Mercury and Mink. II. Experimental methyl mercury intoxication.

Adult female mink were fed rations containing 1.1, 1.8, 4.8, 8.3 and 15.0 ppm mercury as methyl mercury chloride over a 93 day period. Histopathological evidence of injury was present in all groups. Mink fed rations containing 1.8 to 15.0 ppm mercury developed clinical intoxication within the experimental period. The rapidity of onset of clinical intoxication was directly related to the mercury content of the ration. Mercury concentration in tissue of mink which died were similar, despite differences in mercury content of the diets and time of death. The average mercury concentration in the brain of mink which died was 11.9 ppm. The lesions of methyl mercury poisoning are described and criteria for diagnosis are discussed.     

Serology of Haemophilus (Actinobacillus) pleuropneumoniae serotype 5 strains: establishment of subtypes a and b

The serological characteristicis of 14 strains assigned to serotype 5 were examined by the slide agglutination test, the indirect haemagglutination (IHA) test and by gel diffusion.All the strains possessed identical capsular antigenic determinants of polysaccharide (PS) nature and lipopolysaccharide (LPS) nature. However, based upon a capsular antigenic determinant of PS nature the strains could be divided in two subtypes. It is therefore proposed to refer to the H. pleuropneumoniae strains of serotype 5 to two subtypes: subtype a with strain K17 as the subtype strain and subtype b with strain L20 as the subtype strain.     

Summer mastitis in heifers: observations on the effect of insect attacks on the teats of heifers

An estimation of the possible etiology behind summer mastitis in heifers includes an evaluation of the significance of various insects as hosts for the causal microorganism. Under Danish conditions, several species of insects may be considered disease-carriers, such as Simulium sp., Culicoides sp., tabanids and Hydrotaea irritans (Fall.) in particular. In contrast to the other insects mentioned, Hydrotaea irritans is not able to penetrate the skin by itself but depends on one of the species of insects able to carry out the necessary opening of the skin in order to be able to pick up a “blood meal” (cf. Hϕi Sϕensen 1979).     

A mass attack by the biting midge culicoides nubeculosus (Mg.) (Dipteria, Ceratopogonidae) on grazing cattle in Denmark. A new aspect of sewage discharge.

A consequence of sewage discharge into a shallow marsh pool was large-scale hatching of the biting midge Culicoides nubeculosus from the recipient and mass attacks by this blood-sucking insect on grazing cattle. Culicoides nubeculosus is a great nuisance due to the painful bite and in Denmark it is a potential vector of pathogenic agents. In the future, these aspects of sewage discharge must be borne in mind.     

Bordetella bronchiseptica isolations from the nasal cavity of pigs in relation to atrophic rhinitis.

The occurrence of Bordetella bronchiseptica and atrophic rhinitis was studied during a one-year period in four Danish sow herds. In three of the heards, the epidemiological studies revealed a relation between the occurrence of B. bronchiseptica in 3--10-week-old pigs and the presence and severity of atrophic rhinitis at slaughter. In the fourth herd no such relation was found.     

Isolation of porcine reproductive and respiratory syndrome (PRRS) virus in a Danish swine herd and experimental infection of pregnant gilts with the virus

The first case of porcine reproductive and respiratory syndrome (PRRS) in Denmark was diagnosed in March 1992 by the detection of specific antibodies against PRRS virus in serum samples originating from sows in a herd located on the island of Als. Subsequently, PRRS virus was isolated from a 200-sow farrow-to-finish herd with clinical signs consistent with PRRS. The virus was isolated by inoculation of pleural fluid from a stillborn piglet onto porcine pulmonary alveolar macrophages. The isolate was identified as PRRS virus by staining with a specific antiserum. By electron microscopy, the virus particle was found to be spherical and enveloped, measuring 45–55 nm in diameter and containing a 30–35 nm nucleocapsid. Only minor antigenic differences were found between the Danish and a Dutch isolate. Following intranasal inoculation of 3 pregnant gilts with the Danish isolate transplacental infection was demonstrated by the re-isolation of PRRS virus from approximately 45% of the piglets from the experimentally infected gilts. However, the experimental infection produced no significant reproductive disorders or other clinical signs. At autopsy, histopathological examination revealed slight interstitial pneumonia in a few piglets.     

Actinobacillus pleuropneumoniae serotype 5, subtypes a and b: cross protection experiments

Vaccination of pigs with a killed culture of A. pleuropneumoniae serotype 5, strain K17 (subtype a) afforded a high degree of protection against challenge with strains L20 and T928 (subtype b). The reverse experiment showed that strain L20 gave good protection against challenge with strain K17 whereas strain T928 did not afford an acceptable protection against challenge with this strain.The considerable cross immunity shown to exist between strains K17 and L20 indicates a high degree of homogeneity of the antigenic determinants of the two strains involved in induction of protective immunity and suggest that antibodies to capsular subtype specific determinants may not play a significant role in the specific defence against A. pleuropneumoniae strains belonging to serotype 5. The finding that a vaccine prepared from strain T928 did not afford an acceptable protection against challenge with strain K17 indicates a variable expression among serotype 5 strains of the antigenic determinants which induce protective immunity against A. pleuropneumoniae infection.     

The use of a selective medium in the growth-agglutination test for chronic Erysipelothrix insidiosa infections in swine

The use of a phosphate-buffered horse-meat infusion broth (pH 7.8) containing neomycin sulphate 50 pg/ml, kanamycin 400xg/ml and vancomycin 25 pg/ml was compared with the medium without antibiotics in the E. insidiosa growth-agglutination test on sterile and contaminated, positive and negative swine and rabbit serums.The addition of the inhibitory agents to the medium caused no visible growth depression on the 2 antigen strains employed — regardless of the percentage (S 40 %) of specific hyperimmune serum content.The use of the selective medium in testing hyperimmune serum revealed no significant difference in the recorded antibody titer as compared to the ordinarily used medium. The presence of some contaminants in the agglutinating system did not influence the results — provided that the multiplication of these organisms was inhibited (Table 1).The inhibitory efficiency was tested on 161 contaminated sw’ine serum samples and on 12 contaminated rabbit serums. None of the selective broth dilutions of these serums showed multiplication of contaminants during a 24 hrs. preincubation period or in a control tube after 48 hrs. incubation.The inhibitors allow bacteriologic aseptic technique in the procedure of the growth-agglutination test to be deviated to a certain limit. This limit was not exceeded in this material by applying a serum dilution technique otherwise used in agglutination tests with killed antigen.As the described method eliminates the demand of complete aseptic bleeding and serum preparation procedures or an elaborious sterile filtration procedure, and since the test can be used by any laboratory without previous preparation and testing of a killed antigen, the growth-agglutination test is recommended as a fast and reliable aid in the differential diagnosis of erysipelas arthritis on herd basis in swine.     

An evaluation of selected screening tests for bovine paratuberculosis.

The objective of this study was to evaluate the performance of the lipoarabinomannan antigen enzyme-linked immunosorbent assay (LAM-ELISA), carbohydrate antigen complement fixation (CH-CFT), and protein D antigen agar gel immunodiffusion (D-AGID) tests for bovine paratuberculosis, relative to histopathology, and to culture and isolation of Mycobacterium paratuberculosis from tissues and feces. Samples for test evaluation were collected from four sources including blood and tissues from 400 cull cows at three abattoirs in Ontario, blood and feces from a paratuberculosis survey of cattle from 120 dairy farms in Ontario, a serum bank containing samples from cattle from Ontario and Québec, and a bank of sera from cattle from Pennsylvania and the northeastern United States. The data were analyzed using receiver operator characteristic curves, estimates of relative sensitivity and specificity, and kappa statistics of agreement between tests. The LAM-ELISA performed significantly better than both the CH-CFT and the D-AGID tests. The LAM-ELISA was better at predicting fecal shedding status than tissue infection. However, the LAM-ELISA also had limitations. When interpreted as positive or negative (+/-), at a critical optical density of 0.675, its sensitivity and specificity relative to bacteriology were 49% and 87% respectively. Although the serological tests examined in this study provided some information, they did not predict well the infection status of individual animals.