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1.
Vet Pathol ; 47(3): 547-52, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-20472807

RESUMO

Cowpox virus infections have been described in various domestic and exotic animal species. This report is the first on an outbreak of fatal generalized cowpox virus infection among captive banded mongooses (Mungos mungo, suborder Feliformia). All animals of a colony of 8 mongooses showed a fulminant course of disease. The whole population died (n=7) or was euthanized (n=1) within 11 days. Postmortem examinations were performed on 4 animals. All animals showed extensive necrotizing inflammation of retropharyngeal lymph nodes, typical poxviral skin lesions, and multiple necrotic foci in liver and spleen. Three animals exhibited an ulcerating stomatitis. Pulmonary lesions, a common feature of fatal cowpox virus infections in other feliform species, were not obvious. Histopathologically, characteristic cytoplasmic inclusion bodies were detected in all affected organs but the spleen. Based on transmission electron microscopy and cell culture, Orthopoxvirus was identified as the etiology. The virus was further characterized by polymerase chain reaction and sequence analysis, identifying it as cowpox virus. A survey in the habitat suggests wild brown rats (Rattus norvegicus) as the most likely source of infection.


Assuntos
Vírus da Varíola Bovina/isolamento & purificação , Varíola Bovina/veterinária , Herpestidae/virologia , Animais , Varíola Bovina/mortalidade , Varíola Bovina/patologia , Surtos de Doenças , Vetores de Doenças , Feminino , Hepatócitos/ultraestrutura , Hepatócitos/virologia , Intestinos/virologia , Fígado/patologia , Masculino , Ratos , Pele/patologia , Língua/patologia
2.
J Comp Pathol ; 140(2-3): 203-7, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19135211

RESUMO

A Eurasian lynx and a European wildcat from the same wildlife park were submitted for necropsy examination after sudden death and after death following a clinical history of lethargy, respectively. Neither animal had been vaccinated against feline parvovirus (feline panleukopenia virus). Feral domestic cats were widespread in the area of the wildlife park and a number of these animals that had been captured had recently died from parvovirus infection. Gross and microscopical findings in the two non-domestic felids were consistent with feline parvovirus infection and this was confirmed by immunohistochemistry and polymerase chain reaction. The introduction of feline parvovirus into captive non-domestic felid populations could pose a threat to their health and survival. Vaccination of captive non-domestic felids is therefore recommended.


Assuntos
Felis/virologia , Lynx/virologia , Infecções por Parvoviridae/patologia , Infecções por Parvoviridae/veterinária , Animais , Imuno-Histoquímica , Parvovirus/genética , Reação em Cadeia da Polimerase
3.
Matrix Biol ; 19(6): 533-43, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11068207

RESUMO

Aggrecanase cleavage at the Glu(373)-Ala(374) site in the interglobular domain of the cartilage proteoglycan aggrecan is a key event in arthritic diseases. The observation that substrates representing only the aggrecanase cleavage site are not catabolized efficiently by aggrecanase prompted us to investigate the requirement of aggrecanase for additional structural elements of its substrate other than the actual cleavage site. Based on the recombinant substrate rAgg1mut we constructed deletion mutants with successively truncated N- or C-termini of the interglobular domain. Catabolism by aggrecanase activities induced in rat chondrosarcoma cells, porcine chondrocytes, and by human recombinant ADAMTS4 showed a gradually decreasing catabolism of progressively shortened, N-terminal deletion mutants of the substrate rAgg1mut. A reduction to 32 amino acids N-terminal to the aggrecanase site resulted in a decrease of at least 42% of aggrecanase cleavage products as compared with the wild-type substrate. When only 16 amino acids preceded the Glu(373)-Ala(374) site, aggrecanase cleavage was completely inhibited. In contrast, C-terminal deletions did not negatively affect aggrecanase cleavage up to the reduction to 13 amino acids C-terminal to the cleavage site. Unlike aggrecanase(s), membrane type 1-matrix metalloprotease (MT1-MMP), able to cleave rAgg1mut both at the aggrecanase and the MMP site, was insensitive to N-terminal deletions regarding aggrecanase cleavage, indicating that the importance of the N-terminus is characteristic for aggrecanase(s). Taken together, the results demonstrate that the amino-terminus of rAgg1mut, containing the MMP site, plays an important role for efficient cleavage by aggrecanase(s), possibly by serving as a further site of interaction between the enzyme and its substrate.


Assuntos
Endopeptidases/metabolismo , Proteínas da Matriz Extracelular , Proteoglicanas/genética , Proteoglicanas/metabolismo , Proteínas ADAM , Proteína ADAMTS4 , Agrecanas , Sequência de Aminoácidos , Animais , Células Cultivadas , Ensaio de Imunoadsorção Enzimática , Humanos , Imunoglobulina G/genética , Imunoglobulina G/isolamento & purificação , Lectinas Tipo C , Metaloproteinases da Matriz Associadas à Membrana , Metaloendopeptidases/metabolismo , Dados de Sequência Molecular , Oligopeptídeos , Peptídeos/genética , Peptídeos/isolamento & purificação , Pró-Colágeno N-Endopeptidase , Proteoglicanas/isolamento & purificação , Ratos , Proteínas Recombinantes de Fusão/isolamento & purificação , Proteínas Recombinantes de Fusão/metabolismo , Deleção de Sequência , Especificidade por Substrato , Células Tumorais Cultivadas
4.
Biochem Biophys Res Commun ; 241(1): 59-67, 1997 Dec 08.
Artigo em Inglês | MEDLINE | ID: mdl-9405234

RESUMO

We have identified the functional promoter of the translational inhibitor p14.5, the human homologue to a rat perchloric acid-soluble protein (PSP), a mouse heat-responsive protein (Hrp12) and a goat tumor antigen (UK114). Sequence analysis revealed a GC-rich promoter with several consensus sequences for transcription factors, but no TATA- and CAAT-box. To confirm promoter activity, DNA fragments of the p14.5 5'-flanking region were ligated in front of the luciferase gene and were transfected into HeLa and HepG2 cells. A minimal promoter between nt -104 and nt +88 relative to the transcription start site was responsible for basal activity. Furthermore, we observed a head-to-head orientation of p14.5 to the gene for the protein subunit of RNase P and MRP ribonucleoproteins (hPOP1). Luciferase assays with fragments of the hPOP1 5'-flanking region revealed a minimal promoter between nt -20 and nt +98 relative to the start of transcription. These data indicate that the 102 bp region between p14.5 and hPOP1 can act as a bidirectional promoter. The p14.5-hPOP1-cluster was mapped to chromosome 8q22 using in situ hybridization technique.


Assuntos
Cromossomos Humanos Par 8 , Endorribonucleases/genética , Regiões Promotoras Genéticas , RNA Catalítico/genética , Animais , Sequência de Bases , Sítios de Ligação , Mapeamento Cromossômico , Sequência Consenso , Endorribonucleases/biossíntese , Células HeLa , Humanos , Luciferases/biossíntese , Camundongos , Dados de Sequência Molecular , Reação em Cadeia da Polimerase , RNA Catalítico/biossíntese , Ratos , Proteínas Recombinantes de Fusão/biossíntese , Ribonuclease P , Ribonucleoproteínas/genética , Fatores de Transcrição/metabolismo , Transcrição Gênica , Transfecção , Células Tumorais Cultivadas
5.
Eur J Biochem ; 242(2): 339-51, 1996 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-8973653

RESUMO

A trichloroacetic-acid-soluble 14.5-kDa protein (p14.5) has been isolated from human mononuclear phagocytes (MNP) by a combination of trichloroacetic acid extraction, preparative electrophoresis and hydrophobic affinity chromatography; five tryptic peptides were subjected to protein sequencing. The full-length cDNA of the protein was cloned and sequenced from a lambda gt11 human liver library. The cDNA showed a remarkable similarity to a rat protein preferentially expressed in hepatocytes and renal tubular epithelial cells. The encoded protein is 137 amino acids long and similar to members of a new hypothetical family of small proteins with presently unknown function, named YER057c/YJGF. Human recombinant p14.5 inhibits in vitro protein synthesis in a rabbit reticulocyte lysate system. Unlike other inhibitors of protein synthesis, p14.5 is not phosphorylated despite the presence of putative phosphorylation sites. The p14.5 mRNA is weakly expressed in freshly isolated monocytes but is significantly upregulated when these monocytes are subjected to differentiation. This is also reflected by a differentiation-dependent increase in the protein concentration as demonstrated by immunoblots from cytosolic fractions and fluorescence-activated flow cytometry of permeabilized cells. A differentiation-dependent mRNA and protein expression of p14.5 is further suggested by the observation of a low expression in a variety of liver and kidney tumor cells and a high expression in fully differentiated cells as assessed by immunohistochemistry and northern blots. The highest mRNA expression was found in hepatocytes and renal distal tubular epithelial cells and only weak expression was found in other human tissues as evaluated by northern blot analysis. The preferential localization of the immunoreaction product seemed to be cytoplasmatic but, in less differentiated cells, nuclear labeling was occasionally visible. Immunoblotting of subcellular fractions confirmed these data. The high degree of evolutionary conservation of p14.5, the considerable upregulation during cellular differentiation and its potential role as a translational inhibitor may reflect an involvement in basic cellular mechanisms, e.g. a differentiation-dependent regulation of protein synthesis in hepatocytes, renal tubular epithelial cells, smooth muscle cells and MNP.


Assuntos
Proteínas de Choque Térmico/biossíntese , Proteínas de Choque Térmico/farmacologia , Monócitos/metabolismo , Inibidores da Síntese de Proteínas/farmacologia , Transcrição Gênica , Sequência de Aminoácidos , Animais , Sequência de Bases , Diferenciação Celular , Células Cultivadas , Clonagem Molecular , Sequência Consenso , Primers do DNA , Biblioteca Gênica , Proteínas de Choque Térmico/isolamento & purificação , Humanos , Fígado/citologia , Fígado/metabolismo , Fígado/ultraestrutura , Dados de Sequência Molecular , Peso Molecular , Monócitos/citologia , Especificidade de Órgãos , Fragmentos de Peptídeos/química , Fragmentos de Peptídeos/isolamento & purificação , Reação em Cadeia da Polimerase , Biossíntese de Proteínas/efeitos dos fármacos , Inibidores da Síntese de Proteínas/isolamento & purificação , Coelhos , Ratos , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/química , Proteínas Recombinantes/farmacologia , Reticulócitos/metabolismo , Homologia de Sequência de Aminoácidos , Ácido Tricloroacético
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