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1.
Vet Microbiol ; 169(1-2): 8-17, 2014 Feb 21.
Article in English | MEDLINE | ID: mdl-24411658

ABSTRACT

Classical swine fever (CSF) is among the most important viral disease of domestic and feral pigs and has a serious impact on animal health and pig industry. In most countries with industrialized pig production, prophylactic vaccination against CSF is banned, and all efforts are directed towards eradication of the disease, e.g. by culling of infected herds and animal movement restrictions. Nevertheless, emergency vaccination remains an option to minimize the socio-economic impact of outbreaks. For this application, potent vaccines are needed that allow differentiation of infected from vaccinated animals. Among the promising candidates for next generation marker vaccines is the chimeric pestivirus CP7_E2alf. Efficacy studies are usually carried out using highly virulent CSFV strains of genotype 1 that do not mirror the current field situation where strains of genotype 2 predominate. To prove that CP7_E2alf also protects against these strains, efficacy was assessed after single oral vaccination of wild boar and single intramuscular vaccination of domestic pigs using challenge models with recent CSFV strains and the highly virulent strain "Koslov" (genotype 1.1). It could be demonstrated that CP7_E2alf pilot vaccine batches for intramuscular and oral use were able to protect pigs from challenge infection with a highly virulent CSFV. Moreover, solid protection was also achieved in case of challenge infection with recent field strains of genotypes 2.1 and 2.3. Thus, broad applicability under field conditions can be assumed.


Subject(s)
Classical Swine Fever Virus/immunology , Classical Swine Fever/prevention & control , Sus scrofa/immunology , Vaccines, Marker , Viral Vaccines , Administration, Oral , Animals , Antibodies, Viral/blood , Classical Swine Fever/immunology , Classical Swine Fever/virology , Classical Swine Fever Virus/genetics , Classical Swine Fever Virus/isolation & purification , Classical Swine Fever Virus/pathogenicity , Genotype , Injections, Intramuscular , Swine , Vaccination/veterinary , Vaccines, Marker/administration & dosage , Vaccines, Marker/immunology , Vaccines, Synthetic/administration & dosage , Vaccines, Synthetic/immunology , Viral Vaccines/administration & dosage , Viral Vaccines/immunology
2.
Vet Microbiol ; 162(2-4): 360-368, 2013 Mar 23.
Article in English | MEDLINE | ID: mdl-23107658

ABSTRACT

Classical swine fever (CSF) is a multi-systemic disease that can be accompanied by severe haemorrhagic lesions. The underlying pathogenetic mechanisms are still far from being understood, though disseminated intravascular coagulation (DIC) was discussed as a major factor. In the presented study, the direct thrombin inhibitor hirudin was used in an attempt to elucidate the role of the coagulation system in the pathogenesis of CSF-induced haemorrhagic lesions. Two groups of piglets (n=5) were infected with highly virulent CSF virus (CSFV) strain CSF0634. One group underwent daily treatment with hirudin, the other served as untreated challenge infection control. Assessment of clinical signs using a clinical score system, coagulation tests, and blood counts were performed daily. Both groups developed acute-lethal CSF with haemorrhagic lesions. Although changes in the coagulation system were seen in the late stages of CSFV infection, our results strongly suggest that DIC does not present the crucial event in the pathogenesis of haemorrhagic lesions.


Subject(s)
Classical Swine Fever Virus/pathogenicity , Classical Swine Fever/blood , Disseminated Intravascular Coagulation/veterinary , Animals , Classical Swine Fever/pathology , Classical Swine Fever/virology , Disseminated Intravascular Coagulation/blood , Disseminated Intravascular Coagulation/pathology , Fibrinogen/metabolism , Hirudins/blood , Leukocyte Count , Partial Thromboplastin Time/veterinary , Platelet Count , Random Allocation , Sus scrofa , Swine , Thrombocytopenia/blood , Thrombocytopenia/veterinary , Thrombocytopenia/virology
3.
J Virol Methods ; 175(2): 170-4, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21600240

ABSTRACT

Classical swine fever (CSF) is a highly contagious disease, causing severe economic losses in the pig industry worldwide. Vaccination of pigs with lapinized Chinese vaccines is still practised in some regions of the world, where the virus is enzootic, in order to prevent and control the disease. However, a single real-time assay that can detect all lapinized Chinese vaccines used widely, namely, Lapinized Philippines Coronel (LPC), Hog Cholera Lapinized virus (HCLV) and the Riems C-strain is still lacking. This study describes a real-time RT-PCR assay, targeting the N(pro) gene region, for specific detection of these lapinized vaccine strains. The assay is highly sensitive, with a detection limit of 10 genome copies per reaction for HCLV and Riems C-strain and highly specific, as more than 100 strains of wild type CSFV representing all major genotypes were not detected. The assay is also highly repeatable: the coefficient of variation of Ct values in three runs was 2.77% for the detection of 10 copies of the vaccine viral RNA. This study provides a potentially useful tool for specific detection of the lapinized Chinese vaccines, HCLV and C-strain, and the differentiation of these vaccines from wild type CSFV.


Subject(s)
Classical Swine Fever Virus/classification , Classical Swine Fever Virus/isolation & purification , Classical Swine Fever/virology , Polymerase Chain Reaction/methods , Viral Vaccines/administration & dosage , Virology/methods , Animals , Classical Swine Fever/prevention & control , Classical Swine Fever Virus/genetics , Reproducibility of Results , Sensitivity and Specificity , Swine , Vaccines, Attenuated/administration & dosage
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