4.7 Article

Antiviral activity of natural humic substances and shilajit materials against HIV-1: Relation to structure

Journal

ENVIRONMENTAL RESEARCH
Volume 193, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.envres.2020.110312

Keywords

Humic acid; Fulvic acid; Shilajit; Antiviral; HIV; Structure-activity; C-13 NMR; FTICR MS; ChemBL data-mining

Funding

  1. Russian Science Foundation [19-75-00092]
  2. Russian Science Foundation [19-75-00092, 20-63-47070] Funding Source: Russian Science Foundation

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Natural products such as humic substances and shilajit have antiviral activity, with humic substances showing stronger anti-HIV activity compared to shilajit. The presence of aromatic structures in humic substances correlates with their anti-HIV activity, while shilajit exhibits a different mechanism. Aromatic structures with alkyl substituents, terpenoids, N-containing analogs of typical flavonoids, and azapodophyllotoxins were identified as potential carriers of antiviral activity in humic substances.
Natural products, such as humic substances (HS) and shilajit, are known to possess antiviral activity. Humic-like components are often called as carriers of biological activity of shilajit. The goal of this study was to evaluate anti-HIV activity of well characterized HS isolated from coal, peat, and peloids, and compare it to that of water-soluble organic matter (OM) isolated from different samples of Shilajit. The set of humic materials included 16 samples of different fractional composition: humic acid (HA), hymatomelanic acid (HMA), fulvic acid (FA). The set of shilajit OM included 19 samples of different geographic origin and level of alteration. The HIV-1 p24 antigen assay and cell viability test were used for assessment of antiviral activity. The HIV-1 Bru strain was used to infect CEM-SS cells. The obtained EC50 values varied from 0.37 to 1.4 mg L-1 for the humic materials, and from 14 to 142 mg L-1 for the shilajit OM. Hence, all humic materials used in this study outcompeted largely the shilajit materials with respect to anti-HIV activity: For the humic materials, the structure-activity relationships revealed strong correlation between the EC50 values and the content of aromatic carbon indicating the most important role of aromatic structures. For shilajit OM, the reverse relationship was obtained indicating the different mechanism of shilajit activity. The FTICRMS molecular assignments were used for ChEMBL data mining in search of the active humic molecules. As potential carriers of antiviral activity were identified aromatic structures with alkyl substituents, terpenoids, N-containing analogs of typical flavonoids, and azapodophyllotoxins. The conclusion was made that the typical humic materials and Shilajit differ greatly in molecular composition, and the humic materials have substantial preferences as a natural source of antiviral agents as compared to shilajit.

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