加工萝卜蜀萝9号(038A/C9274)的选育与应用

介绍了适合四川蔬菜加工的萝卜品种蜀萝9号的亲本选育经过、组合配制、品比试验、多点试验、生产试验与示范中的表现,结果表明:2年的生产示范产量可达61.02 t/hm2,比对照增产11.60%,增加经济效益显著。并对其理化品质分析的表明,蜀萝9号符合加工萝卜和企业深加工的要求,此外还提出了蜀萝9号的栽培技术与制种技术。     

基于农田温室系统的嵌入式USB主机系统

介绍了一套基于ARM内核处理器开发的USB主机系统,提出了基于S3C44B0X和SL811HST的系统解决方案,该系统成本低廉、运行稳定,适合应用于从温室系统中提取数据到U盘上。为USB在嵌入式领域的应用和实现USB的通信,提供了一个简便、可靠的方法。     

甬优9号在三明市的种植表现及关键栽培技术

甬优9号在三明市试种表现高产稳产、产量潜力大。该文总结了甬优9号在三明市的种植表现,并提出高优关键栽培技术。     

双低三系杂交油菜蜀杂9号选育研究

蜀杂9号为四川大学生命科学学院育成的甘蓝型油菜细胞雄性不育三系中熟杂交种,参加四川省区试产量为1917．0－2256．0kg/hm^2,比对照种中油821增产33．82％,生产示范最高产量2541．0kg/hm^2。品质优良,芥酸含量0．02％,硫甙（含吲哚硫代葡萄糖甙）含量23．03μmol/g,含油量（干基）41．47％,2001年通过四川省农作物品种审定委员会审定。     

Studies on the mechanism of vaccinal immunity to Marek''s disease

Current knowledge of the nature of the antigens and of the host immune responses in vaccinal immunity to Marek's disease is reviewed. It is suggested that a two-step mechanism of resistance operates. The first step involves humoral and cell-mediated responses directed against viral antigens; the second step occurs after challenge with Marek's disease virus and consists of cellmediated responses directed against tumour cells.     

Medical management of biological warfare and bioterrorism: place of the immunoprevention and the immunotherapy

Biological weapons are considered as mass destruction and terror weapons. Terrorism including bioterrorism is the major threat in the future conflicts for our nations. The aim of bioterrorism is more related to the potential disorganisation of the society than to the lethal effects of the agents used. The dramatic consequences cannot be discarded, especially if contagious agents such viral are used. The preparation of specific defence measures is a major challenge for our countries.

The knowledge acquired from the struggle against natural infectious diseases and recent events are essential to improve behaviours to face the biological weapon threats. The defence attitude is based on the anticipation of the threat, the management of the victims, and the restoration of the operational capabilities. This global defence attitude implies six important functions: (i) alert, (ii) detection and diagnosis, (iii) availability of pharmaceutical countermeasures such as vaccine, sera and anti-infectious medicine and products, (iv) medical management of victims, (v) training and information, (vi) research and development.

Passive and active immunoprevention and immuntherapy belong to the approaches discussed in the context of bioterrorism countermeasures. Further researches might be focused on these topics.     

Foot-and-mouth disease virus

Foot-and-mouth disease virus (FMDV) is an aphthovirus of the family Picornaviridae and the etiological agent of the economically most important animal disease. As a typical picornavirus, FMD virions are nonenveloped particles of icosahedral symmetry and its genome is a single stranded RNA of about 8500 nucleotides and of positive polarity. FMDV RNA is infectious and it replicates via a complementary, minus strand RNA. FMDV RNA replication is error-prone so that viral populations consist of mutant spectra (quasispecies) rather than a defined genomic sequence. Therefore FMDV in nature is genetically and antigenically diverse. This poses important challenges for the diagnosis, prevention and control of FMD. A deeper understanding of FMDV population complexity and evolution has suggested requirements for a new generation of anti-FMD vaccines. This is relevant to the current debate on the adequacy of non-vaccination versus vaccination policies for the control of FMD.

Résumé

Le virus de la fièvre aphteuse est un aphtovirus de la famille des Picornaviridae et l'agent de la maladie animale la plus importante sur le plan économique. En tant que picornavirus typique, le virus de la fièvre aphteuse est nu, sous forme d'icosaèdre et son génome comprend un acide ribonucléique monobrin avec environ 8500 nucléotides et une polarité positive. L'acide ribonucléique de ce virus est infectieux et il se réplique par l'intermédiaire d'un brin d'ARN moins, complémentaire. La réplication de l'acide nucléique de ce virus conduit à des erreurs, de telle sorte que les populations virales comprennent un ensemble de mutants (quasi espèce) plutôt qu'une séquence génomique bien définie. Par suite, le virus de la fièvre aphteuse est génétiquement et antigéniquement varié. Ceci entraîne des difficultés importantes pour le diagnostic, la prévention et la maîtrise de la fièvre aphteuse. Une connaissance plus approfondie de la complexité et de l'évolution de la population de ce virus a conduit à des besoins pour une nouvelle génération de vaccines aphteux. Ceci est lié au débat actuel sur le choix d'une politique de vaccination ou de non-vaccination dans la lutte contre la fièvre aphteuse.     

B9对假俭草抗寒性和绿期的影响

用不同浓度比久(B9)(0、1、3、57、g/L)对盆栽假俭草品系E-126进行喷施处理,研究其对假俭草抗寒性和绿期的影响。结果表明,在低温条件下,B9处理的假俭草与对照相比,可溶性糖、脯胺酸含量升高,电导率降低,喷施低浓度的B9可以提高假俭草叶绿素含量,降低叶绿素分解,从而提高其抗寒性。其中效果最好的处理为喷施1 g/L B9,可延长假俭草绿期4-5 d。     

Construction of Full-length cDNA of Recombinant Rabies Virus SRV9 Strain Expressing EgM123 Gene of Echinococcus granulosus

The aim of the experiment was to construct the recombinant rabies virus SRV₉ vaccine strain with EgM123 gene by reverse genetics technology and provide the technical means for effective prevention and control of rabies and hydatidosis in China's agricultural and pastoral areas.In this study,the structural protein N,P and L genes of rabies virus SRV₉ were synthesized using gene synthesis technology,which was based on the complete genome sequence of rabies virus SRV₉ and the fusion fragment of the N-P-M fusion fragment and the rabies G gene,through the carrier of enzyme insertion connection methods,the recombinant rabies virus L gene,N-P-M gene fusion fragment and G+EgM123+eGFP gene fusion fragment were successively recombined on the expression vector pcDNA3.1(-) to construct the full-length cDNA of recombinant rabies virus SRV₉ with EgM123 gene.The synthesized genes were constructed on pcDNA3.1(-) expression vector,and the results of transformation,plasmid digestion and gene sequencing showed that the length of N,P,L,N+P+M and G+EgM123+eGFP gene fragments were 1 365,1 107,6 471,3 160 and 3 256 bp,respectively.The full-length cDNA fragment of EgM123 gene recombinant rabies virus full-length cDNA was 12 465 bp,and the sequencing results of each gene fragment were 100%.In this experiment,the full-length cDNA fragment of recombinant EgM123 rabies and eukaryotic expression vectors of the N,P and L genes of rabies virus were successfully constructed,which could save EgM123 gene recombinant rabies by reverse genetics,it also provided the reference for the development of rabies and hydatid disease combined gene recombinant oral live vaccine.     

鸡白细胞介素-6活性MTT检测方法的建立

采用白细胞介素-6依赖细胞株B9建立了鸡白细胞介素-6活性的MTT检测方法。每孔培养细胞数在2.5×103~4×104范围内D值与细胞数显示有良好的线性关系,MTT的最佳保留时间为4 h,最低检测限为0.1 U/mL。应用该方法检测了健康艾维茵肉鸡25例,血清chIL-6活性为(4.33±0.75)U/mL,而25例葡萄球菌病患鸡血清chIL-6的活性为(14.05±6.87)U/mL,与健康肉鸡比较差异极显著(P<0.01),为该方法进一步临床应用奠定了基础。