Abstract

The Tupaia or tree shrew (Tupaia belangeri), a small mammal of the Tupaiidae family, is an increasingly used and promising infection model for virological and immunological research. Recently, sequencing of the Tupaia whole genome revealed that it is more homologous to the genome of humans than of rodents. Viral infections are a global threat to human health, and a complex series of events are involved in the interactions between a virus and the host immune system, which play important roles in the activation of an immune response and the outcome of an infection. Majority of immune response data in viral infections are obtained from studies using animal models that enhance the understanding of host-virus interactions; a proper understanding of these interactions is very important for the development of effective antivirals and prophylactics. Therefore, animal models that are permissive to infection and that recapitulate human disease pathogenesis and immune responses to viral infections are essential. Several studies have shown the permissiveness of Tupaia to a number of important human viral infections in vitro and in vivo without prior adaptation of the viruses; the immune responses and clinical manifestations were comparable to those observed in human infections. Thus, the Tupaia is being utilized and developed as a promising immunocompetent small animal model for viral infection studies. In this review, we focused on the immune responses, mostly innate, during viral infection and pathogenesis in the Tupaia model; we evaluated the interaction between the virus and the components of host resistance, the usefulness of this model for immunopathogenesis studies, and the vaccines and antivirals available.

Highlights

  • The investigation of the immune response to viruses has provided fundamental insight into the functioning of the host’s immune system

  • The innate immune response safeguards the host against viral infections as the first line of defense, and early and non-specific detection of pathogens are generally mediated by the recognition of pathogen-associated molecular patterns (PAMPs) by different pattern recognition receptors (PRRs), such as Toll-like receptors (TLRs), retinoic acid-inducible gene I (RIG)-like receptors (RLRs), nucleotide-binding oligomerization domain-containing protein (NOD)-like receptors, C-type Lectin, and DNA-sensing receptors [1,2]

  • TLR9 messenger RNA (mRNA) expression was found to be suppressed in Hepatitis B virus (HBV) chronic infection in the Tupaia model, which is consistent with a previous report showing reduced TLR9 expression in peripheral CD14+ monocytes of chronic hepatitis B patients [64]

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Summary

Introduction

The investigation of the immune response to viruses has provided fundamental insight into the functioning of the host’s immune system. In this study, we aimed to address the findings obtained from research on human viral infections using the Tupaia model, which might help to elucidate the underlying mechanisms of host-virus interactions and viral pathogenesis. This may provide an opportunity to evaluate virus-host interactions, host defense mechanisms, immunopathogenesis, and the efficacy of vaccines and antivirals in this animal model. Searching for alternative suitable small animal models for DENV infection study is imperative To this end, we have investigated the susceptibility of Tupaia cells to infection by wild type DENV serotypes 1–4 [24]. DThEiNs mV asyersoutygpgees1t cdoifmfepraernetdfetaotuthreesoothfeDrEsNerVotysepreost.ype 1 compared to the other serotypes

Zika Virus
Epstein–Barr Virus
Conclusions
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