- Open Access
Combination of extracts from Aristolochia cymbifera with streptomycin as a potential antibacterial drug
- Willer F SilvaJr1,
- Samyra G Cecílio2,
- Cintia LB Magalhães†3,
- Jaqueline MS Ferreira†4,
- Antonio H Tótola†5 and
- Jose C de Magalhaes5Email author
© Silva et al.; licensee Springer. 2013
- Received: 3 May 2013
- Accepted: 22 August 2013
- Published: 3 September 2013
The appearance of new antibiotic-resistant bacteria is a societal problem that requires the development of new alternative treatments. Therefore, this work evaluated the antibacterial activity of ethanolic (EHI), dichloromethanic (EDI) and hexanic (EHE) extracts from Aristolochia cymbifera stems and the combination of these extracts with an antimicrobial drug to develop a new antibacterial therapy. The EDI, EHE and EHI extracts were obtained by maceration using three different solvents. The minimal inhibitory concentrations (MIC) of these extracts were determined using the microdilution test to determine the antibacterial potential of these extracts and their combination with streptomycin against Staphylococcus aureus, Bacillus cereus, Klebsiella pneumoniae and Shigella flexneri. The extract dose leading to the cytotoxicity of 50% of the cells (CC50) was evaluated using mammalian cells MA104 and the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay. The extracts had a MIC under 500 mg/L and a CC50 lower than 50 mg/L. The antibiotic/extract proportion influenced the antibacterial activity of the mixtures, and the proportion that optimized the antibacterial activity of streptomycin was a mixture that contained 75 percent of extract. This composition included less than 6.5 mg/L of extract and 2.5 mg/L of streptomycin and has potential as a new antibacterial therapy.
- Aristolochia cymbifera
- Antibacterial activity
- Drug discovery
- Natural products
Longstanding experiments and the popular use of plants as therapeutic tools have helped to introduce chemical entities in modern medicine. Plants, especially those with ethnopharmacological uses, have been the main sources for the discovery of new drugs. Worldwide, natural products have played a prominent role in the prevention and treatment of several diseases for thousands of years (Chin et al. 2006).
Drugs based on natural products have been developed from sources that include terrestrial plants, microorganisms, marine organisms, terrestrial vertebrates and invertebrates (Newman et al. 2000). Brazil has a vast forest and a popular tradition associated with the use of medicinal plants for antimicrobial applications (Sartoratto et al. 2004). Thus, extracts from plants can be used as sources of new drugs or antimicrobial compounds (Alviano and Alviano 2009) and these new therapies are of great importance, as the emergence of resistant strains has increased the difficulty of treating infections (Cole et al. 2003).
Staphylococcus aureus (S. aureus), Bacillus cereus (B. cereus), Klebsiella pneumoniae (K. pneumoniae) and Shigella flexneri (S. flexneri) are known to cause enteric disease. Shigella flexneri causes enteric shigellosis and is responsible for 1.1 million deaths per year, with children being the most affected group (Jennison and Verma 2004). B. cereus is responsible for diarrheal food poisoning due to its toxin production (Ceuppens et al. 2012). Staphylococcus aureus can induce many diseases, such as bovine mastitis, skin disease and gastroenteritis, due to the ingestion of enterotoxins (Reinhardt et al. 2013; Moran et al. 2013; Hyeon et al. 2013) and are often associated with antibiotic resistance. Another species that has been shown to be antibiotic resistant is Klebsiella pneumoniae, including carbapenem-resistant Klebsiella pneumoniae (CRKP) (Tenover 2006), which can inactivate the carbapenems.
In some regions, enteric diseases are treated with teas, infusions or macerated medicinal plants and this folk medical knowledge is transmitted from generation to generation. This alternative treatment, which sometimes represents the only therapy option for many people, is widely used due to its low cost and easy access (Veiga et al. 2005).
Species of the Aristolochia genus are used in traditional medicine, mainly in South America, to treat skin diseases, poisoning, wounds, worms, diarrhea, and also as emmenagogues. The species Aristolochia cymbifera (Aristolochiaceae) is popularly known as jarrinha, papo de peru, cipó mil homens, cassaú and other common names (Wu et al. 2004). Some studies using A. cymbifera extracts have indicated potential antimicrobial properties of this species. In experiments performed by Carvalho et al. (2008), the leaf methanol extract of this species showed strong activity against promastigotes from Leishmania chagasi, and the diterpene copalic acid was isolated using bioassay-guided fractionation and showed high toxicity against the extracellular form of the parasite. Sartorelli et al. (2010) observed that copalic acid was also active against trypomastigotes of Trypanosoma cruzi. Copalic acid maintained its selectivity against T. cruzi, although it showed low toxicity against infected mammalian cells.
In studies conducted by Alviano et al. (2008) that evaluated the antioxidant potential and antimicrobial properties of plants used in Brazilian folk medicine, the crude ethanol-water (1:1) extract from A. cymbifera stems exhibited a significant antibacterial effect. This extract inhibited the growth of the oral bacteria Prevotella intermedia, Porphyromonas gingivalis, Fusobacterium nucleatum, Lactobacillus casei and Streptococcus mutans even in the presence of an artificial biofilm. In experiments using the agar dilution method, the ethanolic extract from A. cymbifera stems inhibited the growth of various staphylococci, including multi-drug resistant endemic Brazilian clones of Staphylococcus aureus. The hexane fraction of the extract proved to be active against Pseudomonas aeruginosa strains Machado et al. 2005).
Thus, based on the potential and promising use of medicinal plants in traditional medicine, the current investigation involved screening the ethanolic (EHI), dichloromethanic (EDI) and hexanic (EHE) extracts of A. cymbifera against important pathogenic bacteria and combining these extracts with streptomycin determine the prospects for a new antibacterial therapy.
Extract absorption outlines
Determination of Minimum Inhibitory Concentration (MIC)
Minimum inhibitory concentration (mg L -1 ) of ethanolic (EHE), dichloromethanic (EDI) and hexanic (EHE) extracts from Aristolochia cymbifera
Extracts from Aristolochia cymbifera
Effect of combination of streptomycin and A. cymbifera extracts
Different effects were observed when the streptomycin/extract proportions were changed, and an increase in the antibacterial activity was observed when the percentage of extracts in the mixture was higher (see Additional file 1). A mixture containing 75% extract reduced the MIC value of streptomycin approximately four-fold against S. aureus, K. pneumoniae, B. cereus and S. flexneri.
The maximum antibacterial activity was obtained in mixtures containing 25% of streptomycin. There were differences in interaction index (II) between the extracts when used against S. aureus and B. cereus (Figures 2a and 2b). The best II values were observed for EHE when used against B. cereus, which was the most susceptible bacteria to the streptomycin/extract mixture.
Evaluation of cytotoxicity in mammalian cells
The MIC results were significant with the exception of EHE against S. aureus, mainly because of the antibacterial activity against S. aureus and K. pneumoniae, which have shown resistance to several antibacterial drugs (Al-Masaudil et al. 1991; Mangeney et al. 2000). The low MIC values of the extracts against B. cereus indicate that the three extracts should be further studied to find active compounds to design new drugs. There were differences in antibacterial activity against S. aureus, S. flexneri and K. pneumoniae based on both extract polarity and bacterial strain. This fact can be associated with physiological differences between the microorganisms and the diversity and amounts of compounds in each extract.
The EHE and EDI extracts contain compounds with similar absorption bands in the UV region, but with different intensities. In the spectra of EHI and EDI, an absorption band at 400 nm was observed that was not found in the EHE spectrum (Figure 1). These data indicated that the use of solvents with different polarities allowed the extraction of distinct constituents in different concentrations. Some compounds have been isolated from Aristolochia cymbifera extracts, including 2-oxopopulifolic acid (Machado et al. 2005), copalic acid, fargesin, hinokinin, kusunokinin, sesamin, epieudesmin, benznidazole (Sartorelli et al. 2010), (5R,8R,9S,10R)-ent-3-cleroden-15-oic acid (Leitão et al. 1992), (5R,8R,9S,10S)-ent-labd-14-en-8ß-ol (Lopes et al. 1988), and (−)-kolavelool (Lopes et al. 1987).
The highest concentrations of EDI, EHE and EHI in the streptomycin/extract mixture that showed a synergistic effect were 10.42 ± 3.61 mg L-1 (50% EDI), 6.25 ± 2.71 mg L-1 (75% EHE) and 6.25 ± 2.71 mg L-1 (75% EHI) against K. pneumonia (Additional file 1). Using the non-linear regression equations obtained from the cytotoxicity assay (Figure 3), the percentage of living cells at the above extract concentrations would be 68.00 ± 11.93, 122.54 ± 0.29 and 80.49 ± 10.77 respectively, each of which resulted in more than 50% living cells.
The in vitro toxic effect of Aristolochia cymbifera extracts on MA104 cells (Figure 3) is similar to that observed in studies that report high toxicity of the Aristolochia genus to human kidney cells, which was associated with aristolochic acids (Chen et al. 2010). However, the checkerboard dilution test used in this study showed that lower extract concentrations improve the antibacterial activity of the mixture (see Additional file 1).
The 75% EHE mixture was generally the most effective solution against the studied bacteria (Additional file 1), containing a streptomycin concentration near the MIC of the antibiotics recommended for the treatment of S. aureus (oxacillin 0.5 mg L-1) (Auwaerter et al. 2013; European Committee on Antimicrobial Susceptibility Testing 2013) and B. cereus (ciprofloxacin 0.25 mg L-1) (Turnbull et al. 2004). Based on these data and in vivo cytotoxicity tests, which must be performed, the mixture of streptomycin plus the hexanic extract from Aristolochia cymbifera has good potential to be used as an alternative treatment against the studied bacteria. Even if the toxic effects of A. cymbifera are related to the aristolochic acids, this damage is associated with high cumulative doses of these compounds (Nortier et al. 2000; Martinez et al. 2002), which are unlikely to occur with the low extract concentration in the streptomycin/extract mixture that demonstrated antibacterial activity in this study. Additionally, the use of A. cymbifera extracts in addition to antibiotic drugs reduces the dose of streptomycin required for treatment, which can decrease the resistance of bacteria to the antibiotic and reduce the costs of antibiotic therapy.
Streptomycin is an aminoglycoside antibiotic that acts on the 30S subunit of the bacterial ribosome and prevents protein synthesis, causing bacterial death (Luzzatto et al. 1968). Thus, one possible hypothesis for the synergic effect between streptomycin and A. cymbifera extracts may be that compounds that are present in the extracts increase membrane fluidity or permeability, helping the streptomycin molecules cross the bacterial membrane to enter the cytoplasm. Some compounds identified in A. cymbifera, such as copalic acid, have been shown to be able to disrupt the cell membrane (Souza et al. 2011).
The popular use of medicinal plants can sometimes be a good indicator of a new product source, as plants have several substances with different proprieties that can cause a specific biological effect. In this study, the antibacterial activity of ethanolic, hexanic and dichloromethane extracts form A. cymbifera stems was studied in addition to the antibacterial activity of streptomycin/extract mixtures. The cytotoxicity of the extracts on mammalian cells was also evaluated.
The results show that A. cymbifera extracts have compounds with potential as antibacterial drugs against S. aureus, K. pneumoniae, B. cereus and S. flexneri. The antibiotic/extract proportion affected the antibacterial activity of the mixture and the proportion that optimized the streptomycin's antibacterial activity contained 75 percent extract. At this percentage, the streptomycin’s activity was increased four-fold.
Although the three extracts were toxic to the mammalian cells, at the concentrations used in the 75 percent extract they were less toxic. Thus, to demonstrate the safety of the use of a mixture of streptomycin/A. cymbifera extracts and the mode of action of these extracts when combined with streptomycin, in vitro and in vivo toxicity assays should be performed in addition to mechanistic studies.
Plant extract preparation
Stem samples from A. cymbifera (Mart. & Zucc) were purchased from Nutri Comércio de Ervas Ltda. Company (São Paulo, Brazil) (Lot: MIH0111DM). Extracts were obtained by maceration using 50 g of the stems in ethanol, dichloromethane or hexane for three weeks (5 × 250 mL of each solvent). The mixtures were filtered and the solvents were removed under reduced pressure in a rotary evaporator at 45°C. The crude extracts (EDI= 1.15 g, EHE= 0.27 g and EHI= 3.38 g) were dissolved in DMSO and stored at −20°C. The extracts were analyzed to determine their absorption spectrum over a range of wavelengths between 200 and 900 nm.
Reference bacterial strains were chosen in accordance with their ability to cause enteric disorders or association with gastrointestinal disorders or food poisoning episodes as follows: Staphylococcus aureus (ATCC 29213), Bacillus cereus (ATCC 11778), Klebsiella pneumoniae (ATCC 4352) and Shigella flexneri (ATCC 12022). The bacteria were reactivated on nutrient agar plates.
Determination of Minimum Inhibitory Concentration (MIC)
The MIC was determined using a microdilution assay in a 96-well microplate, as suggested by National Committee for Clinical Laboratory Standards (NCCLS 2003), with modifications. The inoculum was adjusted to 0.5 on McFarland’s scale and diluted to 106 CFU mL-1 in nutrient broth (HiMedia Laboratories®, India), which was used as the growth medium. The initial concentration of the extracts was 500 mg L-1, which was decreased 50 percent for each subsequent microplate’s column. Streptomycin (Estreptomax®, Eurofarma Laboratories, São Paulo, Brazil) and dimethyl sulfoxide (DMSO) were the positive and negative controls. The plates were incubated for 24 h at 37°C and then 10 μL of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) (Sigma®) was added to each well. A blue color indicated that there were living cells (active metabolism), and a yellow color indicated the absence of living cells.
Checkerboard dilution test
(See the derivation of the equation in Additional file 2).
Assessment of cytotoxicity in mammalian cells
MA104 cells (ATCC) (rhesus monkey kidney cells) were cultured in Dulbecco's Modified Eagle Medium (DMEM) (Sigma®) supplemented with 6 percent of Fetal Bovine Serum (FBS) at 37°C in a 5 percent CO2 atmosphere in 96-well microplate until 95 percent confluence was reached. The wells were washed twice with phosphate-buffered saline (PBS) and 200 μL of extracts from 250 to 1.95 mg L-1 in DMEM with 2 percent of FBS were added. After 48 h of incubation, the medium was discarded and 20 μL of MTT was added to each well. After 1 h, 130 μL of DMSO was added, and the UV/Vis absorbance was measured with a spectrophotometer to determine the concentration of the extract that killed 50 percent of cells (CC50) Twentyman and Luscombe, 1987.
All assays were performed in triplicate in three independent experiments. The mean ± SD were used to describe the results. To analyze the data, descriptive statistics, analysis of variance (ANOVA) and non-linear regression were applied with 95 percent confidence intervals Skoog, 2007.
The authors would like to acknowledge FAPEMIG and MEC/Sesu (Tutorial Education Program-PET) for fellowship support, Universidade Federal de São João Del-Rei for other support, Dra Daniela Leite Fabrino and Dr. Juliano Lemos Bicas, UFSJ, Ouro Branco, MG, Brazil, Dr. Rafael Russo Chagas, UFSJ, Divinopolis, MG, Brazil, Dr Sidney Augusto Vieira Filho, UFOP, Ouro Preto, MG, Brazil, Camila Magalhães Dias, Juliana Gomes Santana and Jéssica dos Santos Diniz (undergraduates), Ouro Branco, MG, Brazil for contributions.
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