计算机实验室病毒流行原因研究简

论证了计算机实验室内研究病毒流行规律的意义,明确了流行规律研究的主要内容.结合计算机实验室的特定环境,从主观和客观两个角度对病毒流行原因进行归纳总结,为建立以还原保护技术为主的系统性防毒方案提供了重要参考资料.     

压水试验在船撞破损桥墩裂缝检测中的应用

通过工程实例,介绍了在对被船只等漂浮物撞击受损的桥墩进行裂缝检测的过程中,运用压水试验计算等价裂缝开度判定桥墩裂缝大小及分布情况的方法.该方法在检测时间紧、桥墩高度大,短时间内无法近距离直接对裂缝进行观测的情况下,不失为一种有效实用的方法,而且可以据此对水下、地面线以下桩基础受损情况作出判断.     

运筹帷幄方能决胜千里

6月上半月,最引人注目的消息当属6月11日世界卫生组织总干事陈冯富珍宣布把甲型H1N1流感警戒级别升至6级,这意味着世卫组织认为疫情已经发展为全球性流感大流行(6月11日新华社).     

Specific in vitro antibody response to influenza virus by human blood lymphocytes.

Advances in understanding of human immune responses depend, for obvious reasons, on the use of in vitro techniques for culture of peripheral blood lymphocytes (PBL). We report here that specific antibody responses to influenza virus can readily be obtained using simple, reproducible methods. The system will be useful for the analysis of the cellular requirements for antibody production, the genetics of immune responsiveness and in clinical studies of immunosuppressed and immunodeficient patients.     

Detection of lymphocystis disease virus infection to flounder gill cells in vitro by monoclonal antibodies

Flounder gill （FG） cells were used to isolate lymphocystis disease virus （LCDV） and two monoclonal antibodies （Mabs） （1A8 and 3G3） against LCDV were used to trace LCDV infection to FG cells. FG monolayer cells was inoculated with LCDV supernatant, obtained from lymphocystis cells of diseased flounder, Paralichthys olivaceus. LCDV infection was detected with Mabs employing immunocytochemical assay （ICA） and indirect immunofluorescence assay test （IIFAT） technique. Detected by IIFAT, they were specifie for LCDV. The results of experimental infection illustrated that FG cells was sensitive to LCDV, and showed virus-infection positive detected by ICA. Cytopathic effect （CPE） occurred 1-2 days post inoculation （PI）, and half tissue culture infection dosage （TCID50） of vires supematant was 2^2.57 per 40μl. Tracing by IIFAT showed that LCDV positive signal first appeared at the cell membrane immediately PI, and then in cytoplasm at 24h PI, it reached the strongest positive at 48-72 h PI, and began to decrease at 96h PI.     

纳米铝佐剂诱导鸡提前产生抗AIVH9体液免疫应答

接种灭活油佐剂疫苗是目前国内防控禽流感主要的措施,为有效防控禽流感的流行发挥了重要的作用,但灭活苗首次接种后需要较长时间抗体才能达到有效保护水平.纳米颗粒具有独特的生物学特性,作为疫苗佐剂能引起机体强烈的免疫应答.本研究用纳米铝颗粒作为AIV H9的佐剂,结果显示,小鸡产生有效免疫保护抗体时间较常规油佐剂疫苗提前4天且无副反应,但抗体峰值和持续时间均低于油佐剂疫苗.氢氧化铝纳米颗粒作为佐剂可能对禽流感等重大传染病的紧急预防接种具有潜在的应用价值.     

2012年山西省承担的国家科技计划项目绩效分析

对2012年山西省承担的国家科技计划项目绩效进行了分析,包括这些项目的实施情况、资金投入情况、参与研究人员情况及取得的效果。     

Non-responsiveness to a foot-and-mouth disease virus peptide overcome by addition of foreign helper T-cell determinants

Study of the immune response to synthetic antigens has shown that uncoupled peptides can realize their potential as vaccines only if they contain domains that react with helper T-cell receptors and Ia antigens in addition to antibody binding sites. Here we consider whether genetically restricted non-responsiveness to an uncoupled peptide could be overcome by synthesizing a peptide with an additional helper T-cell epitope from a different protein. We demonstrate that H-2d mice, which are non-responders to the 141-160 VP1 peptide of foot-and-mouth disease virus (FMDV), can be converted into responders by immunization with peptides containing the FMDV sequence with defined 'foreign' helper T-cell determinants from ovalbumin or sperm whale myoglobin. Furthermore, the virus-neutralizing activity of the antibody raised against peptide was dependent on the determinant used. Thus, FMDV peptides with the added sequences 323-339 from ovalbumin and 132-148 from sperm-whale myoglobin elicited a high degree of neutralizing activity in B10.D2 mice. The sera from mice which received the peptide with the added sequence 105-121 from sperm whale myoglobin did not neutralize the virus, although they had high levels of anti-141-160 FMDV peptide activity. Our data indicate that the T-cell help given by the 'foreign' epitopes is B-cell clone specific. These results are likely to have important implications for the design of peptide vaccines.     

Transduction of endogenous envelope genes by feline leukaemia virus in vitro

Feline leukaemia viruses (FeLV) are exogenous retroviruses that can be detected in most cats with leukaemia, aplastic anaemia, myeloproliferative diseases and fatal immunosuppression. FeLV isolates have been divided into three subgroups, based on the viral envelope-determined properties of interference and host range in vitro. FeLV-A is present in all natural isolates and is generally minimally pathogenic. FeLV-B is found with FeLV-A in isolates from approximately 40% of natural infections and in a higher percentage of cats with lymphoma. Following the fundamental observations of genetic reassortment of avian retroviruses with endogenous viral genes and the origination of lymphomagenic viruses during the ontogeny of AKR mice, we show here that transfection of feline cells with FeLV-A DNA results in its recombination with endogenous FeLV-related sequences to produce viruses with the structural and host range properties of FeLV-B. Thus in vitro propagation of a retrovirus may result in the generation of variants with very different properties.