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副痘病毒(PPV)分离株的比较和回顾性分子分析。

Comparative and retrospective molecular analysis of Parapoxvirus (PPV) isolates.

机构信息

Bavarian Health and Food Safety Authority, Oberschleissheim, Germany.

Laboratory for Functional Genome Analysis (LAFUGA), Gene Centre, Ludwig-Maximilians-Universität München, Munich, Germany.

出版信息

Virus Res. 2014 Mar 6;181:11-21. doi: 10.1016/j.virusres.2013.12.015. Epub 2013 Dec 27.

Abstract

Species members of the genus Parapoxvirus (PPV) within the family Poxviridae cause contagious pustular dermatitis in small ruminants (Orf virus, ORFV) and mostly mild localized inflammation in cattle (bovine papular stomatitis virus, BPSV and pseudocowpox virus, PCPV). All PPVs are known to be zoonotic, leading to circumscribed skin lesions in humans, historically known as milker's nodules. Human PPV isolates are often ill defined concerning their allocation to an animal origin. Here we present a comparative molecular analysis of a unique collection of 21 historic and recent human and animal PPV cell culture isolates (and two PPV DNA samples). Cell culture PPV propagation was restricted to primary ruminant fibroblasts and was strictly kept at low passages to avoid genomic changes by in vitro influences. For molecular arrangement of the isolate DNAs and their attribution to established PPV species DNA fragments of the PPVs were generated by two different discriminating PCR protocols, targeting the major part of the open reading frame (ORF) 011 (B2L gene) and the complete ORF 032. Multiple sequence alignments and phylogenetic analysis of both genes resulted in affiliation to the known PPV species. The sequences from the ORF 032 allowed discrimination of the isolate DNAs at a higher resolution. Human PPV isolates could be clearly assigned to the PPV species belonging to the reported or assumed animal host of transmission. For the first time, a whole PPV genome sequence comparison of a human biopsy derived virus (B029) and its ovine counterpart (B015) originating from a defined Orf outbreak in Germany is provided, revealing their well conserved relationship. Thus human PPVs can be molecularly retraced to the PPV species indicating the animal of transmission. After transmission to the human host, molecular conservation of the animal's virus peculiarities indicative for a PPV species became evident.

摘要

痘病毒科副痘病毒属的种成员引起小反刍动物的接触传染性脓疱性皮炎(口疮病毒,ORFV)和牛的主要是轻度局部炎症(牛丘疹性口炎病毒,BPSV 和假性牛痘病毒,PCPV)。所有副痘病毒都已知是人畜共患的,导致人类出现局限性皮肤损伤,历史上称为挤奶工结节。人类副痘病毒分离株的动物来源分配通常定义不明确。在这里,我们对一组独特的 21 个人类和动物副痘病毒细胞培养分离株(和两个副痘病毒 DNA 样本)进行了比较分子分析。细胞培养副痘病毒的繁殖仅限于原发性反刍动物成纤维细胞,并且严格保持在低传代数,以避免体外影响引起的基因组变化。为了对分离株 DNA 的分子排列及其归属建立的副痘病毒种,我们使用两种不同的区分 PCR 方案生成了 PPV 的 DNA 片段,该方案针对主要开放阅读框(ORF)011(B2L 基因)和完整的 ORF 032 部分。这两个基因的多重序列比对和系统发育分析导致了对已知副痘病毒种的归属。ORF 032 的序列允许在更高分辨率下区分分离株 DNA。人类副痘病毒分离株可以明确分配到属于报道或假定动物宿主传播的副痘病毒种。首次提供了从德国定义的 Orf 爆发中获得的人类活检衍生病毒(B029)及其绵羊对应物(B015)的完整副痘病毒基因组序列比较,揭示了它们良好的保守关系。因此,人类副痘病毒可以通过分子追踪到指示传播动物的副痘病毒种。在传播到人类宿主后,动物病毒特征的分子保守性变得明显,这些特征指示了副痘病毒种。

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