Immunoprophylactic properties of the Corynebacterium pseudotuberculosis-derived MBP:PLD:CP40 fusion protein
Autor(a) principal: | |
---|---|
Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , , , , |
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. |
id |
UNSP_37757b620d962bb72a4eaf22fb3e8758 |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/249381 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
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 |
|
_version_ |
1808129115138555904 |