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杆状病毒感染因子 1 和 2 的 C 末端通过促进 PIF0 和 PIF8 与进入复合物核心的结合来介导 ODV 的口服感染。

The C-termini of the baculovirus infectivity factors 1 and 2 mediate ODV oral infectivity by facilitating the binding of PIF0 and PIF8 to the core of the entry complex.

机构信息

Laboratory of Virology, Wageningen University and Research, The Netherlands.

Summerland Research and Development Centre, 4200 Highway #97, Agriculture and Agri-Food Canada, Summerland, British Columbia, Canada.

出版信息

J Gen Virol. 2020 May;101(5):553-564. doi: 10.1099/jgv.0.001404. Epub 2020 Mar 17.

DOI:10.1099/jgv.0.001404
PMID:32182204
Abstract

Oral infection of caterpillars by baculoviruses is initiated by occlusion-derived virus particles (ODVs) that infect midgut epithelium cells. The ODV envelope therefore contains at least ten different proteins, which are called infectivity factors (PIFs). Nine of these PIFs form the so-called ODV entry complex that consists of a stable core formed by PIF1, 2, 3 and 4, to which the other PIFs [PIF0, 6, 7, 8 and 9 ()] bind with lower affinity. PIF1 and 2 are not only essential for complex formation, but also mediate ODV-binding to the epithelial brush border, probably via the C-termini. To study the involvement of these PIFs during midgut infection in greater detail, we assessed the oral infectivity and the ability to form the complex of a series of PIF1 and PIF2 C-terminal truncation mutants of Autographa californica multiple nucleopolyhedrovirus (AcMNPV), which were constructed in this study. Limited truncation of either PIF1 or 2 already severely impaired the ODV oral infectivity, but did not affect the formation of the core complex. However, the entry complex as a whole was not assembled in these mutants as PIF0 and 8 failed to bind to the core. This suggests that the interactions between the core and the loosely associated PIFs are important for the ODV infectivity and that complex formation complicates the determination of the exact roles of PIF1 and 2 during midgut infection. We also showed that the presence of PIF0, 6 and the ZF-domain of PIF8 are crucial for complex formation.

摘要

昆虫杆状病毒通过由封闭衍生的病毒粒子(ODV)感染中肠上皮细胞来引发对毛毛虫的口腔感染。因此,ODV 包膜至少含有十种不同的蛋白质,这些蛋白质被称为感染性因子(PIF)。这 9 种 PIF 形成了所谓的 ODV 进入复合物,该复合物由 PIF1、2、3 和 4 形成的稳定核心组成,其他 PIF[PIF0、6、7、8 和 9()]以较低的亲和力结合到该核心上。PIF1 和 2 不仅对复合物的形成是必不可少的,而且还介导 ODV 与上皮刷状缘的结合,可能通过 C 末端。为了更详细地研究这些 PIF 在中肠感染中的参与,我们评估了一系列 Autographa californica 多角体病毒(AcMNPV)的 PIF1 和 PIF2 C 末端截短突变体的口腔感染力和形成复合物的能力,这些突变体是在本研究中构建的。PIF1 或 2 的有限截短已经严重损害了 ODV 的口腔感染力,但不影响核心复合物的形成。然而,整个进入复合物在这些突变体中没有组装,因为 PIF0 和 8 未能与核心结合。这表明核心和松散相关的 PIF 之间的相互作用对 ODV 的感染力很重要,并且复合物的形成使确定 PIF1 和 2 在中肠感染过程中的确切作用复杂化。我们还表明,PIF0、6 和 PIF8 的 ZF 结构域的存在对于复合物的形成是至关重要的。

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