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Spatial distribution of orally administered viral fusolin protein in the insect midgut and possible synergism between fusolin and digestive proteases to disrupt the midgut peritrophic matrix

机译:昆虫中肠道口服病毒素蛋白蛋白的空间分布及富士林和消化蛋白酶之间的可能协同作用,破坏中肠脱脂基质

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Oral inoculation of entomopoxvirus spindles, microstructures composed of fusolin protein, causes disruption of the peritrophic matrix (PM), a physical barrier against microbe infection, in the insect midgut. Although the atomic structure of fusolin has been determined, little has been directly elucidated of the mechanism of disruption of the PM. In the present study, we first performed an immunohistochemical examination to determine whether fusolin acts on the PM directly or indirectly in the midgut of Bombyx mori larvae that were inoculated with spindles of Anomala cuprea entomopoxvirus. This revealed that the PM, rather than the midgut cells, was the attachment site for fusolin. Fusolin broadly attached to the PM from the anterior to the posterior region, both to its ectoperitrophic and endoperitrophic surfaces and within the PM. These results likely explain why the whole of the PM is rapidly disintegrated. Second, we administered protease inhibitors mixed with spindles and observed decreased midgut protease activity and reduced disruption of the PM. This suggests that midgut protease(s) is also positively involved in PM disruption. Based on the present results, we propose an overall mechanism for the disruption of the PM by administration of fusolin.
机译:口服接种昆虫痘病毒血管,由Fusolin蛋白组成的微观结构导致卵巢中肠中的脱脂基质(PM),对微生物感染的物理屏障。虽然已经确定了Fusolin的原子结构,但是对PM破坏的机制很少一点被直接阐明。在本研究中,我们首先进行了免疫组化检查,以确定Fusolin是否直接或间接地在Bombyx Mori幼虫中直接或间接地用Anomala Cuprea昆虫毒oxvirus的主轴接种。这揭示了PM,而不是中肠细胞是富士林的附着位点。 Fusolin广泛地附着于从前部到后部到后部的PM,两者渗透渗透性和内骨渗透性表面和PM。这些结果可能解释了为什么整个PM迅速崩解。其次,我们施用蛋白酶抑制剂与主轴混合并观察到的中小蛋白蛋白酶活性降低并降低了PM的破坏。这表明中肠蛋白酶也积极参与PM中断。根据目前的结果,我们提出了通过施用Fusolin来破坏PM的总体机制。

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