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Published on: October 31, 2019
Substrate-dependent metabolites from mangrove-derived Aspergillus ochraceus PLP1F21 exhibit antibacterial and wound
Andi Setiawan1, Fendi Setiawan2, Rosyidatul Lutfiah2
1Department of Chemistry, Faculty of Mathematics and Natural Sciences, Lampung University, Bandar Lampung, Lampung 35145, Indonesia.
Abstract:
Mangrove-derived Aspergillus sp. represents a promising source of bioactive secondary metabolites with potential therapeutic applications. The One Strain-Many Compounds (OSMAC) approach was employed to modulate metabolite production of Aspergillus ochraceus PLP1F21 from Pesawaran, Indonesia, using three agro-industrial waste substrates: shrimp shell (PLP1-SS), rice medium (PLP1-RM), and palm mesocarp fibre (PLP1-PW). Ethyl acetate extracts were evaluated for antibacterial activity against clinically isolated multidrug-resistant (MDR) Staphylococcus aureus and Pseudomonas aeruginosa, and for wound healing efficacy in MDR-infected murine dorsal incision models. PLP1-SS exhibited direct antibacterial activity against both pathogens (minimum inhibitory concentration 250 μg/mL) and promoted superior wound closure in the P. aeruginosa model (0.59 ± 0.03 cm2 on Day 7); liquid chromatography-high resolution mass spectrometry profiling putatively attributed this dual activity to notoamide-class prenylated indole alkaloids. PLP1-PW, despite negligible antibacterial activity, promoted wound contraction in the S. aureus model (0.85 ± 0.03 cm2) with a metabolite profile enriched in terpenoids and polyketides, suggesting host-directed repair mechanisms. PLP1-RM similarly enhanced wound closure (0.32 ± 0.02 cm2), although its chemical basis remains uncharacterised. Histopathological evaluation revealed selective macrophage infiltration without neutrophilic or lymphocytic elevation in the S. aureus model, indicative of a controlled pro-repair immune response, while no significant immune modulation was detected in the P. aeruginosa model. These findings demonstrate that OSMAC cultivation on agro-industrial waste substrates generates metabolically distinct extracts with substrate-dependent activities, highlighting PLP1-SS and PLP1-PW as promising candidates for infected wound management.
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