⮝ Full datasets listing

PXD060892

PXD060892 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleLabel-free quantitative proteomic analysis reveals the effects of biogenic silver nanoparticles on Fusarium keratoplasticum and their therapeutic potential in Galleria mellonella larvae
DescriptionThe increasing problem of antifungal drug resistance is a serious concern, making it necessary to find new treatment options. In this study, we evaluated the antifungal activity and molecular effects of biogenic silver nanoparticles (AgNPs) synthesized using the culture filtrate of Epicoccum nigrum against Fusarium keratoplasticum, a fungal genera with high resistance to antifungal drugs. The AgNPs showed strong antifungal activity, with a MIC50 of 1.79 μg/mL, leading to 92.85% inhibition of fungal growth at the highest concentration tested (5.92 μg/mL). To understand how AgNPs affect F. keratoplasticum, we performed label-free quantitative proteomic mass spectrometric (LFQ-MS) analysis. We identified 853 proteins, 52 of which were significantly altered in abundance after AgNPs treatment. Principal component analysis (PCA) and hierarchical clustering showed a clear difference between the proteomes of control and AgNP-treated samples. Several proteins related to oxidative stress response, mitochondrial function, and riboflavin biosynthesis were affected. Proteins involved in riboflavin biosynthesis and electron transport decreased in abundance, suggesting that AgNPs disrupt fungal metabolism and energy production. On the other hand, proteins related to oxidative stress response and heat shock increased in abundance, showing that the fungus is under strong stress when exposed to AgNPs. To check the toxicity and antifungal activity of AgNPs in vivo, we used the Galleria mellonella larval model. At a dose of 2.58 mg/kg, AgNPs were not highly toxic, with 90% of the larvae surviving after seven days. Hemocyte density increased after AgNPs treatment, showing that there was some immune activation, but it returned to normal levels after 48 hours. Also, proteomic analysis of G. mellonella hemolymph after AgNPs exposure showed only small changes in protein abundance, mostly in immune response and metabolism, confirming that AgNPs do not cause serious damage to the host. The antifungal effect of AgNPs was also tested in G. mellonella larvae infected with F. keratoplasticum. Infection with 10⁵ conidia/mL caused a 90% mortality rate by day seven in untreated larvae. However, AgNP-treated larvae had a fivefold increase in survival, with 50% surviving by day seven, proving that AgNPs can help fight fungal infections in vivo. These results confirm that biogenic AgNPs are effective antifungal agents that act through oxidative stress, metabolic disruption, and mitochondrial damage in F. keratoplasticum. The combination of proteomic analysis and in vivo experiments provides strong evidence that AgNPs are effective and safe in insect model. Future studies should focus on testing long-term toxicity, and exploring their use in medicine and agriculture to help combat the increasing problem of antifungal resistance.
HostingRepositoryPRIDE
AnnounceDate2025-09-08
AnnouncementXMLSubmission_2025-09-07_16:29:08.063.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterGlaucia Caruso
SpeciesList scientific name: Fusarium keratoplasticum; NCBI TaxID: 1328300; scientific name: Galleria mellonella; NCBI TaxID: 7137;
ModificationListmonohydroxylated residue; iodoacetic acid derivatized residue
InstrumentQ Exactive
Dataset History
RevisionDatetimeStatusChangeLog Entry
02025-02-17 14:25:28ID requested
12025-09-07 16:29:08announced
Publication List
Rigotto-Caruso G, Curtis A, Kavanagh K, von Zeska Kress MR, Larvae. ACS Omega, 10(33):37408-37418(2025) [pubmed]
10.1021/acsomega.5c03275;
Keyword List
submitter keyword: proteomics,Fusarium keratoplasticum, biogenic synthesis., antifungal therapy, silver nanoparticles, oxidative stress, Galleria mellonella, metabolic disruption
Contact List
Marcia Regina von Zeska Kress
contact affiliationDepartment of Clinical Analyses, Toxicology, and Food Science, School of Pharmaceutical Sciences of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto, SP, Brazil.
contact emailkress@fcfrp.usp.br
lab head
Glaucia Caruso
contact affiliationDepartment of Clinical Analyses, Toxicology, and Food Science, School of Pharmaceutical Sciences of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto, SP, Brazil.
contact emailg_rigotto@usp.br
dataset submitter
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2025/09/PXD060892
PRIDE project URI
Repository Record List
[ + ]