日粮抗氧化剂减少肉鸡的腹水症

低死亡率和较高的饲料利用率 ,看来是鸡抗氧化状态得到改善的结果。增高日粮维生素E的含量并应用有机硒可减少肺高压 (腹水症 )引起的死亡。     

Diagnosis of mastitis for therapy decisions.

Identifying specific groups of mastitis pathogens by their growth on selective agars can help identify the pathogens that are present in mastitic milk samples. This article addresses issues that are essential in making good use of diagnostic procedures to improve udder health on dairies.     

Synchronization of oestrus with prostaglandins

Luteolytic doses of the Tham salt of PGF₂ or one of its synthetic analogues cause premature regression of, the corpus luteum between the 5th and the 16th day of the oestrous cycle, inducing, 2 to 4 days after the injection, endcrine changes similar to a normal lultolysis and oestrus. After insemination at the time of this oestrus or at predefined times 72 to 96 hours after the injection, fertility is similar to that in controls. The paractical use of prostaglandins for the synchronization of oestrus in a herd of randomly cyclic animals takes account of the fact that only animals between the 5th and the 16th day respond to an injection. Various techniques are proposed, notably a double injection with an interval of 10–12 days.

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Kurzfassung Luteolytische Dosen eines Tham'schen Salzes von PGF₂, oder einer dessen synthetischen Analogen bringen vorzeitige Regressionen des corporis lutei zwischen dem 5ten und dem 16ten Tage hervor. Als Folge dieser Regressionen entwickeln sich innerhalb 2 bis 4 Tage nach der Einspritzung endokrine Veränderungen, die der normalen Luteolyse und Brunst ähnlich sind. Nach einer Besamung zur Zeit dieser Brunst oder zu vorherbestimmten Zeiten und zwar 72 und 92 Stunden nach der Einspritzung wird die gleiche Frunchtbarkeit wie in unbehandelten Kontrollen beobachtet. Nur ein Teil einer zyklischen Herde reagiert auf Prostaglandin, und es werden daher verschiedene Methoden der Viehwirtschaftsführung zur Überwindung dieses Problems erörtert, wie auch den Gebrauch einer Doppeleinspritzung von Prostaglandin mit einem 10 bis 12 tägigen Abstand zwischen den Behandlungen.

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Resume Les doses lutéolytiques de sel Tham de PGF₂ ou d'un de ses analogues synthetiques causent une reégression prématurée du corps jaunne entre le 5ème et le 16ème jour du cycle provoquant, 2 à 4 jours après l'injections, des changements endocriniens semblales à une lutéolyse normale et à un oestrus. Après l'insémination au moment de cet oestrus ou à des temps prédéfinis de 72 à 96 heures après l'injection, la fertilité est semblable à celle des animaux témoins non traités. L'utilisation pratique des prostaß-landinesd pour la synchronisation des chaleurs dans un troupoeau de femelles cyclées tient compte du fait que seules les femelles entre le 5ème et 16ème jour du cycle répondent à une injection. Différentes techniques sont proposées, notamment la double injection à 10–12 jours d'intervalle.

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Riassunto Le dosi luteolitiche del sale Them PGF₂ o di uno dei suoi analoghi sintetioi causano una regressione prematura del corpo giallo tra il 5^o ed il 16^o giorno del ciclo provooando, dopo un periodo che va dai 2 ai 4 giorni dall'iniezione, dei cambiamenti endocrini simili ad una luteolisi normale o ad un estro. Dopo l'inseminazine, nel momento di questo estro oppure in tempi predeterminati, in un periodo compreso tra 72 e 96 ore dopo l'iniezione, la fertilità è simile a quella jdegli animali di controllo non trattati. L'utilizzazione poratioa della prostaglandine per la sincronizzazione dei oalori in una mandria di femmine cicliche dimostra che le femmine rispondono all'iniezione soltanto tra il 5^o ed 16^o giorno del ciclo. Si propongono diverse techniche, in poarticolasre la doppia iniezione ad un intervallo di 10–12 giorni.

     

‘Plantibodies’: a flexible approach to design resistance against pathogens

Engineering resistance against various diseases and pests is hampered by the lack of suitable genes. To overcome this problem we started a research program aimed at obtaining resistance by transfecting plants with genes encoding monoclonal antibodies against pathogen specific proteins. The idea is that monoclonal antibodies will inhibit the biological activity of molecules that are essential for the pathogenesis. Potato cyst nematodes are chosen as a model and it is thought that monoclonal antibodies are able to block the function of the saliva proteins of this parasite. These proteins are, among others, responsible for the induction of multinucleate transfer cells upon which the nematode feeds. It is well documented that the ability of antibodies to bind molecules is sufficient to inactivate the function of an antigen and in view of the potential of animals to synthesize antibodies to almost any molecular structure, this strategy should be feasible for a wide range of diseases and pests.Antibodies have several desirable features with regard to protein engineering. The antibody (IgG) is a Y-shaped molecule, in which the domains forming the tips of the arms bind to antigen and those forming the stem are responsible for triggering effector functions (Fc fragments) that eliminate the antigen from the animal. Domains carrying the antigen-binding loops (Fv and Fab fragments) can be used separately from the Fc fragments without loss of affinity. The antigen-binding domains can also be endowed with new properties by fusing them to toxins or enzymes. Antibody engineering is also facilitated by the Polymerase Chain Reaction (PCR). A systematic comparison of the nucleotide sequence of more than 100 antibodies revealed that not only the 3′-ends, but also the 5′-ends of the antibody genes are relatively conserved. We were able to design a small set of primers with restriction sites for forced cloning, which allowed the amplification of genes encoding antibodies specific for the saliva proteins ofGlobodera rostochiensis. Complete heavy and light chain genes as well as single chain Fv fragments (scFv), in which the variable parts of the light (V_L) and heavy chain (V_H) are linked by a peptide, will be transferred to potato plants. A major challenge will be to establish a correct expression of the antibody genes with regard to three dimensional folding, assembly and intracellular location.     

Studies on the chiral isomers of fonofos and fonofos oxon: II. In vitro metabolism

The in vitro metabolism of the chiral isomers of fonofos and fonofos oxon in the presence of mouse liver mixed-function oxidase and serum esterase was investigated. The metabolism of ³⁵S-labeled phenyl-(S)_P-fonofos mediated by mixed-function oxidase took place stereoselectively, resulting predominantly in (R)_P-fonofos oxon. Similarly, (R)_P-fonofos was converted to (S)_P-oxon. In each case, however, a significant amount of racemization occurred. Other products were diphenyl disulfide and diphenyl disulfide oxide. In addition to stereospecificity, the oxidative metabolism of (R)_P-fonofos proceeded at a rate faster than that of (S)_P-fonofos. Stereoselective rate differences also were observed in mouse or rat serum-catalzyed degradation of the fonofos oxon enantiomers, the (S)_P isomer being degraded about twofold faster than its enantiomer. The differences in toxicities of the isomers of fonofos and fonofos oxon were consistent with the in vitro metabolism data.     

Effects of Latent Infection of Stock Plants and Abundance of Thrips on the Occurrence of <Emphasis Type="Italic">Tomato spotted wilt virus </Emphasis>in Chrysanthemum Fields

DAS-ELISA proved to be reliable enough to detect a latent infection by Tomato spotted wilt virus (TSWV) in asymptomatic stock plants of chrysanthemum. A high density of Frankliniella occidentalis, the predominant vector, in the presence of latently infected stock plants resulted in a high incidence of disease in the chrysanthemum production field. The incidence of disease was low when the vector thrips were not abundant in spite of the presence of latently infected stock plants. These results suggest that an infestation of the vector thrips causes severe secondary spread of TSWV originating from latently infected stock plants in chrysanthemum production fields. Received 27 July 2001/ Accepted in revised form 27 November 2001