PLoS ONE (Jan 2015)

Enterovirus 71 infection causes severe pulmonary lesions in gerbils, meriones unguiculatus, which can be prevented by passive immunization with specific antisera.

  • Fang Xu,
  • Ping-Ping Yao,
  • Yong Xia,
  • Lei Qian,
  • Zhang-Nv Yang,
  • Rong-Hui Xie,
  • Yi-Sheng Sun,
  • Hang-Jing Lu,
  • Zi-Ping Miao,
  • Chan Li,
  • Xiao Li,
  • Wei-Feng Liang,
  • Xiao-Xiao Huang,
  • Shi-Chang Xia,
  • Zhi-Ping Chen,
  • Jian-Min Jiang,
  • Yan-Jun Zhang,
  • Ling-Ling Mei,
  • She-Lan Liu,
  • Hua Gu,
  • Zhi-Yao Xu,
  • Xiao-Fei Fu,
  • Zhi-Yong Zhu,
  • Han-Ping Zhu

DOI
https://doi.org/10.1371/journal.pone.0119173
Journal volume & issue
Vol. 10, no. 3
p. e0119173

Abstract

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Neurogenic pulmonary edema caused by severe brainstem encephalitis is the leading cause of death in young children infected by Enterovirus 71 (EV71). However, no pulmonary lesions have been found in EV71-infected transgenic or non-transgenic mouse models. Development of a suitable animal model is important for studying EV71 pathogenesis and assessing effect of therapeutic approaches. We had found neurological disorders in EV71-induced young gerbils previously. Here, we report severe pulmonary lesions characterized with pulmonary congestion and hemorrhage in a gerbil model for EV71 infection. In the EV71-infected gerbils, six 21-day-old or younger gerbils presented with a sudden onset of symptoms and rapid illness progression after inoculation with 1×105.5 TCID50 of EV71 via intraperitoneal (IP) or intramuscular (IM) route. Respiratory symptoms were observed along with interstitial pneumonia, pulmonary congestion and extensive lung hemorrhage could be detected in the lung tissues by histopathological examination. EV71 viral titer was found to be peak at late stages of infection. EV71-induced pulmonary lesions, together with severe neurological disorders were also observed in gerbils, accurately mimicking the disease process in EV71-infected patients. Passive transfer with immune sera from EV71 infected adult gerbils with a neutralizing antibody (GMT=89) prevented severe pulmonary lesion formation after lethal EV71 challenge. These results establish this gerbil model as a useful platform for studying the pathogenesis of EV71-induced pulmonary lesions, immunotherapy and antiviral drugs.