1. Background
Since the introduction of the antibiotics, they have been known as one of the most important tools against bacterial infections (1). Although, in the past years due to the widespread and in some cases incorrect use of antibiotics we can see dramatic increase in microbial resistance against antimicrobial agents that is a critical reason for finding new drugs with les resistance and side effects (1). The medicinal plants have been used from ancient times especially in Asia, and have been used for the treatment of specific illness (2). In Iran, we can find the history of using these plants in Ibn-Sina (Avicenna, 980-1037) books (3, 4). They contain active components used in the treatment of many human diseases. Many studies showed that some plants contain many components like peptides, unsaturated long chain aldehydes, alkaloid constituents, some essential oils, phenols and soluble compounds in water, ethanol, chloroform, methanol and butanol (5-7).
Cassia fistula (Leguminosae), is distributed in different parts of the world including Asia, South Africa, Mexico, China, East Africa and Brazil. It is an ornamental tree with beautiful bunches of yellow flowers (8). It has been explained in the Indian literatures that C. fistula has advantageous application against some diseases such as skin infection, liver troubles and tuberculous glands and even this plant is used as a drug for rheumatism treatment, hematemesis, pruritus, leucoderma, and diabetes. Also Considerable effects of C. fistula against some microbes have been observed. With respect to these properties, this plant is used as broad-spectrum antimicrobial agent for treatment of some infectious diseases (8, 9).
Bacterial infectious diseases are widespread in Khuzestan (southwest of Iran) meanwhile different studies have reported the emergence of antibiotic resistant strains from this province. Actually, the raise of antibiotic resistant pathogens is a growing concern all over the world and WHO assign it as an emerging public health problem (10). For example some bacteria such as Escherichia coli and Klebsiella spp., the main agents of UTI (urinary tract infection), had high resistance to cephalosporins that is resulted from the production of extended-spectrum beta-lactamases (ESBL). The EBSLs genes are located on transferable plasmids and consequently their distribution will be at high rate (11).
2. Objectives
The aim of this study was to discover the antimicrobial effects of C. fistula flowers, a native plant in Khuzestan, and comparing its properties with commonly used antibiotics. These results can be useful in finding new antibacterial agents.
3. Materials and Methods
3.1. Plant Collection and Identification
C. fistula was freshly collected in April 2011 from Shahid Chamran University farmlands, Ahvaz, Khuzestan province. The taxonomic identification of this plant performed by comparison with existing herbarium in Biology department of Shahid Chamran University.
3.2. Extract Preparation
The flowers of C. fistula were shade dried at room temperature for 7 days and then finely powdered using electronic blender. One gram of powder was extracted using 10 mL of alcohol (ethanol or methanol)-distilled water solution (8:2 v/v), centrifugation (3000 rpm) for 15 minutes and finally harvesting the supernatant (12, 13). This process was repeated for three times. Eventually the extracts were placed at room temperature to evaporate the solvent (12, 13).
3.3. Bacterial Test
A total of 8 bacterial species were tested including 3 Gram positive: Bacillus cereus, Staphylococcus aureus and S. epidermidis and 5 Gram negative: Salmonella Typhi, Kelebsiella pneumoniae, E. coli, Pseudomonas aeruginosa, and Proteus mirabilis. These species were originally isolated from the clinical samples and identified based on standard phenotypic tests according to Bergey’s manual of systematic bacteriology.
3.4. Determination of Antibacterial Activity
Antibacterial activity of the ethanolic and methanolic extracts of the plant were studied by standard paper disc-diffusion method (14). Stock cultures of the bacteria were grown in Muller Hinton broth (MHB, Merck, Germany) medium at 37˚C for 22 hours. Final cell concentrations were adjusted to 105 CFU.mL-1 with reference to the McFarland turbidometry (15). A lawn culture was prepared from bacterial suspension on Muller-Hinton agar (MHA, Merck, Germany) using sterile cotton swab and allowed to remain in contact for 1 minute. Five concentrations of ethanolic and methanolic extracts were prepared as follows 0.05, 0.1, 0.2, 0.4 and 0.6 g/mL. Sterile 6 mm filter paper discs were saturated with 30 µL of different concentrations of extracts (16, 17). So the effective dose of each disc was reached to 1.5, 3, 6, 12 and 18 mg, respectively. Then it was allowed to evaporate the solvents and the discs were placed on bacterial cultures. The plates were left at room temperature for 1 hour, then the petri dishes were subsequently incubated at 37˚C for 24 hours and the inhibition zone of each disc was measured in millimeter.
3.5. Determination of Minimum Inhibitory Concentrations
The minimum inhibitory concentration (MIC) of the extracts was determined for most sensitive bacterial species. A 16-hour culture was diluted with a sterile physiologic saline solution (0.9% (w/v) sodium chloride) with reference to the 0.5 McFarland turbidometry to achievement the inoculum approximately equal to 105 CFU.mL-1 (15). In the tube dilution assay, standard bacterial suspension and different concentration of extracts (5, 10, 20, 40, 80 and 160 mg/mL) were added to tubes containing 1 mL Muller Hinton broth. These tubes were incubated at 37°C for 24 hours. The first tube of the series with no sign of visible growth was considered as the MIC. This process has been done three times (18).
3.6. Determination of Minimum Bactericidal Concentrations
To determine the MBC, for each set of test tubes in the MIC assay, a loop full of broth was collected from the tubes without any visible growth and cultured at 37°C for 18 - 24 hours. The highest dilution that yields no colony formation on solid medium was considered as MBC (19).
3.7. Time-Kill Kinetic Study
The time-kill kinetics was studied by culturing one standard loop of the suspension from the tube possessing MBC on MHA from 0 to 36 hours. This was performed at the first hours of intervals for the first 18-hour study, and then at 2-hour intervals for the later 18 hours (18).
4. Results
Both alcoholic extracts of C. fistula exhibited antibacterial activity against Gram positive and Gram negative species. As a result, both alcoholic extracts efficiently inhibited three Gram positive species including S. aureus, S. epidermidis and B. cereus and two Gram negative bacteria including E .coli and K. pneumoniae. The antimicrobial activity results were shown in Tables 1 and 2. The highest activity (with inhibition zone diameter about 26 mm) was demonstrated in case of ethanolic extract of C. fistula flowers against E. coli while the lowest activity (with inhibition zone diameter about 7 mm) was demonstrated by the ethanolic extract against B. cereus and S. aureus and methanolic extract against B. cereus and S. epidermidis. On the other hand, the ethanolic and methanolic extracts were not active against S. Typhi, P. aeruginosa, K. pneumoniae and P. mirabilis. The results of MIC and MBC of ethanolic and methanolic extracts for 3 bacterial species were shown in Table 3. Time-kill kinetic of ethanolic extract of C. fistula was 4 hours (Table 4).
| Ethanolic Extract (Effective dose, mg) | Methanolic Extract (Effective Dose, mg) | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Bacterial species | 18 | 12 | 6 | 3 | 1.5 | 18 | 12 | 6 | 3 | 1.5 |
| Gram positive | ||||||||||
| B. cereus | 9a | 8 | 7 | - | - | 8 | 7 | - | - | - |
| S. aureus | 13 | 10 | 9 | 7 | - | 12 | 10 | 8 | - | - |
| S. epidermidis | 15 | 14 | 11 | 9 | - | 13 | 13 | 9 | 7 | - |
| Gram negative | ||||||||||
| E. coli | 26 | 20 | 17 | 13 | 11 | 22 | 20 | 18 | 14 | 10 |
| K. pneumoniae | 23 | 22 | 19 | 16 | 12 | 25 | 22 | 18 | 17 | 13 |
Results of Antibacterial Activity of Ethanolic and Methanolic Extracts of Cassia fistula Flowers
| Ethanolic | Methanolic | ||||||
|---|---|---|---|---|---|---|---|
| S. aureus | E. coli | S. epidermidis | K.pneumoniae | S. aureus | E.coli | K.pneumoniae | |
| MIC | 40 | 5 | 40 | 5 | 20 | 10 | 5 |
| MBC | …. | 40 | …. | 160 | 40 | 20 | 160 |
Antibacterial Activity (MIC and MBC, mg.mL -1) of the Ethanolic and Methanolic Extracts of Cassia fistula
The Time-Kill Kinetic of Methanolic Extract of C. fistula at 20 mg/mL Concentration Against E. coil
5. Discussion
About 80% of world population use plant extracts or their active components in traditional therapies (1). In this study, we have studied the ethanolic and methanolic extracts obtained from C. fistula flowers. Both extracts showed significant activity against five of the tested strains. Interestingly, among sensitive strains, the Gram negative bacteria were more sensitive than Gram positive ones. From this finding it can be concluded that the possible target site of these extracts is the structures except the cell wall. It may be affect the outer membrane of Gram negative bacteria or protein synthesis mechanisms.
In any case, these extract can be a proper candidate using against infections caused by Gram negative bacteria. Furthermore, there was a direct relationship between effective dose of these extracts and their antibacterial effects. Also, in some cases, they showed an effective dose 1.5 mg which can be a significant finding. These antibacterial activities were comparable to routinely used antibiotics. Most of the antimicrobial effects of C. fistula is related to their components and secondary metabolites like phenolic compounds (20, 21). Phytochemical studies showed that this plant containing components like saponin, triterpnoids, glycosides, anthraquinore, steroids and flavonoids that inhibit the growth of the tested bacterial strains (22, 23). The presence of this component inhibits the growth of tested bacterial strains.
The antimicrobial activity depends on the contents of phenolic components of the plant extracts. High amounts of phenolic group in the aerial parts of C. fistula implied that these components may be the active compounds, which may be responsible for the antibacterial activity (24). Rizvi et al. observed that Cassia species had a significant activity against Gram positive microorganisms. They claimed that this is the result of some substances like flavonoids and polysaccharides (23). Abo et al. also found that leaves extracts of C. fistula have considerable antimicrobial activity (25). Vasudevan et al. reported that methanolic extracts inhibited Gram positive bacteria more than Gram negative species (24). The result of this study suggests that C. fistula extracts can be useful to treat infectious diseases and must be considered as a new source of antibacterial agents.
