Thermet A, Robaczewska M, Rollier C, Hantz O, Trepo C, Deleage G, Cova L
INSERM U271, 69424 Lyon Cedex 03, France.
J Virol. 2004 Feb;78(4):1945-53. doi: 10.1128/jvi.78.4.1945-1953.2004.
The induction of humoral response in ducks by DNA-based immunization against duck hepatitis B virus (DHBV) core protein (DHBc) was investigated. In addition, the amino acid specificity of the induced response was compared by using peptide scanning to that elicited either by protein immunization or during chronic DHBV infection. Immunization of ducks with a plasmid expressing DHBc protein led to the induction of a long-lasting antibody response able to specifically recognize viral protein in chronically infected duck livers. Peptide scanning analysis of anti-DHBc response induced during chronic DHBV infection allowed us to identify six major antigenic regions (AR1 to AR6). The reactivity spectrum of duck sera elicited by protein immunization appeared narrower and was restricted to only four of these antigenic regions in spite of higher anti-DHBc antibody titers. Interestingly, anti-DHBc antibodies induced by DNA-based immunization recognized five of six antigenic regions, and the epitope pattern was broader and more closely related to that observed in chronic viral infections. To gain more insight into the location of antigenic regions, we built a three-dimensional (3-D) model of DHBc protein based on human and duck core sequence alignment data and the HBc 3-D crystal structure. The results suggest that two identified antigenic regions (AR2, amino acids [aa] (64)T-P(84), and AR5, aa (183)A-R(210)) are located at positions on the protein surface equivalent to those of the two HBc major epitopes. Moreover, we identified another antigenic region (AR3, aa (99)I-I(112)) that was recognized by all sera from chronically infected, DNA- or protein-immunized ducks within the large 45-aa insertion in DHBc protein, suggesting that this region, which lacks HBc, is externally exposed.
研究了基于DNA免疫鸭乙型肝炎病毒(DHBV)核心蛋白(DHBc)对鸭体液免疫反应的诱导作用。此外,通过肽扫描比较了诱导反应的氨基酸特异性与蛋白质免疫或慢性DHBV感染所引发反应的氨基酸特异性。用表达DHBc蛋白的质粒免疫鸭可诱导产生持久的抗体反应,该反应能够特异性识别慢性感染鸭肝脏中的病毒蛋白。对慢性DHBV感染期间诱导的抗DHBc反应进行肽扫描分析,使我们能够确定六个主要抗原区域(AR1至AR6)。尽管蛋白质免疫诱导的鸭血清抗DHBc抗体滴度较高,但其反应谱似乎较窄,仅局限于其中四个抗原区域。有趣的是,基于DNA免疫诱导的抗DHBc抗体识别六个抗原区域中的五个,且表位模式更广泛,与慢性病毒感染中观察到的更为相似。为了更深入了解抗原区域的位置,我们基于人和鸭的核心序列比对数据以及HBc三维晶体结构构建了DHBc蛋白的三维(3-D)模型。结果表明,两个已确定的抗原区域(AR2,氨基酸[aa](64)T - P(84),和AR5,aa(183)A - R(210))位于蛋白质表面,相当于两个HBc主要表位的位置。此外,我们确定了另一个抗原区域(AR3,aa(99)I - I(112)),在DHBc蛋白中45个氨基酸的大插入区内,慢性感染、DNA或蛋白质免疫鸭的所有血清均可识别该区域,这表明该缺乏HBc的区域暴露于外部。