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In the present study, five Penicillium species, namely, P. italicum, P. expansum, P. simplicissimum, P. oxalicum, and P. citrinum, were identified using ITS (internal transcribed spacer) and β-tubulin markers and screened for their in vitro antagonistic potential against a soil-borne fungal pathogen, Macrophomina phaseolina, in a dual-culture plate assay. Among all the tested strains, P. italicum showed the highest antagonistic potential against M. phaseolina by reducing its growth up to 57% over control, followed by P. citrinum (42%), P. simplicissimum (21%), P. expansum (11%), and P. oxalicum (9%). In order to find out the mechanism of action of P. italicum, genomic DNA of M. phaseolina was exposed to P. italicum secondary metabolites. The findings showed that these metabolites completely degraded the fungal DNA after the 48-h incubation period. To further explore the antifungal mechanism of action of P. italicum, chloroform and ethyl acetate fractions of its metabolites were subjected to gas chromatography–mass spectrometry (GC-MS) analysis. The major compounds identified in these fractions were 9,12-octadecadienoic acid (Z,Z)- (25.19%), decane (19.72%), dodecane (18.05%), benzene, nitro- (14.62%), benzene, 1,3,5-trimethyl (14.37%), benzene, 1,4-diethyl (11.62%), 1,2-benzenedicarboxylic acid, mono(2-ethylhexyl) ester (9.02%), and 1-nonadecene (8.99%), which could be responsible for control of M. phaseolina growth. [ABSTRACT FROM AUTHOR]

Bioassays were performed to assess the potential ofCoronopus didymusfor managing collar rot disease of bell pepper, caused bySclerotium rolfsii. In laboratory bioassays, methanolic shoot extract ofC. didymuswas partitioned withn-hexane, chloroform, ethyl acetate andn-butanol. Concentrations from 3.125 to 200 mg ml− 1of each fraction were evaluated against the target fungal species. All concentrations of the ethyl acetate fraction gave complete inhibition of fungal growth. Thin layer chromatography of the ethyl acetate fraction yielded two unidentified compounds1and2withRfvalues of 0.531 and 0.787, respectively. Antifungal activity of these compounds was assessed using the minimum inhibitory concentrations (MICs) technique. Mancozeb was used as a reference compound. Compound2was found to be highly effective againstS. rolfsiiwith MIC value 7.81 μg ml− 1which was at par with the MIC of mancozeb. In a pot trail, dried powdered shoots ofC. didymuswere mixed at 1%, 2% and 3% (w/w) in soil already inoculated with the target fungal pathogen. A negative control with no fungal inoculation or soil amendment and a positive control withS. rolfsiiinoculation but no soil amendment were also included. The treatment with 3% soil amendment significantly suppressed the collar rot disease. There was 50% and 13% disease incidence and mortality, respectively, with 3% treatment compared with 91% and 40%, respectively, in the positive control. This study suggests that collar rot of bell pepper can effectively be managed by exploiting the antifungal potential ofC. didymus. [ABSTRACT FROM AUTHOR]

Methanolic leaf and fruit extracts of Datura metel were found highly effective in suppressing against Macrophomina phaseolina, the cause of charcoal rot disease. These extracts were further subjected to successive fractionation with n-hexane, chloroform, ethyl acetate and n-butanol. All the concentrations (3.125–200 mg mL−1) of chloroform, ethyl acetate and n-butanol fractions of leaf extract, and n-hexane fraction of fruit extract completely inhibited the target fungal growth. Two compounds A and B from the n-hexane fraction of fruit extract and compound C from n-butanol fraction of leaf extract were obtained by TLC. Compound B exhibited the best antifungal activity with an MIC value of 7.81 µg mL−1 that was at par with that of commercial fungicide mancozeb (80% w/w). This study concludes that M. phaseolina can be effectively controlled by natural antifungal compounds in n-hexane fraction of methanolic fruit extract of D. metel. [ABSTRACT FROM PUBLISHER]

Antifungal activity of methanolic extracts of leaves of three tree species, namely Azadirachta indica L., Syzygium cumini (L.) Skeels. and Melia azedarach L. was evaluated against two strains of Alternaria alternata, isolated from dying-back trees of two Eucalyptus spp., namely Eucalyptus citriodora and Eucalyptus globulus. All the concentrations (1, 2, … , 5% w/v) of the methanolic extracts of the three tree species significantly reduced the fungal biomass. There were reductions in the ranges 82–88%, 88–96% and 83–96% in the biomass of A. alternata strains due to different concentrations of the leaf extracts of S. cumini, A. indica and M. azedarach, respectively. Methanolic extract of M. azedarach was subjected to further fractionation using n-hexane, chloroform, ethyl acetate and n-butanol successively in the order of increasing polarity. Aqueous and n-butanol fractions gave promising results in the significant decrease in fungal biomass. This study concludes that aqueous and n-butanol fractions of methanolic leaf extract of M. azedarach can be used as biofungicides for the management of A. alternata. [ABSTRACT FROM PUBLISHER]

Sclerotium rolfsii Sacc. is a pathogen of about 500 plant species. In a laboratory screening bioassay, methanolic extracts of 15 mg mL−1 concentrations of different parts of Coronopus didymus (L.) Sm. (Brassicaceae) namely leaf, stem, inflorescence and root reduced the biomass of S. rolfsii by 67%, 26%, 40% and 58%, respectively. Methanolic root extract was successively fractionated with n-hexane, chloroform, ethyl acetate and n-butanol. All the concentrations (3.125–200 mg mL−1) of ethyl acetate fraction completely inhibited the target fungal growth. Two compounds A and B were separated from this fraction by Thin Layer Chromatography (TLC). TLC fraction A was found highly effective against S. rolfsii with MIC value 15.62 µg mL−1 as compared to MIC value 7.81 µg mL−1 of the commercial fungicide mencozeb. This compound may be used for the synthesis of natural product based fungicide for the control of S. rolfsii. [ABSTRACT FROM PUBLISHER]

A pot experiment was conducted in heat-sterilized soil to evaluate the effect of effective microorganism (EM) application on growth, yield, and nutrient uptake in Vigna radiata (L.) Wilczek var. NIAB Mung 98 in different soil amendment systems. Pot soil was amended with farmyard manure (FYM), Trifolium alexanrinum L. crop residues (TCR), and half (½NPK) and recommended dose (NPK) of chemical fertilizers. The EM application significantly enhanced shoot and root biomass in TCR-amended soil. However, grain yield was significantly enhanced in FYM, TCR, and NPK amendments by 24%, 15%, and 84%, respectively, as a result of EM application. Effect of EM application on nutrient uptake was variable with respect to soil amendment and plant growth stage. In general, EM application enhanced plant nitrogen (N), phosphorus (P), and potassium (K) nutrition in organic amendments while its effect was either negative or insignificant in chemical fertilizer amendments. Effects of EM application on plant nutrient uptake were more pronounced at maturity than at flowering stage. [ABSTRACT FROM AUTHOR]

The herbicidal potential of culture filtrates of four Trichoderma spp., namely Trichoderma harzianum Rifai, Trichoderma pseudokoningii Rifai, Trichoderma reesei Simmons and Trichoderma viride Pers., was evaluated against two problematic weeds of wheat, Phalaris minor L. and Rumex dentatus L. In laboratory bioassays, generally, metabolites of all four Trichoderma species significantly reduced various root and shoot growth parameters of the two target weed species. The original concentrations of the culture filtrates of all Trichoderma spp., except T. harzianum, significantly reduced various parameters of root and shoot growth of wheat seedlings. In a foliar spray bioassay, the culture filtrates of all four Trichoderma spp. significantly diminished root and shoot biomass of R. dentatus. The effect of these filtrates on the shoot growth of P. minor and wheat was not significant. Culture filtrates of the four Trichoderma species were successively extracted with butanol, n-hexane, chloroform and ethyl acetate. In detached leaf injection bioassays, n-hexane fractions (3 mg mL-1) of T. pseudokoningii, T. reesei and T. viride, and ethyl acetate fractions of T. horzianum and T. pseudokoningii were found to be toxic against R. dentatus. This study concludes that the culture filtrates of Trichoderma species have herbicidal potential in the control of R. dentatus. [ABSTRACT FROM AUTHOR]

This study was designed to evaluate the herbicidal activity of Withania somnifera (L.) Dunal against the noxious weed parthenium (Parthenium hysterophorus L.). In a laboratory bioassay, the effect of aqueous, methanol and n-hexane shoot and root extracts of 5%, 10%, 15% and 20% w/v concentrations (on a fresh weight basis) of W. somnifera were tested against the germination and seedling growth of parthenium. In general, aqueous and methanol extracts markedly suppressed the germination, root and shoot growth of parthenium. The shoot extracts were more inhibitory than the root extracts. In a foliar spray bioassay, the aqueous and methanol shoot extracts of 10% w/v (on a dry weight basis) concentration were sprayed on 1-week and 2-week-old pot-grown parthenium seedlings. Two subsequent sprays were carried out 5 and 10 days after the first spray. The aqueous and methanol extracts significantly reduced the length and biomass of parthenium shoots. In a soil amendment bioassay, the crushed shoots of W. somnifera were incorporated in the soil at 1-5% w/w. Parthenium seeds were sown one week after the residue incorporation and plants were harvested 40 days after sowing. All the soil amendment treatments significantly reduced seed germination by 43-89%. The highest dosages of 4% and 5% significantly suppressed the root and shoot biomasses of parthenium. This study concludes that foliar spray of aqueous and methanol extracts, and soil amendment with leaf residue of W. somnifera, can control the germination and growth of parthenium, one of the world's worst weeds. [ABSTRACT FROM AUTHOR]

The antifungal activity of Melia azedarach L. leaves was investigated against Ascochyta rabiei (Pass.) Lab., the cause of destructive blight disease of chickpea (Cicer arietinum L.). Bioassay guided fractionation revealed that the chloroform fraction of the methanolic extract of M. azedarach leaves was highly effective against A. rabiei. Six compounds, namely β-sitosterol (1), β-amyrin (2), ursolic acid (3), benzoic acid (4), 3,5 dimethoxybenzoic acid (5) and maesol (6) were isolated from the chloroform fraction through column chromatography. The in vitro antifungal activity of compounds 2-5 was evaluated against A. rabiei. A commercial fungicide, mancozeb, was used as a positive control. Different concentrations of mancozeb and the isolated compounds, ranging from 0.0039 to 4 mg mL-1, were used in the antifungal bioassay, and data regarding minimum inhibitory concentration (MIC) was recorded 24, 48 and 72 h after incubation. All concentrations of mancozeb inhibited the fungal spore germination at all three incubation periods. The tested compounds exhibited variable antifungal activity against the target fungal pathogens. All compounds showed their highest antifungal activity after 24 h of incubation. Compound 2 was found to be the most effective, with an MIC of 0.0156 mg mL-1, followed by compounds 3, 4 and 5, with MIC values of 0.0312, 0.25 and 0.125 mg mL-1, respectively. [ABSTRACT FROM AUTHOR]

Five flavonoids, namely (-)-epicatechin-3-O-β-glucopyranoside (1), 5-hydroxy-3-(4-hydroxylphenyl)pyrano[3,2-g]chromene-4(8H)-one (2), 6-(p-hydroxybenzyl)taxifolin-7-O-β-D-glucoside (tricuspid) (3), quercetin-3-O-α-glucopyranosyl-(1 → 2)-β-D-glucopyranoside (4) and (-)-epicatechin(2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol (5), were isolated from the leaves of mango (Mangifera indica L.). Antifungal activity of these compounds was evaluated against five fungal species, namely Alternaria alternata (Fr.) Keissler, Aspergillus fumigatus Fresenius, Aspergillus niger van Tieghem, Macrophomina phaseolina (Tassi) Goid. and Penicillium citrii. Six concentrations, namely 100, 300, 500, 700, 900 and 1000 ppm of each of the five flavonoids were employed by means of the poisoned medium technique. All concentrations of the five test flavonoids significantly suppressed fungal growth. However, the specificity of different test compounds was evident against different fungal species. In general, antifungal activity of the flavonoids was gradually increased by increasing their concentrations. The highest concentration (of 1000 ppm) of compounds 1-5 reduced the growth of different target fungal species by 63-97%, 56-96%, 76-99%, 76-98% and 82-96%, respectively. [ABSTRACT FROM AUTHOR]

This study was undertaken to investigate the herbicidal activity of mango (Mangifera indica L.) leaves against parthenium weed (Parthenium hysterophorus L.). The aqueous leaf extract at 15% concentration (on fresh weight basis) significantly reduced germination, shoot length and the shoot and root biomasses of parthenium seedlings. In a leaf residue incorporation pot trial, 2% residue incorporation treatment significantly suppressed the root and shoot biomasses of parthenium, while a 5% residue treatment completely stopped the growth of the weed. Five flavonoids, namely (-)-epicatechin-3-O-β-glucopyranoside (1), 5-hydroxy-3-(4-hydroxyphenyl)pyrano[3,2-g]chromene-4(8H)-one (2), 6-(p-hydroxybenzyl)taxifolin-7-O-β-D-glucoside (tricuspid) (3), quercetin-3-O-α-glucopyranosyl-(1 → 2)-β-D-glucopyranoside (4) and (-)-epicatechin(2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H chromene-3,5,7-triol (5) were isolated from mango leaves. In a laboratory bioassay, 50 ppm solution of compounds 3 and 4 caused yellowing of the parthenium seedlings. A 250 ppm solution of compound 4 also significantly reduced germination and the root and shoot lengths of parthenium seedlings. This study concludes that compound 4 exhibits herbicidal activity against parthenium weed. [ABSTRACT FROM AUTHOR]

The present study was designed to evaluate the herbicidal activity of Datura metel against the noxious weed parthenium (Parthenium hysterophorus L.). In a laboratory bioassay, the effect of aqueous, methanol and n-hexane shoot and root extracts of 5, 10, 15 and 20% w/v (on a fresh weight basis) concentration of D. metel were tested against the germination and seedling growth of parthenium. Both aqueous and methanol extracts markedly suppressed the germination and seedling growth of parthenium. Generally, the effect of shoot extracts was more pronounced than the effect of root extracts. In foliar spray bioassay, aqueous and methanol shoot extracts of 10% w/v (on dry weight bases) concentrations were sprayed on one-week and two-week-old pot-grown parthenium seedlings. Two subsequent sprays were carried out at five day intervals each. Both the aqueous as well as the methanol extracts significantly suppressed shoot length as well as shoot and root biomass of one-week and two-week-old parthenium plants. In residue incorporation bioassay, crushed shoots of D. metel were incorporated in the soil at 1, 2, ... 5% w/w. Parthenium seeds were sown one week after residue incorporation and plants were harvested 40 days after sowing. Incorporation of 2-5% residues significantly reduced germination by 47-89%. Residues of 4 and 5% concentration significantly suppressed plant biomass by 90 and 97%, respectively. The present study concludes that root and shoots of D. metel contain herbicidal constituents for the management of parthenium weed. [ABSTRACT FROM AUTHOR]

Herbicidal activity of Withania somnifera (L.) Dunal. was studied against Phalaris minor Retz., one of the most problematic weeds of wheat in Pakistan. In laboratory bioassays the aqueous, methanol and n-hexane extracts of 5, 10 and 15% w/v (fresh weight basis) of the roots and shoots of W. somnifera were applied. Extracts in the different solvents exhibited markedly variable herbicidal activities against germination and seedling growth of the target weed species. The methanol extracts showed the highest toxicity. Different concentrations of methanol shoot and root extracts declined the germination of P. minor by 21-71%, its shoot length by 40-72%, its root length by 50-99% and the plant biomass by 32-83%. The aqueous extracts proved to be comparatively less toxic than the methanol extracts, where generally the highest concentration of 15% exhibited pronounced toxicity against the target weed species. There was up to 48, 51, 99 and 55% suppression of the weed's germination, shoot length, root length and plant biomass, respectively, due to the 15% aqueous root and shoot extracts. Generally, the n-hexane extracts of both roots and shoots exhibited insignificant or stimulatory effects against weed shoot length and plant biomass. In a foliar spray bioassay, aqueous and methanol shoot extracts of 10% w/v (dry weight basis) concentration were sprayed on one- and two-week old pot grown P. minor seedlings. Two subsequent sprays were carried out at five day intervals each. The aqueous extract significantly reduced the shoot and root dry biomass of one-week old P. minor plants. In a residue incorporation bioassay, crushed shoots of W. somnifera were incorporated in the soil at 1, 2, ... 5% w/w. Phalaris minor seeds were sown one week after residue incorporation and plants were harvested 45 days after sowing. The lower concentrations of 2 and 3% significantly reduced, while higher concentrations of 4 and 5% of residue incorporation completely arrested, the germination of P. minor. The present study concludes that both roots and shoots of W. somnifera contain herbicidal constituents against P. minor. [ABSTRACT FROM AUTHOR]

Aqueous, ethanol and n-hexane extracts from leaves, fruit, root-bark and stem-bark of Syzygium cumini (L.) Skeels were tested for their antifungal activity against Ascochyta rabiei (Pass.) Lab., the cause of blight disease of the chickpea (Cicer arietinum L.). Different concentrations, namely 1, 2, ..., 5% of both aqueous and the two organic solvent extracts were used in this study. Aqueous extracts of all the four test plant parts, namely leaves, fruit, stem-bark and root-bark, showed significant antifungal activity resulting in 7-30%, 22-59%, 23-39% and 21-64% reduction in fungal growth, respectively. Similarly, n-hexane stem-bark extract, and ethanol root- and stem-bark extracts also significantly suppressed the growth of target fungal species, resulting in 17-39%, 24-30% and 12-32% suppression in fungal growth. [ABSTRACT FROM AUTHOR]

A pot experiment was conducted to evaluate the efficacy of aqueous extracts of six plant species, namely Azadirachta indica A. Juss. (neem), Alstonia scholaris (L.) R. Br., Lawsonia alba Lam., Allium cepa L., A. sativum L. and Zingiber officinale Roscoe, and a systemic fungicide carbendazim 50% (w/w) WP, to manage the corm-rot disease of Gladiolus (Gladiolus grandiflorus L.) caused by a fungal pathogen Fusarium oxysporum f.sp. gladioli (Massey) Snyd. & Hans. Fusarium inoculation showed 80% disease incidence with 54 disease lesions per corm. Recommended dose of the chemical fungicide carbendazim significantly reduced the disease incidence to 13% and number of lesions to six per corm. Plant extract treatments exhibited variable effects on the incidence and severity of the disease. In general, all the test plant extracts managed the corm-rot disease to some extent. Aqueous bulb extracts of A. sativum and A. cepa and the rhizome extract of Z. officinale showed better disease management potential than that of the recommended dose of carbendazim. Fusarium inoculation significantly declined shoot growth. In general, carbendazim, as well as aqueous extracts, enhanced shoot growth to variable extents as compared to the Fusarium control. [ABSTRACT FROM AUTHOR]

In the present study, herbicidal activity of culture filtrates of nine phytopathogenic fungi, namely, Alternaria alternata (Fr.) Keissl., Drechslera australiensis (Bugnicourt) Subramanian & Jain, Drechslera hawaiiensis (Curtis and Cooke) Shoemaker, Drechslera biseptata (Saccardo & Roumeguere) Richardson & Fraser., Drechslera rostrata (Drechsler) Ricardson & Fraser, Fusarium oxysporum (Massey) Synd. & Hans., Fusarium solani (Martius) Saccardo., Monilia stophila (Montagne) and Cladosporium sp. (Grey) de Hoff, was evaluated against parthenium weed (Parthenium hysterophorus L.). In laboratory bioassays, the effect of original (100%) as well as lower concentrations (75, 50 and 25%) of these cultural filtrates was studied on germination and early seedling growth of parthenium. Cultural filtrates of different concentrations of A. alternata, Cladosporium sp. and D. rostrata significantly suppressed the germination of parthenium seeds by 70-90, 13-73 and 27-50%, respectively. Cultural filtrates of these fungi also exhibited pronounced adverse effects on the seedling root and shoot growth. Among other fungal species, cultural filtrates of D. australiensis, D. hawaiiensis, F. oxysprium and F. solani significantly reduced the root and shoot length of parthenium seedlings. Foliar spray bioassay was performed using cultural filtrates of three fungal species, namely A. alternata, F. solani and D. rostrata. In this bioassay, three sprays of fungal cultural filtrates, with 4 day intervals each, were carried out on 1 and 2 week-old pot-grown seedlings of parthenium. Cultural filtrates of all the three fungal species markedly suppressed root and shoot growth of parthenium weed. [ABSTRACT FROM AUTHOR]

Arbuscular mycorrhizae (AM) are the symbiotic fungi that predominate in the roots and soils of agricultural crop plants. The most recognized beneficial effect of these fungi is to enhance host plant uptake of relatively immobile nutrients, in particular phosphorus (P), and several micronutrients. The AM fungi absorb inorganic P either from the soluble P pools in the soil, or from insoluble forms such as rock phosphates as well as from insoluble organic sources. Recent studies show that mycorrhizal fungi would have access to rock phosphate through localized alterations of pH and/or by the production of organic acid anions that may act as chelating agents. The AM colonization also improves plant N nutrition. Generally mycorrhizal symbiosis more influences on nitrogen (N) uptake and translocation if ammonium (NH4+) rather than nitrate (NO3-) is the nitrogen source. However, under drought stress the role of mycorrhizae in NO3- transport to the root surface may be significant as the NO3- mobility is severely restricted due to its low concentration and diffusion rate under such circumstances. However, as yet little is known about the mechanism of N uptake by the AM fungi. Uptake of micronutrients is also influenced by mycorrhizal colonization. [ABSTRACT FROM AUTHOR]

Antifungal activity of methanol and n-hexane leaf, stem, root and inflorescence extracts (1, 2, 3 and 4% w/v) of three Chenopodium species (family Chenopodiaceae) namely Chenopodium album L., Chenopodium murale L. and Chenopodium ambrosioides L. was investigated against Macrophomina phaseolina (Tassi) G. Goid., a soil-borne fungal plant pathogen that has a broad host range and wide geographical distribution. All the extracts of the three Chenopodium species significantly suppressed the test fungal growth. However, there was marked variation among the various extract treatments. Methanol inflorescence extract of C. album exhibited highest antifungal activity resulting in up to 96% reduction in fungal biomass production. By contrast, methanol leaf extract of the same species exhibited least antifungal activity where 21-44% reduction in fungal biomass was recorded due to various employed extract concentrations. The various methanol extracts of C. murale and C. ambrosioides decreased fungal biomass by 62-90 and 50-84%, respectively. Similarly, various n-hexane extracts of C. album, C. murale and C. ambrosioides reduced fungal biomass by 60-94, 43-90 and 49-86%, respectively. [ABSTRACT FROM AUTHOR]