毒死蜱与噻嗪酮、吡虫啉混用防治稻飞虱和二化螟田间试验

20 0 2年在安徽省庐江县 4次田间试验结果表明 ,防治 3代和 4代稻飞虱 (Sogatellafurcifera(Horvath)和Nilaparvatalugens(St l) ) ,667m2 用 48%毒死蜱乳油 41 67mL +1 0 %吡虫啉可湿性粉剂 2 0g的处理 7d后防治效果分别为 93 0 3 %和 92 67% ,毒死蜱 5 2 0 8mL +2 5 %噻嗪酮可湿性粉剂 5 0g分别为92 79%和 95 2 2 %。防治 2代和 3代二化螟Chilosuppressalis(Walker) ,667m2 用毒死蜱 41 67mL +吡虫啉2 0g的处理 1 6d后防治效果分别为 73 2 2 %和 80 43 % ,毒死蜱 5 2 0 8mL +噻嗪酮 5 0g分别为 76 81 %和84 80 %。建议交替轮换使用以上混剂及剂量 ,并掌握在稻飞虱低龄若虫高峰期和二化螟卵孵高峰期施药 ,可有效防治稻飞虱和二化螟。     

白化和黄化茶树品种绿茶游离氨基酸、儿茶素类及咖啡碱差异分析

为探究以白化和黄化茶树品种鲜叶为原料制成的绿茶滋味品质和代谢物差异,对广德市6个白化品种绿茶(奶白茶)和14个黄化品种绿茶(黄金芽茶)进行感官审评和代谢物分析。结果表明,奶白茶滋味鲜爽而收敛性略弱;黄金芽茶滋味收敛性强而鲜度低于奶白茶。游离氨基酸总量以及呈现鲜味、甜味的游离氨基酸在奶白茶中的含量显著高于黄金芽茶,而贡献收敛性的儿茶素类化合物和没食子酸含量以及呈现苦味的咖啡碱含量在奶白茶中显著低于黄金芽茶。偏最小二乘法判别分析(PLS-DA)表明导致两种绿茶滋味差异的标志性化合物有7种,分别是茶氨酸、精氨酸、谷氨酸、天冬氨酸、表没食子儿茶素没食子酸酯(EGCG)、表儿茶素没食子酸酯和咖啡碱。味觉活性值(Dot)最高的EGCG在黄金芽茶中的呈味贡献显著高于奶白茶。因此,游离氨基酸、儿茶素类化合物、没食子酸和咖啡碱含量差异导致白化和黄化茶树品种绿茶滋味不同。     

种子散布位置对格氏栲幼苗根系形态及生长特征的影响

种子从母株掉落于地面萌发后,其根系在不同散布位置(凋落物上层、土壤表层和凋落物下层)的生长形态影响幼苗定居及建成,而目前对其根系形态及生长特征的了解并不充分,限制了对幼苗根系在不同散布下适应策略的理解。为此,以格氏栲(Castanopsis kawakamii)为研究对象,通过模拟种子在凋落物中位置,设置凋落物上层(种子下层铺垫2 cm和4 cm凋落物,U2和U4处理)、土壤表层与凋落物下层(种子上层覆盖0、2、4、6 cm和8 cm凋落物,CK、D2、D4、D6和D8处理)等3种散布,探讨不同散布位置对格氏栲幼苗根系9个生长指标的影响。结果表明：(1)种子散布位置对幼苗根干物质质量具有显著影响,D2处理达最大值。(2)D2处理的幼苗根长、根表面积、根尖数、分枝数和比根长高于其它处理;根系平均直径在D6处理达最大值。(3)相关分析表明根长、根表面积、根尖数、分枝数和比根长与根系平均直径呈显著负相关关系。(4)对根系9个生长指标提取主成分后聚类为4个类群,D2与D4处理各划分一类;U2与U4处理划分一类,其余三个处理划分一类。综上所述,凋落物浅层覆盖(D2处理)适宜格氏栲根系生长;凋落物...     

短时低温对茶黄蓟马发育与繁殖的影响

蓟马是芒果的重要害虫,为探明短时低温对蓟马发育与繁殖的影响,以为害芒果的蓟马优势种茶黄蓟马Scirtothrips dorsalis为对象,将其放置于8℃和12℃(RH 75%±10%, 12 L∶12 D)人工气候箱内,分别处理6 h、12 h及24 h,观察若虫的存活率、发育历期及成虫寿命和繁殖力。结果表明：短时低温暴露对茶黄蓟马若虫的发育历期有一定的影响,不同龄期对低温的响应有所不同,若虫期经历短时低温会显著降低成虫寿命;短时低温暴露对所处理龄期及世代的存活能力均造成显著影响,处理温度越低时间越长,存活率下降越显著,其中2龄若虫在8℃下处理24 h,若虫期的累计存活率最低,仅6.86%。结果说明短时低温暴露后对成虫寿命和产卵量均产生不利的影响,处理温度越低时间越长,影响越大。     

基于蛋白序列的IDQD算法预测蛋白质相互作用

基于蛋白质序列组分信息,提出一个离散增量结合二次判别分析法(IDQD)预测蛋白质相互作用的模型,对人类蛋白质相互作用进行预测.自洽检验的识别精度达到75.89%,3-fold交叉检验的敏感性和特异性分别为64.22%和64.68%.结果表明IDQD算法可以用于蛋白质相互作用的预测.     

Low-expression of E-cadherin in leukaemia cells causes loss of homophilic adhesion and promotes cell growth

E-cadherin (epithelial cadherin) belongs to the calcium-dependent adhesion molecule superfamily and is implicated in the interactions of haematopoietic progenitors and bone marrow stromal cells. Adhesion capacity to bone marrow stroma was impaired for leukaemia cells, suggesting that a breakdown of adhesive mechanisms governed by an adhesion molecule may exist in leukaemic microenvironment. We previously found that E-cadherin was low expressed in primary acute leukaemia cells compared with normal bone marrow mononuclear cells. In this study, we investigate the functional importance of low E-cadherin expression in leukaemia cell behaviours and investigate its effects in the abnormal interaction of leukaemic cells with stromal cells. After expression of E-cadherin was restored by a demethylating agent in leukaemia cells, E-cadherin-specific adhesion was enhanced. Additionally, siRNA (small interfering RNA)-mediated silencing of E-cadherin in Raji cells resulted in a reduction of cell homophilic adhesion and enhancement of cell proliferation and colony formation. These results suggest that low expression of E-cadherin contributes to the vigorous growth and transforming ability of leukaemic cells.     

An efficient molecular docking method for adsorbent screening

In this study, with flavonol glycosides (FG) and terpene lactones (TL) in ginkgo biloba extract (GBE) as the targets for separation, we investigated the effectiveness of molecular docking in adsorbent screening. Several polyamine-modified methyl acylate-co-divinylbenzene (MA-co-DVB) adsorbent models were built, and their affinity to rutin, quercetin and ginkgolide B (GB) was evaluated via molecular docking. The model of ethylenediamine-modified adsorbent showed the largest difference in affinity between to GB and to quercetin as well as rutin, and thus this adsorbent could have the best separation performance. The results of the subsequently conducted static adsorption and dynamic adsorption experiments correlated well with docking results. Finally, using ethylenediamine-modified MA-co-DVB adsorbent, nearly complete separation of the FG and TL in GBE was simply achieved by one step of adsorption-desorption. Thus, the reported molecular docking method is expected to be helpful for rapid adsorbent screening.     

Magnetic resonance imaging of bone marrow cell-mediated interleukin-10 gene therapy of atherosclerosis

Background

A characteristic feature of atherosclerosis is its diffuse involvement of arteries across the entire human body. Bone marrow cells (BMC) can be simultaneously transferred with therapeutic genes and magnetic resonance (MR) contrast agents prior to their transplantation. Via systemic transplantation, these dual-transferred BMCs can circulate through the entire body and thus function as vehicles to carry genes/contrast agents to multiple atherosclerosis. This study was to evaluate the feasibility of using in vivo MR imaging (MRI) to monitor BMC-mediated interleukin-10 (IL-10) gene therapy of atherosclerosis.

Methodology

For in vitro confirmation, donor mouse BMCs were transduced by IL-10/lentivirus, and then labeled with a T2-MR contrast agent (Feridex). For in vivo validation, atherosclerotic apoE^−/− mice were intravenously transplanted with IL-10/Feridex-BMCs (Group I, n = 5) and Feridex-BMCs (Group II, n = 5), compared to controls without BMC transplantation (Group III, n = 5). The cell migration to aortic atherosclerotic lesions was monitored in vivo using 3.0T MRI with subsequent histology correlation. To evaluate the therapeutic effect of BMC-mediated IL-10 gene therapy, we statistically compared the normalized wall indexes (NWI) of ascending aortas amongst different mouse groups with various treatments.

Principal Findings

Of in vitro experiments, simultaneous IL-10 transduction and Feridex labeling of BMCs were successfully achieved, with high cell viability and cell labeling efficiency, as well as IL-10 expression efficiency (≥90%). Of in vivo experiments, MRI of animal groups I and II showed signal voids within the aortic walls due to Feridex-created artifacts from the migrated BMCs in the atherosclerotic plaques, which were confirmed by histology. Histological quantification showed that the mean NWI of group I was significantly lower than those of group II and group III (P<0.05).

Conclusion

This study has confirmed the possibility of using MRI to track, in vivo, IL-10/Feridex-BMCs recruited to atherosclerotic lesions, where IL-10 genes function to prevent the progression of atherosclerosis.     

Identification of novel Clostridium perfringens type E strains that carry an iota toxin plasmid with a functional enterotoxin gene

Clostridium perfringens enterotoxin (CPE) is a major virulence factor for human gastrointestinal diseases, such as food poisoning and antibiotic associated diarrhea. The CPE-encoding gene (cpe) can be chromosomal or plasmid-borne. Recent development of conventional PCR cpe-genotyping assays makes it possible to identify cpe location (chromosomal or plasmid) in type A isolates. Initial studies for developing cpe genotyping assays indicated that all cpe-positive strains isolated from sickened patients were typable by cpe-genotypes, but surveys of C. perfringens environmental strains or strains from feces of healthy people suggested that this assay might not be useful for some cpe-carrying type A isolates. In the current study, a pulsed-field gel electrophoresis Southern blot assay showed that four cpe-genotype untypable isolates carried their cpe gene on a plasmid of ～65 kb. Complete sequence analysis of the ～65 kb variant cpe-carrying plasmid revealed no intact IS elements and a disrupted cytosine methyltransferase (dcm) gene. More importantly, this plasmid contains a conjugative transfer region, a variant cpe gene and variant iota toxin genes. The toxin genes encoded by this plasmid are expressed based upon the results of RT-PCR assays. The ～65 kb plasmid is closely related to the pCPF4969 cpe plasmid of type A isolates. MLST analyses indicated these isolates belong to a unique cluster of C. perfringens. Overall, these isolates carrying a variant functional cpe gene and iota toxin genes represent unique type E strains.     

马尾松两广优良家系遗传变异研究

通过调查马尾松中龄林的生长情况,对其群体遗传变异进行分析。结果表明,马尾松两广优良家系中龄林存在丰富的遗传变异,树高、胸径、材积和冠幅等性状在家系层次上有极显著或显著差异,这些差异主要由遗传因素制约,各性状受中度、中低度遗传控制。主成分分析表明,树高、胸径和材积为主要生长性状,它们的累积贡献率达89.54%。采用Structure Version 2.2软件进行群体遗传结构分析,将群体分成5大类,在第4组群中,广东的家系数量最多,且组群生长性状值最高;第2组群中广西的家系数量最多,而生长性状值仅次于第4组群。