SARS-CoV-2-free residual proteins mediated phenotypic and metabolic changes in peripheral blood monocytic-derived macrophages in support of viral pathogenesis.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2023
Historique:
received: 27 10 2022
accepted: 03 01 2023
entrez: 19 1 2023
pubmed: 20 1 2023
medline: 24 1 2023
Statut: epublish

Résumé

The large-scale dissemination of coronavirus disease-2019 (COVID-19) and its serious complications have pledged the scientific research communities to uncover the pathogenesis mechanisms of its etiologic agent, severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). Methods of unveiling such mechanisms are rooted in understanding the viral agent's interactions with the immune system, including its ability to activate macrophages, due to their suggested role in prolonged inflammatory phases and adverse immune responses. The objective of this study is to test the effect of SARS-CoV-2-free proteins on the metabolic and immune responses of macrophages. We hypothesized that SARS-CoV-2 proteins shed during the infection cycle may dynamically induce metabolic and immunologic alterations with an inflammatory impact on the infected host cells. It is imperative to delineate such alterations in the context of macrophages to gain insight into the pathogenesis of these highly infectious viruses and their associated complications and thus, expedite the vaccine and drug therapy advent in combat of viral infections. Human monocyte-derived macrophages were treated with SARS-CoV-2-free proteins at different concentrations. The phenotypic and metabolic alterations in macrophages were investigated and the subsequent metabolic pathways were analyzed. The obtained results indicated that SARS-CoV-2-free proteins induced concentration-dependent alterations in the metabolic and phenotypic profiles of macrophages. Several metabolic pathways were enriched following treatment, including vitamin K, propanoate, and the Warburg effect. These results indicate significant adverse effects driven by residual viral proteins that may hence be considered determinants of viral pathogenesis. These findings provide important insight as to the impact of SARS-CoV-2-free residual proteins on the host cells and suggest a potential new method of management during the infection and prior to vaccination.

Identifiants

pubmed: 36656874
doi: 10.1371/journal.pone.0280592
pii: PONE-D-22-29694
pmc: PMC9851515
doi:

Substances chimiques

Viral Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0280592

Informations de copyright

Copyright: © 2023 Mohammad et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Mohammad G Mohammad (MG)

Department of Medical Laboratory Sciences, Collage of Health Sciences, University of Sharjah, Sharjah, UAE.
Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, UAE.

Naglaa S Ashmawy (NS)

Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, UAE.
Department of Pharmacognosy, Faculty of Pharmacy, Ain Shams University, Abbassia, Cairo, Egypt.

Ahmed M Al-Rawi (AM)

Department of Medical Laboratory Sciences, Collage of Health Sciences, University of Sharjah, Sharjah, UAE.
Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, UAE.

Ameera Abu-Qiyas (A)

Department of Medical Laboratory Sciences, Collage of Health Sciences, University of Sharjah, Sharjah, UAE.
Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, UAE.

Alshaimaa M Hamoda (AM)

Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, UAE.
College of Medicine, University of Sharjah, Sharjah, UAE.
Faculty of Pharmacy, Assiut University, Assiut, Egypt.

Rania Hamdy (R)

Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, UAE.
Faculty of Pharmacy, Zagazig University, Zagazig, Egypt.

Salam Dakalbab (S)

Department of Medical Laboratory Sciences, Collage of Health Sciences, University of Sharjah, Sharjah, UAE.
Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, UAE.

Shahad Arikat (S)

Department of Medical Laboratory Sciences, Collage of Health Sciences, University of Sharjah, Sharjah, UAE.

Dana Salahat (D)

Department of Medical Laboratory Sciences, Collage of Health Sciences, University of Sharjah, Sharjah, UAE.

Mohamed Madkour (M)

Department of Medical Laboratory Sciences, Collage of Health Sciences, University of Sharjah, Sharjah, UAE.

Sameh S M Soliman (SSM)

Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, UAE.
College of Pharmacy, University of Sharjah, Sharjah, UAE.

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Classifications MeSH