Inhibitory Effects of Extracts and Isolates from Kigelia africana Fruits against Pathogenic Bacteria and Yeasts
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Inhibitory Effects of Extracts and Isolates from Kigelia africana Fruits against Pathogenic Bacteria and Yeasts

Authors: Deepak K. Semwal, Ruchi B. Semwal, Aijaz Ahmad, Guy P. Kamatou, Alvaro M. Viljoen

Abstract:

Kigelia africana (Lam.) Benth. (Bignoniaceae) is a reputed traditional remedy for various human ailments such as skin diseases, microbial infections, melanoma, stomach troubles, metabolic disorders, malaria and general pains. In spite of the fruit being widely used for purposes related to its antibacterial and antifungal properties, the chemical constituents associated with the activity have not been fully identified. To elucidate the active principles, we evaluated the antimicrobial activity of fruit extracts and purified fractions against Staphylococcus aureus, Enterococcus faecalis, Moraxella catarrhalis, Escherichia coli, Candida albicans and Candida tropicalis. Shade-dried fruits were powdered and extracted with hydroalcoholic (1:1) mixture by soaking at room temperature for 72 h. The crude extract was further fractionated by column chromatography, with successive elution using hexane, dichloromethane, ethyl acetate, acetone and methanol. The dichloromethane and ethyl acetate fractions were combined and subjected to column chromatography to furnish a wax and oil from the eluates of 20% and 40% ethyl acetate in hexane, respectively. The GC-MS and GC×GC-MS results revealed that linoleic acid, linolenic acid, palmitic acid, arachidic acid and stearic acid were the major constituents in both oil and wax. The crude hydroalcoholic extract exhibited the strongest activity with MICs of 0.125-0.5 mg/mL, followed by the ethyl acetate (MICs = 0.125-1.0 mg/mL), dichloromethane (MICs = 0.250-2.0 mg/mL), hexane (MICs = 0.25- 2.0 mg/mL), acetone (MICs = 0.5-2.0 mg/mL) and methanol (MICs = 1.0-2.0 mg/mL), whereas the wax (MICs = 2.0-4.0 mg/mL) and oil (MICs = 4.0-8.0 mg/mL) showed poor activity. The study concludes that synergistic interactions of chemical constituents could be responsible for the antimicrobial activity of K. africana fruits, which needs a more holistic approach to understand the mechanism of its antimicrobial activity.

Keywords: Kigelia Africana, traditional medicine, antimicrobial activity, Candida albicans, palmitic acid, synergistic interaction.

Digital Object Identifier (DOI): doi.org/10.5281/zenodo.1097140

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References:


[1] V. Roodt, “Kigelia africana” In: The Shell Field Guide to the Common Trees of the Okavango Delta and Moremi Game Reserve. Gaborone, Shell Oil, Botswana, 1992, pp. 176-180.
[2] S. Saini, H. Kaur, B. Verma, S. K. R. Singh, “Kigelia africana (Lam.) Benth. An overview.” Natural Product Radiance, vol. 8, 2009, pp. 190- 197.
[3] P. J. Houghton, “The sausage tree (Kigelia africana): Ethnobotany and recent scientific work.” South African Journal of Botany, vol. 68, 2002, pp. 14-20.
[4] L. S. Gill, “Ethanomedical uses of plants in Nigeria”, Uniben Press, Benin City, Nigeria, 1992, pp. 143.
[5] Oliver-Bever B. (1986). “Medicinal plants in tropical West Africa.” Cambridge University Press; Cambridge, London, New York, New Rochelle, Melbourne, Sydney, pp. 240-245.
[6] J. M. Watt, M. G. Breyer-Brandwijk, “The medicinal and poisonous plants of southern and eastern Africa.” E. and S. Livingstone Ltd. Edinburgh and London, 1962, pp. 52.
[7] M. F. Khan, P. Dixit, N. Jaiswal, A. K. Tamrakar, A. K. Srivastava, R. Maurya, “Chemical constituents of Kigelia pinnata twigs and their GLUT4 translocation modulatory effect in skeletal muscle cells.” Fitoterapia, vol. 83, 2012, pp. 125-129.
[8] P. J. Houghton, D. N. Akunyili, “Iridoids from Kigelia pinnata bark.” Fitoterapia, vol. 64, 1993, pp. 473-474.
[9] Y. G. Gouda, A. M. Abdel-Baky, F. M. Darwish, K. M. Mohamed, R. Kasai, K. Yamasaki, “Iridoids from Kigelia pinnata DC. fruits.” Phytochemistry, vol. 63, 2003, pp. 887-892.
[10] C. R. Weiss, S. V. K. Moideen, S. L. Croft, P. J. Houghton, “Activity of extracts and isolated naphthoquinones from Kigelia pinnata against Plasmodium falciparum.” Journal of Natural Products, vol. 63, 2000, pp. 1306-1309.
[11] D. N. Akunyili, P. J. Houghton, “Monoterpenoids and naphthoquinones from Kigelia pinnata.” Phytochemistry, vol. 32, 1993, pp. 1015-1018.
[12] S. M. El-Sayyad, “Flavonoids of the leaves and fruits of Kigelia pinnata.” Fitoterapia, vol. 52, 1982, pp. 189-191.
[13] T. R. Govindachari, S. J. Patankar, N. Viswanathan, “Isolation and structure of two new dihydroisocoumarins from Kigelia pinnata.” Phytochemistry, vol. 10, 1971, pp. 1603-1606.
[14] K. Inoue, H. Inouye, C. C. Chen, “A naphthoquinone and a lignan from the wood of Kigelia pinnata.” Phytochemistry, vol. 20, 1981, pp. 2271- 2276.
[15] O. T. Asekun, E. Olusegun, O. Adebola, “The volatile constituents of the leaves and flowers of Kigelia africana Benth.” Flavour and Fragrance Journal, vol. 22, 2007, pp. 21-23.
[16] O. M. Grace, M. E. Light, K. L. Lindsey, D. A. Mulholland, J. van Staden, A. K. Jager, “Antibacterial activity and isolation of active compounds from fruit of the traditional African medicinal tree Kigelia africana.” South African Journal of Botany, vol. 68, 2002, pp. 220-222.
[17] R. Jeyachandran, A. Mahesh, “Antimicrobial evaluation of Kigelia africana (Lam).” Research Journal of Microbiology, vol. 2, 2007, pp. 645-649.
[18] M. A. A. Sikder, A. K. M. N. Hossian, A. B. Siddique, M. Ahmed, M. A. Kaisar, M. A. Rashid, “In vitro antimicrobial screening of four reputed Bangladeshi medicinal plants.” Pharmacognosy Journal, vol. 3, 2011, pp. 72-76.
[19] R. Badoni, D. K. Semwal, U. Rawat, “Fatty acid composition and antimicrobial activity of Celtis australis L. fruits.” Journal of Scientific Research, vol. 2, 2010, pp. 397-402.
[20] CLSI, “Clinical and Laboratory Standards Institute, Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically, Approved Standard M7-A6.” National Committee for Clinical Laboratory Standards, 6th edition, Fort Wayne, Ind, USA, 2003.
[21] S. K. Kothiyal, D. K. Semwal, R. Badoni, U. Rawat, “GC-MS analysis of fatty acids and the antimicrobial activity of Ilex dipyrena Wallich leaves.” Asian Journal of Traditional Medicines, vol. 5, 2010, pp. 153- 157.