紫锥菊对临床来源耐多药菌株的抑菌效果评价及植物化学分析

Momen M. Abdelmotaleb, Huessien H. Elshikh, Marwa M Abdel-Aziz, Mahmoud M. Elaasser, Mohammed Yosri
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引用次数: 0

摘要

对抗生素具有耐药性的微生物正在成为全球卫生保健系统的严重威胁。在细菌性疾病的治疗方法中结合具有相当抗菌特性的自然疗法,是很可能替代耐药性可能性的方法。从2016年1月至6月在Al-Zahraa大学医院和开罗专科医院采集的50份临床标本中分离出耐甲氧西林金黄色葡萄球菌(MRSA)、粪肠球菌(E. faecalis)、大肠杆菌(E. coli)、肺炎克雷伯菌(K. pneumoniae)、铜绿假单胞菌(P. aeruginosa)、鲍曼不动杆菌(A. baumannii)、神奇变形杆菌(P. mirabilis)、嗜麦芽窄养单胞菌(S. maltopophilia)。筛选了不同溶剂(己烷、乙酸乙酯、氯仿和水溶液)对临床样品中分离的多重耐药(MDR)菌株的抑菌效果。紫锥菊乙酸乙酯部位对临床菌株的抑菌效果最好,抑菌带范围为16.8 ~ 22.7 mm, MIC范围为15.63 ~ 250µg/mL,而其他部位对MDR的抑菌带较低,最小抑菌浓度(MIC)值高于乙酸乙酯部位。对嗜麦芽葡萄球菌均无抗菌作用。紫红色E. E. purpurea乙酯对MRSA的电镜观察揭示了其裂解致病菌细胞的作用。采用LC-MS对紫荆荆的乙酸乙酯部位进行分析,筛选出紫荆荆荆乙酸乙酯部位中存在的各种分子,其抗氧化活性为IC50 = 14.24±0.58µg/m。紫荆乙酸乙酯部位对Vero细胞的CC50值为1145.97 μg/ml,毒性较小。该研究结果将用于进一步在体内阐明紫荆叶乙酸乙酯部分的潜在药用价值。
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Evaluation of antibacterial efficacy and phytochemical analysis of Echinacea purpurea towards MDR strains with clinical origins
Microbes that are resistant to antibiotics are becoming a severe threat to global healthcare system. The well possible alternative to the possibility of medication resistance is the incorporation of natural remedies with considerable antimicrobial property in the therapeutic approaches of bacterial illnesses. Methicillin-resistant Staphylococcus aureus (MRSA), Enterococcus faecalis (E. faecalis), Escherichia coli (E. coli), Klebsiella pneumoniae (K. pneumoniae), Pseudomonas aeruginosa (P. aeruginosa), Acinetobacter baumannii (A. baumannii), Proteus mirabilis (P. mirabilis), Stenotrophomonas maltophilia (S. maltophilia) were isolated from 50 clinical specimens taken from patients admitted to Al-Zahraa University Hospital and Cairo Specialized Hospital from January 2016 to June 2016. Antimicrobial impacts of various solvents including (hexane, ethyl acetate, chloroform, and aqueous) were screened against multi-drug resistant (MDR) strains isolated from clinical samples. Echinacea Purpurea ethyl acetate fraction showed the most promising antibacterial activity versus bacterial clinical isolates with inhibition zone range 16.8-22.7 mm, and MIC range of 15.63-250 µg/mL, whereas other fractions were found to exhibit lower inhibition zones and higher minimal inhibitory concentration (MIC) values than ethyl acetate fraction against MDR strains. None of fractions have antibacterial action versus S. maltophilia. Electron microscopic investigation of MRSA treated by E. purpurea ethyl acetate reveled its role in lysis of pathogenic bacterial cells. The ethyl acetate fraction of the E. purpurea was analyzed using LC–MS to screen various molecules present in the fraction of E. Purpurea ethyl acetate fraction showed promising antioxidant activity with IC50 = 14.24 ± 0.58 µg/m. E. Purpurea ethyl acetate fraction had CC50 value of 1145.97 μg/ml upon testing on Vero cells highlighted its minimal toxicity. The study's findings will be used to further in vivo elucidate the E. purpurea ethyl acetate fraction for potential medicinal purposes.
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