National Health Research Institutes (NHRI), Zhunan, Taiwan.
PLoS Negl Trop Dis. 2013;7(2):e2067. doi: 10.1371/journal.pntd.0002067. Epub 2013 Feb 14.
Recently, enterovirus 71 (EV71) has caused life-threatening outbreaks involving neurological and cardiopulmonary complications in Asian children with unknown mechanism. EV71 has one single serotype but can be phylogenetically classified into 3 main genogroups (A, B and C) and 11 genotypes (A, B1∼B5 and C1∼C5). In Taiwan, nationwide EV71 epidemics with different predominant genotypes occurred in 1998 (C2), 2000-2001 (B4), 2004-2005 (C4), and 2008 (B5). In this study, sera were collected to measure cross-reactive neutralizing antibody titers against different genotypes.
We collected historical sera from children who developed an EV71 infection in 1998, 2000, 2005, 2008, or 2010 and measured cross-reactive neutralizing antibody titers against all 11 EV71 genotypes. In addition, we aligned and compared the amino acid sequences of P1 proteins of the tested viruses.
Serology data showed that children infected with genogroups B and C consistently have lower neutralizing antibody titers against genogroup A (>4-fold difference). The sequence comparisons revealed that five amino acid signatures (N143D in VP2; K18R, H116Y, D167E, and S275A in VP1) are specific for genogroup A and may be related to the observed antigenic variations.
This study documented antigenic variations among different EV71 genogroups and identified potential immunodominant amino acid positions. Enterovirus surveillance and vaccine development should monitor these positions.
最近,肠道病毒 71 型(EV71)在亚洲儿童中引起了危及生命的爆发,涉及神经系统和心肺并发症,但发病机制尚不清楚。EV71 只有一个血清型,但可以根据系统发生关系分为 3 个主要基因群(A、B 和 C)和 11 个基因型(A、B1~B5 和 C1~C5)。在台湾,1998 年(C2)、2000-2001 年(B4)、2004-2005 年(C4)和 2008 年(B5)曾发生过不同优势基因型的全国性 EV71 流行。在本研究中,收集了血清来测量针对不同基因型的交叉反应中和抗体滴度。
我们收集了 1998 年、2000 年、2005 年、2008 年和 2010 年发生 EV71 感染的儿童的历史血清,并测量了针对所有 11 种 EV71 基因型的交叉反应中和抗体滴度。此外,我们对检测病毒的 P1 蛋白的氨基酸序列进行了比对和比较。
血清学数据显示,感染 B 组和 C 组的儿童对 A 组的中和抗体滴度持续较低(差异超过 4 倍)。序列比较显示,5 个氨基酸特征(VP2 中的 N143D;VP1 中的 K18R、H116Y、D167E 和 S275A)是 A 组特有的,可能与观察到的抗原变异有关。
本研究记录了不同 EV71 基因群之间的抗原变异,并确定了潜在的免疫显性氨基酸位置。肠道病毒监测和疫苗开发应监测这些位置。