不同感染状态下EB病毒核抗原亚型表达的研究

本实验用免疫印迹法纯化的抗ＥＢＮＡ亚型抗体,结合显微荧光分光光度检测技术,检测在不同感染状态下,三种亚型ＥＢＮＡ抗原在细胞中的表达程度。结果表明,处于潜伏感染状态下的Ｒａｊｉ细胞ＥＢＮＡ－１表达量较大,经巴豆油和正丁酸诱导进入钝挫感染状态后ＥＢＮＡ－１表达减少,而ＥＢＮＡ－２的表达增强。Ｂ＿（９５－８）细胞也有相似的趋势。表明ＥＢ病毒的激活可能与不同ＥＢＮＡ亚型表达量的改变有关。     

油藏注入水靶向脱硫潜力的高温脱硫菌群富集驯化

【背景】海上油田见聚后产出水硫化物超标,影响到注聚水的配聚黏度,采用生物脱硫时,由于常规除硫菌难以适应除油后产出液的高温,使得脱硫效果不佳。【目的】分析海上采出液水处理过程的菌群结构,明确生物处理各节点的菌群构成变化;开展耐高温脱硫菌驯化筛选,获得耐高温的高效脱硫菌。【方法】采集来自胜利油田海三站的水样,以16S rRNA基因高通量测序技术分析样本菌群结构,并分别在不同温度(55、60和65℃)下的无机富集培养基中进行多轮转接驯化,结合常压室温等离子体(atmospheric and room temperature plasma, ARTP)诱变技术筛选获得耐高温的脱硫菌群,采用宏基因组测序技术分析富集菌群的组成,并测定其脱硫能力。【结果】处理前的采出液水样含有较多的嗜热菌和硫酸盐还原菌,如Thermodesulfovibrio、Pseudothermotoga、Thermolithobacter、Fervidobacterium、Thermovenabulales和Pseudomonas;以厌氧气浮除油工艺处理的出水中,嗜氢菌属(Hydrogenophilus)成为最主要的优势菌,...     

自由飞行蜜蜂对静止目标形状和颜色的综合识别能力

研究了蜜蜂对相同颜色和不同颜色目标图对的形状以及颜色的综合识别能力实验过程中,蜜蜂始终处于自由飞行状态.做为刺激目标使用的图对分别有相同颜色不同几何形状、相同颜色不同拓扑结构和不同颜色几何形状三组.主要结果有三点:(1)在相同颜色的条件下,蜜蜂可以分辨出图形的几何形状,并且识别能力与图对的相似程度成反比(2)在刺激图形为环形时,蜜蜂对图形平均亮度敏感;在平均亮度相同的情况下,对环形细节变和尺寸大小不敏感.(3)在不同颜色不同几何形状的刺激条件下.蜜蜂视觉信息加工过程中颜色因素会抑制几何形状因素而起主要作用.这三个结果可以视为深入研究颜色加工通道和几何形状加工通道之间内在关系的基础.     

北美水貂和欧亚水獭在东北地区的分布与生态位重叠

作为入侵物种,北美水貂(Neovison vison)在欧洲引起了一系列生态问题,侵占了欧亚水獭(Lutra lutra)的生态空间,其入侵性对当地生物多样性和生态系统构成了严重威胁。水貂引入我国东北地区已有70多年的历史,然而国内对其野外种群却鲜有研究。掌握水貂种群的入侵范围、入侵影响因素以及与本地具有相似生态位的欧亚水獭之间的竞争关系,对水貂的入侵管理和东北地区的生物多样性保护具有重要意义。本研究利用实地调查和文献资料获取的分布信息,通过集合模型识别水貂和水獭的潜在分布区,评估水貂对水獭在地理空间上的入侵风险,并通过主成分分析(principal component analysis,PCA)评估其生态位重叠和影响因素。结果表明:(1)我国东北地区水貂的潜在分布区面积为61,944.57 km²,水獭的潜在分布区面积为83,590.94 km²,两者重叠区域面积为50,544.21 km²,占水獭潜在分布区面积的60.47%;(2)从各省分布情况来看,黑龙江省水獭受水貂入侵的风险最高,潜在分布区重叠的比例达到78.9...     

Low genetic diversity and population connectivity fuel vulnerability to climate change for the Tertiary relict pine Pinus bungeana

Endemic species are important components of regional biodiversity and hold the key to understanding local adaptation and evolutionary processes that shape species distributions. This study investigated the biogeographic history of a relict conifer Pinus bungeana Zucc. ex Endl. confined to central China. We examined genetic diversity in P. bungeana using genotyping-by-sequencing and chloroplast and mitochondrial DNA markers. We performed spatial and temporal inference of recent genetic and demographic changes, and dissected the impacts of geography and environmental gradients on population differentiation. We then projected P. bungeana's risk of decline under future climates. We found extremely low nucleotide diversity (average π 0.0014), and strong population structure (global F_ST 0.234) even at regional scales, reflecting long-term isolation in small populations. The species experienced severe bottlenecks in the early Pliocene and continued to decline in the Pleistocene in the western distribution, whereas the east expanded recently. Local adaptation played a small (8%) but significant role in population diversity. Low genetic diversity in fragmented populations makes the species highly vulnerable to climate change, particularly in marginal and relict populations. We suggest that conservation efforts should focus on enhancing gene pool and population growth through assisted migration within each genetic cluster to reduce the risk of further genetic drift and extinction.     

Structural studies of the capsular polysaccharide and lipopolysaccharide O-antigen of Aeromonas salmonicida strain 80204-1 produced under in vitro and in vivo growth conditions.

Aeromonas salmonicida is a pathogenic aquatic bacterium and the causal agent of furunculosis in salmon. In the course of this study, it was found that when grown in vitro on tryptic soy agar, A. salmonicida strain 80204-1 produced a capsular polysaccharide with the identical structure to that of the lipopolysaccharide O-chain polysaccharide. A combination of 1D and 2D NMR methods, including a series of 1D analogues of 3D experiments, together with capillary electrophoresis-electrospray MS (CE-ES-MS), compositional and methylation analyses and specific modifications was used to determine the structure of these polysaccharides. Both polymers were shown to be composed of linear trisaccharide repeating units consisting of 2-acetamido-2-deoxy-D-galacturonic acid (GalNAcA), 3-[(N-acetyl-L-alanyl)amido]-3,6-dideoxy-D-glucose[3-[(N-acetyl-L-alanyl)amido]-3-deoxy-D-quinovose, Qui3NAlaNAc] and 2-acetamido-2,6-dideoxy-D-glucose (2-acetamido-2-deoxy-D-quinovose, QuiNAc) and having the following structure: [-->3)-alpha-D-GalpNAcA-(1-->3)-beta-D-QuipNAc-(1-->4)-beta-D-Quip3NAlaNAc-(1-]n, where GalNAcA is partly presented as an amide and AlaNAc represents N-acetyl-L-alanyl group. CE-ES-MS analysis of CPS and O-chain polysaccharide confirmed that 40% of GalNAcA was present in the amide form. Direct CE-ES-MS/MS analysis of in vivo cultured cells confirmed the formation of a novel polysaccharide, a structure also formed in vitro, which was previously undetectable in bacterial cells grown within implants in fish, and in which GalNAcA was fully amidated.