期刊论文详细信息
BMC Complementary and Alternative Medicine
Antibacterial constituents of three Cameroonian medicinal plants: Garcinia nobilis, Oricia suaveolens and Balsamocitrus camerunensis
Victor Kuete1  Namrita Lall1  Jacobus J Marion Meyer1  Choudhary M Iqbal3  Shaheen Farzana3  Augustin E Nkengfack2  Celine D Mbazoa2  Armelle T Mbaveng4  Hugues Fouotsa3 
[1] Department of Plant Science, Faculty of Agricultural and Biological Science, Pretoria 0002, South Africa;Department of Organic Chemistry, Faculty of Science, University of Yaoundé 1, Po.box 812, Yaoundé, Cameroon;H. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Pakistan;Department of Organic Chemistry, Higher Teachers Training College, University of Maroua, P.O.Box 46, Maroua, Cameroon
关键词: Balsamocitrus camerunensis;    Oricia suaveolens;    Garcinia nobilis;    Compounds;    Cameroon;    Antibacterial;    Antimycobacterial;   
Others  :  1230111
DOI  :  10.1186/1472-6882-13-81
 received in 2012-08-16, accepted in 2013-04-08,  发布年份 2013
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【 摘 要 】

Background

Multidrug resistance is a worrying cause of treatment failure in bacterial infections. The search of bioactive constituents from medicinal plants against multidrug resistant (MDR) bacteria has significantly evolved in the two last decades. In the present study, twenty-two compounds (three terpenoids, eleven phenolics and eight alkaloids) isolated from three Cameroonian medicinal plants, namely Garcinia nobilis, Oricia suaveolens and Balsamocitrus camerunensis, as well as the crude extracts were tested for their antibacterial activities against Mycobacterium tuberculosis and Gram-negative bacteria amongst which were MDR active efflux pumps expressing phenotypes.

Methods

The microplate alamar blue assay (MABA) and the broth microdilution methods were used to determine the minimal inhibitory concentrations (MIC) and minimal bactericidal concentrations (MBC) of the studied samples.

Results

The results of the MIC determinations indicate that, the best crude extract was that from G. nobilis (GNB), its inhibitory effects being noted against 12 of the 14 tested bacteria. The extract of GNB also exhibited better anti-tuberculosis (MIC of 128 μg/ml M. tuberculosis against ATCC 27294 strain) and antibacterial (MIC of 64 μg/ml against Escherichia coli ATCC10536) activities compared to the extracts of O. suaveolens and B. camerunensis. Interestingly, 4-prenyl-2-(3,7-dimethyl-2,6-octadienyl)-1,3,5,8-tetrahydroxyxanthone (2), isolated from the most active extract GNB, also showed the best activity amongst compounds, inhibiting the growth of all the fourteen tested microorganisms. The lowest MIC value obtained with compound 2 was 8 μg/ml against M. tuberculosis ATCC 27294 and M. tuberculosis clinical MTCS2 strains. Other compounds showed selective activities with 11 of the 14 tested bacteria being sensitive to the xanthone, morusignin I (5) and the alkaloid, kokusaginine (13).

Conclusions

The results of the present investigation provide evidence that the crude extract from G. nobilis, O. suaveolens and B. camerunensis as well as some of their compounds, and mostly compound 2 (isolated from G. nobilis,) could be considered as interesting natural antibacterial products.

【 授权许可】

   
2013 Fouotsa et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Kuete V, Ngameni B, Tangmouo JG, Bolla JM, Alibert-Franco S, Ngadjui BT, Pagès JM: Efflux pumps are involved in the defense of Gram-negative bacteria against the natural products isobavachalcone and diospyrone. Antimicrob Agents Chemother 2010, 54:1749-1752.
  • [2]Kuete V, Alibert-Franco S, Eyong KO, Ngameni B, Folefoc GN, Nguemeving JR, Tangmouo JG, Fotso GW, Komguem J, Ouahouo BM, Bolla JM, Chevalier J, Ngadjui BT, Nkengfack AE, Pagès JM: Antibacterial activity of some natural products against bacteria expressing a multidrug-resistant phenotype. Int J Antimicrob Agents 2011, 37:156-161.
  • [3]Ampofo AS, Waterman GP: Xanthones from three Garcinia species. Phytochemistry 1986, 25:2351-2355.
  • [4]Nguyen LH, Venkatraman G, Sim KY, Harrison LJ: Xanthones and benzophenones from Garcinia griffithii and Garcinia mangostana. Phytochemistry 2005, 66:1718-1723.
  • [5]Abe MO: The occurrence of the alkaloid oricine in the wood of Oricia suaveolens. Phytochemistry 1971, 10:3328-3330.
  • [6]Abe MO, Taylor DAH: A quinolone alkaloid from Oricia suaveolens. Phytochemistry 1971, 10:1167-1169.
  • [7]Letouzey R: Flore du Cameroun No. 1. Rutacées, Zygophyllacées, Balanitacées. Paris: Museum National d'Histoire Naturelle; 1963.
  • [8]Tsassi VB, Hidayat H, Meffo BY, Kouam SF, Dongo E, Schulz B, Green IR, Krohn K: Anti-microbial coumarins from the stem bark of Afraegle paniculata. Nat Prod Commun 2010, 5:559-561.
  • [9]Asase A, Oteng-Yeboah AA, Odamtten GT, Simmonds MSJ: Ethnobotanical study of some Ghanaian anti-malarial plants. J Ethnopharmacol 2005, 99:273-279.
  • [10]Fouotsa H, Meli Lannang L, Djama Mbazoa C, Rasheed S, Marasini BP, Ali Z, Devkota KP, Kengfack AE, Shaheen F, Choudhary MI, Sewald N: Xanthones inhibitors of α-glucosidase and glycation from Garcinia nobilis. Phytochem Lett 2012, 5:236-239.
  • [11]Gella MD, Monako P, Previtera L: Stigmasterols from Typha latifolia. J Nat Prod 1990, 53:1430-1435.
  • [12]Sholichin M, Yamasaki K, Kasai R, Tanaka O: 13C Nuclear Resonance of lupane-type triterpenes, lupeol, betulin and betulinic acid. Chem Pharm Bull 1980, 28:1006-1008.
  • [13]Govindachari TR, Pai BR, Subramaniam PS, Subramanyam V: A synthesis of evoxanthine. Tetrahedron 1967, 23:1827-1829.
  • [14]Ermias D, Abiy Y, Peter GW, Alexander IG: The chemical systematics of the Rutaceae, subfamily Toddalioideae, in Africa. Biochem Syst Ecol 1988, 16:179-188.
  • [15]Vaquette J: Alkaloids from leave of Teclea boiviniaana. Planta Med 1978, 60:78-84.
  • [16]Al-Rehaily AJ, Ahmad MS, Muhammad I, Al-Thukair AA, Perzanowski HP: Furoquinoline alkaloids from Teclea nobilis. Phytochemistry 2003, 64:1405-1411.
  • [17]Wondimu A, Dagne E, Waterman PG: Quinoline alkaloids from the leaves of Teclea simplicifolia. Phytochemistry 1988, 27:959-960.
  • [18]Kuzovkina I, Al’terman I, Schneider B: Specific accumulation and revised structures of acridone alkaloid glucosides in the tips of transformed roots of Ruta graveolens. Phytochemistry 2004, 65:1095-1100.
  • [19]Semwal S, Sharma RK: A new lignan rhamnoside from Bauhinia retusa seed pods (Caesalpiniaceae). Chinese Chem Lett 2011, 22:1081-1083.
  • [20]Barton DHR, Pradhan SK, Sternhell S, Templton JF: T: Part XXV: The constitutions of limonin and related bitter principles. J Chem Soc 1961, 255-275.
  • [21]Chaurasia N, Wichtl M: Sterols and Steryl Glycosides from Urtica dioica. J Nat Prod 1987, 50:881-885.
  • [22]Lin LC, Yang LL, Chou CJ: Cytotoxic naphthoquinones and plumbagic acid glucosides from Plumbago zeylanica. Phytochemistry 2003, 62:619-622.
  • [23]Renmin L, Aifeng L, Ailing S: Preparative isolation and purification of coumarins from Angelica dahurica (Fisch. ex Hoffm) Benth, et Hook. f (Chinese traditional medicinal herb) by high-speed counter-current chromatography. J Chromatograph A 2004, 1052:223-227.
  • [24]Ulubelen A, Oksuz S, Aynehchi Y: Salehi Sormaghi MH, Souri A, Mabry TM: Capillarin and Scaporone from Artemisia lamprocaulos. J Nat Prod 1984, 47:170-171.
  • [25]Shouce ZYC: The Committee of Chinese Herb Information. Beijing: Renmin Weisheng Publisher; 1986.
  • [26]Eloff JN: A sensitive and quick microplate method to determine the minimal inhibitory concentration of plant extracts for bacteria. Planta Med 1998, 64:711-713.
  • [27]Mativandlela SPN, Lall N, Meyer JJM: Antibacterial, antifungal and antitubercular activity of (the roots of) Pelargonium reniforme (CURT) and Pelargonium sidoides (DC) (Geraniaceae) root. S Afr J Bot 2006, 72:232-237.
  • [28]Lacmata ST, Kuete V, Dzoyem JP, Tankeo SB, Teke GN, Kuiate JR, Pages JM: Antibacterial Activities of Selected Cameroonian Plants and Their Synergistic Effects with Antibiotics against Bacteria Expressing MDR Phenotypes. Evid Based Complement Alternat Med 2012, 2012:623723.
  • [29]Kuete V, Ngameni B, Fotso Simo CC, Kengap Tankeu R, Tchaleu Ngadjui B, Meyer JJM, Lall N, Kuiate JR: Antimicrobial activity of the crude extracts and compounds from Ficus chlamydocarpa and Ficus cordata (Moraceae). J Ethnopharmacol 2008, 120:17-24.
  • [30]Tereschuk ML, Riera MVQ, Castro GR, Abdala LR: Antimicrobial activity of flavonoid from leaves of Tagetes minuta. J Ethnopharmacol 1997, 56:227-232.
  • [31]Zgoda JR, Porter JR: A convenient microdilution method screening natural products against bacteria and fungi. Pharmaceut Biol 2001, 39:221-225.
  • [32]Jimenez-Arellanes A, Meckes M, Ramirez R, Torres J, Luna-Herrera J: Activity against multidrug-resistant Mycobacterium tuberculosis in Mexican plants used to treat respiratory diseases. Phytother Res 2003, 17:903-908.
  • [33]Simões M, Bennett RN, Rosa EA: Understanding antimicrobial activities of phytochemicals against multidrug resistant bacteria and biofilms. Nat Prod Rep 2009, 26:746-757.
  • [34]Kuete V: Potential of Cameroonian plants and derived products against microbial infections: a review. Planta Med 2010, 76:1479-1491.
  • [35]Kuete V, Efferth T: Cameroonian medicinal plants: pharmacology and derived natural products. Front Pharmacol 2010, 1:123.
  • [36]Gallo MBC, Sarachine MJ: Biological activities of lupeol. Intl J Biomed Pharma Sci 2009, 3:46-66.
  • [37]Kuete V, Wansi JD, Mbaveng AT, Kana Sop MM, Tcho Tadjong A, Penlap Beng V, Etoa FX, Wandji J, Marion Meyer JJ, Lall N: Antimicrobial activity of the methanolic extract and compounds from Teclea afzelii (Rutaceae). S Afr J Bot 2008, 74:572-576.
  • [38]Kuete V, Komguem J, Penlap Beng V, Meli AL, Tangmouo JG, Etoa FX, Lontsi D: Antimicrobial components of the methanolic extract from the stem bark of Garcinia smeathmannii Oliver (Clusiaceae). S Afr J Bot 2007, 73:347-354.
  • [39]Kim Y-G, Watanabe N, Sano Y, Uraki Y, Sano Y: Extractives of kitakobusi Magnolia kobus DC. var. borealis Sarg. III.: Antibacterial and Antifungal Activity of Extractives. Res Bull Hokkaido Univ For 1998, 55:63-73.
  • [40]Rahman A, Na M, Kang SC: Antilisterial potential of imperatorin and limonin. J Food Biochem 2012, 36:217-223.
  • [41]Sunthitikawinsakul A, Kongkathip N, Kongkathip B, Phonnakhu S, Daly JW, Spande TF, Nimit Y, Rochanaruangrai S: Coumarins and carbazoles from Clausena excavata exhibited antimycobacterial and antifungal activities. Planta Med 2003, 69:155-157.
  • [42]Kuete V, Metuno R, Ngameni B, Tsafack AM, Ngandeu F, Fotso GW, Bezabih M, Etoa FX, Ngadjui BT, Abegaz BM, Beng VP: Antimicrobial activity of the methanolic extracts and compounds from Treculia obovoidea (Moraceae). J Ethnopharmacol 2007, 112:531-536.
  • [43]Olila D, Opuda-Asibo J: Olwa-Odyek: Bioassay-guided studies on the cytotoxic and in vitro trypanocidal activities of a sesquiterpene (Muzigadial) derived from a Ugandan medicinal plant (Warburgia ugandensis). Afr Health Sci 2001, 1:12-15.
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