Arita Minetaro, Nagata Noriyo, Iwata Naoko, Ami Yasushi, Suzaki Yuriko, Mizuta Katsumi, Iwasaki Takuya, Sata Tetsutaro, Wakita Takaji, Shimizu Hiroyuki
Department of Virology II, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashimurayama-shi, Tokyo 208-0011, Japan.
J Virol. 2007 Sep;81(17):9386-95. doi: 10.1128/JVI.02856-06. Epub 2007 Jun 13.
Enterovirus 71 (EV71) is a causative agent of hand, foot, and mouth disease and is also sometimes associated with serious neurological disorders. In this study, we characterized the antigenicity and tissue specificity of an attenuated strain of EV71 [EV71(S1-3')], which belongs to genotype A, in a monkey infection model. Three cynomolgus monkeys were inoculated with EV71(S1-3'), followed by lethal challenge with the parental virulent strain EV71(BrCr-TR) via an intravenous route on day 45 postinoculation of EV71(S1-3'). Monkeys inoculated with EV71(S1-3') showed a mild neurological symptom (tremor) but survived lethal challenge by virulent EV71(BrCr-TR) without exacerbation of the symptom. The immunized monkey sera showed a broad spectrum of neutralizing activity against different genotypes of EV71, including genotypes A, B1, B4, C2, and C4. For the strains examined, the sera showed the highest neutralization activity against the homotype (genotype A) and the lowest neutralization activity against genotype C2. The order of decreasing neutralization activity of sera was as follows: A > B1 > C4 > B4 > C2. To examine the tissue specificity of EV71(S1-3'), two monkeys were intravenously inoculated with EV71(S1-3'), followed by examination of virus distribution in the central nervous system (CNS) and extraneural tissues. In the CNS, EV71(S1-3') was isolated only from the spinal cord. These results indicate that EV71(S1-3') acts as an effective antigen, although this attenuated strain was still neurotropic when inoculated via the intravenous route.
肠道病毒71型(EV71)是手足口病的病原体,有时还与严重的神经系统疾病有关。在本研究中,我们在猴子感染模型中对属于A基因型的EV71减毒株[EV71(S1-3')]的抗原性和组织特异性进行了表征。三只食蟹猴接种了EV71(S1-3'),在接种EV71(S1-3')后第45天,通过静脉途径用亲本强毒株EV71(BrCr-TR)进行致死性攻击。接种EV71(S1-3')的猴子出现了轻微的神经症状(震颤),但在受到强毒株EV71(BrCr-TR)的致死性攻击后存活下来,且症状未加重。免疫后的猴子血清对不同基因型的EV71,包括A、B1、B4、C2和C4基因型,表现出广泛的中和活性。对于所检测的毒株,血清对同型(A基因型)的中和活性最高,对C2基因型的中和活性最低。血清中和活性降低的顺序如下:A > B1 > C4 > B4 > C2。为了检测EV71(S1-3')的组织特异性,两只猴子静脉接种了EV71(S1-3'),随后检测病毒在中枢神经系统(CNS)和神经外组织中的分布。在中枢神经系统中,仅从脊髓中分离出了EV71(S1-3')。这些结果表明,EV71(S1-3')作为一种有效的抗原,尽管这种减毒株通过静脉途径接种时仍具有嗜神经性。