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Maeto Kaoru - One of the best experts on this subject based on the ideXlab platform.
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FIGURE 12 in Taxonomic status of the subgenus Conoblasta Förster 1869 of the genus Glypta Gravenhorst 1829 with revision of Japanese species (Hymenoptera, Ichneumonidae, Banchinae)
2014Co-Authors: Watanabe Kyohei, Maeto KaoruAbstract:FIGURE 12. Distribution of Glypta extincta Ratzeberg, G. flavitarsus sp. nov., G. ichitai sp. nov. and G. kamijoi Momoi
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FIGURE 10 in Taxonomic status of the subgenus Conoblasta Förster 1869 of the genus Glypta Gravenhorst 1829 with revision of Japanese species (Hymenoptera, Ichneumonidae, Banchinae)
2014Co-Authors: Watanabe Kyohei, Maeto KaoruAbstract:FIGURE 10. Distribution of Glypta acares Momoi, G. biauriculata Kuslitzky, G. chinensis (Uchida) and C, G. cognata sp. nov
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FIGURE 8 in Taxonomic status of the subgenus Conoblasta Förster 1869 of the genus Glypta Gravenhorst 1829 with revision of Japanese species (Hymenoptera, Ichneumonidae, Banchinae)
2014Co-Authors: Watanabe Kyohei, Maeto KaoruAbstract:FIGURE 8. Male subgenital plates (ventral view: A, D, G, J, M), right volsellae (mesal view: B, E, H, K, N) and right aedeagi (lateral view: C, F, I, L, O) of Glypta. — A–C, G. biauriculata Kuslitzky; D–F, G. cymolomiae Uchida; G–I, G. extincta Ratzeberg; J–L, G. ichitai sp. nov. (paratype); M–O, G. tumor Momoi
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FIGURE 2 in Taxonomic status of the subgenus Conoblasta Förster 1869 of the genus Glypta Gravenhorst 1829 with revision of Japanese species (Hymenoptera, Ichneumonidae, Banchinae)
2014Co-Authors: Watanabe Kyohei, Maeto KaoruAbstract:FIGURE 2. Head of Glypta, lateral view. ― A, G. biauriculata Kuslitzky; B, G. chinensis (Uchida); C, G. cognata sp. nov.; D, G. cymolomiae Uchida; E, G. daisetsuzana sp. nov.; F, G. densepunctata sp. nov.; G, G. extincta Ratzeberg; H. G. flavitarsus sp. nov.; I, G. ichitai sp. nov.; J, G. kamijoi Momoi; K, G. karasawensis sp. nov.; L, G. nipponica sp. nov.; M, G. shigaensis sp. nov.; N, G. suwai sp. nov.; O, G. touyaensis sp. nov.; P, G. tumor Momoi; Q, G. zenibakoensis sp. nov
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FIGURE 1 in Taxonomic status of the subgenus Conoblasta Förster 1869 of the genus Glypta Gravenhorst 1829 with revision of Japanese species (Hymenoptera, Ichneumonidae, Banchinae)
2014Co-Authors: Watanabe Kyohei, Maeto KaoruAbstract:FIGURE 1. Head of Glypta, dorsal view. ― A, G. biauriculata Kuslitzky; B, G. chinensis (Uchida); C, G. cognata sp. nov.; D, G. cymolomiae Uchida; E, G. daisetsuzana sp. nov.; F, G. densepunctata sp. nov.; G, G. extincta Ratzeberg; H. G. flavitarsus sp. nov.; I, G. ichitai sp. nov.; J, G. kamijoi Momoi; K, G. karasawensis sp. nov.; L, G. nipponica sp. nov.; M, G. shigaensis sp. nov.; N, G. suwai sp. nov.; O, G. touyaensis sp. nov.; P, G. tumor Momoi; Q, G. zenibakoensis sp. nov
Watanabe Kyohei - One of the best experts on this subject based on the ideXlab platform.
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FIGURE 12 in Taxonomic status of the subgenus Conoblasta Förster 1869 of the genus Glypta Gravenhorst 1829 with revision of Japanese species (Hymenoptera, Ichneumonidae, Banchinae)
2014Co-Authors: Watanabe Kyohei, Maeto KaoruAbstract:FIGURE 12. Distribution of Glypta extincta Ratzeberg, G. flavitarsus sp. nov., G. ichitai sp. nov. and G. kamijoi Momoi
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FIGURE 10 in Taxonomic status of the subgenus Conoblasta Förster 1869 of the genus Glypta Gravenhorst 1829 with revision of Japanese species (Hymenoptera, Ichneumonidae, Banchinae)
2014Co-Authors: Watanabe Kyohei, Maeto KaoruAbstract:FIGURE 10. Distribution of Glypta acares Momoi, G. biauriculata Kuslitzky, G. chinensis (Uchida) and C, G. cognata sp. nov
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FIGURE 8 in Taxonomic status of the subgenus Conoblasta Förster 1869 of the genus Glypta Gravenhorst 1829 with revision of Japanese species (Hymenoptera, Ichneumonidae, Banchinae)
2014Co-Authors: Watanabe Kyohei, Maeto KaoruAbstract:FIGURE 8. Male subgenital plates (ventral view: A, D, G, J, M), right volsellae (mesal view: B, E, H, K, N) and right aedeagi (lateral view: C, F, I, L, O) of Glypta. — A–C, G. biauriculata Kuslitzky; D–F, G. cymolomiae Uchida; G–I, G. extincta Ratzeberg; J–L, G. ichitai sp. nov. (paratype); M–O, G. tumor Momoi
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FIGURE 2 in Taxonomic status of the subgenus Conoblasta Förster 1869 of the genus Glypta Gravenhorst 1829 with revision of Japanese species (Hymenoptera, Ichneumonidae, Banchinae)
2014Co-Authors: Watanabe Kyohei, Maeto KaoruAbstract:FIGURE 2. Head of Glypta, lateral view. ― A, G. biauriculata Kuslitzky; B, G. chinensis (Uchida); C, G. cognata sp. nov.; D, G. cymolomiae Uchida; E, G. daisetsuzana sp. nov.; F, G. densepunctata sp. nov.; G, G. extincta Ratzeberg; H. G. flavitarsus sp. nov.; I, G. ichitai sp. nov.; J, G. kamijoi Momoi; K, G. karasawensis sp. nov.; L, G. nipponica sp. nov.; M, G. shigaensis sp. nov.; N, G. suwai sp. nov.; O, G. touyaensis sp. nov.; P, G. tumor Momoi; Q, G. zenibakoensis sp. nov
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FIGURE 1 in Taxonomic status of the subgenus Conoblasta Förster 1869 of the genus Glypta Gravenhorst 1829 with revision of Japanese species (Hymenoptera, Ichneumonidae, Banchinae)
2014Co-Authors: Watanabe Kyohei, Maeto KaoruAbstract:FIGURE 1. Head of Glypta, dorsal view. ― A, G. biauriculata Kuslitzky; B, G. chinensis (Uchida); C, G. cognata sp. nov.; D, G. cymolomiae Uchida; E, G. daisetsuzana sp. nov.; F, G. densepunctata sp. nov.; G, G. extincta Ratzeberg; H. G. flavitarsus sp. nov.; I, G. ichitai sp. nov.; J, G. kamijoi Momoi; K, G. karasawensis sp. nov.; L, G. nipponica sp. nov.; M, G. shigaensis sp. nov.; N, G. suwai sp. nov.; O, G. touyaensis sp. nov.; P, G. tumor Momoi; Q, G. zenibakoensis sp. nov
Brian A. Federici - One of the best experts on this subject based on the ideXlab platform.
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Molecular evidence for the evolution of ichnoviruses from ascoviruses by symbiogenesis
BMC Evolutionary Biology, 2008Co-Authors: Yves Le Bigot, Sylvie Samain, Corinne Augé-gouillou, Brian A. FedericiAbstract:Background Female endoparasitic ichneumonid wasps inject virus-like particles into their caterpillar hosts to suppress immunity. These particles are classified as ichnovirus virions and resemble ascovirus virions, which are also transmitted by parasitic wasps and attack caterpillars. Ascoviruses replicate DNA and produce virions. Polydnavirus DNA consists of wasp DNA replicated by the wasp from its genome, which also directs particle synthesis. Structural similarities between ascovirus and ichnovirus particles and the biology of their transmission suggest that ichnoviruses evolved from ascoviruses, although molecular evidence for this hypothesis is lacking. Results Here we show that a family of unique pox-D5 NTPase proteins in the Glypta fumiferanae ichnovirus are related to three Diadromus pulchellus ascovirus proteins encoded by ORFs 90, 91 and 93. A new alignment technique also shows that two proteins from a related ichnovirus are orthologs of other ascovirus virion proteins. Conclusion Our results provide molecular evidence supporting the origin of ichnoviruses from ascoviruses by lateral transfer of ascoviral genes into ichneumonid wasp genomes, perhaps the first example of symbiogenesis between large DNA viruses and eukaryotic organisms. We also discuss the limits of this evidence through complementary studies, which revealed that passive lateral transfer of viral genes among polydnaviral, bacterial, and wasp genomes may have occurred repeatedly through an intimate coupling of both recombination and replication of viral genomes during evolution. The impact of passive lateral transfers on evolutionary relationships between polydnaviruses and viruses with large double-stranded genomes is considered in the context of the theory of symbiogenesis.
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Molecular evidence for the evolution of ichnoviruses from ascoviruses by symbiogenesis
BMC evolutionary biology, 2008Co-Authors: Yves Le Bigot, Sylvie Samain, Corinne Augé-gouillou, Brian A. FedericiAbstract:Female endoparasitic ichneumonid wasps inject virus-like particles into their caterpillar hosts to suppress immunity. These particles are classified as ichnovirus virions and resemble ascovirus virions, which are also transmitted by parasitic wasps and attack caterpillars. Ascoviruses replicate DNA and produce virions. Polydnavirus DNA consists of wasp DNA replicated by the wasp from its genome, which also directs particle synthesis. Structural similarities between ascovirus and ichnovirus particles and the biology of their transmission suggest that ichnoviruses evolved from ascoviruses, although molecular evidence for this hypothesis is lacking. Here we show that a family of unique pox-D5 NTPase proteins in the Glypta fumiferanae ichnovirus are related to three Diadromus pulchellus ascovirus proteins encoded by ORFs 90, 91 and 93. A new alignment technique also shows that two proteins from a related ichnovirus are orthologs of other ascovirus virion proteins. Our results provide molecular evidence supporting the origin of ichnoviruses from ascoviruses by lateral transfer of ascoviral genes into ichneumonid wasp genomes, perhaps the first example of symbiogenesis between large DNA viruses and eukaryotic organisms. We also discuss the limits of this evidence through complementary studies, which revealed that passive lateral transfer of viral genes among polydnaviral, bacterial, and wasp genomes may have occurred repeatedly through an intimate coupling of both recombination and replication of viral genomes during evolution. The impact of passive lateral transfers on evolutionary relationships between polydnaviruses and viruses with large double-stranded genomes is considered in the context of the theory of symbiogenesis.
Yves Le Bigot - One of the best experts on this subject based on the ideXlab platform.
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Molecular evidence for the evolution of ichnoviruses from ascoviruses by symbiogenesis
BMC Evolutionary Biology, 2008Co-Authors: Yves Le Bigot, Sylvie Samain, Corinne Augé-gouillou, Brian A. FedericiAbstract:Background Female endoparasitic ichneumonid wasps inject virus-like particles into their caterpillar hosts to suppress immunity. These particles are classified as ichnovirus virions and resemble ascovirus virions, which are also transmitted by parasitic wasps and attack caterpillars. Ascoviruses replicate DNA and produce virions. Polydnavirus DNA consists of wasp DNA replicated by the wasp from its genome, which also directs particle synthesis. Structural similarities between ascovirus and ichnovirus particles and the biology of their transmission suggest that ichnoviruses evolved from ascoviruses, although molecular evidence for this hypothesis is lacking. Results Here we show that a family of unique pox-D5 NTPase proteins in the Glypta fumiferanae ichnovirus are related to three Diadromus pulchellus ascovirus proteins encoded by ORFs 90, 91 and 93. A new alignment technique also shows that two proteins from a related ichnovirus are orthologs of other ascovirus virion proteins. Conclusion Our results provide molecular evidence supporting the origin of ichnoviruses from ascoviruses by lateral transfer of ascoviral genes into ichneumonid wasp genomes, perhaps the first example of symbiogenesis between large DNA viruses and eukaryotic organisms. We also discuss the limits of this evidence through complementary studies, which revealed that passive lateral transfer of viral genes among polydnaviral, bacterial, and wasp genomes may have occurred repeatedly through an intimate coupling of both recombination and replication of viral genomes during evolution. The impact of passive lateral transfers on evolutionary relationships between polydnaviruses and viruses with large double-stranded genomes is considered in the context of the theory of symbiogenesis.
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Molecular evidence for the evolution of ichnoviruses from ascoviruses by symbiogenesis
BMC evolutionary biology, 2008Co-Authors: Yves Le Bigot, Sylvie Samain, Corinne Augé-gouillou, Brian A. FedericiAbstract:Female endoparasitic ichneumonid wasps inject virus-like particles into their caterpillar hosts to suppress immunity. These particles are classified as ichnovirus virions and resemble ascovirus virions, which are also transmitted by parasitic wasps and attack caterpillars. Ascoviruses replicate DNA and produce virions. Polydnavirus DNA consists of wasp DNA replicated by the wasp from its genome, which also directs particle synthesis. Structural similarities between ascovirus and ichnovirus particles and the biology of their transmission suggest that ichnoviruses evolved from ascoviruses, although molecular evidence for this hypothesis is lacking. Here we show that a family of unique pox-D5 NTPase proteins in the Glypta fumiferanae ichnovirus are related to three Diadromus pulchellus ascovirus proteins encoded by ORFs 90, 91 and 93. A new alignment technique also shows that two proteins from a related ichnovirus are orthologs of other ascovirus virion proteins. Our results provide molecular evidence supporting the origin of ichnoviruses from ascoviruses by lateral transfer of ascoviral genes into ichneumonid wasp genomes, perhaps the first example of symbiogenesis between large DNA viruses and eukaryotic organisms. We also discuss the limits of this evidence through complementary studies, which revealed that passive lateral transfer of viral genes among polydnaviral, bacterial, and wasp genomes may have occurred repeatedly through an intimate coupling of both recombination and replication of viral genomes during evolution. The impact of passive lateral transfers on evolutionary relationships between polydnaviruses and viruses with large double-stranded genomes is considered in the context of the theory of symbiogenesis.
Michel Cusson - One of the best experts on this subject based on the ideXlab platform.
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ultrastructural and genomic characterization of a second banchine polydnavirus confirms the existence of shared features within this ichnovirus lineage
Journal of General Virology, 2013Co-Authors: Michel Cusson, Catherine Béliveau, Abdelmadjid Djoumad, Brian Boyle, Lisa KuhnAbstract:Polydnaviruses (PDVs) are symbiotic viruses carried by endoparasitic wasps and transmitted to caterpillar hosts during parasitization. Although they share several features, including a segmented dsDNA genome, a unique life cycle where replication is restricted to the wasp host, and immunodepressive/developmental effects on the caterpillar host, PDVs carried by ichneumonid and braconid wasps (referred to as ichnoviruses and bracoviruses, respectively) have different evolutionary origins. In addition, ichnoviruses (IVs) form two distinct lineages, with viral entities found in wasps belonging to the subfamilies Campopleginae and Banchinae displaying strikingly different virion morphologies and genomic features. However, the current description for banchine IVs is based on the characterization of a single species, namely that of the Glypta fumiferanae IV (GfIV). Here we provide an ultrastructural and genomic analysis of a second banchine IV isolated from the wasp Apophua simplicipes, and we show that this virus shares many features with GfIV, including a multi-nucleocapsid virion, an aggregate genome size of ~300 kb, genome segments <5 kb, an impressively high degree of genome segmentation and a very similar gene content (same gene families in both viruses). Altogether, the data presented here confirm the existence of shared characteristics within this banchine IV lineage.
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Genomics of Banchine Ichnoviruses:1 Insights into their Relationship to Bracoviruses and Campoplegine Ichnoviruses
2012Co-Authors: Michel Cusson, Jean-michel Drezen, Renée Lapointe, Catherine Béliveau, Audrey Nisole, Halim Maaroufi, Roger C LevesqueAbstract:Ichneumonid polydnaviruses, referred to as ichnoviruses (IVs), have so far been observed in only two parasitic wasp subfamilies, the Campopleginae and Banchinae. The IVs carried by banchine wasps have received limited attention, and most of what we know about them is based on the characterization of a single virus, the Glypta fumiferanae ichnovirus (GfIV). The latter differs considerably from the more extensively studied campoplegine IVs, both in terms of virion morphology and features of the packaged genome. These differences have in fact raised the question as to whether campoplegine and banchine IVs have a common ancestor. The present chapter provides a brief review of the current state of knowledge on banchine IVs, including results from recent genomic analyses. It also provides suggestions as to how to address, in future research, the question of whether the campoplegine and banchine IVs have a common origin.