
pmid: 28508213
We have established a reverse genetic system for Zika virus (ZIKV). Five shuttle plasmids were constructed and assembled into the full-length cDNA clone of ZIKV genome. To ensure the stability of the cDNA clone, we used a low copy vector (pACYC177) and a set of unique restriction enzyme sites on the ZIKV genome to assemble the full-length cDNA clone. A T7 promoter was engineered in front of the viral 5' UTR for in vitro transcription. A hepatitis delta virus ribozyme (HDVr) sequence was engineered following the viral 3' UTR for generation of the authentic 3' end of the RNA transcript.
DNA, Complementary, Genome, Viral, Viral Plaque Assay, Zika Virus, Transfection, Virus Replication, Reverse Genetics, Chlorocebus aethiops, Animals, Humans, RNA, Viral, Vero Cells, Plasmids
DNA, Complementary, Genome, Viral, Viral Plaque Assay, Zika Virus, Transfection, Virus Replication, Reverse Genetics, Chlorocebus aethiops, Animals, Humans, RNA, Viral, Vero Cells, Plasmids
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 10 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
