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Journal of Venomous Animals and Toxins including Tropical Diseases

versão On-line ISSN 1678-9199

J. Venom. Anim. Toxins incl. Trop. Dis vol.16 no.4 Botucatu  2010

http://dx.doi.org/10.1590/S1678-91992010000400012 

ORIGINAL PAPER

 

Antimicrobial activity of an L-amino acid oxidase isolated from Bothrops leucurus snake venom

 

 

Torres AFCI; Dantas RTII; Menezes RRPPBI; Toyama MHIII; Filho EDIV; Oliveira MFI; Nogueira NAPI; Oliveira MRV; Monteiro HSAII; Martins AMCI

IDepartment of Clinical and Toxicological Analysis, School of Pharmacy, Federal University of Ceará, Fortaleza, Ceará State, Brazil
IIDepartment of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, Ceará State, Brazil
IIILaboratory of Cell Biology and Chemistry for Proteins and Peptides, São Paulo Experimental Coast Campus, São Paulo State University (UNESP - Univ Estadual Paulista), São Vicente, São Paulo State, Brazil; IVDepartment of Biochemistry, Institute of Biology, State University of Campinas, UNICAMP, Campinas, São Paulo State, Brazil
VDepartment of Molecular Biology, Center of Exact Sciences and Nature, Federal University of Paraíba, João Pessoa, Paraíba State, Brazil

Correspondence to

 

 


ABSTRACT

Some snake venom proteins present enzymatic activities, such as L-amino acid oxidase (LAAO). The aim of this paper was to investigate the effect of Bothrops leucurus total venom (BleuTV) and its fraction LAAO (BleuLAAO) on bacteria, yeast, and promastigote forms of Leishmania amazonensis and Leishmania chagasi, and epimastigote forms of Trypanosoma cruzi. BleuTV was isolated with a Protein Pack 5PW® (Waters Corporation, USA), and several fractions were obtained. BleuLAAO was purified to high molecular homogeneity, and its N-terminal amino acid sequence shared a high degree of amino acid conservation with other LAAOs. BleuTV inhibited Staphylococcus aureus growth in a dose-dependent manner, with a minimum inhibitory concentration (MIC) of 25 μg/mL, which corresponded to its minimum lethal concentration (MLC). BleuTV also inhibited the growth of promastigote forms of L. chagasi and L. amazonensis, with respective IC50 values of 1.94 μg/mL and 5.49 μg/mL. Furthermore, it repressed T. cruzi growth with an IC50 of 1.14 μg/mL. However, BleuLAAO did not inhibit the growth of the microorganisms studied and was not toxic to macrophages. BleuTV had low toxicity against macrophages at the concentrations studied. In conclusion, whole venom from Bothrops leucurus inhibited the growth of some microorganisms, including S. aureus, Leishmania sp., and T. cruzi.

Key words: L-amino oxidase, Bothrops leucurus, antimicrobial activity.


 

 

INTRODUCTION

Members of the genus Bothrops are present in several ecosystems and include approximately 20 species. The main snakes of this genus are B. jararaca, B. jararacussu, B. moojeni, B. asper, B. alternatus, B. marajoensis and B. leucurus (1).

Snake venom contains numerous components of biological and/or biotechnological value. Venom is a complex mixture that varies in proportions and characteristics among different species and contains both non-protein and protein components with different structures and specific biochemical activities (2, 3). The major protein components of the venom are neurotoxins, cardiotoxins, lectins, disintegrins, natriuretic peptides, proteases, phospholipases, phosphodiesterases, nucleotidases, and L-amino acid oxidases (2). Venom enzymes induce various pharmacological effects including neurotoxic, myotoxic, cardiotoxic, hemorrhagic, hemolytic, procoagulant and anticoagulant (4, 5).

L-Amino acid oxidase (L-amino acid: O2 oxidoreductase, EC 1.4.3.2) is a flavoenzyme that catalyzes the oxidative deamination of an L-amino acid substrate into an α-keto acid with the production of ammonia and hydrogen peroxide. LAAO is the only FAD-dependent oxidase found in snake venom, and venom toxicity may be related to the hydrogen peroxide generated during reoxidation of the transiently reduced flavin cofactor by molecular oxygen (6, 7).

Various venoms and toxins show antibacterial activity, such as miotoxin II from B. moojeni and venom from B. neuwiedi pauloensis (8, 9). Several bothropic venoms inhibit growth of some intracellular parasites, such as Leishmania sp. and Trypanosoma cruzi. Crotalus durissus venoms inhibit parasite growth; however, Crotalus durissus colillineatus venom increases the promastigote growth rate (10). Moreover, B. jararaca venom inhibits promastigote forms of L. amazonensis and epimastigote forms of T. cruzi, with rupture of the membrane and mitochondrial disruption (11).

In light of the potential biological activities of animal venoms and toxins and the need to understand the molecules involved in the host-parasite interaction, the aim of this paper was to study the effect of B. leucurus venom and its fraction L-amino acid oxidase (LAAO) on bacteria, yeast, promastigote forms of L. amazonensis and L. chagasi, and epimastigote forms of T. cruzi.

 

MATERIAL AND METHODS

Reagents and Venom

The venom was obtained from Butatan Institute, in São Paulo city, SP, Brazil. Chemicals and reagents employed in this work were purchased from Sigma-Aldrich (Sigma Chemical Co., USA), Applied Biosystems, Pierce and Bio Rad (USA).

Purification of L-amino Acid Oxidase from B. leucurus Venom

LAAO from B. leucurus whole venom was purified by two chromatographic steps. First, the whole venom was fractionated by affinity chromatography with immobilized lactose as the stationary phase (Pierce, USA). Approximately 100 mg of whole venom previously dissolved in Tris-buffered saline (TBS, 0.05 M, pH 7.8) was centrifuged and filtered with 0.22-μm filters. The same buffer was used for equilibration of the chromatographic column. The chromatographic profile was determined by measuring the absorbance at 280 nm. LAAO activity was measured with a microplate assay (12). The first fraction that eluted in the first chromatographic step, which contained the majority of LAAO activity, was subjected to a second chromatographic step with a Protein-Pak DEAE 5PW® (Waters Corporation, USA). Proteins were eluted at a constant flow rate of 1.0 mL/minute with a linear gradient (0.05 to 1.0 M) of ammonium bicarbonate, and the elution profile was monitored at 280 nm. The concentrated fraction was then recovered and stored at -20°C. PAGE-SDS electrophoresis was conducted as previously described (13).

Microplate Assay for L-amino Acid Oxidase

The assay was conducted in triplicate in a 96-well microplate; 10 μL/well of the enzyme solution and 90 μL/well of the substrate solution were added to start the reaction. The standard reaction mixture contained 250 mM L-leucine, 2 mM o-phenylenediamine (OPD), 0.81 U/mL horseradish peroxidase and LAAO in 50 mM Tris-HCl buffer (pH 8.0) in a total volume of 100 μL/well. After incubation at 37°C for 60 minutes, the reaction was terminated by adding 50 μL of 2 M H2SO4. The absorbance of the reaction mixture was measured in a SpectraMax Microplate Reader® (Molecular Devices, USA) at 480 nm (12, 14). The enzyme activity was measured by the increase in absorbance after the incubation time and compared with LAAO activity from other venoms. Hydrogen peroxide standards were used and linear regression of the data was calculated with Origin 5.0® software (Microcal, USA). LAAO activity was expressed as nmoles H2O2/minute.

N-terminal Amino Acid Sequence

The N-terminal sequence of LAAO was determined following published protocols (15). Briefly, 10 mg of purified protein was dissolved in 200 μL of 6 M guanidine (final pH 8.15). Nitrogen was flushed over the top of the protein solution for 15 minute, and the protein was then reduced with dithiothreitol (DTT, 6 M, 200 μL) and carboxymethylated with 14C-iodoacetic acid and cold iodoacetic acid. Nitrogen was again flushed over the surface of the solution and the reaction tube was sealed. This solution was incubated in the dark at 37°C for one hour and desalted with a C4 reverse phase HPLC column and the same elution buffer used in the protein purification. The eluted, reduced, and carboxymethylated (RC) proteins were then lyophilized and stored at -20°C. N-terminal sequencing of the reduced and carboxymethylated proteins was conducted using a Procise f automatic sequencer® (USA). Phenylthiohydantoin (PTH) amino acids were identified by comparing their retention times with those of 20 PTH amino acid standards on an Applied Biosystems model 450 Microgradient PTH® analyzer (USA). Peptides containing 14C-CM-Cys were monitored for radioactivity with a Beckman L-250® liquid scintillation counter (USA). The N-terminal analysis of the protein was performed with ClustalW (http://www.clustal.org/).

Antimicrobial Activity of Bothrops leucurus Venom and Fraction

Whole venom (BleuTV; 2 mg/mL) and L-amino acid oxidase (BleuLAAO; 2 mg/mL) were dissolved in sterile phosphate-buffered saline, pH 7.4.

The antimicrobial potential of the whole venom and LAAO was determined by the disk-diffusion method with modifications (16). Five pure microbial cultures (Salmonella choleraesuis subsp. choleraesuis serotype choleraesuis ATCC 10708, Staphylococcus aureus ATCC 6538P, Escherichia coli ATCC 11229, Pseudomonas aeruginosa ATCC 15442 and Candida albicans ATCC 10231 all donated by the Laboratory for Reference Materials of the Oswaldo Cruz Foundation, FIOCRUZ), as well as the refrigerated agar stock were added to brain heart infusion (BHI) broth and incubated at 35°C until they reached a visible turbidity equivalent to 0.5 on the McFarland scale (approximately 108 CFU/mL).

The bacterial inoculums were spread with a sterile cotton swab on the surface of sterile Mueller-Hinton agar (Merck, Germany) for bacteria or sterile Sabouraud-dextrose agar (Merck, Germany) for yeast. After five minutes, wells were made in the agar (5-mm diameter) using a sterile punch. In these wells, 25 μL of varying concentrations (2, 1, 0.5, 0.25 and 0.125 mg/mL) of venom or the venom fraction LAAO were added. Commercial antimicrobials (2 mg/mL amikacin and 1.2 mg/mL ketoconazole) were used as positive controls, and the sample diluent (PBS, pH 7.4) was used as a negative control. After incubation at 35°C for 18 hours, the zone of inhibition was recorded in millimeter diameters.

Determination of Minimum Inhibitory Concentration (MIC)

The MIC was determined using a broth microdilution method as reported by Hecht et al. (17) with modifications. The venom and fractions were prepared as previously described (section: "Antimicrobial Activity of Bothrops leucurus Venom and Fraction), and several concentrations (200, 100, 50, 25 and 12.5 μg/mL) were used. The microbial strains were subcultured, and microbial density was adjusted as previously described. The cultures were diluted to 1:100 (~ 1.5 x 106 CFU/mL). An inoculum of 125 μL of microbial culture was added to 25 μL of each concentration of venom or venom fraction in BHI broth (100 μL) for bacteria or Sabouraud-dextrose broth for C. albicans in 96-well plates. For the negative control, wells contained sterile PBS (pH 7.4) instead of venom or fractions. For the positive controls (growth inhibition), wells contained culture medium, an antimicrobial agent (amikacin for bacteria and ketoconazole for yeast), and an inoculum of microorganisms. The plates were incubated at 35°C for 24 hours, and inhibition of microorganism growth was determined by measuring the absorbance at 490 nm. The MIC was assessed based on the lowest concentration of sample required to inhibit microbial growth (detected by a lack of visible turbidity). Three independent experiments were performed in triplicate.

Determination of Minimum Lethal Concentration (MLC)

For assays of minimum lethal concentration, 25-μL aliquots were removed from wells that did not contain visible turbidity as previously described (section: "Antimicrobial Activity of Bothrops leucurus Venom and Fraction) and were placed on plate count agar (for bacteria) or Sabouraud-dextrose agar (for C. albicans) by the pour-plate method. After incubation at 35°C for 24 hours, colonies were counted. The concentration of samples that resulted in growth < 0.1% of initial inoculum (1.5 x 106 CFU/mL) was recognized as the MLC (17).

Leishmanicidal Effects of B. leucurus Venom and Fraction

The promastigote forms of L. amazonensis (MHOM/IFLA/BR/67/PH8) and L. chagasi (MCAN/BR/99/JP15) were used in ours experiments. The parasites were cultivated in NNN/Schneider medium supplemented with 20% fetal bovine serum (FBS), penicillin (1000 U/mL) and streptomycin (50 μg/mL). The cultures were incubated at 26°C until they reached stationary growth phase (18). Cytotoxicity was evaluated for 1 x 106 cells/mL of parasite culture in the presence of various concentrations of the venom (200, 100, 50, 25, 12.5, 6.25, 3.12 and 1.56 μg/mL) or fraction (6.25, 3.12, 1.56, 0.78 and 0.39 μg/mL). As a negative control, cells were cultivated in the absence of B. leucurus venom or fraction. After 72 hours, qualitative and quantitative analyses of the cells were performed, and the promastigote forms were quantified in a Neubauer chamber. The motion and characteristic form of promastigotes were observed by optical microscopy (40x).

Trypanocidal Effects of B. leucurus Venom and Fraction

The epimastigote form of the Y strain of T. cruzi was cultured in liver infusion tryptose (LIT, Difco, USA) medium according to Camargo (19). Hemin was replaced by hemoglobin. The parasites were kept at 26°C and the medium was replaced every 5 to 6 days until the concentration of parasites in the logarithmic phase reached a density of approximately 5 x 107 to 10 x 108 parasites/mL. Parasites were quantified in a Neubauer chamber after dilution in formaldehyde (2% v/v, in PBS). To evaluate the trypanocidal activity of different concentrations of venom or the fraction (200, 100, 50, 25, 12.5, 6.25, 3.12 and 1.56 μg/mL), the parasites were subcultured in 96-well microplates at a density of 1 x 106 parasites/mL at 26°C for five days. For a negative control, parasites were cultured in PBS (pH 7.4). After the incubation period, the cells were quantified in a Neubauer chamber. The motion and characteristic form of epimastigotes were observed by optical microscopy (40x).

Cytotoxicity in Murine Macrophages

Macrophages were obtained from the peritoneal cavity of Swiss female mice and cultivated in RPMI-1640 medium supplemented with FBS (10%), penicillin, and streptomycin, and 1 x 106 cells/mL were seeded in 96-well microplates for two hours at 37°C with 5% CO2. Cells were washed twice with medium at 37°C and further incubated with venom or venom fraction at the highest concentration (200 μg/mL) for 24 hours at 37°C. The viability of the macrophages was determined using an MTT (3-(4.5-dimethylthiazol-2-yl)-2.5-diphenyltetrazolium bromide) assay (20). After the incubation, 100 μL of the medium was aspirated, 10 μL of MTT was added to the wells, and the plate was incubated for four hours. Following this incubation, 90 μL of a solution of 10% sodium dodecyl sulfate hydrochloride (SDS/HCl) was added to solubilize the MTT-formazan product. After 17 hours, the plate was read with a microplate reader at 570 nm. All measurements were performed in triplicate.

 

RESULTS

LAAO Purification from B. leucurus Venom

LAAO from B. leucurus venom was purified as non-binding material from a lactose affinity column used to purify lectin that was eluted by a TBS buffer containing 0.3 M galactose (Figure 1 - A). The non-binding material containing the LAAO fraction was then subjected to DEAE chromatography on a DEAE 5PW HPLC column (Figure 1 - B). The LAAO from B. leucurus was purified to high molecular homogeneity after this last chromatographic step, and its molecular weight was estimated at approximately 80 kDa by SDS-PAGE (Figure 1 - C). The N-terminal amino acid sequence of the LAAO isolated from B. leucurus was highly conserved with other LAAO from other sources (Figure 1 - D). The enzymatic activities estimated at 480 nm (Vo 480 nm) of B. leucurus LAAO, Bothrops pirajai LAAO and Crotalus durissus cascavella LAAO were 0.31 ± 0.06, 0.36 ± 0.04 and 0.21 ± 0.03. The enzymatic activity of LAAO from Bothrops leucurus was therefore intermediate that of the LAAOs from Crotalus durissus cascavella and Bothrops pirajai. Two-dimensional electrophoresis revealed that the molecular weight of the protein was 80 kDa and its pI was approximately 5.3.

 



 

Antibacterial Activity

Antibacterial activity was evaluated by the presence of an inhibition zone after inoculation in Mueller-Hinton agar for bacteria or Sabouraud-dextrose agar for C. albicans. Inhibition zones were determined by a radial diffusion assay. BleuTV inhibited the growth of S. aureus (Figure 2 - A and B). BleuLAAO did not cause any degree of inhibition of the strains studied.

 


 

The microdilution method was used to determine the MIC and MLC for BleuTV. MIC and MLC values for the venom were 25 μg/mL. When compared with amikacin (MIC = 25 μg/mL and MLC = 50 μg/mL), BleuTV was significantly more efficient (Figure 3).

 

 

Leishmanicidal and Trypanocidal Activity

BleuTV inhibited the promastigote forms of L. amazonensis and L. chagasi after 72 hours of culture (Figure 4), IC50 was 5.49 μg/mL for L. amazonensis and 1.94 μg/mL for L. chagasi. BleuTV also inhibited growth of the epimastigote form of T. cruzi (Figure 5); after five days of culture, the IC50 value was 1.14 μg/mL. The effects of inhibition were dose-dependent, and the cells lost their characteristic morphology, lacking flagella and a spherical format (data not shown). BleuLAAO did not have any inhibitory effect.

 

 

 

 

Cytotoxicity in Murine Macrophages

BleuTV significantly reduced cell viability at 200 μg/mL (IC50 = 175.5 μg/mL) (Figure 6). The venom promoted morphological alterations in the cell surface, including membrane rupture and significant cellular lysis, when compared with the control group (Figure 7). BleuLAAO did not have any cytotoxic effect at the studied concentrations.

 

 

 

 

DISCUSSION

Snake venoms are often targeted for new therapeutic uses, and many pharmacologic activities and biotechnological applications for these venoms have been described. Thus, the isolation and functional characterization of venom components provides a basis for understanding the mechanisms and/or future molecular models of venom action (21, 22).

The N-terminal amino acid sequence of BleuLAAO showed high conservation to other LAAOs, such as those from the Bothrops insularis and Bothrops moojeni venoms.

Some studies have demonstrated an antimicrobial effect of snake venoms and their isolated compounds. In the present study, BleuTV had a significant antibacterial effect on S. aureus, with an MIC equal to the MLC. According to Tavares (23), the value of MLC should be no greater than one or two-fold the MIC value. A large difference between these values suggests that the microorganism is tolerant to the drug, which does not cause therapeutic difficulties for most infections in patients with preserved immunity because the bacteriostatic activity of the drug is sufficient to allow the immune system to eliminate the microorganism.

In this study, antiparasitic effects against L. amazonensis, L. chagasi and T. cruzi were observed for BleuTV. Venoms from Crotalus durissus terrificus and Crotalus durissus cascavella have antiparasitic activity against Xantomonas axonopodis pv. passiflorae, and L. amazonensis (10, 24). Bothrops venoms also have antimicrobial activity against Leishmania major, T. cruzi and S. aureus (25, 11).

L-amino acid oxidases of snake venoms (svLAAO) present antimicrobial activity against several microorganisms. LAAOs from Crotalus adamanteus and Bothrops asper have an antibacterial effect against S. aureus and Proteus mirabilis (26). svLAAOs from Bothrops venoms also have antimicrobial effects (27-29). svLAAO from B. pirajai inhibited the growth of Pseudomonas aeruginosa and E. coli (29). Bactericidal action has also been described for svLAAOs from B. alternatus (30). In our studies, parasites lost their characteristic morphology in the presence of BleuTV.

LAAO from B. jararacussu is significantly active against Leishmania sp. (31). The whole venom of B. moojeni and its LAAO are significantly active against the promastigote forms of L. amazonensis, L. chagasi and L. panamensis, with IC50 values around 1 μg/mL; the hydrogen peroxide generated is a strong inducer of apoptosis, causing oxidative stress, initiating disruption of membranes and cytoplasm and, consequently, cell death (32). Some authors have observed that the antimicrobial action of this enzyme is significantly reduced by catalase, suggesting the importance of enzymatically-produced hydrogen peroxide for biological activity (31, 33, 34). BleuLAAO had no cytotoxic effect on any microorganism studied or on macrophages, which suggests that this fraction does not produce hydrogen peroxide in sufficient quantities at the studied concentrations of enzyme.

The alarming growth of microbial resistance to common therapeutic agents has drawn attention to infectious diseases. These diseases, which are mainly parasitic such as leishmaniasis and Chagas disease, are considered neglected and affect a wide portion of Brazilian populations and other developing countries that have difficulty accessing treatment. In addition, the available treatment options have limited effectiveness and high levels of toxicity. The identification of substances from natural sources with therapeutic potential is an important alternative. Many natural products demonstrate biological activities, including antimicrobial and antiparasitic effects, and snake venom may be a similarly relevant source of antimicrobials. Once molecules with the potential to inhibit microorganisms are identified, chemical modification techniques can be used to develop synthetic analogues with adequate pharmacological and toxicological characteristics.

In conclusion, our results suggest that B. leucurus venom contains some substances of therapeutic value, but LAAO is not responsible for the inhibitory effect of the whole venom.

 

ACKNOWLEDGEMENTS

The authors are thankful to Bruna Regina dos Santos for her technical assistance.

 

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Correspondence to
Alice Maria Costa Martins
Departamento de Análises Clínicas e Toxicológicas, Faculdade de Farmácia, Universidade Federal do Ceará
Rua Capitão Francisco Pedro, 1210
Fortaleza, CE, 60.420-970, Brasil
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Submission status
Received: June 7, 2010.
Accepted: October 21, 2010.
Abstract published online: October 22, 2010.
Full paper published online: November 30, 2010.

Financial Source
This work was supported by the Brazilian research agencies The National Council for Scientific and Technological Development (CNPq) and Coordination for the Improvement of Higher Education Personnel (CAPES).

 

 

CONFLICTS OF INTEREST
There is no conflict.
ETHICS COMMITTEE APPROVAL
The present study was approved by the Animal Ethics Committee of the Federal University of Ceará (process n. 17/09).

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