Inhibition Of Plant Pathogenic Fungi Research Articles

Antimicrobial potential of silver nanoparticles biosynthesized using aerial yam bulbils for control of selected phytopathogens

Silver nanoparticles as antimicrobial agent have vast potential in agriculture for the protection of plants from diseases and increasing crop productivity. In this study, the bulbils of aerial yam (Dioscorea bulbifera L.) were investigated for their potential for biosynthesis of silver nanoparticles. Variation in the absorption spectra of silver nanoparticles synthesized using different concentrations of 10 to 50% (v/v) of plant extract was observed. Phytochemical analysis of aerial yam bulbils revealed high content of flavonoid (4.06 ± 0.44 mg/g), phenols (3.36 ± 0.20 mg/g) and tannins (12.42 ± 0.22 mg/g) with potential role in the bioreduction process. Highest inhibition (98-100%) was recorded against Fusarium oxysporum and Colletotrichum gloeosporioides with 100 ppm silver nanoparticles. The inhibition zone against Bacillus sp. and Enterobacter cloacae ranged from 6.00 ± 0.41 to 11.00 ± 0.87 mm at 100 ppm concentration indicating antibacterial efficacy of biosynthesized silver nanoparticles. Silver nanoparticles biosynthesized using 20% (v/v) extract at higher temperature demonstrated the most effective inhibition of plant pathogenic fungi and bacteria.

Inhibition of plant pathogenic fungi by endophytic Trichoderma spp. through mycoparasitism and volatile organic compounds

Antagonism of plant pathogenic fungi by endophytic fungi is a well-known phenomenon. In plate assays, the antagonism could be due to mycoparasitism, competition for space or antibiosis, involving a chemical diffusate, or a volatile organic compound (VOC). In this study, we demonstrate that besides mycoparasitism, VOCs play a major role in antagonism of pathogenic fungi by four endophytic fungi belonging to the genus Trichoderma. Using a double-plate assay, we show that all the four endophytic Trichoderma species significantly inhibited mycelial growth of three of the four pathogens, (Sclerotinia sclerotiorum-TSS, Sclerotium rolfsii-CSR and Fusarium oxysporum-CFO), while that of Macrophomina phaseolina-CMP was not affected. GC–MS analysis of the pure cultures of one of the endophytic fungi studied, namely, Trichoderma longibrachiatum strain 2 (Acc. No. MK751758) and the pathogens, F. oxysporum-CFO and M. phaseolina-CMP revealed the presence of several VOCs including hydrocarbons, alcohols, ketones, aldehydes, esters, acids, ethers and different classes of terpenes. In mixed double plates, where the endophyte was grown along with either of the two plant pathogens, F. oxysporum-CFO or M. phaseolina-CMP, there was an induction of a number of new VOCs that were not detected in the pure cultures of either the endophyte or the pathogens. Several of these new VOCs are reported to possess antifungal and cytotoxic activity. We discuss these results and highlight the importance of such interactions in endophyte-pathogen interactions.

Antifungal Effects of Silver Nanoparticles (AgNPs) against Various Plant Pathogenic Fungi

This research is concerned with the fungicidal properties of nano-size silver colloidal solution used as an agent for antifungal treatment ofvarious plant pathogens. We used WA-CV-WA13B, WA-AT-WB13R, and WA-PR-WB13R silver nanoparticles (AgNPs) at concentrations of 10, 25, 50, and 100 ppm. Eighteen different plant pathogenic fungi were treated with these AgNPs on potato dextrose agar (PDA), malt extract agar, and corn meal agar plates. We calculated fungal inhibition in order to evaluate the antifungal efficacy of silver nanoparticles against pathogens. The results indicated that AgNPs possess antifungal properties against these plant pathogens at various levels. Treatment with WA-CV-WB13R AgNPs resulted in maximum inhibition of most fungi. Results also showed that the most significant inhibition of plant pathogenic fungi was observed on PDA and 100 ppm of AgNPs.

Bioactive xanthones from the roots of Hypericum perforatum (common St John's wort).

Extracts of Hypericum perforatum L. (common St John's wort; Hypericaceae) are sold as phytopharmaceuticals and herbal supplements to treat mild to moderate depression and as food additives. Extensively cultivated in Europe, plants can be infected by anthracnose (Colletotrichum gloeosporioides), a virulent fungal pathogen that causes tissue necrosis and dramatically decreases crop value. Such infections triggered the production of new secondary metabolites, specifically xanthones, in cell culture experiments. Bioassay-guided fractionation of H. perforatum root extracts, testing for growth inhibition of plant pathogenic fungi from the genera Colletotrichum, Botrytis, Fusarium and Phomopsis, was performed. In vitro anti-inflammatory activity through inhibition of COX-1, COX-2 and 5-LOX-catalyzed LTB(4) formation was also evaluated. Extracts were analyzed by various chromatographic means and structure elucidation was performed using data from nuclear magnetic resonance and mass spectrometry. Researchers have previously described constituents from the aerial parts of this species, but few reports describe secondary metabolites found in underground parts, of particular interest because the lower stem and upper root are often sites of fungal infection. This work resulted in the isolation of three xanthones: 1,6-dihydroxy-5-methoxy-4',5'-dihydro-4',4',5'-trimethylfurano-(2',3':3,4)-xanthone; 4,6-dihydroxy-2,3-dimethoxyxanthone; and cis-kielcorin, one of which possessed novel bioactivity against species of Phomopsis and inhibited 5-LOX-mediated LTB(4) formation.

Bacterial community composition and chitinase gene diversity of vermicompost with antifungal activity

Bacterial communities and chitinase gene diversity of vermicompost (VC) were investigated to clarify the influence of earthworms on the inhibition of plant pathogenic fungi in VC. The spore germination of Fusarium moniliforme was reduced in VC aqueous extracts prepared from paper sludge and dairy sludge (fresh sludge, FS). The bacterial communities were examined by culture-dependent and -independent analyses. Unique clones selected from 16S rRNA libraries of FS and VC on the basis of restriction fragment length polymorphism (RFLP) fell into the major lineages of the domain bacteria Proteobacteria, Bacteroidetes, Verrucomicrobia, Actinobacteria and Firmicutes. Among culture isolates, Actinobacteria dominated in VC, while almost equal numbers of Actinobacteria and Proteobacteria were present in FS. Analysis of chitinolytic isolates and chitinase gene diversity revealed that chitinolytic bacterial communities were enriched in VC. Populations of bacteria that inhibited plant fungal pathogens were higher in VC than in FS and particularly chitinolytic isolates were most active against the target fungi.

Growth inhibition of plant pathogenic fungi by extracts of Allium sativum and Tulbaghia violacea

An important stage in tissue culture is the acclimatising of the in vitro grown plantlets to conditions outside the culture flask. Many plantlets succumb to fungal attack at this stage resulting in significant financial loss. The use of plant extracts as possible antifungal agents is of great interest in this regard. In a pilot study aqueous extracts of Tulbaghia violacea and Allium sativum (Alliaceae) were used to treat plantlets of Harpagophytum procumbens (devils claw) by pre-soaking plantlets in extract before planting out into pots or by applying extracts as a soil drench after planting plantlets into pots. Results obtained after a two-week period showed that plantlets treated with extracts of T. violacea had a higher percentage survival than did those treated with extracts of A. sativum. Applying T. violacea extract as a soil drench was most effective at increasing plantlet survival. In an in vitro assay for antifungal activity, extracts of T. violacea had greater activity than A. sativum against the fungal pathogens: Botrytis cinerea, Pythium ultimum and Rhizoctonia solani. This activity was lower than that obtained for the commercial fungicide used when compared on a concentration basis. Results suggest that aqueous extracts of T. violacea may be used as an alternative to synthetic fungicides to increase plantlet survival of H. procumbens during acclimatisation.

Inhibition of plant-pathogenic fungi by the barley cystatin Hv-CPI (gene Icy) is not associated with its cysteine-proteinase inhibitory properties.

The recombinant barley cystatin Hv-CPI inhibited the growth of three phytopathogenic fungi (Botrytis cinerea, Colletotrichum graminicola, and Plectosphaerella cucumerina) and the saprotrophic fungus Trichoderma viride. Several mutants of barley cystatin were generated by polymerase chain reaction approaches and both their antifungal and their cysteine-proteinase inhibitory properties investigated. Point mutants R38-->G, Q63-->L, and Q63-->P diminished their capacity for inhibiting papain and cathepsin B, retaining their antifungal properties. However, mutant C68-->G was more active for papain and cathepsin B than the wild type. These results indicate that in addition to the consensus cystatin-reactive site, Q63-V64-V65-A66-G67, the A37-R38-F39-A40-V41 region, common to all cereal cystatins, and the C68 residue are important for barley cystatin activity. On the other hand, the K92-->P mutant is inactive as a fungicide, but still retains measurable inhibitory activity for papain and cathepsin B. Against B. cinerea, the antifungal effect of Hv-CPI and of its derived mutants does not always correlate with their activities as proteinase inhibitors, because the Q63-->P mutant is inactive as a cystatin, while still inhibiting fungal growth, and the K92-->P mutant shows the reciprocal effects. These data indicate that inhibition of plant-pathogenic fungi by barley cystatin is not associated with its cysteine-proteinase inhibitory activity. Moreover, these results are corroborated by the absence of inhibition of intra- and extramycelia-proteinase activities by barley cystatin and by other well-known inhibitors of cysteine-proteinase activity in the fungal zymograms of B. cinerea.

Mycelial growth inhibition of plant pathogenic fungi by extracts of South African plant species

SummaryEleven plant species were collected from the Blyde River Canyon area, Mpumalanga, South Africa. Methanolic crude extracts of the plant samples were concentrated to dryness, dissolved in sterile distilled water and bioassayed in the laboratory for their fungicidal potential against seven plant fungal pathogens, namely Botrytis cinerea, Fusarium oxysporum, Sclerotium rolfsii, Rhizoctonia solani, Verticillium dahliae, Botryosphaeria dothidea and Pythium ultimum, at equal concentrations.A modified agar dilution method was used to determine the inhibitory effect of the plant extracts on the mycelial radial growth of the plant pathogens. Antifungal activity was confirmed in all the plants, but not in all plant parts and also not against all the test organisms. The crude extract of Eucomis autumnalis performed best of all the plant extracts tested, as it showed significant antifungal activity against all seven of the plant pathogenic test organisms and compared favourably to the inhibition of the mycelial growth by a broad spectrum synthetic fungicide (carbendazim/ difenoconazole). The crude extract of Schrebera alata came out second best, in the sense that at least one plant part inhibited the mycelial radial growth of four of the seven test organisms by at least 50%.

Growth inhibition of plant pathogenic fungi by hydroxy fatty acids

Hydroxy fatty acids are plant self-defense substances (Masui et al, Phytochemistry1989). Three types of hydroxy fatty acids: 10-hydroxystearic acid (HSA), 7S,10S-dihydroxy-8(E)-octadecenoic acid (DOD), and 12,13,17-trihydroxy-9(Z)-octadecenoic acid (THOA) were tested against the following plant pathogenic fungi: Erysiphe graminis f sp tritici (common disease name, wheat powdery mildew); Puccinia recondita (wheat leaf rust); Pseudocercosporella herpotrichoides (wheat foot rot); Septoria nodorum (wheat glume blotch); Pyricularia grisea (rice blast); Rhizoctonia solani (rice sheath blight); Phytophthora infestans (potato late blight); and Botrytis cinerea (cucumber botrytis). At a concentration of 200 ppm, both HSA and DOD showed no fungal disease control activity. However, THOA at the same concentration showed weak activity and provided disease control (percent) of the following plant pathogenic fungi: Erysiphe graminis 77%; Puccinia recondita 86%; Phytophthora infestans 56%; and Botrytis cinerea 63%. The position of the hydroxy groups on the fatty acids seems to play an important role in activity against specific fungi. Journal of Industrial Microbiology & Biotechnology (2000) 24, 275–276.

In Vitro Growth Inhibition of Plant Pathogenic Fungi, Botrytis spp., by Escherichia coli Transformed with a Chitinolytic Enzyme Gene from a Marine Bacterium, Alteromonas sp. Strain 79401.

Marine bacterium, Alteromonas sp. strain 79401 was shown to suppress the conidial growth of plant pathogenic fungi Botrytis cinerea and B. fabae in vitro by means of its high chitinolytic activity. To use the ability of this bacterium for biocontrol, a DNA fragment (ca. 12kb) carrying the chitinolytic enzyme gene(s) was cloned into the plasmid pBR322. The resulting plasmid, pALCHI1, was introduced into Escherichia coli strain DH5. B. cinerea and B. fabae could not grow in the vicinity of the transformed E. coli colonies in vitro. Conidial germination and hyphal growth were markedly suppressed. Swelling of the conidia and germ tubes and bursting of hyphal tips were observed under a microscope, suggesting that the chitinolytic enzyme affected the fungal cell walls. This chitinolytic enzyme gene might be useful for the biocontrol of Botrytis spp. and other plant pathogenic fungi.

Abstracts of Papers Presented at the Annual Meeting of the Canadian Phytopathological Society Banff, Alberta June 1991

Abstracts of Papers Presented at the Annual Meeting of the Canadian Phytopathological Society Banff, Alberta June 1991