Bacterial leaf streak or black chaff of cereals

The literature related to bacterial leaf streak of cereals, due to various pathovars of Xanthomonas campestris , is confusing and dispersed. This review presents a synthesis of the knowledge that has been accumulated on the disease in cereals since the early reports on barley and wheat. The aim is to present the current status on geographical distribution of the disease, to explain possible confusions in symptoms, and to show the limited quantitative information available on losses and on host/pathogen interactions. Disease etiology and means of control are also reviewed. The objective is to define the present situation of black chaff in wheat, barley and triticale, and to delineate the major research needs in these crops. Difficulties in controlling bacterial leaf streak arise as a result of limited epidemiological knowledge and of the absence of satisfactory seed treatment permitting the eradication of the bacterium. There is an urgent need for a seed certification scheme and for more information on genetic resistance, with a view to limiting outbreaks of this sporadic but devastating disease.     

Skeletal muscle characteristics in young trained and untrained standardbred trotters.

Muscle biopsies were taken from the middle gluteal muscle of 28 Standardbred trotters, 3-4 years of age. The 13 horses in Group T were trained consistently from 18 months of age, whereas the 15 horses in Group UT were not exposed to any systematic training before 3 years of age. Group T horses had a lower percentage of Type IIB fibres (31%) than did Group UT horses (39%). Citrate synthase (CS) activity, representing oxidative capacity, was higher in Group T (72 mmol kg-1 min-1) than in Group UT (47 mmol kg-1 min-1). Biopsies were taken from 4 horses in each group when they were foals and then annually until 3-4 years of age. Results from this study indicate that regular training of Standardbreds from 18 months of age resulted in increased CS activity and a decrease in the percentage of Type IIB fibres. This study shows that training, not growth, is the main factor that induces a high oxidative capacity and a high Type IIA/IIB fibre ratio in muscle of Standardbred trotters.     

Radiological assessment of 50 cases of incisive or maxillary neoplasia in the dog

This paper reviews the radiological features of 50 canine incisive or maxillary tumours and discusses the value of radiological assessment in the diagnosis and staging of these tumours. The 50 tumours examined included 21 sarcomas, 15 carcinomas, three melanomas and an assortment of benign tumours of the oral cavity. There was not any site specificity for the different histological tumour types within the upper dental arcade, although fibrosarcomas had a tendency to be maxillary whereas the squamous cell carcinomas were equally distributed between the incisive and maxillary regions. Seventy-eight per cent of fibrosarcomas, 82 per cent of squamous cell carcinoma and all three melanomas examined showed radiological evidence of bone involvement. Radiographic changes were also seen in the benign tumours. The pattern of growth of tumours correlated with the radiological changes observed. Malignant tumours showed a tendency to irregular or aggressive bone loss whereas bone production predominated in the benign tumours.     

Seroprevalence of porcine and human influenza A virus antibodies in pigs between 1986 and 1988 in Hassia

1,268 sera collected from slaughtered pigs in Hassia (FRG) from 1986 to 1988 were tested for antibodies against porcine and human influenza A virus strains using the single radial haemolysis test (SRHT). Antibodies against the porcine strains (subtype H1N1) A/Swine/Arnsberg/1/81, A/Swine/Iowa/15/30 and A/New Jersey/7/76 were detected in 411 (32.4%), 318 (25.1%) and 304 (24.0%) of sera, respectively. Up to 1988 a slight increase (10%) in the seroprevalence to A/Swine/Arnsberg/1/81 was noticed, whereas the results obtained with the other strains showed little variation. Antibodies against the human H1N1 strain A/Singapore/6/86 were only found in sera collected 1987 and 1988 in rates of 1.6% and 3.0%. Serological indication of infections with the human H3N2 strains A/Victoria/1/75, A/Hong Kong/1/68 and A/Philippines/2/82 could be shown in 286 (22.6%), 178 (14.4%) and 135 (10.6%) of the serum samples. Within the three year period the rate of sera positive for antibodies against A/Philippines/2/82 increased from 6.5% to 23.0%, whereas no variation in the rates were found using the other H3N2 strains. Antibodies simultaneously against porcine (H1N1) and human (H3N2) virus strains were detected in 9.9% of all sera tested.     

An unusual tumor of the nictitating membrane gland of dogs-- a case report]

A tumor of the third eyelid gland was diagnosed in a 13 year old female Chihuahua. Histopathology of the excised tissue revealed an apocrine adnexoma with squamous metaplasia. The literature regarding prolapse and tumors of the third eyelid gland was reviewed. No case with similar morphology to this tumor was described to our knowledge.     

Ionized calcium concentration in horses with surgically managed gastrointestinal disease: 147 cases (1988-1990).

Packed cell volume, total plasma protein, serum sodium, potassium, and ionized Ca2+ concentrations, and blood pH were determined at the time of admission and following surgery in 147 horses with acute abdominal crisis. Horses were allotted to 3 categories on the basis of the surgical lesion: (1) nonstrangulating obstruction of the ascending or descending colon (category A, n = 76), (2) strangulating and nonstrangulating infarction of the cecum or ascending colon (category B, n = 37), and (3) strangulating and nonstrangulating infarction of the small intestine (category C, n = 25). Horses with low serum ionized Ca2+ concentration following surgery were given 23% calcium gluconate (100 to 300 ml) IV to effect, and ionized Ca2+ concentration was determined following treatment. The serum ionized Ca2+ concentrations of horses in categories A, B, and C before and after surgery were lower than our normal laboratory reference range. Prior to surgery, serum ionized Ca2+ concentration measured from horses in category B and C was lower than that in horses in category A. There was no difference in ionized Ca2+ concentration in serum samples obtained before surgery in horses from category B and C, and in serum samples obtained following surgery. There was a decrease in ionized Ca2+ concentration during surgery in horses in category A. There was no change between preoperative and postoperative ionized Ca2+ concentration in the samples obtained from horses in category B and C. After calcium gluconate administration, all horses with low serum ionized Ca2+ after surgery had concentrations within our normal range. Measurement of serum ionized Ca2+ in horses with an acute abdominal crisis is recommended.(ABSTRACT TRUNCATED AT 250 WORDS)     

Progressive Dermal Collagenosis of Male Miniature Swine

Abstract— A unique dermatosis of male miniature swine is described. The disease occurs in post-pubertal pigs, and is characterized by symmetrical, indurated, plaques over the truncal region. Histologically, the dermis and panniculus are effaced by thick, interwoven bundles of collagen resulting in an absence of deep dermal elastin. Hypertrophy and hyperplasia of superficial dermal vessels, fibroblasts and fibrocytes are accompanied by perivascular infiltrates of lymphocytes, plasma cells and eosinophils. The pathogenesis of this unusual dermatosis, designated as “progressive dermal collagenosis of male miniature swine” is unknown. Résumé— Une dermatose originale du cochon nain mâle est décrite. La maladie apparait chez des cochons post pubertaires, et est caractérisée par des plaques sur le tronc, indurées et symétriques. Histologliquement, le derme et le pannicule sont envahis par d‘épais falsceaux de collagène, entrainant l'absence d’élastine dermique. Les vaisseaux du derme superficiei sont hyperplasiés et hypertrophiés, des fibroblastes et des fibrocytes sont accompagnés d'un infiltrat inflammatoire périvasculaire de lymphocytes, éosinophiles et plasmocytes. La pathogénie de cette affection peu commune, appelée “collagénose dermique progressive du cochon nain mâle” est inconnue. Zusammenfassung— Es wird eine einzigartige Hauterkrankung beim männlichen Miniaturschwein beschrieben. Die Krankheit tritt bei postpubertären Schweinen auf und wird durch symmetrische, indurierte Plagues im Rumpfbereich gekennzeichnet. Histologisch treten Dermis und Pannikulus gegenüber dicken, verflochtenen Kollagenbündeln in den Hintergrund, wodurch das tiefe, dermale Elastin verschwindet. Die Hypertrophie und Hyperplasie der oberflächlichen Hautgefäße, Fibroblasten und Fibrozyten wird von perivaskulären Infiltraten aus Lymphozyten, Plasmazellen und eosinophilen Granulozyten begleitet. Die Pathogenese dieser ungewöhnlichen Dermatose, die als “progressive dermale Kollagenose des männlichen Miniaturschweins” bezeichnet wird, ist unbekannt. Resumen El presente artículo es una descripción de una dermatosis única del macho cerdo miniatura. Le enfermedad aparece después de la pubertad, y se caracteriza por la aparición de placas simétricas sobre la región del tronco. El exámen histológico de la dermis y del tejido panicular revela la presencia de gruesas bandas de colágeno entrelazadas, lo cual tiene como resultado la ausencia de la capa de elastina profunda. La hipertrofia e hiperplasia de los vasos superficiales dérmicos, fibroblastos y fibrocitos, se ve acompañadas de infiltrados perivasculares de linfocitos, células plasmáticas y eosinófilos. La patogénesis de esta rara dermatosis Ilamada ‘colagenosis dérmica progresiva del cardo macho miniatura’, es desconocida.     

Distribution of ASFV antigens in pig tissues experimentally infected with two different Spanish virus isolates.

Lymph nodes, spleen, liver, lung and kidney obtained from pigs experimentally infected with two African Swine Fever Virus (ASFV) isolates of differing virulence were fixed by perfusion with glutaraldehyde and embedded in paraffin. An immunoperoxidase technique using a polyclonal anti-ASFV serum was performed on tissue sections in order to detect ASFV antigen. The distribution of ASFV antigen in such infected organs is shown and the differences between both infections compared and discussed. Monocytes, macrophages, hepatocytes, endothelial cells, neutrophils and epithelial cells were found to contain ASFV antigens.     

Insulin-like growth factor I receptor analysis of satellite cell-derived myotube membranes established from two lines of Targhee rams selected for growth rate

Ovine-derived fibroblasts were used to validate an insulin-like growth factor I (IGF-I) membrane-receptor binding assay system. Competitive binding using fibroblasts revealed that half-maximal inhibition of 125I-IGF-I binding by IGF-I was 2.3 nM. SDS-polyacrylamide gel electrophoresis analysis of specific protein-associated 125I-IGF-I was consistent with the migration of 125I-IGF-I-labeled Type I IGF receptor alpha-subunits at Mr 133,000 daltons. Further, the efficiency of two cell solubilization methods was examined and time-dependent binding equilibrium was determined for the membrane assay system. Satellite cell-derived myotubes were subsequently isolated from primary satellite cell cultures established from the semimembranosus muscles of high and low efficiency-of-gain (EOG) Targhee rams, and IGF-I receptor dynamics were measured. A membrane competitive binding study revealed that half-maximal inhibition of 125I-IGF-I binding was achieved by 1-ng IGF-I for low, and 10-ng IGF-I for high, EOG myotube membrane preparations. Kd values were similar between the high EOG (4.78 nM) and low EOG (2.95 nM) groups; however, receptor concentrations (Bmax) appeared to differ between groups. High EOG membrane receptor Bmax was 3.88 pmole/micrograms protein (19.87 pmole/micrograms DNA), whereas low EOG membrane receptor Bmax was 1.22 pmole/micrograms protein (9.28 pmole/micrograms DNA). These preliminary findings support the hypothesis that genetic selection for EOG results in altered satellite cell responsiveness to IGF-I.