Njeru Sospeter Ngoci, Obonyo Meshack, Nyambati Samwel, Ngari Silas, Mwakubambanya Ramadhan, Mavura Hawa
Department of Medicine, Kisii University, P.O. Box. 408-40200, Kisii, Kenya.
Department of Biochemistry & Molecular Biology, Egerton University, P.O. Box. 536-20115, Egerton, Kenya.
J Intercult Ethnopharmacol. 2016 Apr 16;5(3):226-32. doi: 10.5455/jice.20160416122003. eCollection 2016 Jun-Aug.
BACKGROUND/AIM: Clerodendrum myricoides is a Kenyan herbal plant used in the management of respiratory diseases. In the current study, we investigated in vitro antimicrobial activity, cytotoxicity, and phytochemical screening of C. myricoides.
Antimicrobial activities of C. myricoides organic fractions against array of microorganisms including: (i) Mycobacterium tuberculosis (MTB) H37Rv, (ii) Staphylococcus aureus, (iii) Klebsiella pneumoniae, (iv) Escherichia coli, (v) Candida albicans, (vi) Pseudomonas aeruginosa, (vii) Cryptococcus neoformans, (viii) Salmonella typhi, (ix) Shigella sonnei, and (x) Methicillin-resistant S. aureus (MRSA) were investigated by disc diffusion and microdilution techniques. Antituberculous activity was investigated using BACTEC MGIT 960 system while cytotoxicity was analyzed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay on HEp-2 cells. Finally, phytochemicals were screened using standard procedures.
Methanolic fractions exhibited a broad spectrum activity inhibiting 75% of test pathogens. It had the highest activity with minimal inhibition concentration (MIC) values of ≤62.5 µg/ml recorded against 62.5% tested microbes. It yielded the highest zone of inhibition of 20.3 mm (S. aureus), lowest MIC of <12.5 µg/ml (MTB), and the lowest minimal bactericidal concentration of 62.5 µg/ml (C. albicans), within the acceptable toxicity limit (CC50 >90 µg/ml). The phytochemicals largely believed to be responsible for the observed activity included: Alkaloid, phenols, anthraquinones, terpenoids, and flavonoids.
Methanolic fraction had remarkable activity against MRSA, S. aureus, E. coli, S. sonnei, C. albicans, and MTB, which are of public health concerns due to drug resistance and as sources of community and nosocomial infections. To the best of our knowledge, this is the first report exploring the antituberculous activity of C. myricoides and thence a major output in search of novel, safe drug leads to mitigate the global tuberculosis threat.
背景/目的:杨梅臭牡丹是一种肯尼亚草药,用于治疗呼吸道疾病。在本研究中,我们对杨梅臭牡丹进行了体外抗菌活性、细胞毒性及植物化学物质筛查。
采用纸片扩散法和微量稀释法研究杨梅臭牡丹有机提取物对一系列微生物的抗菌活性,这些微生物包括:(i)结核分枝杆菌(MTB)H37Rv、(ii)金黄色葡萄球菌、(iii)肺炎克雷伯菌、(iv)大肠杆菌、(v)白色念珠菌、(vi)铜绿假单胞菌、(vii)新型隐球菌、(viii)伤寒沙门菌、(ix)宋内志贺菌、(x)耐甲氧西林金黄色葡萄球菌(MRSA)。使用BACTEC MGIT 960系统研究抗结核活性,通过在HEp-2细胞上进行的3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐试验分析细胞毒性。最后,采用标准程序对植物化学物质进行筛查。
甲醇提取物表现出广谱活性,可抑制75%的受试病原体。其活性最高,对62.5%的受试微生物的最低抑菌浓度(MIC)值≤62.5μg/ml。它对金黄色葡萄球菌的抑菌圈最大,为20.3mm,对结核分枝杆菌的最低MIC为<12.5μg/ml,对白色念珠菌的最低杀菌浓度为62.5μg/ml,且在可接受的毒性限度内(CC50>90μg/ml)。普遍认为对观察到的活性起作用的植物化学物质包括:生物碱、酚类、蒽醌类、萜类和黄酮类。
甲醇提取物对耐甲氧西林金黄色葡萄球菌、金黄色葡萄球菌、大肠杆菌、宋内志贺菌、白色念珠菌和结核分枝杆菌具有显著活性,这些病原体因耐药性以及作为社区和医院感染源而备受公共卫生关注。据我们所知;这是首篇探索杨梅臭牡丹抗结核活性的报告,因此是寻找新型、安全药物先导物以减轻全球结核病威胁的一项重要成果。