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首页> 外文期刊>Viruses >Interaction of a Densovirus with Glycans of the Peritrophic Matrix Mediates Oral Infection of the Lepidopteran Pest Spodoptera frugiperda
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Interaction of a Densovirus with Glycans of the Peritrophic Matrix Mediates Oral Infection of the Lepidopteran Pest Spodoptera frugiperda

机译:齿状病毒与周围营养的聚糖的相互作用介导鳞翅目害虫Spodoptera frugiperda的口腔感染。

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The success of oral infection by viruses depends on their capacity to overcome the gut epithelial barrier of their host to crossing over apical, mucous extracellular matrices. As orally transmitted viruses, densoviruses, are also challenged by the complexity of the insect gut barriers, more specifically by the chitinous peritrophic matrix, that lines and protects the midgut epithelium; how capsids stick to and cross these barriers to reach their final cell destination where replication goes has been poorly studied in insects. Here, we analyzed the early interaction of the Junonia coenia densovirus (JcDV) with the midgut barriers of caterpillars from the pest Spodoptera frugiperda . Using combination of imaging, biochemical, proteomic and transcriptomic analyses, we examined in vitro, ex vivo and in vivo the early interaction of the capsids with the peritrophic matrix and the consequence of early oral infection on the overall gut function. We show that the JcDV particle rapidly adheres to the peritrophic matrix through interaction with different glycans including chitin and glycoproteins, and that these interactions are necessary for oral infection. Proteomic analyses of JcDV binding proteins of the peritrophic matrix revealed mucins and non-mucins proteins including enzymes already known to act as receptors for several insect pathogens. In addition, we show that JcDV early infection results in an arrest of N -Acetylglucosamine secretion and a disruption in the integrity of the peritrophic matrix, which may help viral particles to pass through. Finally, JcDV early infection induces changes in midgut genes expression favoring an increased metabolism including an increased translational activity. These dysregulations probably participate to the overall dysfunction of the gut barrier in the early steps of viral pathogenesis. A better understanding of early steps of densovirus infection process is crucial to build biocontrol strategies against major insect pests.
机译:病毒经口感染的成功取决于其克服宿主的肠道上皮屏障以跨越根尖,粘液细胞外基质的能力。作为口头传播的病毒,densoviruses也受到昆虫肠道屏障的复杂性的挑战,更具体地说,是衬砌并保护中肠上皮的几丁质营养层基质的挑战。在昆虫中,衣壳如何黏附并越过这些障碍物到达最终的细胞复制目的地的研究很少。在这里,我们分析了Junonia coenia densovirus(JcDV)与来自害虫Spodoptera frugiperda的毛毛虫的中肠屏障的早期相互作用。使用成像,生化,蛋白质组和转录组分析的组合,我们在体外,离体和体内检查了衣壳与营养障碍基质的早期相互作用以及早期口腔感染对整体肠道功能的影响。我们表明,JcDV颗粒通过与包括甲壳质和糖蛋白在内的不同聚糖的相互作用而迅速粘附在营养周质基质上,并且这些相互作用对于口腔感染是必需的。对营养缺陷型基质的JcDV结合蛋白的蛋白质组学分析显示粘蛋白和非粘蛋白蛋白,包括已知可作为几种昆虫病原体受体的酶。此外,我们表明JcDV早期感染导致N-乙酰氨基葡萄糖分泌的停止和周围营养基质的完整性破坏,这可能有助于病毒颗粒通过。最后,JcDV早期感染诱导中肠基因表达发生变化,有利于增加新陈代谢,包括增加翻译活性。这些异常调节可能参与了病毒发病机理的早期阶段肠屏障的整体功能障碍。更好地了解Densovirus感染过程的早期步骤对于建立针对主要害虫的生物防治策略至关重要。

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