Carson Steven D, Tracy Steven, Kaczmarek Zac G, Alhazmi Abdulaziz, Chapman Nora M
Department of Pathology and Microbiology, University of Nebraska College of Medicine, 986495 Nebraska Medical Center, Omaha, NE 68198-6495, USA.
Department of Microbiology, College of Medicine, Jazan University, King Abdullah Street, Jazan 82621, Saudi Arabia.
J Gen Virol. 2016 Jan;97(1):60-68. doi: 10.1099/jgv.0.000319. Epub 2015 Oct 20.
Coxsackievirus B3 strain 28 (CVB3/28) is less stable at 37 °C than eight other CVB3 strains with which it has been compared, including four in this study. In a variant CVB3/28 population selected for increased stability at 37 °C, the capsid proteins of the stable variant differed from the parental CVB3/28 by two mutations in Vp1 and one mutation in Vp3, each of which resulted in altered protein sequences. Each of the amino acid changes was individually associated with a more stable virus. Competition between CVB3/28 and a more stable derivative of the strain showed that propagation of the less stable virus was favoured in receptor-rich HeLa cells.
柯萨奇病毒B3 28株(CVB3/28)在37°C时比与之比较的其他8株CVB3病毒更不稳定,本研究中的4株也包括在内。在为提高37°C稳定性而选择的CVB3/28变异群体中,稳定变异体的衣壳蛋白与亲本CVB3/28的不同之处在于,Vp1有两个突变,Vp3有一个突变,每个突变都导致了蛋白质序列的改变。每一个氨基酸变化都与更稳定的病毒个体相关。CVB3/28与该毒株更稳定的衍生物之间的竞争表明,在富含受体的HeLa细胞中,不稳定病毒的增殖更受青睐。