丛枝菌根真菌对番茄信号物质的诱导效应

盆栽番茄Lycopersicon esculentum幼苗分别接种丛枝菌根(AM)真菌摩西球囊霉Glomus mosseae、地表球囊霉G.versiforme、根内球囊霉G.intraradices、幼套球囊霉G.etunicatum及珠状巨孢囊霉Gigaspora margarita 35d后,开始测定番茄植株内源信号物质水杨酸(SA)、茉莉酸(JA)、一氧化氮(NO)和过氧化氢(H2O2)含量变化,抗性相关酶活性,丙二醛(MDA)含量以及生长量等指标。结果表明,接种AM真菌增加了番茄植株鲜重、株高、地上部和地下部干重、叶片和根系NO、JA、H2O2含量和结合态SA含量,其中,以摩西球囊霉G.mosseae诱导作用最大,叶片和根系内NO、JA、H2O2和结合态SA含量分别比对照增加了3.3和1.9倍、6.8和8.0倍、0.9和1.2倍、1.9和2.6倍,而根系中游离态SA含量一直处于较低水平,只有摩西球囊霉G.mosseae处理在诱导高峰时根系游离态SA含量比对照略有增加。接种AM真菌处理的番茄叶片和根系超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)、苯丙氨酸解氨酶(PAL)活性显著增加,其中以摩西球囊霉G.mosseae的诱导效应最大,与未接种对照相比分别增加了0.6和0.3倍、7.9和3.1倍、0.4和1.2倍、2.3和1.9倍;幼套球囊霉G.etunicatum的诱导效应最小:与未接种对照相比分别增加了0.26和0.14倍、2.3和1.0倍、0.1和0.28倍、0.55和0.31倍;而MDA含量下降,分别降低了66%和68%、34%和41%、51%和50%、12%和26%、18%和29%。表明AM真菌能诱导植物同时产生多种信号物质,而且这些信号参与了AM真菌-番茄共生体系统抗性的表达。     

根瘤菌对土壤铜、锌和镉形态分配的影响

以湖南郴州红壤和河北巩义褐土为供试土壤。制备Cu、Zn、Cd污染土壤。接种大豆根瘤菌(Rhi-zobium fredii)HN01,用连续提取法浸提土壤中不同形态的重金属．结果表明。褐土接种根瘤菌后固相结合态Zn总量降低10％。专性吸附态、氧化锰结合态和有机结合态Zn减少达9％～26％．红壤中结合态Zn的总量变化不显著,但专性吸附态和氧化锰结合态Zn含量显著减少。交换态Zn含量显著增加．褐土中接种根瘤菌抑制了Cu向土壤溶液的释放,固相结合态Cu总量增加18％,可交换态、专性吸附态、氧化锰结合态和有机结合态的Cu增加20％～54％．接种根瘤菌对土壤中Cd的溶解没有明显的抑制或促进作用,但改变了红壤中各形态Cd的含量高低顺序．Cd污染红壤中可交换态和有机结合态Cd含量分别增加22％和11％,专性吸附态和氧化锰结合态Cd分别减少14％和29％．根瘤菌对不同类型重金属及不同土壤中重金属形态影响的差异主要与土壤pH降低有关．     

提取植物叶中水杨酸最佳条件的探讨

在测定植物中游离态水杨酸(salicylic acid,SA)和结合态SA的方法中,高效液相色谱被认为是一种精密度高、重复性好的方法(李兆亮等1997;徐幼平等1997)。结合态SA一般采用测定其水解后SA含量的方法测定,但由于SA易升     

NaCl胁迫对茄子嫁接苗根系多胺代谢的影响

采用高压液相色谱法对80 mmol.L-1NaCl胁迫下营养液栽培茄子嫁接苗和自根苗根系多胺代谢的差异进行了研究。结果表明,胁迫2 d时,嫁接苗根系游离态亚精胺和结合态多胺含量显著高于自根苗,游离态腐胺和束缚态多胺显著低于自根苗,游离态精胺含量两者无显著差异。胁迫10 d时,自根苗3种形态的多胺含量均下降,显著低于对照植株,而嫁接苗根系游离态精胺、结合态腐胺和束缚态多胺含量显著高于对照植株。研究结果表明,NaCl胁迫显著提高了茄子嫁接苗和自根苗根系多胺氧化酶的活性,且自根苗增加幅度显著高于嫁接苗;嫁接苗胁迫初期根系结合态多胺的迅速积累及胁迫后期保持较高的精胺含量有利于其耐盐性的提高。     

盐胁迫下大麦根系多胺代谢与其耐盐性的关系

研究了0～300mmol/LNaCl对大麦(Hordeum-vulgare-L.)幼苗生长速率、根系游离和结合态多胺含量以及多胺生物合成关键酶活性的影响。结果表明,在0～200mmol/L NaCl处理下精氨酸脱羧酶（ADC）、多胺氧化酶(PAO)以及转谷酰胺酶(Tgase)活性明显提高,而在300 mmol/L NaCl处理下活性下降。与之对应,游离腐胺（Put）含量随处理盐浓度的提高一直呈上升趋势,亚精胺(Spd)和在根系内检测到的未知多胺(Pax)在低浓度盐处理时含量上升,随盐浓度的提高含量下降。盐处理前后精胺(Spm)含量变化不明显。低浓度盐处理时游离态（Spd+Pax）/Put上升,随盐浓度的提高比值明显下降。结合态Put、Spd和Pax含量以及结合态多胺总量均在低浓度盐处理时上升,随盐浓度的提高含量明显下降。统计分析显示,大麦相对生长速率与游离态（Spd+Pax）/Put和结合态多胺含量间均呈极显著正相关关系,与游离态多胺和结合态多胺的比值间均呈显著负相关关系,上述结果说明盐胁迫下大麦体内游离态Spd、Pax与Put以及结合态形式之间的平衡与大麦耐盐性关系密切,游离态Put向Spd 、Pax以及结合态形式转化均有利于大麦耐盐性的提高.     

盐胁迫下大麦幼苗多胺的种类和状态与多胺氧化酶活性的关系

200 mmol/L的NaCl胁迫8 d大麦幼苗叶片和根系中的三种形态多胺都有不同程度地下降,其中游离态多胺含量的下降幅度最大;高氯酸不溶性结合态多胺含量变化较小.根系中PAO的活性先上升后下降,而叶片中PAO的活性先下降后上升.游离态多胺中,亚精胺和精胺(Spd Spm)的含量变化与相应部位PAO的活性变化趋势相反,表明PAO在盐胁迫下可能调节了游离态多胺的含量从而影响高氯酸可溶结合态与高氯酸不溶结合态多胺的含量.     

外源亚精胺对盐胁迫下毕氏海蓬子体内多胺含量的影响

用含不同浓度(0、100、200、300、400和500 mmol·L 1)NaCl的Hoagland营养液及叶面喷施0.1 mmol·L-1外源亚精胺(Spd)处理毕氏海蓬子幼苗,研究外源Spd对NaCl胁迫下海蓬子体内游离态、结合态和束缚态3种形态多胺含量的影响,分析内源多胺含量的变化与植物耐盐性的关系.结果表明:(1)随盐胁迫浓度的升高,海蓬子幼苗叶片中3种形态腐胺(Put)含量均先降后升;同期的游离态Spd含量持续上升,结合态和束缚态Spd含量均先升后降;同期的游离和结合态精胺(Spm)含量均先升后降,而其束缚态Spm含量呈上升趋势;游离态和束缚态多胺(PAs)总量变化随盐浓度升高均呈上升趋势,而结合态PAs总量先升后降.(2)3种形态(Spd+ Spm) /Put比值均先升后降,而3种形态Put/PAs比值则均呈先降后升的相反趋势.(3)外源Spd处理提高了海蓬子幼苗叶片中结合态和束缚态PAs总量,也提高了游离态和束缚态(Spd+Spm)/Put比值.研究发现,外源Spd参与了NaCl胁迫下海蓬子内源PAs代谢的调节,可能通过促进盐胁迫植株中Put向Spd和Spm的转化,以及游离态多胺向结合态和束缚态多胺的转化来增强海蓬子耐盐性.     

氯化钠胁迫对嫁接黄瓜叶片多胺含量的影响

以日本耐盐品种‘帝王新土佐’南瓜为砧木,以’新泰密刺’黄瓜为接穗,在100 mmol·L^-1 NaCl胁迫下,对黄瓜嫁接和自根植株不同时期叶片中不同形态多胺含量的变化进行了研究.结果表明：NaCl胁迫下黄瓜嫁接植株游离态腐胺（Put）含量在胁迫2 d时与自根植株无显著差异,其余时间均显著高于自根植株;游离态亚精胺（Spd）和游离态精胺（Spm）含量在整个胁迫期间均显著高于自根植株;游离态多胺总量（PAs）在胁迫第4天出现峰值;嫁接植株游离态Put/PAs值在胁迫4 d时与自根植株无显著差异,其余胁迫时间均显著低于自根植株,而(Spd+Spm)/Put值在整个胁迫期间均显著高于自根植株;嫁接植株结合态和束缚态Put、Spd和Spm含量在整个胁迫期间均显著高于自根植株,结合态和束缚态PAs在胁迫第6天出现峰值;结合态多胺的Put/PAs值和(Spd+Spm)/Put值变化趋势与游离态多胺一致;嫁接植株束缚态Put/PAs值在胁迫6 d时与自根植株无显著差异,其余时间均显著低于自根植株,而(Spd+Spm)/Put值在整个胁迫期间均显著高于自根植株.表明黄瓜嫁接植株表现出较强的耐盐特征.     

盐胁迫下大麦根系多胺代谢与其耐盐性的关系

研究了0－300mmol/L NaCl对大麦（Hordeum vulgare L.)幼苗生长速率,根系游离和结合态多胺含量以及多胺生物合成关键酶活性的影响。结果表明,在0－200mmol/L NaCl处理下精氨酸脱羧酶（ADC）、多胺氧化酶（PAO）以及转谷酰胺酶（TGase)活性明显提高,而在300mol/L NaCl处理下活性下降,与之对应,游离腐胺（Put)含量随处理盐浓度的提高一直呈上升趋势。亚精胺（Spd)和在根系内检测到的未知多胺（PAx）在低浓度盐处理时含量上升,随盐浓度的提高含量下降,盐处理前后精胺（Spm)含量变化不明显,低浓度盐处理时游离态（Spd PAx)/Put上升,随盐浓度的提高比值明显下降,结合态Put,Spd和PAx含量以及结合态多胺总量均在低浓度盐处理时上升,随盐浓度的提高含量明显下降,统计分析显示,大麦相对生长速率与游离态（Spd PAx）／Put和结合态多胺含量间均呈极显著正相关关系,与游离态多胺和结合态多胺的比值间均呈显著负相关关系,上述结果说明盐胁迫下大麦体内游离态Spd,PAx与Put以及结合态形式之间的平衡与大麦耐盐性关系密切,游离态Put向Spd,PAx以及结合态形式转化均有利于大麦耐盐性的提高。     

逆境下拟南芥野生型和突变体sex1游离态水杨酸含量及根形态差异

以拟南芥野生型(WT)和突变体sex1为材料,采用HPLC、显微观察等方法,研究了WT在10个不同生长期时游离态水杨酸(SA)含量的变化,比较了在丁香假单胞菌番茄致病变种(Pst.DC3000)、H2O2、甲基紫精(MV)和SA处理环境下WT和sex1中游离态SA含量及幼苗根形态的差异.结果表明:在花序继续开放期(6.30、6.50)以及长角果出现期(8.0),WT中游离态SA含量处在更低水平;2 mmol·L-1 SA处理能够极显著提高WT和突变体sex1中游离态SA的积累,且突变体sex1中游离态SA水平增加更明显,是其他处理游离态SA水平的10倍左右;在MV和H2O2处理下,WT和sex1主根生长受抑制的程度没有明显差异,而突变体sex1幼苗的根毛在低浓度MV环境中比WT更长但密度差异不明显,且WT和sex1根毛在低浓度H2O2环境中差异情况与对照组相似,但外源SA处理使WT和突变体sex1的主根生长均受到明显的抑制,两者的根毛密度随SA增加逐渐降低甚至消失,且突变体sex1比WT受到的抑制作用更明显.研究发现:拟南芥的开花和结果过程与SA依赖途径有一定关系;外源添加SA比Pst.DC3000、H2O2和MV处理更能直接促使拟南芥突变体sex1产生更多的游离态SA;突变体sex1根的生长发育比WT更易受到生长环境条件的影响,且sex1根形态的生长存在一定的SA浓度依赖模式.     

Protection of tomato seedlings against infection by Pseudomonas syringae pv. tomato by using the plant growth-promoting bacterium Azospirillum brasilense

Pseudomonas syringae pv. tomato, the causal agent of bacterial speck of tomato, and the plant growth-promoting bacterium Azospirillum brasilense were inoculated onto tomato plants, either alone, as a mixed culture, or consecutively. The population dynamics in the rhizosphere and foliage, the development of bacterial speck disease, and their effects on plant growth were monitored. When inoculated onto separate plants, the A. brasilense population in the rhizosphere of tomato plants was 2 orders of magnitude greater than the population of P. syringae pv. tomato (10(7) versus 10(5) CFU/g [dry weight] of root). Under mist chamber conditions, the leaf population of P. syringae pv. tomato was 1 order of magnitude greater than that of A. brasilense (10(7) versus 10(6) CFU/g [dry weight] of leaf). Inoculation of seeds with a mixed culture of the two bacterial strains resulted in a reduction of the pathogen population in the rhizosphere, an increase in the A. brasilense population, the prevention of bacterial speck disease development, and improved plant growth. Inoculation of leaves with the mixed bacterial culture under mist conditions significantly reduced the P. syringae pv. tomato population and significantly decreased disease severity. Challenge with P. syringae pv. tomato after A. brasilense was established in the leaves further reduced both the population of P. syringae pv. tomato and disease severity and significantly enhanced plant development. Both bacteria maintained a large population in the rhizosphere for 45 days when each was inoculated separately onto tomato seeds (10(5) to 10(6) CFU/g [dry weight] of root). However, P. syringae pv. tomato did not survive in the rhizosphere in the presence of A. brasilense. Foliar inoculation of A. brasilense after P. syringae pv. tomato was established on the leaves did not alleviate bacterial speck disease, and A. brasilense did not survive well in the phyllosphere under these conditions, even in a mist chamber. Several applications of a low concentration of buffered malic acid significantly enhanced the leaf population of A. brasilense (>10(8) CFU/g [dry weight] of leaf), decreased the population of P. syringae pv. tomato to almost undetectable levels, almost eliminated disease development, and improved plant growth to the level of uninoculated healthy control plants. Based on our results, we propose that A. brasilense be used in prevention programs to combat the foliar bacterial speck disease caused by P. syringae pv. tomato.     

Differential volatile emissions and salicylic acid levels from tobacco plants in response to different strains of<Emphasis Type="Italic"> Pseudomonas syringae</Emphasis>

Pathogen-induced plant responses include changes in both volatile and non-volatile secondary metabolites. To characterize the role of bacterial pathogenesis in plant volatile emissions, tobacco plants, Nicotiana tabacum L. K326, were inoculated with virulent, avirulent, and mutant strains of Pseudomonas syringae. Volatile compounds released by pathogen-inoculated tobacco plants were collected, identified, and quantified. Tobacco plants infected with the avirulent strains P. syringae pv. maculicola ES4326 (Psm ES4326) or pv. tomato DC3000 (Pst DC3000), emitted quantitatively different, but qualitatively similar volatile blends of (E)-beta-ocimene, linalool, methyl salicylate (MeSA), indole, caryophyllene, beta-elemene, alpha-farnesene, and two unidentified sesquiterpenes. Plants treated with the hrcC mutant of Pst DC3000 (hrcC, deficient in the type-III secretion system) released low levels of many of the same volatile compounds as in Psm ES4326- or Pst DC3000-infected plants, with the exception of MeSA, which occurred only in trace amounts. Interaction of the virulent pathogen P. syringae pv. tabaci (Pstb), with tobacco plants resulted in a different volatile blend, consisting of MeSA and two unidentified sesquiterpenes. Overall, maximum volatile emissions occurred within 36 h post-inoculation in all the treatments except for the Pstb infection that produced peak volatile emissions about 60 h post-inoculation. (E)-beta-Ocimene was released in a diurnal pattern with the greatest emissions during the day and reduced emissions at night. Both avirulent strains, Psm ES4326 and Pst DC3000, induced accumulation of free salicylic acid (SA) within 6 h after inoculation and conjugated SA within 60 h and 36 h respectively. In contrast, SA inductions by the virulent strain Pstb occurred much later and conjugated SA increased slowly for a longer period of time, while the hrcC mutant strain did not trigger free and conjugated SA accumulations in amounts significantly different from control plants. Jasmonic acid, known to induce plant volatile emissions, was not produced in significantly higher levels in inoculated plants compared to the control plants in any treatments, indicating that induced volatile emissions from tobacco plants in response to P. syringae are not linked to changes in jasmonic acid.     

Is Salicylic Acid a Translocated Signal of Systemic Acquired Resistance in Tobacco?

Salicylic acid (SA) is a likely endogenous signal in the development of systemic acquired resistance (SAR) in some dicotyledonous plants. In tobacco mosaic virus (TMV)-resistant Xanthi-nc tobacco, SA levels increase systemically following the inoculation of a single leaf with TMV. To determine the extent to which systemic increases in SA result from SA export from the inoculated leaf, SA produced in TMV-inoculated or healthy leaves was noninvasively labeled with 18O2. Spatial and temporal distribution of 18O-SA indicated that most of the SA detected in the healthy tissues was synthesized in the inoculated leaf. No significant increase in the activity of benzoic acid 2-hydroxylase, the last enzyme involved in SA biosynthesis, was detected in upper uninoculated leaves, although the basal level of enzyme activity was relatively high. No increases in SA level, pathogenesis-related PR-1 gene expression, or TMV resistance in the upper uninoculated leaf were observed if the TMV-inoculated leaf was detached up to 60 hr after inoculation. Apart from the inoculated tissues, the highest increase in SA was observed in the leaf located directly above the inoculated leaf. The systemic SA increase observed during SAR may be explained by phloem transport of SA from the inoculation sites.     

Bacterial non-host resistance: interactions of Arabidopsis with non-adapted Pseudomonas syringae strains

Although interactions of plants with virulent and avirulent host pathogens are under intensive study, relatively little is known about plant interactions with non-adapted pathogens and the molecular events underlying non-host resistance. Here we show that two Pseudomonas syringae strains for which Arabidopsis is a non-host plant, P. syringae pathovar (pv.) glycinea (Psg) and P. syringae pv. phaseolicola (Psp),induce salicylic acid (SA) accumulation and pathogenesis-related gene expression at inoculation sites, and that induction of these defences is largely dependent on bacterial type III secretion. The defence signalling components activated by non-adapted bacteria resemble those initiated by host pathogens, including SA, non-expressor of PR-1, non-race specific disease resistance 1, phytoalexin-deficient 4 and enhanced disease susceptibility 1. However, some differences in individual defence pathways induced by Psg and Psp exist, suggesting that for each strain, distinct sets of type III effectors are recognized by the plant. Although induction of SA-related defences occurs, it does not directly contribute to bacterial non-host resistance, because Arabidopsis mutants compromised in SA signalling and other classical defence pathways do not permit enhanced survival of Psg or Psp in leaves. The finding that numbers of non-adapted bacteria in leaf extracellular spaces rapidly decline after inoculation suggests that they fail to overcome toxic or structural defence barriers preceding SA-related responses. Consistent with this hypothesis, rapid, type III secretion system-independent upregulation of the lignin biosynthesis genes, PAL1 and BCB, which might contribute to an early induced, cell wall-based defence mechanism, occurs in response to non-adapted bacteria. Moreover, knockout of PAL1 permits increased leaf survival of non-host bacteria. In addition, different survival rates of non-adapted bacteria in leaves from Arabidopsis accessions and mutants with distinct glucosinolate composition or hydrolysis exist. Possible roles for early inducible, cell wall-based defences and the glucosinolate/myrosinase system in bacterial non-host resistance are discussed.     

Systemic Responses in Arabidopsis thaliana Infected and Challenged with Pseudomonas syringae pv syringae

Attack of plants by necrotizing pathogens leads to acquired resistance to the same or other pathogens in tissues adjacent to or remotely located from the site of initial attack. We have used Arabidopsis thaliana inoculated with the incompatible pathogen Pseudomonas syringae pv syringae on the lower leaves to test the induction of systemic reactions. When plants were challenged with Pseudomonas syringae pv syringae in the upper leaves, bacterial titers remained stable in those preinfected on the lower leaves. However, there was a distinct decrease in symptoms that correlated with a local and systemic increase in salicylic acid (SA) and in chitinase activity. Peroxidase activity only increased at the site of infection. No changes in catalase activity were observed, either at the local or at the systemic level. No inhibition of catalase could be detected in tissue in which the endogenous levels of SA were elevated either naturally (after infection) or artificially (after feeding SA to the roots). The activity of catalase in homogenates of A. thaliana leaves could not be inhibited in vitro by SA. SA accumulation was induced by H2O2 in leaves, suggesting a link between H2O2 from the oxidative burst commonly observed during the hypersensitive reaction and the induction of a putative signaling molecule leading to system acquired resistance.     

Resistance of Pepper Lines to the Movement of Cucumber Mosaic Virus

The multiplication and the migration of cucumber mosaic virus (CMV) were studied in greenhouse conditions in one susceptible ‘Yolo wonder’ and two resistant ‘Milord’ and ‘Vania’ pepper varieties. DAS-ELISA tests have revealed that the virus is replicated in inoculated leaves of the resistant varieties as high as in the susceptible variety. In the susceptible variety ‘Yolo wonder’, CMV migrated from the leaf lamina to the petiole two days after inoculation and it became systemic three days later regardless the season. In ‘Milord’ the virus migrated from the leaf lamina to the petiole five days after inoculation and it became systemic during the winter 16 days after inoculation. Whereas plants of the same genotype were not infected systemically during the summer. In ‘Vania’, during the two seasons, CMV spread from the blade to the petiole five days after inoculation, but the virus was not detected beyond the inoculated leaf. These results show that ‘Milord’ and ‘Vania’ are resistant to CMV migration. Therefore, the resistance to CMV migration is affected by plant genotype and temperature. The study of effect of pepper plant phenology on infection has revealed that resistance to CMV migration is also affected by the development stage of the plants.