LFA—3和IL—2对机体免疫增强作用

以绵羊红细胞膜提取的ＬＦＡ－３和猪外周血单个核细胞所产生的ＩＬ－２，同时或分别与新城疫Ⅳ系疫苗胸肌注射２２日龄雏鸡，测定鸡体ＨＩ抗体效阶及Ｅｔｇ花环形成率的变化，结果表明，ＬＦＡ－３组抗体效价与对照组差异极显著，ＩＬ－２也可显著提高ＩＶ系苗免疫后ＨＩ抗体效价，且两者的作用具有剂量依赖性。     

根据个体间蛋白质多位点基因型的比较分析中国黄牛的遗传关系

现行群体间遗传距离的度量方法都以等位基因频率的计算为依据，这些方法的缺点之一是在位点不多，多态笥不高时要求群体有较大的取样个体数目，另外，这些方法所建造的树素图不能反映群体是由混血引起还是由长期进化引起这一问题，针对这些问题，本文提出了以个体间蛋白质多位点基因型比较为基础的群体间遗传距离和群体内基因杂合度的度量方法，以十个主要中国黄牛群体的遗传关系分析为例，比较圆满的解决了上面几个问题。     

扬子鳄胚胎背部皮肤及鳞甲的发生

本文观察了１６例不同时间的扬子鳄（Ａｌｌｉｇａｔｏｒｓｉｎｅｎｓｉｓ）胚胎背部皮肤及鳞甲的形态及组织发生过程。孵化第２０天，来自胚胎中胚层生皮节的间充质细胞开始向原始表皮下迁移，表皮仅具周皮层与生发层两层细胞。第２８天背部鳞片开始明显，左右鳞片之间出现很浅的鳞间沟，前后鳞片交界处的原始表皮、真皮层开始向外突出形成鳞甲原基。第３４天鳞甲原基突出伸长，第４０天背鳞的纵崤明显。第３４～５０天中，鳞甲后缘基部的表皮层向鳞甲前缘基部的真皮层不断内陷，鳞甲显著伸长并向体后方水平伸出。背部表皮在孵化第３４天出现三层细胞，第４０天周皮细胞中开始出现色素沉集。第５０天表皮具四层细胞，周皮层细胞中出现大量色素沉集。第６０天表皮分层与成体时相似，周皮层已退化。孵化第３４天真皮层细胞形态出现多样化，第４０天真皮可分上、下两层。第５０天真皮上层中形成交织的胶原纤维网，下层中形成平行走向的胶原纤维。本文简要讨论了扬子鳄鳞甲的形态发生特点。     

改革创新开拓蚕业现代化新局面

“十五”期间蚕业将面临从计划经济走向经济的重大改革。蚕茧流通体制改革、企业制度改革、事业单位改革都会给蚕业生产带来巨大冲击。蚕业必须深改革,加快体制创新和技术创新,从调整结构,形成专业化分工的区域区布局,探索桑地流转机制,扩大生产规模,加强生产基础,加快实用技术创新,实行产业化经营等方面入手,开拓蚕业现代化的新局面。     

波尔山羊与睢宁白山羊杂交羔羊生长性能研究

研究波尔山羊与睢宁白山羊F1 代、F2 代的生长发育情况 ,结果从出生到 3个月不同日龄羔羊的体重体尺均高于纯种睢宁白山羊 ,杂交优势显著 ,F1 代体重的杂种优势率为 18 96 % ,杂种后代生长性能比睢宁白山羊好     

<Emphasis Type="Italic">Echinococcus granulosus</Emphasis>: Immunoprotection accompanyied by humoral and cytokine response against secondary hydatidosis in mice immunized with r<Emphasis Type="Italic">Eg.</Emphasis>myophilin

Objects:  

This study aimed to investigate the immunoprotection of the recombinant Eg.myophilin (rEg.myophilin) and tentatively analyze mechanism of this protection.     

DNA Barcoding:An Effective Tool for Species Identification of Lepidopteran Oak Pests

[Objective] The paper was to improve the efficiency and accuracy of early forecast of Lepidopteran oak-infesting pests.[Method] DNA barcoding technique was established for quick species identification using mitochondrial cytochrome C oxidase subunit Ⅰ(COⅠ) as the standard gene.This barcoding technique was used to amplify and sequence genomic DNA samples from eggs and pupae of 11 species of Lepidopteran pests collected from oak.[Result] The DNA barcoding standard genes of 594-708 bp were determined from eggs and pupae of Lepidopteran insects.There were differences of 0-2 bases in DNA barcode sequences between conspecific eggs and pupae,with the sequence identity of 99.7%-100%.The average content of A,T,G and C of DNA barcode sequences from Lepidopteran insects were 30.7%,38.5%,14.9% and 15.9%,respectively.The obtained DNA barcode sequences had 91.4%-100% identity and 0-8.6% difference degree with GenBank-deposited DNA barcode sequences from organisms of the genetically-closest relationship.Among them,DNA barcode sequences from egg and pupa samples of 10 Lepidopteran insects(No.1-20) had 99%-100% identity and 0-1.0% difference degree with homologous sequences in GenBank database,while the remaining samples(No.21-22) had high difference degree(8.6%) with homologous sequences.[Conclusion] The established DNA barcoding technique is an effeetive tool for species identification of Lepidopteran pests using genomic DNA from eggs and pupae of Lepidopteran insects.     

对上海市区县兽医实验室设置问题的思考

阐述了目前上海市区(县)兽医系统实验室设置情况比较混乱,部分区兽医系统实验室已转/并至农产品检测中心,名称五花八门,由此出现的问题也层出不断的情况.根据《动物防疫法》《应急条例》等法律法规,对动物疫病预防控制机构及兽医系统实验室承担的职责进行梳理,汇总和分析后,得出结论:区(县)兽医系统实验室应依法设置于动物疫病预防控制机构,疫病监测与诊断是兽医系统实验室法律所赋予的主要职能,与以检测为主的农产品安全检测中心有着本质的区别,剥离了兽医实验室的区(县)动物疫病预防控制机构,无法真正履行好其法定职责.并提出了相应的解决方案与建议.     

哺乳动物卵母细胞孤雌激活的研究进展

本文概述了卵母细胞孤雌激活的研究历程,并从激活机制、激活方法及影响因素等方面对孤雌激活的研究意义和发展前景进行了综述。     

High‐level exogenous trans10, cis12 conjugated linoleic acid plays an anti‐lipogenesis role in bovine mammary epithelial cells

Primary bovine mammary epithelial cells (BMECs) were treated by 0, 37.5, 75, 112.5, 150 μmol/L trans10, cis12 conjugated linoleic acid (CLA) to evaluate the effects of different level trans10, cis12 CLA on lipogenesis in BMEC. Addition of 75–150 μmol/L trans10, cis12 CLA reduced significantly the triacylglycerol (TAG) content (P < 0.05), but did not have inhibiting action on cell proliferation (P > 0.05). Treatment with 150 μmol/L trans10, cis12 CLA for 48 h resulted in a 17.1% reduction (P < 0.0001) of medium chain fatty acids (MCFA, C14 < C < C16), a 26.5% reduction (P < 0.0001) of unsaturated fatty acids (UFA) and a corresponding reduction of the mRNA abundance of acetyl coenzyme A (acetylCoA) carboxylase (ACC) (P = 0.046), fatty acid synthase (FAS) (P = 0.017) and stearoylCoA desaturase1 (SCD1) (P = 0.002). Another finding was that trans10, cis12 CLA elevated expression of diacylglycerol acyltransferase2 (DGAT2) (P = 0.020) and long chain acylCoA synthetases (ACSL) (P = 0.032). In conclusion, higher trans10, cis12 CLA, not low trans10, cis12 CLA, inhibited milk fat synthesis and changed fatty acid composition by regulating the expression of FAS, ACC, SCD1, DGAT2 and ACSL.