| Literature DB >> 26855330 |
Rachmat Hidajat1, Brian Nickols1, Naomi Forrester2, Irina Tretyakova1, Scott Weaver2, Peter Pushko3.
Abstract
Chikungunya virus (CHIKV) represents a pandemic threat with no approved vaccine available. Recently, we described a novel vaccination strategy based on iDNA® infectious clone designed to launch a live-attenuated CHIKV vaccine from plasmid DNA in vitro or in vivo. As a proof of concept, we prepared iDNA plasmid pCHIKV-7 encoding the full-length cDNA of the 181/25 vaccine. The DNA-launched CHIKV-7 virus was prepared and compared to the 181/25 virus. Illumina HiSeq2000 sequencing revealed that with the exception of the 3' untranslated region, CHIKV-7 viral RNA consistently showed a lower frequency of single-nucleotide polymorphisms than the 181/25 RNA including at the E2-12 and E2-82 residues previously identified as attenuating mutations. In the CHIKV-7, frequencies of reversions at E2-12 and E2-82 were 0.064% and 0.086%, while in the 181/25, frequencies were 0.179% and 0.133%, respectively. We conclude that the DNA-launched virus has a reduced probability of reversion mutations, thereby enhancing vaccine safety.Entities:
Keywords: Alphavirus; CHIKV; Chikungunya fever; Chikungunya virus; DNA vaccine; Live attenuated vaccine
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Year: 2016 PMID: 26855330 PMCID: PMC4773897 DOI: 10.1016/j.virol.2016.01.009
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616