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对在人血浆中鉴定出的两种人细小病毒PARV4基因型进行分级分离分析。

Analysis of two human parvovirus PARV4 genotypes identified in human plasma for fractionation.

作者信息

Fryer Jacqueline F, Delwart Eric, Bernardin Flavien, Tuke Philip W, Lukashov Vladimir V, Baylis Sally A

机构信息

Division of Virology, National Institute for Biological Standards and Control, Blanche Lane, South Mimms, Potters Bar, Hertfordshire, EN6 3QG, UK.

University of California, San Francisco, CA 94118, USA.

出版信息

J Gen Virol. 2007 Aug;88(Pt 8):2162-2167. doi: 10.1099/vir.0.82620-0.

Abstract

The presence of the novel parvovirus PARV4 and a related variant, PARV5, was recently demonstrated in pooled plasma used in the manufacture of blood and plasma-derived medicinal products. DNA sequence analysis of nearly full-length genomes of four PARV4 and two PARV5 strains from manufacturing plasma pools is now presented. Like PARV4, PARV5 encodes two non-overlapping open reading frames (ORF1 and ORF2), homologous to the non-structural and capsid proteins of other parvoviruses, respectively. A highly conserved region in ORF2 contains phospholipase A2 motifs involved in parvovirus infectivity. Hybridization of strand-specific probes to DNA extracted from high-titre, PARV4-positive plasma revealed that the positive and negative strands are packaged into PARV4 virions in similar quantities. This extended analysis of nearly full-length PARV4 and PARV5 sequences suggests that they are closely related genotypes and the use of a single virus name, PARV4, comprising genotypes 1 and 2 (previously termed PARV5) is proposed.

摘要

最近在用于制造血液和血浆衍生药品的混合血浆中发现了新型细小病毒PARV4和一种相关变体PARV5。本文现展示了来自生产血浆库的4株PARV4和2株PARV5菌株的近全长基因组的DNA序列分析。与PARV4一样,PARV5编码两个不重叠的开放阅读框(ORF1和ORF2),分别与其他细小病毒的非结构蛋白和衣壳蛋白同源。ORF2中的一个高度保守区域包含参与细小病毒感染性的磷脂酶A2基序。用链特异性探针与从高滴度PARV4阳性血浆中提取的DNA杂交,结果显示正链和负链以相似的量包装到PARV4病毒粒子中。对PARV4和PARV5近全长序列的这种扩展分析表明,它们是密切相关的基因型,并建议使用单一病毒名称PARV4,包括基因型1和2(以前称为PARV5)。

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