滇中冷凉山区不同播期反季花椰菜产量效益分析

为摸索滇中高海拔冷凉山区反季节栽培花椰菜的最佳播期以集成高效栽培技术推广应用,于2017—2018年选择海拔2250 m的云南省峨山县塔甸镇大西村地块进行9个播期的2年随机区组试验。结果表明,花椰菜生育期随播期推迟而延长,而花球采收期除播期7月10日外随播期推迟而逐渐增长;花椰菜株高、外叶数、开展度、球高、球径和单球重等农艺性状有随播期延迟呈现先逐渐减小而后又逐渐增大的趋势;莲座期黑腐病和霜霉病的病情指数随着播期的延迟呈现先逐渐升高而后又逐渐下降的趋势;花椰菜小区产量随着播期的延迟呈现先逐渐下降而后又逐渐提高的趋势,播期4月20日和4月30日与其余7个播期产量之间的差异达极显著水平。综合花椰菜在冷凉山区反季节栽培的生产实际和各播期产量产值及商品性表现,推荐滇中高海拔冷凉山区反季节栽培花椰菜的最佳播期为4月20—30日。     

甘露糖修饰的壳聚糖聚乳酸-羟基乙酸共聚物纳米微球作为口蹄疫病毒核酸疫苗递送载体的特性评价

旨在对制备的甘露糖修饰的壳聚糖聚乳酸-羟基乙酸共聚物[poly （D，L-lactide-co-glycolide），PLGA]纳米微球作为口蹄疫病毒（foot-and-mouth disease virus，FMDV）核酸疫苗递送载体进行评价。采用西佛碱反应和元素分析制备具有一定取代度的甘露糖修饰的壳聚糖衍生物（mannose modified chitosan，MCS），然后，经双重乳化挥发法制备得到甘露糖修饰的壳聚糖PLGA纳米微球（MCS-PLGA-NPs）。采用纳米粒径仪检测MCS-PLGA-NPs粒径分布和表面电势（zeta）、扫描电镜考察其形态、琼脂糖凝胶电泳观察其对质粒的吸附和吸附质粒后抵抗核酸酶降解能力、CCK-8法检测MCS-PLGA-NPs的细胞毒性、激光共聚焦观察巨噬细胞对MCS-PLGA-NPs-质粒DNA复合物的摄取、荧光显微镜和Western blot验证MCS-PLGA-NPs加载质粒DNA在细胞中的表达。元素分析结果表明，成功制备了取代度为5%~10%的MCS。纳米粒径测定和扫描电镜结果表明，MCS-PLGA-NPs的zeta为正值、粒径分布均匀且形态规则呈球形。琼脂糖凝胶电泳结果显示，MCS-PLGA-NPs吸附质粒的能力随着其质量的增加而增强并且可以在一定程度上抵抗核酸酶降解质粒DNA。在细胞毒性试验中，不同浓度的MCS-PLGA-NPs与RAW264.7细胞共孵育24 h后，细胞存活率仍在85%以上。在细胞摄取试验中，用激光共聚焦显微镜可以明显观察到质粒DNA结合到纳米微球表面被RAW264.7细胞摄取。荧光显微镜和Western blot试验证明MCS-PLGA-NPs加载质粒DNA可以在细胞中进行表达。综上表明，本研究成功制备了MCS以及具有递送核酸疫苗能力的MCS-PLGA-NPs，为FMDV核酸疫苗的递送研究提供了新的方向和见解，也为该递送载体携带特定抗原靶向抗原递呈细胞表面甘露糖受体以及应用于动物免疫的研究奠定基础。     

不同水肥条件下夏玉米/冬小麦农田生态系统碳平衡研究

农田生态系统碳平衡取决于农作物固定碳量和土壤异养呼吸排放碳量。为揭示水肥用量对农田生态系统碳平衡的综合影响，设置3个灌水水平：高水、中水和低水（W1、W0.85、W0.7夏玉米季分别为90、76.5、63mm，冬小麦季分别为140、119、98mm），4个施氮水平：高氮、中氮、低氮和不施氮（N1、N0.85、N0.7、N0夏玉米季分别为300、255、210、0kg/hm2，冬小麦季分别为210、178.5、147、0kg/hm2），4个施磷水平：高磷、中磷、低磷和不施磷（P1、P0.85、P0.7和P0夏玉米季分别为90、76.5、63、0kg/hm2，冬小麦季分别为150、127.5、105、0kg/hm2）进行了田间试验。结果表明：不同水肥处理下夏玉米/冬小麦农田生态系统表现为碳汇，夏玉米季净生态系统生产力固碳量（CNEP）为6805~7233kg/hm2，冬小麦季CNEP为5842~6434kg/hm2，夏玉米CNEP高于冬小麦。在高、中、低肥水平下，增加灌水量，夏玉米/冬小麦周年净初级生产力固碳量（CNPP）提高2.48%~5.96%，土壤微生物异养呼吸碳释放量（CRm）增加2.15%~15.20%，净生态系统生产力固碳量（CNEP）增加1.16%~6.47%。在高、中、低供水水平下，增加施肥量，夏玉米/冬小麦周年CNPP增加2.95%~3.43%，土壤CRm增加5.23%~18.67%，CNEP增加0.93%~2.79%，CNEP增加比例与供水水平呈负相关。在低水条件下，氮磷肥配施处理夏玉米/冬小麦农田周年CNEP较单施氮、磷肥分别增加4.86%、7.34%，且氮磷肥交互作用显著（P<0.05），水肥供应水平相差15%时对冬小麦农田CNEP有显著的正交互作用。氮磷肥配施、水肥协调供应均有助于促进夏玉米/冬小麦农田生态系统的净碳输入，在节水节肥原则下，夏玉米和冬小麦分别在W0.85N0.85P0.85和W0.7N0.85P0.85水肥供应条件下有利于增加农田CNEP。     

过氧化氢(H2O2)介导的光合诱导系统信号

研究光照玉米幼苗顶部叶片产生的系统信号对底部叶片光合诱导过程的影响,探讨玉米叶片对光斑高效利用可能机制.以玉米(Zea mays L.)幼苗为试验材料,光照其顶部叶片,其余叶片处于遮蔽状态,利用Li-6400便携式光合仪测定玉米幼苗底部叶片光合诱导过程.通过预先光照玉米幼苗顶部叶片,底部叶片光合诱导过程从最低值到达最高值所需时间显著缩短,中间叶片光合诱导过程T50和T90分别下降,底部叶片光合诱导过程T50和T90分别下降29％和37％.玉米叶片全部遮荫条件下,底部叶片喷施过氧化氢(H2O2)促进光合诱导过程.三氯乙酸(TCA)和二苯基碘化钾(DPI)处理玉米顶部叶片基部,即使顶部叶片受到预光照,也无法改变底部叶片光合诱导过程.预先光照玉米顶部叶片,产生系统信号,信号物质为H2O2,通过韧皮部转运,可调节其他叶片光合诱导过程,有利于玉米底部叶片对动态光能利用和碳积累.该系统信号对玉米冠层底部叶片高效利用光斑发挥重要作用.     

Screening and Verification of Low Nitrogen Tolerant and Nitrogen Sensitive Cotton Germplasm

[Objective] The aim of this study is to evaluate nitrogen efficient cotton germplasms and improve nitrogen use efficiency. [Method] Eighty cotton germplasms were selected and evaluated in the hydroponic experiment under low (0.25 mmol·L^－1) and high (5 mmol·L^－1) nitrogen concentration. Different traits for screening were identified and nitrogen use efficiency types were classified. Field experiments were also performed for comparison and confirmation of the identified germplasms. [Result] The results showed that there were significant differences in the total plant dry matter, shoot nitrogen accumulation and nitrogen absorption efficiency in cotton germplasms at the two nitrogen levels. Based on coefficient of variation, principal component analysis and correlation, six traits including total plant dry matter, shoot dry matter, root dry matter, total nitrogen accumulation, shoot nitrogen accumulation and nitrogen absorption efficiency were used as screening indicators. According to the Heatmap clustering analysis and the nitrogen efficiency comprehensive index, two germplasms (Lu05R59 and CCRI 69) were identified as low nitrogen tolerant and nitrogen efficient, and two germplasms (Coker 201 and Xinluzhong 30) as low nitrogen sensitive and nitrogen inefficient. The results of field experiment were consistent with the results of the hydroponic culture at the seedling stage. [Conclusion] It was finally determined that Lu05R59 and CCRI 69 were the low nitrogen tolerant and nitrogen efficient germplasms, and Coker 201 and Xinluzhong 30 were low nitrogen sensitive and nitrogen inefficient germplasms. The results of these studies provide the possibility for screening and rapid identification of nitrogen use efficiency in cotton at the seedling stage, and provide the ideal materials and theoretical basis for further study of cotton nitrogen efficient.     

雪山草鸡感染传染性法氏囊病病毒新型变异株的鉴定

传染性法氏囊病病毒(infectious bursal disease virus,IBDV)新型变异株正在我国广泛蔓延,给商品肉鸡群和蛋鸡群带来了新的威胁。本研究对一个疑似发生非典型传染性法氏囊病的地方品种雪山草鸡群进行了RT-PCR检测,并对分离的3株毒株进行了基因测序及序列分析。结果显示,引起该鸡群发病的病原是IBDV新型变异株,属于A2dB1基因型;这3个毒株的VP2高变区编码蛋白上含有IBDV变异株的特征性氨基酸,也具有IBDV新型变异株的独特氨基酸。结果提示,我国地方品种鸡群中也有IBDV新型变异株的流行,现有的部分商品化IBDV疫苗已不能有效预防IBDV新型变异株的流行。     

2015―2020年国家西北内陆棉区棉花品种区域试验参试品种（系）枯黄萎病抗性评述

对2015－2020年参加西北内陆棉区区域试验的192个棉花品种（系）枯萎病、黄萎病的抗性分析，为棉花抗病育种及品种推广提供依据。结果表明，参试棉花品种（系）未出现对枯萎病和黄萎病免疫的品种；参试棉花品种（系）对枯萎病的抗性水平较高，除2018年高抗和抗病品种（系）占比为 88.2%外，其他年份均在92%以上；参试的品种（系）的黄萎病抗性水平除2017年较高外，其余各年均较低，以耐病为主，6年耐病品种（系）平均占比为56.2%；参试品种的总体抗枯萎病指数（r_F）远大于总体抗黄萎病指数（r_V）和总体兼抗指数（r_FV）,各年份均表现为r_F＞r_V＞r_FV，且三者均呈振荡上升趋势；早中熟常规棉的抗枯萎病、黄萎病性及兼抗性表现均优于早熟常规棉_。可见，黄萎病抗性的提高是西北内陆棉区选育兼抗棉花品种的关键。     

Generation and characterization of aptamers against grass carp reovirus infection for the development of rapid detection assay

Grass carp reovirus (GCRV) causes devastating viral haemorrhagic disease in farmed grass carp (Ctenopharyngon idellus). As novel molecular probes, aptamers have been widely applied in rapid diagnosis and efficient therapies against virus or diseases. In this study, three single‐stranded DNA (ssDNA) aptamers were selected against GCRV‐infected CIK cells via SELEX (systematic evolution of ligands by exponential enrichment technology). Secondary structures predicted by MFOLD indicated that aptamers formed stem‐loop structures, and GVI‐11 had the lowest ΔG value of ?30.84 KJ/mol. Three aptamers could specifically recognize GCRV‐infected CIK cells, with calculated dissociation constants (Kd) of 220.86, 176.63 and 278.66 nM for aptamers GVI‐1, GVI‐7 and GVI‐11, respectively, which indicated that they could serve as specific delivery system for antiviral therapies. The targets of aptamers GVI‐1, GVI‐7 and GVI‐11 on the surface of GCRV‐infected cells could be membrane proteins, which were trypsin‐sensitive. Furthermore, FAM‐labelled aptamer GVI‐7 could be applied to detect GCRV infection in vivo. It is the first time to generate and characterize aptamers against GCRV‐infected cells. These aptamers have great potentials in development of rapid diagnosis technology and antiviral agents against GCRV infection in aquaculture.     

Effects of DHRS3 in C2C12 Myoblast Differentiation and Mouse Skeletal Muscle Injury

Myoblast differentiation is an essential process during skeletal muscle development. C2 C12 myoblast is a commonly used experimental model to study muscle cell differentiation in vitro. Dehydrogenase/reductase(SDR family) member 3(DHRS3) is a highly conserved member in short-chain alcohol dehydrogenase/reductase superfamily and has been shown to be involved in the metabolism of retinol. Previous experimental results showed that the expression of DHRS3 increased significantly during the differentiation of myoblasts differentiation. However, the effect of DHRS3 on mouse muscle cell differentiation was unclear. The objective of current study was to determine if DHRS3 affected muscle cell differentiation, and if DHRS3 was involved in muscle regeneration. Protein expression was determined by western blot and immunofluorescence analysis. The activation and inhibition of DHRS3 increased and decreased C2 C12 myoblast differentiation respectively, which indicated that DHRS3 could affect C2 C12 myoblast differentiation. DHRS3 expression was significantly changed during muscle regeneration, with the regeneration of muscle injury, the expression of DHRS3 tended to increase first and then decrease. It suggested that DHRS3 might be involved in muscle regeneration. In summary, this study confirmed the involvement of DHRS3 in C2 C12 myoblast differentiation and mouse skeletal muscle regeneration and provided a theoretical basis for further elucidating the molecular mechanism of muscle development.     

镇江长江豚类省级自然保护区水域生态修复效果的监测与评价

自2006年以来,长江豚类极度濒危的生存状况得到广泛关注,在其自然保护区实施一系列生态修复工程,为镇江长江豚类省级自然保护区内的江豚提供良好的生存环境。于2015—2018年在和畅洲水域建设生态浮岛、人工鱼巢和放流底栖动物进行水域生态修复,对生态修复工程进行跟踪监测和效果评价。结果表明：生态浮岛的建设可提高区域内浮游植物和浮游动物的生物多样性和群落结构复杂程度;人工鱼巢对产黏性卵鱼类具有一定增殖效果,增殖种类主要为鲤、鲫、䱗和黄尾鲴;生态浮岛和人工鱼巢的建设对鱼类均有较好的聚集效果;底栖动物增殖放流显著增加了放流物种的丰度、生物量及保护区底栖动物群落生物量,增殖放流效果评价为中等。该自然保护区水域生态修复效果明显,为工程施工影响下水生生物保护区生态修复提供科学依据。