Infectious Agents Associated Cancers Epidemiology and Molecular Biology

(Nora) #1

© Springer Nature Singapore Pte Ltd. 2017 225
Q. Cai et al. (eds.), Infectious Agents Associated Cancers: Epidemiology
and Molecular Biology, Advances in Experimental Medicine and Biology 1018,
DOI 10.1007/978-981-10-5765-6_14


Chapter 14


Murine Gammaherpesvirus 68: A Small


Animal Model for Gammaherpesvirus-


Associated Diseases


Sihan Dong, J. Craig Forrest, and Xiaozhen Liang


Abstract Murine gammaherpesvirus 68 (MHV68) is a naturally occurring patho-


gen of murid rodents that is genetically related to the human gammaherpesviruses


Epstein-Barr virus (EBV) and Kaposi sarcoma-associated herpesvirus (KSHV).


Viral, immunologic, and disease parameters following experimental infection of


laboratory mice with MHV68 closely resemble what occurs during primary EBV


infection of humans, which suggests that MHV68 infection of mice offers a small


animal model to study in general the pathogenesis of gammaherpesvirus infections.


Diseases elicited by MHV68 infection include lymphoproliferative diseases, idio-


pathic pulmonary fibrosis, and autoimmune diseases, ailments also associated with


EBV infection of humans. Furthermore, MHV68 infection also is linked to the


development of vasculitis, encephalomyelitis, and other disorders that resemble


pathologies with viral and nonviral etiologies in humans. This review aims to pro-


vide an overview of MHV68-associated diseases in infected mice that may provide


a model for understanding basic mechanisms by which similar diseases in humans


occur and can be treated.


Keywords Animal model • Murine gammaherpesvirus 68 • Epstein-Barr virus •


Kaposi sarcoma-associated herpesvirus


S. Dong • X. Liang (*)
Key Laboratory of Molecular Virology & Immunology, Institut Pasteur of Shanghai, Chinese
Academy of Sciences, Shanghai 200031, People’s Republic of China
e-mail: [email protected]


J.C. Forrest
Department of Microbiology and Immunology and Center for Microbial Pathogenesis and
Host Inflammatory Responses, University of Arkansas for Medical Sciences,
Little Rock, AR, USA

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