Pharmacognostic evaluation and antimicrobial activity of Pteridium aquilinum (L.) Kuhn leaves (Onocleaceae) via in vitro and in silico perspectives.

Oluwatoyin Temilolu Adebayo, Bolaji Bosede Oluremi, Akingbolabo Daniel Ogunlakin, Gideon Ampoma Gyebi, Mubo Adeola Sonibare
Author Information
  1. Oluwatoyin Temilolu Adebayo: Department of Pharmacognosy, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria.
  2. Bolaji Bosede Oluremi: Department of Pharmaceutical Microbiology, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria.
  3. Akingbolabo Daniel Ogunlakin: Department of Biochemistry, Phytomedicine, Molecular Toxicology, and Computational Biochemistry Research Laboratory (PMTCB-RL), Bowen University, Iwo, Nigeria. ORCID
  4. Gideon Ampoma Gyebi: Department of Biotechnology and Food Science, Faculty of Applied Sciences, Durban University of Technology, Durban, South Africa.
  5. Mubo Adeola Sonibare: Department of Pharmacognosy, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria.

Abstract

BACKGROUND AND OBJECTIVE: Traditionally, Pteridium aquilinum L. has been utilized as medicine for ages, however, it is not listed in the Nigerian herbal pharmacopeia, and there is no information regarding its standardization and antimicrobial activity. Therefore, the purpose of this study was to examine the pharmacognostic parameters and antimicrobial activity of Pteridium aquilinum leaf.
METHODS: Macroscopy, chemo-microscopy, fluorescence, and microscopic analyses of the leaf were investigated using standard methods. Qualitative and quantitative phytochemical screening, thin layer chromatography (TLC), GC-MS, and FTIR were also determined using standard procedures. Antioxidants were evaluated using DPPH. The antimicrobial activities of methanol extract and fractions were evaluated using Agar well diffusion method against Candida albicans, Aspergillus niger, Staphylococcus aureus, Salmonella Typhimurium, Escherichia coli, and Pseudomonas aeruginosa. The macroscopic features of P. aquilinum leaf include a bi-pinnate leaflet and alternate pinna arrangement. The GC-MS-identified compounds in the most active (DCM fraction) were docked against Candida albicans Sterol 14-alpha demethylase (5TZ1) and Escherichia coli DNA gyrase subunit B (6YD9).
RESULTS: The macroscopic features and microscopic features such as anomocytic stomata, numerous stomata in the abaxial layer, and absence of stomata in the adaxial layer were observed. Chemomicroscopy of the powdered leaves shows that the leaf contains tannins, starch, and lignin. GC-MS detected eighteen compounds. The antimicrobial test revealed that the dichloromethane fraction of P. aquilinum leaf was most active on all the test strains (bacteria and fungi) at 25 mg/mL to 100 mg/mL concentrations. Through in silico research, the binding of 1,2-benzenedicarboxylic acid, (4-hydroxybenzoyl) hydrazine, octadecadienoyl chloride, and 11,14-Eicosadienoic acid, detected in the DCM fraction by GC-MS analysis, to the active sites of 5TZ1 and 6YD9 was stable.
CONCLUSION: This research gave scientific credence to the traditional medical practice of treating infections with P. aquilinum leaves.

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MeSH Term

Plant Leaves
Plant Extracts
Anti-Infective Agents
Microbial Sensitivity Tests
Antioxidants
Gas Chromatography-Mass Spectrometry
Candida albicans
Molecular Docking Simulation
Computer Simulation

Chemicals

Plant Extracts
Anti-Infective Agents
Antioxidants

Word Cloud

Created with Highcharts 10.0.0aquilinumantimicrobialleafusingPteridiumactivitylayerGC-MSfeaturesPactivefractionstomataleavesLmicroscopicstandardevaluatedCandidaalbicansEscherichiacolimacroscopiccompoundsDCM5TZ16YD9detectedtestsilicoresearchacidBACKGROUNDANDOBJECTIVE:TraditionallyutilizedmedicineageshoweverlistedNigerianherbalpharmacopeiainformationregardingstandardizationThereforepurposestudyexaminepharmacognosticparametersMETHODS:Macroscopychemo-microscopyfluorescenceanalysesinvestigatedmethodsQualitativequantitativephytochemicalscreeningthinchromatographyTLCFTIRalsodeterminedproceduresAntioxidantsDPPHactivitiesmethanolextractfractionsAgarwelldiffusionmethodAspergillusnigerStaphylococcusaureusSalmonellaTyphimuriumPseudomonasaeruginosaincludebi-pinnateleafletalternatepinnaarrangementGC-MS-identifieddockedSterol14-alphademethylaseDNAgyrasesubunitBRESULTS:anomocyticnumerousabaxialabsenceadaxialobservedChemomicroscopypowderedshowscontainstanninsstarchlignineighteenrevealeddichloromethanestrainsbacteriafungi25 mg/mL100 mg/mLconcentrationsbinding12-benzenedicarboxylic4-hydroxybenzoylhydrazineoctadecadienoylchloride1114-EicosadienoicanalysissitesstableCONCLUSION:gavescientificcredencetraditionalmedicalpracticetreatinginfectionsPharmacognosticevaluationKuhnOnocleaceaeviavitroperspectives

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