Construction of an infectious horsepox virus vaccine from chemically synthesized DNA fragments

被引:163
作者
Noyce, Ryan S. [1 ,2 ]
Lederman, Seth [3 ]
Evans, David H. [1 ,2 ]
机构
[1] Univ Alberta, Dept Med Microbiol & Immunol, Edmonton, AB, Canada
[2] Univ Alberta, Li Ka Shing Inst Virol, Edmonton, AB, Canada
[3] Tonix Pharmaceut Inc, New York, NY USA
基金
加拿大创新基金会;
关键词
EVOLUTIONARY RELATIONSHIPS; NUCLEOTIDE-LEVEL; GENOMIC ANALYSIS; RECOMBINATION; REACTIVATION; REPLICATION; RESOLUTION; ORIGINS; BASE;
D O I
10.1371/journal.pone.0188453
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Edward Jenner and his contemporaries believed that his variolae vaccinae originated in horses and molecular analyses show that modern vaccinia virus (VACV) strains share common ancestry with horsepox virus (HPXV). Given concerns relating to the toxicity of modern VACV vaccines, we asked whether an HPXV-based vaccine might provide a superior alternative. Since HPXV may be extinct and the only specimen of HPXV that has been identified is unavailable for investigation, we explored whether HPXV could be obtained by large-scale gene synthesis. Ten large (10 +/- 30 kb) fragments of DNA were synthesized based on the HPXV sequence along with two 157 nt VACV terminal sequences, and were recombined into a live synthetic chimeric HPXV (scHPXV) in cells infected with Shope fibroma virus (SFV). Sequencing of the 212 kbp scHPXV confirmed it encoded a faithful copy of the input DNA. We believe this is the first complete synthesis of a poxvirus using synthetic biology approaches. This scHPXV produced smaller plaques, produced less extracellular virus and exhibited less virulence in mice than VACV, but still provided vaccine protection against a lethal VACV challenge. Collectively, these findings support further development of scHPXV as a novel replication-proficient smallpox vaccine.
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页数:16
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