Publications by authors named "J Rulka"

This study demonstrates the usefulness of PLA and nested-PCR methods for the detection of cattle infection with enzootic bovine leukemia virus. Serological control with PLA was by 1.7% more sensitive than reference ELISA examination.

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In the years 1992 to 2002 the ID and ELISA systemic serological examinations of infected cows from a large farm brought advantageous results. A total of 468 cows from three farms from Opole province were examined. In the years 1997 to 2002 there were four times more positive serological results obtained than in the years 1992 to 1996.

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The bovine leukemia virus (BLV) envelope gene encoding extracellular glycoprotein gp51 and transmembrane glycoprotein gp30 was cloned into a vehicle expression vector under the human cytomegalovirus (CMV) intermediate early promoter. The intramuscular injection of this plasmid vector generated a cellular immune response. Seven out of ten cows vaccinated with the DNA construct resisted a drastic challenge (500 BLV-infected lymphocytes as an infectious dose).

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The Rous-associated virus 1 env gene, which encodes the envelope gp85 and gp37 glycoproteins, was isolated and inserted in place of the v-erbB oncogene into an avian erythroblastosis virus-based vector, carrying the neo resistance gene substituted for the v-erbA oncogene, to generate the pNEA recombinant vector. A helper-free virus stock of the pNEA vector was produced on an avian transcomplementing cell line and used to infect primary chicken embryo fibroblasts (CEFs) or quail QT6 cells. These infected cells, selected with G418 (CEF/NEA and QT6/NEA, respectively) were found to be resistant to superinfections with subgroup A retroviruses.

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Nine groups of sheep have been experimentally infected with different doses of BLV and by various routes. An immunological response of animals, as well as clinical symptoms of leukosis in the experimental sheep were investigated within several years or months. The animals inoculated with the virus showed appearance of BLV-antibodies in 94 per cent of cases, lymphocytosis in 47 per cent and clinical symptoms of the disease in 33 per cent.

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