Insecticidal metabolites from Serratia marcescens associated with the fall armyworm (Spodoptera frugiperda): molecular identification, metabolomic profiling and molecular docking insights
Aug 2026· Scientific Reports· Vol 16· 0 citations· 43 references
Medicine
TL;DR
Findings demonstrate that S. marcescens associated with S. frugiperda produces metabolites with notable insecticidal potential and highlight insect-associated pathogenic bacteria as a valuable source of bioactive compounds for the sustainable management of fall armyworm.
Abstract
The fall armyworm (S. frugiperda) has developed resistance to numerous insecticides and is currently considered one of the most destructive pests threatening global crop production. Consequently, the development of environmentally sustainable pest management strategies has become increasingly important. Insect-associated pathogenic bacteria represent a promising source of bioactive metabolites with potential insecticidal properties. In the present study, pathogenic bacteria associated with S. frugiperda were isolated and molecularly identified as Serratia marcescens strain INS420 based on 16 S rRNA gene sequencing. The secondary metabolites produced by this bacterium demonstrated significant insecticidal activity under both laboratory and field conditions. Metabolic profiling of the extracted compounds was performed using liquid chromatography–mass spectrometry (LC–MS) and gas chromatography–mass spectrometry (GC–MS), revealing the presence of several bioactive compounds, including diketopiperazines, fatty acids and their esters, squalene, phthalate derivatives, and a cardenolide. To gain insights into the potential mechanism of action, molecular docking simulations were conducted to evaluate the binding affinity of the identified metabolites with S. frugiperda acetylcholinesterase (AChE). Among the detected compounds, squalene and several fatty acid derivatives exhibited stable interactions within the active site of the enzyme, suggesting a possible inhibitory effect on AChE activity. Collectively, these findings demonstrate that S. marcescens associated with S. frugiperda produces metabolites with notable insecticidal potential and highlight insect-associated pathogenic bacteria as a valuable source of bioactive compounds for the sustainable management of fall armyworm.
Bacillus velezensis is a promising candidate for the biocontrol of plant pathogens due to its production of broad-spectrum antimicrobial metabolites. The present study evaluates the antifungal potential and metabolic profile of the non-pathogenic rhizobacterial strain Bacillus velezensis 5RB. Modifying the mineral composition across three different growth media (A, B, and C) resulted in distinct secondary-metabolite profiles of B. velezensis 5RB. Notably, the free-cell supernatant of strain 5RB cultivated in medium A and C demonstrated the most potent antifungal activity against the gray mold pathogen Botrytis cinerea. For the first time, the antimicrobial metabolites produced by B. velezensis 5RB across these three media were comprehensively characterized using ultra-performance liquid chromatography-quantitative time-of-flight mass spectrometry (UHPLC-QTOF-MS). Mass spectrometric analyses (LC-ESI-MS) identified predominantly lipopeptides from the surfactin and fengycin families, alongside three classes of polyketides: macrolactins, difficidins, and bacillaenes. Multiple lipopeptide homologues, including a novel surfactin isoform (B*), were confirmed by tandem mass spectrometry (LC-ESI-MS/MS). Additionally, this study provides the first experimental evidence for subtilosin A production by B. velezensis 5RB. The multicomponent fermentation matrix of 5RB conferred robust biocontrol protection to tomato leaves against B. cinerea and Phytophthora infestans in an in vitro disease model, underscoring its strong potential for sustainable agricultural applications.
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A spore-free, high-yield, scalable production platform for oosporein was established, highlighting the potential of rare, protected fungal species as sources for valuable enzymes and bioactive secondary metabolites for efficient microbial biomanufacturing systems.
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