生防棘孢木霉T31菌株的分离筛选及其生物学特性

为评价具有生防潜力的棘孢木霉,采用平板对峙法、对扣培养法、圆盘滤膜法从长白山土样中分离筛选出木霉菌株T31,结合形态学及分子生物学分析对其进行种类鉴定,并采用菌丝生长法研究了该菌株的生物学特性。所分离的菌株T31被鉴定为棘孢木霉Trichoderma asperellum,该菌株对8种靶标菌的抑菌率在44.49%~77.91%之间,其中,对玉米大斑病菌Exserohilum turcicum、核盘菌Sclerotinia sclerotiorum、腐霉菌Pythiumuhtimum sp.及镰刀菌Fusarium sp.均有较强生长竞争优势,对玉米灰斑病菌Magnaporthe oryzae具明显重寄生作用。菌株T31的最适培养基为PDA培养基,最适生长温度为30 ℃、最适产孢温度为25 ℃,最适pH值为6。持续光照可以促进木霉菌孢子产生,Zn²⁺、Mn²⁺、Ca²⁺和Mg²⁺利于菌丝生长,但是高浓度的Fe²⁺和Cu²⁺抑制菌丝生长,Mn²⁺和Mg²⁺可促进产孢。此外,与普通木霉菌相比,该菌株具有耐寒性及耐盐性。     

拟康宁木霉Tk1的分离鉴定、拮抗作用及其生物学特性

为了分离利用高效植物病害生物防治菌株，从广东药用植物金丝皇菊根部分离获得一株木霉菌株Tk1。经过形态观察、rDNA-ITS和EF-1α序列分析明确其为拟康宁木霉Trichoderma koningiopsis。用平板对峙培养法测定，该菌株对金丝皇菊枯萎病菌（尖孢镰刀菌Fusarium oxysporum）和柑橘炭疽病菌（胶胞炭疽菌Colletotrichum gloeosporioides）的抑制率分别为68.5%和77.1%，且在后期能完全覆盖或部分覆盖病原真菌。其无菌发酵液对金丝皇菊枯萎病菌的抑制率为45.55%。该菌株营养生长和产孢的最适碳源分别为乳糖和葡萄糖，最适氮源是酵母膏；在pH 4~11的培养基上均可生长、产孢，最适pH为7；12 h交替光照条件下菌丝的生长速度最快，全光照条件下产孢数量最大；该菌株的致死温度为73℃处理10 min。     

拟康宁木霉T-51菌株生物学特性及其生物防治潜力

为进一步扩宽拟康宁木霉Trichoderma koningiopsis T-51菌株的生防应用范围,该研究测定T-51菌株菌丝生长、产孢和分生孢子萌发的最适温度、光照和碳氮源条件及其对灰葡萄孢Botrytis cinerea菌核的重寄生能力和对12种植物病原真菌的生防潜力。结果表明,拟康宁木霉T-51菌株在26℃下菌丝生长最快,生长速度达到2.5 cm/d,在20℃光照条件下产孢量最大,达到1.64×109个/皿,26～28℃光照条件下适宜T-51菌株分生孢子萌发;供试氮源中硫酸铵和硝酸铵适宜T-51菌株菌丝生长、产孢和分生孢子萌发,供试碳源中葡萄糖和可溶性淀粉适宜T-51菌株菌丝生长和分生孢子萌发,果糖和乳糖适宜T-51菌株产孢;T-51菌株能够重寄生灰葡萄孢菌核,当分生孢子悬浮液浓度为1×108个/mL时,重寄生效果最好;T-51菌株对核盘菌属Sclerotinia和丝核菌属Rhizoctonia植物病原真菌重寄生能力较强,对镰刀菌Fusarium spp.、暹罗刺盘孢菌Colletotrichum siamense、桃褐腐病菌Monilinia fructicola和稻瘟菌Mag...     

木霉菌颗粒剂对玉米茎腐病防治的应用

为明确棘孢木霉菌Trichoderma asperellum不同颗粒剂配方对玉米茎腐病的防效,通过人工接种盆栽试验比较分析其防效,同时进行多基点田间试验以筛选对茎腐病防效明显并具有增产效应的木霉菌生防颗粒剂。结果表明:盆栽试验中,2号木霉菌颗粒剂对于苗期玉米茎腐病的防效最高,为65.57%,3号木霉菌颗粒剂对于成株期玉米茎腐病的防效最好,为40.00%;1~4号4种木霉菌颗粒剂均能提高玉米的出苗率、株高、鲜重、干重和根长,表明木霉菌颗粒剂对玉米生长具有促进作用。在全国10余个综合试验站对1号木霉菌颗粒剂的田间防效试验结果显示,对玉米茎腐病的防效较好,均在50%以上,最高可达80%,玉米增产效果在8%以上。表明木霉菌颗粒剂具有良好的生物防治效果及增产作用。     

主要环境及营养因素对西瓜枯萎病菌生长的影响

采用菌丝生长速率法和产孢量测定研究了不同温度、光照、pH及碳氮源对来源于海南、河北和上海的3株西瓜枯萎病菌Fo-HN-46、Fo-HB-12和Fo-SH-1生长速率和产孢量的影响。结果表明:西瓜枯萎病菌菌株的适宜生长温度为20~30℃,Fo-HN-46最适生长温度为28℃,Fo-HB-12和Fo-SH-1最适生长温度为25℃,产孢的最适温度为28~30℃;光照对西瓜枯萎病菌生长速率无显著影响,对产孢影响显著,Fo-HN-46在黑暗条件下单位面积产孢量最高,Fo-HB-12和Fo-SH-1在半光照条件下产孢量最高;pH对西瓜枯萎病菌菌株的生长速率和产孢量有显著影响,pH 7~9时菌丝生长速率快,pH 8~11时产孢量高;葡萄糖、淀粉和乳糖作为碳源能够显著增加西瓜枯萎病菌的产孢量;蛋白胨作为氮源能显著促进菌丝生长,硝酸钠、酵母粉和蛋白胨均能显著增加西瓜枯萎病菌的产孢量。用最适碳源、氮源培养,Fo-HN-46生长速率大于Fo-HB-12和Fo-SH-1。Fo-SH-1产孢量高于Fo-HN-46和Fo-HB-12。     

木霉对土传病原真菌的拮抗作用

 分别在体外及温室测定了筛选菌株哈茨木霉Trichoderma harzianum(T₈₂)和Tricho-derma sp.(NF9)对土传病原真菌的拮抗作用。体外测定表明,木霉菌株T₈₂和NF₉对白绢病菌Sclerotium rolfsii,立枯丝核菌Rhizoctonia solani,瓜果腐霉Pythium aphanidermatum刺腐霉P.spinosum和尖镰孢Fusarium oxysporum在对崎培养中的拮抗系数分别为2或2~3和2。温室测定表明,用0、6%(W/W)T₈₂麸皮培养物(10⁷cfu/g)处理土壤。在人工接种白绢病菌,立枯丝核菌及瓜果腐霉20天后,黄瓜发病率分别比未用木霉处理的对照减少46、5%,28.4%和81。2%;用T₈₂和NF₉木霉孢子悬浮液(10⁸cfu/ml)处理黄瓜种子,人工接种白绢病菌11天后,黄瓜成苗率分别比未用木霉处理的对照增加14%的20%。分别在光学显微镜和扫描电镜下观察到木霉T₈₂对白绢病菌菌丝和菌核的重寄生以及木霉T₈₂和NF₉对立枯丝核菌菌丝的缠绕。穿入及寄生。作者认为重寄生可能是试验木霉菌株T₈₂和NF₉对白绢病菌和立枯丝核菌的主要拮抗机制。     

木霉对玉米纹枯病的生物防治

为明确木霉菌在玉米纹枯病防治上的作用,研究了从雅安郊区大田玉米根际土壤中分离到的18个木霉菌株对立枯丝核菌的抑制作用及对玉米纹枯病的田间防治效果.对峙培养结果表明,这些木霉菌株对立枯丝核菌的抑制率为39.44%～84.98%;而木霉发酵滤液的抑菌作用为13.48%～85.81%.对峙培养和液体发酵滤液的抑菌测定相结合,筛选出木霉菌株T8、T2、T13,经鉴定分别为哈茨木霉Trichoderma harzianum、黄绿木霉Trichoderma aureoviride和长枝木霉Trichoderma Longibrachiatum.用这3种木霉的固体培养物作进一步的田间防治试验,防治效果分别为62.75%、64.48%、68.52%,比井冈霉素(49.68%)效果高;T13菌株的发酵滤液的防治效果仅为40.07%.3株木霉固体培养物对玉米产量影响显著,增产率依次为29.77%、43.37%、54.21%.     

黄淮海夏玉米主产区穗腐病病原菌的分离鉴定

为明确我国黄淮海夏玉米主产区玉米穗腐病的病原菌种类、优势种群及虫害、年度、省份对病原菌的影响,以形态学为基础,结合分子生物学方法对2013、2015年随机采自河南、河北、山东3省的155份玉米穗腐病样品进行分离鉴定。结果表明,引起黄淮海夏玉米主产区玉米穗腐病的主要致病菌为镰孢菌Fusarium spp.,包括拟轮枝镰孢F.verticillioides、禾谷镰孢F.graminearum、层出镰孢F.proliferatum、木贼镰孢F.equiseti及藤仓镰孢F.fujikuroi,分离频率分别为49.7%、28.4%、12.3%、3.9%和1.3%;其次为木霉菌Trichoderma spp.,包括哈茨木霉T.harzianum、绿色木霉T.viride和棘孢木霉T.asperellum,分离频率分别为8.4%、3.2%和5.2%;青霉菌Penicillium spp.分离频率较低,为14.2%;曲霉菌Aspergillus spp.包括黑曲霉A.niger和黄曲霉A.flavus,分离频率分别为2.6%和1.9%。研究表明,黄淮海主产区玉米穗腐病优势病原菌为拟轮枝镰孢、禾谷镰孢和木霉菌,不同省份不同年度间病原菌种类及优势病原菌存在差异,虫害能加重玉米穗腐病的发生。     

甘肃玉米穗腐病样品中轮枝镰孢菌的分离鉴定及生物学特性

 为了明确甘肃玉米穗腐病的病原种类, 于2009年9月在甘肃省四大生态区采集玉米穗腐病样品, 以组织分离法进行病原物的分离培养, 对分离得到的镰孢菌菌落进行纯化和单孢分离后, 以形态学为基础, 参照Leisle分类系统进行鉴定。结果表明:共分离到271株镰孢菌菌株, 其中以轮枝镰孢菌(Fusarium verticillioides)和黄色镰孢菌(F. culmorum)出现频率高, 属优势种。按照柯赫氏法则对沈单16和金穗96832进行致病性测定, 证实了轮枝镰孢菌对玉米果穗的致病性。选取2株轮枝镰孢菌菌株进行EF-1α(tef) 基因序列分析, 将PCR产物回收测序后在GenBank上比对, 菌株GSLT4-3-2与GenBank中登记的轮枝镰孢菌FN179339、FN179345和FN179338;GSTS24-2-1与轮枝镰孢菌FN179343、FN179346、FN179340、FN179344和 FN252384亲缘关系最近, 序列同源性达100%。轮枝镰孢菌GSYC17-2-1的生长温度范围为15～35℃, 最适温度为28℃, pH 值为8;菌落在pH值为4～10的培养基上能够迅速扩展, pH值为7时产孢量最大;碳源对轮枝镰孢菌菌丝生长影响相对稳定, 而氮源对其营养生长影响的变幅较大;完全黑暗条件下, 菌丝扩展最快, 12 h光暗交替对产孢量有明显的促进作用;病原菌菌丝致死温度为70℃, 10 min。     

木霉分生孢子和厚垣孢子对黄瓜幼苗生理特性及枯萎病防效的影响

采用前期筛选出的对黄瓜枯萎病菌有较好拮抗作用的3株木霉菌,即哈茨木霉Trichoderma harzianum 809、拟康氏木霉Trichoderma pseudokoningii 886和棘孢木霉Trichoderma asperellum 525,利用盆栽试验,测定了木霉菌孢子不同类型施用对黄瓜幼苗生长、生理特性及枯萎病防效的影响。结果表明:哈茨木霉809、拟康氏木霉886、棘孢木霉525分生孢子和厚垣孢子对黄瓜枯萎病的盆栽防效均在66.81%以上,且以拟康氏木霉886厚垣孢子防效最高,达到81.46%。当黄瓜幼苗长至三叶一心时,3株木霉菌分生孢子和厚垣孢子处理的黄瓜幼苗株高、茎粗、根体积、叶面积、全株鲜质量均比CK显著上升,以厚垣孢子886的促进效果最显著,其株高、茎粗、根体积、叶面积、全株鲜质量分别较CK增加了85.33%、108.43%、235.29%、144.38%、272.32%。同时,3株木霉菌分生孢子和厚垣孢子处理的黄瓜幼苗叶绿素含量、根系活力、叶片可溶性糖含量、叶片可溶性蛋白含量也均比CK显著上升,厚垣孢子886的促进效果仍最显著,其叶绿素含量、根系活力、叶片可溶性糖含量、叶片可溶性蛋白含量分别较CK增加了97.47%、86.05%、172.49%、201.91%。     

苏云金芽胞杆菌cry1Ie新基因的克隆、表达与生物活性测定

为获得新的鳞翅目害虫杀虫基因,根据已知cry1I类基因编码区设计简并引物,采用直接克隆法,以苏云金芽胞杆菌(Bacillus thuringiensis,Bt)菌株BN23-5质粒DNA为模板进行扩增,并对得到的基因进行鉴定和分析。结果表明:克隆得到一个完整的cry1Ie基因,全长2 160 bp,由719个氨基酸组成,该氨基酸序列与已知的4种Cry1Ie蛋白不同,与Cry1Ie2和Cry1Ie3的氨基酸序列同源性最高,为95.4%,被国际Bt杀虫晶体蛋白基因命名委员会命名为Cry1Ie5(登录号为KJ710646)。将该基因插入表达载体p ET-28a,转化大肠杆菌BL21(DE3),IPTG低温诱导成功表达,SDS-PAGE电泳验证其大小为81 k D,与预测的分子量相符合。生物活性测定表明,Cry1Ie5表达的包涵体蛋白对小菜蛾和亚洲玉米螟具有杀虫活性,LC_(50)分别为0.43μg/m L和48.39μg/m L;对棉铃虫的致死率不高,但能明显抑制其生长;对甜菜夜蛾没有杀虫活性。     

Three evolutionary lineages of tomato wilt pathogen, Fusarium oxysporum f. sp. lycopersici, based on sequences of IGS, MAT1, and pg1, are each composed of isolates of a single mating type and a single or closely related vegetative compatibility group

Three evolutionary lineages of the tomato wilt pathogen Fusarium oxysporum f. sp. lycopersici were found among a worldwide sample of isolates based on phylogenetic analysis of the ribosomal DNA intergenic spacer region. Each lineage consisted of isolates mainly belonging to a single or closely related vegetative compatibility group (VCG) and a single mating type (MAT). The first lineage (A1) was composed of isolates VCG 0031 and MAT1-1; the second (A2) included VCG 0030 and/or 0032 and MAT1-1; and the third (A3) included VCG 0033 and MAT1-2. Race 1 and race 2 isolates belonged to the A1 or A2 lineages, and race 3 belonged to A2 or A3 lineages, suggesting that there is no correlation between race and lineage. However, for the isolates from Japan, race 1 (with one exception), race 2, and race 3 isolates belonged to A2, A1, and A3 lineages, respectively. These results suggest that the races could have evolved independently in each lineage; and in Japan the present races were likely to have been introduced independently after they had evolved in other locations.     

Identification of Trichoderma SKT-1, a biological control agent against seedborne pathogens of rice

Trichoderma SKT-1 was previously reported as a powerful biological control agent against seedborne pathogens of rice, but the taxonomic disposition of the fungal isolate was not clear. Trichoderma SKT-1 produced irregular pyramidal warts on conidia and had an optimum growth temperature of 30°C. Morphological characteristics and colony growth were identical to those of known species of Trichoderma, including the newly recognized species T. asperellum. The 5.8S rDNA with the internal transcribed spacer (ITS) region (ca. 514 bp) of the fungus was compared with those of known species to determine the phylogenetic placement of the fungus. The length and sequence of the regions from Trichoderma SKT-1 were completely identical to those of an isolate of T. asperellum NRRL 5242 (AJ230669). On the basis of these results, we concluded that Trichoderma SKT-1 was T. asperellum.     

禾谷缢管蚜水通道蛋白基因RpAQP1的克隆、分子特性和表达分析

为探究禾谷缢管蚜Rhopalosiphum padi (Linnaeus)水通道蛋白基因RpAQP1的序列特征及其在不同龄期的表达,利用RT-PCR和RACE技术克隆了RpAQP1基因的cDNA全序列,采用生物信息学软件分析了RpAQP1编码蛋白的特性,利用qRT-PCR分析了RpAQP1在不同龄期的表达量。结果显示:禾谷缢管蚜水通道蛋白基因RpAQP1的cDNA全长为1 216 bp,其750 bp的开放阅读框编码250个氨基酸,蛋白分子量为27.36 kD。RpAQP1属于水通道蛋白亚家族DRIP(果蝇内嵌蛋白Drosophila integral protein)的一员,具有6个跨膜区,2个保守的NPA结构单元和1个压缩区域Ar/R;qRT-PCR结果显示,RpAQP1在整个发育历期均有表达,其在2龄若蚜中表达水平最高,是成蚜表达量的1.432倍;在4龄若蚜中表达量最低,为成蚜表达量的0.444倍,显著低于其它龄期,而其余各龄期RpAQP1表达量无显著差异。     

转cry1Ab/cry2Aj、cry1Ab/vip3DA玉米对棉铃虫、甜菜夜蛾和斜纹夜蛾的抗虫性评价

为评估转cry1Ab/cry2Aj、cry1Ab/vip3DA玉米对棉铃虫Helicoverpa armigera(Hübner)、甜菜夜蛾Spodoptera exigua(Hübner)和斜纹夜蛾Prodenia litura(Fabricius)的抗虫性,在室内测定了3个转cry1Ab/cry2Aj玉米品系和1个转cry1Ab/vip3DA玉米品系对3种害虫幼虫存活和生长发育的影响,研究了该系列Bt玉米不同组织器官对害虫的杀虫活性和控制效果。结果显示,棉铃虫初孵幼虫取食各品系Bt玉米叶片96h后死亡率为87.50%~90.00%,取食花丝和雌穗的幼虫96h后几乎全部死亡;甜菜夜蛾初孵幼虫取食各品系Bt玉米叶片、花丝和雌穗168h后死亡率为22.50%~68.33%,幼虫的生长发育受到明显抑制,体重抑制率达85.00%~95.00%;斜纹夜蛾初孵幼虫取食各品系Bt玉米叶片、花丝和雌穗96 h后死亡率显著高于非转基因亲本对照,168h后幼虫死亡率达90.00%以上。研究表明,转cry1Ab/cry2Aj和cry1Ab/vip3DA玉米品系对棉铃虫和斜纹夜蛾的初孵幼虫表现出较好的抗性,可以作为转多基因抗虫玉米育种的备选材料。     

冬青卫矛内生放线菌Streptomyces flavofuscus G1 发酵液中抑菌活性成分研究

从冬青卫矛内生放线菌Streptomyces flavofuscus G1的发酵液中分离得到化合物G13和G19。经核磁共振波谱及质谱分析,并结合相关文献,两个化合物分别被鉴定为phencomycin(G13)和4'-deacetyl-(-)-griseusin A(G19)。抑菌活性测定结果表明:G19对水稻白叶枯病菌Xanthomonas oryzae pv.oryzae、铜绿假单孢菌Pseudomonas aeruginosa(1.203 1)、蜡状芽孢杆菌Bacillus cereus(1.184 6)及金黄色葡萄球菌Staphyloccocus aureus(1.008 9)等供试病原细菌具有强烈的抑制作用,其最低抑菌浓度(MIC)值均为1.56μg/m L;对苹果树腐烂病菌Valsa mali和小麦赤霉病菌Fusarium graminearum菌丝生长亦有明显的抑制作用,其IC50值分别为14.70和24.35μg/m L。而G13对植物病原真菌油菜菌核病菌Sclerotinia sclerotiorum和苹果树腐烂病菌V.mali菌丝生长有强烈的抑制作用,其IC50值分别为5.21和4.82μg/m L。     

DNA sequence analysis of ribosomal ITS region 1 of Phytophthora vignae f. sp. adzukicola, the pathogen that causes stem rot of adzuki bean

Sequences of the internal transcribed spacer (ITS) region 1 were used to examine the phylogenetic relationships among races of 19 isolates of Phytophthora vignae f. sp. adzukicola and between this forma specialis and three isolates of the closely related P. vignae f. sp. vignae. The ITS 1 sequences were highly conserved (> 98.7% similarity) among representatives of both formae speciales groups. The results of this study indicate that P. vignae is a monophyletic group. The nucleotide sequence data reported are available in the DDBJ/EMBL/GenBank databases under the accession nos. AB120062–AB120080 and AB120122     

Harpin-elicited hypersensitive cell death and pathogen resistance require the NDR1 and EDS1 genes

Plants sprayed with harpin, a bacterial protein that induces hypersensitive cell death (HCD), develop systemic acquired resistance (SAR) without macroscopic necrosis. HCD sometimes accompanies the development of resistance conferred by resistance (R) genes. In Arabidopsis, some R genes require one or both of the signalling components NDR1 and EDS1 for function. This study addresses whether HCD, NDR1 and EDS1 are required for induction of SAR by harpin. When Arabidopsis and tobacco leaves were sprayed with harpin, microscopic hypersensitive response (micro-HR) lesions developed. Systemic expression of PR genes and the development of resistance were accompanied by micro-HR, except in the ndr1-1 mutant, in which harpin induced micro-HR without the development of resistance or expression of the PR-1 gene. Cell death and resistance did not occur following treatment with harpin in plants that could not accumulate salicylic acid. Harpin also failed to induce resistance in Arabidopsis eds1-1 mutants. Therefore, harpin-induced resistance seems to develop concomitantly with cell death and resistance requires NDR1 and EDS1.     

Mating type gene MAT1-2-1 is common among Japanese isolates of Verticillium dahliae

Mating type genes of Verticillium dahliae, a wilt pathogen affecting many plant species, were identified to examine sexual recombination between Japanese pathotypes. We amplified a DNA sequence encoding high mobility group (HMG) box from V. dahliae using PCR. A cloned genomic DNA fragment included a sequence homologous to MAT1-2-1 gene. Despite that sequence's presence in all V. dahliae isolates we used, MAT1-1-1 (an opposite mating type gene) was never amplified. We concluded that V. dahliae is potentially heterothallic. Furthermore, sexual bias practically obviates sexual recombination between Japanese pathotypes. This report describes, for the first time, a mating type gene of phytopathogenic Verticillium.