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本文引用的文献

1
No evidence of human genome integration of SARS-CoV-2 found by long-read DNA sequencing.长读 DNA 测序未发现 SARS-CoV-2 人类基因组整合的证据。
Cell Rep. 2021 Aug 17;36(7):109530. doi: 10.1016/j.celrep.2021.109530. Epub 2021 Jul 28.
2
No evidence of SARS-CoV-2 reverse transcription and integration as the origin of chimeric transcripts in patient tissues.没有证据表明患者组织中嵌合转录本的起源是SARS-CoV-2逆转录和整合。
Proc Natl Acad Sci U S A. 2021 Aug 17;118(33). doi: 10.1073/pnas.2109066118.
3
Comprehensive analysis of RNA-seq and whole genome sequencing data reveals no evidence for SARS-CoV-2 integrating into host genome.RNA测序和全基因组测序数据的综合分析显示,没有证据表明新冠病毒会整合到宿主基因组中。
Protein Cell. 2022 May;13(5):379-385. doi: 10.1007/s13238-021-00861-8.
4
SARS-CoV-2-Host Chimeric RNA-Sequencing Reads Do Not Necessarily Arise From Virus Integration Into the Host DNA.严重急性呼吸综合征冠状病毒2-宿主嵌合RNA测序读数不一定源于病毒整合到宿主DNA中。
Front Microbiol. 2021 Jun 2;12:676693. doi: 10.3389/fmicb.2021.676693. eCollection 2021.
5
Host-Virus Chimeric Events in SARS-CoV-2-Infected Cells Are Infrequent and Artifactual.宿主-病毒嵌合事件在感染 SARS-CoV-2 的细胞中罕见且为人工假象。
J Virol. 2021 Jul 12;95(15):e0029421. doi: 10.1128/JVI.00294-21.
6
Reverse-transcribed SARS-CoV-2 RNA can integrate into the genome of cultured human cells and can be expressed in patient-derived tissues.经逆转录的 SARS-CoV-2 RNA 可整合到培养的人类细胞基因组中,并可在源自患者的组织中表达。
Proc Natl Acad Sci U S A. 2021 May 25;118(21). doi: 10.1073/pnas.2105968118.
7
Retrotransposons as Drivers of Mammalian Brain Evolution.逆转录转座子作为哺乳动物大脑进化的驱动因素
Life (Basel). 2021 Apr 22;11(5):376. doi: 10.3390/life11050376.
8
Exogenous Coronavirus Interacts With Endogenous Retrotransposon in Human Cells.外源性冠状病毒与人类细胞中的内源性逆转录转座子相互作用。
Front Cell Infect Microbiol. 2021 Feb 25;11:609160. doi: 10.3389/fcimb.2021.609160. eCollection 2021.
9
Human Endogenous Retroviruses Are Ancient Acquired Elements Still Shaping Innate Immune Responses.人类内源性逆转录病毒是古老的获得性元件,仍在塑造先天免疫反应。
Front Immunol. 2018 Sep 10;9:2039. doi: 10.3389/fimmu.2018.02039. eCollection 2018.
10
HERV Envelope Proteins: Physiological Role and Pathogenic Potential in Cancer and Autoimmunity.人内源性逆转录病毒包膜蛋白:在癌症和自身免疫中的生理作用及致病潜力
Front Microbiol. 2018 Mar 14;9:462. doi: 10.3389/fmicb.2018.00462. eCollection 2018.

通过逆转录转座子将 SARS-CoV-2 RNA 整合到受感染的人类细胞中:一个不太可能的假设和古老的病毒关系。

Integration of SARS-CoV-2 RNA in infected human cells by retrotransposons: an unlikely hypothesis and old viral relationships.

机构信息

Laboratory of Molecular Virology, Department of Life and Environmental Sciences, University of Cagliari - Cittadella Universitaria di Monserrato, SS554, Monserrato (Cagliari), Italy.

Istituto di Ricerca Genetica e Biomedica (IRGB), CNR - SS554, Monserrato (Cagliari), Italy.

出版信息

Retrovirology. 2021 Oct 29;18(1):34. doi: 10.1186/s12977-021-00578-w.

DOI:10.1186/s12977-021-00578-w
PMID:34715873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8554740/
Abstract

Zhang et al. (Proc Natl Acad Sci 118:e2105968118, 2021) recently reported that SARS-CoV-2 RNA can be retrotranscribed and integrated into the DNA of human cells by the L1 retrotransposon machinery. This phenomenon could cause persistence of viral sequences in patients and may explain the prolonged PCR-positivity of SARS-CoV-2 infected patients, even long after the phase of active virus replication has ended. This commentary does critically review the available data on this topic and discusses them in the context of findings made for other exogenous viruses and ancestral endogenous retroviral elements.

摘要

Zhang 等人(Proc Natl Acad Sci 118:e2105968118, 2021)最近报道称,SARS-CoV-2 RNA 可以通过 L1 反转录转座子机制被逆转录并整合到人类细胞的 DNA 中。这种现象可能导致病毒序列在患者体内持续存在,并可能解释为什么 SARS-CoV-2 感染患者的 PCR 阳性持续时间很长,甚至在病毒复制的活跃阶段结束后很久仍然如此。这篇评论文章批判性地回顾了关于这一主题的现有数据,并在其他外源性病毒和祖先内源性逆转录元件的研究结果的背景下对其进行了讨论。