小麦矮腥黑穗病菌和普通腥黑穗病菌在几种灭活处理中的相关性分析

对小麦矮腥黑穗病菌和小麦普通腥黑穗菌(光腥和网腥)进行了60Co辐照、环氧乙烷熏蒸、直线加速器电子辐射等方法的灭活处理实验并进行了相关性分析.结果表明各处理对几种菌灭活效果基本一致.预示实验中的两种普通腥黑穗菌可做为矮腥黑穗菌的指示菌.     

应用TaqMan MGB探针检测小麦印度腥黑穗病菌和黑麦草腥黑穗病菌

 以小麦印度腥黑穗病菌9个菌株和黑麦草腥黑穗病菌5个菌株及其近似种或相关种:稻粒黑粉菌、狼尾草腥黑粉菌、狗尾草腥黑粉菌、苏玛特腥黑粉菌、狐尾草腥黑粉菌、小麦网腥黑穗病菌和小麦矮化腥黑穗病菌共9种22个菌株为研究对象,通过序列比对分析,设计了检测小麦印度腥黑穗病菌及黑麦草腥黑穗病菌的TaqMan MGB实时荧光PCR引物和探针,优化了反应条件,筛选出特异性探针,分别建立了小麦印度腥黑穗病菌和黑麦草腥黑穗病菌实时荧光单重PCR和实时荧光双重PCR检测方法,其中实时荧光双重PCR检测方法实现了在同一PCR管中仅用5μL的反应体系,进行1次PCR反应就能特异性检测出小麦印度腥黑穗病菌或黑麦草腥黑穗病菌。本研究所建立的检测方法特异性强、结果可靠、检测速度快、成本明显降低,在文际应用中具有推广价值。     

小麦光腥黑粉菌的鉴别及其检测技术的研究进展

小麦光腥黑穗病是小麦上的一种毁灭性病害,其病原菌被列为国内限定非检疫性有害生物,但目前国内对该病菌的认识和研究远远落后于口岸经常截获的小麦矮腥黑穗病菌、小麦网腥黑穗病菌和小麦印度腥黑穗病菌。为早期识别和检测该病菌,从源头上预防该病菌传入、流行和传播,保障我国小麦生产的安全,本综述在总结这4种小麦腥黑粉菌的冬孢子形态和生理特征差异的基础上,分析和比较了目前用于小麦光腥黑粉菌检测的激光共聚焦扫描显微、红外光谱、电子鼻和PCR等主要技术的优劣,为更好地利用这些技术来检测小麦光腥黑粉菌提供了参考。     

小麦矮化腥黑穗病菌侵染能力的研究

中美专家合作在美国犹他州对小麦矮化腥黑穗病菌的侵染能力进行了研究。试验采用不含抗病基因的小麦品种Cheyanne,播种前用溴甲烷对试验小区进行了熏蒸。接种物为含有多种致病型的冬孢子悬浮液,采用土壤表面喷洒冬孢子悬浮液的方法进行接种,接种密度为每cm20、0.88、8.84、88.45、884.49、8844.89、88449个孢子。结果表明,接种密度为每cm20.88个孢子时即可产生0.21％的穗发病率。对试验数据进行分析后表明,小麦矮化腥黑穗病菌的侵染规律符合侵染概率理论,在本试验条件下,单个孢子的侵染概率为0.0002。     

小麦矮腥黑穗病的检验与防治

小麦矮腥黑穗病(Tilletia controversaKnhü.)的传染方式和普通腥黑穗病不尽相同。矮腥黑穗病菌孢子能借土壤传染,在土壤内能存活七、八年,甚至十年以上。矮腥黑穗病菌的侵染期也较长,不限于小麦的胚芽鞘期,从12月到翌年4月均能感病,是一种相当顽强和比较不易防治的病害。因此必须认真处理带菌小麦。 这种黑穗病菌除为害小麦外,其它寄主还有黑麦和60多种禾本科杂草,但在自然环境条件下较少     

河北埧上小表腥黑穗病的鉴定

 为查清河北省坝上发生的小麦腥黑穗病是网腥还是矮腥,按腥黑穗菌标准鉴定方法作了观察比较.     

基于ISSR标记开发的一种用于小麦矮腥黑穗病菌的分子鉴定方法

 小麦矮腥黑穗病菌(Tilletia controversa Kühn, 简称TCK)是小麦上的一种重要检疫性真菌。本研究利用内部简单重复序列(Inter-simple sequence repeat, ISSR)技术研究TCK及其近缘种的DNA多态性,开发了一种可靠而简单的方法用于TCK的分子鉴定。用ISSR引物P4从TCK中扩增出一条1 113 bp的特异性条带,据此设计了一对特异性引物TCKF/TCKR,在12个TCK菌株中均能扩增得到一条882 bp的特异性条带,而其他近缘种包括小麦网腥黑穗病菌(T. caries)和小麦光腥黑穗病菌(T. foetida)及相关黑粉菌的14个菌株均无扩增条带。用该特异性引物检测TCK的下限为25 μL反应体系中可检测到1 ng DNA模板。本研究开发的种特异性引物,可将TCK与其形态上相似的近缘种尤其是小麦网腥黑穗病菌准确区分开,本研究基于ISSR标记建立的小麦矮腥黑穗病菌的分子鉴定方法为腥黑粉菌的检疫提供了一种便捷的方法,是对现有分子鉴定方法的一个补充。     

诱导小麦抗叶锈病生防细菌的筛选、鉴定及其防效评价

小麦叶锈病是小麦生产上的重要病害,防治该病害主要采用抗病品种和喷施化学农药,而探索生物防治是防治该病的一种新方法。本研究使用3株细菌菌悬液对小麦种子进行处理,于小麦一叶期接种叶锈病菌10d后调查其发病率和严重度。结果表明,在盆栽试验中,Sneb1462菌株菌悬液诱导小麦抗叶锈病的效果最好,可使发病率和严重度比对照分别降低27.54%和49.90%;Sneb1462还可促进小麦根部生长,施用后小麦根长和地下部鲜重分别比对照提高30.19%和29.03%。在大田试验中,用Sneb1462菌悬液处理小麦种子后叶锈病的严重度降低38.60%,小麦株高和穗重分别提高16.44%和34.98%,表明该菌株是一株优良的抗病促生菌。经透射电镜观察、16SrDNA序列分析及生理生化的检测,鉴定该菌株为多黏类芽胞杆菌Paenibacillus polymyxa。利用生防细菌Sneb1462进行种子处理防控小麦叶锈病将是一种新型的植保措施,具有重要的研究意义。     

河北埧上小表腥黑穗病的鉴定

为查清河北省坝上发生的小麦腥黑穗病是网腥还是矮腥,按腥黑穗菌标准鉴定方法作了观察比较. 小麦矮腥黑穗病的典型症状是病株矮化(比健株矮25—66%),分蘖增多(比正常植株增加50%).坝上的病株比健株仅矮8.6—29.7%,而分蘖数差异不甚显著. 坝上腥黑穗病瘘质地有疏松也有稍硬,为探明病瘿质地与孢子形态和萌芽特性的关系,曾把疏松和稍硬的病     

小麦矮腥黑穗病菌冬孢子的春眠

由小麦矮腥黑穗病菌 Tilletia contro-versa 引起的小麦矮腥黑穗病尚未在春小麦上发现,即使有时春季气候条件适合冬孢子萌发和侵染。每月从大田采集病穗散落在土壤中的冬孢子,经1—3年,并于室内测定萌芽力。7月到1月采集的冬孢子萌芽量     

西葫芦根腐和茎基腐病新病原-露湿拟漆斑菌Paramyrothecium roridum

 2013年12月,甘肃省白银市水川镇日光温室中的西葫芦发生了严重的根腐和茎基腐,部分棚室病株率达50%,从病根和病茎上分离得到拟漆斑菌属真菌3株,病株分出率27.3%。采用胚根和茎基部接种法测定了菌株FG-62对西葫芦的致病性:茎基部接种后27 d,植株开始出现凋萎;接种后40 d,两种接种法的西葫芦苗均呈现严重根腐和茎基腐症状,茎基部接种的西葫芦凋萎株率达30%;从病根和病茎上均可再分离出原接种菌。菌株FG-62在PDA平板上25℃培养14 d,产生大量墨绿色至黑色分生孢子座,分生孢子无色至淡榄黑色,单胞,杆状或腰鼓状,两端钝圆,大小为(7.04~9.15)μm ×(1.97~2.46)μm,聚集的分生孢子呈黑色。BLASTn分析结果显示,菌株FG-62(GenBank 登录号 MK252098)的rDNA-ITS序列与露湿拟漆斑菌Paramyrothecium roridum分离物E-469 (GenBank 登录号KY582183.1)和CBS 357.89(源自模式材料,GenBank 登录号NR_145077.1)的序列相似性分别达99.65%和96.83%。依据病原菌形态学和rDNA-ITS序列,将其鉴定为露湿拟漆斑菌P. roridum (Basionym:Myrothecium roridum)。这是露湿拟漆斑菌引起西葫芦根腐和茎基腐的首次报道。     

Efficacy of Hypovirulent Binucleate Rhizoctonia sp. to Control Banded Leaf and Sheath Blight in Corn

Water agar, artificially infested soil and leaf sheath inoculation methods were used to assess the suitable time of application, varietal host response and persistence of Rhv7, a hypovirulent, binucleate Rhizoctonia collected from soil in the Philippines, to effectively control virulent Rhizoctonia solani AG1-IA isolate RS35 on corn. With the water agar method, prior inoculation (2 to 3 days) with the biocontrol agent is essential to achieve maximum control of the pathogen. Disease protection was increased from 23 to 70% as the pre-incubation time of Rhv7 prior to the challenge inoculation with virulent isolate was lengthened from 0 to 3 days. Disease severity and incidence of banded leaf and sheath blight (BLSB) on the three corn hybrids were also suppressed in artificially infested soil. In leaf sheath inoculation, the suppressive ability of Rhv7 against BLSB on corn persisted during lesion expansion. This suppression was expressed as slower disease progress in plants with Rhv7 than in plants without Rhv7. Early and timely brace root formation that detached infected sheaths, also aided in reducing the number of diseased plants in Rhv7-treated plots at the final observation. Mycelial growth activity of RS35 was reduced when corn plants were pre-inoculated with Rhv7 before challenge even if there was no contact detected between Rhv7 and RS35, which suggests that Rhv7 protects corn against BLSB by induced resistance. The hypovirulent, binucleate Rhizoctonia Rhv7 strain effectively controlled R. solani AG1-IA isolate RS-35 in corn. Received 30 August 1990/ Accepted in revised form 25 October 1999     

Demonstration of secondary infection by Pythium violae in epidemics of carrot cavity spot using root transplantation as a method of soil infestation

Cavity spot of carrot (CCS), one of the most important soilborne diseases of this crop worldwide, is characterized by small sunken elliptical lesions on the taproot caused by a complex of pathogens belonging to the genus Pythium , notably P. violae . In most soilborne diseases the soil is the source of inoculum for primary infections, with diseased plants then providing inoculum for secondary infections (both auto- and alloinfection). Using fragments of CCS lesions to infest soil, it was demonstrated that CCS lesions on carrot residues can cause primary infection of healthy roots. Using a novel soil infestation method, in which an artificially infected carrot root (the donor plant) was placed close to healthy roots (receptor plants) the formation of typical CCS lesions were induced more efficiently than the use of classical soil inoculum and showed that CCS can spread from root to root by alloinfection from transplanted diseased roots. The method also demonstrated the polycyclic nature of a CCS epidemic caused by P. violae in controlled conditions. Secondary infections caused symptoms and reduced root weight as early as two weeks after transplantation of the diseased carrot. This reproducible method may be used for delayed inoculation and for studying the effect of cropping factors and the efficacy of treatments against primary and secondary cavity spot infections.     

黄芪根腐病病株和健株根围微生物菌群变化分析

通过分析黄芪根腐病病株和健株根围微生物菌群的变化,探究根腐病的发病机理,寻找预警病害发生的生物指示因子,为土壤微生态的生物调控提供依据。试验通过菌落计数、PCR-DGGE和16S rRNA V3区基因测序的方法,分析不同年限下黄芪根围病/健土中微生物区系、多样性及群落结构的变化。结果表明:细菌作为黄芪根围土中的优势种群,是影响病土中微生物数量升高的关键因子,其多样性降低是影响病害加重的主要原因之一。假单胞菌属Pseudomonas和无色杆菌属Achromobacter为土壤中的优势菌群,健土中的1号和4号特异条带分别为未培养的假单胞菌Uncultured Pseudomonas sp.和荧光假单胞菌P.fluorescens;6号未培养假单胞菌Uncultured Pseudomonas sp.的丰度与根腐病发病率负相关,16号无色杆菌Achromobacter sp.的丰度则在3年生土壤中显著升高,随后急剧下降。上述4个菌可作为潜在的土壤健康或发病指示因子进一步研究。     

Evaluation of models to predict take-all incidence in winter wheat as a function of cropping practices,soil, and climate

The incidence and severity of take-all, caused by Gaeumannomyces graminis var. tritici (Ggt), in susceptible crops depend on climate, soil characteristics and cropping practices. Take-all can be controlled by modifying crop rotation, crop management and fungicide treatment. When available, fungicides are used as a seed treatment and are partially effective. There is currently no reliable method for helping farmers to optimise their choice of cropping system to improve take-all control. In this study, we defined 16 models, based on various mathematical functions and input variables, for predicting disease incidence in a wheat crop as a function of soil characteristics, climate, crop rotation and crop management. The parameters of these models were estimated from field experiments carried out at six sites in the north of France over a ten-year period. The root mean squared error of prediction (RMSEP) values of the models were estimated by cross validation and compared. RMSEP was in the range 16.34–65.93% and was higher for the models based on multiplicative functions. The lowest RMSEP value was obtained for a dynamic model simulating disease incidence during the crop cycle and which included among input variables the percentage of diseased plants determined at GS30.     

Temporal Dynamics of Phytophthora Blight on Bell Pepper in Relation to the Mechanisms of Dispersal of Primary Inoculum of Phytophthora capsici in Soil

ABSTRACT The effect of components of primary inoculum dispersal in soil on the temporal dynamics of Phytophthora blight epidemics in bell pepper was evaluated in field and growth-chamber experiments. Phytophthora capsici may potentially be dispersed by one of several mechanisms in the soil, including inoculum movement to roots, root growth to inoculum, and root-to-root spread. Individual components of primary inoculum dispersal were manipulated in field plots by introducing (i) sporangia and mycelia directly in soil so that all three mechanisms of dispersal were possible, (ii) a plant with sporulating lesions on the soil surface in a plastic polyvinyl chloride (PVC) tube so inoculum movement to roots was possible, (iii) a wax-encased peat pot containing sporangia and mycelia in soil so root growth to inoculum was possible, (iv) a wax-encased peat pot containing infected roots in soil so root-to-root spread was possible, (v) noninfested V8 vermiculite media into soil directly as a control, or (vi) wax-encased noninfested soil as a control. In 1995 and 1996, final incidence of disease was highest in plots where sporangia and mycelia were buried directly in soil and all mechanisms of dispersal were operative (60 and 32%) and where infected plants were placed in PVC tubes on the soil surface and inoculum movement to roots occurred with rainfall (89 and 23%). Disease onset was delayed in 1995 and 1996, and final incidence was lower in plants in plots where wax-encased sporangia (6 and 22%) or wax-encased infected roots (22%) were buried in soil and root growth to inoculum or root-to-root spread occurred. Incidence of root infections was higher over time in plots where inoculum moved to roots or all mechanisms of dispersal were possible. In growth-chamber studies, ultimately all plants became diseased regardless of the dispersal mechanism of primary inoculum, but disease onset was delayed when plant roots had to grow through a wax layer to inoculum or infected roots in tension funnels that contained small volumes of soil. Our data from both field and growth-chamber studies demonstrate that the mechanism of dispersal of the primary inoculum in soil can have large effects on the temporal dynamics of disease.     

Response of Hard Red Winter Wheat to Soilborne wheat mosaic virus Using Novel Inoculation Methods

ABSTRACT Soilborne wheat mosaic virus (SBWMV) is an agronomically important pathogen of wheat that is transmitted by the soilborne plasmodiophorid vector Polymyxa graminis. In the laboratory, attempts to generate SBWMV-infected plants are often hampered by poor infectivity of the virus. To analyze the mechanism for virus resistance in wheat cultivars, we developed novel inoculation techniques. A new technique for foliar inoculation of SBWMV was developed that eliminated wound-induced necrosis normally associated with rub inoculating virus to wheat leaves. This new technique is important because we can now uniformly inoculate plants in the laboratory for studies of host resistance mechanisms in the inoculated leaf. Additionally, wheat plants were grown hydroponically in seed germination pouches and their roots were inoculated with SBWMV either by placing P. graminis-infested root material in the pouch or by mechanically inoculating the roots with purified virus. The susceptibility of one SBWMV susceptible and three field resistant wheat cultivars were analyzed following inoculation of plants using these novel inoculation techniques or the conventional inoculation technique of growing plants in P. graminis-infested soil. The results presented in this study suggest that virus resistance in wheat likely functions in the roots to block virus infection.     

Pathogenicity of plant and soil isolates of <Emphasis Type="Italic">Phytophthora parasitica</Emphasis> on tomato and pepper

Crown and root rot of tomato and sweet pepper can be caused by Phytophthora parasitica. In this work, 23 P. parasitica isolates from diseased pepper or tomato plants as well as 54 isolates from 23 monocrop tomato soils (from Spain and Chile) and one from a pepper soil were studied for their host–pathogen response. Results show significant host specificity for the isolates from tomato plants and tomato soils (63 of 64 isolates were unable to cause disease in pepper). None of the pepper plant/soil isolates showed pathogenicity on tomato, and only four of 14 reproduced their pathogenicity on pepper. Only one tomato isolate was pathogenic to both Solanaceae species. Two different inoculation protocols were evaluated (substrate irrigation and stem cutting). All isolates which expressed pathogenicity when stem inoculated also did it when root inoculated, but not vice-versa. Therefore, the recommended test protocol for tomato and pepper breeding programmes is that based on root inoculation by irrigation.     

小麦稈枯病菌(Gibellia cerealis Pass.)子囊孢子萌发试验

 小麦秆枯病过去在国内仅在少数地方零星发现^[1],很少有叹注意。近几年来在华北局部地区有严重发生的趋势。     

Dominant Colonisation of Wheat Roots by Pseudomonas fluorescens Pf29A and Selection of the Indigenous Microflora in the Presence of the Take-all Fungus

Increases in populations of fluorescent pseudomonads on wheat roots are usually associated with take-all decline, natural control of take-all, a disease caused by the fungus Gaeumannomyces graminis var. tritici (Ggt). Colonisation by Pseudomonas fluorescens strain Pf29A was assessed on the roots of healthy plants and of plants with take-all, and the effect of this bacterium on indigenous populations of fluorescent pseudomonads was studied. The efficacy of Pf29A as an agent for the biocontrol of take-all on five-week-old wheat seedlings was tested in non-sterile conducive soil in a growth chamber. RAPD (random amplification of polymorphic DNA) fingerprinting with a decamer primer was used to monitor strain Pf29A and culturable indigenous rhizoplane populations of fluorescent pseudomonad. Pf29A decreased disease severity and accounted for 44.6% of the culturable fluorescent pseudomonads on healthy plant rhizoplane and 75.8% on diseased plant rhizoplane. Fewer RAPD patterns were obtained when Pf29A was introduced into the soil with Ggt. In the presence of Ggt and necrotic roots, Pf29A became the dominant root coloniser and dramatically changed the diversity and the structure of indigenous fluorescent pseudomonad populations. The results show that Ggt and reduced lesion size on roots can trigger a specific increase in antagonist populations and that the introduction of a biocontrol agent in soil influences the structure of indigenous bacterial populations.