樟树(Cinnamomum camphora)幼苗细根形态对氮磷添加和幼苗密度的响应

全球氮沉降对森林生态系统结构和功能的影响已成为现代生态学研究热点之一,我国华南地区氮沉降的增长引起了土壤酸化和磷限制加剧等一系列生态问题。密度制约着植物个体对环境资源的吸收利用,是自然界中十分重要的选择压力之一。因此研究樟树(Cinnamomum camphora)幼苗的细根形态对氮磷添加和密度的响应,有利于了解亚热带树木根系对氮沉降和磷添加与林分密度的响应过程和机制,并为全球变化背景下樟树林生态系统的管理提供依据。本研究以1年生樟树幼苗为试验材料,选择氯化铵(NH_4Cl)作为氮肥以模拟大气氮沉降,并且以二水合磷酸二氢钠(NaH_2PO_4·2H_2O)模拟磷添加,氮磷处理设置4个水平,即对照、施N、施P和施N+P;种植密度设置10、20、40和80株/m~2 4个水平。测定各处理樟树幼苗细根的根长、表面积、体积和根尖数,分析氮磷添加、密度和两者交互作用对樟树幼苗细根的影响。研究结果表明,与对照处理相比,N、P和N+P处理促进了幼苗细根长度、表面积、体积以及根尖数的增加。低密度条件下的N添加对幼苗根系形态的促进效果强于P添加。N+P处理对10、20、40株/m~2幼苗根系形态的促进效果最佳,而各处理对80株/m~2幼苗根系形态的促进效果均无显著性差异。随着种植密度的增大,幼苗细根长度、表面积、体积和根尖数均减少。樟树幼苗的细根长度、表面积、体积和根尖数在各密度间和不同氮磷添加处理间均有显著性差异,密度和氮磷处理间的交互作用对根系形态各指标均无显著影响。     

昆虫病原斯氏线虫SY-5对重组Cip晶体蛋白的营养利用（英文稿）

【目的】初生型Photorhabdus luminescens细菌产生两种胞内晶体蛋白CipA和CipB,为其共生的昆虫病原异小杆线虫提供营养。探索非共生的斯氏线虫对Cip蛋白的营养利用情况。【方法】在已构建重组Cip蛋白大肠杆菌表达体系的基础上,建立重组菌细胞与无菌斯氏SY-5线虫共培养系统,检测线虫的生长发育情况。【结果】Cip蛋白对目标线虫生长有显著支持作用:发育为成虫的比例达到65%-82%,雌虫的怀卵率为80%-95%,平均怀卵量为30-50粒,并显著降低各虫态的死亡率。【结论】Cip蛋白不仅为共生的异小杆线虫提供营养,亦能为斯氏线虫所利用。     

微生物菌剂对楸树幼苗生长及根际土细菌群落结构的影响

为探究球毛壳ND35微生物菌剂对楸树幼苗生长及土壤肥力的作用机制,本研究楸树幼苗为研究对象,采用室内盆栽试验,设计0（CK）,10（T1）,15（T2）,20（T3）4种微生物菌剂施用量,测定幼苗生长情况、土壤微生物组成结构、土壤酶和土壤养分等特征。研究结果如下：（1）球毛壳ND35微生物菌剂可显著促进楸树幼苗的生长,株高、地径、地上及地下生物量显著提高（P<0.05）,T2处理下促生效果最好。（2）施用球毛壳ND35微生物菌剂可显著提高土壤中有机质、硝态氮、铵态氮含量及脲酶、磷酸酶、蔗糖酶活性（P<0.05）。（3）球毛壳ND35微生物菌剂可显著影响土壤细菌群落组成,提高细菌群落的丰富度和多样性,使土壤中β-变形菌纲（Betaproteobacteria）、γ-变形菌纲（Gammaproteobacteria）的相对丰度显著下降,α-变形菌纲（Alphaproteobacteria）、δ-变形菌纲（Deltaproteobacteria）的相对丰度呈显著提高,可使土壤中鞘氨醇单胞菌属（Sphingomonas）的相对丰度显著提高21.88%-103.56%（P<0.05）,芽孢杆菌属（Bacillus）的相对丰度提高66.28%-65.97%（P<0.05）,酸杆菌属（Acidibacter）的相对丰度提高12.76%-38.06%。（4）冗余分析（RDA）结果表明,土壤硝态氮、铵态氮、有机质是影响土壤细菌群落分布和多样性的重要环境因子,土壤细菌群落结构的改变会显著影响土壤脲酶、蔗糖酶、碱性磷酸酶的活性。因此,施用球毛壳ND35微生物菌剂可通过影响植物根际土壤的化学性质及生物性质,促进楸树幼苗的生长。这一研究结果为楸树繁育提供了新的指导方向,亦为将其用于困难立地及退化生态系统植被恢复提供基础理论指导。     

Caveolin-1 identified as a key mediator of acute lung injury using bioinformatics and functional research

Acute lung injury (ALI) is a potentially life-threatening, devastating disease with an extremely high rate of mortality. The underlying mechanism of ALI is currently unclear. In this study, we aimed to confirm the hub genes associated with ALI and explore their functions and molecular mechanisms using bioinformatics methods. Five microarray datasets available in GEO were used to perform Robust Rank Aggregation (RRA) to identify differentially expressed genes (DEGs) and the key genes were identified via the protein-protein interaction (PPI) network. Lipopolysaccharide intraperitoneal injection was administered to establish an ALI model. Overall, 40 robust DEGs, which are mainly involved in the inflammatory response, protein catabolic process, and NF-κB signaling pathway were identified. Among these DEGs, we identified two genes associated with ALI, of which the CAV-1/NF-κB axis was significantly upregulated in ALI, and was identified as one of the most effective targets for ALI prevention. Subsequently, the expression of CAV-1 was knocked down using AAV-shCAV-1 or CAV-1-siRNA to study its effect on the pathogenesis of ALI in vivo and in vitro. The results of this study indicated that CAV-1/NF-κB axis levels were elevated in vivo and in vitro, accompanied by an increase in lung inflammation and autophagy. The knockdown of CAV-1 may improve ALI. Mechanistically, inflammation was reduced mainly by decreasing the expression levels of CD3 and F4/80, and activating autophagy by inhibiting AKT/mTOR and promoting the AMPK signaling pathway. Taken together, this study provides crucial evidence that CAV-1 knockdown inhibits the occurrence of ALI, suggesting that the CAV-1/NF-κB axis may be a promising therapeutic target for ALI treatment.Subject terms: Cell signalling, Respiratory tract diseases     

克氏原螯虾嗜水气单胞菌噬菌体的分离鉴定和应用

为分离获得致病性嗜水气单胞菌烈性噬菌体,鉴定和研究其生物学特性,为克氏原螯虾细菌性疾病的防治和治疗提供依据,研究以患病克氏原螯虾分离到的致病性嗜水气单胞菌为宿主菌,从湖泊水体中分离到多株噬菌体,对其中一株烈性噬菌体Ph-0进行了生物学特性的分析,包括噬菌斑形态的观察,最佳感染复数的测定,一步生长曲线的绘制,热稳定性的测...     

Age‐related memory vulnerability to interfering stimuli is caused by gradual loss of MAPK‐dependent protection in Drosophila

Age‐related memory impairment (AMI) is a common phenomenon across species. Vulnerability to interfering stimuli has been proposed to be an important cause of AMI. However, the molecular mechanisms underlying this vulnerability‐related AMI remain unknown. Here we show that learning‐activated MAPK signals are gradually lost with age, leading to vulnerability‐related AMI in Drosophila. Young flies (2‐ or 3‐day‐old) exhibited a significant increase in phosphorylated MAPK levels within 15 min after learning, whereas aged flies (25‐day‐old) did not. Compared to 3‐day‐old flies, significant 1 h memory impairments were observed in 15‐, 20‐, and 30‐day‐old flies, but not in 10‐day‐old flies. However, with post‐learning interfering stimuli such as cooling or electric stimuli, 10‐day‐old flies had worse memory performance at 1 h than 3‐day‐old flies, showing a premature AMI phenomenon. Increasing learning‐activated MAPK signals through acute transgene expression in mushroom body (MB) neurons restored physiological trace of 1 h memory in a pair of MB output neurons in aged flies. Decreasing such signals in young flies mimicked the impairment of 1 h memory trace in aged flies. Restoring learning‐activated MAPK signals in MB neurons in aged flies significantly suppressed AMI even with interfering stimuli. Thus, our data suggest that age‐related loss of learning‐activated neuronal MAPK signals causes memory vulnerability to interfering stimuli, thereby leading to AMI.