Anouk Lkharrazi, Kurt Tobler, Sara Marti, Anna Bratus-Neuenschwander, Bernd Vogt, Cornel Fraefel
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We have revisited AAV2 DNA replication and specifically compared the formation of AAV2 replication intermediates in the presence of either HSV-1 or AdV5 as the helper virus. The results confirmed that the AAV2 DNA replication mechanism is helper virus-dependent and follows a strand-displacement RHR mechanism when AdV5 is the helper virus and primarily an RCR mechanism when HSV-1 is the helper virus. We also demonstrate that recombination plays a negligible role in AAV2 genome replication. Interestingly, the formation of high-molecular-weight AAV2 DNA concatemers in the presence of HSV-1 as the helper virus was dependent on an intact HSV-1 DNA polymerase.</p><p><strong>Importance: </strong>AAV is a small helper virus-dependent, non-pathogenic parvovirus. The AAV genome replication mechanism was extensively studied in the presence of AdV as the helper virus and described to proceed using RHR. Surprisingly, HSV-1 co-infection facilitates RCR of the AAV2 DNA. We directly compared AdV5 and HSV-1 supported AAV2 DNA replication and showed that AAV2 can adapt its replication mechanism to the helper virus. A detailed understanding of the AAV replication mechanism expands our knowledge of virus biology and can contribute to increase gene therapy vector production.</p>","PeriodicalId":17583,"journal":{"name":"Journal of Virology","volume":" ","pages":"e0128224"},"PeriodicalIF":4.0000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11575299/pdf/","citationCount":"0","resultStr":"{\"title\":\"AAV2 can replicate its DNA by a rolling hairpin or rolling circle mechanism, depending on the helper virus.\",\"authors\":\"Anouk Lkharrazi, Kurt Tobler, Sara Marti, Anna Bratus-Neuenschwander, Bernd Vogt, Cornel Fraefel\",\"doi\":\"10.1128/jvi.01282-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Adeno-associated virus type 2 (AAV2) is a small, non-pathogenic, helper virus-dependent parvovirus with a single-stranded (ss) DNA genome of approximately 4.7 kb. AAV2 DNA replication requires the presence of a helper virus such as adenovirus type 5 (AdV5) or herpes simplex virus type 1 (HSV-1) and is generally assumed to occur as a strand-displacement rolling hairpin (RHR) mechanism initiated at the AAV2 3' inverted terminal repeat (ITR). We have recently shown that AAV2 replication supported by HSV-1 leads to the formation of double-stranded head-to-tail concatemers, which provides evidence for a rolling circle replication (RCR) mechanism. We have revisited AAV2 DNA replication and specifically compared the formation of AAV2 replication intermediates in the presence of either HSV-1 or AdV5 as the helper virus. The results confirmed that the AAV2 DNA replication mechanism is helper virus-dependent and follows a strand-displacement RHR mechanism when AdV5 is the helper virus and primarily an RCR mechanism when HSV-1 is the helper virus. We also demonstrate that recombination plays a negligible role in AAV2 genome replication. 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引用次数: 0
摘要
腺相关病毒 2 型(AAV2)是一种依赖辅助病毒的小型非致病性辅助病毒,其 DNA 基因组单链(ss)约为 4.7 kb。AAV2 DNA 的复制需要辅助病毒(如 5 型腺病毒(AdV5)或 1 型单纯疱疹病毒(HSV-1))的存在,一般认为复制是以 AAV2 3' 倒置末端重复序列(ITR)为起始点的链置换滚动发夹(RHR)机制进行的。我们最近发现,HSV-1 支持的 AAV2 复制会导致双链头尾连接体的形成,这为滚动圈复制(RCR)机制提供了证据。我们重新研究了 AAV2 DNA 复制,特别比较了在 HSV-1 或 AdV5 作为辅助病毒存在的情况下 AAV2 复制中间体的形成。结果证实,AAV2 DNA 复制机制依赖于辅助病毒,当 AdV5 为辅助病毒时遵循链置换 RHR 机制,而当 HSV-1 为辅助病毒时则主要遵循 RCR 机制。我们还证明,重组在 AAV2 基因组复制中的作用微乎其微。有趣的是,在 HSV-1 作为辅助病毒的情况下,高分子量 AAV2 DNA 浓缩物的形成依赖于完整的 HSV-1 DNA 聚合酶:AAV是一种依赖辅助病毒的非致病性小病毒。AAV 的基因组复制机制在有 AdV 作为辅助病毒的情况下进行了广泛研究,并描述了其复制过程是利用 RHR 进行的。令人惊讶的是,HSV-1 共感染促进了 AAV2 DNA 的 RCR。我们直接比较了 AdV5 和 HSV-1 支持的 AAV2 DNA 复制,结果表明 AAV2 可根据辅助病毒调整其复制机制。对 AAV 复制机制的详细了解拓展了我们的病毒生物学知识,有助于提高基因治疗载体的产量。
AAV2 can replicate its DNA by a rolling hairpin or rolling circle mechanism, depending on the helper virus.
Adeno-associated virus type 2 (AAV2) is a small, non-pathogenic, helper virus-dependent parvovirus with a single-stranded (ss) DNA genome of approximately 4.7 kb. AAV2 DNA replication requires the presence of a helper virus such as adenovirus type 5 (AdV5) or herpes simplex virus type 1 (HSV-1) and is generally assumed to occur as a strand-displacement rolling hairpin (RHR) mechanism initiated at the AAV2 3' inverted terminal repeat (ITR). We have recently shown that AAV2 replication supported by HSV-1 leads to the formation of double-stranded head-to-tail concatemers, which provides evidence for a rolling circle replication (RCR) mechanism. We have revisited AAV2 DNA replication and specifically compared the formation of AAV2 replication intermediates in the presence of either HSV-1 or AdV5 as the helper virus. The results confirmed that the AAV2 DNA replication mechanism is helper virus-dependent and follows a strand-displacement RHR mechanism when AdV5 is the helper virus and primarily an RCR mechanism when HSV-1 is the helper virus. We also demonstrate that recombination plays a negligible role in AAV2 genome replication. Interestingly, the formation of high-molecular-weight AAV2 DNA concatemers in the presence of HSV-1 as the helper virus was dependent on an intact HSV-1 DNA polymerase.
Importance: AAV is a small helper virus-dependent, non-pathogenic parvovirus. The AAV genome replication mechanism was extensively studied in the presence of AdV as the helper virus and described to proceed using RHR. Surprisingly, HSV-1 co-infection facilitates RCR of the AAV2 DNA. We directly compared AdV5 and HSV-1 supported AAV2 DNA replication and showed that AAV2 can adapt its replication mechanism to the helper virus. A detailed understanding of the AAV replication mechanism expands our knowledge of virus biology and can contribute to increase gene therapy vector production.
期刊介绍:
Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.