扫描及负染电镜在兔脑炎原虫病诊断中的应用

12只临床表现头颈歪斜、昏睡、震颤、局部或全身轻瘫的可疑为兔脑炎原虫病的獭兔 ,对其肾脏皮髓交界和尿沉渣分别进行了扫描电镜和负染电镜观察 ,看到了大小为 1～ 1 .5× 1 .4～ 2 .5μm,形态呈卵圆形和杆状的兔脑炎原虫。阳性检出率为 1 0 0 %。说明扫描及负染电镜术是诊断兔脑炎原虫病的一种较为可靠的技术。     

奶牛血浆PGFM浓度变化与子宫内膜炎关系的研究

奶牛子宫内膜炎是奶牛产后多发性疾病之一，产后子宫感染是一种非特异性感染，主要的致病菌有分泌型化脓菌（Arcanobacterium pyogenes）、埃希氏大肠杆菌及其他多种革兰氏阴性厌氧菌。子宫内膜炎对奶牛业有重要的经济影响，若能早期识别出对子宫内膜炎易感性较高的奶牛，并提高对子宫内膜炎患牛的诊断率，将会明显的减少因产后子宫感染所带来的损失。     

猪传染性胃肠炎病毒南京株纤突S蛋白基因的克隆与序列分析

参考 Genbank收录的 TGEV- Miller株的基因序列 ,自行设计合成 1对引物 (TGEVP5 /P6 ) ,对不同代次的 TGEV疫苗弱毒 STC3及种毒 、种毒 进行了 RT- PCR扩增 ,产物经琼脂糖凝胶电泳分析 ,均出现 1条大约 12 6 2 bp的目的条带 ,经 Eco R 酶切 ,都产生了 871bp和391bp左右的两个片段 ,与预期大小相符。将种毒 RT- PCR扩增目的条带回收纯化后克隆入PMD18- T载体中 ,转化宿主菌 DH5 α,挑选阳性克隆 (命名为 PTs) ,提取重组质粒 ,用 Hpa 、Eco R 对重组质粒进行酶切鉴定以及 PCR扩增 ,然后进行序列测定 ,并进行了序列分析 ,证实与国外标准毒株 Miller、Fs772 / 70、Purdue、TO14等有较高的同源性     

家兔选育性状典型相关分析

选择日本大耳白和新西兰两个品种家兔的生长、繁殖、以及体尺3组共17个性状，应用多元统计方法进行了典型相关分析，结果表明；日本大耳白兔的初生重、初生窝重、21日龄重、泌乳力、胸围等5个性状，新西兰兔的产活仔数、初生重、21日龄重、泌乳力、断奶窝重、母兔体重等6个性状为主要性状。     

类固醇合成相关酶在小鼠不同组织中的表达

利用RT-PCR和Western-blotting技术分析了胆固醇侧链裂解酶（P450scc）、3β-羟甾脱氢酶（3β-HSD）、C17-20裂解酶（P450c17）、StAR mRNA和蛋白在成年昆明小白鼠心脏、脾、肝、肾中的表达.结果显示,StAR mRNA及其蛋白、P450scc mRNA在以上组织中均有表达;3β-HSD在肾中有较强的表达,在其他组织的表达较弱;P450c17在上述组织中无明显的表达,但在睾丸中有明显的表达.这表明,心脏、脾、肝、肾均具有合成类固醇的能力,但合成类固醇的类型存在一定的差异.     

重视粪污处理 改善养殖环境

近20多年来，我国养殖业发展迅速，取得了可喜的业绩。我国肉类、蛋类总产量连续多年保持世界第一，养殖业为改善我国人民生活水平，调整人们膳食结构、提高农民收入做出了巨大的贡献。但它的发展不可避免地产生了大量的“畜产公害”，畜禽粪便、养殖污水任意堆弃、排放现象普遍存在。     

离子选择电极法测定NBPG与银、镉、汞的配合物组成和稳定常数

本文用离子选择电极法测定了N,N—二甲基膦酸基甘氨酸(NBPG)与银、镉、汞的配合物组成和稳定常数。结果表明,NBPG与Ag~ 、Cd~(2 )、Hg~(2 )均生成组成为1:1的多齿质子型配合物。其lgK_稳值分别为:AgL5.28、CdH_3L3.63、CdH_2L5.16、CdHL7.30、CdL11.56、HgH_3L6.06、HgH_2L7.55、HgHL8.24、HgL12.58。     

加快淮北地区杂交粳稻发展的几个问题

回顾了淮北地区十多年来杂交粳稻示范推广的发展过程，分析了影响杂交粳稻发展的主要原因，并论述了加快该地区杂交粳稻发展的几个主要问题。     

桉树的一个国内新记录病原菌

本文报道了寄生在雷林一号桉“[Eucalyptus leichou NO:1]”叶片上的一个国内新记录病原菌[Fairmaniella leprosa(Fairman)Petrak & Sydow.]的主要特征,并与已知种作了比较;文中讨论了国内外研究状况,寄主及分布。标本采集于广东省雷州林业局林科所人工桉树林。     

‘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.