---|---|---|---|---|---|---|---|---|
[4-14C]CIP
|
[Piperazine-2,3-14C]CIP
|
||||||||||
2 | 4 | 8 | 2 | 4 | 8 | ||||||
Agaricales | Bolbitiaceae | Agrocybe praecox | P1 | Litter, soil | 0.8 ± 0.1 | 1.3 ± 0.1 | 1.6 ± 0.1 | 9.5 ± 7.1 | 19.6 ± 6.2 | 27.3 ± 4.2 | ND |
Strophariaceae | Nematoloma frowardii | DSM 11239 | Wood | 3.5 ± 1.5 | 6.3 ± 2.1 | 9.0 ± 1.8 | 13.9 ± 2.9 | 23.5 ± 0.6 | 30.3 ± 2.1 | ND | |
Panaeolus sphinctrinus | DSM 3356 | Dung | 0.6 ± 0.4 | 0.6 ± 0.4 | 0.7 ± 0.5 | 1.6 ± 0.1b | 2.0 ± 0.3 | 2.2 ± 0.4b | 33 ± 21 | ||
Psilocybe cubensis | DSM 8304 | Dung | 2.5 ± 1.8 | 3.2 ± 1.8 | 4.2 ± 1.9 | 5.3 ± 4.6 | 6.9 ± 5.7 | 9.0 ± 7.1 | 12 ± 9 | ||
Stropharia rugosoannulata | DSM 9616 | Soil, litter | 0.5 ± 0.1 | 0.7 ± 0.1 | 1.2 ± 0.4 | 3.3 ± 1.3b | 4.4 ± 1.6 | 4.9 ± 1.7b | 21 ± 14 | ||
Stropharia rugosoannulata | DSM 11372 | Soil, litter | 0.7 ± 0.4 | 1.5 ± 0.2 | 1.9 ± 0.3 | 5.4 ± 1.7 | 8.1 ± 4.4 | 8.7 ± 5.1 | 3.6 ± 0.5 | ||
Tricholomataceae | Clitocybe odora | WP 0478 | Humus | 13.4 ± 4.6 | 21.3 ± 4.7 | 24.3 ± 4.5 | 18.8 ± 10.9 | 29.8 ± 18.5 | 33.1 ± 20.1 | 0.0 | |
Clitocybula dusenii | DSM 11238 | Wood | 7.4 ± 0.7 | 8.7 ± 0.8 | 9.5 ± 0.9 | 16.5 ± 5.0 | 20.1 ± 4.3 | 24.1 ± 4.3 | ND | ||
Hohenbuehelia rickenii | WP 0715 | Wood | 0.3 ± 0.1 | 0.6 ± 0.1 | 0.9 ± 0.3 | 2.5 ± 0.1 | 3.4 ± 0.5 | 4.1 ± 1.1 | 19 ± 9 | ||
Cantharellales | Hydnaceae | Hydnum repandum | WP 0492 | Mycorrhiza | 0.5 ± 0.2 | 1.3 ± 0.7 | 2.3 ± 1.5 | 4.0 ± 1.2 | 4.4 ± 1.3 | 4.6 ± 1.3 | 16 ± 13 |
Nidulariales | Nidulariaceae | Cyathus stercoreus | DSM 1674 | Dung | 1.9 ± 1.3 | 2.4 ± 1.6 | 5.3 ± 3.2 | 11.3 ± 1.5 | 15.6 ± 3.2 | 19.3 ± 4.5 | ND |
Poriales | Coriolaceae | Bjerkandera adusta | DSM 4708 | Wood | 6.2 ± 1.5 | 6.4 ± 1.7 | 6.6 ± 1.9 | 17.9 ± 2.1 | 20.1 ± 3.3 | 22.1 ± 4.4 | ND |
Coriolopsis rigida | DSM 9596 | Wood | 3.2 ± 2.0 | 4.8 ± 2.3 | 5.6 ± 2.4 | 17.6 ± 5.4 | 23.6 ± 6.6 | 30.4 ± 6.2 | ND | ||
Gloeophyllum trabeum | DSM 3087 | Wood | 7.2 ± 2.1 | 10.4 ± 1.6 | 17.4 ± 2.1 | 5.6 ± 1.4 | 7.5 ± 1.5 | 10.6 ± 1.8 | ND | ||
Trametes versicolor | DSM 11269 | Wood | 4.0 ± 0.6 | 4.7 ± 0.7 | 4.9 ± 0.7 | 24.0 ± 1.9 | 31.5 ± 3.2 | 35.3 ± 4.5 | 2.0 ± 1.1 | ||
Stereales | Meruliaceae | Phanerochaete chrysosporium | DSM 9620 | Wood | 1.3 ± 1.5 | 1.8 ± 2.4 | 2.0 ± 2.7 | 1.6 ± 1.5 | 2.4 ± 2.0 | 3.3 ± 2.4 | ND |
Percentage of the initial CIP concentration (10 ppm) present after 13 weeks; results should be classified apparent because neither unspecific binding of CIP to mycelia nor the absence of endogenous antibacterial activity in fungal species was assessed. ND, not done.
If the inoculum had been precultured for 14 days instead of 7 days, up to threefold activity would have been observed.
Values given are the means ± standard deviations of results from three or (mostly) four replicate cultures.
Culture conditions.
Media and culture conditions enhancing FQ degradation were identical to those reported previously (31), except that the concentration of Mn2+ in mineral medium was increased from 2 to 20 μM (except for G. striatum). Briefly, the organisms were precultured unagitated in 30 ml of malt medium at room temperature for 7 days. Then, mycelia were washed and transferred into a defined mineral medium devoid of carbon, nitrogen, and phosphate at substrate concentrations.
Ciprofloxacin and reference compounds.
The chemical structure of CIP [1-cy-clopropyl-7-(1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid], including the positions of 14C labeling, is shown in Fig. 1. The nonlabeled standard compound had a chemical purity of >99.9%. Chemically synthesized references (Table 2) were kindly provided by W. Hallenbach and U. Petersen (Bayer AG, Leverkusen, Germany). [4-14C]CIP was synthesized by R. Koch (Bayer Corp., Stilwell, Kans.), and [piperazine-2,3-14C]CIP was synthesized by M. Conrad (Bayer AG, Wuppertal, Germany). Both compounds were purified immediately before use by R. Thomas (Bayer AG, Wuppertal). The specific activities of [4-14C]CIP-hydrochloride and [piperazine-2,3-14C]CIP-hydrochloride were 6.13 and 6.96 MBq/mg, while their radiochemical purities were >97% and >99%, respectively, as determined by high-performance liquid chromatography (HPLC).
TABLE 2.
Nomenclature of metabolites generated from ciprofloxacin by G. striatum
Desig-nationa | Chemical name |
---|---|
F-1 | 1-Cyclopropyl-7-(1-piperazinyl)-6-fluoro-3-hydroxy-1H-quinoline-4-one |
F-2 | 1-Cyclopropyl-7-(1-piperazinyl)-1,4-dihydro-6-hydroxy-4-oxo-3-quinolinecarboxylic acid |
F-3 | 1-Cyclopropyl-6-(1-piperazinyl)-5-fluoro-1H-indole-2,3-dione |
F-4b | 1-Cyclopropyl-7-[(2-aminoethyl)-amino]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid |
F-5 | 1-Cyclopropyl-7-(1-piperazinyl)-1,4-dihydro-6,8(5,6)-dihydroxy-4-oxo-3-quinolinecarboxylic acid |
F-6 | 1-Cyclopropyl-7-(1-piperazinyl)-6-fluoro-1,4-dihydro-8-hydroxy-4-oxo-3-quinolinecarboxylic acid |
F-7 | 1-Cyclopropyl-7-(1-piperazinyl)-6-fluoro-1,4-dihydro-5,8-dihydroxy-4-oxo-3-quinolinecarboxylic acid |
F-8b | 1-Cyclopropyl-6-fluoro-1,4-dihydro-7,8-dihydroxy-4-oxo-3-quinolinecarboxylic acid |
F-9b | 7-Amino-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid |
F-10b | Piperazine |
F-12 | 1-Cyclopropyl-7-[(2-aminoethyl)-amino]-1,4-dihydro-6-hydroxy-4-oxo-3-quinolinecarboxylic acid |
The F annotation, introduced for metabolites generated from EFL (31), was also applied to CIP to facilitate comparison.
A chemically prepared reference compound is available.
Experimental procedures.
Test system A, which was described in detail before (31), was employed during screening for degradation of CIP. G. striatum had a concentration of approximately 2 mg (dry weight) of mycelium per ml. For all other organisms, the mycelial mass obtained after 7 days of growth in malt broth was washed and transferred into mineral medium. Each flask received either [4-14C]CIP (7.3 kBq) or [piperazine-2,3-14C]CIP (9.3 kBq), which was supplemented with nonlabeled drug to give a final concentration of 10 ppm. All experiments were carried out at room temperature in the dark to prevent photodegradation of CIP.
Test system B was utilized to produce metabolites (31). Each 250-ml Erlenmeyer flask contained 30 ml of mineral medium, G. striatum DSM 9592 (as mentioned above), and 900 μg of CIP, 14C labeled with 400.6 or 890.3 kBq of [4-14C]CIP or [piperazine-2,3-14C]CIP, respectively. The vessels were kept at 150 rpm. Produced 14CO2 was trapped in NaOH and determined by liquid scintillation counting as described before (31). For structure elucidation, four supernatants of 90-h-old cultures containing [4-14C]CIP were combined and lyophilized. After resuspension in 2 ml of water, this preparation was fractionated by micropreparative HPLC.
Analytical and micropreparative HPLC.
HPLC was performed as described previously (31), although the gradients had to be modified. The eluent was composed of 0.1 mM ammonium formate in 1% formic acid (component A) and acetonitrile (component B). For analytical purposes, gradient method I was employed as follows. Starting at 100% A for 2 min, A was linearly decreased to 94% over 5 min and then to 88% over a further 10 min. Thereafter, A was kept constant for 15 min and then decreased to 72% over 5 min and, finally, to 0% over 10 min. Method II was used for micropreparative isolation of metabolites. Component A contained an additional 1% (vol/vol) 2-propanol. After 2 min, A was decreased to 97% over 3 min and then to 90% over 20 min. Following a decrease to 87% over 18 min, A was reduced to 68% over 10 min and to 0% over 7 min. In order to separate metabolite F-6 from CIP, method II was modified, giving method III, as follows. First, the column temperature was reduced from 30 to 9°C. After 2 min, A was successively decreased to 94% over 3 min, to 92% over 10 min, to 82% over 55 min, to 70% over 10 min, and to 0% over 10 min. The flow rate was 1 ml/min.
Purification and derivation of F-10.
A solid-phase cartridge containing 400 mg of Adsorbex SPE-RP18 (particle size, 40 to 63 μm; Merck, Darmstadt, Germany) was conditioned by washing it twice with 5 ml of methanol followed by 5 ml of 1% aqueous formic acid. Five milliliters of supernatant from a culture of G. striatum degrading [piperazine-2,3-14C]CIP was passed through this device. The effluent volume (containing F-10) was reduced to about 100 μl by freeze drying. To this preparation, 20 μl of borate buffer pH 9.2 (Merck) was added, followed by 50 μl of 0.5% (wt/vol) 2,4-dinitro-1-fluorobenzene in acetonitrile. This solution was incubated at 95°C for 5 min.
Other analytical techniques.
HPLC-electrospray ionization mass spectrometry (HPLC-MS), 1H nuclear magnetic resonance spectroscopy (1H-NMR), and liquid scintillation counting were performed as described in reference 31. High-resolution electrospray mass spectrometry (HR-ESI-MS) was performed on a MAT 900 mass spectrometer (Finnigan-MAT, Bremen, Germany) operated at a resolution of 6,000 (10% valley definition) applying the peak matching mode. The spray needle voltage was 3.8 kV. Nitrogen at 100 kPa served as sheath gas. The capillary was held at 250°C. Samples spiked with the calibration standard, polypropylene glycol 425 (Sigma-Aldrich Chemie, Deisenhofen, Germany), were delivered at a flow rate of 10 μl/min by an infusion pump (no. 22; Harvard Apparatus, Inc., South Natick, Mass.).
Residual antibacterial activity.
Activity of CIP in supernatants of liquid cultures was determined by an agar diffusion procedure with Balanced Sensitivity Test Agar (Difco, Augsburg, Germany) and Escherichia coli ATCC 8739 (MIC, = 0.015 μg of CIP/ml) as the test organism. Samples of 0.1 ml, drawn from quadruplicate cultures of selected fungal strains (Table 1), were transferred into agar wells (diameter, 9.5 mm). Five replicate serial dilutions of a CIP standard were used to construct a reference curve correlating the concentration of CIP (0.05 to 10 μg/ml) with the respective zone of growth inhibition (11 to 34 mm) after 20 h at 37°C.
RESULTS
Kinetics of 14CO2 formation from [14C]CIP.
Precultured mycelia of G. striatum DSM 9592 were resuspended in a defined mineral medium containing 10 ppm CIP 14C labeled either at C-4 or the piperazine moiety (Fig. 1). After 8 weeks, 17.0% ± 2.1% and 10.1% ± 1.0% 14CO2 were produced from both label positions, respectively (Fig. 2). The kinetics were similar to those determined for EFL (31). Cultures of G. striatum DSM 10335 evolved 10.6% ± 3.8% and 7.2% ± 0.6% 14CO2 from the respective compounds. Other species of basidiomycetes, inhabiting either wood, humus, agricultural soils, pastures, or even cattle dung, had formed between 0.7 and 24.3% 14CO2 from [4-14C]CIP after 8 weeks, while 2.2 to 35.3% 14CO2 had been produced from [piperazine-2,3-14C]CIP (Table 1). Despite the relatively small amounts of 14CO2 evolved by some species, all those tested had lowered the apparent residual antibacterial activity of CIP in supernatants to between 0 and 33% ± 21% after 13 weeks (Table 1). Most remarkably, CIP was completely inactivated by the soil-inhabiting fungus Clitocybe odora.
FIG. 2.
Total 14CO2 production from [14C]CIP by G. striatum DSM 9592 (○, □) and DSM 10335 (▵, ◊). Mycelia were incubated in a defined mineral medium containing 10 ppm CIP labeled either at C-4 (○, ▵) or at the piperazine moiety (□, ◊). Values given are the means ± standard deviations for quadruplicate cultures.
Metabolites in supernatants of G. striatum.
Typical HPLC elution profiles obtained from cultures of G. striatum DSM 9592 degrading either [4-14C]CIP or [piperazine-2,3-14C]CIP are shown in Fig. 3. Identical profiles were found for G. striatum DSM 10335 (data not shown). A reference profile, already reported for EFL (31), was included (Fig. 3C) to facilitate a provisional assignment of the metabolites. Molecular weights of major metabolites were determined by HPLC-MS (Table 3) and are also included in Fig. 3. An overall similarity in the profiles is obvious, although the peaks of metabolites generated from CIP were shifted toward the more polar side of the gradient. However, metabolite F-8 had a similar retention time and an identical molecular weight, regardless of whether its source had been CIP or EFL. F-8 was absent from the HPLC trace when piperazine-labeled CIP was used as the substrate (Fig. 3, trace A). Again, a broad, tailing, and oversized peak (designated F-10) appeared at the front of trace A. F-10 was retained by adsorption to the solid-state scintillator of the detector cell, thereby causing such an artificially enlarged signal (31). Micropreparative separation of F-10 and subsequent liquid scintillation counting of the fractions indicated that F-10 accounted for approximately 23% of the initially applied radioactivity.
FIG. 3.
HPLC profiles of 90-h-old supernatants of cultures of G. striatum degrading [piperazine-2,3-14C]CIP (A) and [4-14C]CIP (B). A profile of congeners of [4-14C]EFL (C) was included as a reference (see reference 31; Fig. 4, trace A). Molecular weights of metabolites derived from CIP ought to be reduced by 28, due to the absence of an ethyl group in its piperazine substituent. Note that metabolite F-8 was detected in traces B and C but was absent in trace A (arrow).
TABLE 3.
HPLC retention times, pseudomolecular ions in HPLC-MS, and characteristics of the UV absorption spectra of [4-14C]ciprofloxacin and metabolites
Characteristic | Value for:
|
|||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
CIP | F-1 | F-2 | F-3b | F-4 | F-5 | F-6 | F-7 | F-8 | F-9 | F-10 | F-12b | |
Retention timea (min) | 25.9 | 14.3 | 17.7 | 21.4 | 22.2 | 25.9 | 36.1 | 38.1 | 39.1 | 2.2c | ||
Pseudomolecular iond [M + H]+ (m/z) | 332 | 304 | 330 | 290 | 306 | 346 | 348 | 364 | 280 | 263 | 253e | 304 |
UV absorption (nm) | ||||||||||||
λmax (major) | 278 | 268 | 278 | 278 | 289 | 242 | 358 | 272 | 272 | |||
λmax (minor) | 327, 316 | 337 | 346 | 338 | 260 | 331 | 267 | 250, 328 | 298 | |||
Shoulder | 330 | 270 |
Determined by HPLC method I.
Not detectable by HPLC with either UV or radioactivity detection.
Data derived from [piperazine-2,3-14C]CIP.
[M + H]+ was accompanied by [M + 2 + H]+ resulting from the 14C label.
2,4-Dinitrophenyl derivative; [M + H]+ was accompanied by [M + 2 + H]+ and [M + 4 + H]+ as well as intense cluster ions [M + H + CH3CN]+ m/z 294 and [M + H + 2 × CH3CN]+ m/z 335, each showing the isotope pattern mentioned before.
HPLC profiles of 90-h-old supernatants of G. striatum revealed six further major metabolites (Fig. 3). F-1, F-2, and F-4 had reached maximum concentrations (13% ± 2%, 8% ± 1%, and 9% ± 1%, respectively; values are means ± ranges for five independent cultures) already at 72 h after the shift of mycelia from malt into mineral medium. Half-maximal concentrations were attained at around 40 h. However, metabolites F-5, F-7, and F-8 were not readily detected before 48 h and reached their maximum concentrations of 3% (F-8) to 5% (F-5) at 90 h. Hence, an incubation time of 90 h was used to produce the quantity of metabolites needed for structure elucidation. HPLC-MS analysis of the asymmetric peak assigned to CIP (Fig. 3) indicated the presence of an additional compound, F-6 (see below). CIP and F-6 could not be separated under analytical HPLC conditions; after 1, 2, and 3 weeks, the peak area accounted for 10 to 36%, 1 to 15%, and 0 to 3% of the initially applied radioactivity (with six cultures), respectively. Hence, quantitative transformation of CIP into metabolites was attained after about 3 weeks.
Nonspecific binding of 14C label to mycelia of G. striatum was assessed by generating a series of balances for radioactivity. As observed with EFL (31), recoveries were close to 100% throughout; therefore, the results are not shown in detail. For example, in 90-h-old cultures, the amounts of 14C recorded as (i) nonspecifically bound to mycelium, (ii) liberated as 14CO2, and (iii) remaining in the supernatant, were 8.0% ± 0.9%, 2.6% ± 1.4%, and 91.8% ± 3.8%, respectively (means ± standard deviations for three cultures). This demonstrates almost full bioavailability of CIP and its congeners under our experimental conditions.
Structure determination.
Major metabolites were isolated from supernatants of cultures of G. striatum DSM 9592 in which [4-14C]CIP had been degraded. Their systematic names are given in Table 2; chemical structures are shown in Fig. 4. Retention times, pseudomolecular ions, and characteristics of their UV absorption spectra are compiled in Table 3. Metabolites were assigned to four categories as follows.
FIG. 4.
Proposed network of metabolites generated from CIP by the brown rot fungus G. striatum. Primary hydroxylation of CIP at one of several alternative sites initiates four principal degradation routes (A through D). Further hydroxylation of congeners leads to an extensive branching of those routes. Tentatively identified trace metabolites, detected only by HPLC-MS, were included at reduced size. Metabolite F-12 links routes B and D because it could have been formed in both reaction sequences.
(i) Monohydroxylated congeners.
Metabolites F-1 and F-2 (Table 2) were first characterized by their UV spectra and molecular weights, 303 and 329, respectively (Table 3). The 1H-NMR spectrum of F-1 showed a set of signals which was almost identical to those of CIP, except for an upfield shift of the signal of H-2 (Table 4). This indicated the replacement of the carboxyl group with a hydroxyl group (31). The 1H-NMR spectrum of F-2 (Table 4) revealed singlets of H-5 and H-8, proving the elimination of fluorine (Fig. 4). To isolate F-6 (Table 2) by HPLC, the elution gradient had to be run at lowered temperature. Characteristic UV absorption maxima of F-6, at 242 and 331 nm (Table 3), were almost identical to those observed with F-6 derived from EFL (31). The molecular weight of F-6, 347 (Table 3), suggested monohydroxylation. Its 1H-NMR spectrum contained only one doublet with an H,F coupling constant (J = 11.3 Hz), indicating a proton in the ortho position to fluorine (Table 4). Therefore, hydroxylation had occurred at C-8 (Fig. 4).
TABLE 4.
1H-NMR data for ciprofloxacin and hydroxylated metabolitesa
Proton(s)b | CIP
|
F-1
|
F-2
|
F-6
|
F-12
|
F-5
|
|||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
δ (ppm) | Integral | Multi-plicity | J (Hz) | δ (ppm) | Integral | Multi-plicity | J (Hz) | δ (ppm) | Integral | Multi-plicity | δ (ppm) | Integral | Multi-plicity | J (Hz) | δ (ppm) | Integral | Multi-plicity | δ (ppm) | Integral | Multi-plicity | |
CH2 (cyclopropyl) | 1.26 | 2 | m | 1.21 | 2 | m | 1.25 | 2 | m | 1.22 | 2 | m | 1.21 | 2 | m | 1.21 | 2 | m | |||
CH2 (cyclopropyl) | 1.52 | 2 | m | 1.46 | 2 | m | 1.52 | 2 | m | 1.39 | 2 | m | 1.47 | 2 | m | 1.40 | 2 | m | |||
CH2 (piperazine, H-3′) | 3.53 | 4 | m | 3.50 | 4 | m | 3.53 | 4 | m | 3.45 | 4 | m | 3.58 | 4 | m | ||||||
CH2 (ethylidene, H-3′) | 3.44 | 2 | t | ||||||||||||||||||
CH2 (piperazine, H-2′) | 3.75 | 4 | m | 3.60 | 4 | m | 3.71 | 4 | m | 3.55 | 4 | m | 3.67 | 4 | m | ||||||
CH2 (ethylidene, H-2′) | 3.81 | 2 | t | ||||||||||||||||||
CH (cyclopropyl) | 3.89 | 1 | m | 3.84 | 1 | m | 3.89 | 1 | m | 4.53 | 1 | m | 3.81 | 1 | m | 4.21 | 1 | m | |||
H-8 | 7.71 | 1 | d | 7.0c | 7.62 | 1 | d | 7.5c | 7.69 | 1 | s | 7.21 | 1 | s | 7.29d | 1 | s | ||||
H-5 | 8.14 | 1 | d | 12.5c | 8.00 | 1 | d | 12.5c | 7.80 | 1 | s | 7.75 | 1 | d | 11.3c | 7.61 | 1 | s | |||
H-2 | 9.14 | 1 | s | 8.49 | 1 | s | 9.04 | 1 | s | 9.14 | 1 | s | 8.92 | 1 | s | 8.78 | 1 | s |
Spectra were determined at 500 MHz in 50% trifluoroacetic acid-d1 in D2O; acetone was used as an internal standard (δ = 2.16 ppm). Multiplicities are abbreviated as follows: s, singlet; d, doublet; t, triplet; m, multiplet.
Positioning was as shown in Fig. 1.
JH,F.
Alternatively H-5; data do not permit an unequivocal assignment.
(ii) Dihydroxylated congeners.
Metabolites F-5 and F-8 (Table 2) had molecular weights of 345 and 279, respectively (Table 3). The 1H-NMR spectrum of F-5 contained only two singlets, one of H-2 and another (7.29 ppm) which could have been derived from either H-5 or H-8. Both moieties, piperazinyl and cyclopropyl, were also detected (Table 4). Hence, two alternative structures were feasible, either a 5,6-dihydroxylated or a 6,8-dihydroxylated congener (Fig. 4), as observed for EFL (31). The 1H-NMR spectrum of F-8 was devoid of signals of the piperazinyl moiety. Furthermore, signals of H-2, H-5, and the cyclopropyl group showed chemical shifts and multiplicities identical to those of the reference compound (data not shown). Identification of F-7 (Table 2), due to its instability under our analytical conditions, had to be based on molecular weight (373, suggesting dihydroxylation) and UV absorption spectrum (Table 3). The latter was almost identical to the spectrum observed for F-7 of EFL (31), suggesting identical substitution patterns of both heterocyclic cores.
(iii) Isatin-type congener.
F-3 was present in supernatants at a low concentration, as observed before with EFL (31). However, it could be identified by its ion m/z 290, which was accompanied by m/z 292 generated from [4-14C]CIP (Table 3), as well as by m/z 292 plus 294, if [piperazine-2,3-14C]CIP had served as the substrate. Furthermore, these ions were detected at a relative retention time (between F-2 and F-4) similar to that observed for F-3 derived from EFL and moxifloxacin (30, 31).
(iv) Metabolites indicating either elimination or oxidation of the piperazine moiety.
Due to its polarity, F-10 (piperazine) was hardly retained by the HPLC column. However, piperazine derivatized to give 2,4-dinitro-1-(1-piperazinyl)-benzene was eluted at 20.8 min and could be identified by HPLC-MS. Hence, F-10 was purified from a culture containing degraded [piperazine-2,3-14C]CIP by removing all other major metabolites by solid-phase extraction. After derivation of F-10, the products comprised an ion at m/z 253, which was accompanied by a specific ion pattern (253/255/257 = 10:1:3) caused by the ratio of 12C and 14C atoms (either zero, one, or two) contained in the piperazine moiety. A corresponding pattern was found in [piperazine-2,3-14C]CIP at m/z 332, 334, and 336, proving that F-10 was a specific derivative thereof. Other polar metabolites were not detected. Metabolites F-4 and F-9 (Table 2) were identified by cochromatography by using synthetically prepared reference compounds as standards (Table 3).
A new metabolite, F-12 (Table 2), reached only a low concentration in supernatants. However, after purification, a 1H-NMR spectrum was obtained (Table 4). It contained three singlets (H-2, H-5, and H-8), the latter ones indicating elimination of fluorine. Furthermore, the integral for methylene groups assigned to the piperazinyl moiety was reduced from 8 to 4 (Table 4), in accordance with the elimination of one ethylidene bridge. This was in agreement with its molecular formula, C15H17N3O4, determined by HR-ESI-MS; the measured mass of [M + H]+, m/z 304.1296, closely matched the theoretical value of 304.1297. The resulting structure is shown in Fig. 4.
Metabolites at trace concentrations.
Due to their extremely low concentrations, five additional metabolites of CIP could be detected by HPLC-MS only. All had retained both types of 14C labels and showed specific patterns of pseudomolecular ions. Their hypothetical structures are included in Fig. 4. Oxidative decarboxylation of F-2, F-4, and F-5 would give rise to molecular weights of 301, 277, and 317, respectively. Hydroxylation of F-1 and F-4 at either position C-5 or C-8 would generate molecular masses of 319 and 321 Da, respectively.
DISCUSSION
G. striatum and other species of basidiomycetes indigenous to agriculturally relevant sites were shown to degrade CIP in liquid cultures. The actual extent of inactivation, with G. striatum, for example, could be related to either (i) the amount of 14CO2 produced, e.g., 17% from [4-14C]CIP within 8 weeks, or (ii) the residual concentration of CIP, e.g., at the time of harvest, 90 h. At that point, identified metabolites represented at least 50% of the applied 14C label. Thirdly, for selected species, residual antibacterial activity in supernatants was directly measured by employing an agar diffusion assay (see below).
Rate and extent of 14CO2 production from [4-14C]CIP by G. striatum were apparently twice as high as those from [piperazine-2,3-14C]CIP. The piperazine moiety contains two equivalent ethylidene bridges which are most likely targeted with similar probability. Because the 14C label is located exclusively at positions C-2′ and C-3′ (Fig. 1), produced 14CO2 represents only half of the total ethylidene groups degraded. This explains why metabolite F-4 is detectable at approximately half the relative peak area (compared, e.g., with F-2) in HPLC profiles obtained from supernatants containing degraded [piperazine-2,3-14C]CIP (Fig. 3, traces A and B; see also in reference 31, Fig. 4, traces A and C). Therefore, the rates of 14CO2 formation from C-4 and piperazine-labeled CIP actually indicate that both parts of the molecule, the heteroaromatic core and the aliphatic substituent, were degraded by G. striatum at approximately the same rate.
Identification of metabolites and proposed metabolic scheme.
HPLC profiles of metabolites present in 90-h-old supernatants of cultures of G. striatum (Fig. 3) resembled profiles observed for EFL (31), although metabolite peaks were shifted toward lower retention times. One metabolite was common to CIP and EFL, F-8 (Fig. 4), which had lost its amine moiety (Fig. 3, traces B and C). The turnover of CIP could not be followed directly because, under analytical HPLC conditions, a major metabolite, F-6, was not separable. However, after about 3 weeks, CIP was almost quantitatively transformed into congeners. After purification, metabolites were characterized by combining cochromatography, UV spectroscopy, HPLC-MS, and 1H-NMR spectroscopy. The molecular structures of 6 of 11 metabolites (F-1, F-2, F-4, F-5, F-6, and F-12) were proved by complete 1H-NMR spectra.
The metabolic scheme depicted in Fig. 4 shows four principal degradation routes (A through D) which, due to similar concentrations of primary metabolites (F-1, F-2, F-6, and F-4), appear to be simultaneously employed. They may reflect different sites of initial attack of CIP by hydroxyl radicals. Either reaction, i.e., oxidative decarboxylation, defluorination, hydroxylation at C-8, or oxidation of the amine moiety, will terminate antibacterial activity of CIP (4, 5, 31, 33). Because each primary metabolite offers several sites for further attack, an extensive branching of the basic routes can be expected, resulting in a network of metabolites. Dihydroxylated metabolites, contained in routes A, B, and C, were quite unstable. Tentatively identified trace metabolites (included in Fig. 4) could have been generated either by one-step reactions from firmly identified congeners of CIP or by alternative reaction sequences.
An isatin-type derivative, F-3, proved the elimination of C-2 and suggested an intermittent cleavage of the heterocyclic core of CIP. Isatin is a known intermediate in fungal degradation pathways for indole and tryptophan. Its multiple effects on fungal metabolism have been reviewed previously (16). Hydroxylation of F-6 at C-7 caused elimination of the piperazine moiety, F-10. Such elimination is also feasible for several other metabolites, which may explain the concentration of 23% detected for F-10 at 90 h. Therefore, F-10 was an important indicator of CIP inactivation, compared with approximately 3% 14CO2, which had been formed from [4-14C]CIP at that time. Metabolites homologous to F-4 and F-9 are common in mammals (4). Recently, a variety of soil microbes was also demonstrated to produce F-9 from danofloxacin (3). Such metabolites were reported to have a residual antibacterial activity on the order of ≤3% compared with CIP (4, 33). Hence, they are also important indicators of inactivation of FQs. Most notably, metabolite F-12 was identified here for the first time. It may be formed from F-4 by hydroxylation or from F-2 in a multistep oxidation process. Therefore, it links the principal degradation routes B and D. Overall, the proposed metabolic scheme closely resembles those proposed for EFL and moxifloxacin (30, 31). Our results may further strengthen the hypothesis that brown rot fungi such as G. striatum are able to perform Fenton’s reaction in order to produce hydroxyl radicals (8, 9, 15, 17). Other mechanisms employed by bacteria and fungi in aerobic degradation of N-heterocyclic compounds have been discussed before (31).
Approaching field conditions from in vitro experiments.
Drug residues, excreted by patients under FQ therapy, enter the environment via wastewater (11) and, theoretically, by processed sewage sludge. Unspecific binding to feces (6, 26) and soils (18, 22) restricts the mobility of FQs in the environment and greatly reduces their bioavailability (20, 27). At present, it is unknown whether FQs are degraded during anaerobic and, more specifically, aerobic process steps in sewage sludge treatments. However, FQ degradation is likely to occur during composting procedures. Our screening experiments demonstrated that coprophilous basidiomycetes, such as Cyathus stercoreus, as well as six species inhabiting various soil compartments, have the potential to degrade CIP. All species evolved 14CO2 from CIP labeled at either C-4 or the piperazine moiety. Standard deviations indicated considerable variation in the performance of individual cultures. Moreover, the variable activities between species most likely reflected inappropriate culture conditions rather than principally different degradation potentials. Certainly, the specificity of some relatively low activities needs to be confirmed, after improved culture conditions have become available; such work is currently in progress (28). Despite these reservations, a high inactivation potential for CIP was present in all basidiomycetes tested. Notably, no residual antibacterial activity remained in the supernatant of C. odora after 13 weeks (Table 1). In more recent studies, a residual activity of ≤1% has been determined in 4-week-old cultures of G. striatum DSM 9592 decomposing EFL (28).
High degradation activity for [piperazine-2,3-14C]EFL has recently been found in a population of microorganisms indigenous to rotting wheat straw, which was obtained from an agricultural field. In contrast, degradation of the core of FQs may proceed at a rate resembling turnover rates of the humus matrix (28, 33). Appropriate rates have been observed with EFL and [2-14C]sarafloxacin in agricultural soils (18, 19, 27, 33). Obviously, the piperazine label had a much higher diagnostic potential as an indicator of both inactivation and degradation (33). Wood-rotting fungi play an essential role in the global carbon cycle in degrading lignocellulose, including substances bound to such matrices. G. striatum served as our first model organism in FQ degradation (19, 29–31). Basidiomycetes resembling wood-rotting species in showing lignocellulose degradation were first isolated from aging cattle dung (34, 35). Relatively little is known about similar species from agricultural soils and plant litter (25). In the present study, a few such species were shown to have the potential to degrade even the heterocyclic core of CIP. Just recently, other groups of soil microorganisms, including bacteria, a yeast, and molds, have been reported to degrade the amine moiety of danofloxacin (3). Curvularia lunata, an imperfect ascomycete, even produced 14CO2 from [2-14C]danofloxacin (3). Most likely, such microbes are present at agricultural sites, onto which humus produced from sewage sludge might be spread as fertilizer. Taken together, these results indicate the presence of a broad inactivation potential for FQs in nature.
ACKNOWLEDGMENTS
We thank our colleagues at various chemistry departments at Bayer for providing the labeled and nonlabeled standard compounds and S. Ochtrop, A. Gerhardt, and J. Schneider for excellent technical assistance.
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