鸭大肠杆菌的药物敏感性试验

采用纸片扩散法测定了14株鸭大肠杆菌对10种抗菌药物的敏感性,结果鸭大肠杆菌对头孢唑啉、头孢噻肟、丁胺卡那霉素最为敏感,敏感率均为100%;其次为庆大霉素,敏感率为78.6%;对其他抗菌药物均产生不同程度的耐药性,耐药性最为严重的是四环素、复方新诺明及多西环素,耐药率分别为92.9%、85.7%、78.6%,对阿莫西林、氯霉素、环丙沙星的耐药率分别为57.1%、50.0%、64.3%;78.6%的菌株对10种抗菌药物表现为多重耐药性.耐阿莫西林菌株经碘-淀粉测定法测定均为产β-内酰胺酶菌株,阿莫西林对它们的最小抑菌浓度范围为256～ 1 024 mg/L.     

亚热带牧用草地中威提特东非狼尾草的种子繁殖研究

在3月和4月对全日制放牧的东非狼尾草草地上的风干牛粪取样,进行发芽试验,分别测定其中的东非狼尾草发芽种子数量。结果,3月取样平均432.5 g的牛粪中东非狼尾草平均发芽种子数量为118.25粒,4月取样平均437.8 g的牛粪中东非狼尾草平均发芽种子数量为52.8粒,二者平均牛粪重为435.15 g,平均发芽种子为85.5粒,说明牛粪中东非狼尾草种子数量较多,是其繁殖扩展较快的主要原因;3月取样的种子数量为4月取样数量的1.38倍,说明人工利用牛粪进行东非狼尾草繁殖时,需在有降雨来临前准备,即1～3月进行牛粪的准备工作。     

谷氨酰胺对肉仔鸡脾组织结构发育的影响

160只 1日龄艾维茵肉仔鸡随机分成 4组 ,分别饲喂添加 0 % ,0 2 % ,0 4%和 0 8%谷氨酰胺的饲粮 2 8d。每周末每组取 6只鸡 ,颈静脉放血致死 ,取脾脏 ,Bouin液固定 ,制作石蜡切片 ,HE染色 ,光镜观察 ,显微摄影 ,研究基础日粮中添加谷氨酰胺对肉仔鸡脾组织结构的影响。结果显示 :添加谷氨酰胺的各试验组脾小结增多、增大 ;动脉周围淋巴鞘增厚 ;椭球增多、增大 ,细胞排列疏松 ,鞘毛细血管内皮细胞增高、增多 ;红髓比例降低 ,脾索内浆细胞和巨噬细胞增多。添加 0 8%谷氨酰胺的脾小结变化明显 ,添加 0 4%谷氨酰胺的动脉周围淋巴鞘和椭球变化明显。说明日粮中适量添加谷氨酰胺可促进脾内淋巴细胞的增殖与分化 ,从组织学角度证明 ,谷氨酰胺可促进脾的免疫应答能力 ,提高机体的免疫功能     

猪大肠杆菌水肿毒素SLT-IIeA基因的克隆和序列分析

研究以本地猪水肿病大肠杆分离物ED1株为材料 ,利用 PCR克隆了含猪水肿病大肠杆菌 (VTEC) slt-IIe A基因 987bp的片段 ,并测定了含该克隆片段的 Bam HI、Hind 酶切片段的核苷酸序列。结果表明 ,slt-IIe A基因的编码区全长 960 bp,编码 3 1 9个氨基酸的蛋白质 ,序列与国外报导的 S1 1 79株进行比较发现其核苷酸同源性为 98.9%。经推导的氨基酸序列的同源性为 99.7%。这为进一步研究 slt-IIe A的生物学特性、水肿病的分子诊断及其防制打下基础     

芽孢杆菌绿色荧光蛋白标记及其在小麦体表定殖的初探

 将来自质粒pAD4412的启动子和绿色荧光蛋白基因gfpmut3a插入大肠杆菌-枯草芽孢杆菌穿梭载体pBE2,构建成芽孢杆菌表达载体pGF P4412,用其转化野生型生防芽孢杆菌83-6和A-47等8个菌株,均得到良好的发光表型。质粒稳定性实验表明重组质粒pG FP4412稳定性为92%。借助荧光显微镜对gfp标记的菌株A-47-gfp在小麦体表的定殖进行初步的研究。结果表明:A-47-gfp能够在小麦根际及小麦体表定殖(包括根表和茎叶表面);相对于在茎叶表面定殖的A-47-gf p在根表定殖的菌体与根的结合更为牢固;从根基到根尖A-47-gfp的定殖量有明显的减少趋势。     

黄瓜花叶病毒丹参分离物的鉴定和外壳蛋白基因序列分析

 丹参(Salvia miltorrhiza Bge.)为唇形科鼠尾草属草本植物,以根入药,是我国一种常用大宗中草药。近年来河北安国中药材基地丹参上一种退化病十分严重,该病田间发病率高,有的田块高达60%~80%,表现为花叶、斑驳、卷叶、黄化、矮化等症状,严重影响了丹参的产量和品质。我们利用生物学、电镜观察、血清学方法和基因序列测定等方法对病原进行了初步研究,发现黄瓜花叶病毒(Cucumber mosaic virus,CMV)与该病害密切相关     

梨果实发育过程中石细胞团及几种相关酶活性变化的研究

以梨品种西子绿、菊水及砀山酥梨为试材,对不同发育时期梨果实石细胞团的密度、大小及几种相关酶的活性变化进行了研究。结果表明石细胞团的分布密度在幼果期较高,以后随着果实的发育和膨大,密度逐渐减小,接近成熟前1个月左右基本稳定;石细胞团的直径随果实的生长而逐渐变大;苯丙氨酸解氨酶在果实发育初期表现出较高的活性,随着果实的生长逐渐降低,花后75d后保持低水平不变;过氧化物酶活性高峰出现稍迟于苯丙氨酸解氨酶,高峰后呈现出下降的趋势;多酚氧化酶活性波动较大,总的变化趋势逐渐下降。品种间苯丙氨酸解氨酶、过氧化物酶活性与石细胞团的形成之间表现为正相关。     

显齿蛇葡萄新品种——绿凤

 从中国鄂西地区生长的显齿蛇葡萄植株中选育出优良无性系‘绿凤’, 其叶含总黄酮12.9 % ,总氨基酸16.7 % , 总糖6.92 % , 维生素E 60.1 mg/ kg , 用其叶加工饮品具有保健作用。     

Characteristics in the secretion of liver TNF-α induced by infusion of LPS into veins in goats

AIM: To study the role of liver in immune regulation in experimental endotoxemia. METHODS: 17 castrated male goats were subjected to simultaneously installing catheters in jugular, hepatic and portal veins by surgery. Four days later, lipopolysaccharide (LPS) was infused in term of three groups as followings: In group ①, LPS of 20 EU (endotoxin unit, EU)·kg^-1 was infused into portal vein; In group ②, LPS of 20 EU·kg^-1 was infused into jugular vein and LPS of 1 500 EU·kg^-1 infused into jugular vein in group ③. Before and after infusion, blood samples were collected from the three veins through the catheters for 8 h.The plasma levels of TNF-α were measured by RIA. RESULTS: In group ①, the plasma TNF-α levels of hepatic and portal vein rose to peak value at 5 h, but that of the jugular vein did not changed. In group ②, the plasma TNF-α levels in hepatic vein rose to peak value at 3 h. The TNF-α levels of jugular vein rose to peak value at 1 h and the one in portal vein enhanced continuously between 0-8 h. In group ③, the plasma TNF-α levels in jugular, hepatic and portal vein rose to significant peaks at 1 h simultaneously. CONCLUSION: During experimental endotoxemia,liver showed different dynamic characteristics in TNF-α secretion according to the pathway and doses of LPS delivery.     

Expression of cyclooxygenase-2 in IL-1β-stimulated mesangial cells is medicated by NF-κB/IκB signal pathway

AIM: To investigate the role of NF-κB/IκB signal pathway in the regulation of cyclooxygenase-2 (COX-2) expression in human mesangial cells (HMC). METHODS: The PGE₂ concentration in supernatants of HMC was measured by radioimmunoassay. COX-2 mRNA and protein expression were determined by RT-PCR and Western blot. Electrophoretic mobility shift assay (EMSA) and Western blot were used to detect the activity of NF-κB and degradation of IκB. RESULTS: IL-1β significantly upregulated COX-2 expression and PGE₂ production in HMC. Significant up-regulation of NF-κB activation, nuclear translocation of p65 subunit, and degradation of IκB α and IκB β were observed in IL-1β-induced HMC. CONCLUSION: Expression of COX-2 in IL-1β-induced HMC is mediated by NF-κB/IκB signal pathway.