Search

The effect of seven substances, Copper, CuO, ZnO, AlO NPs (8 mg L−1), CuO, ZnO, AlO (8 mg L−1) and chitosan was evaluated under both greenhouse and field conditions during two growing seasons (2017/2018 and 2018/2019) to control powdery mildew disease caused by Erysiphe cichoracearum on marigold (Calendula officinalis). Results have shown that all the treatments tested had decreased disease severity compared to the non-treated control. In this respect, chitosan showed the best effect in decreasing disease severity followed by ZnO NPs. Meanwhile, CuO gave the lowest effect in this respect. The decrease in disease severity of powdery mildew was positively expressed by an increase in crop parameters, i.e. numbers of inflorescence weight, fresh and dry weights of plants, plant height, number of branches and increased chlorophyll ( a and b) and carotenoids.

The article represents the comprehensive study of the resistance of ornamental plants Phlox paniculata L. to the biotic stress caused by the causative agent of powdery mildew (Erysiphe cichoracearum DC. f. phlogis Jacz.). The aim of the study was to investigate biochemical parameters in leaves of plants with different degree of resistance to the damage. in the conditions of the Forest-Steppe of Ukraine. There were classic common methods of determining the content of anthocyanins, catechins, proline, flavonoids applied in this work study. The varieties of fall phlox were studied: 'Katharine', 'Panianka', 'Tenor', 'Poliarnyi', 'Fiosin', 'Mohuchii', 'Rembrandt', 'Holubka', 'Novinka', 'Fujiyama', 'Detstvo'. The main result of the experiments is to establish a mechanism for the secondary metabolites use (catechins, flavonoids and anthocyanins) in the process of the increased plant resistance formation. As a result, the content of flavonoids is significantly reduced, in the affected plants, and the content of catechins and anthocyanins is significantly increased compared with the intact ones on the contrary. It is noted, that the content of flavonols in plants with powdery mildew is significantly lower in comaprison with unaffected plants from 8.0 to 61.55 %. The flavonols are obviously consumed during anthocyanins and catechins recovery reactions. In addition, there is a tendency for a significant increase in the content of the catechins in the affected powdery mildew plants compared to the non-affected ones generally 8-21 %. The anthocyanin content in the affected plants was also higher on 18˗48 %. Therefore, studies represent that the content of secondary metabolites is a marker of Ph. paniculata plants stability to the cause of powdery mildew unlike proline.

Bacillus amyloliquefaciens YN201732 is an endophytic bacteria with high biocontrol efficiency and broad-spectrum antimicrobial activities. In order to clarify the main active ingredients and their antifungal mechanisms against powdery mildew of tobacco, this study is focused on lipopeptide obtained through acid precipitation and organic solvent extraction. HPLC and LCMS-IT-TOF were used to separate and identify antimicrobial lipopeptides. Findings revealed that bacillomycin D plays an important role against surrogate fungal pathogen Fusarium solani. Synthetic pathways of sfp, bacillomycin D, and fengycin were separately disrupted. The sfp gene knockout mutant B. amyloliquefaciens YN201732M1 only showed minor antagonistic activity against F. solani. While Erysiphe cichoracearum spore germination was inhibited and pot experiments displayed a significant decrease in tobacco powdery mildew. The spore inhibition rate of YN201732M1 was only 30.29%, and the pot experiment control effect was less than 37.39%, which was significantly lower than that of the wild type. The inhibitory effect of mutant YN201732M2 (deficient in the production of bacillomycin D) and mutant YN201732M3 (deficient in the production of fengycin) on the spore germination of E. cichoracearum were 50.22% and 53.06%, respectively, suggesting that both fengycin and bacillomycin D had potential effects on spore germination of powdery mildew. Interestingly, in a greenhouse assay, both B. amyloliquefaciens YN201732M2 and YN201732M3 mutants displayed less of a control effect on tobacco powdery mildew than wild type. The results from in vitro, spore germination, and greenhouse-pot studies demonstrated that antimicrobial lipopeptides especially bacillomycin D and fengycin may contribute to the prevention and control of tobacco powdery mildew. In addition, gene mutation related to lipopeptide synthesis can also affect the biofilm formation of strains.

Powdery mildew disease, caused by Erysiphe cichoracearum, is considered one of the most severe pathogenic threats of sunflower worldwide. This study discusses how to improve the effect of biocontrol agents, as a more economic and eco-friendlier alternative to fungicides, by mixing different bioagents (Trichoderma harzianum and Bacillus subtilis) with different antioxidants (ascorbic acid and salicylic acid), either individually or combined. They were applied to sunflower during two successive seasons to determine their effectiveness in promoting growth and inducing resistance in sunflower against powdery mildew disease under field conditions. Results show that all treatments reduced the severity of powdery mildew disease significantly compared with control. A synergistic effect was noticed when combining T. harzianum and salicylic acid led to a significant decrease in powdery mildew disease severity in sunflower in comparison to control. In general, the results suggested that the integration of antioxidants with bioagents showed a better response to control powdery mildew disease than single treatments. In field experiments, the applied treatments significantly increased all of the studied growth parameters, plant length, fresh and dry weight. All treatments showed a remarkable increase in physiological aspects (enzymes activity and total phenol content).

Diseases are critical factors that affect the yield and quality of crops. Therefore, it is of great research value to develop rapid and quantitative methods for identification of common agricultural diseases. This exploratory study involved data analysis of common fungal pathogens using identification modeling based on terahertz spectrum technology. The selected pathogens were Physalospora piricola, Erysiphe cichoracearum, and Botrytis cinerea, which are common fungal pathogens that cause apple ring rot, cucumber powdery mildew, and grape gray mold blight, respectively. Taking polyethylene as the control, the terahertz time-domain spectra, and frequency-domain spectra of samples of the three pathogens were both measured. The absorption and refraction characteristics of these samples in the range of 0.1-2.0 THz were calculated and analyzed, and samples were then divided using the KS algorithm. Terahertz spectrum-image data blocks of the pathogen samples were preprocessed, and the dimensions of data were reduced using non-local mean filtering and the SPA algorithm, respectively. K-nearest neighbors (KNN), support vector machine (SVM), and BP neural network (BPNN), and other algorithms were used for analysis of terahertz images at characteristic frequencies, and for investigating the identification model. The model was quantitatively evaluated, and its imaging visualization was studied. The results suggest that there are significant differences among P. piricola, E. cichoracearum, and B. cinerea in absorption and refraction in the terahertz band. SVM modeling identification results of the three pathogens at the frequency of 1.376 THz were satisfactory, with an Rp of 0.9649, RMSEP of 0.0273, and a high (93.8212%) comprehensive evaluation index F1-score, and a clearly identifiable visualization effect. This study demonstrated the potential of terahertz spectroscopy to be used for identification of common crop pathogens and has provided technical references for the rapid diagnosis and early warning of agricultural diseases.

Foliar sprays of three plant resistance inducers, including chitosan (CH), potassium sorbate (PS) (C6H7kO2), and potassium bicarbonates (PB) (KHCO3), were used for resistance inducing against Erysiphe cichoracearum DC (powdery mildew) infecting okra plants. Experiments under green house and field conditions showed that, the powdery mildew disease severity was significantly reduced with all tested treatments of CH, PS, and PB in comparison with untreated control. CH at 0.5% and 0.75% (w/v) plus PS at 1.0% and 2.0% and/or PB at 2.0% or 3.0% recorded as the most effective treatments. Moreover, the highest values of vegetative studies and yield were observed with such treatments. CH and potassium salts treatments reflected many compounds of defense singles which leading to the activation power defense system in okra plant. The highest records of reduction in powdery mildew were accompanied with increasing in total phenolic, protein content and increased the activity of polyphenol oxidase, peroxidase, chitinase, and β-1,3-glucanase in okra plants. Meanwhile, single treatments of CH, PS, and PB at high concentration (0.75%, 2.0%, and/or 3.0%) caused considerable effects. Therefore, application of CH and potassium salts as natural and chemical inducers by foliar methods can be used to control of powdery mildew disease at early stages of growth and led to a maximum fruit yield in okra plants.

Powdery mildew (PM), which is mainly caused by Podosphaera xanthii, is a serious biotrophic pathogen disease affecting field-grown and greenhouse-grown cucurbit crops worldwide. Because fungicides poorly control PM, the development and cultivation of PM-resistant varieties is critical. A homolog of SGT1 (suppressor of the G2 allele of skp1), which encodes a key component of the plant disease-associated signal transduction pathway, was previously identified through a transcriptomic analysis of a PM-resistant pumpkin (Cucurbita moschata) inbred line infected with PM. In this study, we have characterized this SGT1 homolog in C. moschata, and investigated its effects on biotic stress resistance. Subcellular localization results revealed that CmSGT1 is present in the nucleus. Additionally, CmSGT1 expression levels in the PM-resistant material was strongly induced by PM, salicylic acid (SA) and hydrogen peroxide (H2O2). In contrast, SA and H2O2 downregulated CmSGT1 expression in the PM-susceptible material. The ethephon (Eth) and methyl jasmonate (MeJA) treatments upregulated CmSGT1 expression in both plant materials. The constitutive overexpression of CmSGT1 in Nicotiana benthamiana (N. benthamiana) minimized the PM symptoms on the leaves of PM-infected seedlings, accelerated the onset of cell necrosis, and enhanced the accumulation of H2O2. Furthermore, the expression levels of PR1a and PR5, which are SA signaling transduction markers, were higher in the transgenic plants than in wild-type plants. Thus, the transgenic N. benthamiana plants were significantly more resistant to Erysiphe cichoracearum than the wild-type plants. This increased resistance was correlated with cell death, H2O2 accumulation, and upregulated expression of SA-dependent defense genes. However, the chlorosis and yellowing of plant materials and the concentration of bacteria at infection sites were greater in the transgenic N. benthamiana plants than in the wild-type plants in response to infections by the pathogens responsible for bacterial wilt and scab. Therefore, CmSGT1-overexpressing N. benthamiana plants were hypersensitive to these two diseases. The results of this study may represent valuable genetic information for the breeding of disease-resistant pumpkin varieties, and may also help to reveal the molecular mechanism underlying CmSGT1 functions.

A double-stranded RNA (dsRNA) HBJZ1506 recovered from the phytopathogenic fungus Erysiphe cichoracearum infecting Calendula officinalis in Jingzhou, Hubei Province, China, was sequenced. HBJZ1506 comprises 11,908 nucleotides (nt) and contains a 11,859-nt-long open reading frame (ORF) coding for a polypeptide that is 61 % identical to that of a putative endornavirus named grapevine endophyte endornavirus (GeEV). The putative polyprotein has an RNA-dependent RNA polymerase (RdRp) domain and an RNA helicase domain, which show homology to and have an arrangement that is similar to that of their counterparts in approved or putative endornaviruses. In a phylogenetic tree constructed using amino acid sequences of the RdRp region of HBJZ1506 and selected endornaviruses, HBJZ1506 clustered with endornaviruses and formed a well-supported monophyletic branch with GeEV. These results suggest that HBJZ1506 might represent a novel endornavirus, for which the name Erysiphe cichoracearum endornavirus (EcEV) is proposed.

In this study, we cloned a new chitinase gene, EuCHIT2, from Eucommia ulmoides Oliver (E. ulmoides) using rapid amplification of cDNA ends (RACE) technology and constructed an overexpression vector, pSH-35S-EuCHIT2, to introduce it into tobacco (Nicotiana tabacum cv. Xanthi). Resistance to Erysiphe cichoracearum de Candolle (E. cichoracearum DC.) and molecular mechanisms in the transgenic tobacco were determined by drop inoculation, spore counting, determination of physicochemical indicators, and analysis of gene expression. The chitinase activity and resistance to E. cichoracearum DC. were significantly higher in the transgenic tobacco than in wild-type tobacco (p < 0.05). The activities of peroxidase (POD) and catalase (CAT), after inoculation with E. cichoracearum DC., were higher in the transgenic tobacco than in the wild-type. Conversely, the malondialdehyde (MDA) content was significantly lower in the transgenic tobacco than the wild-type before and after inoculation. In addition, our study also indicated that the resistance to E. cichoracearum DC. might involve the salicylic acid (SA) and jasmonic acid (JA) pathways, because the expression levels of pathogenesis-related gene 1 (PR-1a) and coronatine-insensitive 1 (COI1) were significantly increased and decreased, respectively, after inoculation with E. cichoracearum DC. The present study supports the notion that PR-1a and POD participate in resistance to E. cichoracearum DC. in the transgenic tobacco plants.

The Robinia pseudoacacia plant extract has been reported to have protective effect against cucumber powdery mildew (Sphaerotheca fuliginea). In this study, the active compound of R. pseudoacacia was isolated from the plant extract, and the structure was identified to be d -Pinitol by nuclear magnetic resonance. d -Pinitol, as a known compound, has important physiological activity on plant osmotic tolerance and medicinal activities on human health. This study is the first to report the antifungal activity of d -pinitol on an obligate parasite S. fuliginea and tried to develop a phytochemical fungicide. The evaluation in the growth chamber showed that the control effect of d -pinitol and its formulation against cucumber powdery mildew disease was 80.7% and 94.4%, at a concentration of 0.5 mg/ml. This formulation was further tested in a greenhouse to evaluate its control effect against cucumber (S. fuliginea) and tobacco (Erysiphe cichoracearum) powdery mildew under natural condition. The efficacy of d -pinitol in both trials was better than that of positive control at the recommended concentration. The content of d -pinitol in this plant was 25 mg/g (w/w, dry leaves weight) as determined by gas chromatography. The abundant biomass of d -pinitol in R. pseudoacacia plant extract makes it more economical in practical use. Our study provides a base for the future exploitation of d -pinitol as a natural phytochemical fungicide.

A series of new N,N'-diacylhydrazine derivatives were designed and synthesized. Their structures were verified by 1H-NMR, mass spectra (MS) and elemental analysis. The antifungal activities of these N,N'-diacylhydrazines were evaluated. The bioassay results showed that most of these N,N'-diacylhydrazines showed excellent antifungal activities against Cladosporium cucumerinum, Corynespora cassiicola, Sclerotinia sclerotiorum, Erysiphe cichoracearum, and Colletotrichum orbiculare in vivo. The half maximal effective concentration (EC50) of one of the compounds was also determined, and found to be comparable with a commercial drug. To further investigate the structure-activity relationship, comparative molecular field analysis (CoMFA) was performed on the basis of antifungal activity data. Both the steric and electronic field distributions of CoMFA are in good agreement in this study.

Resveratrol is a stilbene compound that is synthesized by plants in response to biotic stress and has been linked to health benefits associated with the consumption of certain foods and food products, such as grapes and wine. The final step in the biosynthesis of resveratrol is catalyzed by the enzyme stilbene synthase (STS). Here, we assessed the expression of two STS genes (VqSTS36 and VpSTS36) from the wild grape species Vitis quinquangularis (accession 'Shang-24'; powdery mildew (PM) resistant) and Vitis pseudoreticulata (accession 'Hunan-1'; PM susceptible) following infection by Uncinula necator (Schw.) Burr, the causal agent of PM disease. Some correlation was observed between the relative levels of STS36 transcript and disease resistance. We also cloned the 5' upstream sequence of both VpSTS36 and VqSTS36 and generated a series of 5' VqSTS36 promoter deletions fused to the GUS reporter gene in order to analyze expression in response to wounding, the application of exogenous stress-associated hormones, and biotic stress in tobacco leaves. The promoter was shown to be induced by the hormone salicylic acid (SA), inoculation with the fungal pathogen Erysiphe cichoracearum, and by wounding. These results suggest that VqSTS36 is regulated by biotic stresses and that it plays an important role in mediating disease resistance in grape.

High-performance liquid chromatographic (HPLC) analysis of chloroform fraction (CF) of cow urine showed rich pool of phenolic acids. Antifungal and antibacterial bioassays of CF have shown its tremendous efficacy against some fungal plant pathogens as well as human pathogenic bacteria at very low concentrations. The CF also inhibited powdery mildew (Erysiphe cichoracearum) of balsam (Impatiens balsamania) under field conditions during pre- and post-inoculation treatments. HPLC analysis of pre- and post-inoculation-treated plant leaves indicated that CF induced phenolic acid synthesis as compared to control. The results revealed that CF of cow urine has the potential for controlling some important human diseases. The result on balsam powdery mildew is a good signal that CF may also be effective against other plant diseases in the field.

NAC (for NAM, ATAF1, 2, and CUC2) family genes encode plant-specific transcription factors that play important roles in plant development regulation and in abiotic and biotic stresses. However, the function of NAC genes in grapevines is not clear. A novel NAC transcription factor, designated as VpNAC1, was isolated from Chinese wild Vitis pseudoreticulata. It belongs to the TERN subgroup and is a nuclear-targeting protein and functions as a transcriptional activator. Moreover, VpNAC1 was induced by the fungus Erysiphe necator and the exogenous hormones, particularly salicylic acid, methyl jasmonate and ethylene. Over-expression of VpNAC1 in tobacco plants enhanced their resistance to Erysiphe cichoracearum and Phytophthora parasitica var. nicotianae Tucker. These results suggest that VpNAC1 acts as a positive regulator in biotic stresses.

A series of new N,N'-diacylhydrazine derivatives were synthesized efficiently under microwave irradiation. Their structures were characterized by (1) H NMR, MS, and elemental analysis. Various biological activities of these compounds were tested. Most of them exhibited higher herbicidal activities against dicotyledonous weeds than monocotyledonous weeds. In addition, favorable in vivo fungicidal activities were also found of these compounds against Cladosporium cucumerinum, Corynespora cassiicola, Sclerotinia sclerotiorum(Lib.)de Bary, Erysiphe cichoracearum, and Colletotrichum orbiculare (Berk aLMont) Arx. All compounds displayed excellent plant growth regulatory activities: 100% inhibition was achieved against the radicle growth of cucumber. To further investigate the structure-activity relationship, comparative molecular field analysis was performed on the basis of herbicidal activity data, resulting in a statistically reliable model with good predictive power (r(2) = 0.913, q(2) =0.556). Based on the calculation, five additional novel compounds were designed and synthesized. Satisfyingly, compound 4u displayed excellent herbicidal activity (94.7%) at 1500 g/ha, although it is less active than 2,4-D. Meanwhile, this compound also exhibited good fungicidal activity against C. orbiculare (Berk aLMont) Arx (82.16%).

Neem cake is used as a soil amendment. It releases nutrient into the soil very slowly. It is also an insect repellent. It improves the physical as well as biological conditions of the soil such as soil aeration, water holding capacity and also the microflora in the rhizosphere. Aqueous extract of neem cake was used against powdery mildew (Erysiphe cichoracearum) of balsam (Impatiens balsaminia) in the field at 25, 50, 75 and 100%. The efficacy was observed even at low concentrations (25%). Foliar application of aqueous extract of neem cake induced synthesis of phenolic acids in balsam. Maximum phenolic acid was detected in balsam plant leaves treated with 50% neem cake followed by 75% in both pre-and post-inoculation treatments. The induction of phenolic acid in plants was correlated with the induction of resistance in treated plants against powdery mildew.

Powdery mildew, caused by Erysiphe cichoracearum or Podosphaera fusca, is a common disease of gerbera daisy (Gerbera jamesonii) grown in Florida. Previous studies demonstrated that silicon reduces powdery mildew in Arabidopsis, cucumber, grape, strawberry, and wheat. In this study, two silicon (Si) sources, calcium silicate and potassium silicate, were evaluated for their ability to reduce powdery mildew in gerbera ‘Snow White’. The effect of calcium silicate in flower quality and the silicon uptake was also determined. Calcium silicate was not effective in reducing powdery mildew or in improving flower quality. The silicon content of gerberas treated with potassium silicate was slightly greater than that in plants treated with calcium silicate. However, the severity of powdery mildew was not reduced by potassium silicate. The results suggest that silicon may not be useful for managing this disease of gerbera daisy, possibly due to the low accumulation of silicon by gerbera leaves.

Effectiveness of Azoxystrobin in the Control ofErysiphe CichoracearumandPseudoperonospora Cubensison CucumberThe bioefficacy of azoxystrobin (Amistar 25 SC) was tested against cucumber downy mildew and powdery mildew diseases. The two season trials of field studies revealed that the disease progression of cucumber downy mildew and powdery mildew was successfully arrested by azoxystrobin. Spraying of azoxystrobin at various doses (31.25, 62.50 and 125g a.s./ha) revealed that 125 g a.s./ha (500 ml/ha) was considered as the optimum dose for the control of these diseases of cucumber. The treatment also recorded the highest yield of 13.23 and 14.46 tonnes/ha in the first and second season, respectively. No phytotoxic effect of azoxystrobin was observed in the both field trials even at four times of the recommended dose 125 g a.s./ha. The persistence of azoxystrobin at 250 and 500 g a.s./ha was observed up to seven days after last spraying. However, the persistence of azoxystrobin at 31.25, 62.50 and 125 a.s./ha was observed up to three to five days after last spraying. The safe waiting period for the harvest of cucumber fruits was 1.53 days in the first field trial and 2.37 days in the second field trial, respectively at azoxystrobin 125 g a.s./ha. The residues of azoxystrobin were at below detectable level (BDL) in the harvested cucumber fruits.

Tobacco leaf sections were treated with actin inhibitors, i.e., cytochalasins, to determine the effects of actin depolymerization on tobacco defense responses. Inoculation of the leaf sections with the pathogen Erysiphe cichoracearum, depolymerized the actin cytoskeleton, priming the cells for a hypersensitive response-like cell death. Further, expression of the acidic PR1 and PR2 genes were induced in cytochalasin-treated leaf sections. The intensity of the cytochalasin effects on the defense responses was closely correlated with the extent of actin depolymerization. This suggests that plant cells may perceive perturbation of the actin cytoskeleton, and this stimulus may trigger plant defense responses.

Cross-talk between signal transduction pathways is a central feature of the tightly regulated plant defense signaling network. The potential synergism or antagonism between defense pathways is determined by recognition of the type of pathogen or pathogen-derived elicitor. Our studies have identified WRKY70 as a node of convergence for integrating salicylic acid (SA)- and jasmonic acid (JA)-mediated signaling events during plant response to bacterial pathogens. Here, we challenged transgenic plants altered in WRKY70 expression as well as WRKY70 knockout mutants of Arabidopsis with the fungal pathogens Alternaria brassicicola and Erysiphe cichoracearum to elucidate the role of WRKY70 in modulating the balance between distinct defense responses. Gain or loss of WRKY70 function causes opposite effects on JA-mediated resistance to A. brassicicola and the SA-mediated resistance to E. cichoracearum. While the up-regulation of WRKY70 caused enhanced resistance to E. cichoracearum, it compromised plant resistance to A. brassicicola. Conversely, down-regulation or insertional inactivation of WRKY70 impaired plant resistance to E. cichoracearum. Over-expression of WRKY70 resulted in the suppression of several JA responses including expression of a subset of JA- and A. brassicicola-responsive genes. We show that this WRKY70-controlled suppression of JA-signaling is partly executed by NPR1. The results indicate that WRKY70 has a pivotal role in determining the balance between SA-dependent and JA-dependent defense pathways.

Chitin is a major component of fungal walls and insect exoskeletons. Plants produce chitinases upon pathogen attack and chito-oligomers induce defense responses in plants, though the exact mechanism behind this response is unknown. Using the ATH1 Affymetrix microarrays consisting of about 23,000 genes, we examined the response of Arabidopsis (Arabidopsis thaliana) seedlings to chito-octamers and hydrolyzed chitin after 30 min of treatment. The expression patterns elicited by the chito-octamer and hydrolyzed chitin were similar. Microarray expression profiles for several genes were verified via northern analysis or quantitative reverse transcription-PCR. We characterized T-DNA insertion mutants for nine chito-oligomer responsive genes. Three of the mutants were more susceptible to the fungal pathogen, powdery mildew, than wild type as measured by conidiophore production. These three mutants included mutants of genes for two disease resistance-like proteins and a putative E3 ligase. The isolation of loss-of-function mutants with enhanced disease susceptibility provides direct evidence that the chito-octamer is an important oligosaccharide elicitor of plant defenses. Also, this study demonstrates the value of microarray data for identifying new components of uncharacterized signaling pathways.

The Arabidopsis genome contains six NPR1-related genes. Given the pivotal role played by NPR1 in controlling salicylic acid (SA)-mediated gene expression and disease resistance, functional characterization of other family members appears to be justified. Reverse genetics was used to analyze the role of one NPR1-like gene, which we called NPR4. The NPR4 protein shares 36% identity with NPR1 and interacts with the same spectrum of TGA transcription factors in yeast two-hybrid assays. Plants with T-DNA insertions in NPR4 are more susceptible to the virulent bacterial pathogen Pseudomonas syringe pv. tomato DC3000. This phenotype is complemented by expression of the wild type NPR4 coding region. As determined by the parasite reproduction, the npr4-1 mutant is more susceptible to the fungal pathogen Erysiphe cichoracearum, but does not differ markedly from wild type in its interaction with virulent and avirulent strains of the oomycete Peronospora parasitica. In leaves of wild-type plants, NPR4 mRNA levels increase following pathogen challenge or SA treatment, and decrease rapidly following methyl jasmonic acid (MeJA) treatment. Transcripts of the pathogenesis-related (PR) genes PR-1, PR-2, and PR-5 are only marginally reduced in the npr4-1 mutant following pathogen challenge or SA treatment. This reduction of PR gene expression is more pronounced when leaves are challenged with the bacterial pathogen following SA treatment. Expression of the jasmonic acid-dependent pathway marker gene PDF1.2 is compromised in npr4-1 leaves following application of MeJA or a combination of SA and MeJA. These results indicate that NPR4 is required for basal defense against pathogens, and that it may be implicated in the cross-talk between the SA- and JA-dependent signaling pathways.

*Summary Powdery mildews and other obligate biotrophic pathogens are highly adapted to their hosts and often show limited host ranges. One facet of such host specialization is likely to be penetration of the host cell wall, a major barrier to infection. A mutation in the pmr5 gene rendered Arabidopsis resistant to the powdery mildew species Erysiphe cichoracearum and Erysiphe orontii, but not to the unrelated pathogens Pseudomonas syringae or Peronospora parasitica. PMR5 belongs to a large family of plant-specific genes of unknown function. pmr5-mediated resistance did not require signaling through either the salicylic acid or jasmonic acid/ ethylene defense pathways, suggesting resistance in this mutant may be due either to the loss of a susceptibility factor or to the activation of a novel form of defense. Based on Fourier transform infrared analysis, the pmr5 cell walls were enriched in pectin and exhibited a reduced degree of pectin modification relative to wild-type cell walls. In addition, the mutant had smaller cells, suggesting a defect in cell expansion. A double mutant with pmr6 (defective in a glycosylphosphatidylinositol-anchored pectate lyase-like gene) exhibited a strong increase in total uronic acid content and a more severe reduction in size, relative to the single mutants, suggesting that the two genes affect pectin composition, either directly or indirectly, via different mechanisms. These two mutants highlight the importance of the host cell wall in plant‐microbe interactions.

The diffraction-limited spot size of synchrotron-based IR microscopes provides cell-specific, spectrochemical imaging of cleared leaf, stem and root tissues of the model genetic organism Arabidopsis thaliana, and mutant plants created either by T-DNA insertional inactivation or chemical mutagenesis. Spectra in the wavelength region from 6 to 12 lm provide chemical and physical information on the cell wall polysaccharides of mutants lacking particular biosynthetic enzymes (‘‘Cellulose synthase-like’’ genes). In parallel experiments, synchrotron IR microscopy delineates the role of Arabidopsis cell wall enzymes as susceptibility factors to the fungus Erysiphe cichoracearum, a causative agent of powdery mildew disease. Three genes, pmr4, pmr5, and pmr6 have been characterized by these methods, and biochemical relations between two of the genes suggested by IR spectroscopy and multivariate statistical techniques could not have been inferred through classical molecular biology. In ecological experiments, live plants can also be imaged in small microcosms with mid-IR transmitting ZnSe windows. Small exudate molecules may be spatially mapped in relation to root architecture at diffraction-limited resolution, and the effect of microbial symbioses on the quantity and quality of exudates inferred. Synchrotron IR microscopy provides a useful adjunct to molecular biological methods and underground observatories in the ongoing assessment of the role of root–soil–microbe communication.

Plants attacked by pathogens rapidly deposit callose, a β-1,3-glucan, at wound sites. Traditionally, this deposition is thought to reinforce the cell wall and is regarded as a defense response. Surprisingly, here we found that powdery mildew resistant 4 ( pmr4 ), a mutant lacking pathogen-induced callose, became resistant to pathogens, rather than more susceptible. This resistance was due to mutation of a callose synthase, resulting in a loss of the induced callose response. Double-mutant analysis indicated that blocking the salicylic acid (SA) defense signaling pathway was sufficient to restore susceptibility to pmr4 mutants. Thus, callose or callose synthase negatively regulates the SA pathway.

A transgenic Arabidopsis line containing a chimeric PR-1∷luciferase (LUC) reporter gene was subjected to mutagenesis with activation tags. Screening of lines via high-throughput LUC imaging identified a number of dominant Arabidopsis mutants that exhibited enhanced PR-1 gene expression. Here, we report the characterization of one of these mutants, designated activated disease resistance (adr) 1. This line showed constitutive expression of a number of key defense marker genes and accumulated salicylic acid but not ethylene or jasmonic acid. Furthermore, adr1 plants exhibited resistance against the biotrophic pathogens Peronospora parasitica and Erysiphe cichoracearum but not the necrotrophic fungus Botrytis cinerea. Analysis of a series of adr1 double mutants suggested that adr1-mediated resistance against P. parasitica was salicylic acid (SA)-dependent, while resistance against E. cichoracearum was both SA-dependent and partially NPR1-dependent. The ADR1 gene encoded a protein possessing a number of key features, including homology to subdomains of protein kinases, a nucleotide binding domain, and leucine-rich repeats. The controlled, transient expression of ADR1 conveyed striking disease resistance in the absence of yield penalty, highlighting the potential utility of this gene in crop protection.

The actin cytoskeleton is a key player in defense responses during early stages of infection by fungal pathogens. To investigate molecular mechanisms of actin-related defense responses, a cultured tobacco ( Nicotiana tabacum L.) BY-2 cell system was devised. When conidia were directly deposited on BY-2 cells, neither a pathogen, Erysiphe cichoracearum, nor a non-pathogen, Erysiphe pisi, was able to form appressoria or haustoria on BY-2 cells. On the other hand, conidia of the powdery mildews formed appressoria on BY-2 cells if they were covered with a thin hydrophobic membrane of Formvar. Percentages of appressoria formation of the powdery mildews on the Formvar-covered BY-2 cells were mostly the same as those on leaf epidermal cells. The pathogen successfully penetrated through the membrane into BY-2 cells and formed haustoria, whereas penetration attempts of the non-pathogen were completely rejected by the BY-2 cells similar to attempts on leaf epidermal cells. On the other hand, when BY-2 cells were treated with actin cytoskeleton-depolymerizing agents, cytochalasins, the non-pathogen became able to penetrate and form haustoria in BY-2 cells. Simultaneously, cytochalasin inhibited callose deposition at penetration sites of the non-pathogen. These results demonstrated that the actin cytoskeleton plays an important role in defense mechanisms against fungal penetration, even in the dedifferentiated cultured cells. The newly devised Formvar-covered cultured cell system will be a useful tool for molecular dissection of signal perception and defense mechanisms of plant cells during the early stage of fungal attack.

For obligate parasites like Erysiphe cichoracearum, manipulation of nitrogen (N) and potassium (K) nutrition may provide an alternative control method for powdery mildew in greenhouse crops. Subsequently, Hiemalis begonias “Hilda” and “Renaissance” were grown in separate experiments with a factorial combination of three N (30, 120, 240 mg L−1) and three K (30, 120, 240 mg L−1) rates applied at each irrigation. One‐half the plants in each treatment were inoculated with E. cichoracearum, while the remaining plants were sprayed regularly with the fungicide triadimefon to prevent disease development. Plant growth and powdery mildew incidence in both cultivars were significantly influenced by N fertilization and pathogen inoculation, but relatively unaffected by K fertility. Shoot dry mass in both cultivars increased with increasing N rate up to 120 mg N/L, but decreased from pathogen inoculation. This latter response increased in magnitude with increasing N rate in “Hilda”, but not in “Renaissance”. ...

In Arabidopsis spp., the jasmonate (JA) response pathway generally is required for defenses against necrotrophic pathogens and chewing insects, while the salicylic acid (SA) response pathway is generally required for specific, resistance (R) gene-mediated defenses against both biotrophic and necrotrophic pathogens. For example, SA-dependent defenses are required for resistance to the biotrophic fungal pathogen Erysiphe cichoracearum UCSC1 and the bacterial pathogen Pseudomonas syringae pv. maculicola, and also are expressed during response to the green peach aphid Myzus persicae. However, recent evidence indicates that the expression of JA-dependent defenses also may confer resistance to E. cichoracearum. To confirm and to extend this observation, we have compared the disease and pest resistance of wild-type Arabidopsis plants with that of the mutants coi1, which is insensitive to JA, and cev1, which has constitutive JA signaling. Measurements of the colonization of these plants by E. cichoracearum, P. syringae pv. maculicola, and M. persicae indicated that activation of the JA signal pathway enhanced resistance, and was associated with the activation of JA-dependent defense genes and the suppression of SA-dependent defense genes. We conclude that JA and SA induce alternative defense pathways that can confer resistance to the same pathogens and pests.

Plants of the discovered chlorophyll-deficient mutant of oak (ML) display enhanced disease resistance to the fungus Erysiphe cichoracearum, causal agent of powdery mildew. Quantitative imaging of chlorophyll (Chl) fluorescence revealed that the net photosynthetic rate (PN) declined progressively in both untreated and invaded ML leaves as well as in inoculated wild-type (WT) leaves. Images of non-photochemical fluorescence quenching (NPQ) in both untreated and infected mutant leaves suggested that the capacity of Calvin cycle had been reduced and that there was a complex metabolic heterogeneity within the ML leaf. The ML mutant accumulates reactive oxygen species, ROS (H2O2) from the oxidative burst followed by spontaneous cell death that mimic the hypersensitive response. Reduction in pathogen sporulation on ML leaves correlated with the accumulation of soluble saccharides and a more rapid induction of defence responses including expression of some defence proteins (β-1,3-glucanase and chitinase). Unlike to WT plants, ML- conferred phenotype activates and/or de-represses multiple defence responses, making them more easily induced by pathogens.

We studied the effects of exogenous salicylic acid on the level of endogenous cytokinins and abscisic and salicylic acids in the tissues of leaves of phloxes contrasting in resistance against the powdery mildew causative agent: susceptible Phlox paniculata L. and resistant Ph. setacea L. Studies were carried out under the conditions of biotic stress. The initial level of salicylic and abscisic acids and cytokinins is the highest in the resistant phlox species. After treatment with salicylic species, the total level of cytokinins and endogenous salicylic acid increased in both species. When the treated phlox species were infected by the powdery mildew causative agent, the level of abscisic and salicylic acids increased in the susceptible Ph. paniculata, while that of cytokinins increased in the resistant Ph. setacea. The role of salicylic acid in the induction of plant defense reactions against phytopathogens is discussed.

When supplied via roots to tobacco host plants, aqueous solutions of allopurinol, a specific inhibitor of xanthine oxidase and dehydrogenase, markedly reduced or completely prevented the visible development of tobacco powdery mildew fungus Erysiphe cichoracearum(E. orontii) at concentrations as low as 25–50 μ M administered for periods as short as 2 days. The duration of this allopurinol-dependent protection from the pathogen was of at least 20 days after the last administration. If supplied as foliar sprays at concentrations up to 1600 μ M , allopurinol was not absorbed by the leaf tissues and did not affect the fungal infection. Histological observations revealed that on tobacco plants treated with allopurinol via roots, a sharp reduction inE. cichoracearum mycelial development started only 48 h after inoculation (after formation of the first haustoria) and was accompanied by a strong delay and reduction of sporulation. The proportion of haustoria partially or entirely embedded in thick translucent sheaths (possibly callosic in nature) increased significantly in allopurinol irrigated plants reaching about 41% of the total haustoria (compared to 9% in controls) 7 days post-inoculation. No effects of allopurinol supply was observed on Blumeria graminis and Erysiphe trifolii development on wheat and clover plants, respectively. The present results are consistent with the view that allopurinol affects pathogen growth and sporulation by inhibition of xanthine dehydrogenase in the plant, the pathogen or both organisms.

Tobacco cv. Havana 425 acquired resistance to a compatible isolate of Erysiphe cichoracearum after infection by a strain of potato virus Y (PVYN) that causes veinal necrosis; another common strain (PVYO) that does not cause necrosis gave less protection. Hydroxyproline-rich glycoproteins (HRGPs), believed to be involved in resistance, were determined by analysing hydroxyproline (Hyp) in purified cell walls. Hyp content increased significantly in PVYN-protected leaves, compared with untreated controls, 2–4 days after necrotic lesion symptoms developed. No further increase in Hyp was noted in PVYN-protected leaves after E. cichoracearum challenge. Hyp increases were significantly higher in protected leaves of plants showing symptoms on day 7 than on day 10. Infection with the PVYO strain caused significant decrease in Hyp content, compared with uninoculated controls. Inoculation of virus-free plants with E. cichoracearum induced moderate and transitory Hyp increases on day 2 or 3, followed by a quick decrease associated with a weak response by the compatible host. It is suggested that HRGP accumulation induced by PVYN (but not by PVYO) causes changes in the host cell wall that result in resistance to E. cichoracearum.

A decrease of the polyamine content of tobacco leaves inoculated with fungal, bacterial and viral pathogens differing in symptom severity (mosaic, chlorosis, necrosis) was observed. The extent of the decrease was not related to the type of pathogens but to the severity of damage symptoms; hence, the polyamine decline may be regarded as a common response of tobacco to damage produced by pathogens.

The human lysozyme gene, which is assembled by the stepwise ligation of chemically synthesized oligonucleotides, was introduced into tobacco (Nicotiana tabacum cv `SR1') by the Agrobacterium-mediated method. The introduced human lysozyme gene was highly expressed under the control of the cauliflower mosaic virus 35S promoter, and the gene product accumulated in the transgenic tobacco plants. The transgenic tobacco plants showed enhanced resistance against the fungus Erysiphe cichoracearum - both conidia formation and mycelial growth were reduced, and the size of the colony was diminished. Microscopic observation revealed that the transgenic tobacco plants carried the resistant phenotype, analogous to that of the resistant cultivar `Kokubu' which had been selected by conventional breeding. Growth of the phytopathogenic bacterium Pseudomonas syringae pv. tabaci was also strongly retarded in the transgenic tobacco, and the chlorotic halo of the disease symptom was reduced to 17% of that observed in the wild-type tobacco. Thus, the introduction of a human lysozyme gene is an effective approach to protect crops against both fungal and bacterial diseases.

Changes in lipoxygenase (LOX) protein pattern and/or activity were investigated in relation to acquired resistance of cucumber (Cucumis sativus L.) leaves against two powdery mildews, Sphaerotheca fuliginea (Schlecht) Salmon and Erysiphe cichoracearum DC et Merat. Acquired resistance was established by spraying leaves with salicylic acid (SA) or 2,6-dichloroisonicotinic acid (INA) and estimated in whole plants by infested leaf area compared to control plants. SA was more effective than INA. According to Western blots, untreated cucumber leaves contained a 97 kDa LOX form, which remained unchanged for up to 48 h after pathogen inoculation. Upon treatment with SA alone for 24 h or with INA plus pathogen, an additional 95 kDa LOX form appeared which had an isoelectric point in the alkaline range. For the induction of this form, a threshold concentration of 1 mM SA was required, higher SA concentrations did not change LOX-95 expression which remained similar between 24 h and 96 h but further increased upon mildew inoculation. Phloem exudates contained only the LOX-97 form, in intercellular washing fluid no LOX was detected. dichloroisonicotinic localization revealed LOX protein in the cytosol of the mesophyll cells without differences between the forms.

Plant injuries activate signal transduction cascades mediated by the plant hormones, which lead to enhanced expression of defence related genes and/or to changes in the emission of volatile organic compounds that can act as semiochemicals. In this research we demostrated that infection with the biotrophic pathogen Golovinomyces cichoracearum (DC.) V.P. Heluta (ex Erysiphe cichoracearum DC.), the causal agent of powdery mildew, led in the susceptible host Nicotiana tabacum L. cv Havana 425 to an increased emission of volatile compounds including Methyl-jasmonate (MeJA), (E)-2-hexenal and (E)-β-ocimene. Furthermore we investigated the role of these volatiles in the plant-pathogen interaction. Exogenous application of MeJA induced in tobacco an increase in the transcripts level of the defence related genes lipoxygenase, allene oxide cyclase and defensin and a decrease in the severity of the infection. Qualitative and quantitative differences in volatile compounds emission were showed also in MeJA-treated plants, where the emission of (E)-β-ocimene was significantly increased instead (E)-2-hexenal was not detected. Application of (E)-2-hexenal reduced the severity of powdery mildew while application of (E)-β-ocimene did not. Since (E)-2-hexenal did not activate in tobacco the accumulation of the above reported genes transcripts and the plant cell death, the reduction of the infection severity could be attributable to its inhibitory activity on the fungal germ tube growth. Our data highlight the contributions of natural substances that can act, directly or indirectly, against phytopathogens. In the global context of sustainability, food safety and environmental protection, such semiochemicals represent an alternative and promising approach to integrated pest management.

Local infections of either TMV or TNV in tobacco plants cv. Havana 425 (hypersensitive to TMV) proved effective in inducing systemic resistance to subsequent inoculation with the powdery mildew fungus Erysiphe cichoracearum DC. The proportion of leaf surface invaded by this pathogen and the amount of conidia it produced were both significantly lower in virus inoculated plants than in non-inoculated controls. However, the decrease in sporulation rate was less regularly observed than the reduction in leaf area infected. TMV was more effective than TNV in protecting tobacco plants from powdery mildew. E. cichoracearum is thus added to the list of challenge pathogens to which TMV or TNV are known to induce resistance in the host plants. Necrotic lesions caused to the leaves by local treatment with Ethephon (an ethylene-releasing compound) also conferred to tobacco some degree of systemic resistance to the same fungal pathogen, more frequently visible as a reduction of leaf area invaded. The protection due to the Ethephon lesions was in present experiments less marked than that of TMV. No effects against subsequent powdery mildew infection were obtained when point freeze necrotic lesions were provoked on the plants.

Summary The coumarin umbelliferone was identified as a stress metabolite of the medicinal plant Chamomilla recutita . The increased content of umbelliferone was already observed in leaves 12 hrs after abiotic stress elicitation by CuCl 2 . In 48 hrs this amount rose approximately 10 times. In the same period of time, a decrease of ( Z )- and ( E )-2- β -D-glucopyranosyloxy-4-methoxy cinnamic acid and an increase of herniarin was found. In the leaves infected by powdery mildew Erysiphe cichoracearum DC., the increase of umbelliferone content was also observed.

The effect of soluble potassium silicate applied to cucumber (Cucumis sativus L.), muskmelon (C. melo L.), and zucchini squash (Cucurbita pepo L.) on the severity of powdery mildew was examined. Application methods included amending nutrient solutions to a concentration of 1.7 mM Si and foliar sprays containing 1.7, 8.5, 17, and 34 mM Si. Untreated plants and plants sprayed with distilled water were used as controls. The leaves of all plants were inoculated with known concentrations of conidia of Sphaerotheca fuliginea (Schlecht.:Fr.) Poll. (cucumber and mum Mathai et al., 1978; Volk et al., 1958) and powdery mildew diseases of barley (Erysiphe gruminis DC. f. sp. hordei E m . Marchal on Hordeum vulgare L.) (Jiang et al., 1989), wheat (E. graminis D.C. f. sp. tritici Em. Marchal on Triticum aestivum L.) (Leusch and Buchenauer, 1989), and cucumber (S. fuliginea) (Menzies et al., 1991a). Previous studies of Si effects on plant disease have involved root absorption of Si from either soil or soilless media. Although the amendment of soilless media with Si can be adapted to greenhouse and similar industries (Menzies et al., 1991a; Samuels et al., 1991b), large amounts of Si must be applied to soils to adequately control diseases. For example, basal dressings of 250 and 500 kg sodium silicate/ha were required to reduce sheath blight of rice (Mathai et al., 1978) and an equivalent of 4500 kg SiO2/ha was necessary to control powdery mildew of wheat (Leusch and Buchenauer, 1989). A reduction of the incidence of a wilt pathogen of cucumber requires the application of 2000 to 4000 kg calcium silicate/ha or 2250 to 4500 kg potassium silicate/ ha (Miyake and Takahashi, 1983b). Foliar application of Si to field plants is potentially a viable alternative to root-zone applifor publication 5 Nov. 1991. Accepted for publication 6 May 1992. esearch Station Contribution no. 440. We acknowlege the assistance muels, D. Vianzon, C. Koch, and T. Helmer, the statistical advice , Research Station, Agriculture Canada, Vancouver, B.C., and the the B.C. Greenhouse Vegetable Research Council and the Science B.C. Mention of a trademark or proprietary product does not imply nt of the products named or criticism of other products that may also . The cost of publishing this paper was defrayed in part by the payage charges. Under postal regulations, this paper therefore must be rked advertisement solely to indicate this fact. Scientist. cation. This method of Si application to control disease has been reported only once, to our knowledge. Aleshin et al. (1986) applied sprays of sodium metasilicate (440 mg·liter-1) and 1-ethoxysilatran (180 mg·liter -l) and reduced the degree of rice blast infestation on both resistant and susceptible rice cultivars. The objective of our study was to determine the extent of control of powdery mildew diseases of cucumber, muskmelon, and zucchini squash achieved through foliar or root applications of soluble potassium silicate, and the duration of control that may be obtained with foliar applications. Materials and Methods Long English cucumber (‘Corona’), muskmelon (‘Earlisweet’) and zucchini squash (‘Select’) were used in the experiments. Effective Si concentrations for foliar application. Cucumber, muskmelon, and zucchini squash plants were grown from seed sown in rockwool cubes (Grodan, Roermond, Holland), arranged at random on three greenhouse benches. Eight randomly chosen plants of each species were watered as needed with a nutrient solution containing ( in mM ): 1.75 Si, 13.0 NO3, 1.5 H 2P O4, 7.5 K, 3.5 Ca, 1.0 Mg, and 1.0 to 1.5 SO4; and (in μ M ) 18.8 Fe, 5.5 Mn, 0.9 Zn, 0.2 Cu, 18.1 B, and 1.0 Mo, with a pH of 6.0. Silicon was added in the form of potassium silicate as product K6 (National Silicates Ltd., Toronto, Ont.). The remaining plants were watered with a solution (pH 6.0) containing the same nutrients but without added potassium silicate (the Si and K contents of the solution were 0.05 and 7.0 m M , respectively). Foliar treatments were applied when cucumber and zucchini squash had two fully expanded leaves and muskmelon had three. Treatments included an untreated control, a distilled water spray (pH 5.5), and Si sprays of 1.7, 8.5 (not applied to the zucchini squash), and 17.0 mM (also containing 0.5, 2.5, and 5.0 mM K, respectively). The Si sprays were prepared by diluting the appropriate amount of potassium silicate in distilled water and adjusting to pH 5.5 with phosphoric acid. A drop of Tween 20 J. Amer. Soc. Hort. Sci. 117(6):902-905. 1992. Table 1. The effect of Si treatments on the number of colonies of powdery mildew on cucumber, muskmelon, and zucchini squash. z Colonies established (no.)

Gerbera (Gerbera jamesonii) is one of the most popular ornamental plants in the world, used as cut or vase flower. The experiment aimed to evaluate the effect of milk in natura to control powdery mildew (Erysiphe cichoracearum) on gerbera. The treatments tested were: two concentrations of cow's milk in natura (8 and 16%), with and without adjuvant (vegetal oil), three fungicides (fenarimol -6 g a.i.100 L-1 H2O, chlorothalonil -150 g a.i.100 L-1 H2O and azoxystrobin + mineral oil - 10 g a.i.100 L-1 H2O) and control treatment. The area under the disease progress curve (AUDPC) was calculated for each plot based on disease severity. Milk in natura applied with adjuvant controlled the disease and did not allow the infection and development of pathogen. The addition of adjuvant improves the efficiency of milk in natura, but it requires subsequent washing of plants with H2O + detergent. The fungicide fenarimol promoted the best control and also the best gerbera visual aspect. The fungicide azoxystrobin + mineral oil and the chlorothalonil were phytotoxic to gerbera plants, affecting the aspect of leaves and flowers.A gérbera (Gerbera jamesonii) é uma das mais populares plantas ornamentais do mundo, tanto como flor de corte como de vaso. O objetivo deste trabalho foi avaliar o leite in natura no controle do oídio (Erysiphe cichoracearum) na cultura da gérbera. Foram utilizadas duas concentrações de leite de vaca in natura (8 e 16%), com e sem adição de adjuvante (óleo vegetal), três fungicidas (fenarimol -6 g i.a.100 L-1 H2O, chlorothalonil -150 g i.a.100 L-1 H2O e azoxystrobin + óleo mineral -10 g i.a.100 L-1 H2O) e testemunha. Com os dados de severidade foi calculada a área abaixo da curva de progresso da doença (AACPD). O leite in natura aplicado com o adjuvante controlou o oídio, não permitindo a instalação e o desenvolvimento do patógeno. O uso do adjuvante melhorou a eficiência do leite in natura, no entanto requer a lavagem posterior das plantas com H2O + detergente. O fungicida fenarimol promoveu melhor controle de oídio e aspecto visual das plantas de gérbera. O fungicida azoxystrobin + óleo mineral e o chlorothalonil foram fitotóxicos à planta de gérbera, o que prejudicou a aparência das folhas e flores.

We report a role for the Arabidopsis (Arabidopsis thaliana) RESURRECTION1 (RST1) gene in plant defense. The rst1 mutant exhibits enhanced susceptibility to the biotrophic fungal pathogen Erysiphe cichoracearum but enhanced resistance to the necrotrophic fungal pathogens Botrytis cinerea and Alternaria brassicicola. RST1 encodes a novel protein that localizes to the plasma membrane and is predicted to contain 11 transmembrane domains. Disease responses in rst1 correlate with higher levels of jasmonic acid (JA) and increased basal and B. cinerea-induced expression of the plant defensin PDF1.2 gene but reduced E. cichoracearum-inducible salicylic acid levels and expression of pathogenesis-related genes PR1 and PR2. These results are consistent with rst1's varied resistance and susceptibility to pathogens of different life styles. Cuticular lipids, both cutin monomers and cuticular waxes, on rst1 leaves were significantly elevated, indicating a role for RST1 in the suppression of leaf cuticle lipid synthesis. The rst1 cuticle exhibits normal permeability, however, indicating that the disease responses of rst1 are not due to changes in this cuticle property. Double mutant analysis revealed that the coi1 mutation (causing defective JA signaling) is completely epistatic to rst1, whereas the ein2 mutation (causing defective ethylene signaling) is partially epistatic to rst1, for resistance to B. cinerea. The rst1 mutation thus defines a unique combination of disease responses to biotrophic and necrotrophic fungi in that it antagonizes salicylic acid-dependent defense and enhances JA-mediated defense through a mechanism that also controls cuticle synthesis.

The response of four naturally occurring biotypes of Epilobium ciliatum and four sources of Senecio vulgaris to the herbicide atrazine were compared with their susceptibility to the powdery mildews Sphaerotheca epilobii and Erysiphe cichoracearum. Biotypes that were resistant to atrazine were also resistant to mildew. Mechanisms that might explain the association between atrazine resistance and mildew resistance are discussed, along with possible implications of these findings for farmland ecology and for the production of herbicide- and mildew-resistant crop plants.

Systemic acquired resistance (SAR) is an inducible defence mechanism which plays a central role in protecting plants from microbial pathogen attack. Guided by bioassays, a new chemical inducer of SAR was isolated from the extracts of Strobilanthes cusia and identified to be 3-acetonyl-3-hydroxyoxindole (AHO), a derivative of isatin. Tobacco plants treated with AHO exhibited enhanced resistance to tobacco mosaic virus (TMV) and to the fungal pathogen Erysiphe cichoracearum (powdery mildew), accompanied by increased levels of pathogenesis-related gene 1 (PR-1) expression, salicylic acid (SA) accumulation and phenylalanine ammonia-lyase activity. To study the mode of action of AHO, its ability to induce PR-1 expression and TMV resistance in nahG transgenic plants expressing salicylate hydroxylase, which prevents the accumulation of SA, was analysed. AHO treatment did not induce TMV resistance or PR-1 expression in nahG transgenic plants, suggesting that AHO acts upstream of SA in the SAR signalling pathway. In addition, using two-dimensional gel electrophoresis combined with mass spectrometry, five AHO-induced plant proteins were identified which were homologous to the effector proteins with which SA interacts. Our data suggest that AHO may represent a novel class of inducer that stimulates SA-mediated defence responses.

Aircraft-applied dust and liquid sulfur sprays were evaluated for control of powdery mildew (Erysiphe cichmacearumDC), on rill irrigated potatoes (cv. Russet Burbank). Either form of sulfur applied weekly or biweekly usually controlledE. chichoracearum through September, but not in October. Significant yield increases were obtained in only two of five trials. The small differences in disease severity between weekly and biweekly applications of sulfur were not significant. Sulfur gave very little control if applied after infection was established. Applications of liquid sulfur, the formulation less likely to cause environmental problems, should be started at the first trace of stipples on stems and continued biweekly throughout the season.

We screened for mutants of Arabidopsis thaliana that displayed enhanced disease resistance to the powdery mildew pathogen Erysiphe cichoracearum and identified the edr3 mutant, which formed large gray lesions upon infection with E. cichoracearum and supported very little sporulation. The edr3-mediated disease resistance and cell death phenotypes were dependent on salicylic acid signaling, but independent of ethylene and jasmonic acid signaling. In addition, edr3 plants displayed enhanced susceptibility to the necrotrophic fungal pathogen Botrytis cinerea, but showed normal responses to virulent and avirulent strains of Pseudomonas syringae pv. tomato. The EDR3 gene was isolated by positional cloning and found to encode Arabidopsis dynamin-related protein 1E (DRP1E). The edr3 mutation caused an amino acid substitution in the GTPase domain of DRP1E (proline 77 to leucine) that is predicted to block GTP hydrolysis, but not GTP binding. A T-DNA insertion allele in DRP1E did not cause powdery mildew-induced lesions, suggesting that this phenotype is caused by DRP1E being locked in the GTP-bound state, rather than by a loss of DRP1E activity. Analysis of DRP1E-green fluorescent protein fusion proteins revealed that DRP1E is at least partially localized to mitochondria. These observations suggest a mechanistic link between salicylic acid signaling, mitochondria and programmed cell death in plants.

In two meteorologically quite different years, 2002 and 2003, efficacy of three natural substances with a fungicidal activity (sulphur, soya lecithin, salicylic acid) for control of Erysiphe cichoracearum on chicory was tested. In a block designed field experiment, there were statistically significant differences in the mean index of infection of exterior leaves, in the mean total weight and mean net weight of the plants (= total weight weight of removed damaged leaves). There was also a significant difference in firmness of the heads of nine chicory varieties that was established in both years. In 2002, when no extreme weather conditions occurred, the fungus spread to a substantially larger extent. Yet no statistically significant differences were found in the efficacy of environmentally friendly fungicidal substances for control of the fungus. In the hotter and drier year of 2003, which was less favourable for spread of the pathogen, sulphur-containing fungicide was the most effective. In 2002, chicory yield was lower than in 2003. Generally, yield loss due to removal of damaged leaves was from 30.7 to 45.0% in the first year, and from 11.3 to 24.8% in the second. The highest mean total yield and net yield of chicory were in plants, which were treated three times with sulphur-containing fungicide. In 2002, the most firm heads were in plants treated with sulphur. In 2003, no significant differences among substances were detected. The most infected with the powdery mildew caused by E. cichoracearum, were the less productive varieties of chicory. A statistically significant relationship was not found between the firmness of the heads and the degree of infection. Among different parameters in this experiment, the only relevant and high statistically significant positive correlation (r2 = 0.71) was determined between the total weight of the plants and yield loss of chicory due to infection with the fungus in question.

The plant genes required for the growth and reproduction of plant pathogens are largely unknown. In an effort to identify these genes, we isolated Arabidopsis mutants that do not support the normal growth of the powdery mildew pathogen Erysiphe cichoracearum . Here, we report on the cloning and characterization of one of these genes, PMR6 . PMR6 encodes a pectate lyase–like protein with a novel C-terminal domain. Consistent with its predicted gene function, mutations in PMR6 alter the composition of the plant cell wall, as shown by Fourier transform infrared spectroscopy. pmr6 -mediated resistance requires neither salicylic acid nor the ability to perceive jasmonic acid or ethylene, indicating that the resistance mechanism does not require the activation of well-described defense pathways. Thus, pmr6 resistance represents a novel form of disease resistance based on the loss of a gene required during a compatible interaction rather than the activation of known host defense pathways.

Narceine methyl ester and narceine are potent alkaloids which were isolated from Corydalis longipes were found effective in vitro at very low concentration, i.e., 100~500 ppm against spore germination of some test plant pathogenic fungi (Alternaria solani, A. tagetica, Cercospora abelmoschi, Curvularia maculans, Erysiphe cichoracearum, E. pisi, Fusarium udum, Helminthosporium oryzae, H. penniseti, Ustilago cynodontis). Among the test, phytopathogens the spores of F. udum, C. maculans and H. penniseti were highly sensitive at 200 ppm. However, spores of E. pisi, A. solani and A. tagetica were less sensitive at low concentration followed by other test fungi. Most of the fungi showed zero or nearly zero percent spore germination at 400 and 500 ppm.