A neonatal gnotobiotic pig model of human enterovirus 71 infection and associated immune responses

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Nature Publishing Group


Vaccine development and pathogenesis studies for human enterovirus 71 are limited by a lack of suitable animal models. Here, we report the development of a novel neonatal gnotobiotic pig model using the non-pig-adapted neurovirulent human enterovirus 71 strain BJ110, which has a C4 genotype. Porcine small intestinal epithelial cells, peripheral blood mononuclear cells and neural cells were infected in vitro. Oral and combined oral–nasal infection of 5-day-old neonatal gnotobiotic pigs with 53108 fluorescence forming units (FFU) resulted in shedding up to 18 days post-infection, with viral titers in rectal swab samples peaking at 2.223108 viral RNA copies/mL. Viral capsid proteins were detected in enterocytes within the small intestines on post-infection days (PIDs) 7 and 14. Additionally, viral RNA was detected in intestinal and extra-intestinal tissues, including the central nervous system, the lung and cardiac muscle. The infected neonatal gnotobiotic pigs developed fever, forelimb weakness, rapid breathing and some hand, foot and mouth disease symptoms. Flow cytometry analysis revealed increased frequencies of both CD41 and CD81 IFN-c-producing T cells in the brain and the blood on PID 14, but reduced frequencies were observed in the lung. Furthermore, high titers of serum virus-neutralizing antibodies were generated in both orally and combined oral–nasally infected pigs on PIDs 7, 14, 21 and 28. Together, these results demonstrate that neonatal gnotobiotic pigs represent a novel animal model for evaluating vaccines for human enterovirus 71 and for understanding the pathogenesis of this virus and the associated immune responses.



Immunology, Microbiology, adaptive immune responses, animal model, human enterovirus 71, neonatal gnotobiotic pigs, pathogenesis, vaccine evaluation, SELECTIN GLYCOPROTEIN LIGAND-1, BRAIN-STEM ENCEPHALITIS, HUMAN ROTAVIRUS, MOUTH-DISEASE, ANTIBODY-RESPONSES, CYNOMOLGUS MONKEYS, CLINICAL-FEATURES, CELL RESPONSES, SUBGENOTYPE C4, RHESUS-MONKEYS