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70 results for “entomopathogenic fungi”
ECOBREED WP3 entomopathogenic fungi-wireworm data related to Razinger et al. (2020)
<p>Raw data related to Figures 1 to 5 and Table 1 plus suplementary raw data of the publication Razinger et al. (2020) Frontiers in Plant Science 11:535005; doi: 10.3389/fpls.2020.535005.</p>
Figure 1 in Toxicity and ovicidal activity of different entomopathogenic fungi, Hirsutella extracts on Tetranychus urticae (Acari: Tetranychidae)
Figure 1. Accumulated mortality of T. urticae females at 24, 48 and 72 h after being fed with mulberry leaf discs treated with different concentrations of crude extract, six species of Hirsutella under residual effect bioassay. For each extract and mite, means followed by the same letter are not significantly different (p = 0.05; Tukey HDS test).
Data from: Insect hypovirulence-associated mycovirus confers entomopathogenic fungi with enhanced resistance against phytopathogens
<p>Mycoviruses can alter the biological characteristics of host fungi including decreasing or enhancing virulence or pathogenicity of phytopathogens and entomopathogenic fungi (EPF). As an extensively used EPF, <em>Beauveria bassiana</em> could not only directly control pests, but also improve plant resistance against plant disease through endophytic colonization. However, most studies on the mycoviruses found in <em>B. bassiana</em> have focused on the effects of the viruses on the virulence of host fungi toward insect pests, with relatively few reports on the effects to the host fungi with regard to plant disease resistance in hosts. The present study investigated the effects of the mycovirus <em>Beauveria bassiana</em> chrysovirus 2 (BbCV2) virus infection on host biological characteristics, additionally, we evaluated antagonistic activity of BbCV2 against phytopathogenic fungi (<em>Sclerotinia sclerotiorum</em> and <em>Botrytis cinerea</em>) <em>in vitro</em> and their associated diseases both in <em>in vitro</em> leaves and in pot experiments. Our results showed that the mycovirus, BbCV2, enhanced the growth rate, spore production, and biomass of host fungi <em>B. bassiana</em>. BbCV2 virus infection enhanced the capacity of host fungi and their metabolic products to inhibit phytopathogenic fungi <em>S. sclerotiorum</em> and <em>B. cinerea</em>. BbCV2 virus infection reduced the contents of the two pathogens in tomato plants significantly, and in turn enhanced the plant resistance induced by host fungi colonization against the diseases caused by the two pathogens.</p>
Figure 1 in Diversity of entomopathogenic fungi from soils of eucalyptus and soybean crops and natural forest areas
Figure 1. Entomopathogenic fungi of the genera Aspergillus (A), Beauveria (B), Cordyceps (C), Fusarium (D), Metarhizium (E), Penicillium (F) and Purpureocillium (G) cultivated in Petri dishes with PDA medium.
Figure 4 in A comparative study on the virulence of entomopathogenic fungi against Trogoderma granarium (Everts) (Coleoptera: Dermestidae) in stored grains rice
Figure 4. Mortality (%) of T. granarium grubs exposed to Metarhizium anisopliae at different concentrations. Different letters above the bars represent the significant difference at P=0.05.
Figure 5 in A comparative study on the virulence of entomopathogenic fungi against Trogoderma granarium (Everts) (Coleoptera: Dermestidae) in stored grains rice
Figure 5. Mortality (%) of T. granarium grubs exposed to Isaria fumosoroseus at different concentrations. Different letters above the bars represent the significant difference at P=0.05.
Figure 3 in A comparative study on the virulence of entomopathogenic fungi against Trogoderma granarium (Everts) (Coleoptera: Dermestidae) in stored grains rice
Figure 3. Mortality (%) of T. granarium grubs exposed to Immersion and Food mix method at a conidial concentration of 1x108. Different letters above the bars represent the significant difference at P=0.05.
Figure 7 in A comparative study on the virulence of entomopathogenic fungi against Trogoderma granarium (Everts) (Coleoptera: Dermestidae) in stored grains rice
Figure 7. Mortality (%) of T. granarium grubs exposed to three different fungal strains at different conidial concentrations. Different letters above the bars represent the significant difference at P=0.05.
Figure 2 in A comparative study on the virulence of entomopathogenic fungi against Trogoderma granarium (Everts) (Coleoptera: Dermestidae) in stored grains rice
Figure 2. Mortality (%) of T. granarium grubs exposed to food mix method at 1x108 conidia mL-1. Different letters above the bars represent the significant difference at P=0.05.
Figure 1 in A comparative study on the virulence of entomopathogenic fungi against Trogoderma granarium (Everts) (Coleoptera: Dermestidae) in stored grains rice
Figure 1. Mortality (%) of T. granarium grubs exposed to immersion method at 1x108 conidia mL-1. Different letters above the bars represent the significant difference at P=0.05.
Figure 2 in Indigenous entomopathogenic fungi as potential biological control agents of rose sawfly Arge rosae L. (Hymenoptera: Argidae)
Figure 2. Maximum likelihood tree based on ITS region sequence, showing the phylogenetic relationship between the indigenous isolates of EPF species (B. bassiana, C. rosea and I. farinosa) and other isolates of the respective or related species in the GenBank.
Figure 1 in Indigenous entomopathogenic fungi as potential biological control agents of rose sawfly Arge rosae L. (Hymenoptera: Argidae)
Figure 1. First instar larvae of A. rosae, head capsules of which were black, and their legs were blackish, collected from the infested greenhouse-grown roses in Antalya province.
Figure 4 in New insights on the impact of earthworm extract on the growth of beneficial soil fungi: species-specific alteration of the nematophagous fungal growth and limitation of an entomopathogenic fungus
Figure 4. Growth of Purpureocillium lilacinum after 20 days postexposer to two different earthworm based media: fresh earthworms (FE) (four concentration C1, C2, C3, and C4), and earthworms devoid of gut contents (EDG) (four concentration C1, C2, C3, and C4), C1 = 40 g/L, C2 = 20 g/L, C3 = 10 g/L, C4 = 5 g/L, and two rich media: potato dextrose agar (PDA), and brain heart infusion (BHI).
Figure 5 in New insights on the impact of earthworm extract on the growth of beneficial soil fungi: species-specific alteration of the nematophagous fungal growth and limitation of an entomopathogenic fungus
Figure 5. Evaluation of conidial germination of the fungus Beauveria bassiana exposed to two different earthworm extracts: fresh earthworms (FE) and earthworms without gut contents, EDG, and two conventional media: potato dextrose agar (PDA), and brain heart infusion agar (BHI). A. Percentage germination on conventional and earthworm-based media. B. Percent germination as a function of concentration and earthworm-based medium. Concentrations are equivalent to C1 = 40 g/L, C2 = 20 g/L, C3 = 10 g/L, and C4 = 5 g/L. Results of one-way ANOVA (A) or two-way ANOVA (B), and differences are significant according to Tukey's test (HSD) and groups "a", "b" and "c".
Figure 3 in New insights on the impact of earthworm extract on the growth of beneficial soil fungi: species-specific alteration of the nematophagous fungal growth and limitation of an entomopathogenic fungus
Figure 3. Evaluation of vegetative growth, conidial production and germination in the fungus Purpureocillium lilacinum exposed to two earthworm extracts: fresh earthworm (FE), earthworms devoid of intestinal contents (EDG) and two conventional media: potato dextrose agar (PDA), and brain heart infusion agar (BHI). A. Cumulative growth from 3 to 18 days according to conventional and earthworm-based media. B. Cumulative growth as a function of concentration and earthworm-based medium. C. Conidia production (×10⁵ conidia/mL) according to conventional and earthworm-based media. D. Conidia production (×10⁵ conidia/mL) according to concentration and earthworm-based medium. E. Percent germination on conventional and earthworm-based media. F. Percent germination as a function of concentration and earthworm-based medium. Concentrations are equivalent to C1 = 40 g/L, C2 = 20 g/L, C3 = 10 g/L, and C4 = 5 g/L. Results of one-way ANOVA (A, C, E) or two-way ANOVA (B, D, F), and differences are significant at Tukey's test (HSD) and groups "a", "b" and "c".
Figure 1 in New insights on the impact of earthworm extract on the growth of beneficial soil fungi: species-specific alteration of the nematophagous fungal growth and limitation of an entomopathogenic fungus
Figure 1. Evaluation of vegetative growth, conidial production and germination in the fungus Arthrobotris musiformis exposed to two earthworms' extracts: fresh earthworm (FE), earthworms devoid of intestinal contents (EDG) and two conventional media: potato dextrose agar (PDA), and brain heart infusion agar (BHI). A. Cumulative growth from 3 to 18 days according to conventional and earthworm-based media. B. Cumulative growth as a function of concentration and earthworm-based medium. C. Conidia production (×10⁵ conidia/mL) according to conventional and earthworm-based media. D. Conidia production (×10⁵ conidia/mL) according to concentration and earthworm-based medium. E. Percent germination on conventional and earthworm-based media. F. Percent germination as a function of concentration and earthworm-based medium. Concentrations are equivalent to C1 = 40 g/L, C2 = 20 g/L, C3 = 10 g/L, and C4 = 5 g/L. Results of one-way ANOVA (A, C, E) or two-way ANOVA (B, D, F), and differences are significant at Tukey's test (HSD) and groups "a", "b" and "c".
Fig. 2 in A new methodology to evaluate entomopathogenic fungi and formulated insecticides to control adults of Aedes aegypti (Diptera: Culicidae)
Fig. 2. The mortality proportion of Aedes aegypti females caused by isolates of Beauveria spp. at 20 d afer application. Error bars represent 95% confidence intervals back-transformed from the logistic scale. An asterisk (*) indicates that the treatment was significantly different from the control.
Fig. 1 in A new methodology to evaluate entomopathogenic fungi and formulated insecticides to control adults of Aedes aegypti (Diptera: Culicidae)
Fig. 1. Adults of Aedes aegypti L. contained inside a Petri dish covered with tulle: (a) Petri dish; (b) tulle; (c) straw; (d) natural rubber band.
Fig. 2 in Evaluation of isolates of entomopathogenic fungi in the genera Metarhizium, Beauveria, and Isaria, and their virulence to Thaumastocoris peregrinus (Hemiptera: Thaumastocoridae)
Fig. 2. Daily mean survival curves for adult Thaumastocoris peregrinus exposed to entomopathogenic fungal isolates of the genera Beauveria, Metarhizium, and Isaria for a period of 10 d. The horizontal dotted line indicates insect mortality of 50%.
Fig. 1 in Evaluation of isolates of entomopathogenic fungi in the genera Metarhizium, Beauveria, and Isaria, and their virulence to Thaumastocoris peregrinus (Hemiptera: Thaumastocoridae)
Fig. 1. Percentage of confirmed mortality of Thaumastocoris peregrinus, treat- ed with suspensions of 1 × 108 conidia per mL of entomopathogenic fungal isolates. Different letters above the bars indicate differences between treatments by Tukey's test (P <0.05). Bars represent the error ± 1 × SEM (df = 100).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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