Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion protein

Detalhes bibliográficos
Autor(a) principal: Barral, Thiago Doria
Data de Publicação: 2022
Outros Autores: Kalil, Mauricio Alcantara, Mariutti, Ricardo Barros [UNESP], Arni, Raghuvir Krishnaswamy [UNESP], Gismene, Carolina [UNESP], Sousa, Fernanda Severo, Collares, Tiago, Seixas, Fabiana Kommling, Borsuk, Sibele, Estrela-Lima, Alessandra, Azevedo, Vasco, Meyer, Roberto, Portela, Ricardo Wagner
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s00253-022-12279-1
http://hdl.handle.net/11449/249381
Resumo: Abstract: Caseous lymphadenitis (CLA) is a disease that affects small ruminants, and the best way to prevent its spread on a herd is through immunoprophylaxis. Thus, we aimed to evaluate the MBP:PLD:CP40 fusion protein as a new CLA immunogen. The fusion protein was constructed by combining Corynebacterium pseudotuberculosis PLD and CP40 proteins with maltose-binding protein (MBP) as an intrinsic adjuvant. The antigenicity, allergenic potential, prediction of B epitopes, binding to MHC receptors, and docking on the Toll-Like 2 receptor were evaluated in silico. MBP:PLD:CP40 was expressed and purified. 40 BALB/c were divided into four groups (G1 – control, G2 – Saponin, G3 – MBP:PLD:CP40, and G4 – rPLD + rCP40). Total IgG, IgG1, and IgG2a were quantified, and the expressions of cytokines after splenocyte in vitro stimulation were assessed. Mice were challenged 42 days after the first immunization. The in silico analysis showed that MBP:PLD:CP40 has immunogenic potential, does not have allergic properties, and can dock on the TRL2 receptor. MBP:PLD:CP40 stimulated the production of IgG1 antibodies in a fivefold proportion to IgG2a, and TNF and IL-17 were significantly expressed in response to the antigenic stimuli. When rPLD and rCP40 were used together for immunization, they could induce IFN-γ and IL-12, but with no detectable antibody production. The G3 and G4 groups presented a survival of 57.14% and 42.86%, respectively, while the G1 and G2 mice were all dead 15 days after the challenge. MBP:PLD:CP40 partially protected the mice against C. pseudotuberculosis infection and can be considered a potential new CLA immunogen. Key points: • The fusion protein induced more IgG1 than IgG2a antibodies; • The fusion protein also induced the expression of the TNF and IL-17 cytokines; • Mice inoculated with MBP:PLD:CP40 presented a 57.14% survival.
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spelling Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion proteinCaseous lymphadenitisImmunoinformaticsRecombinant proteinsVaccine developmentAbstract: Caseous lymphadenitis (CLA) is a disease that affects small ruminants, and the best way to prevent its spread on a herd is through immunoprophylaxis. Thus, we aimed to evaluate the MBP:PLD:CP40 fusion protein as a new CLA immunogen. The fusion protein was constructed by combining Corynebacterium pseudotuberculosis PLD and CP40 proteins with maltose-binding protein (MBP) as an intrinsic adjuvant. The antigenicity, allergenic potential, prediction of B epitopes, binding to MHC receptors, and docking on the Toll-Like 2 receptor were evaluated in silico. MBP:PLD:CP40 was expressed and purified. 40 BALB/c were divided into four groups (G1 – control, G2 – Saponin, G3 – MBP:PLD:CP40, and G4 – rPLD + rCP40). Total IgG, IgG1, and IgG2a were quantified, and the expressions of cytokines after splenocyte in vitro stimulation were assessed. Mice were challenged 42 days after the first immunization. The in silico analysis showed that MBP:PLD:CP40 has immunogenic potential, does not have allergic properties, and can dock on the TRL2 receptor. MBP:PLD:CP40 stimulated the production of IgG1 antibodies in a fivefold proportion to IgG2a, and TNF and IL-17 were significantly expressed in response to the antigenic stimuli. When rPLD and rCP40 were used together for immunization, they could induce IFN-γ and IL-12, but with no detectable antibody production. The G3 and G4 groups presented a survival of 57.14% and 42.86%, respectively, while the G1 and G2 mice were all dead 15 days after the challenge. MBP:PLD:CP40 partially protected the mice against C. pseudotuberculosis infection and can be considered a potential new CLA immunogen. Key points: • The fusion protein induced more IgG1 than IgG2a antibodies; • The fusion protein also induced the expression of the TNF and IL-17 cytokines; • Mice inoculated with MBP:PLD:CP40 presented a 57.14% survival.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Laboratory of Immunology and Molecular Biology Universidade Federal da Bahia, Avenida Reitor Miguel Calmon s/n, Bahia StateMultiuser Center for Biomolecular Innovation Universidade Estadual Paulista, São Paulo StateCenter for Technological Development Universidade Federal de Pelotas, Rio Grande do Sul StateLaboratory of Veterinary Pathology School of Veterinary Medicine and Zootechnics Universidade Federal da Bahia, Bahia StateLaboratory of Molecular and Cellular Genetics Universidade Federal de Minas Gerais, Minas Gerais StateMultiuser Center for Biomolecular Innovation Universidade Estadual Paulista, São Paulo StateCAPES: PhD FellowshipCNPq: Research FellowshipCNPq: Techogical Development Fellowship 313350/2019-1Universidade Federal da Bahia (UFBA)Universidade Estadual Paulista (UNESP)Universidade Federal de PelotasUniversidade Federal de Minas Gerais (UFMG)Barral, Thiago DoriaKalil, Mauricio AlcantaraMariutti, Ricardo Barros [UNESP]Arni, Raghuvir Krishnaswamy [UNESP]Gismene, Carolina [UNESP]Sousa, Fernanda SeveroCollares, TiagoSeixas, Fabiana KommlingBorsuk, SibeleEstrela-Lima, AlessandraAzevedo, VascoMeyer, RobertoPortela, Ricardo Wagner2023-07-29T15:14:33Z2023-07-29T15:14:33Z2022-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article8035-8051http://dx.doi.org/10.1007/s00253-022-12279-1Applied Microbiology and Biotechnology, v. 106, n. 24, p. 8035-8051, 2022.1432-06140175-7598http://hdl.handle.net/11449/24938110.1007/s00253-022-12279-12-s2.0-85141964458Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengApplied Microbiology and Biotechnologyinfo:eu-repo/semantics/openAccess2023-07-29T15:14:33Zoai:repositorio.unesp.br:11449/249381Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:45:45.705637Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion protein
title Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion protein
spellingShingle Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion protein
Barral, Thiago Doria
Caseous lymphadenitis
Immunoinformatics
Recombinant proteins
Vaccine development
title_short Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion protein
title_full Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion protein
title_fullStr Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion protein
title_full_unstemmed Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion protein
title_sort Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion protein
author Barral, Thiago Doria
author_facet Barral, Thiago Doria
Kalil, Mauricio Alcantara
Mariutti, Ricardo Barros [UNESP]
Arni, Raghuvir Krishnaswamy [UNESP]
Gismene, Carolina [UNESP]
Sousa, Fernanda Severo
Collares, Tiago
Seixas, Fabiana Kommling
Borsuk, Sibele
Estrela-Lima, Alessandra
Azevedo, Vasco
Meyer, Roberto
Portela, Ricardo Wagner
author_role author
author2 Kalil, Mauricio Alcantara
Mariutti, Ricardo Barros [UNESP]
Arni, Raghuvir Krishnaswamy [UNESP]
Gismene, Carolina [UNESP]
Sousa, Fernanda Severo
Collares, Tiago
Seixas, Fabiana Kommling
Borsuk, Sibele
Estrela-Lima, Alessandra
Azevedo, Vasco
Meyer, Roberto
Portela, Ricardo Wagner
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal da Bahia (UFBA)
Universidade Estadual Paulista (UNESP)
Universidade Federal de Pelotas
Universidade Federal de Minas Gerais (UFMG)
dc.contributor.author.fl_str_mv Barral, Thiago Doria
Kalil, Mauricio Alcantara
Mariutti, Ricardo Barros [UNESP]
Arni, Raghuvir Krishnaswamy [UNESP]
Gismene, Carolina [UNESP]
Sousa, Fernanda Severo
Collares, Tiago
Seixas, Fabiana Kommling
Borsuk, Sibele
Estrela-Lima, Alessandra
Azevedo, Vasco
Meyer, Roberto
Portela, Ricardo Wagner
dc.subject.por.fl_str_mv Caseous lymphadenitis
Immunoinformatics
Recombinant proteins
Vaccine development
topic Caseous lymphadenitis
Immunoinformatics
Recombinant proteins
Vaccine development
description Abstract: Caseous lymphadenitis (CLA) is a disease that affects small ruminants, and the best way to prevent its spread on a herd is through immunoprophylaxis. Thus, we aimed to evaluate the MBP:PLD:CP40 fusion protein as a new CLA immunogen. The fusion protein was constructed by combining Corynebacterium pseudotuberculosis PLD and CP40 proteins with maltose-binding protein (MBP) as an intrinsic adjuvant. The antigenicity, allergenic potential, prediction of B epitopes, binding to MHC receptors, and docking on the Toll-Like 2 receptor were evaluated in silico. MBP:PLD:CP40 was expressed and purified. 40 BALB/c were divided into four groups (G1 – control, G2 – Saponin, G3 – MBP:PLD:CP40, and G4 – rPLD + rCP40). Total IgG, IgG1, and IgG2a were quantified, and the expressions of cytokines after splenocyte in vitro stimulation were assessed. Mice were challenged 42 days after the first immunization. The in silico analysis showed that MBP:PLD:CP40 has immunogenic potential, does not have allergic properties, and can dock on the TRL2 receptor. MBP:PLD:CP40 stimulated the production of IgG1 antibodies in a fivefold proportion to IgG2a, and TNF and IL-17 were significantly expressed in response to the antigenic stimuli. When rPLD and rCP40 were used together for immunization, they could induce IFN-γ and IL-12, but with no detectable antibody production. The G3 and G4 groups presented a survival of 57.14% and 42.86%, respectively, while the G1 and G2 mice were all dead 15 days after the challenge. MBP:PLD:CP40 partially protected the mice against C. pseudotuberculosis infection and can be considered a potential new CLA immunogen. Key points: • The fusion protein induced more IgG1 than IgG2a antibodies; • The fusion protein also induced the expression of the TNF and IL-17 cytokines; • Mice inoculated with MBP:PLD:CP40 presented a 57.14% survival.
publishDate 2022
dc.date.none.fl_str_mv 2022-12-01
2023-07-29T15:14:33Z
2023-07-29T15:14:33Z
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/10.1007/s00253-022-12279-1
Applied Microbiology and Biotechnology, v. 106, n. 24, p. 8035-8051, 2022.
1432-0614
0175-7598
http://hdl.handle.net/11449/249381
10.1007/s00253-022-12279-1
2-s2.0-85141964458
url http://dx.doi.org/10.1007/s00253-022-12279-1
http://hdl.handle.net/11449/249381
identifier_str_mv Applied Microbiology and Biotechnology, v. 106, n. 24, p. 8035-8051, 2022.
1432-0614
0175-7598
10.1007/s00253-022-12279-1
2-s2.0-85141964458
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Applied Microbiology and Biotechnology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 8035-8051
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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