Abstract

During 2001-2002 and 2008-2011, two epidemic outbreaks of infectious hemorrhagic disease have been found in Japanese macaques (Macaca fuscata) in Kyoto University Primate Research Institute, Japan. Following investigations revealed that the causative agent was simian retrovirus type 4 (SRV-4). SRV-4 was isolated by using human cell lines, which indicates that human cells are potently susceptible to SRV-4 infection. These raise a possibility of zoonotic infection of pathogenic SRV-4 from Japanese macaques into humans. To explore the possibility of zoonotic infection of SRV-4 to humans, here we use a human hematopoietic stem cell-transplanted humanized mouse model. Eight out of the twelve SRV-4-inoculated humanized mice were infected with SRV-4. Importantly, 3 out of the 8 infected mice exhibited anemia and hemophagocytosis, and an infected mouse died. To address the possibility that SRV-4 adapts humanized mouse and acquires higher pathogenicity, the virus was isolated from an infected mice exhibited severe anemia was further inoculated into another 6 humanized mice. However, no infected mice exhibited any illness. Taken together, our findings demonstrate that the zoonotic SRV-4 infection from Japanese macaques to humans is technically possible under experimental condition. However, such zoonotic infection may not occur in the real society.

Highlights

  • During 2001-2002 and 2008-2011, two epidemic outbreaks of infectious hemorrhagic disease have been found in Japanese macaques (Macaca fuscata) in Kyoto University Primate Research Institute, Japan

  • These results suggest that simian retrovirus type 4 (SRV-4) is able to replicate in humanized mouse model, while is incapable of inducing a high level of viremia

  • We have previously reported that hemophagocytosis and severe anemia can be induced by Epstein-Barr virus (EBV) infection in NOD/SCID Il2rg–/– (NOG)-hCD34 mice, and that the hemophagocytosis and anemia closely associated with the overproduction of inflammatory cytokines, IFN-γ 23

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Summary

Introduction

During 2001-2002 and 2008-2011, two epidemic outbreaks of infectious hemorrhagic disease have been found in Japanese macaques (Macaca fuscata) in Kyoto University Primate Research Institute, Japan. In order to reproduce and elucidate the infections of human-specific pathogens such as HIV in vivo, we have constructed a humanized mouse model by xenotransplanting human CD34+ hematopoietic stem cells (HSCs) into an immunodeficient NOD/SCID Il2rg–/– (NOG) mouse[19,20,21,22,23,24,25]. In this system, human leukocytes are differentiated de novo and are stably and longitudinally maintained. It is noteworthy that our humanized mice, named NOG-hCD34 mice, are able to recapitulate the pathogenesis of EBV infection including hemophagocytosis and normocytic anemia with high mortality[23]

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