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肠道病毒71型感染会损害雌性小鼠的生殖能力。

Enterovirus 71 infection impairs the reproductive capacity of female mice.

作者信息

Qin Bo, Yan Qiuyue, Chen Xing, Xu Xiuping, Wang Yanan, Chen Jinkun, Dong Xuejun

机构信息

Clinical Laboratory Center, Shaoxing People's Hospital, Shaoxing Hospital of Zhejiang University, Shaoxing, Zhejiang 312000, P.R. China.

Shaoxing Centre for Disease Control and Prevention, Shaoxing, Zhejiang 312000, P.R. China.

出版信息

Exp Ther Med. 2017 Jul;14(1):403-409. doi: 10.3892/etm.2017.4499. Epub 2017 May 23.

Abstract

Enterovirus 71 (EV71) is a major cause of hand, foot and mouth disease (HFMD); however, no clinically approved vaccine or antiviral treatment is currently available for EV71 infection. In the present study, a murine model of EV71 infection was constructed. The clinical isolates of EV71 were amplified in Vero cells and used to challenge adult mice via hydrodynamic injection (HI) and intraperitoneal injection (IP). Following two challenges, >50% of the mice succumbed to EV71 infection. Surviving female mice were identified to have impaired fertility and their litter sizes were significantly decreased compared with the control group. The antibody against EV71-VP1 persisted in the sera of female mice at a high titer for >2 years after challenge. The maternal antibody in the offspring sera also persisted for ~1 year and disappeared after ~2 years. Results from the present study suggest that a high titer of active EV71 was able to impair the reproductivity of adult female mice, and that high levels of maternal antibody persisted in the offspring and protected postnatal mice from EV71-induced mortality. The promising antigenicity, immunogenicity and reactogenicity of EV71 suggests that it a potential vaccine target that may be beneficial to the control of HFMD, through immunizing infants and women of reproductive age.

摘要

肠道病毒71型(EV71)是手足口病(HFMD)的主要病因;然而,目前尚无针对EV71感染的临床批准疫苗或抗病毒治疗方法。在本研究中,构建了EV71感染的小鼠模型。EV71的临床分离株在Vero细胞中扩增,并通过流体动力学注射(HI)和腹腔注射(IP)用于攻击成年小鼠。经过两次攻击后,超过50%的小鼠死于EV71感染。存活的雌性小鼠被确定生育能力受损,与对照组相比,它们的产仔数显著减少。攻击后,抗EV71-VP1抗体在雌性小鼠血清中以高滴度持续存在超过2年。后代血清中的母源抗体也持续存在约1年,并在约2年后消失。本研究结果表明,高滴度的活性EV71能够损害成年雌性小鼠的生殖能力,并且高水平的母源抗体在后代中持续存在,并保护新生小鼠免受EV71诱导的死亡。EV71具有良好的抗原性、免疫原性和反应原性,表明它是一个潜在的疫苗靶点,通过对婴儿和育龄妇女进行免疫接种,可能有助于控制手足口病。

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