土壤铅和镉溶出伏安法检测中影响因素及其削弱方法研究进展

溶出伏安法具有分析速度快、成本低、灵敏度高等优点被广泛应用于检测土壤重金属含量，但在检测土壤重金属时，溶出伏安检测精度会受到多方面因素的影响。该文在介绍溶出伏安法工作原理的基础上，从伏安参数、试验条件和土壤物质成分三方面阐述溶出伏安法检测土壤Pb2+和Cd2+为的影响因素，解析各因素的影响机理，归纳影响削弱方法的研究进展。研究结论为：方波脉冲阳极溶出伏安法最常用于检测土壤Pb2+和Cd2+，伏安参数包括脉冲幅值、电压增量和脉冲频率，试验条件包括沉积时间、沉积电压和支持电解质种类及其pH值，土壤成分主要干扰因素包括非目标重金属和有机质。针对伏安参数和试验条件的影响可以设计优化试验有效削弱。针对非目标重金属和有机质的干扰影响，目前研究还没有提出有效的削弱方法。最后，展望了溶出伏安法检测土壤重金属的未来发展方向。     

草鱼肠系膜脂肪组织高质量总RNA提取方法的研究

基于传统的酸性酚—异硫氰酸胍—氯仿一步提取法,比较分析多种优化操作步骤,摸索出一种高质量提取体质量为80~150 g草鱼肠系膜脂肪组织总RNA的改良方法。试验结果显示,相较于肝脏、脾脏、肠道等脏器组织,草鱼肠系膜脂肪组织RNA丰度低,且极易在样品前处理阶段出现顽固性降解问题。探索发现,将取样量增至约30 mg,可提升RNA产量以满足常规试验需求。针对降解难题,改良常规的样品前处理技术流程,采用鲜样液氮速冻,冻样直接放入TRIzol试剂中裂解,并即刻进行长时间机械匀浆,时长约3 min等核心操作步骤,可显著降低脂肪组织样品RNA的降解。Agilent生物分析仪检测结果显示,改良方法提取的草鱼肠系膜脂肪组织RNA完整度高,关键RIN值为8.7~9.0。研究推测,长时间机械匀浆所形成的持续剪切冲击力或许有助于TRIzol试剂中的异硫氰酸胍等成分突破油滴阻碍而有效抑制内源性RNA酶。本方法提取的草鱼脂肪组织总RNA质量可满足高通量转录组测序要求。     

Identifying and Characterizing a Novel Peritrophic Matrix Protein (MdPM-17) Associated With Antibacterial Response From the Housefly,Musca domestica (Diptera: Muscidae)

Peritrophic matrix/membrane (PM) critically prevents the midgut of insects from external invasion by microbes. The proteins in the peritrophic membrane are its major structural components. Additionally, they determine the formation and function of this membrane. However, the role of PM proteins in immune regulation is unclear. Herein, we isolated a novel PM protein (MdPM-17) from Musca domestica larvae. Further, the function of MdPM-17 in regulating host innate immunity was identified. Results showed that the cDNA of MdPM-17 full is 635 bp in length. Moreover, it consists of a 477-bp open reading frame encoding 158 amino acid residues. These amino acid residues are composed of two Chitin-binding type-2 domain (ChtBD2) and 19 amino acids as a signal peptide. Moreover, tissue distribution analysis indicates that MdPM-17 was enriched expressed in midgut, and moderate levels in the fat body, foregut, and malpighian tubule. Notably, MdPM-17 recombinant protein showed high chitin-binding capacity, thus belongs to the Class III PM protein group. MdPM-17 protein silencing via RNA interference resulted in the expression of antimicrobial peptide (defensin, cecropins, and diptericin) genes, and this occurred after oral inoculation with exogenous microbes Escherichia coli (Enterobacteriales:Enterobacteriaceae), Staphylococcus aureus (Bacillales:Staphylococcaceae), and Candida albicans (Endomycetales:Saccharomycetaceae)). Therefore, all the antimicrobial peptide (AMP) gene expression levels are high in MdPM-17-depleted larvae during microbial infection compared to controls. Consequently, these findings indicate that MdPM-17 protein is associated with the antibacterial response from the housefly.     

农业装备升降装置非接触式光纤位移传感器设计与试验

为了解决农业设备位移的宽量程、高灵敏度非接触测量问题,提出一种基于Peanut-shape迈克尔逊干涉结构的非接触式光纤位移传感器。分析了光纤Peanut-shape迈克尔逊干涉原理,设计了将磁场与Peanut-shape结构形成的全纤式迈克尔逊干涉相结合的传感器结构,并通过磁场仿真,得到磁场强度曲线。建立了传感器应变标定系统和位移测试系统。试验结果表明:Peanut-shape迈克尔逊干涉的光纤传感器应变灵敏度达到1. 82 pm/με,是普通光纤的1. 5倍,线性度为0. 997;位移测试得到的光谱曲线与磁场仿真曲线结果一致,可以实现位移的测量,且线性拟合度达到0. 999。     

东亚小花蝽对草地贪夜蛾幼虫的捕食效应

为探明东亚小花蝽Orius sauteri对草地贪夜蛾Spodoptera frugiperda幼虫的控制潜力,开展了不同温度下东亚小花蝽对不同龄期和密度的草地贪夜蛾幼虫的捕食功能反应与干扰作用研究。结果表明:当东亚小花蝽捕食1龄或2龄草地贪夜蛾幼虫时,其捕食功能反应与HollingⅡ模型拟合度较好。东亚小花蝽对草地贪夜蛾1龄幼虫在20℃、25℃和28℃下的瞬时攻击率分别为0.772 4、1.090 0、0.673 6,处理单头幼虫的时间为0.174 9、0.173 7、0.295 5 d,对2龄幼虫,在20℃、25℃和28℃下的瞬时攻击率分别为0.794 5、1.153 8、0.392 2,处理单头幼虫的时间为0.218 9、0.805 6、0.696 0 d;东亚小花蝽对草地贪夜蛾幼虫的捕食量表现出随着猎物密度增加而上升,随自身密度的增加而下降的趋势;同一温度下,东亚小花蝽对1龄幼虫的日均捕食量和寻找效应均高于2龄幼虫,寻找效应与猎物密度成反比;东亚小花蝽对3龄和4龄草地贪夜蛾幼虫的日均捕食量为0;田间自然状态下东亚小花蝽对草地贪夜蛾幼虫的控制率为34.62%。     

棉铃虫膨胀线粒体基因组的鉴定与分析

以已公布的棉铃虫线粒体DNA序列对来自4头棉铃虫雄蛹的DNA的三代测序数据进行筛选,获得了11条与线粒体DNA有同源性的三代read序列,并根据其中的read 66003鉴定出了一种膨胀的线粒体基因组。该线粒体基因组大小为27 113 bp,其保守区域包含13个蛋白编码基因、2个rRNA基因、22个tRNA基因以及1个AT富集区,与已公布的棉铃虫线粒体基因组的结构相似。膨胀区域位于cox1基因编码区内部,大小为11 467 bp,经预测含有一个完整的真核基因(依赖ATP的RNA解旋酶)以及多种转座元件的片段,但与线粒体DNA无同源性,也无I类或Ⅱ类内含子存在的证据。对田间和室内棉铃虫DNA样品的PCR扩增未能检测到膨胀线粒体基因组的存在。以上结果表明膨胀片段可能是细胞核DNA序列通过偶然的水平转移事件而整合到线粒体基因组中的,且该种膨胀方式的发生概率极低。本文报道的膨胀线粒体基因组为日后动物线粒体基因组学的研究提示了一种独特的变异方式。     

环状RNA及其在畜禽中的研究进展

环状RNA(circular RNA,circRNA)是一类新发现的内源性非编码RNA,是一种由共价键形成闭环结构的RNA分子。circRNA主要来源于外显子或内含子,在生物体内广泛存在,具有种类丰富、保守性强、细胞核组织特异性、稳定存在等特点。目前研究表明,circRNA可通过多种途径发挥作用,在神经发育、免疫、畜禽经济性状调控等过程中扮演重要角色,具有重要的研究价值。对circRNA的特征、形成机制、主要功能及其在畜禽中的研究进展进行综述,旨在为circRNA在畜禽的研究提供一定的理论依据与技术指导。     

Occurrence and genetic diversity of Blackcurrant reversion virus found on various cultivated and wild Ribes in Latvia

A large‐scale survey was carried out to assess the occurrence, natural host range and genetic diversity of Blackcurrant reversion virus (BRV) in cultivated and wild Ribes in Latvia using RT‐PCR and sequence analyses of 3′ NTR of BRV RNA2. The virus was detected in all surveyed habitats in most of the studied Ribes, except gooseberries, Ribes sanguineum, Ribes laxiflorum and crossbreeds between blackcurrants and gooseberries. The overall occurrence of BRV was 27%, although it varied significantly among the surveyed Ribes habitats, exceeding 40% in home gardens and germplasm collections. Among cultivated Ribes, blackcurrants were the most infected and BRV was detected in all commonly grown cultivars. The virus was detected for the first time in Ribes aureum, Ribes fragrans, Ribes nigrum var. pauciflorum and Ribes fasciculatum var. chinense. The sequence identities of the studied fragments of RNA2 3′ NTR varied from 92.8% to 99.7% among 26 BRV isolates from various cultivated, ornamental and wild hosts from Latvia and from 91.1% to 97.1% when they were compared with 27 corresponding sequences from GenBank. Phylogenetic analyses revealed that the major clustering of isolates was not related to host, origin or symptoms. Grouping of BRV isolates based on host or location was identified within the phylogenetic subclusters. Several well‐supported clades were formed within the subclusters, including a group of BRV isolates from redcurrants that had unique nucleotide substitutions. Five putative recombinants were identified for the first time among BRV isolates from Latvia, Finland, Scotland and the Czech Republic.