Delivery of Apoplastic Extracellular Vesicles Encapsulating Green-Synthesized Silver Nanoparticles to Treat Citrus Canker

• Published in: Nanomaterials (Basel, Switzerland) Switzerland), 2023-04, Vol.13 (8), p.1306
• Main Authors: Gaurav, Isha, Thakur, Abhimanyu, Kumar, Gaurav, Long, Qin, Zhang, Kui, Sidu, Rakesh Kumar, Thakur, Sudha, Sarkar, Rajesh Kumar, Kumar, Anoop, Iyaswamy, Ashok, Yang, Zhijun
• Format: Article
• Language: English
• Subjects: Ampicillin; Antiinfectives and antibacterials; Antimicrobial activity; Canker; Citrus canker; Crop damage; drug delivery; Drug delivery systems; Economic impact; Encapsulation; Extracellular vesicles; Ferredoxin; Fruits; green synthesis; Leaves; Mammalian cells; Molecular docking; Nanoparticles; Phyllanthus niruri; Plant cells; Plant diseases; Plant extracts; Reagents; Reductases; Silver; silver nanoparticles; Spectrum analysis; Vesicles; Virulence; Xanthomonas axonopodis
• ISSN: 2079-4991; 2079-4991
• DOI: 10.3390/nano13081306

The citrus canker pathogen has caused severe damage to citrus crops worldwide, resulting in significant economic losses for the citrus industry. To address this, a green synthesis method was used to develop silver nanoparticles with the leaf extract of (GS-AgNP-LEPN). This method replaces the need for toxic reagents, as the LEPN acts as a reducing and capping agent. To further enhance their effectiveness, the GS-AgNP-LEPN were encapsulated in extracellular vesicles (EVs), nanovesicles with a diameter of approximately 30-1000 nm naturally released from different sources, including plant and mammalian cells, and found in the apoplastic fluid (APF) of leaves. When compared to a regular antibiotic (ampicillin), the delivery of APF-EV-GS-AgNP-LEPN and GS-AgNP-LEPN to pv. was shown to have more significant antimicrobial activity. Our analysis showed the presence of phyllanthin and nirurinetin in the LEPN and found evidence that both could be responsible for antimicrobial activity against pv. Ferredoxin-NADP reductase (FAD-FNR) and the effector protein XopAI play a crucial role in the survival and virulence of pv. Our molecular docking studies showed that nirurinetin could bind to FAD-FNR and XopAI with high binding energies (-10.32 kcal/mol and -6.13 kcal/mol, respectively) as compared to phyllanthin (-6.42 kcal/mol and -2.93 kcal/mol, respectively), which was also supported by the western blot experiment. We conclude that (a) the hybrid of APF-EV and GS-NP could be an effective treatment for citrus canker, and (b) it works via the nirurinetin-dependent inhibition of FAD-FNR and XopAI in pv.