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...
Otros Autores: | , , , |
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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. | ||
653 | 0 | |a ANKYRIN | |
653 | 0 | |a ANTHRAX TOXIN | |
653 | 0 | |a CYTOSKELETON PROTEIN | |
653 | 0 | |a TRANSCRIPTION FACTOR | |
653 | 0 | |a APOPTOSIS | |
653 | 0 | |a BACTERIAL STRAIN | |
653 | 0 | |a BACTERIUM ISOLATE | |
653 | 0 | |a BOVINE TUBERCULOSIS | |
653 | 0 | |a CELL DIFFERENTIATION | |
653 | 0 | |a CELL DIVISION | |
653 | 0 | |a GENE EXPRESSION | |
653 | 0 | |a MICROARRAY ANALYSIS | |
653 | 0 | |a MYCOBACTERIUM BOVIS | |
653 | 0 | |a NONHUMAN | |
653 | 0 | |a PERIPHERAL BLOOD MONONUCLEAR CELL | |
653 | 0 | |a REAL TIME POLYMERASE CHAIN REACTION | |
653 | 0 | |a TRANSCRIPTOMICS | |
653 | 0 | |a CATTLE | |
653 | 0 | |a GENE EXPRESSION REGULATION | |
653 | 0 | |a GENETIC TRANSCRIPTION | |
653 | 0 | |a IMMUNOLOGY | |
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 | |
700 | 1 | |a Caimi, Karina |9 72637 | |
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 ^tTranscriptional response of bovine monocyte-derived macrophages after the infection with different argentinean mycobacterium bovis isolates | ||
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900 | |a ^aCaimi, K.^tBiotechnology Institute, INTA Castelar, N. Repetto y Los Reseros s/n (1686), 1712 Hurlingham, Buenos Aires, Argentina | ||
900 | |a ^aBlanco, F.^tBiotechnology Institute, INTA Castelar, N. Repetto y Los Reseros s/n (1686), 1712 Hurlingham, Buenos Aires, Argentina | ||
900 | |a ^aSoria, M.^tCollege of Agronomy, University of Buenos Aires, INBA-CONICET, Av. San Martín 4453, C1417DSE Buenos Aires, Argentina | ||
900 | |a ^aBigi, F.^tBiotechnology Institute, INTA Castelar, N. Repetto y Los Reseros s/n (1686), 1712 Hurlingham, Buenos Aires, Argentina | ||
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900 | |a Vol. 2013 | ||
900 | |a ANKYRIN | ||
900 | |a ANTHRAX TOXIN | ||
900 | |a CYTOSKELETON PROTEIN | ||
900 | |a TRANSCRIPTION FACTOR | ||
900 | |a APOPTOSIS | ||
900 | |a BACTERIAL STRAIN | ||
900 | |a BACTERIUM ISOLATE | ||
900 | |a BOVINE TUBERCULOSIS | ||
900 | |a CELL DIFFERENTIATION | ||
900 | |a CELL DIVISION | ||
900 | |a GENE EXPRESSION | ||
900 | |a MICROARRAY ANALYSIS | ||
900 | |a MYCOBACTERIUM BOVIS | ||
900 | |a NONHUMAN | ||
900 | |a PERIPHERAL BLOOD MONONUCLEAR CELL | ||
900 | |a REAL TIME POLYMERASE CHAIN REACTION | ||
900 | |a TRANSCRIPTOMICS | ||
900 | |a CATTLE | ||
900 | |a GENE EXPRESSION REGULATION | ||
900 | |a GENETIC TRANSCRIPTION | ||
900 | |a IMMUNOLOGY | ||
900 | |a ISOLATION AND PURIFICATION | ||
900 | |a METABOLISM | ||
900 | |a MICROBIOLOGY | ||
900 | |a ANIMALS | ||
900 | |a ARGENTINA | ||
900 | |a MACROPHAGES | ||
900 | |a MONOCYTES | ||
900 | |a TRANSCRIPTION, GENETIC | ||
900 | |a TUBERCULOSIS, BOVINE | ||
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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