Antimicrobial activity of aqueous and ethanolic extracts from Tithonia diversifolia and Bryum coronatum collected from Ogbomoso, Oyo State. Nigeria.
Medicinal plants are gifts of nature to cure limitless number of diseases among human beings (Bushra and Ganga, 2003). The abundance of plants on the earth's surfaces has led to an increasing interest in the investigation of different extracts obtained from traditional medicinal plants as potential sources of new antimicrobial agents. (Bonjar and Farrokhi, 2004).
Researches have shown that all different parts of the plants which include; stem, root, flower, bark, leaves, e.t.c. possess antimicrobial property, work of Jalalpure et al., 2004, showed that the extracts of flowers and seeds of C. auriculata possess antidiabetic activity. Recently several workers have reported antibacterial activities of local plants i.e. Euphorbia hirta (Ogbulie et al, 2007), Kigelia africana (Omokehin et al 2007), Hibiscus sabdariffa (Olaleye 2007) and Mucuna pruriens (Salau and Odeleye, 2007).
Tithonia diversifolia Hemsley. Gray is a plant belonging to the family asteraceae (compositae) found widely distributed" throughout the humid and sub-humid tropics in central and south America, Asia and Africa. Chemical analysis of extracts from the leaf of Tithonia showed that they contain sesquiterpene lactones e.g. Tagitinin which possess insecticidal properties (Liasu and Achakzai 2006). It is not yet known whether these substances have antimicrobial properties.
Bryum coronatum, (Schwaegr) is a lower green plant of the division bryophyta. Which is found growing profusely in moist and shaded microhabitats within rural and urban ecosystems in tropical West Africa e.g. abandoned buildings, open walls of roadside gutters and embankments. An interesting feature of this plant is that quite unlike most mosses often affected by environmental changes brought about by human activities, it persist in habitats within heavily populated human settlements irrespective of industrial emissions. Another unique feature of this moss is that its community is not easily amenable to decomposition after the completion of its annual growth cycle. Hence, the community viewed "in situ" consist of superposed layers of debris of succeeding generations overtopping one another in a descending order of age with the present year's growth lying on the surface. The fact that this moss does not decay in nature, and its persistence in situations when other plants remains must have decayed suggest that it has innate resistance to microbial agents of degradation i.e. bacteria and fungi. No known economic use has been reported for this plant. The present investigation was carried out on stem, leaves and flowers of T. diversifolia and Byrum coronatum in other to determine the antimicrobial activity of their aqueous and ethanolic extracts against five bacterial and four fungal isolates.
Materials and methods
The two plants samples, Tithonia diversifolia and Byrum coronatum used for the work were collected during the rainy season from the bushes around Ladoke Akintola University of Technology, Ogbomoso, Nigeria. Fresh plants were used and all the samples were grounded in a laboratory mortal into fine particles.
The extraction was done with 15 gm powdered samples in distilled water and ethanol by reflux method. The crude extracts were subjected to vapourization to remove excess solvent. The crude extracts were used for bioassay against both gram negative and gram positive bacteria and fungi by agar diffusion method.
The antimicrobial activity of three different parts of T. diversifolia and B. coronatum extracts was tested against five pathogenic bacteria, viz, gram positive, Bacillus subtilis and Staphylococcus sp and gram negative Proteus vulgaris, Pseudomonas aeruginosa and Escherichia coli, while the fungal isolates include Penicillium atrovenetium, Aspergillus niger, Geotrichum candidium and Fusarium flocciferum. The agar diffusion method of Garg and Jain (1988) was followed for the antimicrobial assay. Inoculum was prepared from the 24 hours old culture of bacterial isolates in nutrient broth while mycelia plug was cut off from the 48 hours culture of fungal isolates. Nutrient agar plates were prepared and the inocula were seeded by spread plate method, for the fungal isolates, Potato Dextrose agar were prepared and the mycelia plugs were put at the centre of the prepared plates. The extracts were applied to sterile Whatman No. 1 filter paper discs. All the samples were done in duplicate. Both positive and negative controls were determined, for negative control the two solvents (distilled water and ethanol) were also used to determine their effect on test organisms. While six commonly antibiotics discs were also used to compare the effectiveness of the plants extracts with that of the antibiotics. Antibiotics used include; Amoxicillin, Cotrimoxazole, Ciprofloxacin, Tetracycline, Ofloxacin and Gentamycin. While Clotrimazole was used to compare the effectiveness of the extracts against fungi.
After 24 hours of 37[degrees]c and 48 hours of 25[degrees]c for bacteria and fungi inoculation, the inhibition zone surrounding the discs by the diffusion of compounds was measured in mm diameter.
The minimum inhibitory concentration (MIC) of the extracts against bacteria was also determined. This was done by soaking the paper disc in different concentration of the plant extracts using the same method of agar diffusion. Zones of inhibition in mm were also measured.
Results and discussion
All the plants extracts used in this study possessed antibacterial property except the ethanolic extract of T. diversifolia leaf which is only active against Staphylococcus sp and E. coli with zones of inhibition of 08.00 mm and 15.00 mm respectively (Table 1). Aqueous extract of T. diversifolia stem and the ethanolic extract of its flower had the highest zones of inhibition .The activity of 10mg/ml of both the ethanolic and aqeous extracts of all the plants extracts against Staphylococcus aureus was similar to that of 10[micro]g disc of ciprofloxacin except the ethanolic extract of T. diversifolia which had diameter of zone of inhibition of 08.0mm. The effectiveness of the commercial antibiotics discs used against the test organisms were as follows, 0%, 0%, 100%, 20%, 60%, and 60% for amoxicillin (25[micro]g), cotrimoxazole (25[micro]g), ciprofloxacin (10[micro]g), tetracycline (30[micro]g), ofloxacin (30[micro]g), and gentamycin (10[micro]g) respectively (Table 1). Distilled water and ethanol which served as negative controls produced no zones of inhibition.
Table 2 shows that all the plants extracts used possess antifungal properties. Ethanolic extract of T. diversifolia was able to compare favourably with the standard antifungal agent (Clotrimazole) used. While the MIC for the plants extracts ranged from 0.01 mg/ml to 100 mg/ml. E. coli recorded the least MIC of 0.01 to 1.0 mg/ml (Table 3).
Several workers have reported that many plants possess antimicrobial properties including the parts which include; flower, bark, stem, leaf, e.t.c. It has been shown that when solvents like ethanol, hexane and methanol are used to extract plants, most of them are able to exhibit inhibitory effect on both gram positive and gram negative bacteria (Bushra and Ganga, 2003). Similar work by Omonkhelin et al., showed that ethanolic extract of Kigelia africana has minimum inhibitory concentration of 6.25 +_ 1.07 mg/ml and 7.92 +_ 1.52 mg/ml for S. aureus and C. albicans. This work also showed that all the plants used possessed antimicrobial activity and they can be used as broad spectrum antibiotics since they were active against both Gram positive and Gram negative bacteria. Antibacterial effects of these plants on Staphylococcus aureus, E. coli, and Pseudomonas aeruginosa showed that the plants can be used in the treatment of gastrointestinal infection and darrhoea in man and skin diseases (Rogger et al., 1990) and they can also be used in the treatment of urinary tract infection associated with Proteus sp. (Madigan et al., 2000). Both ethanolic and aqueous extracts of these plants can be used in the treatment of boils, sores and wounds, since Staphylococcus aureus and P. aeruginosa have been implicated as causative agents of these diseases (Braude, 1982).
The low MIC exhibited by these plants extracts against some test organisms showed that they can be used as an alternative to orthodox antibiotics in the treatment of infections caused by these microorganisms and since most microorganisms are developing resistance to the known antibiotics (Singleton, 1991), they will be the best therapeutics option.
Ayo, R.G., J.O. Amupitan and Yimin Zhao, 2007. Cytotoxicity and antimicrobial studies of 1, 6, 8-trihydroxy-3-methyl-anthraquinone (Emodin) isolated from the leaves of Cassia nigricans Vahl. African Journal of Biotechnology, 6(11): 1276-1279.
Bushra Beegum, N.R. and T. Ganga Devi, 2003. Antibacterial activity of selected Seaweeds from Kovalam south West coast of India. Asian Jr. of Microbiol. Biotech. Env. Sc., 5(3): 319-322.
Fransworth, N.R, O. Akerele and A.S. Bingel, 1985. Medicinal plants in therapy. Bull. WHO., 63: 965-981.
Bonjar, Glls and Farrokhi, P.R., 2004. Antibacillus activity of some plants used in traditional medicine of Iran. Niger. J. Nat. Prod. Med., 8: 34-39.
Braude, A.I., 1982. Microbiology. W. B. Sauders Company, London.
Garg, S.C. and R.K. Jain, 1988. Antimicrobial efficacy of Essential oil from Curcuma caesia Indian Journal of Microbiolgy., 38: 168-17.
Jalalpure, S. S., M.B. Patil, A. Aruna, B.N. Shah and M.D. Salahuddin, 2004. Antidiabetic activity of Cassia auriculata seeds in alloxan induced Diabetic rats. Niger. J. Nat. Prod. Med., 8: 22-23.
Liasu, M.O. and A.K.K Achakzai, 2007. Influence of Tithonia diversifolia leaf mulch and fertilizer application on growth and yield of potted tomato plants. American-Eurasian Journal of Agric. and Environmental Science, 2(4): 335-340.
Madigan, M.T., J.M. Martinko and J. Parker, 2000. Brock Biology of Microorganisms. 9th ed. Prentice-Hall, Inc. New Jersey., pp: 783-784.
Ogbulie, J.N., I.C. Okoli and B.N. Anyanwu, 2007. Antibacterial activities and toxicological potentials of crude ethanolic'extracts of Euphorbia hirta. African Journal of Biotechnology., 6(13): 1544-1548.
Olaleye, M.T., 2007. Cytotoxicity and antibacterial activity of methanolic extract of Hibiscus sabdariffa. Journal of Medicinal Plants Research, 1(1): 009-013.
Omonkhelin, J.O., K.I.O. Eric and O. Osohon, 2007. Antifungal and antibacterial Activities of the ethanolic and aqueous extract of Kigelia africana (Bignoniaceae) stem bark, African Journal of Biotechnology, 6(14): 16771680.
Roggers, Y.S., L.I. John and L.W. Mark, 1990. General Microbiology, 5th ed. Macmillan education Ltd London., pp: 626-642.
Salau, A.O. and O.M. Odeleye, 2007. Antimicrobial activity of Mucuna pruriens on selected bacteria. African Journal of Biotechnology, 6(18): 2091-2092.
Singleton, P., 1999. Bacteria in Biology, Biotechnology and Medicine. 4th Edn. John Wiley and Sons Ltd, New York.
Corresponding Author: Liasu, M.O., Department of Pure and Applied Biology, Ladoke Akintola University of Teghnology, Ogbomoso. E-mail: firstname.lastname@example.org
Liasu, M.O. and Ayandele, A.A.
Department of Pure and Applied Biology, Ladoke Akintola University of Teghnology, Ogbomoso.
Liasu, M.O. and Ayandele, A.A.,: Antimicrobial Activity of Aqueous and Ethanolic Extracts from Tithonia diversifolia and Bryum Coronatum Collected from Ogbomoso, Oyo State. Nigeria,: Adv. in Nat. Appl. Sci., 2(1): 31-34, 2008
Table 1: Antibacterial Activity of Plant Exracts Against Tets Organisms DIAMETER OF ZONE OF INHIBITION IN MM Plant Extract Staphylococcus Proteus Bacillus sp. vulgaris subtilis Ethanolic extract of 20.0 10.0 19.0 T. diver flower Aqueous extract of 22.0 -- 20.0 T. diver flower Ethanolic extract of 18.0 -- 15.0 T. diver stem Aqueous extract of 19.0 13.0 24.0 T. diver stem Ethanolic extract of 08.0 -- -- T. diver leaf Aqueous extract of 20.0 11.0 13.0 T. diver leaf Ethanolic extract of Byrum 22.0 -- 17.0 Aqueous extract of Byrum 20 15.0 -- Control(water) -- -- -- Control(ethanol) -- -- -- Amoxicillin 25 [micro]g -- -- -- Cotrimoxazole 25 [micro] -- -- -- Ciprofloxacin 10 [micro]g 21.0 25.5 31.5 Tetracycline 30 [micro]g 13.5 -- -- Ofloxacin 30 [micro]g 17.0 27.0 -- Gentamycin 10 [micro]g 13.5 -- -- DIAMETER OF ZONE OF INHIBITION IN MM Pseudomonas Escherichia Plant Extract aeruginosa coli Ethanolic extract of 12.0 11.0 T. diver flower Aqueous extract of 17.0 12.0 T. diver flower Ethanolic extract of -- 16.0 T. diver stem Aqueous extract of 15.0 14.0 T. diver stem Ethanolic extract of -- 15.0 T. diver leaf Aqueous extract of 14.0 17.0 T. diver leaf Ethanolic extract of Byrum 15.0 14.0 Aqueous extract of Byrum 12.0 18.0 Control(water) -- -- Control(ethanol) -- -- Amoxicillin 25 [micro]g -- -- Cotrimoxazole 25 [micro] -- -- Ciprofloxacin 10 [micro]g 21.0 25.5 Tetracycline 30 [micro]g -- -- Ofloxacin 30 [micro]g -- 26.0 Gentamycin 10 [micro]g 12.5 14.0 Key = no growth Table 2: Antifungal Activity of the Plant Extracts DIAMETER OF ZONE OF INHIBITION IN MM Penicillium Aspergillus atrovenetium niger Ethanolic extract of T. diver flower 16.0 13.8 Aqueous extract of T. diver flower 14.5 10.5 Ethanolic extract of T. diver stem 17.3 14.0 Aqueous extract of T. diver stem 16.5 08.6 Ethanolic extract of T. diver leaf 10.5 07.6 Aqueous extract of T. diver leaf -- 05.6 Ethanolic extract of Byrum 09.0 10.0 Aqueous extract of Byrum -- 06.8 Clotrimazole 21.5 18.0 DIAMETER OF ZONE OF INHIBITION IN MM Geotrichum Fusarium candidium flocciferum Ethanolic extract of T. diver flower 16.0 20.0 Aqueous extract of T. diver flower 13.5 12.5 Ethanolic extract of T. diver stem 18.6 15.0 Aqueous extract of T. diver stem 10.0 08.7 Ethanolic extract of T. diver leaf 09.5 16.5 Aqueous extract of T. diver leaf 05.0 09.0 Ethanolic extract of Byrum 12.0 10.4 Aqueous extract of Byrum 09.5 08.0 Clotrimazole 21.0 19.0 Key: = no growth Table 3: Minimum Inhibition Concentration of Plant Extracts (MIC) MIC (mg/ml) Staphylococcus Proteus Plant Extract aureus vulgaris Ethanolic extract of T. diver flower 1.0 >100 Aqueous extract of T. diver flower 1.0 >100 Ethanolic extract of T. diver stem 10.0 >100 Aqueous extract of T. diver stem 0.01 1.0 Ethanolic extract of T. diver leaf >100 >100 Aqueous extract of T. diver leaf 0.01 100.0 Ethanolic extract of Byrum 0.01 >100 Aqueous extract of Byrum 1.0 0.1 MIC (mg/ml) Bacillus Pseudomonas Plant Extract subtilis aeruginosa Ethanolic extract of T. diver flower 0.01 100.0 Aqueous extract of T. diver flower 0.1 0.01 Ethanolic extract of T. diver stem 100. >100 Aqueous extract of T. diver stem 0.01 0.01 Ethanolic extract of T. diver leaf >100 >100 Aqueous extract of T. diver leaf 10.0 1.0 Ethanolic extract of Byrum 0.1 10.0 Aqueous extract of Byrum >100 100.0 MIC (mg/ml) Plant Extract E. coli Ethanolic extract of T. diver flower 0.01 Aqueous extract of T. diver flower 0.01 Ethanolic extract of T. diver stem 0.1 Aqueous extract of T. diver stem 0.01 Ethanolic extract of T. diver leaf 0.01 Aqueous extract of T. diver leaf 1.0 Ethanolic extract of Byrum 0.1 Aqueous extract of Byrum 0.1
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|Title Annotation:||Original Article|
|Author:||Liasu, M.O.; Ayandele, A.A.|
|Publication:||Advances in Natural and Applied Sciences|
|Date:||Jan 1, 2008|
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