Chia Min-Yuan, Chung Wan-Yu, Chiang Pai-Shan, Chien Yeh-Sheng, Ho Mei-Shang, Lee Min-Shi
National Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan, Taiwan.
Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
PLoS Negl Trop Dis. 2014 Jul 24;8(7):e3044. doi: 10.1371/journal.pntd.0003044. eCollection 2014 Jul.
Enterovirus 71 (EV71) causes life-threatening epidemics in Asia and can be phylogenetically classified into three major genogroups (A ∼ C) including 11 genotypes (A, B1 ∼ B5, and C1 ∼ C5). Recently, EV71 epidemics occurred cyclically in Taiwan with different genotypes. In recent years, human studies using post-infection sera obtained from children have detected antigenic variations among different EV71 strains. Therefore, surveillance of enterovirus 71 should include phylogenetic and antigenic analysis. Due to limitation of sera available from children with EV71 primary infection, suitable animal models should be developed to generate a panel of antisera for monitoring EV71 antigenic variations. Twelve reference strains representing the 11 EV71 genotypes were grown in rhabdomyosarcoma cells. Infectious EV71 particles were purified and collected to immunize rabbits. The rabbit antisera were then employed to measure neutralizing antibody titers against the 12 reference strains and 5 recent strains. Rabbits immunized with genogroup B and C viruses consistently have a lower neutralizing antibody titers against genogroup A (≧ 8-fold difference) and antigenic variations between genogroup B and C viruses can be detected but did not have a clear pattern, which are consistent with previous human studies. Comparison between human and rabbit neutralizing antibody profiles, the results showed that ≧ 8-fold difference in rabbit cross-reactive antibody ratios could be used to screen EV71 isolates for identifying potential antigenic variants. In conclusion, a rabbit model was developed to monitor antigenic variations of EV71, which are critical to select vaccine strains and predict epidemics.
肠道病毒71型(EV71)在亚洲引发危及生命的疫情,在系统发育上可分为三个主要基因组(A~C),包括11个基因型(A、B1~B5和C1~C5)。最近,EV71疫情在台湾地区呈周期性发生,且基因型不同。近年来,利用儿童感染后血清进行的人体研究检测到不同EV71毒株之间存在抗原变异。因此,肠道病毒71型的监测应包括系统发育和抗原分析。由于EV71初次感染儿童的血清有限,应建立合适的动物模型来制备一批抗血清,以监测EV71的抗原变异。代表11种EV71基因型的12株参考毒株在横纹肌肉瘤细胞中培养。纯化并收集具有感染性的EV71颗粒来免疫兔子。然后用兔抗血清检测针对12株参考毒株和5株近期毒株的中和抗体滴度。用B组和C组病毒免疫的兔子对A组病毒的中和抗体滴度始终较低(相差≧8倍),且能检测到B组和C组病毒之间的抗原变异,但没有明确的模式,这与之前的人体研究结果一致。比较人和兔子的中和抗体谱,结果表明,兔子交叉反应抗体比率相差≧8倍可用于筛选EV71分离株,以鉴定潜在的抗原变异株。总之,建立了一种兔模型来监测EV71的抗原变异,这对于选择疫苗株和预测疫情至关重要。