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The 5' untranslated region (5' UTR) of cytopathogenic pestiviruses isolated from two seronegative roe deer (Capreolus capreolus) in northern Germany was partially sequenced and compared with those of 28 other pestiviruses. Due to the occurrence within a narrow location and the complete identity of the sequenced fragments from both roe deer isolates (SH9 and SH11) they seem to belong to the same bovine virus diarrhea virus (BVDV) strain called SH9/11. This strain is highly homologous (up to 93% identity) to "classical" BVDV strains. However, SH9/11 has characteristic variations in its 5' UTR distinct from all other pestiviruses analyzed in this study. Strain SH9/11 is more similar to BVDV group I than to group II, although it is clearly separated from all other cattle isolates tested. In monoclonal antibody (mAb)-typing studies, isolate SH9 reacted with one pestivirus-specific mAb (C16), with two BVDV specific mAbs (N2B12 and D5), and with one mAb (f48) raised against the E2 protein of classical swine fever virus out of a panel of 13 mAbs. The separate position of strain SH9/11 again was demonstrated by the unique reaction pattern of isolate SH9 when compared with other mAb f48-positive BVDV and BDV strains. All these results indicate that indicate that distinct BVDV strains might exist among freeranging roe deer in Germany.

From 1993 to 1995, 100 blood samples and 97 spleen samples of free-ranging rabbits (Oryctolagus cuniculus) from northern Germany were tested for prevalence of different bovine viral diarrhea virus (BVDV) antibodies and BVDV antigen, respectively. Forty sera (40%) were positive for antibodies to one or more of three cytopathogenic BVDV strains (NADL, Grub 313/83, and roe deer isolate SH9/11). Microneutralization test (NT) titers ranged from 5 to 13. Moreover, 13 of 35 NT positive sera also were positive by enzyme-linked immunosorbent assay for detection of anti-BVDV antibodies. Therefore, we assume that the rabbits either had passively acquired antibodies or had experienced natural infection with BVDV. Furthermore, 97 spleen samples were used for attempts to isolate BVDV and tested by reverse transcription polymerase chain reaction for viral nucleic acid using various protocols. Bovine viral diarrhea virus was not identified in these samples.

Twenty-one blood samples of free-ranging mountain zebras (Equus zebra) from Namibia were tested for equine herpesvirus (EHV-1, -2, -3, -4) specific antibodies by immunofluorescence assay (IFA) and neutralization test (NT). Additionally, type-specific nested polymerase chain reactions (nested PCR) were employed for detection of EHV-1, -2 and -4 DNA. Equine herpesvirus-1 antibodies were detected by IFA in all zebras, while only seven serum samples contained EHV-4 IFA antibodies. Sera with high IFA antibodies also were found to neutralize EHV-1 and -4. Furthermore, 20 zebras were EHV-2 seropositive by IFA, and one zebra had EHV-2 neutralizing antibodies. Equine herpesvirus-3 specific antibodies were not detected. We did not amplify EHV-1, -2 or -4 specific DNA sequences in peripheral blood leukocytes of the same zebras using type-specific nested PCR. EHV infections appear to be widespread in free-ranging zebras, as they are in domestic horses.

A study of European brown hare syndrome (EBHS) was conducted in Poland (Czempin). From April 1993 until February 1994, 100 blood and 78 spleen samples of European brown hares (Lepus europaeus) were tested for prevalence of EBHS and rabbit hemorrhagic disease (RHDV) antibodies and EBHS virus antigen with two enzyme-linked immunosorbent assay (ELISA) test kits. Thirty-eight of 100 serum samples were positive for EBHS, and six (7.6%) of 78 of the spleen materials were-antigen positive for EBHS virus. Three (3%) of the sera were positive against RHDV, whereas two of these also were seropositive for EBHSV. European brown hare syndrome virus seropositive hares were most frequently found from April to September. Based on negative staining electron microscopy investigations of liver and spleen homogenates of all antigen-positive hares, we observed caliciviruses in only one animal. For histopathological investigations organ specimens were available from 98 hares. Histopathological findings corresponded with the clinical picture of chronic EBHS. A pathohistological picture consistent with EBHS was found in 22 (22%) of investigated hares and corresponded in 50% of the animals which reacted positively in the EBHSV antigen-ELISA and in 29% of the animals which reacted positively in the EBHSV antibody-ELISA. These results from western Poland are the first that caliciviruses are present in European brown hare population in Eastern Europe and may be one of the causes for increased mortality in the Polish hare population over the past 10 years.

From 1990 until 1992, 355 blood samples of roe deer (Capreolus capreolus) (n = 123), red deer (Cervus elaphus) (n = 60), fallow deer (Dama dama) (n = 87) and other cervid species (n = 85) from three different habitats (n = 180) and 11 wildlife parks or zoos (n = 175) in Germany were tested for prevalence of pestivirus antibodies. Seventeen samples were seropositive for bovine viral diarrhea virus (BVDV); only one animal had antibodies for Border disease virus. Microneutralization test titers ranged from 1:5 to 1:125. We found no significant difference in antibody prevalence among deer in habitats with high, intermediate and low density of cattle. There were significantly more seropositive individuals in roe deer compared to fallow deer. Significantly more seropositive individuals were found among juvenile animals than among adults. Antibody prevalence in free-ranging cervids was significantly higher compared with that of deer in enclosures. Antibody prevalence in summer was significantly higher than in winter.

The organization and structure of data masses including results of scientific research is presented on the base of the morphometric method. The data massif is realized on ESER-1056 large scale computer. Currently, all the results of the universally scientific programme "Statist", designed for mathematical and statistical morphometric data processing, are collected in this data massif. A personal computer is linked with a large-scale computer by a cable for data transfer by telecommunication, the whole system accomplishes distributed ata processing. This enables the scientist to use the data massif directly from his working site.

Tissue of myocardium from (8262) hamsters, 2, 6 and 27 weeks of age, were analyzed with quantitative microscopic techniques. Besides alterations of some other structures, we found the most evident changes in the mitochondrial abnormalities exist at all ages. They may be related to defective energetic mechanism.

A system of automated microscopic picture analysis was used in an examination of 272 gliomas (70 glioblastomas, 91 astrocytomas, 56 pilocytic astrocytomas or spongioblastomas , and 55 oligodendrogliomas). The specimens were prepared as Feulgen sections, 4 microns in thickness. Thirteen morphometric-densitometric parameters of tumor cell nuclei were tested together with two mitotic parameters. Objective and reproducible data on numerical nuclear density ( KRNZ , AREA), nuclear size ( KOFL , KFRL , P250 ), nuclear shape ( FOFK , FOFR , P150), optical density ( EXTU , EXTS , EXSR , EXTM , EXMR ), and mitotic activity ( MITZ , VHMK ) of the gliomas were obtained from the morphometric-densitometric parameters. All gliomas but glioblastomas were subdivided by four tumor grades. The morphometric-densitometric and mitotic data recorded were statistically checked, depending on tumor grade (Student's t-test, Wilcoxon's test, alpha = 0.05). Numerical nuclear density, deformation of nuclei, and mitotic activity were found to grow with significance along with increasing tumor grade up to glioblastoma. The relative standard deviation (SD) of nuclear size ( KFRL ), relative SD of shape factors ( FOFR ), and relative SD of extinction sums ( EXSR ) are high-accuracy parameters for the pathologist to describe variability of sizes, polymorphism, and polychromasia of nuclei. These parameters show a significant increase of values in parallel with rising tumor grade, with maximum values being recordable from cases of glioblastomas. In cases of astrocytomas, optical values of nuclei decrease along with rising tumor grade. The data thus obtained were used as reference values for objective, reproducible automatic glioma grading. The classifier method, described in an earlier publication, proved to be more effective than the regression method.