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源自L35淋巴母细胞系的克隆中2型猪圆环病毒的形态发生

Porcine circovirus type 2 morphogenesis in a clone derived from the l35 lymphoblastoid cell line.

作者信息

Rodríguez-Cariño C, Duffy C, Sánchez-Chardi A, McNeilly F, Allan G M, Segalés J

机构信息

Centre de Recerca en Sanitat Animal, Departament de Sanitat i Anatomia Animals, Campus de la Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain.

出版信息

J Comp Pathol. 2011 Feb-Apr;144(2-3):91-102. doi: 10.1016/j.jcpa.2010.07.001. Epub 2010 Aug 30.

Abstract

Porcine circovirus type 2 (PCV2) is the essential infectious agent of post-weaning multisystemic wasting syndrome (PMWS), one of the most important diseases of swine. Although several studies have described different biological properties of the virus, some aspects of its replication cycle, including ultrastructural alterations, remain unknown. The aim of the present study was to describe for the first time a complete morphogenesis study of PCV2 in a clone of the lymphoblastoid L35 cell line at the ultrastructural level using electron microscopy techniques. Cells were infected with PCV2 at a multiplicity of infection of 10 and examined at 0, 6, 12, 24, 48, 60 and 72h post-infection. PCV2 was internalized by endocytosis, after which the virus aggregated in intracytoplasmic inclusion bodies (ICIs). Subsequently, PCV2 was closely associated with mitochondria, completing a first cytoplasmic phase. The virus entered the nucleus for replication and virus assembly and encapsidation occurred with the participation of the nuclear membrane. Immature virions left the nucleus and formed ICIs in a second cytoplasmic phase. The results suggest that at the end of the replication cycle (between 24 and 48h), PCV2 was released either by budding of mature virion clusters or by lysis of apoptotic or dead cells. In conclusion, the L35-derived clone represents a suitable in-vitro model for PCV2 morphogenesis studies and characterization of the PCV2 replication cycle.

摘要

猪圆环病毒2型(PCV2)是断奶后多系统消耗综合征(PMWS)的主要感染因子,PMWS是猪最重要的疾病之一。尽管多项研究描述了该病毒的不同生物学特性,但其复制周期的一些方面,包括超微结构改变,仍不清楚。本研究的目的是首次使用电子显微镜技术在超微结构水平上描述PCV2在淋巴母细胞样L35细胞系的一个克隆中的完整形态发生研究。细胞以感染复数10感染PCV2,并在感染后0、6、12、24、48、60和72小时进行检查。PCV2通过内吞作用内化,之后病毒聚集在胞质内包涵体(ICI)中。随后,PCV2与线粒体紧密相关,完成第一个细胞质阶段。病毒进入细胞核进行复制,病毒装配和衣壳化在核膜的参与下发生。未成熟病毒粒子离开细胞核,并在第二个细胞质阶段形成ICI。结果表明,在复制周期结束时(24至48小时之间),PCV2通过成熟病毒粒子簇出芽或通过凋亡或死亡细胞的裂解而释放。总之,L35衍生的克隆代表了一个适合用于PCV2形态发生研究和PCV2复制周期表征的体外模型。

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