牦牛源正呼肠孤病毒2型的检测和分离鉴定

旨在调查川西北牦牛哺乳动物正呼肠孤病毒（MRV）的感染情况并分离病毒。采用RT-PCR方法，对采自川西北15个牧场的72份牦牛腹泻粪便样本和其中5个牧场的15份腹泻牦牛血清样本进行MRV检测，阳性样本进一步用分型PCR确定其血清型。结果显示，粪便样本中MRV检出率为20.83%（15/72），血清2型的比例为60%（9/15）；血清样本中MRV检出率为40%（6/15），血清2型的比例为83.33%（5/6）；未检测到其他血清型。成功地从腹泻粪便中分离到1株MRV血清2型毒株（TCID₅₀为4×10^-8.56·mL^-1），并获得长度为23 587 bp的分离株全基因组，该分离株与中国猪源毒株的遗传关系最近；与GenBank中所有的MRV S1基因相比，该分离株有4个独特的氨基酸突变。本研究从牦牛中检测到MRV，并分离到1株牛源MRV血清2型毒株，为进一步研究MRV血清2型生物学特性奠定了基础。     

圈养华南虎血液生化指标正常参考值初步研究

以国内部分圈养的健康华南虎Panthera tigris amoyensis作为研究对象,通过收集华南虎血液生化报告和采集华南虎血液样本检测建立样本数据,血样检测采用自动血液生化分析仪干式试剂片生化技术测定,测定血液生化指标包括血糖(GLU)、总蛋白(TP)、总胆固醇(CHOL)、总胆红素(TBIL)、肌酐(CREA)等。得到华南虎血液生化共38项指标的正常参考值范围(95%概率),其中几项主要指标正常值范围如下:GLU(2.82-11.55)mmol/L、TP(56.58-85.93)g/L、CHOL(3.32-8.66)μmol/L、TBIL(0-5.30)μmol/L、CREA(52-349)μmol/L等。统计结果显示,雌雄华南虎间血液生化指标的部分项目有差异(P <0.05),幼龄组和成年组间各项生化指标差异不显著(P >0.05),与其他虎亚种相关血液生化报道的生化指标部分有差别。华南虎血液生化指标正常参考值范围不同于其他虎亚种,建立华南虎血液生化指标正常值对华南虎的饲养管理、疾病诊治预防和保育繁殖研究工作有重要作用。     

湖南省湘西自治州动物疫病预防控制机构发展现状及建议

为了解湖南省湘西自治州动物疫病预防控制机构发展现状,采用实地走访及问卷调查方式收集数据,对兽医实验室相关人员、主要动物疫病监测经费投入、实验室检测量等情况进行分析,发现湘西州动物疫病预防控制机构存在业务工作衔接不顺畅、专业技术人员缺乏、经费不足、生物安全体系有待完善等问题。针对存在的问题,结合当地实际对湘西州动物疫病预防控制机构的建设、管理等提出了建议,以期为动物疫病预防控制机构的改革发展提供参考。     

芸薹属及其他异源多倍体植物的基因表达特征研究进展

远缘杂交及异源多倍化导致许多重要作物的起源与进化，而芸薹属栽培异源四倍种是研究作物异源多倍化的模式系统之一。异源多倍体是如何调控及协调来自不同二倍体祖先的不同基因组的遗传行为及基因表达，是过去二十年间的研究热点和重要的生物学问题。利用不断发展的分子生物学技术，一方面揭示出芸薹属及其他多倍体物种基因组表现出动态性质，即在形成初期及长期进化过程中持续发生遗传及表观遗传的变化；另一方面发现异源多倍化过程中伴随着大量的基因表达模式改变，包括非加性表达、超亲表达、表达水平显性、部分同源偏向表达、基因剂量平衡效应等现象。上述基因组结构、表观遗传改变以及基因表达模式的调控，使新产生的多倍体得以成功进化为新物种。     

基于SRP模型的南雄丹霞梧桐自然保护区生态脆弱性评价

通过建立生态敏感性-生态恢复力-生态压力度（SRP）模型，利用主成分分析法确定指标权重，对南雄丹霞梧桐自然保护区进行生态脆弱性评价。结果表明:1）从生态敏感性角度，研究区高度脆弱和极度脆弱面积分别为756.50 hm²和773.58 hm²，占比之和>50%，主要集中分布于北部和中部，而主要影响要素为土壤侵蚀强度，其次为距水源距离；2）从生态恢复力角度，研究区不脆弱和轻度脆弱面积分别为777.71 hm²和676.73 hm²，占比之和>50%，主要集中分布于西部和西南部，主要影响要素为生物多样性，其次为植被覆盖度；3）从生态压力度角度，研究区不脆弱和轻度脆弱面积分别为551.33 hm²和1 205.12 hm²，占比之和>60%，主要集中分布于西部及东部，而主要影响要素为GDP密度和人口密度；4）研究区整体生态脆弱性较高，中度及以上脆弱性面积之和达到67.72%，主要集中于研究区的中部和北部，其中生态敏感性对生态脆弱性的影响最大，说明研究区整体生态脆弱性较强，应做好生态保护工作。     

Differential regulation on C5 expression in goose versus mammals by glucose/palmitate provides a potential protection for goose fatty liver

Goose fatty liver is a specific type of nonalcoholic fatty liver that is protected from harmful effects associated with severe steatosis. Our previous findings suggest that suppression of the complement C5 may be relevant, but the mechanism is unclear. Therefore, in this study, we first verified the expression pattern of complement genes (including C5) during goose fatty liver formation and then determined the liver fat content and fatty acid composition by high-performance liquid chromatography (HPLC), followed by selecting the differential metabolites to treat HepG2, goose and mouse primary hepatocytes, aiming to explore the mechanism of C5 and inflammation suppression in goose fatty liver. The data confirmed the suppression of complement genes (including C5) in goose fatty livers. Moreover, fat content was significantly higher in fatty liver versus normal ones, with oleic acid and palmitic acid dominantly accounting for the difference. In line with this, high concentration of palmitate led to down regulation of C5 expression in goose primary hepatocytes whereas upregulation in mouse primary hepatocytes and HepG2 cells. In conclusion, regulation on C5 expression by fatty liver related factors including high level of palmitic acid may contribute to the protection of goose liver from severe hepatic steatosis.     

猫鼻气管炎病毒、怀状病毒、泛白细胞减少症病毒的分离及其其形态学观察

根据病毒的理化特性，从猫三联活疫苗中分离出猫鼻气管炎、猫西洋太和猫泛白细胞减少症病毒；筛选出每种病毒敏感的细胞，并将该3种病毒分别分别在其中传代与扩增；通过电镜观察此3种病毒的形态学特征及其在宿主细胞内增殖部位、分布情况等，并以此对猫3种病毒进行了初步鉴定。     

Genotype evaluation,muscle histopathology and ultrastructure in a Duchenne muscular dystrophy animal model

AIM: To evaluate the genotype , muscle histopathology and ultrastructure in dko mice. METHODS: Dystrophin/Utrophin-deficient double knockouts (dko) mice were obtained from university of Oxford, UK. Genotype of filial generation of heterozygote was evaluated by PCR-SSP. HE staining and fluorescent immunohistochemistry by SABC-Cy3 were used to detect striated muscle of dko mouse, and the muscle ultrastructure was observed by transmission electron microscope(TEM). RESULTS: In 112 filial generation mice, there were 28 mdx (25.0%), 26 dko (23.2%) and 58 heterozygote (51.8%), which coincided with the law of Mendelian inheritance. HE staining showed that the myocytes were not very uniform, there were phenomenon of round outline, centrally nucleated fibers, widening interspace, inflammatory cell infiltration and connective tissue proliferation in dko mice. There were no any immunofluorescent expression of dystrophin and utrophin in sarcolemma in dko mice. TEM showed sarcolemma breakage, separation and edema, and loose myofibril texture, inflammatory cell infiltration and connective tissue proliferation in dko mice. CONCLUSION: PCR-SSP is a very quick and accurate way for genotype evaluation of filial generation. The pathophysiology of dko mouse was very similar to Duchenne muscular dystrophy (DMD), and dko mouse is an ideal animal model for study of DMD clinical therapy.