In vitro studies of Norwegian Red bovine semen immobilized and cryopreserved in alginate solid gel network

Development of new semen cryopreservation techniques improving sperm survival and ensuring availability of viable spermatozoa for a prolonged time‐period after AI is promising tools to reduce sensitivity of timing of AI and enhance overall fertility. The SpermVital^® technology utilizes immobilization of bull spermatozoa in a solid network of alginate gel prior to freezing, which will provide a gradual release of spermatozoa after AI. The objective of this study was to compare post‐thaw sperm quality and in vitro sperm survival over time of Norwegian Red bull semen processed by the SpermVital^® (SV) technology, the first commercialized production line of SpermVital^® (C) and by conventional procedure applying Biladyl^® extender (B). Post‐thaw sperm motility was not significantly different between SV, C and B semen (p > .05). However, sperm viability and acrosome intactness were higher for SV than C and B semen (p < .05). Small differences in DNA quality were observed (p < .05). Sperm viability after storage in uterus ex vivo was higher for SV than for C semen (p < .05). Furthermore, sperm survival in vitro over time at physiological temperature was significantly higher for SV semen than C semen as well as B semen during the incubation period of 48 hr (p < .05). In conclusion, the SpermVital^® technology is improved and is more efficient in conserving post‐thaw sperm quality and results in higher sperm viability over time in vitro for SV than for C and B semen.     

大麦黄矮病毒(BYDV) cDNA的合成、克隆及初步应用

 以大麦黄矮病毒二叉蚜和麦长管蚜专化株的病毒核酸为模板,以小牛胸腺DNA为引物,合成cDNA的第一条链,再用缺口翻译法合成第二条链,然后采用加装BamH₁人工接头的方法将ds-cDNA插入到质粒载体pUC₈中,重组质粒于大肠杆菌JM—83中进行克隆,以克隆的颜色变化选择含有外源DNA的克隆,再用病毒核酸制备的探针筛选真正病毒cDNA插入的克隆。重组质粒中ds-DNA的插入长度在300—1600bp之间。用缺口翻译法制备质粒DNA分子探针检测同源病毒液,反应灵敏度在100pg-1ng之间。应用cDNA探针检测不同病毒和病毒株系,从中筛选出黄矮病毒株系专化克隆系,黄矮病毒专化克隆系和黄矮病毒组专化克隆系.     

Effectiveness of capillary electrophoresis fluoroimmunoassay of blood PrpSc for evaluation of scrapie pathogenesis in sheep.

Management of prion diseases in livestock would benefit greatly from availability of a validated blood test. A promising immunocapillary electrophoresis technique (also known as capillary electrophoresis fluoroimmunoassay) to detect abnormal prion protein in blood from live sheep is evaluated here. Capillary electrophoresis fluoroimmunoassay was applied to analysis of extracted blood from scrapie-exposed sheep (n = 87; 347 samples) at various stages of incubation, and to control sheep (n = 194; 489 samples). Overall, test values for the control and test populations were not significantly different, and a similar proportion of control (7%) and test (10%) sheep were classified as positive. Over 2-3 month intervals from birth until clinical disease, test specificity and sensitivity ranged from 66.7% to 100% and 0% to 66.7%, respectively, indicating poor diagnostic performance at all stages of pathogenesis. In routine application, in its present form, the capillary electrophoresis fluoroimmunoassay procedure proved to be insufficiently robust for use as a blood test for scrapie diagnosis.     

Phenotypic and histological expression of different genetic backgrounds in interactions between lettuce, wild Lactuca spp., L. sativa × L. serriola hybrids and Bremia lactucae

Phenotypic and histological responses of cultivated lettuce (Lactuca sativa) and wild relatives L. saligna, L.␣virosa as well as interspecific crosses derived from L. sativa × L. serriola to two races of Bremia lactucae (CS2, CS9) were investigated. With the exception of L. sativa genotypes, all accessions and hybrids expressed incomplete or complete resistance to both pathogen races, with slight differences at seedling and adult plant stages, respectively. Histological features of the interactions (development of pathogen infection structures and host hypersensitive response to attempted infection) were studied on leaf discs 48 h after inoculation. Interactions with similar phenotypic expression of resistance were characterized by significant variation in rate of development of pathogen infection structures and hypersensitive reactions. Differences found within eight Lactuca spp. accessions and hybrids challenged by two distinct pathogen races are interpreted and discussed.     

The Urinary Excretion of Riboflavin by the Cat

Abstract— The daily riboflavin excretion of five adult cats has been studied for periods ranging from 7 to 11 days. The cats were housed in metabolism cages and were provided with a diet of cooked rabbit meat, wholemeal bread and water. The total amount of riboflavin excreted does not appear to be related to the dietary intake. The concentration of riboflavin in the urine does appear to be characteristic for a given cat under our experimental conditions.
Résumé— L'excrétion quotidienne de riboflavine chez cinq chats adultes a étéétudié pendant des périodes allant de 7 à 11 jours. Les chats étaient casés dans des cages à métabolisme et recevaient un régime de viande de lapin cuite, de pain entier et d'eau. La quantité totale de riboflavine excrétée ne semble pas être en rapport avec la quantité ingérée. Dans les conditions expérimentales que nous avons utilisées la concentration urinaire de riboflavine parait caractéristique pour un chat donné.
Zusammenfassung— In einer von 7 bis zu 11 Tagen reichenden Zeitspanne wurde untersucht, wieviel Laktoflavin fünf ausgewachsene Katzen täglich ausscheiden. Die Katzen wurden in Käfigen untergebracht, in denen der Stoffwechsel ständig überprüft werden kann, und sie wurden mit einer aus gekochtem Kaninchenfleisch, Vollkornbrot und Wasser bestehenden Diät gefüttert. Die Gesamt-menge des ausgeschiedenen Laktoflavins scheint in keiner Beziehung zu der Nahrungsaufnahme zu stehen. Die Konzentration des Laktoflavin im Urin scheint für eine unter unseren Versuchs-bedingungen stehende Katze charakteristisch zu sein.     

Effects of the needle bladder rust (Chrysomyxa rhododendri) on Norway spruce: implications for subalpine forests

Norway spruce trees in the subalpine forests of the European Alps are frequently attacked by the needle rust Chrysomyxa rhododendri. The obligate parasite undergoes a complex life cycle with a host shift between rhododendrons (Rhododendron sp.) and Norway spruce [Picea abies (L.) Karsten] and causes a yellowing and defoliation of the current-year needles in summer. Infected trees show several anatomical, morphological and physiological modifications, including a decrease in pigment content and net photosynthesis of infected needles, lower biomass production and reduced radial and height growth. The consequences are diminished timber yield and cripple growth. Because of repeated heavy infections in recent years, forest managers report increasing difficulties in both natural regeneration and afforestation at high elevation sites, where rhododendrons occur. This review gives a summary of the present knowledge about the effects of C. rhododendri infections on Norway spruce, including so far unpublished findings and with particular attention to the phenomena of resistant trees. Implications for subalpine forests and counter strategies are discussed.     

Uniaxial compression of rotationally symmetric Norway spruce samples: surface deformation and size effect

The influence of size on strength is well known for various materials and testing methods, but not enough data and knowledge of the effect on wood under compressive strength can be found. Therefore, the deformation and compressive strength of hyperboloid Norway spruce samples were tested for different dimensions. To determine the influence of size on the strength, three different approaches were used: “weakest link theory”, “size effect law” and “multifractal scaling law”. Of the three scaling theories, the “size effect law” and the “weakest link theory” predicted the effect well. Additionally, to determine the surface deformation of various samples, DIC3D was used on the largest sample geometry. The experiments show the existence of a possible size effect during compression, while digital image correlation illustrates the expected differences in deformation due to the shape and dependence of the strain distribution on the structure of wood. Additional experiments are proposed to further verify the observed effects and expand the knowledge of the size effect.