Plasma Proteins Associated with COVID-19 Severity in Puerto Rico

Author:

Rosario-Rodríguez Lester J.1ORCID,Cantres-Rosario Yadira M.2,Carrasquillo-Carrión Kelvin3ORCID,Rosa-Díaz Alexandra4ORCID,Rodríguez-De Jesús Ana E.2,Rivera-Nieves Verónica4,Tosado-Rodríguez Eduardo L.3ORCID,Méndez Loyda B.5ORCID,Roche-Lima Abiel3ORCID,Bertrán Jorge6,Meléndez Loyda M.12ORCID

Affiliation:

1. Department of Microbiology and Medical Zoology, University of Puerto Rico, Medical Sciences Campus, San Juan 00935, Puerto Rico

2. Translational Proteomics Center, Research Capacity Core, Center for Collaborative Research in Health Disparities, University of Puerto Rico, Medical Sciences Campus, San Juan 00935, Puerto Rico

3. Integrated Informatics, Research Capacity Core, Center for Collaborative Research in Health Disparities, University of Puerto Rico, Medical Sciences Campus, San Juan 00935, Puerto Rico

4. Interdisciplinary Studies, Natural Sciences, University of Puerto Rico, Río Piedras Campus, San Juan 00925, Puerto Rico

5. Department of Science & Technology, Ana G. Mendez University, Carolina 00928, Puerto Rico

6. Infectious Diseases, Auxilio Mutuo Hospital, San Juan 00919, Puerto Rico

Abstract

Viral strains, age, and host factors are associated with variable immune responses against SARS-CoV-2 and disease severity. Puerto Ricans have a genetic mixture of races: European, African, and Native American. We hypothesized that unique host proteins/pathways are associated with COVID-19 disease severity in Puerto Rico. Following IRB approval, a total of 95 unvaccinated men and women aged 21–71 years old were recruited in Puerto Rico from 2020–2021. Plasma samples were collected from COVID-19-positive subjects (n = 39) and COVID-19-negative individuals (n = 56) during acute disease. COVID-19-positive individuals were stratified based on symptomatology as follows: mild (n = 18), moderate (n = 13), and severe (n = 8). Quantitative proteomics was performed in plasma samples using tandem mass tag (TMT) labeling. Labeled peptides were subjected to LC/MS/MS and analyzed by Proteome Discoverer (version 2.5), Limma software (version 3.41.15), and Ingenuity Pathways Analysis (IPA, version 22.0.2). Cytokines were quantified using a human cytokine array. Proteomics analyses of severely affected COVID-19-positive individuals revealed 58 differentially expressed proteins. Cadherin-13, which participates in synaptogenesis, was downregulated in severe patients and validated by ELISA. Cytokine immunoassay showed that TNF-α levels decreased with disease severity. This study uncovers potential host predictors of COVID-19 severity and new avenues for treatment in Puerto Ricans.

Funder

UPR COVID19 Emergency Funds

National Institutes of Health National Institute of General Medical Sciences (NIGMS) PR-INBRE-Institutional Developmental Award

Research Infrastructure Core components—National Institute of Minority Health and Health Disparities

Translational Proteomics Center

Publisher

MDPI AG

Reference83 articles.

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