BMC Infectious Diseases · 2016 · 25 citations · 21 references
Veterinary MedicineAnimal SciencesInfectious DiseasesHistopathologyMolecular VirologyVirologyAnimal Infectious DiseasesLiver DiseaseViral HepatitisViral InfectionsViral PathologyAnalytical Methods For Liver EnzymesAnimal Disease ModelsAnimal Model EvaluationAntibodiesCapsid Protein DetectionHepatitis E Virus InfectionHistopathologic ExaminationWestern Blot Analysis
BACKGROUND: Hepatitis E virus (HEV) is a major cause of hepatitis in developing countries and poses a threat to public health worldwide. Tree shrew (Tupaia belangeri chinensis) is a useful animal model in studies on hepatitis viruses, such as hepatitis B and C viruses. However, the use of this animal model for HEV research is yet to be developed. METHODS: Tree shrews were intravenously (IV) injected with swine genotype 4 HEV or infected by contact-exposure to IV infected tree shrews. RT-nPCR was performed to detect HEV RNA in the feces, tissues, and blood. HEV capsid protein in the different tissues was detected by Western blot and estimated by quantitative RT-PCR. Anti-HEV antibodies were determined by ELISA. Liver damages were evaluated by histopathologic examination and analysis of liver-specific enzymes activities. RESULTS: Both negative and positive strands of HEV RNA were detected in the feces of the HEV-infected or contact-exposed tree shrews 3-4 days post-inoculation. HEV RNA was detectable in the liver, spleen, kidneys, and bile. Virusemia developed in all the HEV-infected tree shrews. HEV capsid protein was expressed in the liver, spleen, and kidneys. The histological examination and analysis of liver-specific enzymes activities showed that HEV caused acute liver lesions in the tree shrews. Meanwhile, the infected tree shrews showed positive IgG and IgM antibodies. CONCLUSIONS: Tree shrews are susceptible to HEV and may be useful animal models for HEV experimental infection studies on pathogenesis or preclinical drug development.
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F. F. Huang, Gholamreza Haqshenas, D. K. Guenette et al. · Journal of Clinical Microbiology · 2002 · 381 citations · Full text
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