Ramsingh A I, Collins D N
Wadsworth Center for Laboratories and Research, New York State Department of Health, Albany 12201-2002, USA.
J Virol. 1995 Nov;69(11):7278-81. doi: 10.1128/JVI.69.11.7278-7281.1995.
In analyzing the molecular determinants of virulence of coxsackievirus B4, chimeric viruses were constructed from avirulent and virulent viruses. The vCB424 recombinant contained a single nucleotide substitution on an avirulent genetic background, resulting in replacement of Ser-16 of VP4 with Arg-16. Mice infected with vCB424 displayed an intermediate phenotype.
在分析柯萨奇病毒B4毒力的分子决定因素时,从无毒和有毒病毒构建了嵌合病毒。vCB424重组病毒在无毒遗传背景上有一个单核苷酸替换,导致VP4的第16位丝氨酸被第16位精氨酸取代。感染vCB424的小鼠表现出中间表型。