In situ hybridization analysis of ovarian prostaglandin endoperoxide synthase mRNA throughout the periovulatory period of the ewe.

Cellular alterations in level of expression of mRNA encoding for prostaglandin endoperoxide synthase were quantified within ovarian tissues of sheep obtained before, during and after induction of the preovulatory surge of LH and ovulation with LHRH. This was accomplished by isotopic in situ hybridization using a selective cRNA probe to ovine prostaglandin endoperoxide synthase mRNA. A significant elevation in mRNA was detected within the theca interna of the preovulatory follicle at 8, 16 and 24 hr following administration of LHRH. Very close to the time of ovulation (ie., at 24 hr post-LHRH) a marked rise in mRNA was observed in association with epithelial cells covering the apical surface of the follicle. Ovarian cyclooxygenase metabolites of arachidonic acid produced during the ovulatory process in the ewe originate within the thecal layer and germinal epithelium of the follicle destined to ovulate.     

Exposure of Ankole and crossbred cattle to theileriosis in Rwanda

Summary Susceptible Ankole (Sanga:Bos indicus/Bos taurus) and crossbred Ankole x Jersey (B. taurus) and Ankole x Sahiwal (B. indicus) cattle derived from a farm in Rwanda with no recent history of theileriosis, were infected withTheileria parva stocks from Rwanda either by feeding infectedRhipicephalus appendiculatus ticks on the ears, inoculation of tick derived stabilate or natural exposure to tick challenge. The Ankole cattle originated from local stock born and bred in East Coast fever (ECF) endemic areas of Rwanda. Disease, followed by spontaneous recovery, was observed in 49 of the 72 Ankole cattle after infection withT. parva (68%); the other 23 animals (32%) died of ECF. In contrast 21 of the 33 infected crossbred cattle (64%) died of ECF. It is concluded that the partialTheileria tolerance of the Ankole is, to a great extent, genetic. The basis of this partial tolerance seems to be their ability to limit the explosive multiplication of macroschizonts during the acute phase of the disease.

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Resumen Se infectó ganado Ankole susceptible (Sanga:Bos indicus/Bos taurus) y ganado cruzado Ankole x Jersey (Bos taurus) y Ankole x Sahiwal (Bos indicus) proveniente de una finca en Rwanda sin historia reciente de theileriosis, conTheileria parva procedente de Rwanda, mediante la adhesión en la oreja deRhipicephalus appendiculatus infectado, inoculación de estabilados derivados de garrapatas, o exposición natural a la enfermedad a través del vector. El ganado Ankole era originario de un área endémica de theileriosis en Rwanda. Se observó la enfermedad seguida de recuperación, en 49 de 72 animales Ankole infectados conT. parva (68%); los otros 23 animales murieron (32%). En contraste, 21 de los 33 animales cruzados infectados (64%), murieron. Se concluye, que la tolerancia parcial del ganado Ankole es de origen genético. Las bases de ésta tolerancia genética, parece debida a la habilidad para limitar en cierto modo la multiplicación explosiva de macroesquizontes, durante la fase aguda de la enfermedad.

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Résumé On a infecté du bétail sensible, de race Ankolé (Sanga:Bos indicus/Bos taurus) et des croisés Ankolé x Jersey (B. taurus) et Ankolé x Sahiwal (B. indicus), provenant d'une ferme au Rwanda sans cas récents de theilériose, avec des souches deTheileria parva du Rwanda, par l'application de tiques (Rhipicephalus appendiculatus) infectées sur les oreilles, par inoculation de stabilat de tiques infectées ou par l'exposition à un challenge naturel de tiques. La souche d'Ankolé était originaire du cheptel local Rwandais, né et élevé dans les régions où la theilériose est endémique. La maladie suivie par la guérison spontanée fut observée dans 49 des 72 Ankolés (68%), les autres 23 animaux (32%) ont succombé à la theilériose. Par contre 21 des 33 croisées infectées (64%) ont succombé à la theilériose. Nous concluons que la tolérance partielle des Ankolés contre la theilériose, est génétique. La base de cette tolérance semble être leur capacité de limiter la multiplication explosive des macroschizonts pendant la phase aigu de la maladie.

     

Isolation and purification of a diagnostic antigen for bovine cysticercosis by hydrophobic chromatography

An ammonium sulfate fraction of Taenia hydatigena cyst fluid (ThFAS) was further fractionated by hydrophobic interaction chromatography, using alkylagarose and omega-amino alkylagarose columns, in an effort to isolate and purify a specific diagnostic antigen in the ThFAS preparation. The less than 12 kDa antigen was found to have an affinity for immobilized alkanes with chain length of six carbons or greater. The antigen was recovered in an ethylene glycol eluate from a hexylagarose column then analyzed by Western blot; it reacted with bovine and human cysticercosis infection sera and with specific monoclonal antibodies but not with control sera or fascioliasis infection sera. When the eluate was used as coating antigen in a plate ELISA assay no false positive reactions were seen in sera from cattle infected with Fasciola hepatica; false positive reactions were observed for the unfractionated ThFAS antigen preparation.     

Importance of Some Biochemical Parameters in the Quality and Yield of Rapeseed (Brassica napus L.)

Samples of rapeseed from three Italian growing environments (Bologna, Perugia and Palermo) were analysed for glucose content and dry weight of 1000 seeds every three or four days starting from the end of flowering until complete ripening. In addition, the content of oil, soluble and total proteins, glucosinolates and myrosinase activity was determined in samples of mature seeds. The cultivars used were jet Neuf and Lingot (type 0) and Tandem, Jade and Santana (type 00). From the results it emerged that the point of intersection of the two branches of the linear regression plots for different glucose-consumption kinetics found during seed filling, in addition to being strongly affected by the climate of the test environment, is correlated with quantitative and qualitative production, independently of the genotype.     

山羊脑灰质软化症和李氏杆菌病的区别及防治方法

山羊脑灰质软化症 (ＰＯＬＩＯＥＮ ＣＥＰＨＡＬＯＭＡＬＡＣＩＡ)和李氏杆菌病 (ＬＩＳ ＴＥＲＩＯＳＩＳ)是症状相似治疗方法截然不同的两种疾病。山羊饲养者和兽医工作者必须从两种疾病的细微差别中进行鉴别 ,以便正确治疗和处理病羊。多数情况下 ,这两种疾病出现在饲养条件比较好、但饲养方法不当的地方。特别是在快速育肥时。精饲料喂量过多 ,而含粗纤维的饲料喂量过少是诱发两种疾病的重要因素。突然更换饲料常常导致此病突然发作。脑灰质软化症 (通常又称为大脑皮层坏死症 )是缺乏硫胺 (即维生素Ｂ1)而造成的一种代谢性疾病。瘤胃环…     

Immunohistochemical detection of scrapie prion proteins in clinically normal sheep in Pennsylvania.

Following diagnosis of scrapie in a clinically suspect Suffolk sheep, 7 clinically normal flockmates were purchased by the Pennsylvania Department of Agriculture to determine their scrapie status using an immunohistochemical procedure. Two of the 7 euthanized healthy sheep had positive immunohistochemical staining of the prion protein of scrapie (PrP-Sc) in their brains, nictitating membranes, and tonsils. The PrP-Sc was localized in the areas of the brain where, histopathologically, there was neurodegeneration and astrocytosis. The PrP-Sc occurred within germinal centers of the affected nictitating membranes and tonsils and was located in the cytoplasm of the dendrite-like cells, lymphoid cells, and macrophages. These results confirm that immunohistochemical examination of the nictitating membrane can be used as a screen for the presence of scrapie infection in clinically normal sheep at a capable veterinary diagnostic laboratory. In sheep with a PrP-Sc-positive nictitating membrane, the diagnosis of scrapie should be confirmed by histopathology and immunohistochemical examination of the brain following necropsy. Following full validation, immunohistochemistry assays for detection of PrP-Sc in nictitating membrane lymphoid tissues can improve the effectiveness of the scrapie control and eradication program by allowing diagnosis of the disease in sheep before the appearance of clinical signs.     

Antibody directed against Marek's disease-associated tumor surface antigen can be eluted from Marek's disease tumor cells.

Antibody directed against Marek's disease-associated tumor surface antigen (MATSA) was eluted from tumor cells of lymphomas and peripheral blood lymphocytes that were isolated from Marek's disease virus-infected chickens. Feather follicular Marek's disease virus (MDV) antigen could not be demonstrated with this antibody by indirect immunofluorescent (IF) staining. Monoclonal antibody directed against MATSA could completely block the activity of eluted antibody and vice versa. By indirect IF staining using eluted antibody and fluorescein isothiocyanate (FITC) labelled antichicken globulin conjugate. MATSA-bearing cells were detected in MDV infected and herpes virus of turkey (HVT) vaccinated birds. Blocking of immunoglobulin molecules present on B-cells by anti-chicken globulin is critical in this test.     

Ⅱ型猪环状病毒是断奶后全身消耗性综合征的致病因子

Ⅱ型猪环状病毒 (PCV2 )现已被证明是断奶后全身消耗性综合征 (PMWS)的致病因子 ,这一综合征是一种可造成世界各地严重经济损失的猪病。最近的研究还证实此病毒与加拿大和欧洲猪群的繁殖障碍有关。但是 ,绝大多数PCV2感染都是亚临床性的。刺激仔猪免疫系统是感染此病毒后产生临床疾病的重要因子吗 ?     

Effects of monensin on Mg, Ca, P and Zn metabolism and tissue concentrations in lambs

A study consisting of two trials was conducted to determine the effects of monensin on the apparent absorption and retention of magnesium (Mg), phosphorus (P), calcium (Ca) and zinc (Zn) and to determine mineral changes in tissue and ruminal fluid. Eight lambs (39 kg) were used in trial 1, and 10 lambs (37 kg) were used in trial 2. Animals were blocked by weight and fed a high concentrate diet with or without 20 mg/kg monensin. Trials began with a dietary adjustment period lasting 18 d in trial 1 and 21 d in trial 2. Animals were then placed in metabolism stalls for a 10-d stall adjustment period followed by a 12-d collection period. Collections to determine mineral balance were made during the first 10 d of the collection period. Blood and ruminal fluid samples were taken on d 11 of the collection period. Lambs were slaughtered on d 12 of the collection period and tissue samples were collected. Monensin supplementation increased (P less than .05) Mg retention 42.0%. Urinary Ca excretion decreased (P less than .05) 60.0% when monensin was fed. Monensin supplementation decreased (P less than .05) liver Ca and bone Ca, 45.5 and 2.9%, respectively. Apparent P digestibility increased (P less than .05) 40.0% and P retention increased (P less than .10) 26.8% due to monensin supplementation. Both apparent absorption and retention of Zn increased (P less than .01) 50.0 and 45.0%, respectively, with monensin supplementation. Ruminal fluid Zn concentrations decreased (P less than .05) 33.0% with the addition of monensin.(ABSTRACT TRUNCATED AT 250 WORDS)