Clostridium perfringens α and β recombinant toxoids in equine immunization
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Pesquisa Veterinária Brasileira (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2020001000776 |
Resumo: | ABSTRACT: Clostridium perfringens is considered one of the main causative agents of superacute enterocolitis, usually fatal in the equine species, due to the action of the β toxin, and is responsible for causing severe myonecrosis, by the action of the α toxin. The great importance of this agent in the equine economy is due to high mortality and lack of vaccines, which are the main form of prevention, which guarantee the immunization of this animal species. The aim of this study was to evaluate three different concentrations (100, 200 and 400μg) of C. perfringens α and β recombinant toxoids in equine immunization and to compare with a group vaccinated with a commercial toxoid. The commercial vaccine was not able to stimulate an immune response and the recombinant vaccine was able to induce satisfactory humoral immune response in vaccinated horses, proving to be an alternative prophylactic for C. perfringens infection. |
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Clostridium perfringens α and β recombinant toxoids in equine immunizationClostridium perfringensalpha toxinbeta toxinrecombinant toxoidsequineimmunizationvaccinationmyonecrosisenterocolitishorsesABSTRACT: Clostridium perfringens is considered one of the main causative agents of superacute enterocolitis, usually fatal in the equine species, due to the action of the β toxin, and is responsible for causing severe myonecrosis, by the action of the α toxin. The great importance of this agent in the equine economy is due to high mortality and lack of vaccines, which are the main form of prevention, which guarantee the immunization of this animal species. The aim of this study was to evaluate three different concentrations (100, 200 and 400μg) of C. perfringens α and β recombinant toxoids in equine immunization and to compare with a group vaccinated with a commercial toxoid. The commercial vaccine was not able to stimulate an immune response and the recombinant vaccine was able to induce satisfactory humoral immune response in vaccinated horses, proving to be an alternative prophylactic for C. perfringens infection.Colégio Brasileiro de Patologia Animal - CBPA2020-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2020001000776Pesquisa Veterinária Brasileira v.40 n.10 2020reponame:Pesquisa Veterinária Brasileira (Online)instname:Colégio Brasileiro de Patologia Animal (CBPA)instacron:EMBRAPA10.1590/1678-5150-pvb-6677info:eu-repo/semantics/openAccessFreitas,Nayra F.Q.R.Barbosa,José D.Otaka,Denis Y.Ferreira,Marcos Roberto A.Rodrigues,Rafael R.Moreira Jr,ClóvisConceição,Fabricio R.Salvarani,Felipe M.eng2020-12-10T00:00:00Zoai:scielo:S0100-736X2020001000776Revistahttp://www.pvb.com.br/https://old.scielo.br/oai/scielo-oai.phpcolegio@cbpa.org.br||pvb@pvb.com.br0100-736X1678-5150opendoar:2020-12-10T00:00Pesquisa Veterinária Brasileira (Online) - Colégio Brasileiro de Patologia Animal (CBPA)false |
dc.title.none.fl_str_mv |
Clostridium perfringens α and β recombinant toxoids in equine immunization |
title |
Clostridium perfringens α and β recombinant toxoids in equine immunization |
spellingShingle |
Clostridium perfringens α and β recombinant toxoids in equine immunization Freitas,Nayra F.Q.R. Clostridium perfringens alpha toxin beta toxin recombinant toxoids equine immunization vaccination myonecrosis enterocolitis horses |
title_short |
Clostridium perfringens α and β recombinant toxoids in equine immunization |
title_full |
Clostridium perfringens α and β recombinant toxoids in equine immunization |
title_fullStr |
Clostridium perfringens α and β recombinant toxoids in equine immunization |
title_full_unstemmed |
Clostridium perfringens α and β recombinant toxoids in equine immunization |
title_sort |
Clostridium perfringens α and β recombinant toxoids in equine immunization |
author |
Freitas,Nayra F.Q.R. |
author_facet |
Freitas,Nayra F.Q.R. Barbosa,José D. Otaka,Denis Y. Ferreira,Marcos Roberto A. Rodrigues,Rafael R. Moreira Jr,Clóvis Conceição,Fabricio R. Salvarani,Felipe M. |
author_role |
author |
author2 |
Barbosa,José D. Otaka,Denis Y. Ferreira,Marcos Roberto A. Rodrigues,Rafael R. Moreira Jr,Clóvis Conceição,Fabricio R. Salvarani,Felipe M. |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Freitas,Nayra F.Q.R. Barbosa,José D. Otaka,Denis Y. Ferreira,Marcos Roberto A. Rodrigues,Rafael R. Moreira Jr,Clóvis Conceição,Fabricio R. Salvarani,Felipe M. |
dc.subject.por.fl_str_mv |
Clostridium perfringens alpha toxin beta toxin recombinant toxoids equine immunization vaccination myonecrosis enterocolitis horses |
topic |
Clostridium perfringens alpha toxin beta toxin recombinant toxoids equine immunization vaccination myonecrosis enterocolitis horses |
description |
ABSTRACT: Clostridium perfringens is considered one of the main causative agents of superacute enterocolitis, usually fatal in the equine species, due to the action of the β toxin, and is responsible for causing severe myonecrosis, by the action of the α toxin. The great importance of this agent in the equine economy is due to high mortality and lack of vaccines, which are the main form of prevention, which guarantee the immunization of this animal species. The aim of this study was to evaluate three different concentrations (100, 200 and 400μg) of C. perfringens α and β recombinant toxoids in equine immunization and to compare with a group vaccinated with a commercial toxoid. The commercial vaccine was not able to stimulate an immune response and the recombinant vaccine was able to induce satisfactory humoral immune response in vaccinated horses, proving to be an alternative prophylactic for C. perfringens infection. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-10-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2020001000776 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2020001000776 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1678-5150-pvb-6677 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Colégio Brasileiro de Patologia Animal - CBPA |
publisher.none.fl_str_mv |
Colégio Brasileiro de Patologia Animal - CBPA |
dc.source.none.fl_str_mv |
Pesquisa Veterinária Brasileira v.40 n.10 2020 reponame:Pesquisa Veterinária Brasileira (Online) instname:Colégio Brasileiro de Patologia Animal (CBPA) instacron:EMBRAPA |
instname_str |
Colégio Brasileiro de Patologia Animal (CBPA) |
instacron_str |
EMBRAPA |
institution |
EMBRAPA |
reponame_str |
Pesquisa Veterinária Brasileira (Online) |
collection |
Pesquisa Veterinária Brasileira (Online) |
repository.name.fl_str_mv |
Pesquisa Veterinária Brasileira (Online) - Colégio Brasileiro de Patologia Animal (CBPA) |
repository.mail.fl_str_mv |
colegio@cbpa.org.br||pvb@pvb.com.br |
_version_ |
1754122240467664896 |