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The Journal of Immunology, 2003, 170: 3828-3834.
Copyright © 2003 by The American Association of Immunologists

Differential {gamma}-Herpesvirus Distribution in Distinct Anatomical Locations and Cell Subsets During Persistent Infection in Mice1

Emilio Flaño, In-Jeong Kim, John Moore, David L. Woodland and Marcia A. Blackman2

Trudeau Institute, Saranac Lake, NY 12983

Murine {gamma}-herpesvirus 68 (MHV-68) provides an important experimental model for analyzing {gamma}-herpesvirus latent infection. After intranasal infection with MHV-68, we analyzed the distribution of the virus in different anatomical locations and purified populations of cells. Our data show that long-term latency is maintained in a variety of anatomical locations and cell populations with different frequencies. Importantly, we demonstrate that although latency in the lung is established in a variety of cell subsets, long-term latency in the lung is only maintained in B cells. In contrast, splenic latency is maintained in macrophages and dendritic cells, as well as in B cells. In blood, isotype-switched B cells constitute the major viral reservoir. These results show that the cell subsets in which latency is established vary within different anatomical sites. Finally, we demonstrate that long-term latency is accompanied by a low level of infectious virus in lung and spleen. These data have important implications for understanding the establishment and maintenance of latency by {gamma}2-herpesviruses.




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