Identification of Datura innoxia as a potential source of antimycobacterial components

<i>Datura innoxia</i> is a medicinal plant from the Solanaceae family, having medicinal properties and some toxic effects. It is widely distributed across Asia, Africa, Europe, the Americas, and other tropical and subtropical regions, where it is utilized by local pharmaceutical industries. In this study, bioassay-guided fractionation and LC-MS/MS analysis were used for the identification of secondary metabolites with anti-tuberculosis activity in methanolic leaf extracts of <i>D. innoxia</i>. Bioassay-guided fractionation was conducted using normal and reverse phase column chromatography, and the fractions were assayed for antituberculosis activity <i>in vitro</i> by serial dilution in <i>Mycobacterium tuberculosis</i> H37Ra cultures. The structures of known secondary metabolites in the purified extracts were identified using LC-ESI-MS/MS mass spectroscopy. A purified fraction of the methanolic extract of <i>D. innoxia</i> leaves inhibited <i>M. tuberculosis</i> growth at concentrations as low as 25 μg/mL. Metabolic profiling with LC-ESI-MS/MS enabled the identification of the purified extract of 16 known metabolites, including loliolide, scopolamine, kuromanin, isoquercitrin, moupinamide, methyl isoquinoline-3-carboxylate, trans-3-Indoleacrylic acid, tyramine, (3β,5ξ,9ξ)-3,6,19-trihydroxyurs-12-en-28-oic acid, milbemycin A3 oxime, methyl jasmonate, nicotinamide, methyl ferulate, trifolin, 2-[(1S,2S,4aR,8aS)-1-hydroxy-4a-methyl-8-methylidene-decahydronaphthalen-2-yl]prop-2-enoic acid, and methyl 4-hydroxycinnamate. These results indicate that <i>D. innoxia</i> is a rich natural source of potential antitubercular secondary metabolites.

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Publication Details

Journal
Frontiers in Microbiology
Published
2025-07-01
DOI
https://doi.org/10.3389/fmicb.2025.1553282
Citations
1
Primary Topic
Antibiotics Pharmacokinetics and Efficacy
Type
article
Field-Weighted Citation Impact
1.39

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article

Identification of Datura innoxia as a potential source of antimycobacterial components

Sajjad Ahmed Khan, Sabira Tahseen, Peter W. Villalta, Muzafar Ahmad Rather et al.
1 citations
Frontiers in Microbiology
Antibiotics Pharmacokinetics and Efficacy
1.39
article

Identification of Datura innoxia as a potential source of antimycobacterial components

Sajjad Ahmed Khan, Sabira Tahseen, Peter W. Villalta, Muzafar Ahmad Rather, Syed Mehmood Qadir, W. Thomas Shier, Muhammad Ahmad, Anthony D. Baughn, Sajid Iqbal, Ziyi Jia, Muhammad Umer Khan
article en
1 citations

Abstract

<i>Datura innoxia</i> is a medicinal plant from the Solanaceae family, having medicinal properties and some toxic effects. It is widely distributed across Asia, Africa, Europe, the Americas, and other tropical and subtropical regions, where it is utilized by local pharmaceutical industries. In this study, bioassay-guided fractionation and LC-MS/MS analysis were used for the identification of secondary metabolites with anti-tuberculosis activity in methanolic leaf extracts of <i>D. innoxia</i>. Bioassay-guided fractionation was conducted using normal and reverse phase column chromatography, and the fractions were assayed for antituberculosis activity <i>in vitro</i> by serial dilution in <i>Mycobacterium tuberculosis</i> H37Ra cultures. The structures of known secondary metabolites in the purified extracts were identified using LC-ESI-MS/MS mass spectroscopy. A purified fraction of the methanolic extract of <i>D. innoxia</i> leaves inhibited <i>M. tuberculosis</i> growth at concentrations as low as 25 μg/mL. Metabolic profiling with LC-ESI-MS/MS enabled the identification of the purified extract of 16 known metabolites, including loliolide, scopolamine, kuromanin, isoquercitrin, moupinamide, methyl isoquinoline-3-carboxylate, trans-3-Indoleacrylic acid, tyramine, (3β,5ξ,9ξ)-3,6,19-trihydroxyurs-12-en-28-oic acid, milbemycin A3 oxime, methyl jasmonate, nicotinamide, methyl ferulate, trifolin, 2-[(1S,2S,4aR,8aS)-1-hydroxy-4a-methyl-8-methylidene-decahydronaphthalen-2-yl]prop-2-enoic acid, and methyl 4-hydroxycinnamate. These results indicate that <i>D. innoxia</i> is a rich natural source of potential antitubercular secondary metabolites.

Frontiers in MicrobiologyVol. 16
Quaid-i-Azam University (PK), National Tuberculosis Institute (IN), University of Minnesota (US), University of Lahore (PK), Pir Mehr Ali Shah Arid Agriculture University (PK), University of Minnesota Medical Center (US), Abdus Salam Centre for Physics (PK)
Higher Education Commision, Pakistan
Openalex Percentile: Top 19%
Antibiotics Pharmacokinetics and Efficacy
1.39
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