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F. Oxysporum (f + oxysporum)
Selected AbstractsVolatile organic compounds: a potential direct long-distance mechanism for antagonistic action of Fusarium oxysporum strain MSA 35ENVIRONMENTAL MICROBIOLOGY, Issue 4 2009Daniela Minerdi Summary Fusarium oxysporum MSA 35 [wild-type (WT) strain] is an antagonistic Fusarium that lives in association with a consortium of bacteria belonging to the genera Serratia, Achromobacter, Bacillus and Stenotrophomonas in an Italian soil suppressive to Fusarium wilt. Typing experiments and virulence tests provided evidence that the F. oxysporum isolate when cured of the bacterial symbionts [the cured (CU) form], is pathogenic, causing wilt symptoms identical to those caused by F. oxysporum f. sp. lactucae. Here, we demonstrate that small volatile organic compounds (VOCs) emitted from the WT strain negatively influence the mycelial growth of different formae speciales of F. oxysporum. Furthermore, these VOCs repress gene expression of two putative virulence genes in F. oxysporum lactucae strain Fuslat10, a fungus against which the WT strain MSA 35 has antagonistic activity. The VOC profile of the WT and CU fungus shows different compositions. Sesquiterpenes, mainly caryophyllene, were present in the headspace only of WT MSA 35. No sesquiterpenes were found in the volatiles of ectosymbiotic Serratia sp. strain DM1 and Achromobacter sp. strain MM1. Bacterial volatiles had no effects on the growth of the different ff. spp. of F. oxysporum examined. Hyphae grown with VOC from WT F. oxysporum f. sp. lactucae strain MSA 35 were hydrophobic whereas those grown without VOCs were not, suggesting a correlation between the presence of volatiles in the atmosphere and the phenotype of the mycelium. This is the first report of VOC production by antagonistic F. oxysporum MSA 35 and their effects on pathogenic F. oxysporum. The results obtained in this work led us to propose a new potential direct long-distance mechanism for antagonism by F. oxysporum MSA 35 mediated by VOCs. Antagonism could be the consequence of both reduction of pathogen mycelial growth and inhibition of pathogen virulence gene expression. [source] Diagnosis and detection of host-specific forms of Fusarium oxysporum,EPPO BULLETIN, Issue 3-4 2000R. P. Baayen Diagnosis and detection of host-specific forms of Fusarium oxysporum are traditionally based on the combination of diagnostic symptoms on the host with the presence of the fungus in the affected tissues. The classical approach is becoming increasingly problematic because more than one forma specialis may occur on a given host, along with non-pathogenic strains which are common soil and rhizosphere inhabitants. Neither formae speciales nor pathogenic races within formae speciales can be distinguished morphologically. Although united by joint pathogenicity to a given host, strains belonging to the same forma specialis need not be phylogenetically related. Development of diagnostics for host-specific groups in F. oxysporum requires monophyletic target groups. Recent studies on gene-genealogy and AFLP-based phylogenies show that the majority of formae speciales in F. oxysporum are polyphyletic (unnatural) and do not offer any prospects for the development of molecular diagnostics. In contrast, highly specific PCR primers have been developed for formae speciales (or races) that consist of a single clonal lineage, and for monophyletic groups of lineages within a forma specialis. Among others, specific PCR primers have thus been developed for F. oxysporum f. sp. basilici, specific races in F. oxysporum ff. spp. dianthi and gladioli, and for the EPPO A2 (EU II/A1) quarantine fungus F. oxysporum f. sp. albedinis which can reliably replace conventional isolation and pathogenicity testing procedures. [source] Genetic variation among Fusarium oxysporum isolates from cucumberEPPO BULLETIN, Issue 2 2000D. J. Vakalounakis Isolates of Fusarium oxysporum obtained from cucumber worldwide were classified into 3 groups by random amplified polymorphic DNA-polymerase chain reaction (RAPD-PCR). All isolates of f. sp. radicis-cucumerinum fall into one group. Isolates of races 1 and 2 of f. sp. cucumerinum fall into a second group related to isolates of f. sp. melonis and niveum. Isolates of race 3 fall into a third group, related to f. sp. momordicae. Because f. sp. radicis-cucumerinum has relatively recently been introduced into Greece, where it is actively spreading and very damaging, RAPD-PCR may be valuable in monitoring populations of F. oxysporum. [source] Leaf fungi of two wild plants in Assiut, EgyptFEDDES REPERTORIUM, Issue 7-8 2004S. K. Hemida Leaves of two wild species of the flora of Egypt: Calotropis procera (Ait.) Ait., Asclepiadaceae and Chrozophora plicata (Vahl) A.Juss. ex Spreng., Euphorbiaceae have been studied morphologically and mycologically, in addtion to air borne fungi. Fifty five species and two varieties belonging to 26 genera of phyllosphere and phylloplane fungi were isolated from both plant species on glucose- and cellulose-agar media. Mycological analysis was done monthly over six months (July to December, 2003). Alternariaalternata, Aspergillus fumigatus, A. flavus and A. niger were the basic fungal species found on leaf surfaces. Phylloplane of C. plicata caught specifically Chaetomiumglobosum, C.,spirale, Cochliobolus lunatus, Drechslera halodes, Fusarium incarnatum, F. oxysporum, Memnoniella echinata and Papulaspora sepedonioides. The total counts of phyllosphere fungi of C.,plicata were nearly twice as much as those of C.,procera regardless medium's type. Forty species and one variety belonging to 22 genera of air borne fungi were recovered all over the experimental period (six months). Alternaria, Aspergillus, Cladosporium and Penicillium were the most frequently isolated species. The presented results revealed that, leaf shape and density (hair density and type) may be the most important factors of the biodiversity of the fungal species on the studied taxa. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) Die Blätter zweier Wildarten aus der Flora Ägyptens: Calotropis procera (Ait.) Ait., Asclepiadeceae, und Chrozophora plicata(Vahl) A.Juss. ex Spreng., Euphorbiaceae, wurden in Bezug auf ihre Morphologie und Mykologie untersucht sowie zusätzlich auf ihre "luftgeborenen" Pilze. Auf beiden Arten wurden auf einem Glukose- bzw. Cellulose-Medium insgesamt 55 Arten und zwei Varietäten aus 26 Gattungen phyllosphärer und phylloplaner Pilze nachgewiesen. Die mykologischen Analysen wurden über einen Zeitraum von sechs Monaten (Juli bis Dezember 2003) durchgeführt. Alternariaalternata, Aspergillus fumigatus, A. flavus und A. niger waren die Basis-Pilzarten, die auf den Blattoberflächen ermittelt wurden. Auf C. plicata waren Chaetomiumglobosum, C. spirale, Cochliobolus lunatus, Drechslera halodes, Fusarium incarnatum, F. oxysporum, Memnoniella echinata und Papulaspora sepedonioides die häufigsten phylloplanen Arten. Ungeachtet des Mediumtyps war die Anzahl phyllosphärischer Pilze auf C. plicata etwa zweimal so hoch wie auf C. procera. Über die gesamte Versuchszeit von sechs Monaten wurden 40 Arten und eine Varietät aus 22 Gattungen "luftgeborener" Pilze beobachtet. Mit Alternaria, Aspergillus, Cladosporium und Penicillium fanden sich die am häufigsten isolierten Arten. Aus den erzielten Ergebnissen kann man ableiten, dass Blattform und Haare (Dichte und Typ) die wichtigsten Faktoren für die Biodiversität der untersuchten Pilzarten sind. [source] Composition and antifungal activity of essential oils isolated from Hypericum hyssopifolium and Hypericum heterophyllumFLAVOUR AND FRAGRANCE JOURNAL, Issue 1 2004A. Cakir Abstract The composition of the hydrodistilled essential oils obtained from the aerial parts of Hypericum hyssopifolium subsp. elongatum var. elongatum and H. heterophyllum Vent. were analysed by means of GC and GC,MS, and 66 compounds were determined in total. The oils showed remarkable differences in chemical composition. The oil of H. hyssopifolium, which is rich in monoterpenes, consists primarily of , -pinene (57.3%), , -pinene (9.0%), limonene (6.2%) and , -phellandrene (4.4%). The oil of H. heterophyllum was a complex mixture consisting mainly of sesquiterpenes (72.9% of the total oil). In this oil, isocaryophyllene (17.1%), , -pinene (11.6%), , -cadinene (9.5%), , -muurolene (8.2%), n -decane (5.8%), , -cadinene (5.5%) and , -caryophyllene (4.5%) were found to be major constituents. The two essential oils were tested for antifungal activity using microbial growth inhibition assays in vitro against 10 agricultural pathogenic fungi, which consisted of ,ve Fusarium species (F. oxysporum, F. culmorum, F. sambucinum, F. solani and F. acuminatum) and ,ve anastomosis groups of Rhizoctonia solani (AG-3, AG-4, AG-5, AG-9 and AG-11). In general, the oils showed moderate activity against several fungal species, viz F. acuminatum, AG-5 and AG-11. The most signi,cant results were obtained against AG-11 for H. heterophyllum oil. However, both oils increased the growth of some fungal species. In addition, the antifungal activity of 13 pure compounds identi,ed as major components in the essential oils of the Hypericum species studied were determined using microbial growth inhibition assays against the 10 fungal species mentioned above. Among these compounds, both , -caryophyllene oxide and , -terpineol were inhibitory to the growth of all fungi. Copyright © 2003 John Wiley & Sons, Ltd. [source] Pathogenicity of Fusarium verticillioides and Fusarium oxysporum on Pinus nigra seedlings in northwest SpainFOREST PATHOLOGY, Issue 2 2008P. Martín-Pinto Summary Fusarium verticillioides may be responsible for causing significant damping-off damage similar to that incited by F. oxysporum on forest seedlings, resulting in considerable losses in nurseries in northwest of Spain. Traditionally, F. oxysporum has been considered the most important agent of this disease in Spanish forest nurseries. However, recent studies have showed that F. verticillioides also has been frequently isolated from diseased plants. This has increased the necessity for a more comprehensive knowledge of the behaviour and pathogenicity of both Fusarium spp. isolated from these sites. The effect of Fusarium spp. on seed germination and on seedling mortality was analysed by inoculating the fungus at seeding. The in vitro growth of the two species was studied and is discussed in relation to in vivo virulence. Both species caused a reduction in seed germination and an increase in seedling mortality. Mortality caused by F. verticillioides treatments occurred sooner than that for F. oxysporum and the growth rate of F. verticillioides was also greater. [source] In vitro Selection for Fusarium Wilt Resistance in GladiolusJOURNAL OF INTEGRATIVE PLANT BIOLOGY, Issue 5 2008Idrees Ahmad Nasir Abstract Cormels pieces of four Fusarium susceptible Gladiolus cultivars (Friendship, Peter Pears, Victor Borge and Novalux) formed friable calli when cultured in vitro on Murashige and Skoog basal medium containing various concentrations of auxin and cytokinin. The friable calli established cell suspensions. Plantlet regeneration was obtained from the control callus, control cell suspension derived callus and in vitro selected Fusarium oxysporum Schlecht. resistant cell-lines of Friendship. The in vitro cormlets showed 85,95% germination after breaking dormancy of 8 weeks at 4 °C. Cell suspensions of all four Gladiolus cultivars were found to be highly sensitive to fusaric acid. Gradual increase in fusaric acid concentrations to the cell-suspension cultures decreased cell growth considerably. One albino plant was found from the second generation of the in vitro selected cell line of Friendship. The albino plant was found to be highly susceptible to F. oxysporum. The cormlets of all in vitro selected cell lines of Friendship were inoculated with a conidial suspension of the F. oxysporum before planting and were also sprayed with the same spore suspension for further characterization when the height of plants was about 6 cm. The four selected cell lines showed the same response whether or not they were inoculated with conidia of the F. oxysporum. Plantlets of all of the selected cell lines exhibited significant growth as compared with the control after application of conidia of the F. oxysporum. [source] Use of RAPD and ISSR Markers in Detection of Genetic Variation and Population Structure among Fusarium oxysporum f. sp. ciceris Isolates on Chickpea in TurkeyJOURNAL OF PHYTOPATHOLOGY, Issue 3 2008H. Bayraktar Abstract Genetic variation among the isolates of Fusarium oxysporum f. sp. ciceris, the causal agent of chickpea wilt worldwide, was analysed using pathogenicity tests and molecular markers , random amplified polymorphic DNA (RAPD) and inter-simple sequence repeat (ISSR) polymorphism. Hundred and eight isolates were obtained from diseased chickpea plants in 13 different provinces of Turkey, out of which 74 isolates were assessed using 30 arbitrary decamer primers and 20 ISSR primers. Unweighted pair-grouped method by arithmetic average cluster analysis of RAPD, ISSR and RAPD + ISSR datasets provided a substantially similar discrimination among Turkish isolates and divided into three major groups. Group 1, 2 and 3 consisted of 41, 18 and 15 isolates, respectively. These methods revealed a considerable genetic variation among Turkish isolates, but no correlation with regard to the clustering of isolates from different geographic regions. Analysis of molecular variance confirmed that most genetic variability resulted from the differences among isolates within regions. Our results also indicated that the low-genetic differentiation (FST) and high gene flow (Nm) among populations had a significant effect on the emergence and evolutionary development of F. oxysporum f. sp. ciceris. This is the first report on genetic diversity and population structure of F. oxysporum isolates on chickpea in Turkey. [source] Identification and Regulation of Genes from a Biocontrol Strain of Fusarium oxysporumJOURNAL OF PHYTOPATHOLOGY, Issue 9 2007D. R. Fravel Abstract Differential display with three time points revealed that thiram altered expression of numerous genes in the biocontrol fungus Fusarium oxysporum CS-20. Of the 101 bands purified from the differential display gel, 86 were successfully cloned, and 64 sequenced. Based on nucleic acid sequences, homology to known products was found using BLASTn for 26 sequences and homology to hypothetical proteins was found for six sequences, also from Gibberella zeae. One band (BM1 24-1) showed homology to an ABC transporter from three different fungi. Because of its association with detoxification functions, the ABC transporter was selected for further study. Mycelia of CS-20 were exposed to 25 ,g active ingredient (a.i.) thiram in liquid culture for various times from 0 to 8 h. Quantitative real-time PCR was used to evaluate gene expression. At 30 min after treatment with thiram, the ABC transporter was upregulated 20- to 25-fold relative to the control treatment. The ABC transporter was upregulated 15-fold at 1 h after treatment and 10-fold at 2 h. At 8 h after treatment, there was no difference between treated and non-treated for expression of the ABC transporter. Transcription of the gene encoding EST BM1 24-1 is induced in response to thiram treatment and may function in providing resistance in F. oxysporum isolate CS-20 to fungicides and other toxins. Tolerance to toxins may be critical to the successful inclusion of CS-20 in disease control strategies in cropping systems. [source] Chromatographic Characterization and Phytotoxic Activity of Fusarium oxysporum f. sp. albedinis and Saprophytic Strain ToxinsJOURNAL OF PHYTOPATHOLOGY, Issue 4 2005H. Amraoui Abstract The bayoud disease, vascular fusariosis of date palm tree (Phoenix dactylifera L.), is caused by the pathogenic fungus Fusarium oxysporum f. sp. albedinis. The characteristic symptoms of the bayoud disease were elicited on detached leaves of F. oxysporum f. sp. albedinis -susceptible cultivars of date palm trees, which were treated either with the FII (F. oxysporum f. sp. albedinis) fraction purified from the organic extracts of a F. oxysporum f. sp. albedinis liquid culture, or with a solution of fusaric acid. Enniatins, which are secreted by several Fusarium species, were tested at different concentrations and were not capable of inducing symptoms on such detached leaves. The FII (F. oxysporum f. sp. albedinis) fraction was unable to induce necrosis of potato slices, which indicates that it does not contain significant amounts of enniatins. The high-performance liquid chromatography (HPLC) profiles of the FII (F. oxysporum f. sp. albedinis) fraction showed toxic peaks different from fusaric acid. A fraction, named FII (AZ4), was obtained from culture filtrates of a saprophytic Fusarium strain maintained in the same cultural conditions as for the F. oxysporum f. sp. albedinis. The HPLC profile of the FII (AZ4) fraction did not show the characteristic phytotoxic peaks present in the FII (F. oxysporum f. sp. albedinis) fraction. This finding well agrees with the fact that the FII (AZ4) fraction is not toxic to detached date palm leaves. Moreover, the HPLC profiles of FII fractions obtained from other special forms of F. oxysporum are different the FII (F. oxysporum f. sp. albedinis) profile. The phytotoxic compounds purified from the FII (F. oxysporum f. sp. albedinis) fraction are probably new molecules that may help in understanding the pathogenesis of bayoud disease. [source] Isozyme Analysis and Soluble Mycelial Protein Pattern in Iranian Isolates of Several formae speciales of Fusarium oxysporumJOURNAL OF PHYTOPATHOLOGY, Issue 5 2004M. Mohammadi Abstract A total of 13 representative isolates of Fusarium oxysporum f. sp. melonis (FOM) from Iran, USA and France, eight isolates of seven formae speciales from Iran and one isolate of F. oxysporum f. sp. niveum from the USA were compared based on isozyme analysis and soluble mycelial protein pattern. Isozyme analyses of alkaline phosphatase (ALP), catalase (CAT), esterase (EST), malate dehydrogenase (MDH), superoxide dismutase (SOD) and xanthine dehydrogenase (XDH) revealed polymorphism among the F. oxysporum isolates in which 22 electrophoretic phenotypes (EP) were determined. At least 10 putative loci for these six enzymes were detected and they were all polymorphic. Maximum genetic diversity was observed in CAT, EST and XDH loci. Using UPGMA, the 22 isolates were separated into three main groups with one of the groups divided into two subgroups. Group I included isolates belonging to five formae speciales from Iran, whereas group II that included FOM isolates from both Iran and the USA was divided into two subgroups each containing the vast majority of the respective isolates from either country. Group III constituted FOM isolates from France and one pathogenic isolate on pepper from Iran. FOM isolates representing five different geographical regions from Iran belonged to two different races of 1 and 1,2Y and one vegetative compatibility group (VCG)0134 and thus were genetically homologous. Isozyme polymorphism in these isolates was highly correlated with VCG and geographical origins and to a lesser extent with races. Variations in soluble protein profile in FOM isolates were correlated with genetic distances determined in isozyme analysis. This study suggests that isozyme analysis could be a useful tool for identifying genetic diversity not only in FOM but also several formae speciales of F. oxysporum. [source] Micro-scale Systematic Sampling of Soil: Heterogeneity in Populations of Fusarium oxysporum, F. solani, F. roseum and F. moniliformeJOURNAL OF PHYTOPATHOLOGY, Issue 11-12 2000M. C. Rodríguez-Molina Abstract The variability of Fusarium spp. density in soil was studied in a field located in Badajoz (south-western Spain). The upper 40 cm of each side of a 1 m × 1 m × 1 m pit were sampled intensively, taking soil samples from points 10 cm apart. The species isolated were F. oxysporum, F. solani, F. roseum and F. moniliforme. For all four sides of the pit population densities of F. oxysporum, F. solani and F. roseum significantly decreased with increasing soil depth and for all the four layers significant differences were detected between sides of the pit. Horizontal variability also occurred on a smaller sampling scale: when a layer of a side was sampled, densities might be significantly different between points in the layer. However, no clear trend in horizontal variability was observed for any species. These findings demonstrate that Fusarium spp. populations were heterogeneously distributed in this reduced soil volume. Zusammenfassung Die Variabilität der Dichte von Fusarium spp. im Boden wurde in einem Feld in Badajoz (Südwestspanien) untersucht. Die oberen 40 cm jeder Seite einer 1 m × 1 m × 1 m großen Grube wurden intensiv beprobt, wobei im Abstand von jeweils 10 cm Bodenproben entnommen wurden. Aus den Proben wurden F. oxysporum, F. solani, F. roseum und F. moniliforme isoliert. An allen vier Seiten der Grube nahmen die Populationsdichten von F. oxysporum, F. solani und F. roseum mit zunehmender Bodentiefe signifikant ab. Bei allen vier Schichten wurden signifikante Unterschiede zwischen den Seiten der Grube festgestellt. Bei kleinerem Beprobungsmaßstab wurde auch horizontale Variabilität festgestellt: Wenn eine Schicht einer Seite beprobt wurde, unterschieden sich die Dichten zwischen den einzelnen Punkten der Schicht teilweise signifikant. Für keine Art war jedoch eine deutliche Tendenz bei der horizontalen Variabilität feststellbar. Die Ergebnisse zeigten, daß die Populationen von Fusarium spp. in diesem kleinen Bodenvolumen heterogen verteilt waren. [source] Survival of Sclerotium cepivorum Sclerotia and Fusarium oxysporum Chlamydospores in Soil Amended with Cruciferous ResiduesJOURNAL OF PHYTOPATHOLOGY, Issue 6 2000U. SmolinskaArticle first published online: 28 JUN 200 Abstract The use of cruciferous plant residues to reduce the amount of sclerotia of Sclerotium cepivorum and chlamydospores of Fusarium oxysporum f. sp. lycopersici in soil was investigated. Air-dried and crushed mustard (Brassica juncea) added to the soil effectively reduced the viability of fungal propagules. Consequently, the reduction of white rot of onion, caused by S. cepivorum and wild of tomato caused by F. oxysporum was observed. The addition of rapeseed (Brassica. napus cv. Bolko and B. napus cv. Gorczanski) residues to soil also resulted in a significant decrease of number of S. cepivorum sclerotia but the effect on F. oxysporum chlamydospores was variable. Introduction of the plant material increased the total number of bacteria, spore-forming bacteria, fluorescent pseudomonads, actinomycetes, and fungi in soil. One year after the soil amendment, the amount of sporeforming bacteria in treatments with cruciferous residues was higher as compared to the control soil without plant residues. The possible contribution of the decomposition of plant residues and soil micro-organisms to the reduction of the pathogens population is discussed. Zusammenfassung Untersucht wurde die Eignung von Kreuzblütler-Pflanzenresten zur Reduktion der Zahl der Sklerotien von Sclerotium cepivorum und der Chlamydosporen von Fusarium oxysporum f. sp. lycopersici im Boden. Wurden luftgetrocknete und zerkleinerte Senfpflanzen (Brassica juncea) als Bodenzusatz verwendet, so war die Lebensfähigkeit der pilzlichen Überdauerungsorgane deutlich verringert. Entsprechend wurde ein Rückgang der durch S. cepivorum hervorgerufenen Weißfäule der Zwiebel und der durch F. oxysporum hervorgerufenen Tomatenwelke beobachtet. Der Zusatz von Raps-Pflanzenresten (Brassica napus cv. Bolko und B. napus cv. Gorczanski) zum Boden führte ebenfalls zu einer signifikanten Abnahme der Zahl von S.-cepivorum -Sklerotien, doch die Wirkung auf die Chlamydosporen von F. oxysporum war unterschiedlich. Die Einbringung des Pflanzenmaterials erhöhte die Gesamtzahl an Bakterien, sporenbildenden Bakterien, fluoreszierenden Pseudomonaden, Actinomyceten und Pilzen im Boden. Ein Jahr nach der Bodenanreicherung war die Zahl sporenbildender Bakterien in den Varianten mit Kreuzblütler-Resten höher als in den Böden der Kontrollvariante ohne Pflanzenreste. Der mögliche Einfluß der Zersetzung der Pflanzenreste und der Bodenmikroorganismen auf die Reduktion der Pathogenpopulation wird diskutiert. [source] Increased effectiveness of the Trichoderma harzianum isolate T-78 against Fusarium wilt on melon plants under nursery conditionsJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 5 2009Agustina Bernal-Vicente Abstract BACKGROUND: The use of isolates of the genus Trichoderma to control Fusarium wilt in melon plants is one of the most recent and effective alternatives to chemical treatments. In this work we have studied the immobilization of the isolate Trichoderma harzianum T-78 on different carriers as an efficient method to control vascular Fusarium wilt of melon in nurseries. Different formulations were developed: liquids (spore suspension, guar gum and carboxymethylcellulose) and solids (bentonite, vermiculite and wheat bran). RESULTS: The introduction of F. oxysporum resulted in a significant decrease in seedling fresh weight. The treatments which gave a lesser reduction in weight and showing a greater biocontrol effect were the liquid conidial suspension and the solid treatments with bentonite and superficial vermiculite. Microbiological analyses revealed that the conidial suspension and all the solid treatments, except wheat bran, significantly decreased F. oxysporum populations. Of all the treatments assayed, bentonite produced the greatest decline in the F. oxysporum population. CONCLUSIONS: The most effective treatments against Fusarium wilt on melon plants were the solid treatments bentonite and superficial vermiculite. These two treatments gave the greatest plant weight, the lowest percentage of infected plants and the greatest T. harzianum population throughout the assay. Copyright © 2009 Society of Chemical Industry [source] Antifungal effects of aminosulphoxide and disulphide derivativesMYCOSES, Issue 3 2006Veerle Wittebolle Summary 2-Benzenesulphinyl-(1,4)-naphtoquinone and 14 derivatives were synthesised and were used to evaluate their cytotoxicity against a human myelomonocyte cell line and their antifungal activity against two yeast, i.e. Candida albicans and C. tropicalis and against two filamentous fungi such as Aspergillus niger and Fusarium oxysporum and against one dermatophyte, namely Trichophyton tonsurans. The cytotoxicity and antifungal activities were investigated in comparison with amphotericin B as reference drug. No compound was significantly more toxic than amphotericin B at 0.2 ,g ml,1. The best results of antifungal activity were obtained with GFL 10, GFL 13 and GFL 30 on C. tropicalis, F. oxysporum and T. tonsurans. For C. albicans and A. niger, there was no difference between amphotericin B and the other molecules. The sterol quantitation, the time-kill curves were carried out for these three compounds in order to confirm their action in ergosterol synthesis. Time-kill curves showed a fungistatic activity. For C. tropicalis GFL 10, GFL 13 and GFL 30 increased the growth delay better than amphotericin B, in contrast to F. oxysporum. As for T. tonsurans, GFL10 and GFL13 gave a delay, but the effect of GFL 30 was a bit less marked. [source] Allelochemical tricin in rice hull and its aurone isomer against rice seedling rot diseasePEST MANAGEMENT SCIENCE (FORMERLY: PESTICIDE SCIENCE), Issue 9 2010Chui-Hua Kong Abstract BACKGROUND: One promising area of rice disease management is the potential of exploiting biological control agents. Rice seedling rot disease caused by soil-borne pathogenic fungi has become a dominant disease problem because of greater use of direct seeding. Rice hull has been potentially used to control paddy weeds, but little information is available on rice disease. This study was conducted to investigate the relationships between disease incidence and soil amended with tricin-releasing rice hull, and to assess fungicidal activity of tricin and its synthesised aurone isomer, with an attempt to develop an allelochemical-based fungicide against rice seedling rot disease. RESULTS: Tricin was detected in all hulls of 12 rice cultivars tested, but its contents in rice hulls varied greatly with the cultivar and genotype. Tricin in rice hulls was released into the soil once amended. Disease incidence was significantly reduced by soil amended with rice hull. Tricin-rich rice hull amendment greatly suppressed soil-borne pathogenic fungi Fusarium oxysporum Schlecht. and Rhizoctonia solani Kühn which cause rice seedling rot disease. In attempting to obtain enough tricin for further experiments, the aurone isomer (5,7,4,-trihydroxy-3,,5,-dimethoxyaurone) of tricin rather than tricin itself was unexpectedly synthesised. This aurone isomer had much stronger fungicidal activity on both F. oxysporum and R. solani than tricin itself. CONCLUSION: Soil amended with tricin-rich rice hull was associated with reduced risk of developing seedling rot disease. The tricin isomer, aurone, is more effective against rice seedling rot disease than tricin itself, making it an ideal lead compound for new fungicide discovery. Copyright © 2010 Society of Chemical Industry [source] Recent developments in the molecular discrimination of formae speciales of Fusarium oxysporumPEST MANAGEMENT SCIENCE (FORMERLY: PESTICIDE SCIENCE), Issue 8 2008Bart Lievens Abstract Rapid and reliable detection and identification of potential plant pathogens is required for taking appropriate and timely disease management measures. For many microbial species of which all strains generally are plant pathogens on a known host range, this has become quite straightforward. However, for some fungal species this is quite a challenge. One of these is Fusarium oxysporum Schlechtend:Fr., which, as a species, has a very broad host range, while individual strains are usually highly host-specific. Moreover, many strains of this fungus are non-pathogenic soil inhabitants. Thus, with regard to effective disease management, identification below the species level is highly desirable. So far, the genetic basis of host specificity in F. oxysporum is poorly understood. Furthermore, strains that infect a particular plant species are not necessarily more closely related to each other than to strains that infect other hosts. Despite these difficulties, recently an increasing number of studies have reported the successful development of molecular markers to discriminate F. oxysporum strains below the species level. Copyright © 2008 Society of Chemical Industry [source] Fungitoxic phenols from carnation (Dianthus caryophyllus) effective against Fusarium oxysporum f. sp. dianthiPHYTOCHEMICAL ANALYSIS, Issue 1 2003Paolo Curir Abstract The phenol compositions of two cultivars of carnation (Dianthus caryophyllus) namely "Gloriana" and "Roland", which are partially and highly resistant, respectively, to Fusarium oxysporum f. sp. dianthi have been investigated with the aim of determining if endogenous phenols could have an anti-fungal effect against the pathogen. Analyses were performed on healthy and F. oxysporum -inoculated in vitro tissues, and on in vivo plants. Two benzoic acid derivatives, protocatechuic acid (3,4-dihydroxybenzoic acid) and vanillic acid (4-hydroxy-3-methoxybenzoic acid), were found within healthy and inoculated tissues of both cultivars, together with the flavonol glycoside peltatoside (3-[6-O-(,- L -arabinopyranosyl)-,- D -glucopyranosyl] quercetin). These molecules proved to be only slightly inhibitory towards the pathogen. 2,6-Dimethoxybenzoic acid was detected in small amounts only in the inoculated cultivar "Gloriana", while the highly resistant cultivar "Roland" showed the presence of the flavone datiscetin (3,5,7,2,-tetrahydroxyflavone). The latter compound exhibited an appreciable fungitoxic activity towards F. oxysporum f. sp. dianthi. Copyright © 2003 John Wiley & Sons, Ltd. [source] Wounding induces resistance to pathogens with different lifestyles in tomato: role of ethylene in cross-protectionPLANT CELL & ENVIRONMENT, Issue 11 2007DORIANA FRANCIA ABSTRACT Many reports point to the existence of a network of regulatory signalling occurring in plants during the interaction with micro-organisms (biotic stress) and abiotic stresses such as wounding. However, the focus is on shared intermediates/components and/or common molecular outputs in differently triggered signalling pathways, and not on the degree and modes of effective influence between abiotic and biotic stresses nor the range of true plant,pathogen interactions open to such influence. We report on local and systemic wound-induced protection in tomato (Solanum lycopersicum L.) to four pathogens with a range of lifestyles (Botrytis cinerea, Fusarium oxysporum f.sp. lycopersici, Phytophthora capsici and Pseudomonas syringae pv. tomato). The role of ethylene (ET) in the phenomenon and in the induction by wounding of several markers of defense was investigated by using the never-ripe tomato mutant plants impaired in ET perception. We showed that PINIIb, PR1b, PR5, PR7 and peroxidase (POD) are influenced locally and/or systemically by wounding and, with the exception of POD activity, by ET perception. We also demonstrated that ET, although not essential, is positively (B. cinerea, P. capsici) or negatively (F. oxysporum, P. syringae pv. tomato) involved not only in basal but also in wound-induced resistance to each pathogen. [source] Plant defence reactions against fusarium wilt in chickpea induced by incompatible race 0 of Fusarium oxysporum f.sp. ciceris and nonhost isolates of F. oxysporumPLANT PATHOLOGY, Issue 6 2002J. M. Cachinero Germinated seeds of ,kabuli' chickpea cv. ICCV 4 were inoculated with a conidial suspension of the incompatible race 0 of Fusarium oxysporum f.sp. ciceris (Foc) or of nonhost F. oxysporum resistance ,inducers', and 3 days later were challenged by root dip with a conidial suspension of highly virulent Foc race 5. Prior inoculation with inducers delayed the onset of symptoms and/or significantly reduced the final amount of fusarium wilt caused by race 5. However, the extent of disease suppression varied with the nature of the inducing agent; the nonhost isolates of F. oxysporum were more effective at disease suppression than the incompatible Foc race 0. Inoculation with the inducers gave rise to synthesis of maackiain and medicarpin phytoalexins in inoculated seedlings; these did not accumulate in plant tissues but were released into the inoculum suspension. Inoculation with inducers also resulted in accumulation of chitinase, ,-1,3-glucanase and peroxidase activities in plant roots. These defence-related responses were induced more consistently and intensely by nonhost isolates of F. oxysporum than by incompatible Foc race 0. The phytoalexins and, to a lesser extent, the antifungal hydrolases, were also induced after challenge inoculation with Foc race 5. However, in this case the defence responses were induced in both preinduced and noninduced plants infected by the pathogen. It is concluded that the suppression of fusarium wilt in this study possibly involved an inhibitory effect on the pathogen of preinduced plant defences, rather than an increase in the expression of defence mechanisms of preinduced plants following a subsequent challenge inoculation. [source] Vegetative compatibility and heterokaryon stability in Fusarium oxysporum f.sp. radicis-lycopersici from ItalyPLANT PATHOLOGY, Issue 3 2001P. Di Primo Fusarium crown and root rot, caused by Fusarium oxysporum f.sp. radicis-lycopersici (Forl), is one of the most destructive soilborne diseases of tomato in Italy. Chlorate-resistant, nitrate-nonutilizing (nit) mutants were used to determine vegetative compatibility among 191 isolates of Forl collected in five geographic regions (Calabria, Emilia-Romagna, Liguria, Sardinia, Sicily) in Italy. The isolates were assigned to five vegetative compatibility groups (VCGs): 65 isolates to VCG 0090; 99 to VCG 0091; 23 to VCG 0092; two to VCG 0093; and two to VCG 0096. The population structure of Forl in Italy is similar to that reported for Israel, and differs from that found in North Atlantic European countries, where VCG 0094 is predominant. The stability of prototrophic heterokaryons originating from hyphal anastomosis between compatible complementary nit mutants was assessed through conidial analysis and mycelial mass transfer. Most monoconidial cultures (84%) recovered from 117 prototrophic heterokaryons were nit mutants, indicating that heterokaryons generally do not proliferate well through conidiation; most of the 177 prototrophic heterokaryons examined were unstable, and only 9% sustained prototrophic growth through the tenth mycelial transfer upon subculturing. The prototrophic growth is proposed to be maintained through restoration of the heterokaryotic state by continual anastomosis between adjacent homokaryotic hyphae. Since heterokaryosis is a prerequisite for parasexual recombination, we speculate that this mechanism is unlikely to play a major role in generating the VCG diversity found among Forl or other strains of F. oxysporum. [source] Disease complex in coffee involving Meloidogyne arabicida and Fusarium oxysporumPLANT PATHOLOGY, Issue 3 2000B. Bertrand Coffee corky-root disease, also called corchosis, was first detected in 1974 in a small area of Costa Rica where the root-knot nematode Meloidogyne arabicida is the dominant species. An epidemiological study revealed a constant association between Meloidogyne spp. and Fusarium sp. in cases of corky root. No corky root appears to have been reported in association with Meloidogyne exigua, which is the prevalent root-knot nematode on coffee in Costa Rica. Fusarium spp. are often cited as components of disease complexes in association with nematodes. Combined inoculations using M. arabicida or M. exigua with Fusarium oxysporum under controlled conditions showed that only the combination with M. arabicida produced corky-root symptoms on Coffea arabica cvs Caturra or Catuai. Fusarium oxysporum alone was nonpathogenic. Meloidogyne exigua or M. arabicida alone caused galls and reduction in shoot height, but no corky-root symptoms. When cultivars susceptible and resistant to M. arabicida were studied under field conditions for 5 years, all the susceptible cultivars exhibited corky-root symptoms on 40,80% of their root systems. Cultivars that were resistant to M. arabicida but not to M. exigua showed no corky root. These observations lead to the conclusion that corky-root disease has a complex etiology, and emphasize the dominant role of M. arabicida as a predisposing agent to subsequent invasion by F. oxysporum. Consequently, genetic resistance to M. arabicida appears to provide an effective strategy against the disease. [source] PCR detection of Fusarium oxysporum f.sp. gladioli race 1, causal agent of Gladiolus yellows disease, from infected cormsPLANT PATHOLOGY, Issue 1 2000De Haan Fusarium oxysporum f.sp. gladioli (FOG) race 1 infects both large- and small-flowered Gladiolus cultivars. Race 2 isolates infect only small-flowered cultivars but can be present as epiphytes on large-flowered plants. When 160 arbitrary 10-mer oligonucleotide primers were tested on FOG by PCR to find RAPD markers specific for race 1, the RAPD primer G12 amplified two discriminating DNA fragments, AB (609 bp) and EF (1196 bp), in race 1 isolates only. Both fragments were cloned and sequenced. Two pairs of race 1-specific primers for multiplex PCR were designed. Tests of 112 F. oxysporum isolates by PCR showed that, in almost all cases, race 1 isolates of vegetative compatibility group 0340 could be distinguished with these primers. Seven putative race 1 isolates did not react in multiplex PCR; hybridization studies with labelled AB and EF DNA fragments showed that these isolates belong to separate groups. A bioassay was developed to detect corms that were latently infected with FOG race 1. Gladiolus corms were homogenized and incubated for 5 days at 28°C in a semiselective medium to induce growth of Fusarium. Cultivated mycelium was isolated and subjected to the developed multiplex PCR after standard DNA isolation or disruption by microwave treatment. [source] Chemical modification of chitosan: synthesis and biological activity of new heterocyclic chitosan derivativesPOLYMER INTERNATIONAL, Issue 2 2008Mohamed EI Badawy Abstract BACKGROUND: Numerous works have been published on the chemical modification of chitosan; this polymer is still being modified, leading to various derivatives with improved properties. In the present study, heterocyclic aldehydes including furan-2-carbaldehyde, 5-methylfuran-2-carbaldehyde, 3-pyridine carboxyaldehyde, benzo[d][1,3]dioxole-5-carbaldehyde and 4-oxo-4H -chromene-3-carbaldehyde were reacted with chitosan by a reductive alkylation reaction to produce for the first time five new N -heterocyclic chitosan derivatives to improve the biological activity of chitosan against the most important economic plant pests including fungi and insects, in particular the cotton leafworm Spodoptera littoralis. RESULTS: The chemical structures of the synthesized compounds were confirmed by 1H NMR spectroscopy and the degree of substitution ranged from 0.30 to 0.43. The fungicidal assessment was investigated in vitro using a mycelia radial growth inhibition technique against soil-borne pathogenic fungi Fusarium oxysporum and Pythium debaryanum and the rice leaf blast Pyricularia grisea. The results showed that N -[(5-methylfuran-2-yl)methyl] chitosan was the most active against P. grisea with an EC50 value of 0.919 mg mL,1 while N -(benzo[d][1,3]dioxol-5-ylmethyl) chitosan and N -(methyl-4H -chromen-4-one) chitosan exhibited the most potent fungicidal activity against P. debaryanum and F. oxysporum. An insecticidal bioassay against the larvae of S. littoralis showed that N -(methyl-4H -chromen-4-one) chitosan exhibited a significant growth inhibition and antifeedant activity among the synthesized compounds. CONCLUSION: The chemical modification of chitosan molecule with a heterocyclic moiety led to an enhancement in the biological activity against the plant pathogenic fungi F. oxysporum, P. debaryanum and P. grisea and the cotton leafworm insect S. littoralis. Copyright © 2007 Society of Chemical Industry [source] Isotopologue fractionation during N2O production by fungal denitrificationRAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 24 2008Robin L. Sutka Identifying the importance of fungi to nitrous oxide (N2O) production requires a non-intrusive method for differentiating between fungal and bacterial N2O production such as natural abundance stable isotopes. We compare the isotopologue composition of N2O produced during nitrite reduction by the fungal denitrifiers Fusarium oxysporum and Cylindrocarpon tonkinense with published data for N2O production during bacterial nitrification and denitrification. The fractionation factors for bulk nitrogen isotope values for fungal denitrification were in the range ,74.7 to ,6.6,. There was an inverse relationship between the absolute value of the fractionation factors and the reaction rate constant. We interpret this in terms of variation in the relative importance of the rate constants for diffusion and enzymatic reduction in controlling the net isotope effect for N2O production during fungal denitrification. Over the course of nitrite reduction, the ,18O values for N2O remained constant and did not exhibit a relationship with the concentration characteristic of an isotope effect. This probably reflects isotopic exchange with water. Similar to the ,18O data, the site preference (SP; the difference in ,15N between the central and outer N atoms in N2O) was unrelated to concentration during nitrite reduction and, therefore, has the potential to act as a conservative tracer of production from fungal denitrification. The SP values of N2O produced by F. oxysporum and C. tonkinense were 37.1,±,2.5, and 36.9,±,2.8,, respectively. These SP values are similar to those obtained in pure culture studies of bacterial nitrification but quite distinct from SP values for bacterial denitrification. The large magnitude of the bulk nitrogen isotope fractionation and the ,18O values associated with fungal denitrification are distinct from bacterial production pathways; thus multiple isotopologue data holds much promise for resolving bacterial and fungal production. Our work further provides insight into the role that fungal and bacterial nitric oxide reductases have in determining site preference during N2O production. Copyright © 2008 John Wiley & Sons, Ltd. [source] Molecular detection of dermatophytes and nondermatophytes in onychomycosis by nested polymerase chain reaction based on 28S ribosomal RNA gene sequencesBRITISH JOURNAL OF DERMATOLOGY, Issue 5 2009M. Ebihara Summary Background, Onychomycosis is often caused by dermatophytes, but the role of nondermatophytes is underestimated due to the difficulty of identifying them by conventional direct microscopy and culture. Objectives, This study aims to detect nondermatophytes, as well as dermatophytes, in the nail samples of patients with onychomycosis using a polymerase chain reaction (PCR)-based culture-independent method. Materials and methods, The nested PCR assay targeting the sequence of the 28S ribosomal RNA gene was used to amplify fungal DNAs from 50 microscopy-positive nail specimens. Newly designed primer sets for dermatophyte universal, Trichophyton rubrum, T. mentagrophytes, Aspergillus spp., Scopulariopsis brevicaulis, Fusarium solani, F. oxysporum, F. verticillioides, Candida albicans and C. tropicalis were used after confirmation of their specificity. Results, Forty-seven cases (94%) were positive for fungal DNA, among which dermatophytes were detected in 39 cases (83·0%): T. rubrum in 35 cases (74·5%) and T. mentagrophytes in eight cases (17·0%). Surprisingly, nondermatophytes were detected in 18 cases (38·3%), both dermatophytes and nondermatophytes in 10 cases (21·3%) and nondermatophytes alone in eight cases (17·0%). Aspergillus spp. alone was observed in five cases (10·6%). Conclusions, This study indicates that most of the affected nail plates of patients with onychomycosis were positive for specific fungal DNAs, and suggests that nondermatophytes detected at high rates may be involved in the pathogenesis of onychomycosis. [source] Cloning and molecular characterization of the Hevea brasiliensis allergen Hev b 11, a class I chitinaseCLINICAL & EXPERIMENTAL ALLERGY, Issue 3 2002G. O'Riordain Background In the last 10 years type-I allergy against proteins from Hevea brasiliensis latex has become an acknowledged medical issue. Fruit-allergic patients represent one risk group for developing latex allergy. Class I chitinases have been identified from chestnut, avocado and banana as relevant allergens. The chitin binding (hevein) domain from these class I chitinases has been postulated to bear the important IgE binding epitopes. Objective To clone the cDNA of an allergenic latex class I chitinase, to express the recombinant protein and to determine its IgE cross-reactivity with hevein (Hev b 6.02). Methods A full-length cDNA coding for a class I chitinase has been isolated from Hevea latex RNA by reverse transcription followed by PCR. The chitinase encoding sequence has been subcloned into the pMAL expression vector and expressed in E. coli as a fusion protein to maltose binding protein. The highly enriched recombinant protein fraction has been tested for its IgE binding capacity in immunoblots and ELISA. Furthermore, the pathogenesis-related function of the recombinant protein was tested in a fungal growth inhibition assay. Results The Hevea brasiliensis latex chitinase, designated Hev b 11, displays 70% identity to the endochitinase from avocado and its hevein-domain 58% to hevein (Hev b 6.02). The recombinant Hev b 11-maltose binding protein is recognized by latex- and fruit-allergic patients with IgE binding in both, ELISA and immunoblots. Pre-incubation of sera with rHev b 11-maltose binding protein showed an overall 16% inhibition of subsequent binding to rHev b 6.02-maltose binding protein on solid phase. The growth of F. oxysporum was inhibited in a dose dependent manner by addition of rHev b 11-maltose binding protein to the culture. Conclusions Hev b 11, a class I chitinase, is another allergen from Hevea latex with a chitin binding domain and displays a different IgE binding capacity compared with hevein. [source] | ||||||||||||||||||||||||||||