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The Porcine Deltacoronavirus Replication Organelle Comprises Double-Membrane Vesicles and Zippered Endoplasmic Reticulum with Double-Membrane Spherules

机译:猪Deltacoronavirus复制细胞器包括双膜囊泡和具有双膜球的双膜内质网

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摘要

Porcine deltacoronavirus (PDCoV) was first identified in Hong Kong in 2012 from samples taken from pigs in 2009. PDCoV was subsequently identified in the USA in 2014 in pigs with a history of severe diarrhea. The virus has now been detected in pigs in several countries around the world. Following the development of tissue culture adapted strains of PDCoV, it is now possible to address questions regarding virus−host cell interactions for this genera of coronavirus. Here, we presented a detailed study of PDCoV-induced replication organelles. All positive-strand RNA viruses induce the rearrangement of cellular membranes during virus replication to support viral RNA synthesis, forming the replication organelle. Replication organelles for the Alpha-, Beta-, and Gammacoronavirus genera have been characterized. All coronavirus genera induced the formation of double-membrane vesicles (DMVs). In addition, Alpha- and Betacoronaviruses induce the formation of convoluted membranes, while Gammacoronaviruses induce the formation of zippered endoplasmic reticulum (ER) with tethered double-membrane spherules. However, the structures induced by Deltacoronaviruses, particularly the presence of convoluted membranes or double-membrane spherules, are unknown. Initially, the dynamics of PDCoV strain OH-FD22 replication were assessed with the onset of viral RNA synthesis, protein synthesis, and progeny particle release determined. Subsequently, virus-induced membrane rearrangements were identified in infected cells by electron microscopy. As has been observed for all other coronaviruses studied to date, PDCoV replication was found to induce the formation of double-membrane vesicles. Significantly, however, PDCoV replication was also found to induce the formation of regions of zippered endoplasmic reticulum, small associated tethered vesicles, and double-membrane spherules. These structures strongly resemble the replication organelle induced by avian Gammacoronavirus infectious bronchitis virus.
机译:Porcine Deltacoronavirus(PDCOV)于2012年在香港确定,2009年从猪中取出的样本.PDCOV随后于2014年在美国在具有严重腹泻病史的猪中确定。现在在世界各国的猪中检测到病毒。在发展PDCOV的组织培养改性菌株之后,现在可以解决该属性冠状病毒的病毒 - 宿主细胞相互作用问题。在这里,我们介绍了对PDCOV诱导的复制细胞器的详细研究。所有正链RNA病毒诱导病毒复制期间细胞膜的重新排列,以支持病毒RNA合成,形成复制细胞器。已经表征了α,β-和γ-和γ-和γ-和γ-和γ-和γ-和γ-和γ-的复制细胞器。所有冠状病毒属,均诱导双膜囊泡(DMV)的形成。此外,α-和甲状腺蛋白捕获剂诱导染色膜的形成,而γAviruses诱导具有束双膜球的拉链内质网(ER)的形成。然而,德拉克罗腔捕获剂诱导的结构,特别是络合膜或双膜球的存在是未知的。最初,利用病毒RNA合成,蛋白质合成和确定后代颗粒释放来评估PDCOV菌株OH-FD22复制的动态。随后,通过电子显微镜在感染的细胞中鉴定病毒诱导的膜重排。如图所示,对于迄今为止研究的所有其他冠状病毒,发现PDCOV复制被发现诱导双膜囊泡的形成。然而,显着地,还发现PDCOV复制诱导诱导拉链内质网的区域,小相关的系叠囊泡和双膜球的形成。这些结构强烈类似于禽类伽马科病毒感染性支气管炎病毒引起的复制细胞器。

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