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47 results for “Entomopathogenic fungus”
Fig. 1 in Neem oil increases the efficiency of the entomopathogenic fungus Metarhizium anisopliae for the control of Aedes aegypti (Diptera: Culicidae) larvae
Fig. 1 Dacls survcval curves of Aedes aegypti larvae exposed to dcfferent concentratcons of neem ocl. Note: Results are the means (± SE) of three expercments for each treatment wcth 30 cnsects used per treatment for each expercment
Fig. 2 in Neem oil increases the efficiency of the entomopathogenic fungus Metarhizium anisopliae for the control of Aedes aegypti (Diptera: Culicidae) larvae
Fig. 2 Dacls survcval curves of Aedes aegypti larvae exposed to dcfferent concentratcons of Metarhizium anisopliae concdca. Note: Results are the means (± SE) of three expercments for each treatment wcth 30 cnsects used per treatment for each expercment
Figure 2. A in Susceptibility of Agriotes spp. larvae (Coleoptera: Elateridae) to stress-and-kill strategies using spinosad and the entomopathogenic fungus Metarhizium brunneum
Figure 2. A: MetarhIzIum brunneum strain ART2825 growth in the tracheae of AgrIotes obscurus 22 days posttreatment. B: ART2825 fungal colonization in the integument of A. obscurus 22 days posttreatment.
Figure 3. A in Susceptibility of Agriotes spp. larvae (Coleoptera: Elateridae) to stress-and-kill strategies using spinosad and the entomopathogenic fungus Metarhizium brunneum
Figure 3. A: Sporulation of MetarhIzIum brunneum strain 16P on AgrIotes sordIdus 21 days posttreatment (zoom ×6.7). B: M. brunneum strain 16P primary and secondary fungal growth, with melanotic spots (black arrow) on A. sordIdus (×6.7). C: ART2825 fungal growth on the cuticle of A. obscurus 22 days posttreatment. D: Fungal growth on the cuticle of A. obscurus, which could correspond to the secondary growth on the sclerites.
Figure 1. A in Susceptibility of Agriotes spp. larvae (Coleoptera: Elateridae) to stress-and-kill strategies using spinosad and the entomopathogenic fungus Metarhizium brunneum
Figure 1. A: Leg of AgrIotes obscurus exposed to MetarhIzIum brunneum strain ART2825 48 h posttreatment. B: intersegment area of A. obscurus exposed to M. brunneum strain F52 36 h posttreatment, C: Depression at the base of a setae of A. obscurus with F52 conidia 24 h posttreatment, D: Melanization on A. sordIdus exposed to M. brunneum strain 16P 21 days posttreatment (zoom x 6.7).
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".
Data Analysis for "Effects of an Entomopathogenic Fungus on the Reproductive Potential of Drosophila males"
<p>Dataset and code used for data analyses and visualization in our manuscript:</p> <p>"Effects of an Entomopathogenic Fungus on the Reproductive Potential of Drosophila Males"</p> <p>by Aijuan Liao, Fanny Cavigliasso, Loriane Savary and Tadeusz J. Kawecki</p> <p>Published in Ecology and Evolution</p>
Effects of the entomopathogenic fungus Mucor hiemalis BO-1 on the physical functions and transcriptional signatures of Bradysia odoriphaga larvae
<p><em><span>Mucor hiemalis</span></em><span> BO-1 is an entomopathogenic fungus that infects <em>Bradysia</em> <em>odoriphaga</em>, a destructive root maggot. <em>M</em>. <em>hiemalis</em> BO-1 possesses stronger pathogenicity to the larvae than to other stages of <em>B</em>. <em>odoriphaga</em> and provides satisfactory field control. However, the physiological response of <em>B</em>. <em>odoriphaga</em> larvae to infection and the infection mechanism of <em>M</em>. <em>hiemalis</em> are unknown. We detected some physiological indicators of diseased <em>B</em>. <em>odoriphaga</em> larvae infected by <em>M</em>. <em>hiemalis</em> BO-1. These included changes in consumption, nutrient contents and digestive and antioxidant enzymes. We performed transcriptome analysis of diseased <em>B</em>. <em>odoriphaga</em> larvae and found that M. <em>hiemalis</em> BO-1 showed acute toxicity to <em>B</em>. <em>odoriphaga</em> larvae and was as toxic as some chemical pesticides. The food consumption of diseased <em>B</em>. <em>odoriphaga</em> after inoculation with <em>M</em>. <em>hiemalis</em> spores decreased significantly, and there was a significant decrease in total protein, lipid and carbohydrates in diseased larvae. Key digestive enzymes (protease, </span>α<span>-amylase, lipase and cellulase) were significantly inhibited during infection. Peroxidase maintained high activity, and the activity of other antioxidant enzymes (catalase, superoxide dismutase and glutathione S-transferases) first increased and then decreased. Combined with the transcriptional signatures of diseased <em>B</em>. <em>odoriphaga</em> larvae, <em>M</em>. <em>hiemalis</em> BO-1 infection resulted in decreased food consumption, reduced digestive enzyme activity and altered energy metabolism and material accumulation. Infection was also accompanied by fluctuations in immune function, such as cytochrome P450 and the Toll pathway. Therefore, our results laid a basis for the further study of the interactions between <em>M</em>. <em>hiemalis</em> BO-1 and <em>B</em>. <em>odoriphaga</em> and promoted the genetic improvement of entomopathogenic fungi.</span></p>
Data from: First report of Fusarium citri as an entomopathogenic fungus mediating plant resistance against insect pests and phytopathogens
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Effects of the entomopathogenic fungus Mucor hiemalis BO-1 on the physical functions and transcriptional signatures of Bradysia odoriphaga larvae
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FIGURES 29–35 in Thitarodes namnai sp. nov. and T. caligophilus sp. nov. (Lepidoptera: Hepialidae), hosts of the economically important entomopathogenic fungus Ophiocordyceps sinensis in Bhutan
FIGURES 29–35. Thitarodes caligophilus, genitalia: 29–31. caudal, 32–35. latero-caudal view; 29. & 32. holotype, male, label 10027; 30. & 33. paratype, male, label 10025; 31. & 34. paratype, male, label 100026; 35. paratype, female, label 10028.
FIGURES 1–5 in Thitarodes namnai sp. nov. and T. caligophilus sp. nov. (Lepidoptera: Hepialidae), hosts of the economically important entomopathogenic fungus Ophiocordyceps sinensis in Bhutan
FIGURES 1–5. Thitarodes namnai: 1. holotype, male, label 10005; 2. & 3. holotype genitalia in caudal (2) and laterocaudal (3) view; 4. paratype, female, label 10010; 5. female paratype genitalia.
FIGURES 25–28 in Thitarodes namnai sp. nov. and T. caligophilus sp. nov. (Lepidoptera: Hepialidae), hosts of the economically important entomopathogenic fungus Ophiocordyceps sinensis in Bhutan
FIGURES 25–28. Thitarodes caligophilus: 25. holotype, male, label 10027; 26. paratype, female, label 10028; 27. paratype, male, label 10025; 28. paratype, male, label 100026.
FIGURES 6–13 in Thitarodes namnai sp. nov. and T. caligophilus sp. nov. (Lepidoptera: Hepialidae), hosts of the economically important entomopathogenic fungus Ophiocordyceps sinensis in Bhutan
FIGURES 6–13. Thitarodes namnai: 6–10. paratypes males; 6. label 10001; 7. label 10006; 8. label 10007; 9. label 10008; 10. label 10009; 11–13. paratypes females; 11. label 10002; 12. label 10003; 13. label 10004.
FIGURES 14–23 in Thitarodes namnai sp. nov. and T. caligophilus sp. nov. (Lepidoptera: Hepialidae), hosts of the economically important entomopathogenic fungus Ophiocordyceps sinensis in Bhutan
FIGURES 14–23. Thitarodes namnai, male genitalia, paratypes: 14–18. caudal view; 19–23. latero-caudal view; 14. & 19. label 10001; 15. & 20. label 10006; 16. & 21. label 10007; 17. & 22. label 10008; 18. & 23. label 10009.
FIGURE 4. A in Ophiocordyceps highlandensis, a new entomopathogenic fungus from Yunnan, China
FIGURE 4. A transversal section of the fertile portion of Ophiocordyceps highlandensis, showing the immersed perithecia.
FIGURE 3 in Ophiocordyceps highlandensis, a new entomopathogenic fungus from Yunnan, China
FIGURE 3. Morphological characters of Ophiocordyceps highlandensis. a. Mature stromata on the heads of the host (larvae of Scarabaeidae, Coleoptera). b. Immature asci at different stages of development. c. Ascus with mature ascospores. d. Mature ascospores showing the four part-spores. e. Longitudinal section of stipe, showing the cortex and the interior.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.