Silicon induced resistance in cucumber plants against Pythium ultimum

The effect of the amendment of nutrient solutions with soluble potassium silicate on the response of cucumber (cv. Corona) root and hypocotyl tissues infected by Pythium ultimum was examined by light and electron microscopy, and by energy dispersive X-ray analysis (EDX). Plants were grown in 0 or 1·7 m Si-amended nutrient solutions, and root and hypocotyl samples were collected at different times after inoculation with P. ultimum. By 48 h after infection, striking differences in the expression of defence reactions were observed between Si-amended and Si-free cucumber plants. Treatment of plants with Si markedly stimulated the accumulation of an electron-dense, phenolic-like material in infected host tissues, and significantly increased the percentage of cells filled with this material. Fungal hyphae colonizing occluded host cells were seriously damaged, and were often reduced to empty hyphal shells. Additionally, Si-treated cucumber plants responded to P. ultimum infection by forming electron-dense layers along primary and secondary cell walls, as well as over pit membranes of xylem vessels. EDX analysis failed to reveal the presence of silica deposits in P. ultimum-infected plants grown in Si-supplemented media. Our results suggest that a relationship exists between Si treatment, resistance to P. ultimum attack, and expression of plant defence mechanisms.     

The anatomy of the leaf surface: The first line of defence

The epidermis and its cuticle are the first line of defence of the plant against a hostile environment. They reduce desiccation, the assaults of pathogens and insects and, more recently, the attacks of toxic sprays and aerial pollution. All aerial surfaces of a plant have a cuticle and there may sometimes be found internal cuticles as well. The epidermal cell/cuticle sandwich is as diverse in structure, dimensions and chemistry as the plants on which it is found. Examples of many of these diverse structures are described and illustrated and their possible roles discussed.     

Sugar beet extract induces defence against Phytophthora infestans in potato plants

The aim of this study was to find a natural and cheap agent that could induce defence responses in potato plants to combat Phytophthora infestans, which causes late blight disease that is one of the most devastating plant pathogens in agriculture. We tested whether a sugar beet extract (SBE), derived through a simple extraction procedure from a large-scale plant waste product, induced resistance under green-house conditions. In three potato genotypes differing in their level of resistance to P. infestans (two susceptible genotypes: Desiree and Bintje and one partially resistant: Ovatio), treatment with SBE resulted in significant reduction of the size of the infection lesions in a pattern similar to that seen with application of a known defence-inducing compound, β-aminobutyric acid (BABA). Lower sporangial production was also observed on SBE-treated leaves, but the reduction in sporangial production was more pronounced after BABA treatment. SBE had no apparent toxic effect on the hyphal growth of the pathogen or on the germination of sporangia. Instead, SBE triggered pathogenesis-related protein (PR-1 and PR-2) induction which suggests that the protection conferred by SBE could be via induced resistance. An array of phenolic metabolites was found in the SBE that may contribute to the defence response.     

Role of methyl jasmonate in the expression of mycorrhizal induced resistance against Fusarium oxysporum in tomato plants

Arbuscular mycorrhiza (AM) colonization led to a decrease in the severity of fusarium wilt disease caused by Fusarium oxysporum f. sp. lycopersici in tomato plants. The involvement of two plant defense hormones, namely methyl jasmonate (MeJA) and salicylic acid (SA), in the expression of mycorrhiza induced resistance (MIR) against this vascular pathogen was studied in the AM colonized and non-colonized (controls) plants. Activity of lipoxygenase (LOX), which plays a role in jasmonic acid (JA) biosynthesis, as well as levels of methyl jasmonate (MeJA) increased in AM colonized plants as compared to controls, but did not show any further changes in response to F. oxysporum inoculation. On the other hand, activity of phenylalanine ammonia lyase (PAL), which is an enzyme from salicylic acid (SA) biosynthetic pathway, as well as SA levels, increased in both controls and AM colonized plants in response to application of F. oxysporum spores. Hence the JA and not the SA signalling pathway appeared to play a role in the expression of MIR against this vascular pathogen. The resistance observed in AM colonized plants was completely compromised when plants were treated with the JA biosynthesis inhibitor salicylhydroxamic acid (SHAM). This confirmed that the AM-induced increase in JA levels was involved in the expression of resistance toward F. oxysporum. The SA response gene pathogenesis-related 1 (PR1) showed an increased expression in response to F. oxysporum infection in SHAM treated AM colonized plants as compared to plants that were not treated with this JA inhibitor. This suggested the possibility that JA inhibited SA responses, at least in the roots. AM colonization therefore appeared to prime plants for improved tolerance against the vascular pathogen F. oxysporum, which was mediated through the JA signalling pathway.     

内生细菌EBS05对烟草诱导抗性的信号转导途径研究

 樟树内生枯草芽胞杆菌EBS05是一株对多种植物病原菌具有较强拮抗活性,并能诱导烟草系统抗性的生防菌株。本文以缺失Surfactin A合成相关基因的突变菌株EBS05^T为材料,研究了内生细菌EBS05对烟草诱导系统抗性的激发子及其信号转导途径。结果表明,菌株EBS05产生的Surfactin A是诱导烟草对TMV系统抗性的有效激发子;Surfactin A诱导处理后,SA信号转导途径下游的关键调节基因NPR1首先被激活,并持续超量表达,进而触发PR1b和PR1a基因持续超量表达,表明Surfactin A诱导烟草对TMV的系统抗性是通过激活SA信号转导途径实现的。同时,Surfactin A诱导处理后24~72 h,JA/ET信号转导途径调节基因PDF1.2被激活,且超量表达,表明在Surfactin A诱导烟草对TMV系统抗性的信号转导过程中,可能存在SA信号途径和JA/ET信号途径的交叉协同作用。     

Pseudomonas-induced defence molecules in rice plants against leaffolder (Cnaphalocrocis medinalis) pest

Fluorescent pseudomonad strains Pf1, TDK1 and PY15 individually and in combination were evaluated against leaffolder, Cnaphalocrocis medinalis Guen., in rice under in vitro, glasshouse and field conditions. Among the various treatments used, a combination of Pf1, TDK1 and PY15 strains effectively reduced the incidence of leaffolder pest in rice plants to an extent comparable with chlorpyrifos-methyl. In addition, morphogenesis of the insect pest in all stages, larval, pupal and adult, was greatly affected by a combination of Pseudomonas Pf1, TDK1 and PY15 strains. Further, the induction of defence-related molecules was demonstrated. An increased accumulation of defence molecules such as chitinase and proteinase inhibitors was observed with a combined Pf1, TDK1 and PY15 treatment compared with all other treatments. Western blot analysis of chitinase revealed the extra induction of 18, 28 and 35 kDa isoforms in rice plants treated with a mixture of Pf1, TDK1 and PY15 strains against leaffolder pest. The study revealed that a combination of fluorescent pseudomonad strains affects the development of leaffolder pest by inducing defence molecules in rice plants which in turn enhance resistance to leaffolder attack.     

Evidence of early defence to Ascochyta lentis within the recently identified Lens orientalis resistance source ILWL180

In plant–pathogen interactions, strong structural and biochemical barriers may induce a cascade of reactions in planta, leading to host resistance. The kinetic speed and amplitudes of these defence mechanisms may discriminate resistance from susceptibility to necrotrophic fungi. The infection processes of two Ascochyta lentis isolates (FT13037 and F13082) on the recently identified ascochyta blight (AB)‐resistant Lens orientalis genotype ILWL180 and two cultivated genotypes, ILL7537 (resistant) and ILL6002 (susceptible), were assessed. Using histopathological methods, significant differences in early behaviour of the isolates and the subsequent differential defence responses of the hosts were revealed. Irrespective of virulence, both isolates had significantly lower germination, shorter germ tubes and delayed appressorium formation on the resistant genotypes (ILWL180 and ILL7537) compared to the susceptible genotype (ILL6002); furthermore, these were more pronounced on genotype ILWL180 than on genotype ILL7537. Subsequently, host perception of pathogen entry led to the faster accumulation and notably higher amounts of reactive oxygen species and phenolic compounds at the penetration sites of the resistance genotypes ILWL180 and ILL7537. In contrast, genotype ILL6002 responded slowly to the A. lentis infection and reaffirmed previous gross disease symptomology reports as highly susceptible. Interestingly, quantification of H₂O₂ was markedly higher in ILWL180 particularly at 12 h post‐inoculation compared to ILL7537, potentially indicative of its superior resistance capability. Faster recognition of A. lentis is likely to be a major contribution to the superior resistance observed in genotype ILWL180 to the highly aggressive isolates of A. lentis assessed.     

Molecular and biochemical mechanisms of defence induced in pea by Rhizobium leguminosarum against Orobanche crenata

Orobanche species (broomrapes) are parasitic weeds which dramatically decrease the yields of many economically important dicotyledonous crops, including pea (Pisum sativum), in Mediterranean areas. Previously, we identified some Rhizobium leguminosarum strains, including P.SOM, which could both promote pea development and significantly reduce infection by Orobanche crenata, notably through induction of necrosis of attached parasites. In the present study, induced resistance against broomrape in the nodulated pea was shown to be associated with significant changes in rates of oxidative lipoxygenase (Lox) and phenylpropanoid/isoflavonoid pathways and in accumulation of derived toxins, including phenolics and pisatin (pea phytoalexin). Changes were followed for 5 weeks after inoculation and attack by Orobanche. In contrast to non‐inoculated plants or Orobanche only infected plants, polyphenoloxidase (PPO) activity and hydrogen peroxide content increased in response to bacteria inoculation indicating the involvement of oxidative processes. In parallel, the nodulated roots displayed high Lox activity related to the overexpression of the lox1 gene. Similarly, the expression of phenylalanine ammonia lyase (PAL) and 6a‐hydroxymaackiain 3‐O‐methyltransferase (Hmm6a) genes were induced early during nodule development, suggesting the central role of the phenylpropanoid/isoflavonoid pathways in the elicited defence. As a consequence, the derived products, phenolics and pisatin, accumulated in response to rhizobacteria and conferred mechanical and chemical barriers to the invading parasite. These results highlight the likely role of signalling pathways in induced resistance and suggest these mechanisms should be enhanced through integrated Orobanche management practices.     

Cultivar‐dependent partial resistance and associated defence mechanisms in wheat against Zymoseptoria tritici

Septoria tritici blotch caused by the fungus Zymoseptoria tritici is one of the most devastating foliar diseases of wheat. Knowledge regarding mechanisms involved in resistance against this disease is required to breed durable resistances. This study compared the expression of defence and pathogenicity determinants in three cultivars in semicontrolled culture conditions. The most susceptible cultivar, Alixan, presented higher necrosis and pycnidia density levels than Altigo, the most resistant one. In Premio, a moderately resistant cultivar, necrosis developed as in Alixan, while pycnidia developed as in Altigo. In noninfectious conditions, genes coding for PR1 (pr1), glucanase (gluc) and allene oxide synthase (aos) were constitutively expressed at a higher level in both Altigo and Premio than in Alixan, while chitinase2 (chit2), phenylalanine ammonia‐lyase (pal), peroxidase (pox2) and oxalate oxidase (oxo) were expressed at a higher level in Premio only. Except for aos, all genes were induced in Alixan during the first steps of the symptomless infection phase. Only pox2, oxo, gluc and pal genes in Altigo and pal, chs and lox genes in Premio were up‐regulated at some time points. Basal cultivar‐dependent resistance against Z. tritici could therefore be explained by various gene expression patterns rather than high expression levels of given genes. During the necrotrophic phase, Z. tritici cell wall‐degrading enzyme activity levels were lower in Altigo and Premio than in Alixan, and were associated more with pycnidia than with necrosis. Similar tissue colonization occurred in the three cultivars, suggesting an inhibition of the switch to the necrotrophic lifestyle in Altigo.     

Induced resistance against leafminer eggs by extrusion in young potato plants

Abstract

Egg extrusion patterns were investigated as an inducible defensive mechanism in potato plants against the leafminer Liriomyza huidobrensis (Blanchard) (Diptera: Agromyzidae). Increased multiplication rates in leaf cells surrounding an egg of L. huidobrensis leads to its exposure through the leaf cuticle, which might increase the risk of mortality. Extrusion rates were evaluated in laboratory tests, in relation to plant and leaf age in Solanum tuberosum L. var. Spunta. Stratified field sampling was also carried out in order to assess leafminer distribution on new and old leaves. Extrusion was higher in young plants, being restricted in older ones to new, still expanding leaves. Plant reaction was independent of egg density. In the field, damage was concentrated in older foliage, in line with the extrusion results. The relevance of egg extrusion for pest management is discussed.     

Evidence of induced systemic resistance against Botrytis elliptica in lily

Lily leaf blight, caused by Botrytis elliptica, is an important fungal disease in Taiwan. In order to identify an effective, nonfungicide method to decrease disease incidence in Lilium formosanum, the efficacy of rhizobacteria eliciting induced systemic resistance (ISR) was examined in this study. Over 300 rhizobacteria were isolated from the rhizosphere of L. formosanum healthy plants and 63 were identified by the analysis of fatty acid profiles. Disease suppressive ability of 13 strains was demonstrated by soil drench application of bacterial suspensions to the rhizosphere of L. formosanum seedlings. Biocontrol experiments were carried out with Bacillus cereus and Pseudomonas putida strains on L. formosanum and Lilium Oriental hybrid cvs. Acapulco and Star Gazer in greenhouse and field studies. Plants treated with B. cereus strain C1L showed that protection against B. elliptica on L. formosanum could last for at least 10 days and was consistent with high populations of B. cereus on lily roots. Analysis of the expression of LfGRP1 and LsGRP1, encoding glycine-rich protein associated with L. formosanum and cv. Star Gazer, respectively, revealed different responses induced by B. cereus or by the pathogen B. elliptica, suggesting that plant defense responses elicited by each follows a different signaling pathway. According to the results of biocontrol assays and LfGRP1/LsGRP1 gene expression analyses with culture filtrates of B. cereus strain C1L, we propose that eliciting factors of ISR are generated by B. cereus and some of them exhibit thermostable and heat-tolerant traits. This is the first report about ISR-eliciting rhizobacteria and factors effective for foliar disease suppression in lily.     

Silicon-enhanced resistance to rice blast is attributed to silicon-mediated defence resistance and its role as physical barrier

A series of experiments were performed to study the effects of silicon (Si) on rice blast development, H₂O₂ accumulation and lipid peroxidation in a controlled rice—Magnaporthe grisea pathosystem. Rice plants supplied with Si as a single dose immediately after pathogen inoculation (−/+Si) exhibited the same high protection against disease as plants treated continuously with Si for the whole growth period (+/+Si), with disease severity indices of 20.8% and 19.6%, respectively, which were significantly lower than that for the control treatment with no Si supplied (63.7%). A single application of Si to rice plants before inoculation (+/−Si) conferred partial protection (disease severity index of 33.3%) compared with the control treatment. Silicon induced a rapid but transient burst of H₂O₂ at 24 h after inoculation. The addition of Si to rice plants significantly altered the activities of catalase and lipoxygenase and the concentration of malodialdehyde (indicative of lipid peroxidation) in rice plants. We propose that rice plants may respond to Si by increased H₂O₂ accumulation and lipid peroxidation. In turn, these responses are linked to host defence mechanisms such as lignin production, oxidative cross-linking in the cell wall, phytoalexin production, and the hypersensitive reaction. Thus, the mechanisms of Si-stimulated plant disease protection may extend beyond its established role in physically strengthening cell walls.     

Effectiveness of systemic resistance in bean against foliar and soilborne pathogens as induced by biological and chemical means

Unifoliate leaves of 9-day-old green bean, Phaseolus vulgaris cv. Redlands Pioneer, were inoculated with 10⁴ conidia/ml Colletotrichum lindemuthianum , causing local lesions, or sprayed with 20 μg 2, 6-dichloro-isonicotinic acid/ml formulated by Ciba-Geigy Ltd as CGA 41396. At various times afterwards (7–16 days), first, second or third trifoliate leaves of these plants were challenge-inoculated with 10⁵ conidia/ml C. lindemuthianum or with the rust pathogen, Uromyces appendiculatus. The numbers of anthracnose lesions or rust uredinia resulting from challenge-inoculation were reduced to similar extents by both pre-treatments compared with control plants. Halo blight, caused by Pseudomonas syringae pv. phaseolicola , was reduced in first trifoliates following treatment of unifoliate leaves 6 days earlier with CGA 41396. Induced resistance to root-infecting pathogens was not observed when stems of either 14- or 16-day-old plants were inoculated with mycelial plugs of Fusarium solani f. sp. phaseoli , or when 11- and 15-day-old plants were inoculated with Rhizoctonia sp., Treatment with CGA 41396 did not protect seedlings when they were transplanted into a mix containing the Fusarium sp. 1 day later.     

拮抗细菌诱导番茄植株抗灰霉病机理研究

 拮抗细菌多粘类芽孢杆菌(Paenibacillus polymyxa) W3菌株悬浮液及其滤液可以诱导番茄叶片对灰霉病(Botrytis cinerea)的系统抗性。W3及其滤液诱导处理后,植株叶内苯丙氨酸解氨酶(PAL)、过氧化物酶(POD)、多酚氧化酶(PPO)和超氧化物歧化酶(SOD)活性明显增强。诱导后1 d,PAL活性最大,是对照的3.8~3.9倍,6 d后仍为对照的2.5倍;POD和PPO诱导后3 d活性最高,分别比对照增加34.7%~54.1%和78.5%~78.7%,6 d后仍比对照高;SOD活性诱导后2d达高峰,6 d后稍高于对照。活性氧(O₂^-)产生速率诱导后1 d最大,比对照增加85.6%~88.6%,以后急剧下降,6 d后接近对照。此外,W3诱导后1 d或2 d,处理叶和上一叶位叶片水杨酸含量明显上升,分别是对照的2.6倍和1.6倍,这表明该拮抗细菌诱导的系统抗性可能与水杨酸介导有关。     

The relation of mansonones to resistance against dutch elm disease and their accumulation,as induced by several agents

No evidence was found that mansonones E and F, which accumulated in elms after infection withCeratocystis ulmi, were responsible for resistance against Dutch elm disease inUlmus hollandica cl. 390. Furthermore, production of mansonones inU. americana was only about one-fifteenth of that inU. hollandica cl. Belgica. Yet both are susceptible to Dutch elm disease.Induction of these compounds was not specific, for accumulation occurred not only after introduction of crude toxin ofC. ulmi, but also after inoculation withVerticillium albo-atrum and after introduction of H₂SO₄ or ethanol.The dark discolouration of the wood after toxin treatment was restricted to the lower part of the stem. No mansonones could be detected in the non-discoloured higher parts of the stem or from the necrotic or wilted leaves.Samenvatting Er werd geen aanwijzing gevonden dat mansononen E en F, die na infectie metC. ulmi gevormd worden, verantwoordelijk zijn voor de resistentie tegen de iepziekte inU. hollandica cl. 390 (Tabel 1). U. americana bevat ongeveer 15 maal zo weinig van deze stoffen alsU. hollandica cl. Belgica, terwijl beide vatbaar zijn.De inductie van de synthese van deze stoffen bleek niet specifiek te zijn, omdat bij chemische beschadiging met H₂SO₄ of ethanol ook mansononen gevormd werden.De donkere verkleuring van het hout bleek na toxine toediening beperkt tot het onderste gedeelte van de stam. Geen mansononen werden gevonden in hoger gelegen, niet verkleurde stamgedeelten of in de necrotische en verwelkte bladeren.     

Development of resistance in tomato plants grafted onto Solanum torvum against bacterial wilt disease

Journal of Plant Diseases and Protection - The bacterial wilt disease caused by Ralstonia solanacearum is a major constraint in the cultivation of tomato in Saint Lucia. The limited options and...     

Silicon induced resistance against powdery mildew of roses caused by Podosphaera pannosa

Powdery mildew, caused by Podosphaera pannosa, is a very common disease in greenhouse potted roses, resulting in poor marketing value and hence economic losses. Alternatives to chemical control are necessary, and therefore the ability of silicon (Si) applied to roots to control the disease was investigated, as well as the mechanisms behind the observed disease reductions. Four genotypes of miniature potted roses representing different genetic backgrounds and susceptibility to disease were studied. Plants were watered with a nutrient solution containing either 3·6 mm Si (100 ppm) supplied as K₂SiO₃ (Si+) or no Si (Si?) before inoculation with P. pannosa. Si application increased leaf Si content two‐ to four‐fold compared to control plants. Confocal microscopy showed that Si deposition was larger in Si+ than in Si? plants and that deposition mainly occurred in the apoplast, particularly in epidermal cell walls. Si application delayed the onset of disease symptoms by 1–2 days and disease severity was reduced by up to 48·9%. The largest reduction was found in the two most resistant genotypes, which also had the highest increase in Si uptake. The Si‐induced disease protection was accompanied by increased formation of papillae and fluorescent epidermal cells (FEC) as well as deposition of callose and H₂O₂, especially at the sites of penetration and in FEC, which are believed to represent the hypersensitive response. Si treatment reduced powdery mildew development by inducing host defence responses and can therefore be used as an effective eco‐friendly disease control measure.     

苯并噻二唑诱发水稻对纹枯病的抗性

研究了苯并噻二唑(B1H)诱发水稻产生对纹枯病的抗性。离体条件下，1．0mmol／L BTH对纹枯病菌菌丝生长无明显抑制作用。BTH叶面或灌根处理四叶一心期水稻幼苗，并将植株第2、3和4叶离体接种纹枯病菌，水稻叶片纹枯病病斑长度明显下降，BTH诱发苗期水稻产生抗性的最佳诱导期在处理后的3—5天，最佳浓度为0．1mmol／L，BTH灌根处理诱发抗性的效果较好。用BTH溶液叶面喷雾处理成株期水稻倒二叶后离体接种纹枯病菌，倒二叶、倒一叶和剑叶上病斑长度显著低于对照，最佳诱导期在处理后3—5天。用BTH处理苗期水稻第2叶或成株期倒二叶，可使未经处理的苗期水稻第3和4叶以及成株期水稻倒一叶和剑叶上纹枯病病斑长度显著下降。     

Fusarium oxysporum Fo47 confers protection to pepper plants against Verticillium dahliae and Phytophthora capsici,and induces the expression of defence genes

The application of the nonpathogenic isolate Fusarium oxysporum 47 (Fo47) reduced the symptoms of verticillium wilt, phytophthora root rot and phytophthora blight in pepper plants. Botrytis cinerea was also tested on the leaves of plants treated with Fo47, but no protection was observed. Verticillium dahliae colonies cultured in the presence of Fo47 grew slower than control cultures, but Phytophthora capsici growth was unaffected by Fo47. At least part of the protection effect observed against V. dahliae could therefore be due to antagonism or competition. In order to search for induced resistance mechanisms, three defence genes previously related to pepper resistance were monitored over time. These genes encode a basic PR‐1 protein (CABPR1), a class II chitinase (CACHI2) and a sesquiterpene cyclase (CASC1) involved in the synthesis of capsidiol, a phytoalexin. These three genes were transiently up‐regulated in the roots by Fo47 in the absence of inoculation with the pathogen, but in the stem only CABPR1 was up‐regulated. In plants that were inoculated with V. dahliae after the Fo47 treatment, the three genes had a higher relative expression level than the control in both the roots and the stem.     

Early defence responses induced by AVR9 and mutant analogues in tobacco cell suspensions expressing the Cf-9 resistance gene

The interaction between the fungal leaf pathogen Cladosporium fulvum and its only host, tomato, fits the gene-for-gene model. In tomato, the Cf-9 resistance gene product mediates specific recognition of the fungal avirulence gene product AVR9, resulting in a hypersensitive response and resistance. Cf9 tomato leaves respond with necrosis after injection with AVR9, whereas Cf9 tomato cell suspensions do not show defence responses after treatment with AVR9. Here we report on early defence responses induced in Cf-9 transgenic tobacco leaves and Cf-9 transgenic tobacco cell suspensions after treatment with synthesized AVR9 and mutant analogues R08K, F10A and F21A. The necrosis-inducing activity of the AVR9 peptides increased in the order F21A, F10A, AVR9, R08K. An oxidative burst was induced at a much lower AVR9 peptide concentration as compared to medium alkalization and necrosis. Interestingly, the mutant peptide F21A failed to induce necrosis and medium alkalization but did induce an oxidative burst. In all assays, the relative differential activities of the AVR9 peptides were similar to those observed in Cf9 tomato leaves. Both AVR9 and F21A activated a MAP kinase in Cf-9 transgenic tobacco cell suspensions. AVR9 also induced specific cell death in these suspensions. The relation between the induction of early defence responses and necrosis is discussed.