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一种在福尔马林固定、石蜡包埋的猪组织中鉴定支持猪圆环病毒2型复制的细胞类型的新方法。

A new method to identify cell types that support porcine circovirus type 2 replication in formalin-fixed, paraffin-embedded swine tissues.

作者信息

Pérez-Martín Eva, Rovira Albert, Calsamiglia Maria, Mankertz Annette, Rodríguez Fernando, Segalés Joaquim

机构信息

Centre de Recerca en Sanitat Animal (CReSA), 08193 Bellaterra, Spain.

出版信息

J Virol Methods. 2007 Dec;146(1-2):86-95. doi: 10.1016/j.jviromet.2007.06.005. Epub 2007 Jul 20.

Abstract

Porcine circovirus type 2 (PCV2) is detected in high amounts within the characteristic microscopic lesions of postweaning multisystemic wasting syndrome (PMWS) affected pigs. In spite of recent advances on disease pathogenesis, the precise cell types that support viral replication are still a major issue of scientific discussion. In this study, a new methodology to detect cell types that support PCV2 replication was designed. For this purpose, two in situ hybridisation (ISH) methods were developed and applied on tissues of PMWS naturally affected pigs using two probes designed from the ORF1 sequence of the virus. While the complementary probe (CP) detected ssDNA, ORF1 mRNA and replicative form (RF) of PCV2, the RF probe (RFP) exclusively hybridised with the RF of the virus, thus, only labelling cells where PCV2 replication is taking place. Both probes demonstrated to be specific and equally sensitive by an in vitro Southern blot hybridisation assay. ISH labelling with the CP was extensive in lymphoid tissues and of variable amount in other non-lymphoid tissues. With this probe, mainly macrophage-like cells were labelled but also other cell types such as hepatocytes and other epithelial cells. Tissues in which RFP labelling was found more frequently were lung, inguinal and mesenteric lymph nodes, tonsil and liver. Labelling with the RFP was always nuclear, and found in the same cell types as with the CP, although in a relatively low proportion of them; labelling of macrophage-like cells was infrequent. Therefore, the results indicate that at least a certain proportion of macrophages may support PCV2 replication, but main cells where PCV2 replicates are of epithelial/endothelial origin. In summary, the present study permitted the study of cell types that support PCV2 replication by the use of ISH on formalin-fixed, paraffin-embedded tissues of PMWS affected pigs.

摘要

在受断奶后多系统消耗综合征(PMWS)影响的猪的特征性微观病变中大量检测到2型猪圆环病毒(PCV2)。尽管在疾病发病机制方面取得了最新进展,但支持病毒复制的精确细胞类型仍是科学讨论的一个主要问题。在本研究中,设计了一种检测支持PCV2复制的细胞类型的新方法。为此,开发了两种原位杂交(ISH)方法,并使用从病毒ORF1序列设计的两种探针应用于自然感染PMWS的猪的组织。互补探针(CP)可检测PCV2的单链DNA、ORF1 mRNA和复制型(RF),而RF探针(RFP)仅与病毒的RF杂交,因此,仅标记发生PCV2复制的细胞。通过体外Southern印迹杂交试验证明,两种探针均具有特异性且灵敏度相同。用CP进行ISH标记在淋巴组织中广泛存在,在其他非淋巴组织中的数量各不相同。使用该探针,主要标记巨噬细胞样细胞,但也标记其他细胞类型,如肝细胞和其他上皮细胞。发现RFP标记更频繁的组织是肺、腹股沟和肠系膜淋巴结、扁桃体和肝脏。用RFP标记总是在细胞核中,并且在与CP相同的细胞类型中发现,尽管比例相对较低;巨噬细胞样细胞的标记很少见。因此,结果表明至少一定比例的巨噬细胞可能支持PCV2复制,但PCV2复制的主要细胞是上皮/内皮来源的。总之,本研究通过对受PMWS影响的猪的福尔马林固定、石蜡包埋组织进行ISH,允许研究支持PCV2复制的细胞类型。

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