Effects of three esca-associated fungi on Vitis vinifera L.: II. Characterization of biomolecules in xylem sap and leaves of healthy and diseased vines

Secondary metabolites and host defense compounds were shown to occur in xylem sap, and leaves of Vitis vinifera cv. Italia and cv. Matilde naturally infected by the esca-associated fungi Phaeomoniella chlamydospora (Pch), Togninia minima (Tmi) and Fomitiporia mediterranea (Fme). Samples of xylem sap and leaves were collected from healthy vines and from vines showing severe symptoms of brown wood-streaking caused by Pch and Tmi, or from vines with symptoms of both brown wood-streaking and white rot caused by Fme. Xylem sap collection was carried out during the early spring of 2003 and 2004, corresponding to the phenological phases: (A) cotton bud; (B) green tip; (C) leaves out; (D) stretched out leaves; and (E) visible clusters. In the present work we have studied the accumulation of biomolecules (pentaketides and α-glucans), host defense compounds (benzaldehydes, benzoic acid and cinnamic acid derivatives, flavonols, flavanols, flavan-3-ol derivatives and stilbenes) at different stages of grapevine development. Accumulation and changes in total phenolics and recurring phenolics, and of three phytotoxic secondary metabolites (scytalone, isosclerone and pullulan) were analyzed by HPLC. On comparing results for cv. Italia and cv. Matilde, it can be seen that phenolic concentrations are strongly related to the cv.     

基于多重分形去趋势移动平均分析的油菜叶片氮素营养诊断建模

为识别和诊断不同施氮水平下油菜叶片纹理特征,利用多重分形去趋势移动平均分析(MF-DMA),分别计算θ=0,θ=0.5,θ=1下油菜叶片图像的11个全局广义Hurst指数和其他6种相关的多重分形特征参数。利用不同的特征参数组合分别对基部叶片、中部叶片和顶部叶片进行氮素营养诊断识别。结果表明θ=0时诊断效果优于θ=0.5和θ=1;并且在θ=0时,基部叶片和中部叶片诊断效果优于顶部叶片,表明基部和中部叶片对氮素敏感性强于顶部。对3个部位混合的油菜样本进行施氮适中和亏缺两类定性诊断,结果表明支持向量机和随机森林这2种分类方法最佳,最佳识别准确率分别为95.81%和96.63%。说明该模型具有良好的有效性。     

铁皮石斛PRC2复合体成员的鉴定及对胁迫响应的表达分析

为了探讨PRC2复合体在铁皮石斛生长发育和胁迫响应中的功能,通过生物信息学方法筛选了铁皮石斛PRC2核心成员DcCLF、DcSWN、DcEMF2、DcFIE和DcMSI1,借助酵母双杂交技术分析了它们之间的互作关系,利用半定量PCR分析了PRC2核心成员的组织表达谱,通过荧光定量PCR检测了它们对非生物胁迫(低温、高温、脱水)和病害胁迫(齐整小核菌、灰葡萄孢霉菌)的响应情况。结果表明,铁皮石斛PRC2复合体包含5个成员:E(z)同源基因DcCLF和DcSWN、Su(z)12基因DcEMF2、ESC基因DcFIE、p55基因DcMSI1,且这5个成员间的互作关系基本符合模式植物的互作模式,也存在物种特异性,表明PRC2复合体在进化中既有保守性也有特殊性。PRC2核心成员在铁皮石斛根、茎、叶、花蕾、成花中均有表达,但不同基因的表达存在组织差异性。同时,PRC2成员响应不同的环境和病害胁迫:DcCLF受低温、高温和脱水等各种环境胁迫的显著诱导;DcMSI1和DcEMF2在齐整小核菌侵染下表达明显上调,而DcSWN在灰葡萄孢霉菌侵染下受诱导程度最大。铁皮石斛PRC2复合体在生长发育和胁迫应答中...     

香龙血树真菌病害的鉴定

1997-2000年在广州地区的香龙血树[Dracaena fragrans(L.)Ker-Gaw.]种植单位共调查到9种真菌病害，即：可可球二孢茎枯病，顶多毛孢叶斑病，弯孢霉灰斑病，弯孢霉褐斑病，炭疽病，拟盘多毛孢叶斑病，拟茎点霉灰斑病，拟茎点霉叶斑病和球壳孢叶枯病，其病原菌分别被鉴定为：可可球二孢（Botryodiplodia theobromaePat.)、龙血树顶多毛孢（Bartalinia dracaenaeaP.G.Xi,Z.D.JiangetP.K.Chi)，弯孢霉[Gurvularia lunata(Walker)Boedijn]、塞河弯孢霉[Curvularia senegalensis(Speg.)Subram]、围小丛壳[Glomerella cingulata(Stonem)Spauld,etSchrenk]，棒孢拟盘多毛孢[Pestalotiopsis clavispora(Atk)Stey]、龙血树拟茎点霉（phomopsis dracaenae Sahni)，龙血树生拟茎点霉（Phomop-sis dracaenicola Z.D.Jiang,P.G.XietP.K.Chi)，龙血树球壳孢（Sphaeropsis dracaenaeP.G.XietP.K.Chi)，对生产影较大的是由可可球二孢引起的茎枯病和由围小丛壳引起的叶部炭疽病。     

禽坦布苏病毒研究进展

禽坦布苏病毒(avian Tembusu virus,ATMUV)是一种主要引起蛋鸭发病的新发病毒性传染病,该病毒自2010年4月以来给中国东南沿海地区的养鸭业造成了巨大经济损失,该病毒也可感染鸡、鹅等多种家禽发病.文章综述了ATMUV的病原学、流行病学、生物学特性、基因组学、诊断技术和疫苗研发的研究现状及前景,为进一步研究ATMUV提供参考.     

Multilocus sequence typing detects new Piscirickettsia salmonis hybrid genogroup in Chilean fish farms: Evidence for genetic diversity and population structure

Piscirickettsia salmonisis the causative bacterial pathogen of piscirickettsiosis, a salmonid disease that causes notable mortalities in the worldwide aquaculture industry. Published research describes the phenotypic traits, virulence factors, pathogenicity and antibiotic‐resistance potential for various P. salmonisstrains. However, evolutionary and genetic information is scarce for P. salmonis. The present study used multilocus sequence typing (MLST) to gain insight into the population structure and evolution of P. salmonis. Forty‐two Chilean P. salmonisisolates, as well as the type strain LF‐89^T, were recovered from diseased Salmo salar, Oncorhynchus kisutchand Oncorhynchus mykissfrom two Chilean Regions. MLST assessed the loci sequences of dnaK, efp, fumC, glyA, murG, rpoD and trpB. Bioinformatics analyses established the genetic diversity among P. salmonis isolates (H = 0.5810). A total of 23 sequence types (ST) were identified, 53.48% of which were represented by ST1, ST5 and ST2. Population structure analysis through polymorphism patterns showed few polymorphic sites (218 nucleotides from 4,010 bp), while dN/dS ratio analysis indicated purifying selection for dnaK, epf, fumC, murG, and rpoD but neutral selection for the trpB loci. The standardized index of association indicated strong linkage disequilibrium, suggesting clonal population structure. However, recombination events were detected in a group of seven isolates. Findings included genogroups homologous to the LF‐89^T and EM‐90 strains, as well as a seven‐isolate hybrid genogroup recovered from both assessed regions (three O. mykiss and four S. salar isolates). The presented MLST scheme has comparative potential, with promising applications in studying distinct P. salmonis isolates (e.g., from different hosts, farms, geographical areas) and in understanding the epidemiology of this pathogen.     

福建省水牛巴贝斯焦虫病调查研究 Ⅱ.病原鉴定

1981～1986年调查福建省崇安县水牛巴贝斯焦虫病,该病病原初步鉴定为牛巴贝斯焦虫Babesia boris(Babes,1988)。病原各类虫体形态所占比例分别为:单梨形虫体占37.21％,双梨形虫体占35.03%,椭圆形虫体占16.73%,环形虫体占7.67％,圆形虫体占1.34%和变形虫形虫体占2.01％。红细胞染虫数1～4个,多数1～2个。带虫红细胞平均直径5.25μm。梨形虫体平均长度1.98μm。虫体指数为1:1.04～2.76。红细胞染虫率x4.33%,S1.97％。虫体位于红细胞中部占78.55％,位子红细胞边缘占21.45％。双梨形虫体尖端排列形成钝角、锐角和直线分别为80.19％、14.15％和5.66％。     

Development and application of molecular methods (PCR) for detection of Tasmanian Atlantic salmon reovirus

Molecular (PCR) diagnostic tests for the detection and identification of aquareovirus in general, and Tasmanian Atlantic salmon reovirus (TSRV) specifically, were developed, and their diagnostic sensitivity and specificity were determined and compared with virus isolation in cell culture. Intralaboratory and interlaboratory comparison of PCR (conventional hemi‐nested RT‐PCR & RT‐qPCR) and virus isolation in cell culture using finfish cell lines, CHSE‐214 and EPC, was carried out for the detection and identification of TSRV using field samples of farmed Atlantic salmon Salmo salar, L. from various aquaculture sites around Tasmania. The interlaboratory comparison of diagnostic methods was carried out between two laboratories, AAHL‐CSIRO and DPIPWE‐Tasmania. A total of 144 fish from nine sites (12–33 fish per site) were sampled from two regions of Tasmania (Tamar River estuary in the north and Huon River estuary in the south‐east) during late spring to early summer of 2009, and the data were analysed using different statistical approaches. The prevalence of TSRV ranged from 6% to 22% in both regions. All the diagnostic methods (data from both laboratories) had high specificity, while the estimated sensitivity varied between tests with RT‐qPCR being the most sensitive (95.2%) method followed by virus isolation and then conventional hemi‐nested RT‐PCR.     

两例犬化脓性子宫内膜炎的病原分离鉴定及药敏试验

本研究对两例确诊为化脓性子宫内膜炎的犬进行了病原的研究。用阴道采样法采集子宫分泌物进行细菌培养和生化鉴定,结果第1例因连续使用抗生素,而分离不到细菌;第2例分离到葡萄球菌和链球菌;药敏试验结果表明,犬子宫内膜炎的主要病原菌对临床使用较多的青霉素和链霉素有很大的耐药性,而对头孢唑啉、环丙沙星、恩诺沙星等药物较为敏感,为临床首选药物。     

Studies on the Epidemiology of Tropical Theileriosis (Theileria annulata Infection) in Cattle in Central Anatolia,Turkey

An epidemiological survey for Theileria annulata infection was conducted in 12 selected villages around Ankara in Central Anatolia, Turkey, during the period April 1990 to January 1993. During the survey, 198 cattle of 30 local breeds, 84 Holstein-Friesian×local breeds and 84 Holstein-Friesian breed were examined for antibodies to T. annulata and the presence of the vector ticks. Four species of Hyalomma ticks were identified: Hyalomma anatolicum anatolicum, Hyalomma anatolicum excavtum, Hyalomma detritum and Hyalomma marginatum marginatum. Salivary gland staining indicated that infected adult ticks of all four species were present and, therefore, were implicated in the transmission of tropical theileriosis in the field. Generally, the Hyalomma infestation rate was low, with the heaviest infestations occurring on the older animals. Young adults and calves had very low infestation rates. Most ticks seen on cattle were adults, very few nymphs were found. The blood smear and serological examination of the 198 cattle conducted in March, before the start of the first disease season, showed that the prevalence of piroplasmosis was 11.1% (22 out of 198) and the seroprevalence of T. annulata was 10.6% (21 out of 198). Forty-three animals were then excluded from the study because they were seropositive and/or harboured piroplasms. Ninety-two seronegative animals showed piroplasmosis (92 out of 155) and 34 seronegative animals became seropositive for T. annulata (34 out of 155) during the three disease seasons. One animal became clinically ill with tropical theileriosis and required treatment. The incidence of cattle showing piroplasmosis and disease in the total study sample was 50.7% and 0.5% per disease season, respectively. The seroconversion rate of new infection with T. annulata in the total study was 14.3% per animal season. The number of cattle showing piroplasmosis was much greater than the number of seropositive cattle, which may indicate the presence of another species of Theileria. The two different management systems encountered in the study were considered to have influenced the tick infestation levels.