骨碎补科植物叶表皮特征及其系统学意义

基于骨碎补科(Davalliaceae)植物属的界定和属下等级的划分一直存在较大争议,本研究首次对骨碎补科6属39种(秦仁昌系统)植物的叶表皮进行了扫描电镜观察。结果显示,骨碎补科有9种类型的角质层,其中,阴石蕨属(Humata)的角质层有密集的孔状凹陷结构;Wibelia条纹突起较厚,排列整齐且细密紧致;广义钻毛蕨属(Davallodes)内存在多种角质层类型,需要在属下进一步细分。本研究还根据角质层特征讨论了骨碎补科与一些近缘种类的关系。角质层特征是骨碎补科内种属分类的重要依据,而保卫细胞形状和气孔密度,均不能用来界定骨碎补科的属和种。本研究按角质层分类的结果与Kato和Tsutsumi的分子系统学分类观点一致。     

Efficient Dicer processing of virus-derived double-stranded RNAs and its modulation by RIG-I-like receptor LGP2

The interferon-regulated antiviral responses are essential for the induction of both innate and adaptive immunity in mammals. Production of virus-derived small-interfering RNAs (vsiRNAs) to restrict virus infection by RNA interference (RNAi) is a recently identified mammalian immune response to several RNA viruses, which cause important human diseases such as influenza and Zika virus. However, little is known about Dicer processing of viral double-stranded RNA replicative intermediates (dsRNA-vRIs) in mammalian somatic cells. Here we show that infected somatic cells produced more influenza vsiRNAs than cellular microRNAs when both were produced by human Dicer expressed de novo, indicating that dsRNA-vRIs are not poor Dicer substrates as previously proposed according to in vitro Dicer processing of synthetic long dsRNA. We report the first evidence both for canonical vsiRNA production during wild-type Nodamura virus infection and direct vsiRNA sequestration by its RNAi suppressor protein B2 in two strains of suckling mice. Moreover, Sindbis virus (SINV) accumulation in vivo was decreased by prior production of SINV-targeting vsiRNAs triggered by infection and increased by heterologous expression of B2 in cis from SINV genome, indicating an antiviral function for the induced RNAi response. These findings reveal that unlike artificial long dsRNA, dsRNA-vRIs made during authentic infection of mature somatic cells are efficiently processed by Dicer into vsiRNAs to direct antiviral RNAi. Interestingly, Dicer processing of dsRNA-vRIs into vsiRNAs was inhibited by LGP2 (laboratory of genetics and physiology 2), which was encoded by an interferon-stimulated gene (ISG) shown recently to inhibit Dicer processing of artificial long dsRNA in cell culture. Our work thus further suggests negative modulation of antiviral RNAi by a known ISG from the interferon response.     

野生大豆抗感大豆孢囊线虫材料内生细菌多样性分析

【目的】对抗感野生大豆材料根内生细菌的多样性进行比较分析,为研究野生大豆内生细菌与大豆孢囊线虫之间的相互关系奠定基础。【方法】在野生大豆抗大豆孢囊线虫3号生理小种筛选基础上,利用扩增核糖体DNA限制性分析(Amplified ribosomal DNA restriction analysis,ARDRA)和16S rDNA克隆文库测序相结合的方法,对抗感野生大豆根系内生细菌多样性及群落结构进行分析。【结果】野生大豆根内生细菌分属于6大类群,其中变形菌门(Proteobacteria)和厚壁菌门(Firmicutes)为优势类群,相对丰度分别为46.8%和13.6%,另外有少量的放线菌门(Actinobacteria)、拟杆菌门(Bacteroidetes)、酸杆菌门(Acidobacteria)、异常球菌-栖热菌门(Deincoccus-Thermus)和古细菌(Archaea),18.8%克隆序列与环境中未培养细菌的16S rDNA序列有较高的相似性。野生大豆高抗材料内生细菌的多样性比高感材料更为丰富,且抗感材料内生细菌优势菌群存在明显差异,中慢生根瘤菌(Mesorhizobium tamadayense)、肠杆菌(Enterobacter ludwigii)和巨大芽孢杆菌(Bacillus megaterium)为野生大豆高抗材料特有的可操作分类单元(Operational Taxonomic Units,OTUs)中的优势种群。【结论】研究结果表明抗感野生大豆根内生细菌的优势种群存在明显差异,而内生细菌的优势种群与大豆孢囊线虫的相互关系正在深入分析研究。     

Numerical simulation of the effect of superparamagnetic nanoparticles on microwave rewarming of cryopreserved tissues

In this study, the microwave rewarming process of cryopreserved samples with embedded superparamagnetic (SPM) nanoparticles was numerically simulated. The Finite Element Method (FEM) was used to calculate the coupling of the electromagnetic field and the temperature field in a microwave rewarming system composed of a cylindrical resonant cavity, an antenna source, and a frozen sample phantom with temperature-dependent properties. The heat generated by the sample and the nanoparticles inside the electromagnetic field of the microwave cavity was calculated. The dielectric properties of the biological tissues were approximated using the Debye model, which is applicable at different temperatures. The numerical results showed that, during the rewarming process of the sample phantom without nanoparticles, the rewarming rate was 29.45 °C/min and the maximum temperature gradient in the sample was 3.58 °C/mm. If nanoparticles were embedded in the sample, and the cavity power was unchanged, the rewarming rate was 47.76 °C/min and the maximum temperature gradient in the sample was 1.64 °C/mm. In the presence of SPM nanoparticles, the rewarming rate and the maximum temperature gradient were able to reach 20.73 °C/min and 0.68 °C/mm at the end of the rewarming under the optimized cavity power setting, respectively. The ability to change these temperature behaviors may prevent devitrification and would greatly diminish thermal stress during the rewarming process. The results indicate that the rewarming rate and the uniformity of temperature distribution are increased by nanoparticles. This could be because nanoparticles generated heat in the sample homogeneously and the time-dependent parameters of the sample improved after nanoparticles were homogeneously embedded within it. We were thus able to estimate the positive effect of SPM nanoparticles on microwave rewarming of cryopreserved samples.     

微生物原生质体融合育种技术及其应用

工业微生物菌种选育在发酵工业中占有重要地位。微生物原生质体融合(microbial protoplast fusion)技术具有重组频率高、受结合型或致育型限制小以及遗传物质传递完整等优点,是微生物育种最常用的方法之一。结合相关研究进展,分析了原生质体融合技术的组成,包括制备、再生、融合的影响因素以及融合子的筛选方法,重点评述了原生质体融合技术应用在微生物育种中的最新进展,以及微生物原生质体融合技术的发展前景。     

PVA颗粒超选择栓塞支气管动脉治疗急性大咯血

目的:探讨应用介入技术,超选择支气管动脉,行PVA颗粒栓塞治疗急性大咯血的治疗价值.方法:对我院2001年以来34例采用PVA颗粒栓塞的大咯血病人的术后反应.并发症发生情况及止血情况进行随访和回顾性分析.结果:所有病人均为一次性栓塞成功,术后随访时间长迭36个月,随访率达100%.除一例肺癌病人因咯血死亡外,未发现复发性咯血.术后病人出现胸部疼痛症状,短期内对证治疗可以缓解.未见明显并发症发生.结论:应用PVA颗粒栓塞支气管动脉是治疗急性大咯血的一种有效方法.     

广东省南昆山伯乐树群落特征及其保护策略

在广东省南昆山自然保护区内调查了中国特有珍稀植物伯乐树种群的分布格局、龄级结构和伴生群落的物种组成.结果表明:该种群的分布范围狭窄且集中;龄级不完整,Ⅱ、Ⅲ级幼树少见,结构呈衰退型;伴生群落呈典型的亚热带植物区系的特点,其组成不稳定、优势种不显著.建议将伯乐树幼树作为就地保护的重点,适当去除周围的罗浮槭、羊角杜鹃和黄樟等速生树种,以创造有光照和水肥条件的生境;对于Ⅳ级以上成株,应注意拟赤杨和华润楠等空间生态位相近树种的数量和密度,适当疏剪枝条,以帮助成株占据较好的空间位;同时再积极引入异龄的伯乐树幼苗,促进种群恢复和发展.     

以潮霉素B抗性为选择标记的深黄被孢霉原生质体转化

利用亚硝基胍(MNNG)诱变方法筛选了一株深黄被孢霉潮霉素B敏感型菌株M6-22-4。采用PEG介导的方法,将含有E.coli潮霉素B抗性标记的PD4质粒转入敏感株M6-22-4原生质体,并在潮霉素B浓度为400μg/mL的选择培养基上筛选转化子,获得了1.6~2.8个转化子/μg质粒DNA的转化频率。稳定性实验表明,质粒线性化后所获得的转化子在PDA培养基上传代10代以后,转接到选择平板上有31.6%仍具有HmB抗性;随机挑选了3个转化子,通过PCR方法检测到潮霉素抗性基因的存在,Southern杂交发现,潮霉素抗性基因已经以1~2拷贝数整合到深黄被孢霉M6-22-4染色体上,这是深黄被孢霉转化系统的首次报道。