Transcriptional response of bovine monocyte - derived macrophages after the infection with different argentinean mycobacterium bovis isolates

Infection of bovines with Mycobacterium bovis causes important financial hardship in many countries presenting also a risk for humans. M. bovis is known to be adapted to survive and thrive within the intramacrophage environment. In spite of its relevance, at present the information about macrophage...

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Detalles Bibliográficos
Otros Autores: Caimi, Karina, Blanco, Federico Carlos, Soria, Marcelo Abel, Bigi, Fabiana
Formato: Artículo
Lenguaje:Inglés
Materias:
Acceso en línea:http://ri.agro.uba.ar/files/download/articulo/2013caimi.pdf
LINK AL EDITOR
Aporte de:Registro referencial: Solicitar el recurso aquí
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245 1 0 |a Transcriptional response of bovine monocyte - derived macrophages after the infection with different argentinean mycobacterium bovis isolates 
520 |a Infection of bovines with Mycobacterium bovis causes important financial hardship in many countries presenting also a risk for humans. M. bovis is known to be adapted to survive and thrive within the intramacrophage environment. In spite of its relevance, at present the information about macrophage expression patterns is scarce, particularly regarding the bovine host. In this study, transcriptomic analysis was used to detect genes differentially expressed in macrophages derived from peripheral blood mononuclear cells at early stages of infection with two Argentinean strains of M. bovis, a virulent and an attenuated strains. The results showed that the number of differentially expressed genes in the cells infected with the virulent strain [5] was significantly lower than those in the cells infected with the attenuated strain [172]. Several genes were more strongly expressed in infected macrophages. Among them, we detected encoding transcription factors, anthrax toxin receptor, cell division and apoptosis regulator, ankyrin proteins, cytoskeleton proteins, protein of cell differentiation, and regulators of endocytic traffic of membrane. Quantitative real-time PCR of a selected group of differentially expressed genes confirmed the microarrays results. Altogether, the present results contribute to understanding the mechanisms involved in the early interaction of M. bovis with the bovine macrophage. 
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653 0 |a MICROARRAY ANALYSIS 
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653 0 |a REAL TIME POLYMERASE CHAIN REACTION 
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653 0 |a GENETIC TRANSCRIPTION 
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653 0 |a ISOLATION AND PURIFICATION 
653 0 |a METABOLISM 
653 0 |a MICROBIOLOGY 
653 0 |a ANIMALS 
653 0 |a ARGENTINA 
653 0 |a MACROPHAGES 
653 0 |a MONOCYTES 
653 0 |a TRANSCRIPTION, GENETIC 
653 0 |a TUBERCULOSIS, BOVINE 
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700 1 |9 70699  |a Blanco, Federico Carlos 
700 1 |9 49057  |a Soria, Marcelo Abel 
700 1 |9 48059  |a Bigi, Fabiana 
773 |t BioMed Research International  |g vol.2013 (2013), p.1-9 
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900 |a CELL DIFFERENTIATION 
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900 |a MYCOBACTERIUM BOVIS 
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900 |a Infection of bovines with Mycobacterium bovis causes important financial hardship in many countries presenting also a risk for humans. M. bovis is known to be adapted to survive and thrive within the intramacrophage environment. In spite of its relevance, at present the information about macrophage expression patterns is scarce, particularly regarding the bovine host. In this study, transcriptomic analysis was used to detect genes differentially expressed in macrophages derived from peripheral blood mononuclear cells at early stages of infection with two Argentinean strains of M. bovis, a virulent and an attenuated strains. The results showed that the number of differentially expressed genes in the cells infected with the virulent strain [5] was significantly lower than those in the cells infected with the attenuated strain [172]. Several genes were more strongly expressed in infected macrophages. Among them, we detected encoding transcription factors, anthrax toxin receptor, cell division and apoptosis regulator, ankyrin proteins, cytoskeleton proteins, protein of cell differentiation, and regulators of endocytic traffic of membrane. Quantitative real-time PCR of a selected group of differentially expressed genes confirmed the microarrays results. Altogether, the present results contribute to understanding the mechanisms involved in the early interaction of M. bovis with the bovine macrophage. 
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