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Proteomic analysis identifies a signature of disease severity in the plasma of COVID-19 pneumonia patients associated to neutrophil, platelet and complement activation

Most patients infected with SARS-CoV-2 display mild symptoms with good prognosis, while 20% of patients suffer from severe viral pneumonia and up to 5% may require intensive care unit (ICU) admission due to severe acute respiratory syndrome, which could be accompanied by multiorgan failure. Plasma p...

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Autores principales: Ciccosanti, Fabiola, Antonioli, Manuela, Sacchi, Alessandra, Notari, Stefania, Farina, Anna, Beccacece, Alessia, Fusto, Marisa, Vergori, Alessandra, D’Offizi, Gianpiero, Taglietti, Fabrizio, Antinori, Andrea, Nicastri, Emanuele, Marchioni, Luisa, Palmieri, Fabrizio, Ippolito, Giuseppe, Piacentini, Mauro, Agrati, Chiara, Fimia, Gian Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641302/
https://www.ncbi.nlm.nih.gov/pubmed/36348270
http://dx.doi.org/10.1186/s12014-022-09377-7
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author Ciccosanti, Fabiola
Antonioli, Manuela
Sacchi, Alessandra
Notari, Stefania
Farina, Anna
Beccacece, Alessia
Fusto, Marisa
Vergori, Alessandra
D’Offizi, Gianpiero
Taglietti, Fabrizio
Antinori, Andrea
Nicastri, Emanuele
Marchioni, Luisa
Palmieri, Fabrizio
Ippolito, Giuseppe
Piacentini, Mauro
Agrati, Chiara
Fimia, Gian Maria
author_facet Ciccosanti, Fabiola
Antonioli, Manuela
Sacchi, Alessandra
Notari, Stefania
Farina, Anna
Beccacece, Alessia
Fusto, Marisa
Vergori, Alessandra
D’Offizi, Gianpiero
Taglietti, Fabrizio
Antinori, Andrea
Nicastri, Emanuele
Marchioni, Luisa
Palmieri, Fabrizio
Ippolito, Giuseppe
Piacentini, Mauro
Agrati, Chiara
Fimia, Gian Maria
author_sort Ciccosanti, Fabiola
collection PubMed
description Most patients infected with SARS-CoV-2 display mild symptoms with good prognosis, while 20% of patients suffer from severe viral pneumonia and up to 5% may require intensive care unit (ICU) admission due to severe acute respiratory syndrome, which could be accompanied by multiorgan failure. Plasma proteomics provide valuable and unbiased information about disease progression and therapeutic candidates. Recent proteomic studies have identified molecular changes in plasma of COVID-19 patients that implied significant dysregulation of several aspects of the inflammatory response accompanied by a general metabolic suppression. However, which of these plasma alterations are associated with disease severity remains only partly characterized. A known limitation of proteomic studies of plasma samples is the large difference in the macromolecule abundance, with concentration spanning at least 10 orders of magnitude. To improve the coverage of plasma contents, we performed a deep proteomic analysis of plasma from 10 COVID-19 patients with severe/fatal pneumonia compared to 10 COVID-19 patients with pneumonia who did not require ICU admission (non-ICU). To this aim, plasma samples were first depleted of the most abundant proteins, trypsin digested and peptides subjected to a high pH reversed-phase peptide fractionation before LC–MS analysis. These results highlighted an increase of proteins involved in neutrophil and platelet activity and acute phase response, which is significantly higher in severe/fatal COVID-19 patients when compared to non-ICU ones. Importantly, these changes are associated with a selective induction of complement cascade factors in severe/fatal COVID-19 patients. Data are available via ProteomeXchange with identifier PXD036491. Among these alterations, we confirmed by ELISA that higher levels of the neutrophil granule proteins DEFA3 and LCN2 are present in COVID-19 patients requiring ICU admission when compared to non-ICU and healthy donors. Altogether, our study provided an in-depth view of plasma proteome changes that occur in COVID-19 patients in relation to disease severity, which can be helpful to identify therapeutic strategies to improve the disease outcome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12014-022-09377-7.
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spelling pubmed-96413022022-11-14 Proteomic analysis identifies a signature of disease severity in the plasma of COVID-19 pneumonia patients associated to neutrophil, platelet and complement activation Ciccosanti, Fabiola Antonioli, Manuela Sacchi, Alessandra Notari, Stefania Farina, Anna Beccacece, Alessia Fusto, Marisa Vergori, Alessandra D’Offizi, Gianpiero Taglietti, Fabrizio Antinori, Andrea Nicastri, Emanuele Marchioni, Luisa Palmieri, Fabrizio Ippolito, Giuseppe Piacentini, Mauro Agrati, Chiara Fimia, Gian Maria Clin Proteomics Research Most patients infected with SARS-CoV-2 display mild symptoms with good prognosis, while 20% of patients suffer from severe viral pneumonia and up to 5% may require intensive care unit (ICU) admission due to severe acute respiratory syndrome, which could be accompanied by multiorgan failure. Plasma proteomics provide valuable and unbiased information about disease progression and therapeutic candidates. Recent proteomic studies have identified molecular changes in plasma of COVID-19 patients that implied significant dysregulation of several aspects of the inflammatory response accompanied by a general metabolic suppression. However, which of these plasma alterations are associated with disease severity remains only partly characterized. A known limitation of proteomic studies of plasma samples is the large difference in the macromolecule abundance, with concentration spanning at least 10 orders of magnitude. To improve the coverage of plasma contents, we performed a deep proteomic analysis of plasma from 10 COVID-19 patients with severe/fatal pneumonia compared to 10 COVID-19 patients with pneumonia who did not require ICU admission (non-ICU). To this aim, plasma samples were first depleted of the most abundant proteins, trypsin digested and peptides subjected to a high pH reversed-phase peptide fractionation before LC–MS analysis. These results highlighted an increase of proteins involved in neutrophil and platelet activity and acute phase response, which is significantly higher in severe/fatal COVID-19 patients when compared to non-ICU ones. Importantly, these changes are associated with a selective induction of complement cascade factors in severe/fatal COVID-19 patients. Data are available via ProteomeXchange with identifier PXD036491. Among these alterations, we confirmed by ELISA that higher levels of the neutrophil granule proteins DEFA3 and LCN2 are present in COVID-19 patients requiring ICU admission when compared to non-ICU and healthy donors. Altogether, our study provided an in-depth view of plasma proteome changes that occur in COVID-19 patients in relation to disease severity, which can be helpful to identify therapeutic strategies to improve the disease outcome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12014-022-09377-7. BioMed Central 2022-11-08 /pmc/articles/PMC9641302/ /pubmed/36348270 http://dx.doi.org/10.1186/s12014-022-09377-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ciccosanti, Fabiola
Antonioli, Manuela
Sacchi, Alessandra
Notari, Stefania
Farina, Anna
Beccacece, Alessia
Fusto, Marisa
Vergori, Alessandra
D’Offizi, Gianpiero
Taglietti, Fabrizio
Antinori, Andrea
Nicastri, Emanuele
Marchioni, Luisa
Palmieri, Fabrizio
Ippolito, Giuseppe
Piacentini, Mauro
Agrati, Chiara
Fimia, Gian Maria
Proteomic analysis identifies a signature of disease severity in the plasma of COVID-19 pneumonia patients associated to neutrophil, platelet and complement activation
title Proteomic analysis identifies a signature of disease severity in the plasma of COVID-19 pneumonia patients associated to neutrophil, platelet and complement activation
title_full Proteomic analysis identifies a signature of disease severity in the plasma of COVID-19 pneumonia patients associated to neutrophil, platelet and complement activation
title_fullStr Proteomic analysis identifies a signature of disease severity in the plasma of COVID-19 pneumonia patients associated to neutrophil, platelet and complement activation
title_full_unstemmed Proteomic analysis identifies a signature of disease severity in the plasma of COVID-19 pneumonia patients associated to neutrophil, platelet and complement activation
title_short Proteomic analysis identifies a signature of disease severity in the plasma of COVID-19 pneumonia patients associated to neutrophil, platelet and complement activation
title_sort proteomic analysis identifies a signature of disease severity in the plasma of covid-19 pneumonia patients associated to neutrophil, platelet and complement activation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641302/
https://www.ncbi.nlm.nih.gov/pubmed/36348270
http://dx.doi.org/10.1186/s12014-022-09377-7
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