Abstract

The treatment of infectious diseases with antimicrobial agents continues to present problems in modern-day medicine with many studies showing significant increase in the incidence of bacterial resistance to several antibiotics. The screening of antimicrobial activity of plant extracts and natural products has shown that medicinal plants are made up of a potential source of new anti-infective agents. The aim of this study was to evaluate the antimicrobial and antioxidant activities of extracts and compounds from the whole plant Trifolium baccarinii Chiov. and to determine their modes of antibacterial action. The plant extracts were prepared by maceration in organic solvents. The antimicrobial activities were evaluated using the broth microdilution method. The antioxidant activity was evaluated using the 2,2′-diphenyl-1-picrylhydrazyl radical (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) diammonium salt (ABTS) assays. The mechanisms of antibacterial action were determined by lysis, salt tolerance assays, and antioxidant enzyme activities. The cytotoxic effect on the erythrocytes was determined by a spectrophotometric method. Biochanin A, formononetin, luteolin, luteolin-4′-O-β-D-glucopyranoside, 4,7,2′-trihydroxy-4′-methoxyisoflavanol, sissotrin, 1-methyl-β-D-glucopyranoside, ononin, D-mannitol, and 3-O-β-D-glucuronopyranosylsoyasapogenol B were isolated from Trifolium baccarinii. The MeOH, EtOAc, and n-BuOH extracts as well as biochanin A, formononetin, luteolin, luteolin-4′-O-β-D-glucopyranoside, 4,7,2′-trihydroxy-4′-methoxyisoflavanol, and sissotrin from Trifolium baccarinii displayed the highest antimicrobial and antioxidant activities. The MeOH extract and 4,7,2′-trihydroxy-4′-methoxyisoflavanol exhibited antibacterial activity through the bacteriolytic effect and reduction of the antioxidant defenses in the bacterial cells. The present study portrays Trifolium baccarinii as a potential natural source of antibacterial, antifungal, and antioxidant agents.

Highlights

  • The treatment of infectious diseases with antimicrobial agents continues to present problems in modern-day medicine with many studies showing significant increase in the incidence of bacterial resistance to several antibiotics [1]

  • The Minimum Inhibitory Concentration (MIC) values of MeOH and EtOAc extracts were in the range of 3264 μg/mL, whereas the n-BuOH extract was active in the range of 128-512 μg/mL towards the tested bacteria and yeasts

  • The lowest MIC value of 8 μg/mL was recorded on Cryptococcus neoformans with compound 3 and on Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus ATCC25923, Candida albicans, and Cryptococcus neoformans with compound 5 whereas the lowest minimum microbicidal concentration (MMC) value was obtained on Pseudomonas aeruginosa, Staphylococcus aureus ATCC25923, and Cryptococcus neoformans with compound 5

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Summary

Introduction

The treatment of infectious diseases with antimicrobial agents continues to present problems in modern-day medicine with many studies showing significant increase in the incidence of bacterial resistance to several antibiotics [1]. Since MRSA is capable of resisting a beta-lactam group of antibiotics, this explains the emergent challenge in the treatment of this highly prevalent pathogen. The organism produces free radicals such as reactive oxygen species (ROS) which are formed during cell respiration and have a vital role in cell signaling [4]. It is generally known that the production of ROS increases during infections, enhancing pathogen clearance, as well as contributing to signaling cascades related to inflammation, cell proliferation, and immune responses [5]. High amounts of the free radicals produced during infection can cause oxidative stress, which further complicates the patient’s prognosis

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