The effect of ethanolic and aqueous extracts of Berberies vulgaris on multidrug- resistant gram-negative pathogenic bacteria
الموضوعات : مجله گیاهان داروییزهرا عطائی کچوئی 1 , سیما یحیی آبادی 2 , منیر دودی 3
1 - گروه میکروبیولوژی، دانشگاه آزاد اسلامی واحد فلاورجان، اصفهان
2 - گروه فیزیولوژی گیاهی، دانشگاه آزاد اسلامی واحد فلاورجان، اصفهان
3 - گروه میکروبیولوژی، دانشگاه آزاد اسلامی واحد فلاورجان، اصفهان
الکلمات المفتاحية: Berberis vulgaris Gram negative bacteria Minimum Bactericidal Concentrations (MBC) Minimum Inhibitory Concentration (MIC) Multidrug resistant (MDR),
ملخص المقالة :
Background and Aim: In recent years, due to the indiscriminate and irrational use of synthetic drugs, the resistance of pathogenic microorganisms has increased; therefore, new compounds are vitally needed. The purpose of this study was to investigate the effect of ethanolic and aqueous extracts of Berberis vulgaris on Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Citrobacter frundi, Enterobacter aerugenes, Pseudomonas aeruginosa and Acinetobacter baumannii in standard conditions. Material and methods: Ethanolic and aqueous extracts of B. vulgaris were prepared by maceration method. After the bacteria were identified, antibiotic resistance was determined by agar disk diffusion method. Antibacterial effect of ethanolic and aqueous extracts of B. vulgaris on multidrug resistant bacteria was examined at four concentrations of 50, 100, 400 and 800 mg/ml, and (MIC) and (MBC) of these extracts on macro dilution method was also used. The collected data were analyzed using SPSS Software and Kruskal-Wallis and Mann-Whitney tests. Results and Conclusion: The results showed that ethanolic and aqueous extracts of B. vulgaris had an antibacterial effect on a multi-drug-resistant bacteria (MDR). The MIC and MBC of the extracts were reported 50 and 100 mg/ml, respectively. Industrial and practical recommendations: After further investigations, extract B. vulgaris was recommended to be utilized as an alternative to antibiotics for treatment.
Amalaradjou, M., Venkitanarayanan, K. 2011. Natural Approaches for Controlling Urinary Tract Infections. Urinary Tract Infections, 227-244.
Ghareeb, A., Abeer, E., El-Wahab, A., Eman, E., Sarhan, M., Marwa, M., 2013. Abu-SerieandMaha A. El Demellawy. Biological assessment of Berberis vulgaris and its active constituent, berberine: Antibacterial, antifungaland anti-hepatitis C virus (HCV) effect. Journal of Medicinal Plants Research, 7(21): 1529-1536.
Kathleen, A. 2008. Natural Approaches to Prevention and Treatment of Infections of the Lower Urinary Tract. Alternative Medicine Review, 3: 244-227.
Kiani, A., Mazandarani, M. Ghaemi, A. 2011. The effect of ethanol extracts of seven medicinal plants against bacteria isolated from patients with urinary tract infection in Gorgan city. Journal of Medicinal Plants, 2 (34): 74-83
Kognou, A., Ngane. R., Kuiate, J. 2011. An Antibacterial and antioxidant properties of the methanolic extract of the stem bark of Pteleopsishylodendron (Combretaceae). Chemotherapy Research and Practice, 10: 7-1.
Kumar, A. 2012. Antibacterial activity of some Medicinal Plants used against UTI causing Pathogens. International Journal of Drug Development & and Research, 4(2): 278-283.
Motamedi, H., Darabpour. E., Gholipour, M., Seyyednejd, SM. 2010. Antibacterial effect of ethanolic and methanolic extracts of plantago ovaa and oliveria decumbens endemic in Iran against some pathogenic bacteria. International Journal of Pharmacology, 6(2):117-22.
Pasrija, A., Singh, R., Katiyar, C. K. 2011. Comparative study on the antimicrobial activity of berberis aristata from different region and berberine in vitro. International journal of life science and Pharma Research, 1 (1): 17-20.
Priti V. 2012. Use ofessential oils against gram negative pathogen. Journal of Drug Delivery and Therapeutics, 2(6): 137-134.
Pradeep, S., and Kanu P.2013. Pharmacognostical, Phytochemical and Antibacterial Evaluation of BerberisTinctoriaLesch. (Stem Wood and Stem Bark). Research Journal of Pharmaceutical, Biological and Chemical Sciences, 4(4): 899-905.