Hu Jiafen, Cladel Nancy M, Pickel Martin D, Christensen Neil D
Department of Pathology, The Jake Gittlen Cancer Research Institute, Pennsylvania State University, Hershey, Pennsylvania 17033, USA.
J Virol. 2002 Dec;76(23):11801-8. doi: 10.1128/jvi.76.23.11801-11808.2002.
Previous studies have identified two different strains of cottontail rabbit papillomavirus (CRPV) that differ by approximately 5% in base pair sequence and that perform quite differently when used to challenge New Zealand White (NZW) rabbit skin. One strain caused persistent lesions (progressor strain), and the other induced papillomas that spontaneously regressed (regressor strain) at high frequencies (J. Salmon, M. Nonnenmacher, S. Caze, P. Flamant, O. Croissant, G. Orth, and F. Breitburd, J. Virol. 74:10766-10777, 2000; J. Salmon, N. Ramoz, P. Cassonnet, G. Orth, and F. Breitburd, Virology 235:228-234, 1997). We generated a panel of CRPV genomes that contained chimeric and mutant progressor and regressor strain E6 genes and assessed the outcome upon infection of both outbred and EIII/JC inbred NZW rabbits. The carboxy-terminal 77-amino-acid region of the regressor CRPV strain E6, which contained 15 amino acid residues that are different from those of the equivalent region of the persistent CRPV strain E6, played a dominant role in the conversion of the persistent CRPV strain to one showing high rates of spontaneous regressions. In addition, a single amino acid change (G252E) in the E6 protein of the CRPV progressor strain led to high frequencies of spontaneous regressions in inbred rabbits. These observations imply that small changes in the amino acid sequences of papillomavirus proteins can dramatically impact the outcome of natural host immune responses to these viral infections. The data imply that intrastrain differences between separate isolates of a single papillomavirus type (such as human papillomavirus type 16) may contribute to a collective variability in host immune responses in outbred human populations.
先前的研究已鉴定出两种不同的棉尾兔乳头瘤病毒(CRPV)毒株,它们的碱基对序列相差约5%,在用于攻击新西兰白兔(NZW)皮肤时表现也大不相同。一种毒株会引起持续性病变(进展毒株),另一种则诱导乳头瘤以高频率自发消退(消退毒株)(J. 萨尔蒙、M. 诺嫩马赫、S. 卡泽、P. 弗拉芒、O. 克罗斯唐、G. 奥尔特和F. 布赖特布德,《病毒学杂志》74:10766 - 10777,2000年;J. 萨尔蒙、N. 拉莫兹、P. 卡索内、G. 奥尔特和F. 布赖特布德,《病毒学》235:228 - 234,1997年)。我们构建了一组CRPV基因组,其中包含嵌合和突变的进展毒株及消退毒株E6基因,并评估了对远交和EIII/JC近交NZW兔感染后的结果。消退型CRPV毒株E6的羧基末端77个氨基酸区域,其中有15个氨基酸残基与持续性CRPV毒株E6的等效区域不同,在将持续性CRPV毒株转变为显示高自发消退率的毒株过程中起主导作用。此外,CRPV进展毒株E6蛋白中的单个氨基酸变化(G252E)导致近交兔中出现高频率的自发消退。这些观察结果表明,乳头瘤病毒蛋白氨基酸序列的微小变化可显著影响天然宿主对这些病毒感染的免疫反应结果。数据表明,单一乳头瘤病毒类型(如人乳头瘤病毒16型)不同分离株之间的株内差异可能导致远交人群宿主免疫反应的总体变异性。