母羊妊娠期添加多不饱和脂肪酸对新生行为的改变

研究目的确定妊娠母羊日粮中添加长链脂肪酸（n-3）鱼油,以及维生素E是否会改变羊的初生行为。将Twin-（n=36）和triplet-（n=12）的妊娠103d的母羊分成4组．4种日粮处理．包括2种脂肪资源[Megalac,棕桐油提取物或鱼油混合物,20：5（n-3）和22：6（n-3）],2种维生素E浓度（50或500mg／kg）进行2×2设计。饲喂鱼油妊娠期延长2d,初生羊血浆中22：6（n-3）的比例增加5．1-fold．大脑中的比例增加10％,而大脑中的20：5（n-3）的比例增加5％。母羊饲喂鱼油而不是Megalac时,日粮高浓度的维生素E缩短羔羊站立的潜在期．而添加鱼油同样缩短出生至哺乳之间的时间43至34min。添加鱼油可降低初乳分泌率（ml／h）和脂肪及蛋白质的产量（g／h）。我们得出以下结论：母羊日粮添加鱼油可缩短出生至哺乳的时间,延长妊娠期,并且初生大脑中22：6（n-3）：20：4（n-6）的比率增加,同时能提高羔羊存活率。但是如何减少鱼油给初乳产量带来的负面影响有待进一步的研究。     

Het Blauw Worden Van Aardappelen

Ohne Zusammenfassung     

Binucleate Rhizoctonia sp. AG G causing root rot in yacon (Smallanthus sonchifolius) in Brazil

A new rot caused by a binucleate Rhizoctonia sp. affecting the tuberous root cortex of the domesticated yacon ( Smallanthus sonchifolius ) has been observed in Brazil. Isolates of a binucleate Rhizoctonia sp. were collected from roots with rot symptoms and characterized by the number of nuclei per cell, hyphal anastomosis, RAPD molecular markers, ITS-5·8S rDNA sequence and pathogenicity tests. All isolates had a mean of 1·9–2·2 nuclei per cell and anastomosed with the binucleate Rhizoctonia sp. AG G-tester strain. RAPD analysis was carried out between 11 isolates recovered from yacon and 11 AG (A, Ba, Bb, Bo, C, D, F, G, O, P, Q) standard testers of binucleate Rhizoctonia sp. Genetic similarities of 94·8–100% were observed among isolates of the binucleate Rhizoctonia sp. from yacon and all isolates were genetically more closely related to the AG G tester than other strains according to upgma analysis using RAPD markers. Homologies of complete ITS nucleotide sequences were 100% between binucleate isolates of Rhizoctonia sp. from yacon and the AG G tester. According to pathogenicity tests, the isolates caused typical rot symptoms of yacon tubers 90 days after inoculation     

PCR-based detection of Xanthomonas campestris pathovars in Brassica seed

Xanthomonas campestris is a seedborne bacterium that causes black rot of crucifers. Substantial crop losses may result from the rapid spread of the bacteria under favourable conditions, especially those occurring during seedling production. A PCR-based method has been developed for the rapid and sensitive detection of the pathovars of X. campestris that affect crucifers. Primers were designed to specifically amplify a 619 bp fragment of the hrpF gene from X. campestris . Amplification products were not detected from other Xanthomonas species, or from other pathogenic or epiphytic bacteria occurring on these plants. To avoid false-negative results arising from the presence of amplification inhibitors in plant extracts, primers targeting a 360 bp section of the internal transcribed spacer (ITS) region from Brassica spp. were included in a multiplex PCR. The assay readily detected X. campestris pv. campestris infections in diseased plants and from bacterial colonies isolated on growth media, and was more sensitive and specific than traditional plating methods and a commercially available ELISA. A seed-washing protocol was optimized to allow the detection of a single artificially infected seed among 10 000 healthy seeds using the multiplex PCR.