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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.
  • Bastos TSB; Department of Pathology, Federal University of Parana, Curitiba, Brazil.
  • de Paula AGP; Department of Pathology, Federal University of Parana, Curitiba, Brazil.
  • Dos Santos Luz RB; Department of Pathology, Federal University of Parana, Curitiba, Brazil.
  • Garnique AMB; Department of Cell Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
  • Belo MAA; Brasil University, Descalvado, São Paulo, Brazil.
  • Eto SF; Center of Excellence in New Target Discovery (CENTD) Special Laboratory, Butantan Institute, São Paulo, Brazil.
  • Fernandes DC; Center of Innovation and Development, Laboratory of Development and Innovation, Butantan Institute, São Paulo, Brazil.
  • Ferraris FK; Veterinarian, São Paulo, Brazil.
  • de Pontes LG; Department of Pharmacology and Toxicology, Oswaldo Cruz Foundation, FIOCRUZ, Rio de Janeiro, Brazil.
  • França TT; Laboratory of Human Immunology, Department Immunology, Institute Biomedical Sciences, University São Paulo, São Paulo, Brazil.
  • Barcellos LJG; Laboratory of Human Immunology, Department Immunology, Institute Biomedical Sciences, University São Paulo, São Paulo, Brazil.
  • Veras FP; Laboratory of Fish Physiology, Graduate Program of Bioexperimentation, University of Passo Fundo, Santa Maria, Brazil.
  • Bermejo P; Graduate Program of Pharmacology, Federal University of Santa Maria, Santa Maria, Brazil.
  • Guidelli G; Center of Research in Inflammatory Diseases, Ribeirão Preto Medical School, University of Sao Paulo, Ribeirão Preto, São Paulo, Brazil.
  • Maneira C; Department of Pharmacology, Ribeirao Preto Medical School, University of São Paulo, Ribeirao Preto, São Paulo, Brazil.
  • da Silveira Bezerra de Mello F; Laboratório de Genômica e bioEnergia (LGE), Institute of Biology - Unicamp, Campinas, Brazil.
  • Teixeira G; Laboratório de Genômica e bioEnergia (LGE), Institute of Biology - Unicamp, Campinas, Brazil.
  • Pereira GAG; Laboratório de Genômica e bioEnergia (LGE), Institute of Biology - Unicamp, Campinas, Brazil.
  • Fernandes BHV; Laboratório de Genômica e bioEnergia (LGE), Institute of Biology - Unicamp, Campinas, Brazil.
  • Sanches PRS; Laboratório de Genômica e bioEnergia (LGE), Institute of Biology - Unicamp, Campinas, Brazil.
  • Braz HLB; Laboratório de Genômica e bioEnergia (LGE), Institute of Biology - Unicamp, Campinas, Brazil.
  • Jorge RJB; Laboratório de Controle Genético e Sanitário, Diretoria Técnica de Apoio ao Ensino e Pesquisa, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
  • Malafaia G; Instituto de Química, Universidade Estadual Paulista, Araraquara, SP, Brazil.
  • Cilli EM; Department of Physiology and Pharmacology, School of Medicine, Federal University of Ceará, Fortaleza, CE, Brazil.
  • Olivier DDS; Department of Physiology and Pharmacology, School of Medicine, Federal University of Ceará, Fortaleza, CE, Brazil.
  • do Amaral MS; Biological Research Laboratory, Goiano Federal Institute, Urutai Campus, Urutaí, GO, Brazil.
  • Medeiros RJ; Instituto de Química, Universidade Estadual Paulista, Araraquara, SP, Brazil.
  • Condino-Neto A; Integrated Sciences Center, Federal University of Tocantins, Araguaína, TO, Brazil.
  • Carvalho LR; Institute of Physics, Federal University of Mato Grosso do Sul, Campo Grande, MS, 79070-900, Brazil.
  • Machado-Santelli GM; Laboratory of Physiology, INCQS/Fiocruz Zebrafish Facility, Department of Pharmacology and Toxicology, National Institute for Quality Control in Health, Rio de Janeiro, Brazil.
  • Charlie-Silva I; Laboratory of Human Immunology, Department Immunology, Institute Biomedical Sciences, University São Paulo, São Paulo, Brazil.
  • Galindo-Villegas J; Laboratório de Controle Genético e Sanitário, Diretoria Técnica de Apoio ao Ensino e Pesquisa, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
  • Braga TT; Laboratory of Cellular and Molecular Biology, Department of Cell and Developmental Biology, Institute of Biomedical Science, University of Sao Paulo, University of São Paulo, São Paulo, Brazil.
Sci Rep ; 13(1): 8060, 2023 05 17.
Article in English | MEDLINE | ID: covidwho-2321900
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies / Prognostic study Limits: Animals / Humans Language: English Journal: Sci Rep Year: 2023 Document Type: Article Affiliation country: S41598-023-29588-8

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies / Prognostic study Limits: Animals / Humans Language: English Journal: Sci Rep Year: 2023 Document Type: Article Affiliation country: S41598-023-29588-8