PXD032333 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Proteomic snapshot of saliva samples reveals new pathways implicated in SARS-CoV-2 pathogenesis |
Description | Variations in the susceptibility to SARS-CoV-2 infection and risk of severe disease are yet not well understood. The information on the human pathways and active members of the microbiome that can affect SARS-CoV-2 susceptibility and disease progression in the saliva is very scarce. Here, we studied 10 hospitalized patients with severe and moderate COVID-19 (Scov and Mcov) at an early stage of the disease during April to June 2020, compared to 10 uninfected individuals, including healthcare workers with repeated high-risk exposures to the virus but not infected (Non-susceptible, Nsus) and subjects who became infected during the follow-up (susceptible, Non-COVID, Ncov). We performed high-throughput proteomic profiling in saliva to determine the human pathways and active members of the microbiome across individuals. We detected differentially expressed proteins between groups, being the differences especially remarkable in the comparison between the non-infected vs the non-susceptible groups. In a functional analysis to correlate the putative protein biomarkers with relevant biological functions, we found increased expression of proteins related to inflammatory responses and central cellular processes and decreased expression of molecules involved in antiviral activity. The most noteworthy are the Cystatin family, protective molecules present at the oral cavity, the Calprotectin family involved in cell cycle progression, or the Histone family related to nucleosome functions. Furthermore, since proteomics allows checking microbiome functionality, we explored bacterial products and found in the COVID-19+ group 4 overrepresented genera and 2 phyla together with 4 main functional features (KOs) related to ribosomal proteins. Finally, we studied correlations with the plasma activity of the molecular target of SARS-CoV-2, ACE2, and found a link with two proteins related to protein transport through the microtubules in the cytoplasm (DYBC1 and MAPR1). Our study delineates new mechanisms of SARS-CoV-2 susceptibility and progression to severe disease that may help find better therapies for COVID-19. |
HostingRepository | PRIDE |
AnnounceDate | 2024-05-31 |
AnnouncementXML | Submission_2024-05-31_09:16:00.697.xml |
DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD032333 |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Supported dataset by repository |
PrimarySubmitter | Sergio Ciordia |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | No PTMs are included in the dataset |
Instrument | Orbitrap Exploris 240 |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2022-03-16 09:17:56 | ID requested | |
⏵ 1 | 2024-05-31 09:16:01 | announced | |
Publication List
10.1186/s12014-024-09482-9; |
Moreno E, Ciordia S, F, á, tima SM, Jim, é, nez D, Mart, í, nez-Sanz J, Vizcarra P, Ron R, S, á, nchez-Conde M, Bargiela R, Sanchez-Carrillo S, Moreno S, Corrales F, Ferrer M, Serrano-Villar S, Proteomic snapshot of saliva samples predicts new pathways implicated in SARS-CoV-2 pathogenesis. Clin Proteomics, 21(1):37(2024) [pubmed] |
10.6019/PXD032333; |
Keyword List
ProteomeXchange project tag: Sars-cov-2, Covid-19 |
submitter keyword: functional analysis,proteomics, SARS-CoV-2, saliva, pathogenesis |
Contact List
Sergio Serrano-Villar |
contact affiliation | Department of Infectious Diseases, Hospital Universitario Ramón y Cajal, IRYCIS. AND CIBERInf, Instituto de Salud Carlos III. Madrid, Spain |
contact email | sergio.serrano@salud.madrid.org |
lab head | |
Sergio Ciordia |
contact affiliation | Spanish National Center for Biotechnology |
contact email | sciordia@cnb.csic.es |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD032333
- Label: PRIDE project
- Name: Proteomic snapshot of saliva samples reveals new pathways implicated in SARS-CoV-2 pathogenesis