Rotula aquatica Lour. inhibits growth and biofilm formation of clinically isolated uropathogenic Escherichia coli

التفاصيل البيبلوغرافية
العنوان: Rotula aquatica Lour. inhibits growth and biofilm formation of clinically isolated uropathogenic Escherichia coli
المؤلفون: Ninan Jisha, V. Vijeesh, Sebastian Jose Midhun, A. Vysakh, Kuriakose Jayesh, Mathew Jyothis, Latha
المصدر: Asian Pacific Journal of Tropical Biomedicine, Vol 10, Iss 12, Pp 547-554 (2020)
بيانات النشر: Wolters Kluwer Medknow Publications, 2020.
سنة النشر: 2020
مصطلحات موضوعية: Minimum bactericidal concentration, lcsh:Arctic medicine. Tropical medicine, biology, rotula aquatica, escherichia coli, urinary tract infections, anti-bacterial activity, lcsh:RC955-962, Biofilm, Resazurin, biology.organism_classification, medicine.disease_cause, Biochemistry, Genetics and Molecular Biology (miscellaneous), Molecular biology, Minimum inhibitory concentration, chemistry.chemical_compound, chemistry, lcsh:Biology (General), Rotula aquatica, medicine, MTT assay, Propidium iodide, Escherichia coli, lcsh:QH301-705.5
الوصف: Objective: To evaluate the anti-bacteria! and anti-biofilm activity of ethyl acetate fraction of Rotula aquatica Lour. (EFRA) against clinically isolated uropathogenic Escherichia coli. Methods: In vitro antibacterial and anti-biofilm studies were employed. The antimicrobial activity of EFRA was assayed by the well diffusion method. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of the active fraction were determined by Resazurin method. The time-kill kinetic assay, acridine orange-ethidium bromide staining, propidium iodide uptake assay, and scanning electron microscopic (SEM) analysis were done to evaluate the efficacy of EFRA in killing uropathogenic Escherichia coli. The anti-biofilm activity was determined by 3-[4,5- dimethyl-2-thiazolyl]-2, 5-diphenyl-2H-tetrazolium-bromide (MTT) assay and specific biofilm formation assay. Results: The well diffusion assay of EFRA showed a very clear zone of inhibition against Escherichia coli BRL-17. The MIC and MBC of EFRA were 2.5 mg/mL and 5 mg/mL, respectively. The time-kill kinetic assay, fluorescence microscopic analysis, propidium iodide uptake assay, and SEM analysis displayed the effect of EFRA in killing the bacteria. The MTT assay and specific biofilm formation assay showed that EFRA prevented the formation of biofilms. Conclusions: The results of the present study confirm that EFRA could prevent bacterial growth and inhibit its biofilm formation.
اللغة: English
تدمد: 2588-9222
2221-1691
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a4c9b34e372cb1273e8eb07ded552c9
http://www.apjtb.org/article.asp?issn=2221-1691;year=2020;volume=10;issue=12;spage=547;epage=554;aulast=Vysakh
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....5a4c9b34e372cb1273e8eb07ded552c9
قاعدة البيانات: OpenAIRE