This revised project will define the role of positive-acting virus-encoded chemokines and chemokine receptors as determinants of host cell trafficking that facilitate virus infection and dissemination in the host. During the past period, this grant supported the discovery and characterization of human CMV chemokine homologs (UL146 and UL147), demonstrating that one (UL146) is a functional chemokine (denoted vCXC-1) that attracts neutrophils via a specific interaction with the receptor hCXCR2. In addition, the murine CMV chemokine homolog, MCK-1, was shown to be a bone fide positive-acting chemokine that signals to macrophages and facilitates inflammation to attract cells for virus dissemination in the host animal. This proposal will focus on understanding how virus-encoded homologs of chemokines and chemokine receptors influence dissemination in the course of acute or latent infection.
The first aim will be to study human CMV vCXC-1 (pUL 146) as a potential recruiter of host cells important in acute or latent infection. The impact of vCXC-1 on hCXCR2-bearing cell types will be investigated in cultured human and mouse cells as well as in mice by engineering vCXC-1 into the murine CMV genome. To model the behavior of human CMV, dissemination behavior will be evaluated in mice engineered to express hCXCR2 in the granulocyte-macrophage lineage, an approach that is possible because mice lack natural vCXC-1 responsive leukocyte populations.
The second aim of this proposal will be to investigate the role of murine CMV MCK-2 in trafficking behavior of monocyte/macrophage cell populations. MCK-2 is a positively-acting, monocyte-attracting chemokine that influences a monocyte-associated viremia and influences inflammation and dissemination in mice.
The aim will identify cell type(s) that respond to MCK-2 and that mediate viral dissemination by cell surface markers as well as by functional properties such as antigen presentation and immune clearance properties. Recombinant MCK-2 will be employed to identify the murine receptor(s) that recognize MCK-2. In order to determine the spectrum of modulatory functions carried out by MCK-2, animals and cells with a variety of immune and chemokine receptor defects will be employed to assess MCK-2 impact on the innate immune response to virus.
The third aim of this proposal will be to investigate signalling and cell migration control via the human CMV US28 chemokine receptor, relying on a recombinant human and murine CMV, as well as cell lines expressing US28 in the absence of viral infection. Microarray analysis has shown that US28-expressing virus induces gene expression consistent with reorganization of cytoskeletal components and these will be dissected during the next grant period. The overall goals of the project will greatly increase the understanding of human CMV dissemination and pathogenesis critical to its success as a ubiquitous pathogen.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI030363-12
Application #
6872896
Study Section
Experimental Virology Study Section (EVR)
Program Officer
Beisel, Christopher E
Project Start
1991-01-01
Project End
2006-03-31
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
12
Fiscal Year
2005
Total Cost
$277,562
Indirect Cost
Name
Stanford University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
McCormick, A Louise; Mocarski, Edward S (2015) The immunological underpinnings of vaccinations to prevent cytomegalovirus disease. Cell Mol Immunol 12:170-9
Mocarski, Edward S; Kaiser, William J; Livingston-Rosanoff, Devon et al. (2014) True grit: programmed necrosis in antiviral host defense, inflammation, and immunogenicity. J Immunol 192:2019-26
Kaiser, William J; Sridharan, Haripriya; Huang, Chunzi et al. (2013) Toll-like receptor 3-mediated necrosis via TRIF, RIP3, and MLKL. J Biol Chem 288:31268-79
Crosby, Lynsey N; McCormick, A Louise; Mocarski, Edward S (2013) Gene products of the embedded m41/m41.1 locus of murine cytomegalovirus differentially influence replication and pathogenesis. Virology 436:274-83
Kaiser, William J; Upton, Jason W; Mocarski, Edward S (2013) Viral modulation of programmed necrosis. Curr Opin Virol 3:296-306
Upton, Jason W; Kaiser, William J; Mocarski, Edward S (2012) DAI/ZBP1/DLM-1 complexes with RIP3 to mediate virus-induced programmed necrosis that is targeted by murine cytomegalovirus vIRA. Cell Host Microbe 11:290-7
Tandon, Ritesh; Mocarski, Edward S (2012) Viral and host control of cytomegalovirus maturation. Trends Microbiol 20:392-401
Daley-Bauer, Lisa P; Wynn, Grace M; Mocarski, Edward S (2012) Cytomegalovirus impairs antiviral CD8+ T cell immunity by recruiting inflammatory monocytes. Immunity 37:122-33
Livingston-Rosanoff, Devon; Daley-Bauer, Lisa P; Garcia, AnaPatricia et al. (2012) Antiviral T cell response triggers cytomegalovirus hepatitis in mice. J Virol 86:12879-90
Kaiser, William J; Upton, Jason W; Long, Alyssa B et al. (2011) RIP3 mediates the embryonic lethality of caspase-8-deficient mice. Nature 471:368-72

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