Serological diagnosis of visceral leishmaniasis by an enzyme immunoassay using protein A in naturally infected dogs
Autor(a) principal: | |
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Data de Publicação: | 2005 |
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=S0100-736X2005000400005 |
Resumo: | A rapid indirect enzyme-linked immunosorbent assay (ELISA) was developed for measuring antibodies against Leishmania chagasi using total antigen from lysed promastigotes. Fifty symptomatic mixed breed dogs from a region of high incidence of visceral leishmaniasis in Brazil were examined. The results showed that in the positive animals, diagnosed by cytological examination, the ELISA using protein A assay system (mean optical density ± SD / 2.078 ± 0.631) detected more antibodies than the anti-IgG assay (mean optical density ± SD / 1.008 ± 0.437), while in the negative animals, the results by both systems were similar. These results suggest that the ELISA assay using protein A peroxidase conjugated could be useful to detect early infected animals in endemic areas, and thus help to control the spread of the infection. |
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Serological diagnosis of visceral leishmaniasis by an enzyme immunoassay using protein A in naturally infected dogsLeishmania chagasivisceral leishmaniasisprotein AdogsA rapid indirect enzyme-linked immunosorbent assay (ELISA) was developed for measuring antibodies against Leishmania chagasi using total antigen from lysed promastigotes. Fifty symptomatic mixed breed dogs from a region of high incidence of visceral leishmaniasis in Brazil were examined. The results showed that in the positive animals, diagnosed by cytological examination, the ELISA using protein A assay system (mean optical density ± SD / 2.078 ± 0.631) detected more antibodies than the anti-IgG assay (mean optical density ± SD / 1.008 ± 0.437), while in the negative animals, the results by both systems were similar. These results suggest that the ELISA assay using protein A peroxidase conjugated could be useful to detect early infected animals in endemic areas, and thus help to control the spread of the infection.Colégio Brasileiro de Patologia Animal - CBPA2005-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2005000400005Pesquisa Veterinária Brasileira v.25 n.4 2005reponame:Pesquisa Veterinária Brasileira (Online)instname:Colégio Brasileiro de Patologia Animal (CBPA)instacron:EMBRAPA10.1590/S0100-736X2005000400005info:eu-repo/semantics/openAccessLima,Valéria Marçal Felix deBiazzono,LucianeSilva,Ana CláudiaCorrea,Ana Paula Ferreira LopesLuvizotto,Maria Cecília Ruieng2006-02-01T00:00:00Zoai:scielo:S0100-736X2005000400005Revistahttp://www.pvb.com.br/https://old.scielo.br/oai/scielo-oai.phpcolegio@cbpa.org.br||pvb@pvb.com.br0100-736X1678-5150opendoar:2006-02-01T00:00Pesquisa Veterinária Brasileira (Online) - Colégio Brasileiro de Patologia Animal (CBPA)false |
dc.title.none.fl_str_mv |
Serological diagnosis of visceral leishmaniasis by an enzyme immunoassay using protein A in naturally infected dogs |
title |
Serological diagnosis of visceral leishmaniasis by an enzyme immunoassay using protein A in naturally infected dogs |
spellingShingle |
Serological diagnosis of visceral leishmaniasis by an enzyme immunoassay using protein A in naturally infected dogs Lima,Valéria Marçal Felix de Leishmania chagasi visceral leishmaniasis protein A dogs |
title_short |
Serological diagnosis of visceral leishmaniasis by an enzyme immunoassay using protein A in naturally infected dogs |
title_full |
Serological diagnosis of visceral leishmaniasis by an enzyme immunoassay using protein A in naturally infected dogs |
title_fullStr |
Serological diagnosis of visceral leishmaniasis by an enzyme immunoassay using protein A in naturally infected dogs |
title_full_unstemmed |
Serological diagnosis of visceral leishmaniasis by an enzyme immunoassay using protein A in naturally infected dogs |
title_sort |
Serological diagnosis of visceral leishmaniasis by an enzyme immunoassay using protein A in naturally infected dogs |
author |
Lima,Valéria Marçal Felix de |
author_facet |
Lima,Valéria Marçal Felix de Biazzono,Luciane Silva,Ana Cláudia Correa,Ana Paula Ferreira Lopes Luvizotto,Maria Cecília Rui |
author_role |
author |
author2 |
Biazzono,Luciane Silva,Ana Cláudia Correa,Ana Paula Ferreira Lopes Luvizotto,Maria Cecília Rui |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Lima,Valéria Marçal Felix de Biazzono,Luciane Silva,Ana Cláudia Correa,Ana Paula Ferreira Lopes Luvizotto,Maria Cecília Rui |
dc.subject.por.fl_str_mv |
Leishmania chagasi visceral leishmaniasis protein A dogs |
topic |
Leishmania chagasi visceral leishmaniasis protein A dogs |
description |
A rapid indirect enzyme-linked immunosorbent assay (ELISA) was developed for measuring antibodies against Leishmania chagasi using total antigen from lysed promastigotes. Fifty symptomatic mixed breed dogs from a region of high incidence of visceral leishmaniasis in Brazil were examined. The results showed that in the positive animals, diagnosed by cytological examination, the ELISA using protein A assay system (mean optical density ± SD / 2.078 ± 0.631) detected more antibodies than the anti-IgG assay (mean optical density ± SD / 1.008 ± 0.437), while in the negative animals, the results by both systems were similar. These results suggest that the ELISA assay using protein A peroxidase conjugated could be useful to detect early infected animals in endemic areas, and thus help to control the spread of the infection. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-12-01 |
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=S0100-736X2005000400005 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2005000400005 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0100-736X2005000400005 |
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.25 n.4 2005 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_ |
1754122228238123008 |