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Pathogenesis of Modoc Virus (Flaviviridae; Flavivirus) in Persistently Infected Hamsters

A. Paige AdamsCenter for Biodefense and Emerging Infectious Diseases and Department of Pathology, University of Texas Medical Branch, Galveston, Texas

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Amelia P. A. Travassos da RosaCenter for Biodefense and Emerging Infectious Diseases and Department of Pathology, University of Texas Medical Branch, Galveston, Texas

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Marcio R. NunesCenter for Biodefense and Emerging Infectious Diseases and Department of Pathology, University of Texas Medical Branch, Galveston, Texas

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Shu-Yuan XiaoCenter for Biodefense and Emerging Infectious Diseases and Department of Pathology, University of Texas Medical Branch, Galveston, Texas

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Robert B. TeshCenter for Biodefense and Emerging Infectious Diseases and Department of Pathology, University of Texas Medical Branch, Galveston, Texas

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The long-term persistence of Modoc virus (MODV) infection was investigated in a hamster model. Golden hamsters (Mesocricetus auratus) were infected by subcutaneous inoculation with MODV, in which fatal encephalitis developed in 12.5% (2 of 16). Surviving hamsters shed infectious MODV in their urine during the first five months after infection, and infectious MODV was recovered by co-cultivation of kidney tissue up to eight months after infection. There were no histopathologic changes observed in the kidneys despite detection of viral antigen for 250 days after infection. Mild inflammation and neuronal degeneration in the central nervous system were the primary lesions observed during early infection. These findings confirm previous reports of persistent flavivirus infection in animals and suggest a mechanism for the maintenance of MODV in nature.

Author Notes

* Address correspondence to A. Paige Adams, Department of Pathology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-0609. E-mail: apadams@utmb.edu

Financial support: This study was supported in part by National Institutes of Health contracts N01 AI25489 and N01 AI30027 to Robert B. Tesh. A. Paige Adams was supported by the James W. McLaughlin fellowship fund.

Authors' addresses: A. Paige Adams, Amelia P. A. Travassos da Rosa, and Robert B. Tesh, Department of Pathology, University of Texas Medical Branch, Galveston, TX, E-mails: apadams@utmb.edu, aptravas@utmb.edu, and rtesh@utmb.edu. Marcio R. Nunes, Instituto Evandro Chagas/SVS/MS, Levilândia, Belém, Pará, Brazil, E-mail: marcionunes@iec.pa.gov.br. Shu-Yuan Xiao, University of Chicago, Chicago, IL, E-mail: Shu-Yuan.Xiao@uchospitals.edu.

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