应用镰形扇头蜱及巴贝斯虫病水牛的染虫血感染黄牛试验

从非流行区购进无蜱寄生的健康黄牛５头与水牛犊１头，其中３头成年黄牛（２～８岁）在畜舍内用从流行区水牛身上采得的镰形扇头蜱Ｒｈｉｐｉｃｅｐｈａｌｕｓｈａｅｍａｐｈｙｓａｌｏｉｄｅｓｈａｅｍａｐｈｙｓａｌｏｉｄｅｓ成虫，置于牛耳壳内叮咬；１头运至流行区放牧，让蜱上身叮咬；１头黄牛犊（１０年龄）去蜱后２周，用液氮保存的患病水牛染虫血４ｍｌ（４×１０ ８个虫体）皮下注射；另一头去蜱水牛犊亦同时注射相同剂量的染虫血，作为对照。５头黄牛在试验期间其体温、精神、食欲正常，未出现任何临床症状，感染后１０～１２ｄ外周血液中出现少量不典型的牛巴贝斯虫，红细胞染虫率在０．１％以下，持续３～５６消失；对照牛则体温升高（３９．８～４１．１℃），出现贫血、黄疸等症状，红细胞压积（ＰＣＶ）降至２６％，外周血液中出现典型的牛巴贝斯虫，红细胞染虫率（ＰＰＥ）高达１２％。对采用蜱叮咬及注射来自病水牛的染虫血为何不能使黄牛感染发病，文中进行了讨论。     

Phylogenetic analysis of S1 gene of infectious bronchitis virus isolates from China

Between 2006 and 2009, seven strains of infectious bronchitis (IB) virus (IBV) were isolated from vaccinated chicken flocks on different chicken farms in China. The pathogenic characters of seven IBV strains were assessed. Each of the seven strains was infective to the test chickens and could induce an immune response. The results from chicken embryo cross-neutralization assays showed that these strains were antigenically distinct from classic IBV strains of H120, M41, Conn, and Gray. Compared to H120 vaccine strain, point mutation, short insertion, and deletion occurred at many positions in the S1 protein of the seven strains. Five of the seven strains had the motif (HRRRR), which was identical to that of the epidemic IBV strains in China. Two new motifs (HRLRR and RRIRR) emerged in the isolated strains. The homology of the nucleotide and amino acid sequences of the S1 gene among the seven isolates was 81.7%-99.7% and 79.0%-99.4%, respectively. These seven strains were also genetically different from the vaccine strains and non-China IBV strains but closely related to large numbers of Chinese strains. The seven isolates and 36 reference IBV strains were clustered into six distinct groups (I-VI). The seven strains were categorized into groups I, II, and III, forming a big phylogenetic branch, which is closely related to Chinese IBVs, whereas the vaccine strains belonging to group VI are genetically distant from groups I, II, and III. The results from this study indicate that different IBV strains cocirculate in the chicken population in China.     

山羊子宫内肽能神经分布及妊娠时的变化

采用免疫组化方法，研究了山羊子宫内含P物质（SP）和含血管活性肠肽（VIP）神经的分布。结果，妊娠及未妊娠山羊子宫颈内有粗细不等的神经束行经于外膜和肌层中，神经分支形成丛状分布于血管壁，子宫颈部未见SP神经元胞体及VIP神经元胞体；未妊娠山羊子宫角内SP神经和VIP神经均呈丛状围绕血管并分布于血管壁；妊娠中期的孕角和非孕角均有胎盘形成，除胎盘内无神经分布外，SP神经及VIP神经同样分支形成丛状分布于血管壁。结果提示，山羊子宫内SP神经和VIP神经主要支配子宫内血管，妊娠时除胎盘内无神经分布外，SP神经及VIP神经的分布无明显变化。     

家蚕对核型多角体病的抗性及遗传规律的研究

试验研究了家蚕对ＮＰＶ病的抵抗性及其遗传规律，结果表明：家蚕品种间存在抗性差异，幼虫期的攻毒发病率与全龄虫蛹率成极显著的负相关，抗性对感性呈不完全显性，是由两对以上基因控制的，至少有一对为主效基因，再一次证明有偏父遗传现象，其狭义遗传力为３６．１％。     

细胞凋亡的常用调控基因研究近况

细胞凋亡主要受基因的控制，现已发现许多基因对细胞凋亡均有直接或间接的调控作用。通常将这些基因分为两大类，即细胞生存基因和细胞死亡基因。一般认为与细胞生存有关的基因包括C－myc,C-abl,Ras,V-src,Bcl-2,EIB,LMW5-HL,C-kit和Bcl-x等；与细胞死亡有关的基因包含P^35,P^53,RB,DCC,WT-1,CpGv,Bcr-abl,V-erb-A,tats20,DAD1,ADO/Fas,TGF-β，TRP－2，RP－8，TRPM－2，SGP－2，TIA，Bax,ICE,C-rel,irrecrst等。本文对目前使用较多研究较深入的几种凋亡调控基因，即C－myc基因，Bcl-2基因，P^53基因，ICE基因，Fas基因及FasL和Cdc2基因的来源，作用和相互间关系的研究近况，予以综述，做一简介。     

赤霉酸与杀菌剂处理对蒜薹贮存期品质的影响

研究旨在通过赤霉酸和杀菌剂处理,在降低蒜薹病害发生的同时较好地保持其品质.以金乡蒜薹为研究对象,分别设置赤霉酸GA3 50 mg/L(S2)、赤霉酸GA4+7 50 mg/L(S3)、赤霉酸GA4+7 25 mg/L(S4)、咪鲜胺800倍液(S5)、吡唑醚菌酯1500倍液(S6)、GA4+7 25 mg/L+GA32...     

外来物种琵琶鼠鱼与本地物种鲫鱼混养的初步研究

试验探究了外来物种琵琶鼠鱼(Pterygoplichthys multiradiatus)和本地物种鲫鱼(Crucian carp)混养时的关系,研究入侵物种对生物多样性和生态环境的破坏。结果表明,琵琶鼠鱼与鲫鱼在不同配比的混养情况下,体重均表现为降低,其中琵琶鼠鱼的体重下降更多,但均有正增长的趋势。琵琶鼠鱼与鲫鱼之间存在空间竞争关系,且鲫鱼表现出更强的竞争优势。     

Sequence Analysis and Prokaryotic Expression of NSP1 Gene of Bovine Rotavirus UK Strain

Rotavirus is a major cause of acute diarrhea in both many kinds of young animals and children under 5 years old.Rotavirus NSP1, a 55 ku RNA binding protein, is the product of gene 5, which can subvert innate immune responses and be one of virulent determinant factors.According to the sequence in GenBank, specific primers targeting to NSP1 gene were designed and the gene was amplified by RT-PCR, following by being cloned into the pET-28a(+) vector.It showed that the full length of NSP1 gene was 1 473 bp, encoding 491 amino acids.The NSP1 shared the highest identity with WC3 strain.The recombinant protein was induced in E.coli Rosetta(DE3) by IPTG and was analyzed by SDS-PAGE and Western blotting.The results revealed that NSP1 recombinant protein existed in the form of inclusion body with the molecular weight of 55 ku.The purified recombinant protein could be recognized by His-tag antibody.This study laid the foundation for further research on the relationship between the intracytoplasmic location of NSP1 protein and its activity.