中华绒螯蟹血淋巴细胞的超微结构

改进常规血液细胞电镜制样技术 ,直接取中华绒螯蟹 (Eriocheirsinensis)血淋巴液固定、脱水、包埋、电镜观察。结果显示 ,中华绒螯蟹血淋巴具有 3类细胞 ,即无颗粒细胞、小颗粒细胞和大颗粒细胞。其中 ,无颗粒细胞的核质比最大 ,异染色质高度浓缩、边缘化 ,几乎没有常染色质 ,胞质内线粒体数目相对较多 ,与高等动物的中幼红细胞结构很相似 ,该细胞数目在中华绒螯蟹血淋巴中最多 ,可能担负着血液的能量转换功能 ;小颗粒细胞核内常染色质较多 ,内质网、高尔基体发达 ,胞质中存在 0 .2～ 0 .4 μm的电子致密颗粒 ,而且胞质中有许多大小不一的空泡 ,细胞表面有许多突起似伪足 ,类似高等动物的单核细胞 ,可能具有吞噬和消化异物的功能 ;大颗粒细胞胞质中的颗粒较大 ,直径 1.4～ 2 .0 μm ,胞质中具空泡 ,细胞表面也常见伪足突起 ,类似高等动物的嗜酸性粒细胞     

尼罗罗非鱼行为习性及其捕捞渔具的设计

尼罗罗非鱼(OreochromisniloticaL.)属热带性鱼类,为我国1978年从国外引进的优良海淡水养殖对象,具有食性杂、生长速度快、肉质鲜美、经济价值高等优点[1]。目前已在我国数个省、市开展养殖。尼罗罗非鱼性喜群游,其最适生长水温为24～32℃,水温降至14℃时,活动迟缓,停止摄食,水温降至12℃以下时便逐渐死亡[2]。因此,在我国北方地区养殖的尼罗罗非鱼,一般在严冬前开始进行捕捞。水温达到20℃以上时,雄鱼会在池边或者池底挖洞,当遇到外界刺激或拉网捕捞受惊后,便潜入洞中或软泥中。尼罗罗非鱼的这一行为习性给捕捞造成很大困难,因此各地一般…     

兰州地区部分奶牛场子宫内膜炎病原菌分离鉴定及抗生素耐药性研究简

为了探明兰州地区奶牛子宫内膜炎病原菌区系分布及抗生素耐药情况,指导临床合理用药。笔者对从兰州地区3个规模化奶牛场采集的47份奶牛子宫内膜炎样品进行了细菌分离鉴定,同时对分离鉴定出的4种主要病原菌采用纸片扩散法（K-B法）进行了抗生素耐药性检测。病原菌区系分布结果表明,引起兰州地区奶牛子宫内膜炎的病原菌主要为化脓隐秘杆菌（37.1%）、大肠杆菌（24.2%）、屎肠球菌（22.6%）和无乳链球菌（16.1%）。抗生素耐药性结果表明,4种主要病原菌对大部分抗生素均产生了不同程度的耐药性,尤其是对青霉素、复方新诺明、奥复星和杆菌肽耐药性最为严重,其耐药率为60%～100%。对4种病原菌均较敏感的药物主要有头孢他啶、先锋霉素V和氟苯尼考,其敏感度达100%。     

Cloning and Sequence Analysis of Major Histocompatibility Complex Ⅰ Gene from Goose F1 of Fast-growth Lines

According to the multiple alignments identified major histocompatibility complex Ⅰ (MHC Ⅰ) gene conserved sequence registered in GenBank from the family ducks (Anatidae) anser waterfowl, a pairs of specific primers for the fragments of MHCⅠgene of goose F1 from fast-growth lines were designed and synthesized by Primer Premier 5.0. Using the genome DNA of goose F1 from fast-growth lines, the target gene fragment was obtained by PCR. To conduct sequencing of the fragments of MHCⅠgene of goose F1 from fast-growth lines and make sequence alignment and analysis of protein structure and function by bioinformatics, and research the characteristics of MHCⅠgene of goose F1 and the physicochemical properties of the protein. Bioinformatics was analyzed the nucleic acid data, deduced amino acid sequence and phylogenetic trees. The result of sequence analysis showed that the fragments of MHCⅠgene of goose F1 from fast-growth lines was 1036 bp in length, which coded 96 amino acids polyprotein. The homology were 93% and 83% with MHC Ⅰ gene and coding sequence of Wulong goose in NCBI respectively. There were 72 different bases sequence and 16 amino acids change. There also was higher homology with other poultry, and existed genetic relationship of Siji goose > chickens > ducks.The homology segment sequences corresponding to the fragments of MHCⅠ gene of goose F1 coded 96 amino acids protein, which molecular weight, PI, positively or negatively charged amino acid, estimated half-life, instability index, aliphatic index and average hydrophobicity were 11.342 ku, 5.32, 14, 17, 2.8 h, 34.92, 42.81, -1.066, respectively, and appeared 9 B cell epitopes, but contained no signal peptide. These results indicated that the protein for hydrophilic non-secreted proteins, had the high immunogenicity. In addition, The protein structure study indicated that alpha-helix, beta-sheet, beta-turn and random coil were 31.25%,16.67%, 14.58% and 37.50%, respectively. There existed amino terminal domain and carboxyl terminal domain in the tertiary structure. Therefore, MHC gene had significant difference between species and populations of individuals by the pathogen pressure in environment, and there were the interaction between polymorphism of MHC molecules and the diversity of antigenic peptide. MHC determined the differences of individual susceptibility to disease, and could be treated as a candidate gene for disease resistance.     

Association Analysis between Differences of GnRHR-Ⅱ Gene Expression with Reproduction Traits Heterosis in Duck Populations

The objective of this study was to clone the sequence of duck type Ⅱ gonadotropin releasing hormone receptor (GnRHR-Ⅱ) gene, and to analyze the association of its expression levels with reproduction trait heterosis. RT-PCR method was used to clone GnRHR-Ⅱ gene fragments, and the expression levels during early laying days and laying fastigium period in Gaoyou duck, Jinding duck and crossed populations were tested by Real-time PCR method. Sequencing and homology analysis showed that the cloned duck GnRHR cDNA was about 500 bp in length, and it belonged to the avian type Ⅱ GnRHR isoforms. It was 96% identical to the cGnRHR-Ⅱ sequence reported in domestic chicken. From the early laying days to laying fastigium period, expression levels of GnRHR-Ⅱ gene in pituitary increased for Jinding duck, Gaoyou duck and crossed populations, with the highest expression levels in Jinding×Gaoyou hybrid group (P<0.01) . The expression levels of GnRHR-Ⅱ gene in hypothalamus also increased for Jinding duck, Gaoyou duck, however, it decreased in two crossed populations. The expression levels of GnRHR-Ⅱ gene in ovary were significantly higher for Jinding duck and two crossed populations than Gaoyou duck (P<0.01), but it decreased during laying fastigium period. Compared to Jinding duck and Gaoyou duck breeds, the two crossed populations had positive heterosis in 42-week production and 42-week egg fertilization percent, and negative heterosis in the first laying age and 42-week fertilized egg hatching rate traits. It suggested that the short-lived higher expression of ovary GnRHR-Ⅱ gene before early laying days be correlated with heterosis of the first laying age and 42-week production traits, and its higher expression levels in pituitary could aid to keep laying fastigium.     

Vero E6细胞酵母双杂交cDNA文库的构建及鉴定

To seek out proteins which interact with structural proteins of porcine epidemic diarrhea virus （PEDV） in Vero E6 cells and study the mechanisms of viral infection.We created a Vero E6 cDNA yeast hybrid library. The total RNA of Vero E6 was extracted using Trizol method, and double strands cDNA was synthesized by SMART technique. We created a Vero E6 cDNA library by using homologous recombination in yeast. The results showed that the titer of cDNA library was 9.7×10⁸ CFU with the average of inserted fragments about 1.6 kb, and the recombination rate was 87%. These data indicated that the yeast two-hybrid cDNA library of Vero E6 was successfully constructed and might be useful for screening the host proteins interacting with structure protein of PEDV.     

池塘中水草覆盖度对中华绒螯蟹生长的影响

为筛选青海地区池塘养殖中华绒螯蟹最佳的水草覆盖度,对中华绒螯蟹在不同水草覆盖度下的体重、成活率及生长发育情况进行了比较。结果表明,当池塘水草覆盖度在60%~80%时,有利于中华绒螯蟹的生长发育,且成活率较高,规格较大。     

低蛋白日粮对育肥猪养分消化率和排泄量的影响

试验旨在探讨低蛋白日粮对育肥猪养分消化率和排泄量的影响。选用42头初始体重为(91.13±1.64)kg的杜长大育肥猪分为2组,每组3个重复,分别饲喂粗蛋白水平为15.49%(对照组)和12.59%(低蛋白组)的日粮。试验期30d。结果表明:(1)低蛋白组干物质、粗脂肪消化率显著提高(P0.01),粗蛋白、钙、磷消化率无显著变化;(2)低蛋白组精氨酸、天冬氨酸、异亮氨酸消化率比对照组分别低2.02%(P0.05)、5.42%(P0.05)、2.97%(P0.05),苏氨酸、蛋氨酸、脯氨酸消化率较对照组分别提高2.93%(P0.05)、1.43%(P0.05)、1.19%(P0.05);(3)低蛋白组育肥猪每天的氮排泄量比对照组低23.96%(P0.05),而有机物、磷、钙排泄量无显著差异(P0.05)。试验结果显示,日粮蛋白水平降低2.9个百分点可以改善养分的消化率,减少氮排放,但降低了精氨酸的消化率。     

2012年全国家畜血吸虫病疫情状况

本文通报了2012年全国家畜血吸虫病疫情状况。在2012年,湖南省、湖北省、江西省、四川省、安徽省、云南省、江苏省等7省共有存栏牛1 033 056头,存栏羊2 024 512只,其他家畜存栏数891 301头（匹、只）。2012年共检查了684 899头牛,其中牛血吸虫病阳性3961头,阳性率0.58%,比2011年的阳性数下降了42.57%;检查了71 473只羊,其中羊血吸虫病阳性406只,阳性率0.57%,比2011年的阳性数下降了4.19%,并对142 976头其他家畜进行了检查,其中血吸虫病阳性为21头,阳性率0.01%。湖南省和江西省的病牛数占到了全国病牛数的80.06%。2012年,全国家畜血吸虫病疫情较之2011年继续下降,但是洞庭湖和鄱阳湖地区依然是今后家畜血吸虫病疫情控制的难点和重点。     

p53调控Nfkbiz基因表达的研究

核因子-κB（NF-κB）在炎症反应中起着关键的促进作用,并且受其他多种因素的调节。Nfkbiz基因编码的IκB？蛋白是IκB家族成员之一,在炎症反应中起着调节NF-κB的作用。本研究采用荧光实时定量PCR分析Nfkbiz基因的表达情况,发现在p53特定刺激源作用下Nfkbiz基因mRNA丰度显著降低。分析Nfkbiz基因序列,发现其基因中存在可能的p53反应元件,通过构建荧光素酶报告质粒及双荧光素酶报告试验和染色质免疫共沉淀试验,证明Nfkbiz基因中含有p53反应元件并且受p53蛋白调节。以上结果初步证明Nfkbiz是受p53蛋白负向调控的靶基因。