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PXD074601-1

PXD074601 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleProteomic remodeling of the chicken spleen during chicken astrovirus infection reveals coordinated interferon activation and stromal restructuring
DescriptionChicken astrovirus (CAstV) is an enteric pathogen associated with white chick syndrome (WCS), a condition characterized by reduced hatchability, hypopigmentation, developmental delay, and increased early mortality. While transcriptomic studies have provided insight into host responses to CAstV infection, protein-level alterations underlying systemic pathology remain poorly defined. Here, we performed label-free quantitative proteomic profiling of the chicken spleen, a central lymphoid organ coordinating systemic immune regulation. Twenty-one-day-old SPF White Leghorn chickens were orally infected with CAstV strain PL/G059/2014 or inoculated with PBS. Spleens collected at 4 days post-infection were analyzed by nanoLC–MS/MS, and relative protein abundance was compared between infected (CA) and control (K) groups. In total, 2,529 proteins were identified (≥2 unique peptides, FDR≤1%), of which 1,118 met criteria for quantitative comparison. Among these, 33 proteins (~3%) exhibited significant differential abundance (q≤0.05), indicating a selective proteomic response to infection. Proteins with increased abundance formed a coherent type I interferon–associated antiviral module, including IFI27L1 (ISG12), OASL, STAT1, MOV10, and IFITM1. In contrast, proteins with reduced abundance were enriched for extracellular matrix components and cytoskeletal regulators, including the small leucine-rich proteoglycans decorin, lumican, and mimecan, as well as actin-associated structural proteins, indicating decreased cytoskeletal tension and stromal remodeling. Increased abundance of HSP90, together with discordant transcript–protein regulation of selected chaperones and metabolic enzymes, suggested selective modulation of proteostasis and mitochondrial metabolism. Functional enrichment and protein interaction analyses revealed two distinct response modules: a transcriptionally driven interferon-mediated antiviral program and a post-transcriptionally regulated structural and metabolic remodeling program. Integration with previously generated RNA-seq data confirmed concordant transcript–protein induction of interferon-stimulated genes, alongside transcript–protein decoupling for extracellular matrix, cytoskeletal, and mitochondrial proteins. Together, these findings demonstrate that CAstV infection induces a systemic antiviral state accompanied by stromal and metabolic reprogramming, providing a mechanistic framework linking splenic proteome remodeling to the pathogenesis of white chick syndrome.
HostingRepositoryPRIDE
AnnounceDate2026-06-08
AnnouncementXMLSubmission_2026-06-08_08:27:20.490.xml
DigitalObjectIdentifierhttps://doi.org/10.6019/PXD074601
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportSupported dataset by repository
PrimarySubmitterAgata Malinowska
SpeciesList scientific name: Gallus gallus (Chicken); NCBI TaxID: NEWT:9031;
ModificationListmonohydroxylated residue; iodoacetamide derivatized residue
InstrumentQ Exactive
Dataset History
RevisionDatetimeStatusChangeLog Entry
02026-02-18 11:49:01ID requested
12026-06-08 08:27:21announced
Publication List
10.6019/PXD074601;
Keyword List
submitter keyword: label-free proteomics,chicken astrovirus, spleen
Contact List
Joanna Sajewicz-Krukowska
contact affiliationDepartment of Virology and Viral Animal Diseases, National Veterinary Research Institute - State Research Institute, Pulawy, Poland
contact emailjoanna.sajewicz@piwet.pulawy.pl
lab head
Agata Malinowska
contact affiliationIBB PAS
contact emailesme@ibb.waw.pl
dataset submitter
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