海南冬季西瓜病毒病的发生及绿色防控

分析海南冬季西瓜病毒病的病原、发生原因与症状表现，提出开展绿色防控的必要性和技术措施。     

陕西省小麦不同部位镰刀菌分离鉴定及毒素化学型分析

为明确陕西省小麦不同部位镰刀菌种群结构及其毒素化学型，于2022年小麦灌浆期分别从陕西省渭南市、宝鸡市、咸阳市、西安市采集小麦穗部、茎秆以及茎基部具有明显病状的样品，采用单孢分离法获得镰刀菌菌株，并使用分子生物学鉴定其种群结构及毒素化学型。结果表明，从采集的样本中共分离到156株镰刀菌菌株，其中发生在穗部的赤霉病以及发生在茎秆的秆腐病的优势病原菌均为禾谷镰刀菌（Fusarium graminearum），主要以15-ADON化学型为主；发生在茎基部的茎基腐病的优势病原菌为假禾谷镰刀菌（F.pseudograminearum），其15-ADON和3-ADON化学型占比差异不大；未检测到NIV毒素化学型的镰刀菌。以上结果说明，小麦不同部位对镰刀菌毒素化学型可能不存在选择性，小麦茎基部与穗部和茎秆的镰刀菌毒素化学型不同，原因可能是由优势病原菌不同造成的。     

红树植物—白骨壤黑斑病病原菌的分离与鉴定

<正>红树林是生长在热带、亚热带海岸潮间带,可海陆两栖的特殊木本植物群落,具有防风御浪、净化环境、维护沿海湿地生物多样性等生态功能,为珍稀植物群落。有报道认为红树植物生长在海边又富含抗菌等活性物质,不利于病害发生,但近年来本实验室在广东雷州半岛等地红树林发现有多种病害发生~([1,2]),仅白骨壤(Avicennia marina)上就发现有黑茎病、灰斑病等病害。2014年我们在该区白骨壤小苗     

Pathogen Analysis of Goat's Respiratory Diseases

To investigate the pathogens of goat's respiratory disease from a goat farm in Guangxi province, the epidemiological investigation, clinic observation, pathological examination, bacterium isolation and identification, biochemical test, PCR and animal experiment test were conducted.The preventive and control measures were taken on the basis of pathogen epidemiological characteristics and drug sensitive test results.The results showed that Mycoplasma, influenza virus and parasite were negative by isolation and culture or PCR, however, two strains of gram-negative bacteria named MS1 and MS2 were isolated from lung.MS1 was identified as Serratia marcescens by biochemical test and 16S rRNA sequencing, which shared 99% nucleotide homology with other Serratia marcescens in GenBank.And MS2 was identified as E.coil by the same methods that shared 99% nucleotide homology with other E.coli in GenBank.Animal experiment showed that two strains could cause death in mice.The drug sensitive tests showed two strains were highly sensitive to spectinomycin, amikacin, kanamicin and neomycin.Kanamycin and dexamethasone were used to treat the sick goats, and achieved good results.     

波叶大黄白粉病病原菌的鉴定

正波叶大黄Rheum rhabarbarum L.隶属于蓼科Polygonaceae大黄属Rheum,是一种重要的药用植物。白粉病多发生在波叶大黄的叶部,会影响其光合作用进而降低其药用价值。据笔者统计,目前关于蓼白粉菌Erysiphe polygoni DC.在世界范围内的报道有很多~([1~9]),但其中关于蓼科Polygonaceae波叶大黄白粉病病原菌的报道较少,目前仅有1个     

Transgenic expression of a sorghum gene (SbLRR2) encoding a simple extracellular leucine-rich protein enhances resistance against necrotrophic pathogens in Arabidopsis

Plant leucine-rich repeat (LRR) domain-containing proteins are known to play important roles in signaling transduction and defense responses. In sorghum, SbLRR2 is pathogen-inducible gene encoding a simple extracellular LRR protein. Here, we demonstrated an earlier and stronger expression of SbLRR2 in a sorghum resistant genotype in comparison to a susceptible genotype following inoculation with the anthracnose pathogen (Colletotrichum sublineolum). In addition, SbLRR2 expression was found to be induced strongly by methyl-jasmonate treatment. Functional analysis was performed in SbLRR2 over-expression (OE) Arabidopsis plants, which showed enhanced resistance against the necrotrophic pathogens Botrytis cinerea and Alternaria brassicicola. In addition, the OE lines were found to have elevated expression of several jasmonate acid (JA)-associated genes and higher endogenous JA contents. Hence, the SbLRR2-mediated defense responses in transgenic Arabidopsis are likely to be dependent on JA-signaling through increased JA production. On the other hand, the OE lines remained susceptible to Pseudomonas syringae pv. tomato like the wild type plants. Consistently, there was no up-regulation of salicylic acid (SA) defense marker gene expression or SA levels in the OE lines. Our results suggested that SbLRR2 is potentially useful for enhancing resistance against necrotrophic pathogens in transgenic dicot crops.     

Analysis of Mycosporine-Like Amino Acids in Selected Algae and Cyanobacteria by Hydrophilic Interaction Liquid Chromatography and a Novel MAA from the Red Alga Catenella repens

Mycosporine-like amino acids (MAAs), a group of small secondary metabolites found in algae, cyanobacteria, lichens and fungi, have become ecologically and pharmacologically relevant because of their pronounced UV-absorbing and photo-protective potential. Their analytical characterization is generally achieved by reversed phase HPLC and the compounds are often quantified based on molar extinction coefficients. As an alternative approach, in our study a fully validated hydrophilic interaction liquid chromatography (HILIC) method is presented. It enables the precise quantification of several analytes with adequate retention times in a single run, and can be coupled directly to MS. Excellent linear correlation coefficients (R² > 0.9991) were obtained, with limit of detection (LOD) values ranging from 0.16 to 0.43 µg/mL. Furthermore, the assay was found to be accurate (recovery rates from 89.8% to 104.1%) and precise (intra-day precision: 5.6%, inter-day precision ≤6.6%). Several algae were assayed for their content of known MAAs like porphyra-334, shinorine, and palythine. Liquid chromatography-mass spectrometry (LC-MS) data indicated a novel compound in some of them, which could be isolated from the marine species Catenella repens and structurally elucidated by nuclear magnetic resonance spectroscopy (NMR) as (E)-3-hydroxy-2-((5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-((2-sulfoethyl)amino)cyclohex-2-en-1-ylidene)amino) propanoic acid, a novel MAA called catenelline.     

提高二倍体马铃薯原始栽培种原生质体分离与分裂频率的研究

为获得较高的原生质体分离和分裂频率,试验以马铃薯二倍体原始栽培种‘47-33’‘5-19’试管苗叶片为材料,进行了原生质体游离和培养的研究.结果表明:培养21d的两品系试管苗叶片均在含有2.0%纤维素酶+0.5%果胶酶+0.25%离析酶,渗透压为0.35mol/L的酶解液中解离效果最好,原生质体产量分别为2.31×106个/gFW和2.52×106个/gFW;在28℃酶解温度条件下缓慢摇动14h或1h静置+13h缓慢摇动的,可促进叶片原生质体的大量释放.此外,1.0mg/L NAA+0.5mg/L 2,4-D+0.4mg/L BAP外源激素组合有利于叶片原生质体的分裂,‘47-33’‘5-19’原生质体一次分裂频率分别达到8.85%和12.56%.在0.35mol/L渗透压的液体培养基中,‘47-33’叶片原生质体分裂更早,分裂频率达13.85%.研究获得了稳定的原生质体分离体系以及较好的原生质体培养条件,为马铃薯二倍体原始栽培种的体细胞融合奠定了基础.     

椭圆嗜蓝层孔菌子实体化学成分研究

椭圆嗜蓝层孔菌(Phellinus ellipsoidea)子实体甲醇提取物依次用石油醚和乙酸乙酯萃取,其乙酸乙酯分部经柱层析分离得到11个化合物。经鉴定这11个化合物分别为:苯并(1,2-b,5,4-b′)二呋喃-3,5-二酮-8-甲酸甲酯(1)、原儿茶酸(2)、4-(3,4-二羟苯基)-3-丁烯-2-酮(3)、原儿茶醛(4)、Hispidin(5)、Hispolon(6)、Inoscavin A(7)、Phelligridin K(8)、Inoscavin C(9)、Inoscavin E(10)和Inonoblins B(11),其中化合物2、4、7、10为首次从该物种中分离得到。     

1株猫杯状病毒的分离鉴定及其ORF2序列的遗传演化分析

为了解猫杯状病毒形态特征及遗传演化情况,采用F81细胞从患病宠物猫的鼻拭子样品中分离获得1株猫杯状病毒(feline calicivirus,FCV),命名为SH1。经电镜观察,病毒粒子呈球形,无囊膜,符合FCV的形态特征。采用RT-PCR方法扩增了该毒株的全基因组,并进行了序列测定和衣壳蛋白基因(ORF2)序列的分析。结果显示:分离株与国内外参考株的ORF2序列的核苷酸和氨基酸同源性分别为74.1%~79.7%和84.5%~90.9%;ORF2基因的遗传演化分析显示,30株FCV毒株形成两大分支,即基因群Ⅰ和Ⅱ,分离株属于基因群Ⅰ;进一步分析发现,基因群Ⅰ和Ⅱ主要在377、539和557氨基酸位点存在差异,基因群Ⅰ和Ⅱ分别为N、A、G和K、V、S。研究结果为FCV感染的防控提供科学依据。