Windows2000的安全防护

从操作系统的设置、维护、管理和病毒防御等方面，介绍了Windows2000使用中的安全防护问题。     

地震前兆信息网安全管理的几个问题

从主机系统安全、服务软件配置、网络系统安全、木马和病毒防范以及安全管理制度等几个方面进行了探讨，总结了基于NT技术的前兆网络安全防范问题，给出了加强前兆网络安全的一些措施和建议。     

如何防范网络病毒

计算机病毒已成为信息社会的公害，被病毒攻击的有些数据是不可恢复的，一旦破坏就永远消失，造成不可估量的损失，管理好计算机网络是预防计算机病毒的最好方法。     

关于局域网建设的几点思考

通过对局域网建设中一些问题的分析,提出了从设备安装、运用技术措施、采用各种策略加强网络的管理等方面入手来建设局域网,从而保证局域网络的正常运行.     

蜱虫致死原因：新致命病毒

蜱虫是去年最令中国人恐慌的一种虫子，现在研究人员已经发现了蜱虫盯咬致死的原因。     

In vivo neutralization assays by monoclonal antibodies against white spot syndrome virus in crayfish(Cambarus proclarkii)

The neutralizing activities of eight monoclonal antibodies （MAbs） against white spot syndrome virus （WSSV） （2D2, 2B2,1D2, 1D5, 1C2, 4A1, 6A4 and 6B4） were analyzed by in vivo experiments. Gills from WSSV-infected shrimp were homogenized and ten-fold serially diluted by PBS, and then incubated with MAbs （hybridoma culture supernatant）, respectively. The mixture of WSSV and MAbs were injected into crayfish （Procambarus clarkii）. After challenge, the death rates of crayfish were counted to determine the neutralizing activities of MAbs. At the same time, the mixture of myeloma culture supernatant and WSSV or PBS was served as positive or negative control, respectively. The results showed that, at each virus dilution, the mean time to death of the crayfish injected with MAb-treated virus was significantly longer than that in the positive control, though they all showed 100% mortality within 25 d, and meanwhile, few crayfish died in the negative control. Among the eight MAbs, 2D2, 2B2, 1D2 and 1D5, especially the former two, delayed the mortality significantly, and 1 C2, 4A1 and 6A4 delayed the mortality as well but not so efficiently, while MAb 6IM was efficient only when the virus concentration increased. The results indicated that the anti-WSSV MAbs can neutralize WSSV in different virus dilutions.     

对虾传染性皮下及造血组织坏死病毒衣壳蛋白基因的克隆表达及抗体制备

本文根据GenBank登录的对虾传染性皮下及造血组织坏死病毒(IHHNV)的全基因组序列(NC-002190),设计出主要结构蛋白基因的相应引物,从厦门发病的对虾中,提取DNA,以此为模板,利用PCR扩增目的基因.再将目的基因分别与pGEX-6p1载体和pET-28a载体连接,构建重组表达载体pGEX-Ⅳ、pET-Ⅳ,重组子经酶切和测序鉴定后导入表达型大肠杆菌BL21,IPTG诱导表达,SDS-PAGE检测,大小约为62KDa和41KDa,与预测大小一致.将pET-Ⅳ表达重组蛋白经纯化,免疫小鼠,Western免疫印迹反应结果表明其抗体均可与pGEX-Ⅳ和pET-Ⅳ表达的蛋白发生特异性反应.本研究的结果为对虾IHHNV的快速检测及其免疫提供了研究基础.     

运用荧光显微技术分析北黄海夏季浮游病毒的分布

运用荧光显微技术(Epifluorescence Microscopy,EFM),对2006年夏季北黄海水域31个站点的病毒丰度进行了检测,对浮游病毒丰度在水平分布,垂直分布和昼夜变化上进行了探讨.北黄海水域浮游病毒直接检测量(Virus Direct Count,VDC)为(1.58×106～1.38×107)/mL,平均为5.86×106/mL.在水平分布上,表层、30 m和底层水在辽东半岛头部附近出现了病毒较高区域,近海水域的病毒丰度较中部水域高(P＜0.05).在垂直分布上,表层浮游病毒丰度高于30 m水层和底层(P＜0.05).在昼夜变化上,表层水体中浮游病毒量有明显的变化,10 m水层和30 m水层的病毒丰度昼夜变化较明显,底层病毒丰度昼夜趋势平缓.利用多元相关分析可知,北黄海夏季浮游病毒丰度与站位总水深(P＜0.01)和盐度(P＜0.05)成一定的负相关性,与温度无明显相关性(P＞0.05).     

Sequence analysis and quantitative detection of Norwalk-like viruses in cultured oysters of China

We isolated 4 Norwalk-like viruses (NLVs) contaminated oysters from 33 Chinese oysters collected from local commer-cial sources of Shandong Province. After amplification of the RNA-dependent RNA polymerase (RdRp) region of NLVs genomes with RT-PCR, the open reading frame 1 (ORF1) of the RdRp was sequenced and subjected to multiple-sequence alignment. The re-suits showed that NLVs in the four isolates belong to genogroup Ⅱ. The sequence comparison showed that the similarity between four Chinese oyster isolates were higher than 99.0%, which indicated that NLVs prevalent in close areas have high homogeneity in genome sequences. In addition, the most conserved sequences between diverse NLVs were used to design primers and TaqMan probes, then the real-time quantitative PCR assay was performed. According to the standard curve of GII NLVs, the original amounts (copies) of NLVs in positive patient's fecal isolate, positive Japanese oyster isolate, and the Chinese oyster isolate were 8.9×108, 1.25×108 and 4.7×101 respectively. The detecting limit of NLVs was 1×101 copies. This study will be helpful for routine diagnosis of NLVs pathogens in foods and thus for avoiding food poisoning in the future.     

三疣梭子蟹几丁质酶基因(PtCht6)的克隆及其在免疫中的功能分析

几丁质酶(chitinase)在甲壳动物的蜕皮、消化和免疫等很多生物学过程中发挥重要功能,为深入探讨几丁质酶的免疫防御机制,本实验利用RACE技术克隆了三疣梭子蟹(Portunus trituberculatus)PtCht6基因。该基因cDNA全长2736bp,开放阅读框(ORF)2103bp,编码700个氨基酸,具有几丁质酶GH18家族典型特征。利用实时荧光定量技术分析PtCht6在三疣梭子蟹不同组织、不同蜕皮阶段、不同病原感染以及低盐胁迫(11)下的表达特征,结果显示:PtCht6在各组织中均有表达且在肝胰腺中的表达量最高;在不同蜕皮时期的肝胰腺中,其表达量由蜕皮后期(A/B)、蜕皮间期(C)、蜕皮前期(D)依次递减(P0.05);人工感染WSSV和副溶血弧菌后.PtCht6的表达量在肝胰腺中分别于12h、72h达到最大值,在血细胞中均于12h达到最大值,且相较于对照组,整体显著上调表达(P0.05);低盐胁迫能够显著抑制该基因的表达,最高抑制73倍(P0.05)。同时发现,低盐环境下感染WSSV后,该基因达到峰值的时间明显延迟(至少延迟12h.P0.05)。该研究结果预示PtCht6作为免疫因子参与三疣梭子蟹的病原防御,且低盐胁迫在一定程度上抑制了该基因的免疫功能。