Pathological changes in the lumbar spine of pigs: gross findings.

The lumbar vertebral columns from 60 sows and 30 slaughter weight pigs were examined grossly for pathological changes. Asymmetry of lumbar articular facets and minor periarticular osteophytes were seen in the slaughter weight group. Degeneration of intervertebral discs or vertebral osteophytes were not present. In contrast, 38% of 60 sows had vertebral osteophytes and 40% had degeneration of intervertebral discs. Extensive ankylosing spondylosis was present in two sows. Other vertebral lesions observed in sows include asymmetry and arthrosis of articular facets, fissures and areas of cavitation in the annulus fibrosus and vertebral end plate, and vertebral osteomyelitis and/or vertebral fracture. Extravertebral skeletal lesions, some of which could be related to a clinical history of lameness or posterior paralysis, include sacroiliac arthrosis, pelvic deformity, polyarthritis, femoral osteomyelitis, sacroiliac dislocation and epiphyseolysis involving the femoral head or tuber ischii.     

Investigation into the pathogenesis of Atrophic Rhinitis in pigs

Summary

In two groups of swine herds, herds with and without clinical AR the presence of Atrophic Rhinitis (AR) correlated with the presence of toxinogenic Pasteurella multocida (PM) and not with the Bordetella bronchiseptica (BB) infection.

Six BB‐ and eighteen PM‐strains have been investigated for AR pathogenicity. Broth cultures were injected intradermally in guinea‐pigs (GPST) orintranasally in 3‐week‐old colostrum deprived specific pathogen free (SPF) piglets.

The average atrophy of the ventral conchae (A VC) correlated with the GPST in 4BB‐ and 7 PM‐strains. One BB‐ and 2 PM‐strains were qualified as doubtful, the others as non‐AR pathogenic. With AR pathogenic BB‐ and PM‐strains clinical AR could be induced in 3‐ and 6‐week‐old piglets. AVC lesions (gradation> 1) could be induced with BB in piglets of 6 and with pathogenic PM in 16‐week‐old piglets. Six of seven AR pathogenic PM‐strains resembled Carter‐type D and one resembled type A. No significance was found between AR pathogenicity and somatic serotypes.

Intranasal instillations of cell‐free broth culture filtrates of AR pathogenic PM‐strains also caused AR in piglets. These filtrates also caused lethality in piglets and in mice lethalitytest (MLT) and induced a positive GPST. After heating the pathogenic effects of the filtrates disappeared. The name AR toxin has been introduced for this thermolabile, haemorrhagic dermonecrotic (HDNT) fraction of the AR inducing filtrates. The severity of the AR lesions depended on the amount of the AR toxin intranasally instilled in pigs.

Cross protecting antibodies obtained in rabbits against the AR toxins of two PM strains could be demonstrated by a toxin neutralisation test in the MLT and the GPST.

Broth cultures were injected intradermally in guinea‐pigs (GPST) or intranasally in 3‐week‐old colostrum deprived specific pathogen free (SPF) piglets.     

Canine atopic disease: investigations of eosinophils and the nasal mucosa

Blood eosinophil counts were comparable in dogs with and without canine atopic disease. Eosinophils were not observed in the nasal smears of any of the dogs studied. Of 46 dogs with atopic disease, a significant increase (P less than 0.001) in nasal airway resistance was observed in 2 dogs after nasal provocation with nebulized allergens of grasses and in 1 dog after provocation with summer weed extracts.     

Pseudorabies virus infections in explants of porcine nasal mucosa.

The spread of infection and the morphogenesis of three pseudorabies virus strains were studied in explants of porcine nasal mucosa. Virulent NIA-3 virus was compared with a deletion mutant 2.4N3A, and with a non-virulent Bartha virus. All three virus strains infected nasal epithelial cells. NIA-3 virus particles were enveloped mainly at the inner nuclear membrane; the virus rapidly invaded the stroma, causing widespread necrosis. In contrast, 2.4N3A virus particles were enveloped mainly at the endoplasmic reticulum and the infection spread more slowly. Bartha virus particles were enveloped mainly at the endoplasmic reticulum; the infection spread slowly and remained restricted to the epithelial cells. In situ DNA hybridisation showed an accumulation of Bartha virus DNA in the nucleus 24 hours after inoculation. In nasal mucosa viral virulence seemed directly related to the speed of replication and release of virus from infected cells.     

A method for the collection of nasal epithelial cells and secretion from domestic animals.

A method for aspirating nasal and genital epithelial cells and secretion using a vacuum pump is described. The samples obtained are suitable for diagnosis of infectious diseases by isolation of bacteria and viruses and by demonstration of the organisms by immunofluorescent techniques.     

A method for bronchoalveolar lavage in live pigs

In order to isolate porcine alveolar macrophages and to quantitatively study the components of recovered lung fluid, a bronchoalveolar lavage technique in living pigs was developed. Lung lavage was performed after introducing a catheter through the mouth via the trachea in the diaphragmatical lobe. Thirty ml of phosphate-buffered saline (PBS) was introduced into the lung and the fluid was aspirated after one minute. Following this, another 15 ml of PBS was introduced into the lung and aspirated after one minute. The recovered volume of the second lavage averaged 15 ml (+/- 0.4 S.E.M.). Cells thus obtained from specific-pathogen-free (SPF) pigs were composed of 98% macrophages. Lavage fluids from conventionally bred pigs contained 67% macrophages, 17% neutrophilic granulocytes and about 16% lymphocytes, demonstrated by their morphology and acid phosphatase activity. The viability of the recovered cells was over 98% in both SPF and conventionally bred pigs. The dilution of the aspirated lung liquid was determined by using methylene blue in the introduced fluid. The calculated dilution factor of the recovered lavage fluid was 0.58 (S.E.M. 0.02). No influence was noticed on the number or composition of cells nor on the dilution factor when lung lavage was done in SPF pigs twice a week during a four week period. The protein concentration in lavage fluid from SPF pigs was 142 (SD +/- 26) mcg/ml. In conventionally bred pigs, however, a wide variation (276 +/- 229 mcg/ml) in protein content was noted. Lavage fluid supernatant of some animals had a bactericidal effect on Haemophilus pleuropneumoniae strain 13261, whereas no bactericidal effect was noted in other lavage samples.     

A novel method for lifting weanling research pigs

It is possible to modify lifting techniques in small laboratory pigs to evoke less of a fear response, strengthen the human–animal bond, and improve welfare. The authors hypothesized that recently weaned pigs lifted with a ventral (belly) scoop method would show less fear of new humans and less fear during treatment than pigs lifted vertically by their hind limbs. To evaluate this hypothesis, 32 Yorkshire-cross pigs (age 3 weeks) were divided into 8 groups of 4. All pigs were acclimated to humans for 11 days and uniformly enriched prior to any lifting tests. Pigs were randomly assigned to 1 of 4 different combinations of ventral and/or vertical lifting techniques that varied by consecutive day (1 ventral-ventral; 2 ventral-vertical; 3 vertical-ventral; 4 vertical-vertical). Each day, data were collected regarding pigs’ aversion to lifting and willingness to be caught multiple times. Two hours later, their time to approach a new person and proportion of time spent hiding from the new person were also measured. Aversion scores were assigned based on duration of squealing, shaking, and freezing responses during lifting. Pigs that were lifted using alternate methods on consecutive days showed significantly less aversion when being scooped ventrally (P = 0.008) as compared to lifted vertically by their hind limbs. Additionally, behavioral trends were identified during the study. Based on standardized aversion scores, this research shows that the ventral scoop method induces less fear than the vertical lift method.     

Immunohistochemical detection of canine distemper virus in haired skin, nasal mucosa, and footpad epithelium: a method for antemortem diagnosis of infection.

A reliable antemortem diagnostic method is needed for determining infection with canine distemper virus (CDV). The utility of immunohistochemical detection of CDV antigen was examined was examined for samples of nasal and footpad epithelium and haired skin in dogs with and without detectable CDV antigen in the lung and/or brain. Tissues from 57 dogs at risk of CDV infection were tested. Viral antigen was found in the lung and/or brain of 28 dogs. Among these dogs, viral antigen was demonstrated in the epithelial cells of the nasal mucosa in 24 of 27 dogs, in the footpad epithelium in 24 of 26 dogs, and in the haired skin of the dorsal neck in 26 of 27 dogs. Among the 29 dogs without CDV antigen in either the lung or brain, 1 dog had positive staining for viral antigen in the skin and nasal mucosa. Biopsies of haired skin of the dorsal neck, which is relatively simple to sample, can be used for immunohistochemical testing for acute and subacute infection with CDV.     

Avian tibial dyschondroplasia: a comparison of the incidence and severity as assessed by gross examination and histopathology.

The assessment of avian tibial dyschondroplasia (TD) in many recent studies is based on examination of slices of the proximal tibiotarsus with the naked eye. This study examines the incidence and severity of TD in broilers under four different dietary regimes and compares the efficacy of naked eye assessment with histopathological examination. The diets contained reduced levels of calcium relative to phosphorus with adequate (diet 1) and high (diet 2) levels of vitamin D3 supplementation; a very low calcium diet (diet 3) and a standard diet (diet 4) were also included. Gross examination suggested that TD was present in 80 per cent, 79 per cent and 27 per cent of tibiotarsi from birds on diets 1, 2 and 4, respectively. However, histological examination indicated TD, correspondingly, to be present in 18 per cent, 39 per cent and 6 per cent of tibiotarsi. Some birds on diet 1 exhibited physeal changes consistent with mild hypocalcaemic rickets. Many of the bone extremities which, grossly, were considered dyschondroplastic (diets 1, 2 and 4), histologically were shown to have an extensive hypertrophied zone with poor metaphyseal vessel penetration, but no cellular or matrix changes consistent with TD. This cast doubt on the validity of earlier studies of TD which relied solely on naked eye examination. The birds on diet 3 all demonstrated histopathology considered consistent with severe hypocalcaemic rickets and the present study suggests that in three-week-old broilers a moderately hypocalcaemic diet with a high level of vitamin D3 will not cause rickets but will increase the incidence and severity of TD.(ABSTRACT TRUNCATED AT 250 WORDS)     

Epithelium lining the rostral portion of the porcine nasal mucosa

Epithelial tissues from the rostral half of the pig nasal cavity were prepared for light and electron microscopy. The predominant epithelial cell type at the luminal surface was cuboidal with surface microplicae or microvilli and a multilobate nucleus. Pinocytotic vesicles were a common feature of the adluminal cytoplasmic zone of these superficial cuboidal cells. Other cell types included basal cells, intermediate cells and, occasionally, goblet and ciliated cells. Basal cells contained vesicles located adjacent to the basal lamina. This transitional mucosa may be specialised for sampling substances from the luminal surface preliminary to releasing cytokines and, or, presenting immunogens to intraepithelial lymphocytes.     

Rabies virus in the salivary glands and nasal mucosa of naturally infected skunks.

Several salivary glands and the nasal mucosa of rabid skunks (Mephitis mephitis) contained rabies virus. Generally titers were high in the submandibular, moderate in the parotid and low to moderate in the zygomatic, molar and sublingual salivary glands. The nasal mucosa (glands and epithelium) contained virus at low to moderate titers that occasionally were equal to titers in brain.     

Bordetella rhinitis in pigs: serum and nasal antibody response to Bordetella bacterins.

The nasal and serum antibody response of two groups of pigs, vaccinated with adjuvant containing formalinized or sonicated Bordetella bronchiseptica bacterins was compared with the response of a nonvaccinated group. The tube agglutination test was used to determine agglutinin titers. Following vaccination, all pigs were challenged intranasally with the vaccine strain of Bordetella, after which the nasal Bordetella flora of vaccinated and nonvaccinated pigs was investigated. Sera and nasal secretions from both vaccinated groups exhibited markedly higher agglutinin titers than the control group and serum titers were higher than those in nasal secretions. No differences in agglutinating antibody response were evident between the two vaccines. Serum antibody titers exceeded nasal titers and persisted over a longer period of time. Systemic vaccination resulted in an increased nasal clearance of the vaccine strain by the groups of pigs vaccinated with sonicated or formalined bacterin, whereas no such clearance was evident in the nonvaccinated control group.     

A chick growth test for the evaluation of protein quality in cereal-based diets. 2. Comparison of the total protein efficiency method with the gross protein value method

Various protein concentrates have been evaluated by the Gross Protein Value (GPV) method and by the Total Protein Efficiency (TPE) method.

The new method discriminated between the samples better than did the GPV, and correlations between the two tests were significant at the 1 per cent level for leaf protein concentrates and at the 5 per cent level for fish meals.