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An increasing number of indigenous cases of hepatitis E caused by genotype 3 viruses (HEV-3) have been diagnosed all around the word, particularly in industrialized countries. Hepatitis E is a zoonotic disease and accumulating evidence indicates that domestic pigs and wild boars are the main reservoirs of HEV-3. A detailed analysis of HEV-3 subtypes could help to determine the interplay of human activity, the role of animals as reservoirs and cross species transmission. Although complete genome sequences are most appropriate for HEV subtype determination, in most cases only partial genomic sequences are available. We therefore carried out a subtype classification analysis, which uses regions from all three open reading frames of the genome. Using this approach, more than 1000 published HEV-3 isolates were subtyped. Newly recovered HEV partial sequences from hunted German wild boars were also included in this study. These sequences were assigned to genotype 3 and clustered within subtype 3a, 3i and, unexpectedly, one of them within the subtype 3b, a first non-human report of this subtype in Europe.

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The aim of this study was to investigate the uptake of new spherical and cuboid baits by wild boar and domestic pigs and to evaluate the stability of lyophilised C-strain vaccine stored at different environmental temperatures. New baits were designed to improve the consumption of the vaccine against classical swine fever by young wild boar. Our uptake studies showed that neither wild boar nor domestic pigs at the age of 2 months picked up the baits at all. Although the animals began to pick up the baits incompletely at the age of 3 months, a complete uptake of both the new baits and the older ones was only observed from the age of 4 (domestic pigs) and 4.5 (wild boar) months on. Nevertheless, the larger spherical baits with a diameter of 3 cm were taken up more effectively than the recent vaccine baits. As expected, lyophilised vaccine showed a higher stability than liquid vaccine, especially at temperatures ≥24°C. Independently of the stabiliser (GS4 or TSM) used, there are no differences between the virus titres detected within a storage period of 7 days. As the lyophilised C-strain vaccine was more stable at higher temperatures than the liquid vaccine formulation, we recommend to use lyophilised vaccine for oral immunisation of wild boar in the future, as oral vaccination is also carried out in the summertime.

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The virulence of two isolates of the classical swine fever virus (CSFV) was studied in experimentally infected wild boars of different ages. The isolates, originating from wild boars shot in Mecklenburg-Western Pomerania (isolate '1829-NVP') and in Rhineland-Palatinate (isolate '11722-WIL'), belong to the genetic subgroup 2.3 Rostock. Clinical picture, transient viraemia, virus excretion and gross lesions at necropsy as well as a failure of virus detection at the end of the experiment revealed that this virus subtype was only moderately virulent. Whereas one subadult wild boar and both 7-week-old wild boar piglets infected intranasally became sick and died, only one of three 8-week-old animals which survived after contact infection remained CSFV positive until the end of the experiment [34 days post infection (dpi)], although neutralizing antibodies were present. This underlines the role of young boars in CSF epidemics. The isolate '11722-WIL' was shed by an infected adult wild boar and was transmitted to susceptible piglets. Interestingly, all animals which became sick and died also were found to be infected with a secondary pathogen. Therefore, we assume that after infection with moderately virulent CSFV simultaneous infections with other pathogens may be important for the clinical course and the outcome of the disease as well as for a spread of the virus in field.

The objective of this study was to retrospectively evaluate the occurrence of porcine parvovirus (PPV)