双向电泳结合蛋白质印迹技术分析猪囊尾蚴乳酸脱氢酶

为了研究猪囊尾蚴乳酸脱氢酶(LDH)的表达,试验选择四川省雅江县呷拉乡猪带绦虫病患者,给其口服槟榔-南瓜子驱虫,收集、制备虫卵悬液(8万个/mL),再给3头20日龄三元杂交乳猪猪灌胃虫卵悬液,每头1 mL,40 d后收集、制备猪囊尾蚴蛋白,进行双向电泳(2-DE)分析,将凝胶蛋白斑点转移至聚偏氟乙烯膜(PVDF膜),用自制的大鼠抗猪带绦虫LDH血清作为一抗、健康大鼠血清作为阴性对照进行蛋白质印迹(Western-blotting)分析。结果表明:双向电泳凝胶共检测到(207±9)个蛋白质斑点,相对分子质量(Mr)为14 400～94 000,等电点(pI)为3.0～10.0;试验组特异性抗原抗体阳性杂交斑点为1个,阴性对照未见阳性杂交斑点;将Western-blotting检测的抗原抗体阳性杂交斑点与原双向电泳凝胶斑点进行比对,找到对应蛋白斑点,经ImageMaster 2D Platinum 5.0软件分析后初步确定该蛋白斑点的pI/Mr为7.03/35 368,与猪带绦虫LDH的pI/Mr理论推导值接近,说明猪囊尾蚴表达LDH。     

镁的营养作用研究进展

镁是生物体内重要的阳离子,参与了体内所有的能量代谢,催化或激化300多种酶体系。本文综述了镁对动物体脂质过氧化、应激及脂类代谢等方面影响的研究近况,并探讨了其可能的作用机制。     

杂交狼尾草打浆后饲喂早中期妊娠母猪效果研究

开展以沼液浇灌的“闽牧6号”杂交狼尾草（Pennisetum americarum×P．purpureum cv．Minmu 6）打浆不同比例饲喂怀孕早中期母猪(0～80 d)效果研究,试验设4个饲喂量处理,处理1（CK）~处理4,妊娠早中期分别饲喂打浆鲜草0、2、4、6 kg/(头·d),牧草以折合成干物质等量替代配合饲料。结果表明,4个处理的母猪窝产仔数分别为13.42、10.60、13.64和11.50头,窝活仔数分别为12.42、10.30、12.73和9.92头,饲喂2和4 kg/（头·d）打浆鲜草在活仔数方面与对照差异不显著,而饲喂6 kg/（头·d）打浆鲜草则显著低于不饲喂鲜(P<0.05)。饲喂牧草的处理仔猪初生体质量、健仔率都比对照得到不同程度的提高,试验结果还表明,怀孕早中期母猪通过饲喂2～4 kg/（头·d）狼尾草草浆来补充纤维来源,可提高母猪的生产性能和仔猪品质,尤其以饲喂4 kg/（头·d）打浆鲜草,饲粮粗纤维含量为8.24%～9.41%,效果最佳。     

隐性乳房炎试验(CMT)及防治方案

[目的]为找出陕西地区奶牛隐型乳房炎的临界点。[方法]采用生产上常用的乳房炎诊断方法,通过间接测定乳中体细胞数来诊断乳房炎的发生。[结果]找出体细胞数在47.46万以上时才依次表现出弱阳性、阳性、强阳性的特征。[结论]从而依据以上结果制定出两种方案用于预防和治疗乳房炎的发生。     

高效液相色谱法测定猪血浆及组织中喹赛多及其脱二氧代谢物

建立了测定猪血浆及肝脏、肾脏、肌肉等组织中的喹赛多及其代谢物脱二氧喹赛多的高效液相色谱(HPLC)法.血浆样用甲醇沉淀蛋白后离心取上清液进样测定.组织样先用乙腈匀浆,用正己烷脱脂后作HPLC检测.色谱柱为ODS C18柱;流动相血浆样测定为乙腈水(2080),组织样测定为甲醇水(4258),流速为1.0 mL/min;紫外检测波长305 nm.药物工作液质量浓度范围为0.005～0.500 mg/L时,血浆样品及组织样品测定条件下药物质量浓度与响应值均具良好线性关系,相关系数＞0.999.血浆中药物质量浓度为0.02、0.10、0.50 mg/L时,喹赛多及脱二氧喹赛多的回收率均大于70%,组织中药物含量为0.05、0.20、1.00μg/g时,肌肉样品的回收率均大于70%,肝脏、肾脏样品则为50%～80%.本试验条件下,喹赛多及其脱二氧代谢物的最低检出质量浓度,血浆样品分别为0.01、0.02mg/L,组织样品2种检测物均为0.025μg/g.测定了工作液3种质量浓度0.01、0.05、0.25 mg/L的仪器精密度,日内相对偏差＜8.0%,日间相对偏差＜17.0%.     

Effect of Fagopyrum dibotrys (D.Don) Hara on Growth Performance,Immune Function and Intestinal Structure of Broilers

This experiment was conducted to investigate the effects of Fagopyrum dibotrys (D.Don) Hara on growth performance,immune function and intestinal structure of broilers. A total of 270 one-day-old healthy Tiejiaoma broilers were chosen and randomly divided into 3 groups with 6 replicates per group and 15 broilers per replicate.Control group was fed with the basal diet,group Ⅱ was fed with basal diet adding 8% flavomycin 60 mg/kg +15% aureomycin 270 mg/kg and group Ⅲ was fed with basal diet adding 1% Fagopyrum dibotrys (D.Don) Hara. The trial period lasted for 21 days. The results showed as follow:① At 21 days of age,the average daily feed intake of group Ⅲ was significantly lower than that of groups Ⅰ and Ⅱ (P<0.05).However,there was no significant difference in the average daily gain and F/G among the three groups (P>0.05).②At 21 days of age,the thymus and bursa of Fabricius indexes of groups Ⅱ and Ⅲ were significantly higher than that of group Ⅰ (P<0.05);But the spleen index were not significantly different among the three groups (P>0.05).③ At 21 days of age,the content of IgA and IgM in serum of groups Ⅲ were significantly higher than that of group Ⅰ (P<0.05),and the content of IgG in serum of groups Ⅱ and Ⅲ were significantly higher than that of group Ⅰ (P<0.05).④At 21 days of age,the content of IL-2,TNF-α and sIgA in intestinal mucosa of groups Ⅱ and Ⅲ were significantly higher than that of group Ⅰ (P<0.05),and the content of IL-6 in intestinal mucosa of group Ⅲ were significantly higher than that of groups Ⅰ and Ⅱ (P<0.05).⑤At 21 days of age,the villus height of jejunum in groups Ⅱ and Ⅲ were significantly higher than that of group Ⅰ (P<0.05),the villus height/crypt depth of jejunum in group Ⅱ was significantly higher than that of groups Ⅰ and Ⅲ (P<0.05). However,the crypt depth was not significantly different among the three groups (P>0.05).In conclusion,that Fagopyrum dibotrys (D.Don) Hara could not affect the growth performance of broilers,but it could improve the development of immune organs,increase the secretion of serum immunoglobulin, promote the immune function of intestinal mucosa and intestinal morphology of jejunum.     

2例犬死亡原因的实验室诊断

对昆明某犬场2例死亡犬的死亡原因进行实验室鉴定。采集犬肠内容物分别做细菌和病毒检测。细菌检测包括:犬肠内容物划线培养,纯化,分离,革兰氏染色,镜检,生化试验,血清试验,药敏试验。病毒检测包括:提取病料的总DNA,用犬细小病毒的特异引物进行PCR扩增,扩增产物经胶回收后克隆到pMD18-T载体,转化受体菌DH5α,挑取阳性克隆质粒进行序列测定,并与已知参考毒株序列进行比对,分析核苷酸的同源性。分离到一株有部分耐药性的侵袭性大肠埃希菌;检测到一株犬细小病毒,由引物P1/P2扩增的基因与参考毒株CPV-b同源性为98.58%,由引物P3/P4扩增的基因与参考毒株CPV-b同源性为92.1%。结果表明,2例死亡犬的死亡原因分别为侵袭性大肠埃希菌感染和犬细小病毒感染。     

改造鼠荒地,改善草原生态环境

鼠荒地是害鼠破坏草原植被以后形成的次生裸地。在鼠荒地上 ,原生植被破坏率达80 %～ 90 % ,并滋生一、二年生杂草 ,植被稀疏 ,群落结构简化 ,植被盖度不及 10 % ,地上植物量为37.5～ 152 .5kg/hm2 。土壤侵蚀严重 ,地表形态支离破碎 ,并出现沙化特证 ,对周边草场构成沙尘暴和扬沙威胁。进一步对鼠荒地的发生与发展、鼠荒地的生态环境特征等问题作了深入论述 ,并针对鼠荒地提出了几项有效的改造措施。