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Evidence for the Failure of Adeno-associated Virus Serotype 5 to Package a Viral Genome ≥8.2 kb

机译:腺相关病毒5型血清未能包装≥8.2kb的病毒基因组的证据

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摘要

Limited packaging capacity hinders adeno-associated virus (AAV) gene therapy. A recent study seems to have provided a solution to this problem. Allocca et al. reported that AAV-5 could package an 8.9 kb vector genome. Here we tested whether this approach can be used to deliver a large genome for Duchenne muscular dystrophy (DMD) gene therapy. We first evaluated AAV-5 packaging of an 8.2 kb genome. This vector carries two independent reporter gene cassettes, one for alkaline phosphatase (AP) and another for LacZ. Viral yield was log-fold lower than that of a regular AAV-5. Nevertheless, both AP and LacZ genes were detected in purified virus. Injection to dystrophic muscle resulted in both AP and LacZ expression. On electron microscopy, virion structure appeared normal. Surprisingly, we did not find the full-length single-stranded viral genome by alkaline gel electrophoresis. Neither did we see the full-length double-stranded replication forms in adenovirus coinfected cells. We suspect that AP and LacZ expression may have come from partially packaged 5′ or 3′-half of the genome. Additional studies revealed failure of AAV-5 to package and express an 8.7 kb minidystrophin gene cassette. In summary, our results do not support the extraordinary packaging capacity of AAV-5.
机译:有限的包装能力阻碍了腺相关病毒(AAV)基因治疗。最近的一项研究似乎为该问题提供了解决方案。 Allocca等。报道说AAV-5可以包装一个8.9kb的载体基因组。在这里,我们测试了这种方法是否可以用于为杜氏肌营养不良症(DMD)基因治疗提供大的基因组。我们首先评估了8.2kb基因组的AAV-5包装。该载体带有两个独立的报告基因盒,一个用于碱性磷酸酶(AP),另一个用于LacZ。病毒产量比常规AAV-5低了几倍。尽管如此,在纯化的病毒中同时检测到了AP和LacZ基因。向营养不良的肌肉注射导致AP和LacZ表达。在电子显微镜下,病毒体结构似乎正常。出乎意料的是,我们没有通过碱性凝胶电泳找到全长的单链病毒基因组。我们也没有在腺病毒共感染的细胞中看到全长的双链复制形式。我们怀疑AP和LacZ的表达可能来自基因组的部分包装的5'或3'一半。进一步的研究表明AAV-5无法包装和表达8.7kb的小肌营养不良蛋白基因盒。总而言之,我们的结果并不支持AAV-5的超凡包装能力。

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