GroEL protein of the Leptospira spp. interacts with host proteins and induces cytokines secretion on macrophages

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dc.contributorLab. Bacteriologiapt_BR
dc.contributorCentro Bioindustrialpt_BR
dc.contributorIniciação Científicapt_BR
dc.contributorPrograma de Pós-Doutoradopt_BR
dc.contributor.authorHo, Joana Diaspt_BR
dc.contributor.authorTakara, Luiz Eduardo Massaopt_BR
dc.contributor.authorMonaris, Denizept_BR
dc.contributor.authorGonçalves, Aline Patríciapt_BR
dc.contributor.authorSouza-Filho, Antonio Franciscopt_BR
dc.contributor.authorSouza, Gisele Oliveira dept_BR
dc.contributor.authorHeinemann, Marcos Bryanpt_BR
dc.contributor.authorHo, Paulo Leept_BR
dc.contributor.authorAbreu, Patricia Antonia Estimapt_BR
dc.date.accessioned2021-04-07T18:40:51Z-
dc.date.available2021-04-07T18:40:51Z-
dc.date.issued2021pt_BR
dc.identifier.citationHo JD, Takara LEM, Monaris D, Gonçalves AP, Souza-Filho AF, Souza GO, et al. GroEL protein of the Leptospira spp. interacts with host proteins and induces cytokines secretion on macrophages. BMC Microbiol.. 2021 Mar;21:99. doi:10.1186/s12866-021-02162-w.pt_BR
dc.identifier.urihttps://repositorio.butantan.gov.br/handle/butantan/3652-
dc.description.abstractBackground: Leptospirosis is a zoonotic disease caused by infection with spirochetes from Leptospira genus. It has been classified into at least 17 pathogenic species, with more than 250 serologic variants. This wide distribution may be a result of leptospiral ability to colonize the renal tubules of mammalian hosts, including humans, wildlife, and many domesticated animals. Previous studies showed that the expression of proteins belonging to the microbial heat shock protein (HSP) family is upregulated during infection and also during various stress stimuli. Several proteins of this family are known to have important roles in the infectious processes in other bacteria, but the role of HSPs in Leptospira spp. is poorly understood. In this study, we have evaluated the capacity of the protein GroEL, a member of HSP family, of interacting with host proteins and of stimulating the production of cytokines by macrophages. Results: The binding experiments demonstrated that the recombinant GroEL protein showed interaction with several host components in a dose-dependent manner. It was also observed that GroEL is a surface protein, and it is secreted extracellularly. Moreover, two cytokines (tumor necrosis factor-α and interleukin-6) were produced when macrophages cells were stimulated with this protein. Conclusions: Our findings showed that GroEL protein may contribute to the adhesion of leptospires to host tissues and stimulate the production of proinflammatory cytokines during infection. These features might indicate an important role of GroEL in the pathogen-host interaction in the leptospirosis.pt_BR
dc.description.sponsorship(CAPES) Coordenação de Aperfeiçoamento de Pessoal de Nível Superiorpt_BR
dc.description.sponsorship(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulopt_BR
dc.description.sponsorship(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológicopt_BR
dc.format.extent99pt_BR
dc.language.isoEnglishpt_BR
dc.relation.ispartofBMC Microbiologypt_BR
dc.rightsOpen accesspt_BR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_BR
dc.titleGroEL protein of the Leptospira spp. interacts with host proteins and induces cytokines secretion on macrophagespt_BR
dc.typeArticlept_BR
dc.rights.licenseCC BYpt_BR
dc.relation.datasethttps://repositorio.butantan.gov.br/handle/butantan/3635pt_BR
dc.identifier.doi10.1186/s12866-021-02162-wpt_BR
dc.identifier.urlhttps://doi.org/10.1186/s12866-021-02162-wpt_BR
dc.contributor.external(USP) Universidade de São Paulopt_BR
dc.identifier.citationvolume21pt_BR
dc.subject.keywordLeptospirapt_BR
dc.subject.keywordLeptospirosispt_BR
dc.subject.keywordChaperonin 60pt_BR
dc.subject.keywordGroELpt_BR
dc.subject.keywordHSP60pt_BR
dc.subject.keywordJ774.1 cellspt_BR
dc.subject.keywordMoonlighting proteinpt_BR
dc.relation.ispartofabbreviatedBMC Microbiolpt_BR
dc.identifier.citationabntv. 21, 99, mar. 2021pt_BR
dc.identifier.citationvancouver2021 Mar;21:99pt_BR
dc.contributor.butantanHo, Joana Dias|:Aluno Egresso|:Iniciação Científica|:Lab. Bacteriologia|:PrimeiroAutorpt_BR
dc.contributor.butantanTakara, Luiz Eduardo Massao|:Aluno Egresso|:Iniciação Científica|:Lab. Bacteriologiapt_BR
dc.contributor.butantanMonaris, Denize|:Pós-Doc Egresso|:Programa de Pós-Doutorado|:Lab. Bacteriologiapt_BR
dc.contributor.butantanGonçalves, Aline Patrícia|:Aluno|:Lab. Bacteriologiapt_BR
dc.contributor.butantanHo, Paulo Lee|:Pesquisador|:Centro Bioindustrialpt_BR
dc.contributor.butantanAbreu, Patricia Antonia Estima|:Pesquisador|:Lab. Bacteriologia|:Autor de correspondênciapt_BR
dc.sponsorship.butantan(CAPES) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior¦¦001pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2010/51215–9pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2019/00546–0pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2019/09804–1pt_BR
dc.sponsorship.butantan(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico¦¦pt_BR
dc.identifier.bvsccBR78.1pt_BR
dc.identifier.bvsdbIBProdpt_BR
dc.description.dbindexedYespt_BR
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