黑胫病菌（Leptosphaeria biglobosa）在油菜叶片和茎中的侵染过程观察

为明确黑胫病菌（Leptosphaeria biglobosa）在甘蓝型油菜叶片和茎中的侵染及扩展过程，利用绿色荧光蛋 白（GFP）标记的黑胫病菌株接菌油菜叶片，利用激光共聚焦显微镜观察菌株在油菜叶片和茎中的侵染过程。结果 表明，接种油菜叶片7 h后，分生孢子萌发并长出芽管；17 h后，芽管侵入气孔；24 h后，分生孢子全部萌发；36 h后萌 发的芽管形成菌丝；120 h后，菌丝在叶片表皮细胞间隙蔓延，并侵入叶肉细胞。13 d后，菌丝侵入茎部皮层组织； 15 d后，菌丝在皮层细胞间隙蔓延，并侵染至茎表皮；21 d后，菌丝侵染至维管组织；23 d后，菌丝侵染至茎韧皮部； 25 d后，茎导管被侵染，并向木质部扩展。本研究发现的L. biglobosa 在油菜叶片和茎中的侵染过程，可为油菜与黑 胫病菌互作的研究、黑胫病致病机理及防治提供参考。     

Establishment and application of an accurate identification method for fragrant soybeans

In order to screen the aroma characteristics of soybean,a new method was established which can quickly quantify the content of 2-acetyl-1pyrroline (2-AP),an important compound related to soybean aroma,using gas chromatography-mass spectrometry (GC-MS).Based on peak profile,total peak area and retention time as test indexes,an accurate identification method for fragrant soybeans was established.The optimum parameters of the protocol consisted of column temperature70°C,sample injector temperature 180°C,optimum extraction alcohol content 1 m L,Na Cl content 0.1 g,ultrasonication time10 min,and extraction time 1 h,which were established by using the orthogonal test of single factors and three factors with four levels (L_9(3)~4).2-AP content of leaves had significant correlations with seeds,which were easier to measure.The protocol was simple and easy to carry out,consumed only small amounts of reagents,and provided accurate and reliable results with good reproducibility.A total of 101 soybean genotypes from different geographical sources were analyzed using this protocol.The results showed that the average content of 2-AP was 0.29 mg L~(–1),ranging from 0.094 to 1.816 mg L~(–1),and the genetic diversity index was 0.54.Among all genotypes-tested,they were classified into three grades,including seven elite genotypes identified as"grade one fragrant soybeans",which were Zhonglong 608,Heinong 88,Ha13-2958,Hongmiandou,Heinong 82,Huangmaodou,and Jiyu 21.These results provide both an identification technique and several elite aroma genotypes for gene discovery and good quality breeding in soybean.     

基于SLAF-seq技术鉴定苹果砧木耐涝候选基因

【背景】苹果（Malus×domestica Borkh）是我国主要栽培果树树种之一,但部分苹果产区由于夏、秋季的大量集中降雨和排水不良等造成果园涝害频繁发生,导致苹果树叶片黄化、脱落,果实品质和产量下降。【目的】鉴定苹果耐涝相关基因,为苹果耐涝分子标记辅助育种和优质高产栽培提供依据。【方法】以耐涝苹果砧木G41和不耐涝苹果砧木新疆野苹果（M. sieverii (Ledeb) Roem.）及其构建的包含495个F₁杂交后代为材料,从F₁杂交群体中挑选出耐涝和不耐涝株系各50株,构建两个极端性状DNA混池,采用简化基因组测序（SLAF-seq）技术,开发SLAF标签和SNP标记,结合苹果基因组信息和遗传关联性分析,对苹果耐涝基因进行定位及候选基因预测,并对候选基因在耐涝差异的株系中进行淹水胁迫下的表达分析。【结果】以‘金冠’苹果为参考基因组,共开发119 072个SLAF标签,其中多态性SLAF有11 133个。通过序列分析和检测SNP位点,共获得6 237 071个SNP,其中高质量SNP有170 617个。通过ED和SNP-index方法关联分析,获得一个与耐涝性状紧密关联的候选区域,位于苹果第10号染色体1.94—3.25 Mb,关联区域大小为1.31 Mb,关联区域内包含120个基因。对该区域内基因进行功能注释,发现一个与呼吸代谢相关的基因—乙醇脱氢酶基因ADH1（MD10G1014500）,在淹水处理后1、2、4和6 d,该基因在耐涝植株中的表达量显著高于不耐涝植株。【结论】将苹果耐涝基因定位于第10号染色体1.94—3.25 Mb处,筛选到可能与苹果耐涝相关的候选基因MD10G1014500,可用于苹果耐涝基因的克隆和功能解析。     

Up-regulation of miR-181a attenuates releases of CSE-induced pro-inflammatory factors and expression of collagen IV,fibronectin and α-SMA in human bronchial epithelial cells

AIM: To investigate the effect and potential mechanism of microRNA-181a (miR-181a) on cigarette smoke extract (CSE)-induced the productions of pro-inflammatory factors and the expression of collagen IV, fibronectin and α-smooth muscle actin (α-SMA) in human bronchial epithelial cells (HBECs). METHODS: CSE-induced miR-181a expression was detected by RT-qPCR in the HBECs. After tansfected with miR-181a mimic, the releases of tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), IL-6 and transforming growth factor-β1 (TGF-β1) were measured by ELISA, the protein expression of collagen IV, fibronectin and α-SMA was determined by Western blot. The activation of NF-κB/TGF-β1/Smad3 pathway was also evaluated by Western blot. RESULTS: CSE increased the levels of TNF-α, IL-1β, IL-6 and TGF-β1 and the expression of collagen IV, fibronectin and α-SMA, and decreased the expression of miR-181a in the HBECs (P<0.05). However, transfected with miR-181a mimic partially prevented the releases of TNF-α, IL-1β, IL-6 and TGF-β1, and inhibited the expression of collagen IV, fibronectin and α-SMA (P<0.05). Additionally, the activation of NF-κB/TGF-β1/Smad3 evoked by CSE was attenuated after transfected with miR-181a mimic. CONCLUSION: Up-regulation of miR-181a prevents the releases of CSE-induced pro-inflammatory factors and expression of collagen IV, fibronectin and α-SMA in the HBECs, and its mechanism may be related to the inhibition of NF-κB/TGF-β1/Smad3 pathway.     

重要农业文化遗产价值体系构建及评估(I):价值体系构建与评价方法研究

重要农业文化遗产是一类典型的资源可持续利用保护地，其水土管理方式、知识体系、文化内涵等对于协调社区生计与生态保护具有积极作用。这类传统生计区域往往与自然保护地毗邻或在其范围内，对其蕴含的价值进行识别与保护，不仅是提升农业文化遗产管理的诉求，也能够支持自然保护地体系优化与功能区划管理。本研究对重要农业文化遗产价值进行系统识别，基于农业文化遗产的广义概念与全球重要农业文化遗产的狭义概念，借鉴多类型自然保护地与世界遗产、生态系统服务功能、自然资源资产等价值体系，从农业文化遗产的复合性、活态性与战略性特点出发，把握其核心价值，构建重要农业文化遗产的价值体系。在充分吸收生态系统服务价值评估、自然资源资产价值核算、自然文化遗产价值评估、品牌价值评估等定量或定性评价方法的基础上，提出一套完整的重要农业文化遗产货币价值评价方法。以系统科学和可持续发展理论为基础，重要农业文化遗产价值主要包括存在价值和潜在价值，其中存在价值以载体价值和服务价值为核心，服务价值则可细分为产品价值、生态价值、社会价值等9类，25个具体指标。研究进一步提出存在价值的评价方法与潜在指标可能测算路径。构建的重要农业文化遗产价值体系以及所提出的评价方法，可为以价值保护为基础进行农业文化遗产管理提供理论依据，为管理决策者在区域保护与发展协调决策中提供科学基础。     

基于SEPLS模型的GIAHS恢复力评估框架及其在保护成效评估中的应用

由联合国粮农组织认定的全球重要农业文化遗产(GIAHS)是一类典型的社会生态生产景观(SEPLS),在传统知识传承保护、粮食与食物安全保障、农业生物多样性保护、气候变化应对等诸多方面具有重要意义。为了更好、更有效地开展GIAHS保护及管理工作,本文在分析GIAHS评估重要性和恢复力概念的基础上,以联合国大学(UNU)等团队开发的社会生态生产景观恢复力评估框架(SEPLS模型)为基础,构建了GIAHS恢复力评估框架(GIAHS-RAF),明确了其评估及计算过程。并以中国第1个GIAHS项目——浙江青田稻鱼共生系统(Qingtian Rice-Fish Culture System in Zhejiang Province, RFC)为例,通过对核心保护区——龙现村在2004年(GIAHS项目授牌前)和2016年(GIAHS授牌11年)的恢复力状况进行评估,探讨模型在GIAHS保护成效评估中的适用性。研究结果显示:1)2016年龙现村恢复力整体状况相对较弱,各项资本评估得分为:物质资本(0.75)经济资本(0.63)人类资本(0.61)社会资本(0.57)自然资本(0.38);2)虽然农户收入来源多样且社会经济基础设施能较好地满足社区需求,但是遗产地内部农业物种较少,农户对于系统提供的粮食多样性尚不是非常满意; 3)相较于2004年,经过11年的保护工作,研究区恢复力有所提高,说明GIAHS项目的实施对该遗产的恢复力有积极影响,尤其是物质资本和经济资本两方面。评估结果与该区域相关研究结果及实地调查情况一致,说明所构建的GIAHS恢复力评估框架可以很好地应用于对GIAHS项目及其他相关农业文化遗产的保护成效评估工作。     

均腐土不同亚纲典型土系土壤细菌群落多样性研究

为研究中国土壤系统分类(CST)体系下均腐土不同亚纲土壤细菌群落结构的多样性，以 4个干润均腐土[富牧西系(DFm)、春雷南系(DCl)、保国系(DBg)、明水系(DMs)]和 4个湿润均腐土[大西江系(MDx)、新发北系(MXf)、卫星农场系(MWx)、裴德系(MPd)]的腐殖质层(Ah层)为研究对象，采用高通量测序技术研究细菌群落多样性，分析细菌群落结构与环境因子间的关系，以探讨影响均腐土不同亚纲群落结构的主要环境因子。结果表明:均腐土 8个土系样品共获得 1 674 634条基因序列，Shannon指数和 Chao1指数表现为:干润均腐土 >湿润均腐土。均腐土 8个土系细菌群落主要包括 10个门类，其中变形菌门(Proteobacteria)、放线菌门(Actinobacteria)、酸杆菌门(Acidobacteria)为富牧西系、春雷南系、保国系、大西江系、新发北系、卫星农场系、裴德系优势菌门，明水系以绿湾菌门(Chloroflexi)、变形菌门(Proteobacteria)、放线菌门(Actinobacteria)为优势菌门；属水平上，均腐土各土系的群落差异较大。样品热图分析将 8个土系细菌群落聚为 2类，其中干润均腐土聚为一类，湿润均腐土聚为一类。pH、交换性 Ca、CEC、交换性 Mg、SOC和 TP是影响均腐土细菌群落结构发生变化的主要因子( P<0.05)。此外，RDA分析发现，土壤 pH为影响均腐土细菌群落结构的主导因子，而 pH、交换性 Ca、CEC为驱动干润均腐土细菌群落结构发生变化的主要影响因素，交换性 Mg、SOC、TP为驱动湿润均腐土细菌群落发生变化的主要影响因素。     

NRF2 attenuates oxidative stress and lysosomal dysfunction in doxorubicin-induced H9C2 cells

AIM:To study the effect of nuclear factor E2-related factor 2 (NRF2) on oxidative stress injury and lysosomal dysfunction in doxorubicin (DOX)-induced rat myocardial H9C2 cells. METHODS:The H9C2 cells were treated with DOX. The expression of NRF2 at mRNA and protein levels was determined by real-time PCR and Western blot. The H9C2 cells stably over-expressing NRF2 were established by lentiviral infection. Real-time PCR and Western blot were used to identify the efficiency of over-expression. After DOX treatment, the cell viability was measured by CCK-8 assay, the activity of lactate dehydrogenase (LDH), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and catalase (CAT), and the content of malondialdehyde (MDA) in the cell supernatant were detected. FITC-dextran was used to analyze lysosomal pH, and the protein expression of lysosomal-associated membrane protein 1 (LAMP1) and cathepsin B was determined by Western blot.RESULTS:The expression of NRF2 at mRNA and protein levels in DOX-treated H9C2 cells was significantly decreased (P<0.05). Over-expression of NRF2 significantly up-regulated the mRNA and protein expression of NRF2 in DOX-treated H9C2 cells (P<0.05). After DOX treatment, the cell viability was decreased, and LDH activity was increased. The activity of SOD, GSH-Px and CAT was decreased, and the content of MDA was increased (P<0.05). The lysosomal pH was increased, and the protein expression of LAMP1 and cathepsin B decreased (P<0.05). Over-expression of NRF2 increased the cell viability, decreased LDH activity, increased the activity of SOD, GSH-Px and CAT, and decreased the content of MDA in cell supernatant (P<0.05). Over-expression of NRF2 also decreased the lysosomal pH, and increased the protein expression of LAMP1 and cathepsin B (P<0.05). CONCLUSION:DOX inhibits the expression of NRF2 in the myocardial H9C2 cells. Over-expression of NRF2 attenuates oxidative stress and lysosomal dysfunction in the H9C2 cells induced by DOX.