Anti-colon cancer activity of endophytic fungal strains from Terminalia chebula Rezt
Abstract
Endophytic microorganisms are fungi or bacteria that live inside the healthy tissues of the host plants causing no apparent symptoms of diseases. Five endophytic fungal strains labeled as IR-1, IR-2, IR-4, IR-6 and IR-7 (identified as Penicillium thiomii) were isolated from the medicinal plant of Terminalia chebula Retz by culture and subculture. The ethyl acetate extract of fungal strains, IR-4, IR-6 and IR-7 inhibited the growth of CaCo-2 colon cancer cell lines in MTT assay with IC50 values of 55, 44 and 67 µg/mL respectively.
Introduction
The word endophyte means inside the plant and refers to microorganisms, i.e. fungi and bacteria that spend the whole or parts of their life cycle colonizing inter or intracellularly inside the healthy tissues of the host plants, typically causing no apparent symptoms of diseases (Petrini, 1991). Endophytic fungi have been shown to produce pharmaceutically important plant metabolites, with the most prominent example being paclitaxel, better known as taxol. Taxol was originally isolated from the bark of the Pacific yew tree Taxus brevifolia (Strobel et al., 2004). Later, it was discovered that the fungal endophyte Taxomyces andreanae, associated with this tree, also produces taxol upon fermentation (Stierie and Strobel, 2003). This example illustrates the biotechnological potential of endophytic fungi, since unlike their plant hosts they are amenable to fermentation, which could represent a sustainable source for unlimited supply of natural products. Endophytic fungi also are a highly diverse source of new chemical entities on their own right, with almost 300 new natural products being reported between 1987 and 2006 (Tan and Zou, 2001; Zhang et al., 2006).. Thus, endophytic microorganisms are a rich source of bioactive compounds with a great potential to discover new lead structures for drug discovery. The bioactive strains are possible to cultivate in large scale by fermentation to isolate the active compound(s) in larger amount rather than destroying natural plant resources. Terminalia chebula Retz (Haritaki) is one of the important medicinal plants of Bangladesh. As a part of our ongoing research on endophytic fungi, two new compounds terminatol and 4, 7-dimethyl-1,3-dioxa-cyclohepta-2-one and several known secondary metabolites were isolated from endophytes of T. chebula earlier (Rob et al., 2005; Shoeb et al., 2010). We, now report the in vitro anti-colon cancer activity of the extracts of fungal strains from T. chebula.
Materials and Methods
Plant collection and sterilization
The medicinal plant, Terminalia chebula Retz, locally known as Haritaki was collected from a nursery of Dhaka city. Different parts (leaves, stems and roots) of the plant were cut into small pieces. Each plant part was surface sterilized with 70% ethanol, 3% sodium hypochlorite and sterile water (Schulz et al., 1983). The agar media was autoclaved at 120ºC at 1 atmosphere pressure for 30 min.
Isolation of endophytic fungi
The surface sterilized plant materials were inoculated on autoclaved potato dextrose agar media on a sterilized petridish (90 mm in diameter) and after 21 days, twenty one fungal strains were isolated for identification. By dereplication of common fungi, five strains labeled as IR-1, IR-2, IR-4, IR-6 and IR-7 were found to have optimum growth for further cultivation. IR-7 was identified as Penicillium thiomii by Prof. Barabara Shultz, Technical University of Braunschweig, Germany. The fungal strains IR-4, IR-6 and IR-7 were selected for cytotoxic studies.
Culture and extraction
The fungal strains IR-4, IR-6 and IR-7 were separately fermented in a large scale (450 Petri dishes of 90 mm in diameter) in the potato dextrose agar semi solid medium at ~22-25ºC. After 21 days the fungi were collected in a round bottom flask and the content was freeze-dried. The dried powdered material was extracted with ethyl acetate (3 x 1500 mL for 24 hours, at room temperature). The ethyl acetate extract was evaporated to dryness. A small part of dried materials from IR-6 was also extracted with 70% ethanol.
Cryopreservation of cancer cells
CaCo-2, human colon cancer cell line was obtained from the European collection of cell cultures. Cells were cryopreserved to ensure the continuous supply of a cell line during this study. Healthy and viable cells 4-10 x 106 per ampoule were used for this purpose. Freezing medium was prepared from the growth medium containing 10% (v/v) sterile dimethyl sulphoxide. Cell pellets dissolved in 1 mL freezing medium were poured into a sterile plastic screw-top cryotubes and immediately cooled at a rate of between 1-5°C per min. Normally the cryotubes were placed in the –20°C freezer for 3-4 hours and transferred to the -80°C for approximately 16 hours (overnight). After freezing, the ampoules were preserved in liquid nitrogen.
Thawing of frozen cells
The ampoule was removed from storage and unscrewed the cap¼ turn to release any residual nitrogen. After 1-2 min (to let gas escape) it was placed in the water bath at 37°C. Special care was taken in order to prevent water entering the ampoule and contaminating the cells. When ampoules were fully thawed, they were taken to the laminar flow hood. Then contents of ampoule were transferred into a 30 mL sterile universal bottle. The growth medium (10 mL) was added slowly to the universal bottle, shaken slowly and centrifuged. After decanting the supernatant, the pelleted cells were resuspended in fresh Earle’s minimum essential
medium and transferred to a culture flask.
Cell counting
Cells were counted by hemocytometer and particle size distributor. Similar results were obtained in both cases and constant cell density was maintained for all cell culture work in this study.
Cell viability assay
CaCo-2 cells were maintained in Earle’s minimum essential medium, supplemented with 10% (v/v) foetal calf serum, 2 mM L-glutamine, 1% (v/v) non-essential amino acids, 100 IU/mL penicillin and 100 m g/mL streptomycin. Exponentially growing cells were seeded on 96-well plates at 1 × 104 cells per well and incubated for 24 hours before the addition of extracts. Stock solution of samples was initially dissolved in DMSO and further diluted with serum free medium. Following a 24 hours incubation at 37°C, 5% CO2, 100 mL of various concentration of test extracts (100, 80, 40, 20, 4, 0.4, 0.04 and 0.004 m g/mL) were added in each well in triplicates and cells were further incubated for 72 hours (Mosmann, 1983). After 72 hours of incubation at 37°C, the medium was removed, and 100 mL of MTT reagent (1 mg/mL) in serum free medium was added to each well. The plates were incubated at 37°C for 4 hours. At the end of the incubation period, the supernatants were removed and, pure DMSO (200 mL) was added to each well and plates were shaken gently for 15 min. The metabolized MTT product dissolved in DMSO was quantified by reading the absorbance at 560 nm using a micro plate reader (Dynex Technologies, USA,). IC50 values are calculated from the equation of the logarithmic line determined by fitting the best line (Microsoft Excel) to the curve formed from the data. The IC50 value was obtained from the equation y = 50 (50% value).
Result and Discussion
The fungal strains, IR-4, IR-6 and IR-7 were tested in MTT cytotoxicity assay (Mosmann, 1983) using the CaCo-2 colon cancer cell lines for possible cytotoxic activities. The MTT assay is a well-documented cell viability assay and has been modified by several investigators since it was first developed by Mosmann (Mosmann, 1983; Monks et al., 1991). This assay is based on the transformation of tetrazolium salt, 3-[4,5- dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide (MTT) by mitochondrial succinic dehydrogenases in viable cells yielding purple formazan crystals that are not soluble in aqueous solution. The amount of formazan generated by dehydrogenase enzyme is directly proportional to the number of viable cells in culture and is measured at 560 nm. The ethyl acetate extracts of fungal strains IR-4, IR-6, IR-7 and ethanol extract of IR-6 showed significant cytotoxic activities with IC50 values of 55, 44, 67 and 71 mg/mL, respectively (Table I). As crude extract may contain several compounds, further work is necessary to isolate the active principles for the cytotoxicity of these extracts. The isolation of endophytic fungi from medicinal plants and their study for bioactive secondary metabolites by fermentation in large scale can produce potential drug candidates and help to conserve the biodiversity of medicinal plants in the country.
Table I: MTT cytotoxicity assay of extracts of endophytic fungi from T. chebula
| Extracts | Cytotoxicity (µg/mL) |
|---|---|
| Ethyl acetate extract of IR-4 | 55 |
| Ethyl acetate extract of IR-6 | 44 |
| Ethyl acetate extract of IR-7 | 67 |
| Ethanol extract of IR-6 | 71 |
Conclusion
This is the first report on the assessment of the extracts of these fungal strains for their cytotoxicity towards the CaCo-2 in vitro colon cancer cell line.
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