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Am. J. Trop. Med. Hyg., 78(4), 2008, pp. 675-680
Copyright © 2008 by The American Society of Tropical Medicine and Hygiene

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Dhori Virus (Orthomyxoviridae: Thogotovirus) Infection of Mice Produces a Disease and Cytokine Response Pattern Similar to That of Highly Virulent Influenza A (H5N1) Virus Infection in Humans

Guangyu Li, Nan Wang, Hilda Guzman, Elena Sbrana, Tomoki Yoshikawa, Chien-tek Tseng, Robert B. Tesh, AND Shu-Yuan Xiao*
Department of Pathology and Center for Biodefense and Emerging Infectious Diseases and Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas

Mice infected with Dhori virus (DHOV) develop a fulminant, systemic, and uniformly fatal illness that has many of the clinical and pathologic findings seen in H5N1 influenza A virus infection. However, the role of host’s immune response in DHOV infection remains unclear. In this study, the concentrations of 23 inflammatory cytokines and chemokines were measured in the liver, lungs, and sera of mice during the course of DHOV infection. Liver function, level of viremia, and hematologic response were also monitored. Infected animals exhibited significant leucopenia and lymphopenia, which directly correlated with the disease progression. High yields of infectious virus along with strikingly elevated expression of various inflammatory mediators, including tumor necrosis factor (TNF)-{alpha}, inter-leukin (IL)-1, IL-6, IL-10, macrophage inflammatory protein (MIP)-1{alpha}, manocyte chemoattractant protein (MCP)-1, and interferon (IFN)- {alpha}, indicate that these responses play an important role in the observed disease and pathology. The overall clinical, pathologic, and immunologic responses of ICR mice to DHOV infection closely resemble those described for highly virulent influenza A virus infection in humans, thereby offering a realistic, safe, and alternative animal model for studying the pathogenesis and treatment of highly pathogenic avian influenza virus.


Received October 4, 2007. Accepted for publication January 18, 2008.

Acknowledgments: The authors thank Dora Salinas for help in preparing the manuscript and Patrick Newman for preparing the histologic sections.

Financial support: This work was supported by National Institutes of Health Contracts NO1-AI25489 and NO1-AI 30027.

* Address to Shu-Yuan Xiao, Department of Pathology, Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-0588. E-mail: syxiao{at}utmb.edu

Authors’ addresses: Guangyu Li, Hilda Guzman, Elena Sbrana, Rob-ert B. Tesh, and Shu-Yuan Xiao, Department of Pathology, University of Texas Medical Branch; 301 University Boulevard; Galveston, TX 77555-0609, Telephone: 409-772-2853, Fax: 409-747-0060, E-mail: syxiao{at}utmb.edu. Nan Wang, Tomoki Yoshikawa, and Chien-tek Tseng, Department of Microbiology and Immunology, University of Texas Medical Branch; 301 University Boulevard; Galveston, TX 77555-0609, Telephone: 409-772-2853, Fax: 409-747-0060, E-mail: syxiao{at}utmb.edu.

Reprint requests: Shu-Yuan Xiao, Department of Pathology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-0609, E-mail: syxiao{at}utmb.edu.







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