Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3426763 | Virology | 2007 | 12 Pages |
Human cytomegaloviruses (HCMVs) are important pathogens in immunocompromised patients and newborns. The viral chemokine, vCXCL-1, of the Toledo (Tol) strain of HCMV has been implicated in HCMV virulence. Chimpanzee CMV (CCMV) has several genes with similarity to the vCXCL-1Tol gene, UL146. In order to test whether the CCMV viral chemokine, vCXCL-1CCMV, is similar to vCXCL-1Tol, we characterized its function in vitro. Receptor binding, activation, chemotaxis, signaling, and apoptosis in neutrophils were compared between vCXCL-1Tol and vCXCL-1CCMV and host chemokines. Although the homologues had similar activation potentials, chemotactic properties, and signaling, vCXCL-1CCMV had a ∼ 70-fold lower affinity for CXCR2 and displayed differences in integrin upregulation and neutrophil apoptosis. These data demonstrate that in spite of extensive amino acid variability in vCXCL-1, CCMV may provide a model for assessing the role of vCXCL-1 in CMV pathogenesis in vivo.