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A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity

Authors :
Thais Sibioni Berti Bastos
André Guilherme Portela de Paula
Rebeca Bosso dos Santos Luz
Anali M. B. Garnique
Marco A. A. Belo
Silas Fernandes Eto
Dayanne Carla Fernandes
Fausto Klabund Ferraris
Leticia Gomes de Pontes
Tábata Takahashi França
Leonardo José Gil Barcellos
Flavio P. Veras
Pamela Bermejo
Giovanna Guidelli
Carla Maneira
Fellipe da Silveira Bezerra de Mello
Gleidson Teixeira
Gonçalo Amarante Guimarães Pereira
Bianca H. Ventura Fernandes
Paulo R. S. Sanches
Helyson Lucas Bezerra Braz
Roberta Jeane Bezerra Jorge
Guilherme Malafaia
Eduardo M. Cilli
Danilo da Silva Olivier
Marcos Serrou do Amaral
Renata J. Medeiros
Antonio Condino-Neto
Luciani R. Carvalho
Glaucia M. Machado-Santelli
Ives Charlie-Silva
Jorge Galindo-Villegas
Tárcio Teodoro Braga
Source :
Scientific Reports, Vol 13, Iss 1, Pp 1-15 (2023)
Publication Year :
2023
Publisher :
Nature Portfolio, 2023.

Abstract

Abstract Despite all efforts to combat the pandemic of COVID-19, we are still living with high numbers of infected persons, an overburdened health care system, and the lack of an effective and definitive treatment. Understanding the pathophysiology of the disease is crucial for the development of new technologies and therapies for the best clinical management of patients. Since the manipulation of the whole virus requires a structure with an adequate level of biosafety, the development of alternative technologies, such as the synthesis of peptides from viral proteins, is a possible solution to circumvent this problem. In addition, the use and validation of animal models is of extreme importance to screen new drugs and to compress the organism's response to the disease. Peptides derived from recombinant S protein from SARS-CoV-2 were synthesized and validated by in silico, in vitro and in vivo methodologies. Macrophages and neutrophils were challenged with the peptides and the production of inflammatory mediators and activation profile were evaluated. These peptides were also inoculated into the swim bladder of transgenic zebrafish larvae at 6 days post fertilization (dpf) to mimic the inflammatory process triggered by the virus, which was evaluated by confocal microscopy. In addition, toxicity and oxidative stress assays were also developed. In silico and molecular dynamics assays revealed that the peptides bind to the ACE2 receptor stably and interact with receptors and adhesion molecules, such as MHC and TCR, from humans and zebrafish. Macrophages stimulated with one of the peptides showed increased production of NO, TNF-α and CXCL2. Inoculation of the peptides in zebrafish larvae triggered an inflammatory process marked by macrophage recruitment and increased mortality, as well as histopathological changes, similarly to what is observed in individuals with COVID-19. The use of peptides is a valuable alternative for the study of host immune response in the context of COVID-19. The use of zebrafish as an animal model also proved to be appropriate and effective in evaluating the inflammatory process, comparable to humans.

Subjects

Subjects :
Medicine
Science

Details

Language :
English
ISSN :
20452322
Volume :
13
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Scientific Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.4accb29875b6439dba15e1534dfe5ee0
Document Type :
article
Full Text :
https://doi.org/10.1038/s41598-023-29588-8