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Photodynamic treatment of adenoviral vectors with visible light: an easy and convenient method for viral inactivation.

机译:用可见光对腺病毒载体进行光动力处理:一种简便且便捷的病毒灭活方法。

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Recombinant adenovirus vectors are popular tools for gene transfer and gene therapy. However biosafety constraints require that all handling of the vectors and vector-containing samples is restricted to dedicated containment laboratories, unless they had undergone a validated virus-inactivation procedure, which decontaminates the samples from any active virus. In this study we evaluated the feasibility of photodynamic treatment (PDT) with visible light to inactivate recombinant adenovirus vectors in biological samples, with minimum associated effects on other biological activities. Several photosensitizers were tested for their capacity to inactivate a model human adenovirus vector, AdCMVLuc, upon illumination. Four photosensitizers (methylene blue (MB), rose bengal (RB), uroporphyrin (UP) and aluminum phthalocynine tetrasulphonate (AIPcS4)) could inactivate the adenovirus, as measured by expression of the luciferase reporter gene and by plaque assay. Of these, MB demonstrated to be the most effective sensitizer in phosphate-buffered saline (PBS), giving > 7 log10 inactivation of the adenovirus. DNA isolated from MB- and light-treated virions was inefficient as a template for transcription. Furthermore, Southern blot analysis revealed fragmentation of the viral DNA. Based on its preference for DNA, MB is suited for adenovirus inactivation in blood plasma. Spiking experiments in which AdCMVLuc was added to plasma samples demonstrated a reduction (> 4 log10-fold) of reporter gene expression to almost background levels. In contrast to MB, photodynamic treatment with RB, UP or AIPcS4 did not lead to DNA damage. Although alterations of the viral capsid could not be detected, the binding pattern of the particles to target cells was significantly changed. Taken together, our data demonstrate that PDT is an efficient, convenient and useful method for the inactivation of adenovirus vectors in biological samples.
机译:重组腺病毒载体是用于基因转移和基因治疗的流行工具。但是,生物安全性约束要求将载体和含载体的样品的所有处理都限于专用的容纳实验室,除非它们已经过验证的病毒灭活程序,该程序使样品免受任何活性病毒的污染。在这项研究中,我们评估了用可见光进行光动力处理(PDT)灭活生物样品中重组腺病毒载体的可行性,而对其他生物活性的相关影响最小。测试了几种光敏剂在照射后使模型人腺病毒载体AdCMVLuc失活的能力。通过荧光素酶报告基因的表达和噬菌斑测定,四种光敏剂(亚甲基蓝(MB),孟加拉红(RB),尿卟啉(UP)和酞菁铝四磺酸铝(AIPcS4))可以灭活腺病毒。其中,MB被证明是磷酸盐缓冲盐水(PBS)中最有效的敏化剂,可使腺病毒> 7 log10失活。从MB和光处理的病毒粒子分离的DNA作为转录模板效率低下。此外,Southern印迹分析揭示病毒DNA的片段化。基于对DNA的偏爱,MB适用于血浆中腺病毒的灭活。向血浆样品中添加AdCMVLuc的加标实验表明,报告基因的表达降低到了几乎本底水平(> 4 log10倍)。与MB相比,用RB,UP或AIPcS4进行光动力处理不会导致DNA损伤。尽管无法检测到病毒衣壳的改变,但颗粒与靶细胞的结合模式却发生了显着变化。综上所述,我们的数据表明,PDT是一种用于灭活生物样品中腺病毒载体的有效,便捷和有用的方法。

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