Antimalarial Activity Screening from Endophytic Fungus of Red Ginger (Zingiber officinale): in vitro and in silico Studies; [Pemeriksaan Aktiviti Antimalaria daripada Kulat Endofit Halia Bara (Zingiber officinale): Kajian in vitro dan in silico]

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Muh Ade Artasasta, Diandra Mytha Faradilla, Herlina Rasyid, Dwi Listyorini, Wira Eka Putra, Dian Handayani, Riga Riga, Ping-Chung Kuo, Hao-Ze Li, Pei-Hung Chang, Loeki Enggar Fitri, Harwoko Harwoko, Heni Endrawati

2025 Sains Malaysiana Vol. 54 Issue 6 Article Cited by 2 Quartile

Abstract

Diversity exploration of secondary metabolite compounds from plant endophytic fungi is expected to yield novel compounds that can efficiently overcome Plasmodium resistance. This study aimed to assess the antimalarial activity of the endophytic fungus derived from red ginger Zingiber officinale against Plasmodium berghei. Subsequently, the endophytic fungus was isolated from the sample using the dilution method, followed by evaporation. Nine isolates of endophytic fungi were successfully isolated that were assigned as JMR1, JMR2, JMR3, JMR5, JMB1, JMB2, JMB3, JMD1, and JMD2. The antimalarial efficacy showed that the JMR5 isolate exhibited significant activity in suppressing the proliferation of P. berghei. This activity was quantified by a per cent inhibition of 83.01% and an IC50 value of 5.81 µg/mL. The detected antimalarial activity of the JMR5 extract can be related to the presence of several phytochemicals, including alkaloids, flavonoids, and terpenoids. In addition, molecular identification was conducted using ITS primers on the JMR5 isolate, showing a complete genetic similarity of 100% with Aspergillus flavus. GNPS analysis was conducted using LCMS-MS data on ethyl acetate extract. Surafactin c, surafactin c14 and erucamide were probably secondary metabolites in the JMR5 extract. Furthermore, drug-likeness and molecular docking analysis were conducted. The result showed that erucamide is a potential antimalarial due to the fulfil of Lipinski’s rule of five and also the binding affinity (-4.2 kcal/mol) against Plasmepsin I. Based on the results obtained, the development of secondary metabolites from Aspergillus flavus JMR5 as potential antimalarial compounds is important to carry out. © 2025, Penerbit Universiti Kebangsaan Malaysia. All rights reserved.

Affiliations

Biotechnology Program, Department of Applied Science, Faculty of Mathematics and Natural Science, Universitas Negeri Malang, Malang, Indonesia; Chemistry Department, Faculty of Mathematics and Natural Sciences, Hasanuddin University, Makassar, Indonesia; Laboratory of Sumatran Biota, Faculty of Pharmacy, Universitas Andalas, Padang, Indonesia; Department of Chemistry, Faculty of Mathematics and Natural Science, Universitas Negeri Padang, Padang, Indonesia; School of Pharmacy, Collage of Medicine, National Cheng Kung University, Tainan, Taiwan; Department of Clinical Parasitology, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia; Department of Pharmacy, Faculty of Health Sciences, Universitas Jenderal Soedirman, Purwokerto, Indonesia