Estudo comparativo entre as provas de imunodifusao em placa e em lamina na deteccao de anticorpos contra o virus da leucose enzootica bovina []. Contagem linfocitaria e anticorpos contra o virus da leucose enzootica bovina em rebanhos do Rio de Janeiro []. Ferreira, M.I. Romero, C.H. Rowe, C.A. Ocorrência do vírus da leucose enzoótica dos bovinos (BLV) e de anticorpos contra herpesvírus bovino tipo-1 (BoHV-1) e vírus da diarreia viral bovina (BVDV) .

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Comparison of agar gel immunodiffusion test, enzyme-linked immunosorbent assay and western bovjna for the detection of BLV antibodies. The predictive Leucokit-La Plata values recommend its application in the commercialization of live cows export cow selection for hemo-vaccines and implementation of control and eradication programmes. The Apparent Prevalence was Analysing cell division in vivo and in vitro using flow cytometric measurement of CFSE dye dilution.

Some long term studies may be necessary, as there appears to be a correlation in instances of cancer among butchers and slaughterhouse workers.

In Europe attempts were made to eradicate the virus by culling infected animals. In accordance with Reichel et al. Only some animals later develop a B-cell leukemia called enzootic bovine leukosis. The natural host of BLV is cattle. Latorre II ; B. In our case ID test has high specificity and unequivocally defines as positive the sample which is clearly reactive in the test. Bovine Leukosis Virus EBLV is a widely distributed pathogen agent in the bovine population of many countries, especially in dairy cattle.

The cut-off value of a diagnostic test is the scale point of measure from which the quantitative results are classified as positive or negative and it is the value from which the quantitative data are categorised.


How to cite this article. With reference to the application of Kappa coefficient or concordance proportion beyond chance, a value of 0.

Enzootic bovine leukosis: performance of an indirect ELISA applied in serological diagnosis

In general BLV causes only a benign mononucleosis -like disease in cattle. In more recent years, different ELISAs have been used in eradication programs and there are several commercial kits available to detect antibodies ezootica the principal viral proteins gp51 and p24 WB is an other serologycal test which is highly specific and suitable to be introduced as confirmatory test at late stages in the eradication programs 9.

Transmission via colostrummilk, and in utero exposure is generally considered to account for a relatively small proportion of infections.

A persistent antibody response can also be detected after experimental infection in deer, rabbits, rats, guinea-pigs, cats, dogs, sheep, rhesus monkeys, chimpanzees, antelopes, pigs, goats and buffaloes.

Once the bovine is infected, it remains as a virus carrier for life and such state is correlated with a specific antibody detectable level. Serological test has been used for a number of years to identify infected cattle and traditionally the ID has been used. Frontiers in Biosciencev. Bovine Leukosis Virus BLV is a pathogenic agent of significant importance in bovines from the American continent since it is widely distributed mainly in dairy cattle.

Rabbits get a fatal AIDS like disease similar to rabbit-snufflesdifferent from the benign human snuffles. On the other hand, the infected individuals are classified as true positives TP and as false negatives FN unless the test is perfectly sensitive where only TP results are obtained. In these cases and as pointed out by Kozaczynska 15sample analyses should be repeated, keeping the animals as no leucoose until the definite confirmation of the result is obtained.

Possibilities and limitations for use of the polymerase chain reaction PCR in the diagnosis of bovine leukemia virus BLV infection in cattle. Soon the United Kingdom followed. peucose


The interpretation of the Kappa value in this case has restrictions since it was applied to lehcose different serological tests ID and indirect ELISA and Kappa implicates that challenged tests are equivalent Saunders Elsevier,p. Mostly farm workers drinking raw milk were tested for disease, especially for leukemia.

Leucose enzoótica bovina

Consultado em 17 de agosto de In this case the value was 0. Determination of lymphocyte division by flow cytometry. Bovnia Kappa and Jouden’s Index J coefficients an almost perfect concordance was obtained between both kits. But neither leukemia nor other signs of infection could be detected.

Leucose enzoótica bovina – Wikipédia, a enciclopédia livre

Agar gel immunodiffusion test for the detection of bovine leukemia virus antibodies: Bovine leukaemia virus-induced lymphocytoosis in sheep is associated with reduction of spontaneous B cell apoptosis. In our study we considered a normal distribution, according with the previous descriptive analysis of the original values. A rapid and sensitive diagnosis of bovine leukaemia virus infection using the nested shuttle polymerase chain reaction. Caniceiro II ; M. The PCR is a technique especially appropiated for the diagnosis of virus infection where virus specific antibodies cannot be detected and the presence of viral genome is the only evidence of infection An international comparison of different laboratory test for the diagnosis of bovine leukosis: According to the OIE 19 the analysis of the test results allows us the following considerations: Once infected, the bovine remains as a virus carrier for life and such state correlates with the specific antibody detectable level.