Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles.

Detalhes bibliográficos
Autor(a) principal: BIGI, M.
Data de Publicação: 2019
Outros Autores: VAZQUEZ, C. L., CASTELÃO, A. B. C., GARCÍA, E. A., CATALDI, A. A., JACKSON, M., MAcNEIL, M., SORIA, M., ZUMÁRRAGA, M. J., MATIAS, C., GAGO, G., BLANCO, F. C., NISHIBEF, C., ALMEIDA, N. F., ARAUJO, F. R., BIGI, F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
Texto Completo: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1117921
Resumo: Mycobacterium bovis (M. bovis) is the causative agent of bovine tuberculosis, a chronic infectious disease that can affect cattle, other domesticated species, wild animals and humans. This disease produces important economic losses worldwide. Two M. bovis strains (04-303 and 534) have been isolated in Argentina. Whereas the 04-303 strain was isolated from a wild boar, the 534 strain was obtained from cattle. In a previous study, six weeks after infection, the 04-303 strain induced 100% mortality in mice. By contrast, mice infected with the 534 strain survived, with limited tissue damage, after four months. In this study we compared all predictive proteins encoded in both M. bovis genomes. The comparative analysis revealed 141 polymorphic proteins between both strains. From these proteins, nine virulence proteins showed polymorphisms in 04-303, whereas five did it in the 534 strain. Remarkably, both strains contained a high level of polymorphism in proteins related to phthiocerol dimycocerosate (PDIM) synthesis or transport. Further experimental evidence indicated that only mutations in the 534 strain have an impact on PDIM synthesis. The observed reduction in PDIM content in the 534 strain, together with its low capacity to induce phagosome arrest, may be associated with the reported deficiency of this strain to replicate and survive inside bovine macrophages. The findings of this study could contribute to a better understanding of pathogenicity and virulence aspects of M. bovis, which is essential for further studies aiming at developing new vaccines and diagnostic techniques for bovines.
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spelling Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles.MutationsGeneMycobacterium bovis BCGGenomeVirulenceMycobacterium bovis (M. bovis) is the causative agent of bovine tuberculosis, a chronic infectious disease that can affect cattle, other domesticated species, wild animals and humans. This disease produces important economic losses worldwide. Two M. bovis strains (04-303 and 534) have been isolated in Argentina. Whereas the 04-303 strain was isolated from a wild boar, the 534 strain was obtained from cattle. In a previous study, six weeks after infection, the 04-303 strain induced 100% mortality in mice. By contrast, mice infected with the 534 strain survived, with limited tissue damage, after four months. In this study we compared all predictive proteins encoded in both M. bovis genomes. The comparative analysis revealed 141 polymorphic proteins between both strains. From these proteins, nine virulence proteins showed polymorphisms in 04-303, whereas five did it in the 534 strain. Remarkably, both strains contained a high level of polymorphism in proteins related to phthiocerol dimycocerosate (PDIM) synthesis or transport. Further experimental evidence indicated that only mutations in the 534 strain have an impact on PDIM synthesis. The observed reduction in PDIM content in the 534 strain, together with its low capacity to induce phagosome arrest, may be associated with the reported deficiency of this strain to replicate and survive inside bovine macrophages. The findings of this study could contribute to a better understanding of pathogenicity and virulence aspects of M. bovis, which is essential for further studies aiming at developing new vaccines and diagnostic techniques for bovines.Mercedes Bigi, Universidad de Buenos Aires, Facultad de Agronomía, Cátedra de Microbiología Agrícola, INBA-CONICET; Cristina Lourdes Vazquez, Universidad de Buenos Aires, Facultad de Agronomía, Cátedra de Microbiología Agrícola, INBA-CONICET; Ana Beatriz C Castelão, Universidad de Buenos Aires, Facultad de Agronomía, Cátedra de Microbiología Agrícola, INBA-CONICET; Elizabeth Andrea García, Instituto de Biotecnología, IABIMO, CICVyA/INTA; Angel A Cataldi, Instituto de Biotecnología, IABIMO, CICVyA/INTA; Mary Jackson, Colorado State University, Dept. of Microbiology, Immunology and Pathology; Michael McNeil, Colorado State University, Dept. of Microbiology, Immunology and Pathology; Marcelo Soria, Universidad de Buenos Aires, Facultad de Agronomía, Cátedra de Microbiología Agrícola, INBA-CONICET; Martín J Zumárraga, Instituto de Biotecnología, IABIMO, CICVyA/INTA; Matias Cabruja, Laboratory of Physiology and Genetics of Actinomycetes, Instituto de Biología Molecular y Celular de Rosario (IBR-CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario; Gabriela Gago, Laboratory of Physiology and Genetics of Actinomycetes, Instituto de Biología Molecular y Celular de Rosario (IBR-CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario; Federico C Blanco, Instituto de Biotecnología, IABIMO, CICVyA/INTA; Christiane Nishibef, Universidade Federal de Mato Grosso do Sul - UFMS/Faculdade de Computação; Nalvo F Almeida, Universidade Federal de Mato Grosso do Sul - UFMS/Faculdade de Computação; FLABIO RIBEIRO DE ARAUJO, CNPGC; Fabiana Bigi, Instituto de Biotecnología, IABIMO, CICVyA/INTA.BIGI, M.VAZQUEZ, C. L.CASTELÃO, A. B. C.GARCÍA, E. A.CATALDI, A. A.JACKSON, M.MAcNEIL, M.SORIA, M.ZUMÁRRAGA, M. J.MATIAS, C.GAGO, G.BLANCO, F. C.NISHIBEF, C.ALMEIDA, N. F.ARAUJO, F. R.BIGI, F.2019-12-31T00:37:05Z2019-12-31T00:37:05Z2019-12-3020192019-12-31T00:37:05Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleVeterinary Microbiology, v. 239, 2019.http://www.alice.cnptia.embrapa.br/alice/handle/doc/1117921enginfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)instacron:EMBRAPA2019-12-31T00:37:12Zoai:www.alice.cnptia.embrapa.br:doc/1117921Repositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestopendoar:21542019-12-31T00:37:12falseRepositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestcg-riaa@embrapa.bropendoar:21542019-12-31T00:37:12Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)false
dc.title.none.fl_str_mv Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles.
title Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles.
spellingShingle Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles.
BIGI, M.
Mutations
Gene
Mycobacterium bovis BCG
Genome
Virulence
title_short Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles.
title_full Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles.
title_fullStr Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles.
title_full_unstemmed Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles.
title_sort Analysing nonsynonymous mutations between two Mycobacterium bovis strains with contrasting pathogenic profiles.
author BIGI, M.
author_facet BIGI, M.
VAZQUEZ, C. L.
CASTELÃO, A. B. C.
GARCÍA, E. A.
CATALDI, A. A.
JACKSON, M.
MAcNEIL, M.
SORIA, M.
ZUMÁRRAGA, M. J.
MATIAS, C.
GAGO, G.
BLANCO, F. C.
NISHIBEF, C.
ALMEIDA, N. F.
ARAUJO, F. R.
BIGI, F.
author_role author
author2 VAZQUEZ, C. L.
CASTELÃO, A. B. C.
GARCÍA, E. A.
CATALDI, A. A.
JACKSON, M.
MAcNEIL, M.
SORIA, M.
ZUMÁRRAGA, M. J.
MATIAS, C.
GAGO, G.
BLANCO, F. C.
NISHIBEF, C.
ALMEIDA, N. F.
ARAUJO, F. R.
BIGI, F.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Mercedes Bigi, Universidad de Buenos Aires, Facultad de Agronomía, Cátedra de Microbiología Agrícola, INBA-CONICET; Cristina Lourdes Vazquez, Universidad de Buenos Aires, Facultad de Agronomía, Cátedra de Microbiología Agrícola, INBA-CONICET; Ana Beatriz C Castelão, Universidad de Buenos Aires, Facultad de Agronomía, Cátedra de Microbiología Agrícola, INBA-CONICET; Elizabeth Andrea García, Instituto de Biotecnología, IABIMO, CICVyA/INTA; Angel A Cataldi, Instituto de Biotecnología, IABIMO, CICVyA/INTA; Mary Jackson, Colorado State University, Dept. of Microbiology, Immunology and Pathology; Michael McNeil, Colorado State University, Dept. of Microbiology, Immunology and Pathology; Marcelo Soria, Universidad de Buenos Aires, Facultad de Agronomía, Cátedra de Microbiología Agrícola, INBA-CONICET; Martín J Zumárraga, Instituto de Biotecnología, IABIMO, CICVyA/INTA; Matias Cabruja, Laboratory of Physiology and Genetics of Actinomycetes, Instituto de Biología Molecular y Celular de Rosario (IBR-CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario; Gabriela Gago, Laboratory of Physiology and Genetics of Actinomycetes, Instituto de Biología Molecular y Celular de Rosario (IBR-CONICET), Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario; Federico C Blanco, Instituto de Biotecnología, IABIMO, CICVyA/INTA; Christiane Nishibef, Universidade Federal de Mato Grosso do Sul - UFMS/Faculdade de Computação; Nalvo F Almeida, Universidade Federal de Mato Grosso do Sul - UFMS/Faculdade de Computação; FLABIO RIBEIRO DE ARAUJO, CNPGC; Fabiana Bigi, Instituto de Biotecnología, IABIMO, CICVyA/INTA.
dc.contributor.author.fl_str_mv BIGI, M.
VAZQUEZ, C. L.
CASTELÃO, A. B. C.
GARCÍA, E. A.
CATALDI, A. A.
JACKSON, M.
MAcNEIL, M.
SORIA, M.
ZUMÁRRAGA, M. J.
MATIAS, C.
GAGO, G.
BLANCO, F. C.
NISHIBEF, C.
ALMEIDA, N. F.
ARAUJO, F. R.
BIGI, F.
dc.subject.por.fl_str_mv Mutations
Gene
Mycobacterium bovis BCG
Genome
Virulence
topic Mutations
Gene
Mycobacterium bovis BCG
Genome
Virulence
description Mycobacterium bovis (M. bovis) is the causative agent of bovine tuberculosis, a chronic infectious disease that can affect cattle, other domesticated species, wild animals and humans. This disease produces important economic losses worldwide. Two M. bovis strains (04-303 and 534) have been isolated in Argentina. Whereas the 04-303 strain was isolated from a wild boar, the 534 strain was obtained from cattle. In a previous study, six weeks after infection, the 04-303 strain induced 100% mortality in mice. By contrast, mice infected with the 534 strain survived, with limited tissue damage, after four months. In this study we compared all predictive proteins encoded in both M. bovis genomes. The comparative analysis revealed 141 polymorphic proteins between both strains. From these proteins, nine virulence proteins showed polymorphisms in 04-303, whereas five did it in the 534 strain. Remarkably, both strains contained a high level of polymorphism in proteins related to phthiocerol dimycocerosate (PDIM) synthesis or transport. Further experimental evidence indicated that only mutations in the 534 strain have an impact on PDIM synthesis. The observed reduction in PDIM content in the 534 strain, together with its low capacity to induce phagosome arrest, may be associated with the reported deficiency of this strain to replicate and survive inside bovine macrophages. The findings of this study could contribute to a better understanding of pathogenicity and virulence aspects of M. bovis, which is essential for further studies aiming at developing new vaccines and diagnostic techniques for bovines.
publishDate 2019
dc.date.none.fl_str_mv 2019-12-31T00:37:05Z
2019-12-31T00:37:05Z
2019-12-30
2019
2019-12-31T00:37:05Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv Veterinary Microbiology, v. 239, 2019.
http://www.alice.cnptia.embrapa.br/alice/handle/doc/1117921
identifier_str_mv Veterinary Microbiology, v. 239, 2019.
url http://www.alice.cnptia.embrapa.br/alice/handle/doc/1117921
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv reponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
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instname_str Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
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repository.name.fl_str_mv Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
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