熊蜂为温室茄子授粉试验

通过对温室茄子应用熊蜂授粉、人工蘸花授粉和空白对照的比较研究,结果表明熊蜂组的座果数比人工组和对照组分别增加了17.84%和33.32%,产量比人工组和对照组分别提高了27.93%和41.98%,果实含糖量比人工组和对照组分别增加了18.33%和21.16%,而且,熊蜂组的果实大而充实,商品性较好.说明利用熊蜂为温室茄子授粉,不仅能够促进座果,提高产量,而且可以改善果实品质,提升产品的附加值.     

徐州地区烟粉虱发生规律及治理措施初探

通过近2a观察表明,徐州地区烟粉虱在田间消长大致分4个阶段,成虫有4个主要迁移期;其喜干热、耐高湿的生活习性、冬季保护地栽培面积的扩大、外来虫源的传入及防治不力是烟粉虱种群数量累积并引起暴发的主要原因;主要寄主有9科20余种栽培作物;寄主植株上虫量垂直分布:棉花上部>中部>下部,温室蔬菜一般中、下部>上部。可采取严格检疫、清洁田园、轮作换茬、黄板诱杀、覆盖防虫网、保护和利用天敌、药剂防治等措施进行治理。     

Relation between TNF-α,TNFR I expression and apoptosis in oral lichen planus

AIM: To examine the expression and distribution of tumor necrosis factor-α (TNF-α), tumor necrosis factor receptor I (TNFR I) and apoptosis in oral lichen planus, and evaluate their roles and relation in the oral lichen. METHODS: Immunohistochemical technique and TUNEL were employed to study the expression of TNF-α, TNFR I and apoptosis in 50 cases of oral lichen planus and 10 normal oral mucosa specimens. RESULTS: Compared with the normal control group, TNF-α expression was upregulated in mononuclear cells in lamina propria and decreased in keratinocytes in oral lichen planus lesion (P<0.05). On the contrary, TNFR I expression was increased in keratinocytes and decreased in lamina propria in oral lichen planus lesion (P<0.05). The increased apoptosis index in keratinocytes and the decreased apoptosis index in lamina propria were found in oral lichen planus (P<0.05). CONCLUSION: The accelerated apoptosis of keratinocytes and the inhibition of lymphocytes apoptosis may contribute to the formation and progression of oral lichen planus.     

Effect of EGFP gene transfection on the cell cycle distribution of primary cultured human chondrocytes

AIM: To investigate the effect of enhanced green fluorescence protein (EGFP) gene transfection on the cell cycle distribution of primary cultured human chondrocytes in order to establish a tracking method of cultured human nasoseptal chondrocytes. METHODS: pEGFP-N1 plasmid was amplified in E.coli, and purified by high purity kit. Primary cultured human chondrocytes,which were initially obtained from the nasoseptal cartilage, were cultured in vitro and transferred with pEGFP-N1 by means of electroporation with Amaxa nucleofector device. Transfering process and transient expression were evaluated by laser scanning confocal microscope (LSCM), the transfer efficiency and the cell cycle distribution were evaluated by flow cytometry. RESULTS: There was significant expression of EGFP at 24 h after transferring. The transfection efficiency of pEGFP-N1 into primary cultured human chondrocytes reached 35.37％ at 48 h. It didn't affect the process of cell adherance and had no effect on the cell cycle distribution. CONCLUSION: Primary cultured human chondrocytes, which were transfected with pEGFP, are alive in vitro, and the transferring process doesn't affect the cell cycle distribution. These results suggest that pEGFP-N1 is an ideal transient expression vector for primary cultured human chondrocytes and it might be a well tracer in construction tissue engineered cartilage.     

猪瘟病毒及其全长cDNA在猪肾细胞中增殖表达特性的比较研究

以猪瘟C-株弱毒疫苗株、经典强毒石门株和C-株全长cDNA为试验材料，以免疫荧光技术为主；结合ELISA和RT-PCR检测技术，对其在培养细胞中的增殖特性和表达规律进行了比较研究。同时筛选猪瘟病毒及其全长cDNA的敏感细胞，探索其增殖表达规律，以便为猪瘟病毒反向遗传操作提供技术方法和可操作的条件。     

Differential gene expression of Eph‐ephrin A1 and LEPR‐LEP with high or low number of embryos in pigs during implantation

The objective of this study was to ascertain whether mRNA and protein expressions of implantation‐related genes (erythropoietin‐producing hepatocellular receptor–ligand A1, Eph‐ephrin A1 and leptin receptor–leptin, LEPR‐LEP) differed between pigs with high and low number of embryos, and whether these differences in gene expression might affect embryo implantation. Experimental pig groups (n = 24) for high and low number of embryos were prepared by altering the number of eggs ovulated in pre‐pubertal gilts treated with 1.5 × (High) or 1.0 × (Low) PG600 ([400 IU PMSG + 200 IU hCG]/dose, AKZO‐NOBEL). Gilts expressing oestrus were artificially inseminated twice and maintained in breeding and gestation until the reproductive tract was collected on day 22 of pregnancy. At slaughter, the reproductive tracts from each pregnant gilt from each treatment were immediately processed to collect samples for RNA and protein analysis. Within each gilt, three conceptus points were sampled, one from each horn and then a random conceptus within the tract. At each conceptus point, endometrial attachment site, chorion–allantois and embryo were collected and immediately frozen in liquid nitrogen. Number of corpus luteum (CL) (35.4 vs. 12.6) and total embryo number (18.8 vs. 10.2) were greater in the high‐embryo compared to the low‐embryo group, respectively (p < .05). Real‐time qPCR results showed that Eph‐ephrin A1 mRNA expression was less in the high‐embryo (p < .05) compared to the low‐embryo group. In addition, Western blotting analysis indicated that Eph‐ephrin A1 and LEP protein expression at endometrial attachment site in high‐embryo was less (p < .05) compared to low‐embryo group. It was also noted that mRNA expression of Eph‐ephrin A1 and LEPR‐LEP was greater in pregnant than non‐pregnant gilts (p < .05). Moreover, mRNA expression of Eph‐ephrin A1 (p < .05) and LEPR‐LEP was greatest at endometrial attachment site among all three tissues. There was a positive correlation between expressions of Eph‐ephrin A1, LEPR‐LEP and embryo length with the correlation coefficient 0.31–0.59. For Eph‐ephrin A1, the highest correlation coefficient appeared between Eph A1 expression and normal embryo number, between ephrin A1 expression and embryo length. For LEPR‐LEP, the highest correlation coefficient appeared between LEPR‐LEP expression and ovary weight (0.79 for both, p < .05), followed by embryo length and weight. The results of this study suggest that low expression of Eph‐ephrin A1 and LEPR‐LEP is somehow related to increased embryo number during implantation and that endometrial attachment site might be the main target tissue of these gene products. Yet, the increased expression of Eph‐ephrin A1 and LEPR‐LEP appeared associated with increased embryo growth (length and weight) and ovary weight, Eph‐ephrin A1 and LEPR‐LEP might play roles in the regulation of embryo implantation in pigs.     

紫茎泽兰对萨能奶山羊血常规及重要脏器病理学的影响

紫茎泽兰(Eupatorium adenophorum)在中国作为入侵物种,可造成食草动物中毒死亡,并给畜牧业带巨大的损失。为研究反刍动物采食紫茎泽兰后的中毒机理,本研究探讨了日粮中添加不同剂量的紫茎泽兰对萨能奶山羊(Saanen goat)血常规及肝、脾、肾的病理学影响。选择16只5~6月龄健康萨能奶山羊,随机分成对照组(日粮中未添加紫茎泽兰)和试验Ⅰ、Ⅱ、Ⅲ组(日粮配比中分别添加紫茎泽兰40%、60%和80%),每组4只。试验Ⅰ、Ⅱ、Ⅲ组分别饲喂含40%、60%和80%紫茎泽兰的混合日粮3个月,每两周检测一次血常规,试验末屠宰奶山羊,并观察其肝、肾、脾的病理学变化。结果表明,与对照组相比,各试验组血液中的白细胞(white blood cell,)和中性粒细胞(neutrophil,NEUT)均显著升高(P0.05),试验后期极显著高于对照组(P0.01);而各试验组血液中淋巴细胞(lymphocyte,LY)与血红蛋白(hemoglobin,HGB)均呈下降趋势,试验后期均极显著低于对照组(P0.01)。肝和脾肿大,肝组织出现淤血,肝细胞发生水泡变性及脂肪变性等,肾组织伴有出血、坏死、颗粒变性及水泡样变性的现象。因此,本研究结果说明紫茎泽兰对萨能奶山羊血液指标有显著影响,且长期摄入紫茎泽兰可引起动物肝、肾、脾等主要实质器官不同程度的损伤。     

紫花苜蓿9个盐响应相关基因表达模式

紫花苜蓿(Medicago sativa)是世界上种植面积最大、应用最广泛的豆科牧草。由于其耐盐性中等,其在我国北方地区的产量和种植受到土壤盐渍化的限制。因此提高紫花苜蓿的耐盐性具有重要的科学和生产意义。为此,以龙牧801紫花苜蓿(M.sativa‘Longmu 801’)为试验材料,采用实时荧光定量PCR技术分析了不同浓度NaCl胁迫下9个盐胁迫蛋白质组筛选出的盐响应相关基因的表达模式。结果显示,处理时间和处理浓度对9个基因的相对表达量均有显著性影响,表明这9个基因均在紫花苜蓿盐胁迫应答中发挥着一定作用。处理1h时,G6PI、ABP19a、Trx-h1、PR bet 1、FBPA、6PGDH和ALDH这7个基因的相对表达量在不同NaCl胁迫浓度处理的紫花苜蓿中均显著上调,RRM和GDPD在NaCl处理2h后开始上调。除G6PI基因,其他8个基因在0.4%NaCl处理下相对表达量显著高于0.2%和0.8%NaCl处理。这些基因参与糖代谢、信号转导和胁迫响应。以上结果表明,紫花苜蓿的耐盐性极其复杂,涉及到多基因的表达和代谢通路的调控。研究结果有助于全面研究并了解紫花苜蓿的盐响应相关基因的表达模式,促进紫花苜蓿耐盐分子育种。