三角帆蚌肝脏瘟病感染期抑制性消减cDNA文库的构建与分析

采用抑制性消减杂交技术构建了三角帆蚌肝脏瘟病感染期抑制性消减cDNA文库。经检验,差异表达基因均被富集了 2¹⁰倍左右,证明构建的 cDNA 消减文库具有很强的消减效率。PCR 鉴定发现,在随机挑取的阳性克隆中,95% 的克隆均含有 0.2～1.0 kb 的插入片段,这些片段可能是三角帆蚌瘟病病毒感染后差异表达基因的cDNA片段。测序共获得 214 个有效 cDNA 序列,分别属于8 大类,共 98 个基因。其中细胞分裂基因 2个、细胞结构与运动基因 9 个、代谢基因 10 个、信号传导基因 7 个、细胞防疫基因 10 个、基因与蛋白表达基因 20 个、未知功能蛋白基因 26 个,GenBank中找不到任何同源序列的基因 14 个。结果说明,构建的差异表达cDNA文库,可较好地反映三角帆蚌瘟病病毒对三角帆蚌影响的基因信息。     

肌醇对氨氮应激下团头鲂幼鱼免疫的影响

为了研究氨氮应激下肌醇对团头鲂幼鱼免疫的影响,实验选择初均重为(3.40±0.07)g的健康团头鲂幼鱼450尾,随机分为6组,每组3个重复,分别投喂含肌醇0、101.2、202.3、404.8、809.1和1 616.4 mg/kg的精制饲料,实验期为90 d。结果表明:与对照组相比,氨氮应激前,404.8 mg/kg肌醇添加组显著提高了团头鲂幼鱼淋巴细胞百分比、补体3、补体4和血液呼吸爆发活性(P0.05);氨氮应激12 h,404.8和809.1 mg/kg肌醇添加组的血液白细胞、红细胞、淋巴细胞百分比、血红蛋白和血清补体3、补体4水平显著升高(P0.05),皮质醇水平显著降低(P0.05),202.3和404.8 mg/kg肌醇添加组的血细胞呼吸爆发活性显著提高(P0.05);氨氮应激72 h,404.8 mg/kg肌醇添加组的血液白细胞、红细胞、淋巴细胞百分比、血红蛋白、血清补体3和血细胞呼吸爆发活性显著升高(P0.05),皮质醇水平显著下降(P0.05),809.1 mg/kg肌醇添加组的血清补体4水平显著升高(P0.05)。研究表明,饲料中添加适量的肌醇(404.8 mg/kg)即可增强团头鲂幼鱼的免疫力,对团头鲂幼鱼抗氨氮应激起到了一定的保护作用。     

全程投喂配合饲料条件下池养中华绒螯蟹的生长性能及其性腺发育

于2012年5月至2013年11月,对池养中华绒螯蟹(Eriocheir sinensis)全程投喂配合饲料,观测扣蟹和成蟹阶段的生长规律、成活率、早熟率、性腺发育速度、产量、规格分布和饲料系数等。结果表明:(1)扣蟹阶段雌雄生长差异不显著(P0.05),增重率(WG)和特定增长率(SGR)为先上升后下降,整个扣蟹培育阶段的平均SGR为1.9%/d左右;平均成活率和早熟率分别为10.0%和4.9%,雌体的早熟率显著高于雄体(P0.05);一龄早熟蟹和正常扣蟹的平均体重分别为19.8 g和7.5 g左右,一龄早熟蟹和正常扣蟹的平均产量分别为229 kg/hm~2和2433 kg/hm~2;扣蟹培育阶段饲料投喂主要发生在7—10月,占全部饲料用量的80%以上,饲料投喂量与扣蟹体重及池塘水温具有一定的关系,扣蟹阶段饲料系数(FCR)为2.15。(2)成蟹养殖过程中,自6月份起雄体体重大于雌体,整个养殖阶段雄体的SGR显著高于雌体(P0.05);雌雄成蟹最终平均体重分别为126.1 g和181.1 g,雌、雄及总体成活率分别为61.30%、53.47%和58.4%,产量分别为412.20 kg/hm~2、536.10 kg/hm~2和950 kg/hm~2;成蟹养殖的饲料消耗主要发生在7—10月,其中育肥前期(9—11月)的饲料用量占50%左右,整个成蟹养殖阶段的FCR为2.63。(3)池养成蟹的生殖蜕壳主要发生在8—9月,雌体比雄体早20 d左右;雌体的性腺发育主要发生在生殖蜕壳后的9—10月,雄体的性腺发育时间跨度较长,生殖蜕壳前性腺指数已达0.8%左右;雌雄成蟹性腺发育期间肝胰腺指数均呈下降趋势。综上,全程投喂配合饲料能保证池养中华绒螯蟹的正常生长发育,可大规模推广应用于中华绒螯蟹养殖产业。     

中华绒螯蟹核糖体DNA全序列分析

核糖体DNA通常被选作系统发育研究的分子标记,核糖体DNA中IGS部分序列的变异在一定程度上影响着生物的生长。报道了中华绒螯蟹核糖体DNA全序列的分离和序列特征。中华绒螯蟹核糖体DNA全长11660bp,包括18S(1873bp),ITS1(317bp),5.8S(163bp),ITS2(614bp),28S(4461bp)和IGS(4240bp);不同部分AT含量在40.1%～48.6%之间,低于果蝇(55.8%～80.0%),高于鲤(22.0%～43.7%)。平均100个核苷酸含简单重复序列(SSR)数由高到低依次为ITS2(0.98%),IGS(0.49%),28S(0.38%),ITS1(0.32%),18S(0.21%),5.8S(0%)。个体内差异分析结果表明,中华绒螯蟹个体内存在两类ITS2序列,其中一类在405nt处有一12bp(CGCAGGACCACC)插入序列。中华绒螯蟹rDNA的IGS部分长4240bp,AT含量为42.6%。IGS部分包含一个有约7个连续136～139bp单元组成的重复序列区,重复序列单元中存在XhoⅠ内切酶位点,为河蟹特有的重复序列;重复序列区后有一个由182个碱基对...     

Jagged1 knocking down in endothelial cells accelerates PDGF induced proliferation and migration of vascular smooth muscle cells in rats

AIM: To investigate the effect of Jagged1 expression in endothelial cells (EC) on platelet derived growth factor (PDGF) induced proliferation and migration of vascular smooth muscle cells (VSMC) in rat.METHODS: Rat aorta EC was inoculated in the lower chamber and VSMC were in the upper chamber of the cell coculture system. Three groups were divided: control, sicontrol and siJagged1. The EC Jagged1 protein expression was assayed by Western blotting to evaluate small RNA interfering (RNAi) efficiency. After the cells were cocultured with PDGF for 24 h, the proliferation and migration of VSMC were respectively evaluated by ［3H］-TdR incorporation and migrating cells counting. Protein expression of α-SM-actin in VSMC was assayed by Western blotting. RESULTS: The Jagged1 protein expression in EC was significantly lower in siJagged1 group than that in control group (0.26±0.02 vs 0.67±0.02, P<0.05), and no statistic significance was observed between control and sicontrol groups. The VSMC ［3H］-TdR incorporation and migration were higher in PDGF +siJagged1 group than those in PDGF group {［3H］-TdR incorporation (23 074±2 702) counts·min-1·well-1 vs (16 442±1 803)counts·min-1·well-1, n=5, P<0.05; migration (27±4) cells/field vs (15±3)cells/field, n=5, P<0.05}. The α-SM-actin protein in VSMC was lower in PDGF + siJagged1 group than that in PDGF group (0.25±0.06 vs 0.49±0.04, n=3, P<0.05).CONCLUSION: Jagged1 knock down in rat EC accelerates PDGF induced proliferation and migration of VSMC. These results suggest that Jagged1 expression in EC plays an important role in maintaining VSMC contract phenotype and inhibiting VSMC overgrowth after arterial injury.     

黄瓜果实曲直性评价方法及相关性分析

以48份黄瓜品种为试材,采用刨分法测量其果实弯曲度,通过黄瓜果实形态指标和相关分析可知弯曲度与果长、果柄长、果柄长/果长、果长/果横径显著正相关,与种腔大小、种腔/果横径极显著负相关,与果横径显著负相关,与果肉厚不相关。依据果形指数和弯曲度对黄瓜进行了分级。筛选出顺直品种8份,次弯曲品种9份,弯曲品种31份。     

两种籽粒镉含量不同水稻的镉吸收转运及其生理效应差异初探

以籽粒镉(Cd)含量不同的两个水稻品种为材料,采用水培和盆栽试验,研究了水稻不同生育期Cd吸收转运,生理效应对籽粒Cd浓度的影响.盆栽试验结果表明,在Cd含量为1.57 mg/kg的上壤中,中香1号(A16,低Cd 品种)和IR65610-38-2-4-2-6-3(A54,高Cd品种)糙米中Cd含量分别为0.88和0....     

基于NDVI密度分割的冬小麦种植面积提取

为解决作物面积遥感监测中常遇的混合像元问题,选用江苏省沭阳县冬小麦扬花期HJ-1A卫星遥感影像,基于不同地物光谱信息的差异性与可分割性,提出基于归一化植被指数(NDVI)密度分割的冬小麦种植面积提取方法。在利用GPS实地取样调查和建立解译标志的基础上,对HJ-1A卫星影像进行了几何与大气校正。利用NDVI灰度影像提取混合像元训练样本的NDVI值和小麦种植面积,计算小麦面积权重,确定混合像元的NDVI阈值。利用NDVI再归一化结果对NDVI灰度影像进行密度分割,依据不同密度分割系数下像元总面积及其所对应的小麦面积权重关系,最终得到沭阳县冬小麦种植面积。结果表明,根据NDVI密度分割法提取冬小麦面积为8.37×104 hm2,面积精度为92.37%,样本精度为93.31%。基于密度分割系数(P0.5)制作沭阳县冬小麦种植分布图,获取了全县冬小麦空间分布特征信息。以上结果说明NDVI密度分割法能较准确地提取研究区内冬小麦种植面积,可有效解决农作物种植面积提取中混合像元问题。     

鹅肠道微生物研究进展

肠道微生物是当前研究的热点,鹅肠道微生物的组成与丰富程度不仅和鹅的生长性能密切相关,而且在鹅机体生理活动中具有一定的调节作用,同时与疾病的发生和发展具有密切的联系.通过研究鹅肠道微生物的调节,从而达到促生长或者治疗疾病的目的,是目前鹅研究探寻的新方向.文章主要综述了鹅肠道微生物的组成及其变化规律,以期为鹅产业生物饲料的...     

Suppression of Rice Stem Borer, Chilo suppressalis by Mass Trapping Using Synthetic Sex Pheromone in Paddy Field

Suppressing effects of mass trapping using synthetic sex pheromone with main active ingredients of Z-11-hexadece-nal, Z-13-octadecenal and Z-9-hexadecenal on the rice stem borer, Chilo suppressalis were investigated during the flight periods of the overwintering and 1^st generation in the paddy area of 60 ha in 1999. Population density of C. suppressalis in the pheromone-treated fields was lower than that in control. The egg masses decreased by 74. 39% and population size of adult males of the 1^st generation decreased by 61.64% in the treated fields as compared to control. Meanwhile, the damage by C.suppressalis larvae was significantly lower in the treated fields than control (t-test, P=0.05). Percentages of brownish leaf sheath, dead heart, and white head in the treated fields were decreased by 70.90%, 57.01% and 44.30%, respectively in contrast to control. The present study demonstrated that mass trapping to C. suppressalis using synthetic sex pheromone shows great potential as an alternative measure in an environment-friendly pest management and at the same challenging the insecticide use that has some environment impacts.