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1.
Rev. argent. microbiol ; 35(1): 19-23, ene.-mar. 2003.
Artigo em Espanhol | LILACS | ID: lil-356644

RESUMO

El diagnóstico serológico es de gran importancia para la detección de la infección con el virus de la diarrea viral bovina (BVDV), importante patógeno asociado a fallas reproductivas entre otras. Las técnicas más utilizadas para la detección de anticuerpos contra BVDV son la seroneutralización en cultivos celulares (SN) y el ELISA. El objetivo del presente trabajo fue estandarizar un ELISA de esquema indirecto comparando sus resultados con la SN. Con resultados de sensibilidad de diagnóstico mayores o iguales que 98,31 por ciento y de especificidad de diagnóstico igual a 100 por ciento, el ELISA-BVDV resultó ser un método sensible, específico y repetible. Además es una técnica de realización rápida, sencilla, económica y de fácil transferencia.


Assuntos
Animais , Argentina , Vírus da Diarreia Viral Bovina , Ensaio de Imunoadsorção Enzimática , Testes de Neutralização , Testes Sorológicos
2.
Rev. argent. microbiol ; 34(3): 150-156, jul.-sept. 2002.
Artigo em Espanhol | LILACS | ID: lil-331790

RESUMO

To establish if BTV was circulating in Argentina, 94 bovines from the Santo TomÚ and Ituzaingó Departments of Corrientes Province were sampled every 30-60 days during 14 months. Red blood cells from those animals that showed seroconvertion with a c-ELISA were processed for virus isolation by inoculation in embryonated chicken eggs and cell cultures. Cells with CPE were positive by direct and indirect immunofluorescence with BTV specific reagents. These samples examined by electron microscopy showed virus particles with BTV morphological characteristics. Blood samples and tissue culture supernantants were positive by RT-PCR technique with primers corresponding to the segment 3 of the BTV genome. Haematophagous insects were captured in one farm using light traps and Culicoides insignis Lutz was the predominant species detected. This is the first isolation of BTV in Argentina from northeastern bovines without any disease symptom.


Assuntos
Animais , Bovinos , Bluetongue , Ceratopogonidae , Doenças dos Bovinos/virologia , Insetos Vetores , Vírus Bluetongue/isolamento & purificação , Anticorpos Antivirais , Argentina , Bluetongue , Células Cultivadas/virologia , Galinhas , Doenças dos Bovinos/epidemiologia , Doenças dos Bovinos/transmissão , Ovos , Ensaio de Imunoadsorção Enzimática , Genoma Viral , RNA Viral , Estações do Ano , Vírus Bluetongue/genética , Vírus Bluetongue/imunologia , Cultura de Vírus
3.
Rev. argent. microbiol ; 33(2): 122-132, abr.-jun. 2001.
Artigo em Espanhol | LILACS | ID: lil-332490

RESUMO

Bluetongue (BT) is a viral disease of domestic and wild ruminants. It is particularly damaging in sheep, where up to half of infected animals may die, showing inflammation and hemorrhages of the mucous membranes of the mouth, nose, and intestines. In cattle and goats, BT rarely causes disease, however it can affect the animal's reproductive ability, so that losses are not easily estimated. Bluetongue virus spreads from animal to animal by biting insects of the genus Culicoides; and this is the reason why the disease is more prevalent in geographic areas where climate conditions are favourable for their development. The disease was first recognized in South Africa in the late 1700's, but it was not until the early 1900's that it was described in detail, and at present, epizootiology and pathogenesis studies are still being carried on.


Assuntos
Animais , Masculino , Feminino , Bluetongue , Vírus Bluetongue , Aborto Animal , Antígenos Virais/imunologia , Argentina , Bluetongue , Ceratopogonidae , Doenças Fetais/veterinária , Doenças Fetais/virologia , Infertilidade Masculina , Insetos Vetores , Proteínas Virais/imunologia , RNA Viral , Ruminantes , Vacinas Virais , Vírus Bluetongue/classificação , Vírus Bluetongue/isolamento & purificação , Vírus Bluetongue/fisiologia
4.
Rev. argent. microbiol ; 32(1): 27-32, ene.-mar. 2000.
Artigo em Espanhol | LILACS | ID: lil-332541

RESUMO

Fetal bovine serum (FBS) used in cell culture may be contaminated with viruses, among them bovine viral diarrhea virus (BVDV) affecting the production of biological reagents and the results of diagnosis. The filtration process used in the preparation of commercial FBS abrogates most viral agents that may be present in raw FBS, but BVDV may pass through the filters because of its small size and its pleomorphism. While detection of bovine herpes virus-1 and parainfluenza-3 (PI-3) is determined by observation of the cytopathic effect, and also by hemadsorption in the case of PI-3, the most frequently isolated BVDV is non cytopathic, and infects cells without morphological alterations, inducing problems that arise after several cell generations. Batches of raw and processed FBS were analyzed. Frequencies of BVDV detection in raw serum in Argentina were similar to those published for USA. By conventional methods for BVDV detection, only 2 of 20 commercial batches of FBS had BVDV. Using cell cultures maintained with high concentrations of the serum under study for at least 2 weeks, with detection of viral antigen by indirect immunofluorescence, the percentage of BVDV detection was 80. This method shows that most lots of commercial FBS contain BVDV. RT-PCR allows faster detection of the viral genome, but it must be validated, as it does not show viral replication. To eliminate the problem of BVDV contamination in FBS, only gamma irradiated FBS is used in our laboratory.


Assuntos
Animais , Bovinos , Sangue , Vírus da Diarreia Viral Bovina/isolamento & purificação , Meios de Cultura
5.
Rev. argent. microbiol ; 14(1): 31-6, 1982.
Artigo em Espanhol | LILACS | ID: lil-10295

RESUMO

Se determino la estabilidad termica, densidad de flotacion y morfologia de la cepa L-114 de virus de la rinotraqueitis infecciosa bovina, aislada recientemente en el pais. La morfologia correspondio a un virus con envoltura, de 200 mm de diametro total y 90 mm de diametro del "core". La estructura de este ultimo fue de tipo icosaedrica, observandose particulas vacias y completas en la preparaciones purificadas de virus. A 37o C, cepa L-114 perdio mas del 90% de su infectividad en 15 hs. y a 56o C se inactivo muy rapidamente, perdiendo 3 log en 24 minutos. La densidad de flotacion en cloruro de cesio, luego de su concentracion por sedimentacion a traves de sacarosa al 47% (p/v), indica que el virus purificado tiene una densidad estimada de 1,25 g/ml, correspondiente a los virus herpes denominados livianos


Assuntos
Herpesvirus Bovino 1 , Microscopia Eletrônica
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