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Biomedical subjects

T M Ellis

Publications and source records attributed to T M Ellis.

At least 127 records · Page 7Linked to original sources

The role of Corynebacterium pseudotuberculosis lung lesions in the transmission of this bacterium to other sheep.

Five groups of 5 shorn and 5 unshorn caseous lymphadenitis (CLA)-free Merino wether weaners were each placed in feedlot pens with 6 Merino ewes, 2 or more of which had CLA lung lesions but no discharging superficial lesions. The sheep were kept together for 5 months. Twenty-eight per cent of the shorn weaners and 20% of the unshorn weaners developed antibodies to Corynebacterium pseudotuberculosis. At slaughter, 8% of the shorn weaners and 12% of the unshorn weaners had CLA lesions in either lungs, lymph nodes or both. In the absence of contact with CLA-infected ewes, a control group of 5 shorn and 5 unshorn weaners failed to develop antibodies to C. pseudotuberculosis or CLA lesions in the same period. This showed that sheep with CLA abscesses in the lungs but no discharging superficial abscesses were a source of C. pseudotuberculosis infection to other sheep.

Animals↗

Evaluation of an enzyme-linked immunosorbent assay for the detection of Corynebacterium pseudotuberculosis infection in sheep.

Two enzyme-linked immunosorbent assays to measure antibody to the cell wall antigen (C-ELISA) and toxin antigen (T-ELISA) of C. pseudotuberculosis were evaluated on serum from 6 separate groups of sheep. For sheep naturally infected with C. pseudotuberculosis the sensitivity and specificity of the C-ELISA was 76% and 73% respectively and for the T-ELISA 67% and 77% respectively. For sheep slaughtered one year after artificial infection the sensitivity of both tests was greater than or equal to 83% and the specificity greater than or equal to 72%. For sheep slaughtered 4 months after artificial infection the specificity of both tests was less than 30% while the mean sensitivity was 85%. The C-ELISA in conjunction with the T-ELISA detected 92% of sheep with lung lesions.

Animals↗

The effect of colostrum-derived antibody on neo-natal transmission of caprine arthritis-encephalitis virus infection.

Two groups of 6 newborn goat kids were artificially fed colostrum containing antibody to caprine arthritis-encephalitis (CAE) virus, obtained from clinically affected does. Kids in group A were fed the colostrum from birth until 7 days of age, while kids in group B were fed colostrum from 1 to 3 days after birth for 7 days. Kids were fed cow's milk at all other times. Serum antibody resulting from the consumption of colostrum, detected by agar gel immunodiffusion (AGID) tests, lasted for up to 8 weeks in group A, but none was detected in group B. Four kids from each group became infected with CAE virus as demonstrated by the emergence of active immunity and by virus isolation procedures. It appeared that uptake of colostral antibody by group A did not prevent viral transmission, interfere with development of active immunity, or modify the outcome of the CAE virus infection.

Animals↗

Emergency preparedness: a survey of dental practitioners.

A total of 6,505 questionnaires were mailed to practicing dentists in Florida and Kentucky. The dentists represented all dental specialties and had been graduated from 72 different dental schools. The results of the survey indicate that improvement is needed in training, office organization, and advanced preparation for the emergency management of patients. The results also indicate that dentists encounter many medical emergencies in their offices.

Dental Care↗

Characteristics of cell fusion induced by a caprine retrovirus.

The mechanism of cell-fusion induced by caprine arthritis-encephalitis virus (CAEV) was investigated. Following infection with concentrated CAEV, cell fusion occurred prior to the production of infectious progeny virus. The time of initial detection of cell fusion was dependent on the multiplicity of infection and was not detected until 5 hours after infection. The virus-induced cell fusion was only partially inhibited by ultraviolet irradiation of the virus and was not inhibited by cytosine arabinoside. The results indicated that fusion by CAEV was a slow response to direct interaction of input virus with cells (fusion from without) and that virus replication was not required.

Animals↗

Detection and prevalence of serotypes of feline syncytial spumaviruses.

Three serotypes of feline syncytial virus (FSV) were detected by neutralisation tests: 906, a serotype of low prevalence and 702 and 951 which were serotypes of higher prevalence, between which a minor one-way antigenic difference was detected. Serum antibody in naturally-infected cats in some cases neutralised 951 but not 702 or 906 which suggested that 951 could be considered as a major distinct serotype. An increase in prevalence of antibody to FSV in cats over a 5 year period from 1977-1981 was detected by neutralisation, agar gel immunodiffusion, and fluorescent antibody techniques. Over the 5 year period the prevalence of antibody to the 951 serotype increased and the overall increase in prevalence of antibody to FSV during this period appeared to relate to dissemination of the 951 serotype.

Animals↗

In vitro evidence for defective afferent immune function in long-term renal allograft recipients.

Experiments were designed to evaluate afferent immune functions in 21 long-term (greater than or equal to 3 years) renal allograft recipients by using in vitro assays that included autologous and allogeneic mixed lymphocyte reactions (AMLR and allo-MLR), proliferative responses to a soluble antigen (tetanus toxoid), and the ability to generate cytotoxic T lymphocytes (CTL) following stimulation in an AMLR. The results showed that allograft recipients generated responses in the allo-MLR (means = 84,789 +/- 8242) that were comparable to those exhibited by normal controls (means = 86,082 +/- 7423). Likewise, mean responses in the AMLR were similar in recipients and controls (14,937 +/- 3243 versus 16,101 +/- 3005), although a greater percentage of recipients generated AMLRs below 5000 cpm than did normals (8/21 versus 4/20). However, 13 recipients analyzed for responsiveness to tetanus toxoid were shown to generate mean proliferative responses that were significantly depressed below normal (18,095 +/- 5545 versus 48,935 +/- 8813, P less than 0.001). Furthermore, despite significant proliferation in the AMLR means = 27,648 +/- 5168), 8 recipients generated significantly lower CTL activity in AMLR cultures than normal controls (mean percentage of cytotoxicity = 10.3 +/- 4.7 versus 24.9 +/- 4.7, P less than 0.05). These recipients generated normal CTL levels against allogeneic target cells following stimulation in an allo-MLR. Thus, these studies provide experimental support for the existence of altered T helper cell-mediated functions in long-term renal allograft recipients.

Humans↗

Phospholipid composition of human monocytes and alterations occurring due to culture and stimulation by C3b.

The phospholipid composition of human peripheral blood monocytes has not been previously reported, due to difficulty in isolating these cells in a purified state. In this study, monocytes were purified by counterflow centrifugation without selective adherence, and were characterized with the use of fluorescent monoclonal antibodies to T and B lymphocytes and monocytes by flow cytometry. These platelet-free cell preparations contained less than 5% T cells and less than 3% B cells. Isolated monocytes, which were rapidly frozen after isolation, contained phospholipids (in order of decreasing concentrations) as follows: phosphatidylcholine greater than phosphatidylethanolamine greater than sphingomyelin greater than phosphatidylserine greater than phosphatidylinositol greater than cardiolipin. A small amount of lyso-PC, but no lyso-PE, phosphatidic acid or lyso-PI, was found. The effect of culturing these cells in the presence or absence of a known stimulant of monocyte prostaglandin E and thromboxane release, the C3b fragment of the third component of human complement (C3), was studied with regard to phospholipid composition. Monocytes cultured without stimulant for 24 h contained 3-4% more sphingomyelin than did uncultured cells, and lyso-PC concentrations were consistently elevated. The addition of the stimulant C3b to cultured cells resulted in enhancement of release of immunoreactive prostaglandin E into culture supernatants, without affecting the release of lysosomal enzymes. Analysis of the phospholipid content of cells cultured in the presence of C3b revealed that there was a significant decrease in total PI compared to cells cultured in the absence of C3b, in addition to an increased concentration of sphingomyelin and lyso-PC when compared to freshly isolated cells. These changes occurred in the absence of elevated concentrations of phosphatidic acid.

Acetylglucosaminidase↗

The pathological features of an interstitial pneumonia of goats.

An interstitial pneumonia in goats which predominantly affects the caudal lung lobes is described. It is characterized microscopically by hypertrophy of type 2 pneumocytes, the presence of an abundant eosinophilic, PAS-positive material within alveolar spaces, and a diffuse and focal lymphoid infiltration of alveolar septa. The material present within alveolar spaces is considered to be composed of surfactant and fibrin. Although the aetiology is not known the gross and microscopic appearance suggests that a retro-virus may be involved.

Animals↗

Effects of feeding lupin seed naturally infected with Phomopsis leptostromiformis to sheep and pigs.

Lupin seed, 10% of which was naturally infected with Phomopsis leptostromiformis was obtained from 2 different sources and stored either conventionally, or in a warm and humid environment, for 45 weeks. Only very low levels of toxicity were apparent during the storage period and in the warm, humid environment the level of infection of P. leptostromiformis was gradually reduced and eventually eliminated. The 2 batches of infected seed, and non-infected lupin seed, were fed to sheep as sole rations for 40 weeks, or as part of feedlot rations for 10 weeks, and to baconer pigs as part of grower and finisher rations for 16 weeks. In the 40-week feeding trial mild lupinosis developed in sheep fed from one batch of infected seed, but there was no evidence of lupinosis in sheep fed the feedlot rations, or pigs fed the grower and finisher rations. It is suggested that lupin seed with levels of Phomopsis-infection of up to 10% could be safely fed to sheep and pigs under commercial conditions.

Animal Feed↗

Detection of leptospires in tissue using an immunoperoxidase staining procedure.

An immunoperoxidase technique for the localisation of leptospires in sections of formalin fixed paraffin embedded kidney tissue is described. The procedure utilises a two-layered antibody sandwich with rabbit anti-leptospiral immunoglobin. Using antiserum to specific leptospiral serovars the presence and distribution of specific serovar in the tissue could be determined. The technique was also used to detect leptospires of given serovars in smears made from infected tissues and fluids. There was good correlation between culture results and results of the immunoperoxidase staining method on kidneys infected with leptospires. The diagnostic possibilities of the technique on formalin fixed tissue specimens are discussed.

Animals↗