离体条件下水稻种衣剂对串珠镰刀菌生长及形态毒理影响

 检测了黑龙江水稻主产区4个当地主栽品种的种子内部镰刀菌寄藏情况,测定了20%克福甲和20%克多甲种衣剂对种子带菌消毒处理效果及对水稻串珠镰刀菌(Fusarium moniliforme)的抑菌作用和联合毒力,并借助扫描电镜观察了上述2种混配种衣剂对串珠镰刀菌的形态毒理影响。结果表明,种子内部镰刀菌的分离频率高达56.7%~96.0%,其中串珠镰刀菌的分离频率为32.6%~48.2%,2种种衣剂对带菌种子具有显著的消毒处理效果。20%克福甲和20%克多甲种衣剂对镰刀菌F.moniliforme的毒力指数分别为457.11和802.04,增效倍数分别为6.53和0.13。20%克多甲种衣剂(多菌灵:甲基立枯磷为5:5,W/W)对串珠镰刀菌的抑菌作用优于20%克福甲种衣剂(福美双:甲基立枯磷为8:6,W/W),增效作用低于20%克福甲种衣剂。电镜观察表明,种衣剂低浓度至高浓度处理下均可引起串珠镰刀菌菌丝不同程度的异常生长,表现为主菌丝局部膨大或形成菌丝束,菌丝顶端异常膨大、缢缩或形成穗状和花絮状分枝。     

棉铃虫性诱剂诱捕器的改进及其应用研究

利用废弃的食用油油壶制成棉铃虫诱捕器,可提高诱蛾的效果。挡板距诱捕器器口的距离以3cm的效果最佳。与常规水钵、水盆诱捕器相比较,全年诱蛾总量分别增加116.3％和减少79.8％,但诱蛾灵敏度均高出18.72％。     

不同抗性的大豆品种感染细菌性疫病后POD、PPOD的研究

 大豆细菌性瑾病(Pseudomonas syringae pv.glycinea简称PSG)是我国和世界大豆产区的主要病害在适宜的发病条件下可使大豆减产18%~22%,最高可达到29%以上。     

在中国发现巴氏杆菌寄生柑桔根线虫

 柑桔根线虫(Tylenchulus semipenetrans)病是普遍发生于世界柑桔产区的重要病害,引起柑桔"缓慢性衰退"、被害树地上部表现明显逐步衰颓,不结实或失去经济价值。在我国四川等柑桔主产区柑桔根线虫发病率高达94.7%、重病园约占15%,严重制约柑桔生产的发展。目前尚无有效的防治措施。     

莲子草假隔链格孢的寄主范围及对空心莲子草的控制作用

 空心莲子草(Alteranthera philoxeroides)由于具有繁殖迅速、适应性强等特点,于20世纪50年代被引人我国江苏和浙江等地作为牲畜饲料植物栽培,随后相继传人全国各地并引起危害,成为我国大部分省区旱地和水域的恶性杂草之一。其微生物防治目前仍处于生物防治物的调查筛选阶段,已发现的病原真菌有假隔链格孢菌(Nimbya alternantherae)、炭疽菌(Colletotrichum gloeosporioides)、立枯丝核菌(Rhizoctonia solani)及链格孢(Alternaria sp.)等。     

以固氮树种发展食用菌专用林的建议

许多固氮树种速生丰产，萌生能力强，叶片，木屑含氮率较高，可为食用菌栽培提供理想原料，而且固氮树种在绿花荒山，保持水土，提高地力方面作用显著，以固氮树种发展短轮伐期食用菌专用林，具有较高的经济效益和生态效益，本文介绍了银合欢，黑荆，大叶相思，银荆，桤木，南洋楹和马占相思等在食用菌栽培上的应用概况，各地可因地制宜栽培合适的固氮树种作为食用菌专用林。     

Role of angiotensin II and angiotensin II receptors in vascular smooth muscle cells migration

AIM:To determine the effects of Angiotensin II(AngII) on migration of rat smooth muscle cells and to investigate the mechanisms underlying Ang II action in the development of injured vascular disease. METHODS:VSMCs isolated from aortic media of Wistar rats and cultured by the modified explant method were adopted. In prersence and absence of AngII, the expression of AngII receptor and reorganization of the actin cytoskeleton of VSMCs were studied by immunocytochemistry technique, fluorocytochemistry technique. The migration assays were performed by a modified Boyden's chamber. And the effects of AT₁R antagonist (CV-11974), AT₂R antagonist (PD123319) on aforementioned target were studied.RESULTS:VSMCs migration was stimulated by addition of AngII. The dynamic reorganization of actin cytoskeleton may be an important mechanism by which AngII facilitates VSMC motility. The expression of AT₁R in VSMCs can be upregulated after treatment with AngII initially, then decreased gradually. The expression of AT₁R was downregulated by AT₁R antagonist. The effect of AngII on VSMCs migration was mediated by AT₁R, while AT₂R had no significant effect.CONCLUSION:The dynamic reorganization of actin cytoskeleton is required for AngII-induced VSMC migration, and this effect is mediated by AT₁R .     

Mechanism of exogenous nitric oxide in attenuating endotoxin-induced increase of rat pulmonary microvascular permeability

AIM and METHODS:The animal model of acute lung injury (ALI) caused by intratracheal instillation of lipopolysaccharides(LPS) in vivo and human peripheral blood polymorphonuclear neutrophil (PMN) in vitro were used to study the effects of sodium nitroprusside (SNP), nitric oxide (NO) donor, on LPS-induced PMN accumulation, microvascular permeability and PMN apoptosis. RESULTS:①In vivo, PMN accumulation in lung, the protein content in bronchoalveolar lavage fluid (BALF) and the Evans blue dye and monastral blue dye extravasation in lung tissue of LPS group were markedly higher than those of both sham operation group and LPS+SNP group. ②In vitro, the apoptotic percentage of SNP group was much higher than that of control group, while compared with LPS group, SNP+LPS group has significantly higher apoptotic percentage. CONCLUSIONS:SNP intratracheal instillation attenuated LPS-induced microvascular permeability and alleviated ALI. PMN apoptosis induced by SNP may be one of the potential mechanisms underlying the decrease of PMN accumulation in lung tissue.     

Preparation of gfp-bcl-XL-contained recombinant adenovirus vector by the homologous recombination in bacteria

AIM: To prepare gfp-bcl-X_L-contained recombinant adenovirus(rAd-gfp-bcl-X_L).METHODS: Bcl-X_L gene was amplified from pEGFP-C₃-bcl-X_L, subcloned into shuttle plasmid and formed transfer plasmid of pAdTrack-CMV-bcl-X_L. Then pAdTrack-CMV-bcl-X_L was linealinzed with PmeI and co-transformed into BJ5183 bacteria with adenovirus genomic plasmid of pAdEasy-1. The identified recombinant adenovirus plasmid was digested with PacI and transfected into 293 cells to package recombinant adenovirus particles. The target gene was detected by PCR.RESULTS: There were about 35% positive recombinant bacterial clones after the co-transformation of pAdTrack-CMV-bcl-X_L and pAdEasy-1 into BJ5183. Recombinant adenovirus particle were produced and further amplified after the transfection of pAdEasy-1-gfp-bcl-X_L into 293 cells. PCR test indicated that the recombinant Ad contained bcl-X_L gene. The titer of the purified rAd-gfp-bcl-X_L was 6.5×10¹² PFU/L. CONCLUSIONS: The homologous recombination in bacteria is a convenient and high efficient method to prepare rAd-gfp-bcl-X_L. This affords a good gene transfer vector for the gene therapy in human’s diseases.