Proteomic analysis capsule synthesis and redox mechanisms in the intracellular survival of group B Streptococcus in fish microglia

Detalhes bibliográficos
Autor(a) principal: Eto, Silas Fernandes
Data de Publicação: 2021
Outros Autores: Fernandes, Dayanne Carla, Baldassi, Amanda Cristina [UNESP], Balbuena, Thiago Santana [UNESP], da Costa Alecrim, João Victor, Almeida de Carvalho, Fabíola Christian, Lima, Carla, Lopes-Ferreira, Monica, Pizauro, João Martins [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.fsi.2021.08.019
http://hdl.handle.net/11449/222324
Resumo: Group B Streptococcus (GBS) causes meningitis in neonates and Nile tilapia (Oreochromis niloticus). The molecular mechanisms regulating the intracellular survival of this pathogen in the host cell are complex and crucial for the progression of infection. Thus, we propose the use of GBS-infected Nile tilapia microglia as an in vitro model system simulating infection caused by homologous bacteria in humans. We used this model to evaluate the phagocytic activity, as well as the functional aspects of the capsular proteins A, B, C, and D and the major redox enzymes, and the synergistic role of mechanisms/proteins involved in blocking phagocytic process. We observed that in the intracellular phase, GBS showed enhanced synthesis of the polysaccharide capsule and used superoxide dismutase, thioredoxin, NADH oxidase, and alkyl hydroperoxide reductase to scavenge reactive oxygen species and reactive nitrogen species produced by the host cell. Furthermore, although these virulence mechanisms were effective during the initial hours of infection, they were not able to subvert microglial responses, which partially neutralized the infection. Altogether, our findings provided important information regarding the intracellular survival mechanisms of GBS and perspectives for the production of new drugs and vaccines, through the druggability analysis of specific proteins. In conclusion, tilapia microglia serve as a potent in vitro experimental model for the study of meningitis.
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spelling Proteomic analysis capsule synthesis and redox mechanisms in the intracellular survival of group B Streptococcus in fish microgliaBrainDruggabilityMeningitisProteomicsVaccineGroup B Streptococcus (GBS) causes meningitis in neonates and Nile tilapia (Oreochromis niloticus). The molecular mechanisms regulating the intracellular survival of this pathogen in the host cell are complex and crucial for the progression of infection. Thus, we propose the use of GBS-infected Nile tilapia microglia as an in vitro model system simulating infection caused by homologous bacteria in humans. We used this model to evaluate the phagocytic activity, as well as the functional aspects of the capsular proteins A, B, C, and D and the major redox enzymes, and the synergistic role of mechanisms/proteins involved in blocking phagocytic process. We observed that in the intracellular phase, GBS showed enhanced synthesis of the polysaccharide capsule and used superoxide dismutase, thioredoxin, NADH oxidase, and alkyl hydroperoxide reductase to scavenge reactive oxygen species and reactive nitrogen species produced by the host cell. Furthermore, although these virulence mechanisms were effective during the initial hours of infection, they were not able to subvert microglial responses, which partially neutralized the infection. Altogether, our findings provided important information regarding the intracellular survival mechanisms of GBS and perspectives for the production of new drugs and vaccines, through the druggability analysis of specific proteins. In conclusion, tilapia microglia serve as a potent in vitro experimental model for the study of meningitis.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Postgraduate in Health Sciences-PROCISA Federal University of Roraima (UFRR)Immunochemistry Laboratory Butantan Institute (CeTICs/FAPESP), Vital Brazil Avenue, 1500Department of Technology School of Agrarian and Veterinary Sciences Sao Paulo State University (Unesp)Immunoregulation Unit of the Laboratory of Applied Toxinology (CeTICs/FAPESP) Butantan Institute, Vital Brazil Avenue, 1500Department of Technology School of Agrarian and Veterinary Sciences Sao Paulo State University (Unesp)Federal University of Roraima (UFRR)(CeTICs/FAPESP)Universidade Estadual Paulista (UNESP)Butantan InstituteEto, Silas FernandesFernandes, Dayanne CarlaBaldassi, Amanda Cristina [UNESP]Balbuena, Thiago Santana [UNESP]da Costa Alecrim, João VictorAlmeida de Carvalho, Fabíola ChristianLima, CarlaLopes-Ferreira, MonicaPizauro, João Martins [UNESP]2022-04-28T19:44:03Z2022-04-28T19:44:03Z2021-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article34-50http://dx.doi.org/10.1016/j.fsi.2021.08.019Fish and Shellfish Immunology, v. 118, p. 34-50.1095-99471050-4648http://hdl.handle.net/11449/22232410.1016/j.fsi.2021.08.0192-s2.0-85114027149Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengFish and Shellfish Immunologyinfo:eu-repo/semantics/openAccess2022-04-28T19:44:03Zoai:repositorio.unesp.br:11449/222324Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-28T19:44:03Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Proteomic analysis capsule synthesis and redox mechanisms in the intracellular survival of group B Streptococcus in fish microglia
title Proteomic analysis capsule synthesis and redox mechanisms in the intracellular survival of group B Streptococcus in fish microglia
spellingShingle Proteomic analysis capsule synthesis and redox mechanisms in the intracellular survival of group B Streptococcus in fish microglia
Eto, Silas Fernandes
Brain
Druggability
Meningitis
Proteomics
Vaccine
title_short Proteomic analysis capsule synthesis and redox mechanisms in the intracellular survival of group B Streptococcus in fish microglia
title_full Proteomic analysis capsule synthesis and redox mechanisms in the intracellular survival of group B Streptococcus in fish microglia
title_fullStr Proteomic analysis capsule synthesis and redox mechanisms in the intracellular survival of group B Streptococcus in fish microglia
title_full_unstemmed Proteomic analysis capsule synthesis and redox mechanisms in the intracellular survival of group B Streptococcus in fish microglia
title_sort Proteomic analysis capsule synthesis and redox mechanisms in the intracellular survival of group B Streptococcus in fish microglia
author Eto, Silas Fernandes
author_facet Eto, Silas Fernandes
Fernandes, Dayanne Carla
Baldassi, Amanda Cristina [UNESP]
Balbuena, Thiago Santana [UNESP]
da Costa Alecrim, João Victor
Almeida de Carvalho, Fabíola Christian
Lima, Carla
Lopes-Ferreira, Monica
Pizauro, João Martins [UNESP]
author_role author
author2 Fernandes, Dayanne Carla
Baldassi, Amanda Cristina [UNESP]
Balbuena, Thiago Santana [UNESP]
da Costa Alecrim, João Victor
Almeida de Carvalho, Fabíola Christian
Lima, Carla
Lopes-Ferreira, Monica
Pizauro, João Martins [UNESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Federal University of Roraima (UFRR)
(CeTICs/FAPESP)
Universidade Estadual Paulista (UNESP)
Butantan Institute
dc.contributor.author.fl_str_mv Eto, Silas Fernandes
Fernandes, Dayanne Carla
Baldassi, Amanda Cristina [UNESP]
Balbuena, Thiago Santana [UNESP]
da Costa Alecrim, João Victor
Almeida de Carvalho, Fabíola Christian
Lima, Carla
Lopes-Ferreira, Monica
Pizauro, João Martins [UNESP]
dc.subject.por.fl_str_mv Brain
Druggability
Meningitis
Proteomics
Vaccine
topic Brain
Druggability
Meningitis
Proteomics
Vaccine
description Group B Streptococcus (GBS) causes meningitis in neonates and Nile tilapia (Oreochromis niloticus). The molecular mechanisms regulating the intracellular survival of this pathogen in the host cell are complex and crucial for the progression of infection. Thus, we propose the use of GBS-infected Nile tilapia microglia as an in vitro model system simulating infection caused by homologous bacteria in humans. We used this model to evaluate the phagocytic activity, as well as the functional aspects of the capsular proteins A, B, C, and D and the major redox enzymes, and the synergistic role of mechanisms/proteins involved in blocking phagocytic process. We observed that in the intracellular phase, GBS showed enhanced synthesis of the polysaccharide capsule and used superoxide dismutase, thioredoxin, NADH oxidase, and alkyl hydroperoxide reductase to scavenge reactive oxygen species and reactive nitrogen species produced by the host cell. Furthermore, although these virulence mechanisms were effective during the initial hours of infection, they were not able to subvert microglial responses, which partially neutralized the infection. Altogether, our findings provided important information regarding the intracellular survival mechanisms of GBS and perspectives for the production of new drugs and vaccines, through the druggability analysis of specific proteins. In conclusion, tilapia microglia serve as a potent in vitro experimental model for the study of meningitis.
publishDate 2021
dc.date.none.fl_str_mv 2021-11-01
2022-04-28T19:44:03Z
2022-04-28T19:44:03Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.fsi.2021.08.019
Fish and Shellfish Immunology, v. 118, p. 34-50.
1095-9947
1050-4648
http://hdl.handle.net/11449/222324
10.1016/j.fsi.2021.08.019
2-s2.0-85114027149
url http://dx.doi.org/10.1016/j.fsi.2021.08.019
http://hdl.handle.net/11449/222324
identifier_str_mv Fish and Shellfish Immunology, v. 118, p. 34-50.
1095-9947
1050-4648
10.1016/j.fsi.2021.08.019
2-s2.0-85114027149
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Fish and Shellfish Immunology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 34-50
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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