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A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity
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 technol...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191404/ https://www.ncbi.nlm.nih.gov/pubmed/37198208 http://dx.doi.org/10.1038/s41598-023-29588-8 |
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author | Bastos, Thais Sibioni Berti de Paula, André Guilherme Portela dos Santos Luz, Rebeca Bosso Garnique, Anali M. B. Belo, Marco A. A. Eto, Silas Fernandes Fernandes, Dayanne Carla Ferraris, Fausto Klabund de Pontes, Leticia Gomes França, Tábata Takahashi Barcellos, Leonardo José Gil Veras, Flavio P. Bermejo, Pamela Guidelli, Giovanna Maneira, Carla da Silveira Bezerra de Mello, Fellipe Teixeira, Gleidson Pereira, Gonçalo Amarante Guimarães Fernandes, Bianca H. Ventura Sanches, Paulo R. S. Braz, Helyson Lucas Bezerra Jorge, Roberta Jeane Bezerra Malafaia, Guilherme Cilli, Eduardo M. Olivier, Danilo da Silva do Amaral, Marcos Serrou Medeiros, Renata J. Condino-Neto, Antonio Carvalho, Luciani R. Machado-Santelli, Glaucia M. Charlie-Silva, Ives Galindo-Villegas, Jorge Braga, Tárcio Teodoro |
author_facet | Bastos, Thais Sibioni Berti de Paula, André Guilherme Portela dos Santos Luz, Rebeca Bosso Garnique, Anali M. B. Belo, Marco A. A. Eto, Silas Fernandes Fernandes, Dayanne Carla Ferraris, Fausto Klabund de Pontes, Leticia Gomes França, Tábata Takahashi Barcellos, Leonardo José Gil Veras, Flavio P. Bermejo, Pamela Guidelli, Giovanna Maneira, Carla da Silveira Bezerra de Mello, Fellipe Teixeira, Gleidson Pereira, Gonçalo Amarante Guimarães Fernandes, Bianca H. Ventura Sanches, Paulo R. S. Braz, Helyson Lucas Bezerra Jorge, Roberta Jeane Bezerra Malafaia, Guilherme Cilli, Eduardo M. Olivier, Danilo da Silva do Amaral, Marcos Serrou Medeiros, Renata J. Condino-Neto, Antonio Carvalho, Luciani R. Machado-Santelli, Glaucia M. Charlie-Silva, Ives Galindo-Villegas, Jorge Braga, Tárcio Teodoro |
author_sort | Bastos, Thais Sibioni Berti |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10191404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101914042023-05-19 A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity Bastos, Thais Sibioni Berti de Paula, André Guilherme Portela dos Santos Luz, Rebeca Bosso Garnique, Anali M. B. Belo, Marco A. A. Eto, Silas Fernandes Fernandes, Dayanne Carla Ferraris, Fausto Klabund de Pontes, Leticia Gomes França, Tábata Takahashi Barcellos, Leonardo José Gil Veras, Flavio P. Bermejo, Pamela Guidelli, Giovanna Maneira, Carla da Silveira Bezerra de Mello, Fellipe Teixeira, Gleidson Pereira, Gonçalo Amarante Guimarães Fernandes, Bianca H. Ventura Sanches, Paulo R. S. Braz, Helyson Lucas Bezerra Jorge, Roberta Jeane Bezerra Malafaia, Guilherme Cilli, Eduardo M. Olivier, Danilo da Silva do Amaral, Marcos Serrou Medeiros, Renata J. Condino-Neto, Antonio Carvalho, Luciani R. Machado-Santelli, Glaucia M. Charlie-Silva, Ives Galindo-Villegas, Jorge Braga, Tárcio Teodoro Sci Rep Article 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. Nature Publishing Group UK 2023-05-17 /pmc/articles/PMC10191404/ /pubmed/37198208 http://dx.doi.org/10.1038/s41598-023-29588-8 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Article Bastos, Thais Sibioni Berti de Paula, André Guilherme Portela dos Santos Luz, Rebeca Bosso Garnique, Anali M. B. Belo, Marco A. A. Eto, Silas Fernandes Fernandes, Dayanne Carla Ferraris, Fausto Klabund de Pontes, Leticia Gomes França, Tábata Takahashi Barcellos, Leonardo José Gil Veras, Flavio P. Bermejo, Pamela Guidelli, Giovanna Maneira, Carla da Silveira Bezerra de Mello, Fellipe Teixeira, Gleidson Pereira, Gonçalo Amarante Guimarães Fernandes, Bianca H. Ventura Sanches, Paulo R. S. Braz, Helyson Lucas Bezerra Jorge, Roberta Jeane Bezerra Malafaia, Guilherme Cilli, Eduardo M. Olivier, Danilo da Silva do Amaral, Marcos Serrou Medeiros, Renata J. Condino-Neto, Antonio Carvalho, Luciani R. Machado-Santelli, Glaucia M. Charlie-Silva, Ives Galindo-Villegas, Jorge Braga, Tárcio Teodoro A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity |
title | A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity |
title_full | A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity |
title_fullStr | A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity |
title_full_unstemmed | A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity |
title_short | A novel insight on SARS-CoV-2 S-derived fragments in the control of the host immunity |
title_sort | novel insight on sars-cov-2 s-derived fragments in the control of the host immunity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191404/ https://www.ncbi.nlm.nih.gov/pubmed/37198208 http://dx.doi.org/10.1038/s41598-023-29588-8 |
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