PXD021144 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Mapping the Host Circulating Exosome Response to SARS-CoV-2 |
Description | The knowledge of the host response to the novel coronavirus SARS-CoV-2 is still limited, slowing the understanding of COVID-19 pathogenesis and the development of therapeutic strategies. During the course of a viral infection, host cells release exosomes and other extracellular vesicles carrying viral and host components, which can modulate the immune response. The present study used a shotgun proteomic approach to mapping the host circulating exosomes response to SARS-CoV-2 infection. We investigated how SARS-CoV-2 modulates extracellular vesicles content, their involvement in disease progression and the potential use of plasma exosomes as biomarkers of disease severity. Proteomic analysis of patients derived exosomes identified several molecules involved in immune response, inflammation, activation of coagulation and complement pathways, the main mechanisms of COVID-19-associated tissue damage and multiple organ dysfunctions. In addition, several potential exosomal biomarkers such as C-reactive protein, Fibrinogen gamma chain, C4b-binding protein alpha chain and Alpha-1-acid glycoprotein 1, presenting an area under the curve (AUC) of 1, were identified. Proteins correlated to the severity of the disease were also detected. These data indicate the existence of a significant contribution of circulating exosomes to inflammation, coagulation, and immunomodulation during SARS-CoV-2 infection. |
HostingRepository | PRIDE |
AnnounceDate | 2021-03-18 |
AnnouncementXML | Submission_2021-03-18_02:00:22.539.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Marcello Manfredi |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | monohydroxylated residue; iodoacetamide derivatized residue |
Instrument | TripleTOF 5600 |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2020-08-26 07:54:10 | ID requested | |
⏵ 1 | 2021-03-18 02:00:23 | announced | |
Publication List
Barberis E, Vanella VV, Falasca M, Caneapero V, Cappellano G, Raineri D, Ghirimoldi M, De Giorgis V, Puricelli C, Vaschetto R, Sainaghi PP, Bruno S, Sica A, Dianzani U, Rolla R, Chiocchetti A, Cantaluppi V, Baldanzi G, Marengo E, Manfredi M, Circulating Exosomes Are Strongly Involved in SARS-CoV-2 Infection. Front Mol Biosci, 8():632290(2021) [pubmed] |
Keyword List
submitter keyword: SARS-CoV-2 |
plasma exosomes |
host response |
biomarkers |
Contact List
Marcello Manfredi |
contact affiliation | Biological Mass Spectrometry Lab, Department of Translational Medicine, University of Piemonte Orientale |
contact email | marcello.manfredi@uniupo.it |
lab head | |
Marcello Manfredi |
contact affiliation | University of Eastern Piedmont |
contact email | marcello.manfredi@uniupo.it |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD021144
- Label: PRIDE project
- Name: Mapping the Host Circulating Exosome Response to SARS-CoV-2