An infectious clone of enterovirus 71(EV71) that is capable of infecting neonatal immune competent mice without adaptive mutations. Issue 1 (1st January 2020)

• Record Type: Journal Article
• Authors: Zhang, Huiying; Song, Zhigang; Zou, Jingyi; Feng, Yanling; Zhang, Jing; Ren, Lehao; Zhang, Xiaonan; Hu, Yunwen; Yuan, Zhenghong; Yi, Zhigang
• Is Part Of: Emerging microbes & infections. Volume 9:Issue 1(2020)
• Page Start: 427
• Page End: 438
• Publication Date: 2020-01-01
• Subjects: Enterovirus 71 -- infectious clone -- mouse model -- adaptive mutation -- myolysis -- pulmonary pathology; Medical microbiology -- Periodicals; Communicable diseases -- Periodicals; Infection -- Periodicals; 616.9041
• DOI: 10.1080/22221751.2020.1729665
• Languages: English
• ISSNs: 2222-1751

Abstract

ABSTRACT: Enterovirus 71 (EV71) is a major pathogen that causes hand, foot and mouth disease (HFMD), which is a life threatening disease in certain children. The pathogenesis of EV71-caused HFMD is poorly defined due to the lack of simple and robust animal models with severe phenotypes that recapitulate symptoms observed in humans. Here, we generated the infectious clone of a clinical isolate from a severe HFMD patient. Virus rescued from the cDNA clone was infectious in cell lines. When administrated intraperitoneally to neonatal ICR, BALB/c and C57 immune competent mice at a dosage of1.4 × 10 4 pfu per mouse, the virus caused weight loss, paralysis and death in the infected mice after 4–5 days of infection. In the infected mice, detectable viral replication was detected in various tissues such as heart, liver, brain, lung, kidney, small intestine, leg skeletal muscle and medulla oblongata. The histology of the infected mice included massive myolysis, glomerular atrophy, villous blunting in small intestine, widened alveolar septum, diminished alveolar spaces and lymphocytes infiltration into the lung. By using the UV-inactivated virus as a control, we elucidated that the virus first amplified in the leg skeletal muscle tissue and the muscle tissue served as a primary viral replication site. In summary, we generated a stable EV71 infectious clone that is capable of infecting neonatal immune competent mice without adaptive mutations and provide a simple, valuable animal model for the studies of EV71pathogenesis and therapy.