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人1型免疫缺陷病毒对单核母细胞样细胞的持续感染会导致自身整合病毒DNA的积累以及缺陷病毒粒子的产生。

Persistent human immunodeficiency virus type 1 infection of monoblastoid cells leads to accumulation of self-integrated viral DNA and to production of defective virions.

作者信息

Pauza C D, Galindo J

机构信息

Developmental Biology Laboratory, Salk Institute for Biological Studies, San Diego, California 92138-9216.

出版信息

J Virol. 1989 Sep;63(9):3700-7. doi: 10.1128/JVI.63.9.3700-3707.1989.

DOI:10.1128/JVI.63.9.3700-3707.1989
PMID:2760979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC250961/
Abstract

Cell-free virus preparations from persistently infected monoblastoid cells (HU937) become progressively less infectious during long-term passage. This effect is specific for cell lines derived from U937 and is not observed in persistently infected T-cell lines. Reduced infectivity is correlated with accumulation of unusual, high-molecular-weight, extrachromosomal forms of the human immunodeficiency virus type 1 (HIV-1) DNA. These DNA molecules contain multiple copies of the viral genome, and their structures are highly variable. Of 17 subclones of the HU937 cell line, 15 unique restriction fragment patterns were observed for the HIV-1 viral DNA. Structural analysis of these viral DNA species indicated that they were formed by sequential rounds of long terminal repeat-mediated integration of one circular DNA form into preexisting monomeric or multimeric structures. These viral DNA structures are termed nested self-integrates. Once formed, self-integrates prove to be stable and can be maintained for several months in culture. The unusual structures of HIV-1 DNA in persistently infected monoblastoid cells attest to an alternative to the accepted retrovirus life cycle. The self-integrated viral DNA species reported here may explain some aspects of the mechanism controlling establishment and maintenance of persistent HIV-1 infection in cells of the monocyte/macrophage lineage.

摘要

来自持续感染的单核细胞样细胞(HU937)的无细胞病毒制剂在长期传代过程中传染性逐渐降低。这种效应是U937衍生细胞系所特有的,在持续感染的T细胞系中未观察到。感染性降低与1型人类免疫缺陷病毒(HIV-1)DNA异常的高分子量染色体外形式的积累相关。这些DNA分子包含病毒基因组的多个拷贝,并且其结构高度可变。在HU937细胞系的17个亚克隆中,观察到HIV-1病毒DNA有15种独特的限制性片段模式。对这些病毒DNA种类的结构分析表明,它们是由一种环状DNA形式通过长末端重复序列介导的连续轮次整合到预先存在的单体或多聚体结构中形成的。这些病毒DNA结构被称为嵌套自整合体。一旦形成,自整合体被证明是稳定的,并且可以在培养物中维持数月。持续感染的单核细胞样细胞中HIV-1 DNA的异常结构证明了公认的逆转录病毒生命周期之外的另一种情况。本文报道的自整合病毒DNA种类可能解释了控制单核细胞/巨噬细胞谱系细胞中持续性HIV-1感染的建立和维持机制的某些方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/558c/250961/b536ad532ce4/jvirol00076-0160-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/558c/250961/7c9bbc8a2ca5/jvirol00076-0159-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/558c/250961/069d06001525/jvirol00076-0159-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/558c/250961/b536ad532ce4/jvirol00076-0160-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/558c/250961/7c9bbc8a2ca5/jvirol00076-0159-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/558c/250961/069d06001525/jvirol00076-0159-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/558c/250961/b536ad532ce4/jvirol00076-0160-a.jpg

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