کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5673118 1593437 2017 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Efficient production of an avian adeno-associated virus vector using insect cell/baculovirus expression system
ترجمه فارسی عنوان
تولید کارآمد یک ویروس با ویروس عدوانی پرندگان با استفاده از سیستم بیان سلول های حشرات / باقلوویروس
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ویروس شناسی
چکیده انگلیسی


• The AAAV proteins can be expressed efficiently in the rBac-infected insect cells.
• The AAAV particles can be assembled correctly in insect cells without the helper viruses.
• The AAAV vector produced in insect cells can mediate the expression of GFP in chicken cells.
• The titer of rAAAV produced in insect cells is greatly improved.
• A scalable and efficient platform for producing rAAAV has been established.

Recombinant avian adeno-associated virus (rAAAV) is a promising gene transfer vector for avian cells. Although rAAAV can be produced by co-transfection of HEK293 cells with three plasmids, both scalability and productivity of the transient transfection method can not meet the demand for large-scale in vivo experiments. In this study, a scalable rAAAV production method was established by using insect cell/baculovirus expression system. Three recombinant baculoviruses, namely BacARep, BacAVP and BacAGFP, were generated by transfection of Sf9 cells with the three plasmids expressing AAAV Rep genes, modified VP gene or the inverted terminal repeats-flanked green fluorescent protein (GFP) gene. After demonstration of the correct expression of AAAV genes, rAAAV-GFP was produced by triple infection of insect cells or triple transfection of HEK293 cells for comparison purpose. Electron microscopy revealed the formation of typical AAAV particles in the insect cells. Western blotting showed the correct assembly of rAAAV particles with a VP protein ratio similar to that of AAAV. Quantitative PCR showed that the insect cell-produced rAAAV yield was almost 25-fold higher than that produced by HEK293 cells. Fluorescent microscopy showed that the insect cell-produced rAAAV could transfer GFP reporter gene into two avian cell types with similar transfer efficiency to that of HEK293 cell-produced rAAAV. These data suggest that insect cell/baculovirus expression system could be used for scalable production of rAAAV, and the viral vector produced could be used as the gene transfer vehicle for avian cells.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Virological Methods - Volume 240, February 2017, Pages 26–31