猪传染性胃肠炎病毒南京株纤突S蛋白基因的克隆与序列分析

参考 Genbank收录的 TGEV- Miller株的基因序列 ,自行设计合成 1对引物 (TGEVP5 /P6 ) ,对不同代次的 TGEV疫苗弱毒 STC3及种毒 、种毒 进行了 RT- PCR扩增 ,产物经琼脂糖凝胶电泳分析 ,均出现 1条大约 12 6 2 bp的目的条带 ,经 Eco R 酶切 ,都产生了 871bp和391bp左右的两个片段 ,与预期大小相符。将种毒 RT- PCR扩增目的条带回收纯化后克隆入PMD18- T载体中 ,转化宿主菌 DH5 α,挑选阳性克隆 (命名为 PTs) ,提取重组质粒 ,用 Hpa 、Eco R 对重组质粒进行酶切鉴定以及 PCR扩增 ,然后进行序列测定 ,并进行了序列分析 ,证实与国外标准毒株 Miller、Fs772 / 70、Purdue、TO14等有较高的同源性     

鸡霍乱口服弱毒疫苗的研究

用经过选择的禽多杀巴氏杆菌自然弱毒菌株Ｒ１－２３菌株制成的鸡霍乱固体培养口服弱毒疫苗，其安全剂量接近于２００个免疫剂量。该口服苗两次饮水免疫的最适总剂量为每羽５０亿个活菌，最佳间隔时间为４８小时。免疫鸡第二次饮苗后第３天即可产生较好的免疫保护率（７／８）。免疫鸡对异型强毒株Ｐ１０５９（８∶Ａ）、Ｐ２７２３（９∶Ａ）和同型强毒株Ｃ４８－１（５∶Ａ）滴鼻攻击的近期保护率平均为５／１０、６／１０和９／１０。６个月免疫期的平均保护率为７６．７０％（４６／６０），一万多羽鸡田间试验结果表明，免疫后２个月的平均保护率为９３．１０％（２７／２９），６个月的平均保护率为７３．５０％（２５／３４），除对产蛋率有轻度影响（下降１．２７％）外，无其它不良反应。野外大面积使用结果表明，该口服苗不但性能稳定，免疫原性优良，而且安全可靠，适用于鸡口服免疫。     

鸡马立克氏病琼扩抗原的研制及应用

将马立克氏病死鸡的皮肤或羽囊捣碎，制成MD琼扩抗原。试验结果表明，自制MD皮肤和羽囊琼扩抗原与标准抗的检测MD抗体的敏感性和特异性相同，但皮肤琼扩抗原制造方法相对比较简单，产量也较高。     

潍坊市农机化发展现状及对策分析

总结了山东省潍坊市农机化发展概况和特点．分析了农机化发展中存在的问题，提出了潍坊市加快农机化发展的对策建议。     

提高农用潜水电泵修复可靠性的方法

对以QY系列为主体的农用潜水电泵修复可靠性低、寿命短的问题，提出了改进措施，从而有效提高潜水电泵修复可靠性，并延长使用寿命。     

“七五”国家科技攻关项目——蔬菜新品种选育研究Ⅳ.甜(辣)椒专题育成的新品种(系)简介

本文介绍了1986-1990年甜(辣)椒专题8个单位育成的15个甜椒、半辛辣椒新品种(系),其抗病性、品质、产量均优于对照品种,并已通过了农业部主持的专家组验收。     

Preliminary results of using in vitro axillary and adventitious buds in mutation breeding of Chinese gooseberry

Summary Aseptically cultured shoots of Chinese gooseberry exhibited growth disorder and morphological aberrances, and some died after being exposed to sufficient gamma-ray irradiation. The death rate was dose dependant and the LD₅₀ was 80–90 Gy and 50–60 Gy respectively for cv. Hayward and clone 4. All petiole explants irradiated with gamma-ray could form calli as the control, but the rate of differentiation of adventitious shoots of the petiole explants decreased and was dependant on dose. Sensitivity of the shoot or petiole explants to gamma-ray irradiation varied with species. Gamma-ray irradiation did not deter either the 2-node segments from producing axillary shoots M₁, M₂, and M₃ or the advantitious shoots originating in the petiole explants and the M₃ shoots from forming advantitious roots. Therefore, using aseptically cultured axillary or adventitious buds for mutation breeding of Chinese gooseberry is feasible. A bacterium surviving in the explants lessened the efficiency of these two in vitro techniques in mutation breeding of Chinese gooseberry.Abbreviations IAA 3-indole acetic acid - IBA -indole butyric acid - MS Murashige & Skoog (1962)     

早熟春甘蓝新品种春冠的选育

春冠亲本之一493是将国外引进的资源96011、9502杂交后，经系统选育，采用露地越冬栽培加大耐先期抽薹性的选择强度选育出的自交不亲和系。另一亲本711是从国外引进的资源B-21经多代自交选育出的自交不亲和系。该品种耐寒，露地越冬不易先期抽薹，早熟，叶球尖桃形，肉质脆嫩，品质佳。单球质量1.5kg左右，每667m^2产量3500kg左右。在南方地区可露地越冬栽培，已在长江流域示范推广。     

架子牛肥育综合技术研究

该文从架子牛的选购、驱虫、肥育期的饲养管理、日粮营养等方面做了系统的研究。结果表明,选择2～3岁的夏洛来牛或西门塔尔牛的改良后代,采用高能量高蛋白质日粮可以获得较高的经济效益。     

Role of p38MAPK in production of pro-inflammatory cytokines in Kupffer cells from severe acute pancreatitis rats

AIM:To investigate the role of p38 mitogen-activated protein kinase (p38MAPK) signaling pathway in the Kupffer cells (KCs) production of pro-inflammatory cytokines, tumor necrosis factor-α(TNF-α) and interleukin-1β(IL-1β), in severe acute pancreatitis (SAP) rats.METHODS:Sprague-Dwaley rats were randomized into three groups:①sham operation rats, ②SAP rats, ③SAP rats given the p38 MAPK inhibitor CNI-1493(10 mg/kg, iv). The SAP model was induced by the bili-pancreatic duct infusion with 5% sterile soduim taurocholate solution. Rats from each group were killed at 12 h after sham operation or SAP and Kupffer cells (KCs) were isolated. The mRNA expressions of TNF-α and IL-1β (by quantitative real-time RT-PCR) and p38 MAPK activity (by Western blot analysis) in KCs were examined. The levels of TNF-α and IL-1β in plasma were determined by ELISA.RESULTS:There was a significant acvitation of p38 MAPK in KCs harvested from SAP rats than those from sham operation rats. SAP also promoted the mRNA expressions of TNF-α and IL-1β in KCs and the plasma levels of TNF-α and IL-1β. These events were significantly inhibited by treatment with CNI-1493.CONCLUSIONS:p38 MAPK activation is one important aspect of the signaling events that may mediate the KCs production of pro-inflammatory cytokines, TNF-α and IL-1β, in SAP rats. The inhibition of the p38 MAPK may be a potential target in the prevention and treatment of SAP.