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The growing phenomenon of antibiotic resistance to pathogenic microorganisms has led to the concern of scientists on finding novel antimicrobial agents from natural sources. Datura species is a medicinal plant that has significant antibacterial properties and has been widely used to treat various diseases such as diabetes, leucoderma, skin disorders, ulcers, bronchitis, jaundice, hysteria, insanity, heart disease, fever, piles, etc. In this review, we focused on the antibacterial characteristics of plant with special reference to phytocompounds studied by various scientists in different species of Datura. Studies showed that maximum antibacterial work has been done on Datura metal, Datura inoxia and Datura stramonium against Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa. Leaves were found to be most promising part as a source for antibacterial activities. Steroidal (5¹, 7¹ dimethyl 6¹-hydroxyl 3¹, phenyl 3 α-amine β-yne sitosterol) and β-carboline(1,7 dihydroxy-1-methyl 6,8dimethoxy β-carboline) alkaloids are the two antibacterial compounds isolated from D. metel. Research showed that the Datura species are very promising plants for isolation of new antibacterial compounds.

Background: Dinoxin B Withanolide was isolated from Datura inoxia and identified with its cytotoxic activity. But its antibacterial properties are not yet evaluated. We have previously reported the broad-spectrum antibacterial property of Dinoxin B Withanolide extracted from D.inoxia on standard strains. Objective: This research has focused to evaluate the efficacy of Dinoxin B Withanolide against infectious Staphylococcus aureus, including resistant strains. Methods: Electrospray Ionization-Mass Spectrometry is used to depict the presence of Dinoxin B withanolide from the chromatographic ethanolic leaf fraction. Antibacterial activity of different concentrations of Dinoxin B(12500-100000 μg/ml) was assessed using the agar diffusion, macro broth dilution, and time-kill assay methods. Docking studies and Drug likeness properties were analyzed. Result: Electrospray Ionization-Mass Spectrometry depicted the presence of Dinoxin B. All the isolates were susceptible to Dinoxin B within the range of 15±0.5mm to 24±0.5mm, and the bacteria were susceptible at a concentration rate of ≤12.5mg/ml. Time-kill assay showed that 25mg/ml of Dinoxin B displayed the highest inhibitory activity after four hours. The MBC values were compatible with the cidal concentration as seen in the time-kill study's growth curve. Computer-aided techniques resulted in a good Docking score towards Quorum-signaling Sar A protein (-7.82)and Penicillin Binding Protein(-6.9). Conclusion: Dinoxin B with its bactericidal properties and significant affinity towards Quorum-signaling Sar A protein and Penicillin Binding Protein can be considered as an effective bioactive compound against Methicillin Resistance Staphylococcus aureus.

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