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85 results for “Diaphorina”
High quality, chromosome-scale genome assemblies: Comparisons of three Diaphorina citri (Asian Citrus Psyllid) geographic populations
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Diaphorina citri new genome annotations and GO terms (2021)
<p>Additional genome annotations for the <em>Diaphorina citri</em> genome (Diaci_v3) including: TEs, intergenic regions and putative promotors, also additional gene ontology terms annotated using EGGnog. </p>
Fig. 1 in Feeding behavior of Diaphorina citri (Hemiptera: Liviidae) and its acquisition of 'Candidatus Liberibacter asiaticus', on huanglongbing-infected Citrus reticulata leaves of several maturity stages
Fig. 1. Sketches of citrus leaves at several maturity stages.
Infection with 'Candidatus Liberibacter asiaticus' improves the fecundity of Diaphorina citri aiding its proliferation: a win-win strategy
<p>The coevolution between insect vectors and pathogens has long been of interest in molecular ecology and evolutionary biology, and <em>Diaphorina citri</em> is the main insect vector of the bacterium, ‘<em>Candidatus</em> Liberibacter asiaticus’ (<em>C</em>Las), the putative cause of the severe Asian form of huanglongbing. <em>C</em>Las-positive <em>D. citri</em> are more fecund than their <em>C</em>Las-negative counterparts; however, the molecular mechanism underlying of increased fecundity remains unclear. Here, we found that <em>C</em>Las promoted ovarian development and increased the expression of the <em>vitellogenin</em> <em>receptor</em> (<em>Dc</em><em>VgR</em>) in ovaries. <em>Dc</em><em>VgR</em> RNAi significantly decreased fecundity and <em>C</em>Las titer in ovaries, extended the preoviposition period, shortened the oviposition period, and blocked ovarian development. Combined <em>in vivo</em> and <em>in vitro</em> experiments showed that miR-275 suppressed <em>Dc</em><em>VgR</em> expression by binding to its 3’ untranslated region. Overexpression of miR-275 resulted in a decline of <em>Dc</em><em>VgR</em> expression and <em>C</em>Las titer in ovaries and caused reproductive defects that mimicked <em>Dc</em><em>VgR</em> knockdown phenotypes. After infection with <em>C</em>Las, the juvenile hormone (JH) signaling pathway was upregulated thereby increasing <em>Dc</em><em>VgR</em> expression via the JH receptor, <em>methoprene-tolerant</em> (Met), and downstream key transcription factor <em>Krüppel homolog 1</em>. As a result, <em>C</em>Las hijacks the JH signaling pathway and host miR-275 that targets <em>Dc</em><em>VgR</em> to improve <em>D. citri</em> fecundity, while simultaneously increasing the replication of <em>C</em>Las itself, suggesting a mutualistic interaction in <em>D. citri </em>ovaries with <em>C</em>Las.</p>
Data from: Insect-microbe-fungus interplay in citrus agro-ecosystems: Cuticular symbionts mediate <em>Diaphorina citri</em> resistance to <em>Beauveria bassiana</em>
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FIGURES 13–16. Diaphorina spp., fifth instar immature. 13. Habitus. 14–16. Caudal plate. 13, 14. D in The jumping plant-louse Diaphorina teucrii sp. nov. (Hemiptera, Liviidae) associated with Teucrium (Lamiaceae) and its parasitoid Tamarixia dorchinae sp. nov. (Hymenoptera, Eulophidae) from the Negev desert, Israel
FIGURES 13–16. Diaphorina spp., fifth instar immature. 13. Habitus. 14–16. Caudal plate. 13, 14. D. teucrii sp. nov. 15. D. chobauti. 16. D. luteola.
FIGURES 23–27. Tamarixia spp. 23. T in The jumping plant-louse Diaphorina teucrii sp. nov. (Hemiptera, Liviidae) associated with Teucrium (Lamiaceae) and its parasitoid Tamarixia dorchinae sp. nov. (Hymenoptera, Eulophidae) from the Negev desert, Israel
FIGURES 23–27. Tamarixia spp. 23. T. bicolor Mercet, right antenna, female. 24. T. flaviventris Kostjukov, right antenna female. 25–26. T. pronomus (Walker). 25—left antenna, female; 26—left forewing, female. 27. T. upis Walker, left antenna, female.
FIGURES 1–6. Diaphorina spp. 1 in The jumping plant-louse Diaphorina teucrii sp. nov. (Hemiptera, Liviidae) associated with Teucrium (Lamiaceae) and its parasitoid Tamarixia dorchinae sp. nov. (Hymenoptera, Eulophidae) from the Negev desert, Israel
FIGURES 1–6. Diaphorina spp. 1. Head and thorax, dorsal view. 2–4. Head. 5, 6. Forewing. 1, 2, 5. D. teucrii sp. nov. 3, 6. D. chobauti. 4. D. lycii.
FIGURES 7–12 in The jumping plant-louse Diaphorina teucrii sp. nov. (Hemiptera, Liviidae) associated with Teucrium (Lamiaceae) and its parasitoid Tamarixia dorchinae sp. nov. (Hymenoptera, Eulophidae) from the Negev desert, Israel
FIGURES 7–12. Diaphorina teucrii sp. nov. 7. Male terminalia, in profile. 8. Paramere, inner face. 9. Distal portion of aedeagus. 10. Female terminalia, in profile. 11. Section of circumanal ring. 12. Antenna of fifth instar immature.
FIGURES 17–22 in The jumping plant-louse Diaphorina teucrii sp. nov. (Hemiptera, Liviidae) associated with Teucrium (Lamiaceae) and its parasitoid Tamarixia dorchinae sp. nov. (Hymenoptera, Eulophidae) from the Negev desert, Israel
FIGURES 17–22. Tamarixia dorchinae sp. nov. 17. Habitus, female. 18. Habitus, male. 19. Left antenna, female. 20. Left forewing, female. 21. Right antenna, male. 22. Left forewing, male.
Host Finding Disruption of Diaphorina Citri by Guava Shoot Extract and Menochilus Sexmaculatus
<div> <p>This material has presented on 2nd International Conference on Advance Research in Agriculture and Food 2023 in October 25, 2023.</p> </div>
Figure 2 in Shamshevia, a new genus of long-legged flies from Namibia (Diptera: Dolichopodidae: Diaphorinae)
Figure 2. Shamshevia hoanibensis Grichanov sp. nov., body in alcohol, general aspect (transmitted light).
Figure 1 in Shamshevia, a new genus of long-legged flies from Namibia (Diptera: Dolichopodidae: Diaphorinae)
Figure 1. Shamshevia hoanibensis Grichanov sp. nov., body in alcohol, general aspect (reflected light).
Figure 5 in Shamshevia, a new genus of long-legged flies from Namibia (Diptera: Dolichopodidae: Diaphorinae)
Figure 5. Shamshevia hoanibensis Grichanov sp. nov., hypopygium, left lateral aspect. Abbreviations: cer, cercus; ep, epandrium; epl, epandrial lobe; hyp, hypandrium; pgt, postgonite; ph, phallus; dsur; vsur, surstylus (dorsal and ventral lobes).
Figure 5 in Diaphorina pfanderae Aléné and Burckhardt sp. nov. (Hemiptera: Psylloidea: Psyllidae) and its association with ants on Ozoroa pulcherrima (Anacardiaceae)
Figure 5. Diaphorina pfanderae Aléné and Burckhardt sp. nov., egg and immatures. (a) Habitus of fifth instar, left side; (b) egg clusters and immatures; (c) caudal plate; (d) colony covered in honeydew; (e) circumanal ring.
Figure 4 in Diaphorina pfanderae Aléné and Burckhardt sp. nov. (Hemiptera: Psylloidea: Psyllidae) and its association with ants on Ozoroa pulcherrima (Anacardiaceae)
Figure 4. Diaphorina pfanderae Aléné and Burckhardt sp. nov., terminalia and egg. (a) Male terminalia, in profile; (b) inner face of paramere; (c) distal two segments of aedeagus; (d) female terminalia, in profile; (e) section of circumanal ring; (f) egg, in profile.
Figure 1 in Diaphorina pfanderae Aléné and Burckhardt sp. nov. (Hemiptera: Psylloidea: Psyllidae) and its association with ants on Ozoroa pulcherrima (Anacardiaceae)
Figure 1. Host plant, habitat and associated ants of Diaphorina pfanderae Aléné and Burckhardt sp. nov. (a) Ozoroa pulcherrima; (b) study site; (c, d) immatures with Camponotus congolensis.
Figure 2 in Diaphorina pfanderae Aléné and Burckhardt sp. nov. (Hemiptera: Psylloidea: Psyllidae) and its association with ants on Ozoroa pulcherrima (Anacardiaceae)
Figure 2. Maps of the study site. (a) Cameroon with its regions; light grey = West Region. (b) West Region with departments; grey = Department of Noun, subdivided into communes; dark grey = commune of Koutaba; star = study site.
Figure 3 in Diaphorina pfanderae Aléné and Burckhardt sp. nov. (Hemiptera: Psylloidea: Psyllidae) and its association with ants on Ozoroa pulcherrima (Anacardiaceae)
Figure 3. Diaphorina pfanderae Aléné and Burckhardt sp. nov., adults. (a) Habitus, in profile, of male; (b) habitus, in profile, of female; (c) head, dorsal view; (d) antenna; (e) fore wing.
Fig. 2 in Feeding behavior of Diaphorina citri (Hemiptera: Liviidae) and its acquisition of 'Candidatus Liberibacter asiaticus', on huanglongbing-infected Citrus reticulata leaves of several maturity stages
Fig. 2. Visual representation of EPG waveforms E1 (phloem salivation), E2 (phloem ingestion) and G (xylem ingestion) produced by adult Diaphorina citri feeding on HLB-infected Citrus sunki leaves.
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