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The genetic stability of recombinant adenovirus expressing human rotavirus VP6 gene which used Ad41 as vector / 中华实验和临床病毒学杂志
Chinese Journal of Experimental and Clinical Virology ; (6): 422-424, 2012.
Article in Chinese | WPRIM | ID: wpr-305020
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the genetic stability of non-replicating recombinant adenovirus which used Ad41 as vector and could express VP6 gene of group A rotavirus during continous passage, in order to develop the vaccine of rotavirus.</p><p><b>METHODS</b>The recombinant adenovirus rvAd41-VP6 (o) was prepared by our laboratory early, it then was continuously propagated on 293TE7 cells for 14 passages. After that samples of the infected cells were collected at every 2 passages for the detection of the integration of the VP6 gene by PCR, and the expression of the target protein was detected by Western Blot analysis.</p><p><b>RESULTS</b>Analysis by PCR revealed that, there was stable integration of specific VP6 gene in the rvAd41-VP6 (o), Western Blot analysis confirmed that rvAd41-VP6 (o) could stably expressed the group-specific antigen structural protein VP6 (o), and it had preferable genetic stability.</p><p><b>CONCLUSION</b>The recombinant adenovirus rvAd41-VP6 (o) which could stably express the VP6 (o) gene had favorable biological property in vitro, and it has provided a basis for further research of animal immunization.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Rotavirus Infections / Virology / Gene Expression / Cell Line / Adenoviridae / Rotavirus / Capsid Proteins / Genetic Vectors / Genetics / Metabolism Limits: Humans Language: Chinese Journal: Chinese Journal of Experimental and Clinical Virology Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Rotavirus Infections / Virology / Gene Expression / Cell Line / Adenoviridae / Rotavirus / Capsid Proteins / Genetic Vectors / Genetics / Metabolism Limits: Humans Language: Chinese Journal: Chinese Journal of Experimental and Clinical Virology Year: 2012 Type: Article