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Foot-and-mouth disease (FMD) is the most contagious disease of mammals and has great potential for causing severe economic losses in susceptible cloven-hoofed animals. FMD is caused by a virus of the genus Aphthovirus, family Picornaviridae. Serological tests in laboratories have identified seven different serotypes as O, A, C, SAT 1, SAT 2, SAT 3 and Asia 1. FMD is diagnosed by the virus isolation or demonstration of FMD viral antigen or nucleic acid in samples of biological specimens. The purpose of the study was to apply the isolation test in cell culture and a RT-PCR assay for the detection of foot-and-mouth disease virus in biological materials. Out of the total of 14 examined samples, 6 (42.8%) were found positive using these methods. The antigen ELISA was used for the confirmation of specificity of the isolation assay. Primary bovine thyroid cells were found the most sensitive cell culture system for the detection of foot-and-mouth disease virus, followed by secondary lamb kidney and certain IB-RS-2 cells.
Swine vesicular disease virus (SVDV) is a member of the genus Enterovirus in the family Picornaviridae. This virus appears to have evolved from human coxsackievirus B5. Pigs infected with this virus show almost identical clinical signs to foot-and-mouth disease in pigs. Vesicular diseases must be differentiated with laboratory tests. The purpose of the study was to apply the isolation test in cell culture and RT-PCR assay for the detection of swine vesicular disease virus in the epithelial and fecal samples. Out of a total of 11 examined samples, 10 were found positive using these methods. The antigen ELISA was used for the confirmation of specificity of isolation assay. Primary piglet kidney cells and certain IB-RS-2 cells were a sensitive cell culture system for the detection of swine vesicular disease virus, whereas secondary lamb kidney cells not.
The purpose of the paper was to present current knowledge on the epizootiology and diagnosis of respiratory infections caused by BRSV. This virus is one of the major infectious agents causing diseases in young cattle. BRSV can be the main cause of a respiratory infection or it can be one of the etiological agents of respiratory disease complex. The results of serological examinations and virus isolation showed that BRSV is widely distributed in cattle population all over the world. Economic losses caused by BRSV are associated mainly with high costs of treatment, decreased growth rates and calf mortality. A rapid diagnosis of the disease is crucial for further therapeutic management and the treatment should be concentrated on limiting losses within the herd. During recent years several papers concerning the diagnosis of BRSV have been published. This review describes not only the classical methods of virus detection (virus isolation in a cell culture, immunofluorescence, immunohistochemistry) but also the recently applied PCR assay.
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