蓝莓腐霉根腐病的病原菌

在山东青岛新发现一种蓝莓根腐病害,症状最初出现在根部,病根腐烂坏死,根状茎维管束和皮层变黑,导致根数量减少,叶片变黄、变红,植株生长不良,严重时叶片全部脱落,植株死亡。通过组织分离法和菌丝段分离法获得纯化菌株HMQAU 180018,经柯赫氏法则验证,综合形态学特征及ITS区和cox I基因序列分析,菌株HMQAU 180018被鉴定为畸雌腐霉Pythium irregulare。这是国内首次描述畸雌腐霉引起蓝莓根腐病的报道。     

内蒙古天竺葵腐霉枯萎病病原菌

为了明确天竺葵腐霉枯萎病的病原菌种类,从内蒙古通辽采集天竺葵腐霉枯萎病样品,对病原物进行了分离、纯化和致病性测定,并对病原物进行形态学和rDNA-ITS序列分析鉴定。结果表明,从10个植物样品中分离得到16个腐霉菌株,分别属于终极腐霉Pythium ultimum var. ultimum、瓜果腐霉P. aphanidermatum和两个与P. ultimum var. ultimum相似的待定种。其中,P. ultimum var. ultimum的分离频率为75%、P. aphanidermatum的分离频率为12.5%,两个腐霉待定种的分离频率均为6.25%;P. ultimum var. ultimum是优势类群。致病性测定结果表明,4种腐霉菌都能引起天竺葵腐霉枯萎病,与自然发病症状相同,其中P. ultimum var. ultimum和P. aphanidermatum的致病性较强,发病率分别为71.4%和85.7%。     

内生真菌对羽茅抗病性的影响

为探讨不同种类内生真菌对宿主植物羽茅(Achnatherum sibiricum)抗病性的影响, 以感染不同内生真菌的天然禾草羽茅为实验材料, 进行了体外纯培养的内生真菌、感染内生真菌的离体叶片和在体叶片对3种植物病原真菌的抑菌实验。结果表明: 体外纯培养条件下, 分离自羽茅的内生真菌Neotyphodium sibiricum、Neotyphodium gansuensis和Epichloë gansuensis对新月弯孢霉(Curvularia lunata)、根腐离蠕孢(Bipolaris sorokiniana)和枝孢霉(Cladosporium sp.)等3种病原真菌都具有抑制作用, 其中N. sibiricum的抑制作用最强, 对新月弯孢霉、根腐离蠕孢和枝孢霉的抑菌率分别为47.8%、40.1%、39.4%; 内生真菌培养滤液也可以有效抑制这3种病原真菌的孢子萌发, 其中N. gansuensis的抑制作用最强, 新月弯孢、根腐离蠕孢和枝孢霉的孢子萌发率分别为9.8%、8.7%、8.5%。对于离体叶片, N. sibiricum和N. gansuensis感染可以有效降低叶片受3种病原真菌侵染后的病斑数和孢子浓度, 其中N. sibiricum对根腐离蠕孢的抑制作用显著高于N. gansuensis, 而E. gansuensis只降低新月弯孢和枝孢霉侵染的病斑数以及枝孢霉侵染的孢子浓度。在体条件下, 内生真菌均可以显著降低病原真菌侵染羽茅后的病斑数、病斑长度和孢子浓度, 其中E. gansuensis的抑菌作用趋于最弱, 而N. sibiricum的抑菌作用趋于最强。     

我国桔梗上一种新病害匍柄霉叶斑病的病原

2013年在内蒙古赤峰市喀喇沁旗发现桔梗匍柄霉叶斑病,该病害在2014-2017年均再次发生。采用单孢分离法在病叶上得到病原菌,于PCA培养基上培养后,在光学显微镜下观察记录病原菌形态学特征。同时将病原菌的rDNA ITS、gpd和EF-1α的PCR产物测序后做BLAST分析。结果表明该菌与桔梗匍柄霉Stemphylium platycodontis基本一致。这是国内桔梗匍柄霉叶斑病的首次详细报道。     

木霉属5个中国新记录种及2种木霉在中国的新分布

对来自北京、广东、黑龙江、河南、湖北、湖南、吉林、内蒙古、浙江的木霉属资源进行系统分类研究,报道了该属5个中国新记录种：桤木木霉Trichoderma alni,絮状木霉T. floccosum,近洋大戟草木霉T. parapiluliferum,普丽西拉木霉T. priscilae和森吉木霉T. songyi,并提供了其宏观和微观特征的详细描述及图示。基于联合rpb2和tef1基因序列的系统发育分析,为确定上述种的分类地位提供了佐证。此外,表明近渐绿木霉T. paraviridescens和西蒙斯木霉T. simmonsii在我国广泛分布。     

白及根部内生真菌多样性研究

白及是地生兰科多年生草本植物,是常见的中草药之一。白及根是白及植株吸收养分和水分的主要场所,开展其根部内生真菌的群落组成及多样性分析,对了解云南原生境白及与根部内生真菌间的共生关系具有重要意义。本研究采用形态学和ITS rDNA分子系统发育分析相结合的方法进行菌株鉴定。结果表明,3个采样点的白及根部分离到可培养内生真菌32株,包括9个目、13个科、16个属。其中木霉属Trichoderma、镰刀菌属Fusarium、拟盘多毛孢属Pestalotiopsis为优势类群,分别占总物种数的21.88%、18.75%、9.38%;中碳垫菌属Nemania、丛赤壳属Nectria、炭角菌属Xylaria、紫霉属Purpureocillium、刺盘孢属Colletotrichum、黑孢子菌属Nigrospora、Biscogniauxia、腐质霉属Humicola、脉孢菌属Neurospora、拟茎点霉属Phomopsis、植物腐霉Phytopythium、毛霉属Mucor、伞状霉属Umbelopsis为常见内生真菌类群。α多样性指数分析表明：各采样点的白及根部内生真菌物种多样性最高的是昆明市水源保护区采样点（D=0.799,H’=1.698）,保山市龙陵县采样点物种多样性最低（D=0.787,H’=1.580）。β多样性分析采样点之间的Jaccard（0.912-0.993）、Bray-Curtis（0.838-0.986）和UniFrac（加权0.618-0.631;不加权0.770-0.799）距离,结果表明3个采样点之间的内生真菌群落组成存在差异。3个采样点的不同地理环境和土壤类型给白及提供了不同的生境条件,是影响白及根部内生真菌物种丰度和群落组成差异的主要因素之一。     

梵净山山顶苔藓矮林AM真菌多样性

为探析和比较梵净山国家自然保护区矮林生态系统中丛枝菌根（arbuscular mycorrhizal,AM）真菌群落特征,对6种山顶苔藓矮林群落（山樱-山矾Prunus-Symplocos、杜鹃-槭树Rhododendron-Acer、花楸-杜鹃Sorbus-Rhododendron、槭树Acer、黔稠Cyclobalanopsis stewardiana、杜鹃Rhododendron）土壤进行AM真菌分离、鉴定和分析。结果表明：梵净山山顶苔藓矮林群落共有13属32种AM真菌,包括无梗囊霉属Acaulospora 13种、球囊霉属Glomus 5种、近明球囊霉属Claroideoglomus 2种、多样孢囊霉属Diversispora 2种、隔球囊霉属Septoglomus 2种、原囊霉属Archaeospora 1种、双型囊霉属Ambispora 1种、内养囊霉属Entrophospora 1种、和平囊霉属Pacispora 1种、硬囊霉属Sclerocystis 1种、西维丁囊霉属Sieverdingia 1种、盾巨孢囊霉属Scutellospora 1种和巨孢囊霉属Gigaspora 1种,其中无梗囊霉属的分离频率、相对多度和重要值最高,分别是100%、65.90%和82.95%,为矮林区域的优势属,柯氏无梗囊霉为该区域的优势种;不同矮林间AM真菌群落结构组成差异显著,槭树矮林的孢子密度、菌根侵染率和Shannon-Wiener指数显著高于其他5种植物群落,黔稠矮林的孢子密度和物种丰富度最低,杜鹃矮林的AM真菌Shannon-Wiener指数和Simpson指数均为所有植物群落中最低,表明不同矮林类型对AM真菌群落结构具有重要影响。     

软枣猕猴桃镰孢菌根腐病的病原

在辽宁丹东新发现一种软枣猕猴桃根腐病害,罹病植株叶片枯萎,老叶变干凋谢,最后干枯死亡。通过组织分离法和单孢分离法获得纯化菌株HMQAU150043和HMQAU150044。经形态学观察、ef‐1a序列分析、mt SSU序列分析及柯赫氏法则验证,确定两株病原菌均为多见镰孢Fusarium commune。这是该菌所致软枣猕猴桃根腐病的首次发现。     

一种土壤中大豆疫霉菌分离新方法*

由于腐霉菌的干扰,土壤中大豆疫霉菌的分离十分困难。利用大豆疫霉菌的致病性和大豆对病原菌的选择作用排除腐霉菌,我们建立了一种简单、有效的土壤中大豆疫霉菌的分离方法。该方法用不含抗大豆疫霉根腐病基因的大豆叶碟诱钓大豆疫霉菌的游动孢子,将诱钓叶碟直接接种不含抗大豆疫霉菌基因的大豆植株,再对病株进行选择性或非选择性分离获得大豆疫霉菌。此方法能十分有效地排除腐霉菌干扰和细菌的污染,直接获得纯化菌株。应用该方法我们在以前未报道有大豆疫霉根腐病发生的山东、河南、安徽、江苏和浙江分离到大豆疫霉菌。     

青海豌豆根腐病病原菌种类及致病性的研究

豌豆极腐病是青海东部干旱地区豌豆生产上的一种新病害,近年来危害逐年加重,致使豌豆产量遭受严重损失。根据分离鉴定和致病性测定结果,青海豌豆根腐病病原真菌是由茄镰刀菌、尖孢镰刀菌、豌豆丝囊霉、根串珠霉、立枯丝核菌、腐霉、链孢粘帚霉等复合反染所引起的。经回接试验：镰刀菌和豌豆丝囊霉对豌豆具有较强的致病力;腐霉及其他病原菌则有加强腐烂作用。     

生姜共生真菌的分离及其体外抑菌效应初探

为筛选得到优良植物病害生防菌,对广西生姜Zingiber officinale种植区健康生姜根系和叶片中的共生真菌进行了组织分离,以生姜茎腐病菌群结腐霉Pythium myriotylum和香蕉枯萎病菌尖孢镰刀菌古巴专化型4号生理小种Fusarium oxysporum f. sp. cubense race 4为指示菌,通过平板对峙培养法和发酵液菌落直径法试验进行筛选评价,并结合形态学观察及ITS序列分析对筛选出的生防效果最好的共生真菌进行了鉴定。结果表明,从生姜植株共分离得到34株共生真菌,其中根系分离22株,叶片分离12株;对峙培养发现有6株共生真菌对生姜茎腐病菌和香蕉枯萎病菌均有抑制作用;其中菌株SBM-11拮抗作用最强,对生姜茎腐病菌抑制率达到93%,对香蕉枯萎病菌抑制率达到82%;SBM-11的发酵液对生姜茎腐病菌和香蕉枯萎病菌抑制率分别为82%、73%,与其他菌株发酵液抑制效果相比差异明显;结合形态和分子鉴定结果表明SBM-11菌株为绿色木霉Trichoderma viride,极具生防潜力。     

苹果轮纹病病害名称之规范

苹果轮纹病(apple ring rot)为苹果重要病害,严重危害果实和枝干,甚至造成幼树枯死等。苹果轮纹病可引起果实腐烂、枝干疣突、溃疡、粗皮等症状,导致苹果轮纹病病害汉语名称使用混乱,如苹果轮纹病、苹果干腐病、苹果果实轮纹病、苹果枝干轮纹病、轮纹烂果病等。病原拉丁学名的使用亦相当混乱,葡萄座腔菌Botryosphaeria dothidea、贝林格葡萄座腔菌B. berengeriana、贝林格葡萄座腔菌梨生专化型B. berengeriana f. sp. pyricola、七叶树壳梭孢Fusicoccum aesculi、锹冢大茎点霉Macrophoma kuwatsukai、梨生囊孢Physalospora pyricola和梨生球座菌Guignardia pyricola等学名都在被使用。本文根据近些年来国内外的研究新进展,认为苹果轮纹病是一类复合病害,与欧美国家发生的白腐病为同一种病害,其病原包括葡萄座腔菌B. dothidea和锹冢葡萄座腔菌B. kuwatsukai。建议将该复合病害汉语统称为苹果轮纹病,英文采用apple ring rot。鉴于两种病原在我国苹果产区的普发性,建议在病害发生规律及抗病育种等研究中,对于葡萄座腔菌和锹冢葡萄座腔菌均需充分重视。     

Sensitive and specific detection of Xanthomonas campestris pv campestris by PCR using species-specific primers based on hrpF gene sequences

A sensitive and specific assay was developed to detect bacterial black rot of crucifers caused by Xanthomonas campestris pv. campestris (X. c. pv. campestris), in cabbage seed and plant. Primers XCF and XCR from hrpF homologous to nolX, host recognition protein, were used to amplify a 525 bp DNA fragment. PCR technique was applied to detect the pathogen in naturally infected seed and plant of cabbage. The PCR product was only produced from X. c. pv. campestris among 40 isolates of Xanthomonas strains, Escherichia coli (O157:H7), Pectobacterium carotovorum subsp. carotovorum, and other reference bacteria.     

Effects of Pseudomonas chlororaphis on Pythium aphanidermatum and Root Rot in Peppers Grown in Small-scale Hydroponic Troughs

The ability of Pseudomonas (Ps.) chlororaphis isolate Tx-1 to suppress Pythium aphanidermatum and control root rot was investigated in sweet peppers grown in small-scale hydroponic trough units with recirculating nutrient solution. The agent was introduced to the nutrient solution 3 days after the peppers were inoculated with P. aphanidermatum, or 4 days before and 3 days after inoculation, or 4 days before and 3 and 10 days after. Controls either received no agent or pathogen, or the agent only (applied once, 4 days before the time of pathogen inoculations), or the pathogen only. The experiment was conducted in a greenhouse with repetitions beginning in January, March, and May. Severity of root browning associated with P. aphanidermatum, in the absence of Ps. chlororaphis, increased in the first, second and third repetitions, respectively, to 74% at 21 days, 28% at 21 days, and 68% at 11 days. In treatments with one, two, or three applications of Ps. chlororaphis, respectively, areas under root browning progress curves were reduced by 18-48%, 50-73%, and 62-79% compared to the pathogen controls, and recovery incidence of the pathogen from roots at 21 days after inoculation was reduced by 14-47%, 62-82%, and 60-89%. Roots not inoculated with P. aphanidermatum were whitish and not colonized by the pathogen. Density of Ps. chlororaphis in treated plants was usually 2×10³-1.2×10⁵ cfu g^-1 fresh roots. The Ps. chlororaphis treatments almost invariably prevented reductions in plant height, leaf area, fresh mass and dry mass of the shoots and of the roots, and root volume associated with P. aphanidermatum and root browning. It is concluded that Ps. chlororaphis Tx-1 strongly antagonized P. aphanidermatum in the pepper roots and that the agent has considerable potential for controlling root rot and maintaining productivity in commercial hydroponic peppers.     

凤梨小果芯腐病病原菌凤梨镰孢菌在中国的首次发现

近年,在广东徐闻凤梨种植基地生产的凤梨果实在采后贮藏过程中发生一种果肉腐烂病害,发病率达10%左右,并有逐年加重危害的趋势。为了明确该病的病原菌,本文通过果实组织分离和接种试验获得1个致病菌株,通过形态学观察和TEF-1α序列分析,确定该病的病原菌为凤梨镰孢菌Fusarium ananatum,这是该菌所致凤梨小果芯腐病在国内的首次报道。     

绿色荧光蛋白标记下镰刀菌侵染地黄的组织学观察

为分析对地黄有较强致病性的尖孢镰刀菌的侵染机制,本研究采用携带有潮霉素抗性标记的强组成型表达载体pCT74,经PEG-CaCl₂介导的原生质体转化法导入镰刀菌,获得荧光信号强烈的sGFP标记菌株,并采用喷施接种和根部灌根接种。研究发现镰刀菌首先在地黄外部聚集繁殖,并通过伤口或气孔等通道侵入地黄维管组织,后逐渐导致周围海绵组织破裂,进而致使地下根茎逐渐变黑腐烂;由于地黄叶部气孔发达,使得镰刀菌由叶部侵入速度要快于根部灌根接种;不同孢子浓度接种实验表明镰刀菌对寄主的致害程度与其在叶部与根部的接种浓度并不呈相关性。进一步在接种处理后采集地黄叶部、茎部和根部组织提取真菌DNA后进行PCR扩增发现：在根部接种60h后即能检测到镰刀菌的侵入,经84h后侵入到地黄茎部组织,经96h后侵入到地黄叶部组织。该标记菌株可为今后探索地黄连作栽培中真菌病害大规模爆发的根际生物学过程提供研究材料。     

变孔异担子菌随进境针叶木传入中国的风险分析

变孔异担子菌Heterobasidion irregulare原产于北美,能引起针叶树根部和根基干部的白色腐朽病,严重时导致树木死亡。目前已扩散至欧洲部分国家,在我国尚未有分布。本研究按照植物检疫的国际标准措施之有害生物风险分析原则(ISPMNo.11),从地理分布、定殖可能性、扩散可能性、经济重要性和管理难度等方面对该病菌进行了定性分析,同时按照有害生物危险性评价指标体系及赋值标准,获得该病菌风险R值。结果显示：变孔异担子菌风险评估R值为2.35,属于高度危险林业有害生物,传入风险较高、危害大,目前尚未列入我国禁止进境检疫性有害生物名录中。因此,建议将该种真菌尽快列入名录中,加强口岸检疫。     

进境美国大豆中值得关注的真菌Diaporthe novem

采用常规平板分离法,从一批进境的美国大豆样品中获得1株可疑的间座壳属菌株MDD57.经形态学观察发现,该菌株在PDA培养基上产生分生孢子器,且同时产生大量α型和β型分生孢子,未见有性阶段.经ITS和tef1α基因扩增、核酸序列比对分析,发现该菌株同GenBank中2株Diaporthe novem菌株的基因序列同源性达...     

茄病镰刀菌单克隆抗体的制备及胶体金免疫层析试纸条的研发*

Objective: The cell lines secreting specific monoclonal antibodies (McAbs) were prepared by using Fusarium solani, one of the pathogenic fungi causing root rot of Fritillaria thunbergii, and the colloidal gold immunochromatographic test strip based on McAbs was developed to provide scientific basis for detecting root rot of F. thunbergii. Methods: Hybridoma technology was used to obtain cell lines that could secrete specific McAbs against F. solani using the whole protein extract of F. solani as the antigen. The specificity, titer, sensitivity and binding protein of McAbs were detected by indirect ELISA and Western blot. Colloidal gold particles were prepared by trisodium citrate reduction method and McAbs were labeled to prepare colloidal gold immunochromatographic strip. Results: Three cell lines secreting specific McAbs against F. solani were obtained, which were named as FsA3, FsG6 and FsD4. The detection sensitivity of FsA3 was 24.41 ng / mL, and that of both FsG6 and FsD4 was 12.21 ng / mL. FsA3, FsG6 and FsD4 had strong reactions to F. solani, and had no cross-reaction to Alternaria tenuissima, A. alternata, Botrytis cinerea, F. equiseti, F. incarnatum, F. oxysporum, Phoma sp., and Phomopsis oblonga. The colloidal gold immunochromatographic strip based on FsG6 showed only a quality control line when detecting the tissue culture seedlings of F. thunbergii. When 100 ng F. solani antigen or the samples of F. thunbergii infested with root rot disease were detected, there were visible quality control lines and test lines. Conclusion: The specificity and sensitivity of the McAbs and test strip are sufficient to detect F. solani isolated from diseased strains of F. thunbergii, which provides the technical support for the rapid detection of root rot of F. thunbergii in the field.