Immune response to Mycobacterium bovis-an5 infection in genetically selected mice (selection IV-A)

Detalhes bibliográficos
Autor(a) principal: Cavalheiro, Juliana Semim [UNESP]
Data de Publicação: 2007
Outros Autores: Trindade, B. C. [UNESP], Balderramas, H. A. [UNESP], Haanwinckel, M. C. [UNESP], Pinto, J. G G [UNESP], Oliveira, S. L. [UNESP], Paes, A. C. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S1678-91992007000300006
http://hdl.handle.net/11449/69932
Resumo: Mice genetically selected for high (H) and low (L) antibody production (Selection IV-A) were used as murine experimental model. The aim of the present work was to evaluate the macrophagic activity and to characterize the immune response in Mycobacterium bovis-AN5 infected mice (3×10 7 bacteria). The response profile previously observed in such strains was not similar to that obtained during M. bovis infection; however, it corroborated works carried out using Selection I, which is very similar to Selection IV-A regarding infection by M. tuberculosis and Bacillus Calmette-Guérin (BCG). Considering bacterial recovery, LIV-A mice showed higher control of the infectious process in the lungs than in the spleen, whereas HIV-A mice presented more resistance in the spleen. With respect to macrophagic activity, hydrogen peroxide (H2O 2) was probably not involved in the infection control since there was an inhibition in the production of this metabolite. Nitric oxide (NO) and TNF-α production seemed to be important in the control of bacterial replication and varied according to the strain, period and organ. Evaluation of the antibody production indicated that the multi-specific effect commonly observed in these strains was not the same in the response to M. bovis. Antibody concentrations were higher in LIV-A than in HIV-A mice at the beginning of the infection, being similar afterwards. Such data were compared with delayed-type hypersensitivity (DTH), which was more intense in HIV-A than in LIV-A mice, indicating that antibody production is independent of the capability to trigger DTH reactions and that cellular and humoral responses to M. bovis antigens show a polygenic control and an independent quantitative genetic regulation. Differences were observed among organs and metabolites, suggesting that different mechanisms play an important role in this infection in natural heterogeneous populations, indicating that NO, TNF-α and Th1 cytokines are involved in the infection control.
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spelling Immune response to Mycobacterium bovis-an5 infection in genetically selected mice (selection IV-A)Biozzi miceImmune responseMycobacterium bovisBacteria (microorganisms)Human immunodeficiency virusMurinaeMusMycobacterium bovis BCGMycobacterium tuberculosisMice genetically selected for high (H) and low (L) antibody production (Selection IV-A) were used as murine experimental model. The aim of the present work was to evaluate the macrophagic activity and to characterize the immune response in Mycobacterium bovis-AN5 infected mice (3×10 7 bacteria). The response profile previously observed in such strains was not similar to that obtained during M. bovis infection; however, it corroborated works carried out using Selection I, which is very similar to Selection IV-A regarding infection by M. tuberculosis and Bacillus Calmette-Guérin (BCG). Considering bacterial recovery, LIV-A mice showed higher control of the infectious process in the lungs than in the spleen, whereas HIV-A mice presented more resistance in the spleen. With respect to macrophagic activity, hydrogen peroxide (H2O 2) was probably not involved in the infection control since there was an inhibition in the production of this metabolite. Nitric oxide (NO) and TNF-α production seemed to be important in the control of bacterial replication and varied according to the strain, period and organ. Evaluation of the antibody production indicated that the multi-specific effect commonly observed in these strains was not the same in the response to M. bovis. Antibody concentrations were higher in LIV-A than in HIV-A mice at the beginning of the infection, being similar afterwards. Such data were compared with delayed-type hypersensitivity (DTH), which was more intense in HIV-A than in LIV-A mice, indicating that antibody production is independent of the capability to trigger DTH reactions and that cellular and humoral responses to M. bovis antigens show a polygenic control and an independent quantitative genetic regulation. Differences were observed among organs and metabolites, suggesting that different mechanisms play an important role in this infection in natural heterogeneous populations, indicating that NO, TNF-α and Th1 cytokines are involved in the infection control.Department of Animal Health School of Veterinary Medicine and Animal Husbandry São Paulo State University - UNESP, Botucatu, São Paulo StateBotucatu Institute of Biosciences UNESP, Botucatu, São Paulo StateDepartamento de Microbiologia e Imunologia Instituto de Biociências de Botucatu UNESP, 18.618-000, Rubiao Junior, Botucatu, SPDepartment of Animal Health School of Veterinary Medicine and Animal Husbandry São Paulo State University - UNESP, Botucatu, São Paulo StateBotucatu Institute of Biosciences UNESP, Botucatu, São Paulo StateDepartamento de Microbiologia e Imunologia Instituto de Biociências de Botucatu UNESP, 18.618-000, Rubiao Junior, Botucatu, SPUniversidade Estadual Paulista (Unesp)Cavalheiro, Juliana Semim [UNESP]Trindade, B. C. [UNESP]Balderramas, H. A. [UNESP]Haanwinckel, M. C. [UNESP]Pinto, J. G G [UNESP]Oliveira, S. L. [UNESP]Paes, A. C. [UNESP]2014-05-27T11:22:37Z2014-05-27T11:22:37Z2007-10-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article620-639application/pdfhttp://dx.doi.org/10.1590/S1678-91992007000300006Journal of Venomous Animals and Toxins Including Tropical Diseases, v. 13, n. 3, p. 620-639, 2007.1678-9199http://hdl.handle.net/11449/6993210.1590/S1678-91992007000300006S1678-91992007000300006WOS:0002496942000062-s2.0-348488783952-s2.0-34848878395.pdf8418958338241095Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Venomous Animals and Toxins Including Tropical Diseases1.7820,573info:eu-repo/semantics/openAccess2023-10-04T06:02:59Zoai:repositorio.unesp.br:11449/69932Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-04T06:02:59Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Immune response to Mycobacterium bovis-an5 infection in genetically selected mice (selection IV-A)
title Immune response to Mycobacterium bovis-an5 infection in genetically selected mice (selection IV-A)
spellingShingle Immune response to Mycobacterium bovis-an5 infection in genetically selected mice (selection IV-A)
Cavalheiro, Juliana Semim [UNESP]
Biozzi mice
Immune response
Mycobacterium bovis
Bacteria (microorganisms)
Human immunodeficiency virus
Murinae
Mus
Mycobacterium bovis BCG
Mycobacterium tuberculosis
title_short Immune response to Mycobacterium bovis-an5 infection in genetically selected mice (selection IV-A)
title_full Immune response to Mycobacterium bovis-an5 infection in genetically selected mice (selection IV-A)
title_fullStr Immune response to Mycobacterium bovis-an5 infection in genetically selected mice (selection IV-A)
title_full_unstemmed Immune response to Mycobacterium bovis-an5 infection in genetically selected mice (selection IV-A)
title_sort Immune response to Mycobacterium bovis-an5 infection in genetically selected mice (selection IV-A)
author Cavalheiro, Juliana Semim [UNESP]
author_facet Cavalheiro, Juliana Semim [UNESP]
Trindade, B. C. [UNESP]
Balderramas, H. A. [UNESP]
Haanwinckel, M. C. [UNESP]
Pinto, J. G G [UNESP]
Oliveira, S. L. [UNESP]
Paes, A. C. [UNESP]
author_role author
author2 Trindade, B. C. [UNESP]
Balderramas, H. A. [UNESP]
Haanwinckel, M. C. [UNESP]
Pinto, J. G G [UNESP]
Oliveira, S. L. [UNESP]
Paes, A. C. [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Cavalheiro, Juliana Semim [UNESP]
Trindade, B. C. [UNESP]
Balderramas, H. A. [UNESP]
Haanwinckel, M. C. [UNESP]
Pinto, J. G G [UNESP]
Oliveira, S. L. [UNESP]
Paes, A. C. [UNESP]
dc.subject.por.fl_str_mv Biozzi mice
Immune response
Mycobacterium bovis
Bacteria (microorganisms)
Human immunodeficiency virus
Murinae
Mus
Mycobacterium bovis BCG
Mycobacterium tuberculosis
topic Biozzi mice
Immune response
Mycobacterium bovis
Bacteria (microorganisms)
Human immunodeficiency virus
Murinae
Mus
Mycobacterium bovis BCG
Mycobacterium tuberculosis
description Mice genetically selected for high (H) and low (L) antibody production (Selection IV-A) were used as murine experimental model. The aim of the present work was to evaluate the macrophagic activity and to characterize the immune response in Mycobacterium bovis-AN5 infected mice (3×10 7 bacteria). The response profile previously observed in such strains was not similar to that obtained during M. bovis infection; however, it corroborated works carried out using Selection I, which is very similar to Selection IV-A regarding infection by M. tuberculosis and Bacillus Calmette-Guérin (BCG). Considering bacterial recovery, LIV-A mice showed higher control of the infectious process in the lungs than in the spleen, whereas HIV-A mice presented more resistance in the spleen. With respect to macrophagic activity, hydrogen peroxide (H2O 2) was probably not involved in the infection control since there was an inhibition in the production of this metabolite. Nitric oxide (NO) and TNF-α production seemed to be important in the control of bacterial replication and varied according to the strain, period and organ. Evaluation of the antibody production indicated that the multi-specific effect commonly observed in these strains was not the same in the response to M. bovis. Antibody concentrations were higher in LIV-A than in HIV-A mice at the beginning of the infection, being similar afterwards. Such data were compared with delayed-type hypersensitivity (DTH), which was more intense in HIV-A than in LIV-A mice, indicating that antibody production is independent of the capability to trigger DTH reactions and that cellular and humoral responses to M. bovis antigens show a polygenic control and an independent quantitative genetic regulation. Differences were observed among organs and metabolites, suggesting that different mechanisms play an important role in this infection in natural heterogeneous populations, indicating that NO, TNF-α and Th1 cytokines are involved in the infection control.
publishDate 2007
dc.date.none.fl_str_mv 2007-10-08
2014-05-27T11:22:37Z
2014-05-27T11:22:37Z
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/10.1590/S1678-91992007000300006
Journal of Venomous Animals and Toxins Including Tropical Diseases, v. 13, n. 3, p. 620-639, 2007.
1678-9199
http://hdl.handle.net/11449/69932
10.1590/S1678-91992007000300006
S1678-91992007000300006
WOS:000249694200006
2-s2.0-34848878395
2-s2.0-34848878395.pdf
8418958338241095
url http://dx.doi.org/10.1590/S1678-91992007000300006
http://hdl.handle.net/11449/69932
identifier_str_mv Journal of Venomous Animals and Toxins Including Tropical Diseases, v. 13, n. 3, p. 620-639, 2007.
1678-9199
10.1590/S1678-91992007000300006
S1678-91992007000300006
WOS:000249694200006
2-s2.0-34848878395
2-s2.0-34848878395.pdf
8418958338241095
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Venomous Animals and Toxins Including Tropical Diseases
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0,573
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 620-639
application/pdf
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)
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