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1.
本试验以苹果砧木平邑甜茶幼苗为试材,通过温室与露地盆栽两种方式,研究不同浓度(0、0.1、0.2、0.4 g·kg-1)棉隆熏蒸对连作土壤微生物环境和平邑甜茶幼苗生长的影响。结果表明:不同浓度的棉隆熏蒸均能促进连作土壤中平邑甜茶幼苗的生长,其中以0.2 g·kg-1处理的效果最显著。0.2 g·kg-1棉隆熏蒸下,平邑甜茶幼苗在温室和露地条件下的株高、地径、地上部干质量、地下部干质量分别比连作对照提高了192.9%和91.8%、72.8%和60.1%、196.8%和195.0%、138.5%和130.7%;幼苗根系相关指标(根长、根面积、根体积、根系呼吸速率)也明显优于其他处理;幼苗根系的超氧化物歧化酶、过氧化物酶、过氧化氢酶活性分别比连作对照提高了114.6%和118.5%、123.5%和107.6%、164.6%和175.6%;幼苗根系的丙二醛含量也显著低于其他处理。随着棉隆施用浓度的增加,土壤细菌含量、真菌含量、尖孢镰孢菌基因拷贝数、土壤酶活性均显著降低,连作土壤真菌群落结构也发生了不同程度的改变。综上,0.2 g·kg-1棉隆熏蒸可以提高连作平邑甜茶幼苗生物量,改善土壤环境,有效缓解平邑甜茶的连作障碍。在苹果老果园重茬建园时,可以优先考虑0.2 g·kg-1的棉隆熏蒸处理。  相似文献   

2.
以苹果连作障碍病原真菌层出镰刀菌、串珠镰刀菌、尖孢镰刀菌和腐皮镰刀菌为靶标菌,通过平板对峙法对分离自苹果根际土壤的细菌进行反复筛选比较,对筛选出的拮抗效果最优的菌株进行形态学、生理生化特征和16S rDNA序列分析鉴定,并于盆栽条件下探讨其菌肥对平邑甜茶幼苗生长及连作土壤环境的影响.结果表明: 菌株B6对上述4种病原真菌的抑菌率最高,分别达到71.8%、70.1%、72.6%、91.5%.经鉴定,菌株B6为甲基营养型芽孢杆菌.盆栽试验表明,与连作处理(CK1)相比,B6菌肥处理(T)可以不同程度地促进平邑甜茶幼苗生物量的增加,其中地径、鲜质量和干质量分别显著增加18.3%、51.2%;显著提高连作土壤中可培养细菌和放线菌数量,使真菌数量下降为连作土壤的37.7%,促使土壤类型向细菌型转化;显著提高连作土壤中的蔗糖酶、磷酸酶、脲酶和过氧化氢酶的活性,增长率分别为37.3%、24.0%、42.9%、49.4%.表明B6菌肥可以优化苹果连作障碍土壤中可培养微生物群落结构,提高土壤酶活性,增加平邑甜茶幼苗生物量.  相似文献   

3.
甲壳素对连作条件下平邑甜茶幼苗生长及土壤环境的影响   总被引:2,自引:0,他引:2  
研究在苹果连作土壤中添加甲壳素对苹果幼苗生长、土壤酶及土壤真菌群落结构的影响,探讨甲壳素缓解苹果连作障碍的可能性,为防控苹果连作障碍提供依据。盆栽条件下,以平邑甜茶幼苗为试材,在苹果连作土壤中分别添加0,0.5,1.0和2.5g/kg的甲壳素,测定了连作土壤中添加不同量的甲壳素后,幼苗生物量、根系保护酶活性、土壤主要酶(蔗糖酶、脲酶、磷酸酶等)活性以及土壤中真菌群落结构的变化。9月份结果表明,与对照相比,1.0 g/kg的甲壳素处理连作土,可显著提高平邑甜茶幼苗株高和干鲜重,分别比对照增加了36.8%、82.1%和100.8%;甲壳素处理能增加幼苗根系保护酶活性,其中1.0 g/kg甲壳素处理SOD、POD和CAT活性最高,其次为0.5 g/kg,而2.5 g/kg甲壳素处理显著抑制了幼苗根系保护酶活性。1.0 g/kg甲壳素处理可提高土壤中细菌/真菌值,并且提高了土壤中蔗糖酶、脲酶、蛋白酶、磷酸酶、过氧化氢酶和多酚氧化酶活性,分别比对照提高了8.6%、40.5%、81.1%、15.3%、18.7%和49.8%,2.5 g/kg甲壳素处理则降低土壤酶活性或者使土壤酶活性与对照相当。根据T-RFLP的图谱中OUT的数量、种类及丰度,分别计算了不同处理土壤的真菌多样性,发现1.0 g/kg甲壳素处理的连作土具有最高的多样性、均匀度和丰富度指数,分别比对照增加了52.2%、8.0%和87.1%。主成分分析(PCA)结果显示,不同剂量甲壳素处理的连作土壤中真菌被PC2分成了两部分,其中0.5 g/kg和1.0 g/kg的甲壳素添加量分布在PC2的负方向上,而CK和2.5g/kg的甲壳素处理分布在PC2的正方向上,这说明添加不同量的甲壳素对连作土壤真菌群落多样性有显著影响,添加量太多或者太少均会造成土壤真菌多样性下降,只有适量的甲壳素可提高真菌群落结构多样性。实验结果表明1.0 g/kg的甲壳素可提高连作平邑甜茶幼苗生物量,改善连作土壤环境,有效缓解平邑甜茶的连作障碍。  相似文献   

4.
有机物料厌氧发酵液(AFOF)能显著改善苹果再植障碍.本研究对AFOF中能拮抗苹果再植障碍主要病原菌(腐皮镰刀菌、层出镰刀菌、尖孢镰刀菌、串珠镰刀菌)的细菌进行了分离筛选,并对其作用效果进行了盆栽验证.结果表明: AFOF能显著抑制病原真菌的生长繁殖;对峙试验共得到4株具有较强拮抗作用的细菌(L11、L12、L13、L14),最高抑菌率达到57.3%,鉴定发现这4株细菌均属于芽孢杆菌属,相互之间没有明显的拮抗作用;在盆栽条件下,与连作土相比,溴甲烷熏蒸处理和拮抗菌菌液处理对平邑甜茶幼苗的生物量均有不同程度的促进作用;在幼苗的长势上,溴甲烷熏蒸处理效果要好于拮抗菌菌液处理;在根系活力上,拮抗菌菌液处理效果要好于溴甲烷熏蒸处理,根系长度、根尖数分别增加了25.1%、70.9%.与连作土处理相比,拮抗菌菌液和溴甲烷熏蒸均能显著降低土壤中的真菌数量,分别降低了71.2%和64.2%,拮抗菌菌液处理能显著增加土壤中的细菌和放线菌数量,分别增加了48.0%和140.2%,使土壤微生物结构向“细菌型”转化;而溴甲烷熏蒸处理显著降低了土壤中的细菌和放线菌数量,说明拮抗菌的确能够抑制土壤中病原真菌的生长.  相似文献   

5.
在盆栽条件下,研究残次苹果发酵产物对连作土壤环境及平邑甜茶幼苗生长的影响,为减轻苹果连作障碍提供理论依据。试验以连作土壤为对照(CK),设置溴甲烷灭菌连作土壤(T1)、连作土壤施加苹果发酵产物(T2)、连作土壤施加灭菌苹果发酵产物(T3)处理,测定了土壤和平邑甜茶幼苗的相关指标。结果表明: T1、T2、T3能显著促进平邑甜茶幼苗的生长,其中以T1和T2的效果较好,其根系呼吸速率、株高、地径、鲜质量、干质量分别比CK提高了107.3%、50.6%、42.4%、171.7%、225.3%和104.4%、50.6%、42.3%、171.8%、225.5%。T2和T3提高了连作土壤中养分转化相关酶的活性,过氧化氢酶、脲酶、中性磷酸酶和蔗糖酶活性分别比CK提高了44.5%、169.5%、23.4%、169.3%和23.7%、72.6%、1.5%、121.5%;T1处理的过氧化氢酶和蔗糖酶活性与CK无显著差异,脲酶和中性磷酸酶活性分别降低了40.8%和41.6%。T2土壤铵态氮、硝态氮、速效磷和速效钾含量分别较CK提高了18.6%、50.6%、14.0%和36.7%;T3只提高了速效氮的含量,铵态氮和硝态氮含量分别提高了7.0%和23.6%;T1与CK相比速效养分含量有所降低。T1和T2显著降低了土壤放线菌和真菌数量,增加了细菌数量;T3处理的细菌、放线菌和真菌数量均较CK显著降低。实时荧光定量PCR分析发现,T1、T2和T3处理的层出镰孢菌、串珠镰孢菌、腐皮镰孢菌和尖孢镰孢菌基因拷贝数均较CK有不同程度的降低。表明苹果发酵产物处理能抑制连作土壤病原菌,改善土壤环境,促进平邑甜茶幼苗生长,可作为一种减轻苹果连作障碍的方法。  相似文献   

6.
为探讨不同有机物料的发酵流体(厌氧发酵产物)和堆肥(有氧发酵产物)对苹果连作土壤环境的影响,以盆栽平邑甜茶幼苗为试验材料,分别设置猪粪+秸秆、鸡粪+秸秆、羊粪+秸秆、猪粪+鸡粪+羊粪+秸秆4个不同有机物料组合并进行厌氧发酵和有氧发酵,并将发酵产物分别施入连作土中,研究其对平邑甜茶幼苗生物量、连作土壤中微生物、土壤酶活性、土壤酚酸等的影响。结果表明:与有机物料堆肥相比,各有机物料发酵流体处理的平邑甜茶幼苗干重、鲜重较高,其中猪粪发酵流体处理显著提高了幼苗干、鲜重,7月份为对照的1.57、1.26倍,9月份为CK的1.55、1.86倍;两类发酵产物均增加了土壤微生物的数量,且发酵流体处理显著增加了土壤中细菌和放线菌的数量,其中羊粪发酵流体效果最明显,分别为CK的2.95倍和2.37倍,在堆肥处理中,真菌数量显著增高;两类发酵产物也影响了土壤中酚酸总量,表现为猪粪、鸡粪发酵流体和猪粪堆肥处理含量下降,至9月份分别下降到CK的0.45、0.39倍和0.36倍。  相似文献   

7.
连作苹果土壤酚酸对平邑甜茶幼苗的影响   总被引:4,自引:0,他引:4  
为探讨连作(重茬)苹果土壤中酚酸类物质的积累与苹果连作障碍的关系,在砂培条件下,取连作果园土壤中实际浓度的酚酸类物质处理平邑甜茶幼苗,探讨了连作2a的果园土壤中实测浓度的根皮苷、间苯三酚、根皮素、对羟基苯甲酸和肉桂酸对平邑甜茶幼苗根系线粒体指标、抗氧化酶活性、膜过氧化程度及活性氧(ROS)含量的影响。结果表明:连作土壤中实际浓度的5种酚酸类物质均使平邑甜茶幼苗生长受到抑制,根系受影响程度高于地上部分,表现为根冠比降低;线粒体膜通透性转换孔(MPTP)开放程度增大,线粒体膜电位降低,细胞色素Cyt c/a比值下降;降低了幼苗根系中超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)活性,增加了过氧化氢(H2O2)、超氧阴离子自由基(O·-2)以及丙二醛(MDA)的含量。土壤浓度的5种酚酸类物质中,以根皮苷处理抑制效果最显著,间苯三酚处理抑制力最小。因此,根皮苷是引起苹果连作障碍的主要酚酸,实践中应重点考虑对根皮苷的降解以缓解苹果连作障碍。  相似文献   

8.
《植物生态学报》2013,37(10):942
为探讨土壤碳氮比(C:N)对苹果(Malus pumila)植株生长和碳氮分配特性的影响, 采用碳氮双标记示踪技术, 以二年生平邑甜茶(Malus hupehensis)幼苗为试验材料, 研究了6个不同土壤C:N处理(T1-T6分别为4.70、9.78、14.70、19.96、25.60和28.83)下平邑甜茶的生长状况和氮素吸收、利用分配以及碳水化合物的运转特性。结果表明, 随着土壤C:N的逐渐增大, 平邑甜茶幼苗根系干重逐渐增加, 而株高、茎粗、地上部干重和植株总干重呈先增加后降低的趋势, 以T4处理最大。土壤C:N显著影响了平邑甜茶幼苗的 15N利用率, 从T1到T4处理, 植株的 15N利用率逐渐升高, T4处理(18.46%)是T1处理(10.65%)的1.73倍; 随着土壤C:N的进一步增加, 植株的 15N利用率逐渐降低, T5和T6处理分别比T4处理降低了1.59%和2.58%。土壤C:N较低的T1和T2处理, 平邑甜茶幼苗各器官从肥料中吸收分配到的 15N量对该器官全氮量的贡献率(Ndff)大小顺序为根>叶>茎, 随着土壤C:N的进一步增大, 叶片的Ndff均为最大, 其次是根, 茎最少。随着土壤C:N的增大, 叶片 15N分配率逐渐升高, 13C分配率逐渐降低; 而根系 15N分配率逐渐降低, 13C分配率逐渐升高。综合考虑植株生长和氮素利用状况, 本试验条件下适宜平邑甜茶生长的土壤C:N为21-23。  相似文献   

9.
放线菌制剂对人参生长及根域土壤微生物区系的影响   总被引:4,自引:0,他引:4  
以小兴安岭地区人参为研究对象,探索放线菌制剂对人参的促生效应及对人参根区、根表土壤微生物区系的影响.结果表明:经放线菌制剂Streptomyces pactum(Act12)处理后,人参药用部分产量增加,品质改善;叶片诱导酶活性提高,根系活力增强;土壤中细菌、放线菌的数量和比例显著增加,真菌的数量和比例减少.与对照相比,土壤微生物区系结构改变:优势菌荧光假单胞菌、韩国假单胞菌和氧化微杆菌在根区、根表土壤中的数量大幅提高;病原真菌烟色织孢霉在根区土壤中减少,在根表土壤中消失.表明施用放线菌制剂Act12能够改善土壤微生物区系,提高人参植株的抗性和根系活力,增加产量并改善品质.  相似文献   

10.
采用有机物料添加、土壤灌水和表土覆盖相结合的土壤生物消毒方法来防控甘肃省中部沿黄灌区马铃薯连作障碍,系统性地评估生物消毒对连作马铃薯块茎产量、植株生长发育及土传病害抑制、微生物区系和酶活性等土壤生化性质的影响.结果表明:生物消毒处理比对照块茎产量和植株生物量分别显著增加16.1%和30.8%,植株发病率和病薯率分别下降68.0%和46.7%.生物消毒处理显著提高了连作马铃薯叶绿素含量和主茎分枝数,改善了根系形态结构.在播前土壤生物消毒处理过程中,土壤p H值和细菌/真菌显著增加,真菌和镰刀菌数量大幅度下降,而细菌和放线菌数量则变化不明显.在马铃薯各生育时期,生物消毒处理土壤真菌数量均远低于对照,镰刀菌数量也低于对照,但随着生育进程的推进,镰刀菌数量呈现逐渐回升的趋势.无论是在生物消毒处理过程中还是马铃薯整个生育期,生物消毒处理的土壤相关酶活性与对照相比变化均不明显.总体上,土壤生物消毒的方法在克服马铃薯连作障碍上具有较大的应用潜力.  相似文献   

11.
连作对芝麻根际土壤微生物群落的影响   总被引:16,自引:0,他引:16  
华菊玲  刘光荣  黄劲松 《生态学报》2012,32(9):2936-2942
采用稀释平板计数法研究了不同连作年限处理芝麻根际土壤细菌、真菌、放线菌、芽孢杆菌、尖孢镰刀菌(FO)和青枯劳尔氏菌(RS)数量的变化情况。结果表明,随着连作年限的增加,芝麻根际土壤中细菌和放线菌的数量下降,而真菌的数量则呈上升趋势。新种芝麻地根际土壤芽孢杆菌数量显著高于连作2a处理和连作5a处理,而连作2a处理又显著高于连作5a处理;连作5a芝麻根际土壤尖孢镰刀菌数量显著高于新种地、轮作1a和连作2a等3个处理;轮作1a、连作2a及连作5a等3个处理青枯劳尔氏菌数量显著高于新种地处理。说明连作导致土壤微生物环境恶化,引起根际微生物区系结构发生定向改变。连作2a与轮作1a相比,各菌群(类群)数量差异均不显著。  相似文献   

12.
Early events of mycorrhizal and nonmycorrhizal fungal colonization in newly-emerging roots of mature apple (Malus domestica Borkh) trees were characterized to determine the relationship of these events to fine root growth rate and development. New roots were traced on root windows to measure growth and then collected and stained to quantify microscopically the presence of mycorrhizal and nonmycorrhizal fungal structures. Most new roots were colonized by either mycorrhizal or nonmycorrhizal fungi but none less 25 days old were ever internally colonized by both. Compared to nonmycorrhizal colonization, mycorrhizal colonization was associated with faster growing roots and roots that grew for a longer duration, leading to longer roots. While either type of fungi was observed in roots as soon as 3 days after root emergence, intraradical colonization by mycorrhizal fungi was generally faster (peaking at 7 to 15 days) than that by nonmycorrhizal fungi and often occurred more frequently in younger roots. Only 15 to 35% of the roots had no fungal colonization by 30 days after emergence. This study provides the first detailed examination of the early daily events of mycorrhizal and nonmycorrhizal fungal colonization in newly emerging roots under field conditions. We observed marked discrimination of roots between mycorrhizal and nonmycorrhizal fungi and provide evidence that mycorrhizal fungi may select for faster growing roots and possibly influence the duration of root growth by non-nutritional means.  相似文献   

13.
连作花生田根际土壤优势微生物的分离和鉴定   总被引:2,自引:0,他引:2  
【目的】从不同连作年限的花生田根际土壤中分离优势微生物并进行鉴定,为研究花生连作后优势微生物的变化奠定基础。【方法】采用土壤稀释分离法从不同连作年限花生根际土壤中分离优势细菌、真菌和放线菌,结合菌株形态特征、培养性状、生理生化特征及16S rDNA序列分析对细菌、放线菌进行鉴定,通过形态特征、培养特征和分子鉴定方法对优势真菌进行鉴定。【结果】从连作花生田根际土壤中分离鉴定出7种优势细菌、7种优势真菌和7种优势放线菌。7种优势细菌分别为Leifsonia xyli、氯酚节杆菌(Arthrobacterchlorophenolicus)、黄色微杆菌(Microbacterium flavescens)、鞘氨醇单胞菌属(Sphingomonas sp.)、巴斯德菌属(Pasteurella sp.)、简单芽孢杆菌(Bacillus simplex)和巨大芽孢杆菌(Bacillus megaterium)。7种优势真菌分别为枝状枝孢菌(Cladosporium cladosporioides)、产紫青霉(Penicillium purpurogenum)、哈茨木霉有性型(Hypocrea lixii)、Exophiala pisciphila、微紫青霉(Penicillium janthinellum)、曲霉(Aspergillus sp.)和大丽轮枝菌(Verticillium dahliae)。7种优势放线菌分别为紫红链霉菌(Streptomyces violaceoruber)、华丽黄链霉菌(Streptomyces flaveus)、Streptomyces panaciterrae、不产色链霉菌(Streptomyces achromogenes)、假浅灰链霉菌(Streptomyces pseudogriseolus)、纤维素链霉菌(Streptomyces cellulosae)和金色链霉菌(Streptomyces aureus)。【结论】本研究是第一次系统的从连作花生根际土中分离鉴定优势微生物,种植花生后根际土壤中优势微生物的种类发生了明显变化,但变化没有规律。  相似文献   

14.
通过盆栽试验,研究了内生真菌拟茎点霉B3(Phomopsis liquidambari)及苍术(Atractylodes lancea)粉联合施用对连作花生根际土壤微生物区系、酶活性及有效态微量元素(Mo、B、DTPA-Fe、Zn、Cu、Mn)含量的影响。结果表明:内生真菌B3和苍术粉复合处理比内生真菌B3处理的荚果和秸秆产量分别增加10.28%和14.11%,内生真菌B3处理与正常施肥相比显著提高了根瘤数量、荚果和秸秆产重,各处理组与正常施肥对照相比分枝数和根长无显著差异。B3处理与对照相比显著提高了种子期、结荚期和成熟期根际土壤可培养细菌和放线菌数量,B3和苍术粉复合处理与对照相比显著提高种子期、花期和成熟期可培养真菌和放线菌数量;细菌DGGE指纹图谱聚类分析表明,B3和苍术粉复合处理相对于正常施肥处理,显著改变种子期、苗期、花期和成熟期花生根际土壤细菌群落结构,同时苗期、花期和结荚期的细菌条带数和香农指数也有所提高,真菌DGGE指纹图谱聚类分析表明,B3和苍术粉复合处理对真菌群落影响较大,除种子期以外的生育期真菌条带数和香农指数都有明显提高,花期真菌群落结构变化最大,相似度仅为49.6%。花生关键生育期(花期和结荚期)根际土壤脲酶和蔗糖酶活性B3处理和复合处理都显著高于正常施肥对照,促进了连作花生生态系统的物质循环和能量流动。B3和苍术粉复合处理促进了花生生长发育必需微量元素Mo、B、Fe、Zn、Mn的活化,花生叶片和籽粒中微量元素Mo、B、Fe的积累显著增加。研究结果表明,内生真菌和苍术粉联合施用能有效改善连作花生根际微生物区系,提高土壤酶活性,促进微量元素的活化和吸收,对缓解花生连作障碍具有重要意义。  相似文献   

15.
In recent years, the interest in the use of bacteria for biological control of plant-pathogenic fungi has increased. We studied the possible side effects of coating barley seeds with the antagonistic strain Pseudomonas fluorescens DR54 or a commercial fungicide, imazalil. This was done by monitoring the number of indigenous Pseudomonas organisms and actinomycetes on barley roots during growth in soil, harvest after 50 days, and subsequent decomposition. Bacteria were enumerated by traditional plate spreading on Gould's S1 agar (Pseudomonas) and as filamentous colonies on Winogradsky agar (actinomycetes) and by two quantitative competitive PCR assays. For this we developed an assay targeting Streptomyces and closely related genera. DR54 constituted more than 75% of the Pseudomonas population at the root base during the first 21 days but decreased to less than 10% at day 50. DR54 was not successful in colonizing root tips. Initially, DR54 affected the number of indigenous Pseudomonas organisms negatively, whereas imazalil affected Pseudomonas numbers positively, but the effects were transient. Although plate counts were considerably lower than the number of DNA copies, the two methods correlated well for Pseudomonas during plant growth, but after plant harvest Pseudomonas-specific DNA copy numbers decreased while plate counts were in the same magnitude as before. Hence, Pseudomonas was 10-fold more culturable in a decomposition environment than in the rhizosphere. The abundance of actinomycetes was unaffected by DR54 or imazalil amendments, and CFU and quantitative PCR results correlated throughout the experiment. The abundance of actinomycetes increased gradually, mostly in numbers of DNA copies, confirming their role in colonizing old roots.  相似文献   

16.
Summary Effect of pretreatment of root of maize seedlings with gibberellic acid, maleic hydrazide and urea was investigated. Gibberellic acid at 1 ppm stimulated the growth of fungi, bacteria, and actinomycetes in the rhizosphere region of maize seedlings while at 5 ppm concentration population of bacteria and actinomycetes were suppressed. Maleic hydrazide treatment stimulated all the three groups at 5 ppm concentration but at 1 ppm there was increase in population of only fungi and actinomycetes. Urea stimulated the growth of fungi, bacteria, and actinomycetes. The order of predominance of different groups also changed with treatments. It was fungi > bacteria > actinomycetes in case of gibberellic acid at 1 ppm and 5 ppm and maleic hydrazide at 1 ppm; and bacteria > fungi > actinomycetes in case of maleic hydrazide at 5 ppm, urea at 0.1M and in control.  相似文献   

17.

Background

To monitor the richness in microbial inhabitants in the phyllosphere of apple trees cultivated under various cultural and environmental conditions, we developed an oligo-DNA macroarray for major pathogenic and non-pathogenic fungi and bacteria inhabiting the phyllosphere of apple trees.

Methods and Findings

First, we isolated culturable fungi and bacteria from apple orchards by an agar-plate culture method, and detected 32 fungal and 34 bacterial species. Alternaria, Aureobasidium, Cladosporium, Rhodotorula, Cystofilobasidium, and Epicoccum genera were predominant among the fungi, and Bacillus, Pseudomonas, Sphingomonas, Methylobacterium, and Pantoea genera were predominant among the bacteria. Based on the data, we selected 29 major non-pathogenic and 12 phytopathogenic fungi and bacteria as the targets of macroarray. Forty-one species-specific 40-base pair long oligo-DNA sequences were selected from the nucleotide sequences of rDNA-internal transcribed spacer region for fungi and 16S rDNA for bacteria. The oligo-DNAs were fixed on nylon membrane and hybridized with digoxigenin-labeled cRNA probes prepared for each species. All arrays except those for Alternaria, Bacillus, and their related species, were specifically hybridized. The array was sensitive enough to detect 103 CFU for Aureobasidium pullulans and Bacillus cereus. Nucleotide sequencing of 100 each of independent fungal rDNA-ITS and bacterial 16S-rDNA sequences from apple tree was in agreement with the macroarray data obtained using the same sample. Finally, we analyzed the richness in the microbial inhabitants in the samples collected from apple trees in four orchards. Major apple pathogens that cause scab, Alternaria blotch, and Marssonina blotch were detected along with several non-phytopathogenic fungal and bacterial inhabitants.

Conclusions

The macroarray technique presented here is a strong tool to monitor the major microbial species and the community structures in the phyllosphere of apple trees and identify key species antagonistic, supportive or co-operative to specific pathogens in the orchard managed under different environmental conditions.  相似文献   

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