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Human cytomegalovirus infected human endothelial cells. Multicolor Immunofluorescence (IF).Blue: DAPI = cellular DNA, Green = GFP (green fluorescence protein), Red + Magenta = two different viral proteins.Live cell microscopy combined with 3D projection of a late stage Human cytomegalovirus infected human fibroblast. Green = GFP (green fluorescence protein).Human cytomegalovirus infected human fibroblast. Immunofluorescence (IF). Green = viral protein, Red: DAPI = cellular DNA.Nucleus of a Human cytomegalovirus infected human fibroblasts. Immunofluorescence (IF). Blue: DAPI = cellular DNA, Green = viral protein, magenta = Golgy apparatus.
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Cytomegaloviruses are members of the herpes virus family. Human cytomegalovirus (HCMV) infections are widespread and subclinical in the vast majority of cases, but the virus exhibits increased virulence in the very young and old and in immunocompromised individuals. Congenital infections cause life-long disabilities in a significant number of children. Transplant recipients, cancer patients, and AIDS patients, all of whom can exhibit decreased immune function, suffer a variety of clinical manifestations resulting from cytomegalovirus infection, including mononucleosis and pneumonia. There are also suggestions in the literature that HCMV might serve as a cofactor in certain cancers, atherosclerosis and immune senescence. The HCMV particle carries a viral genome comprised of linear double-stranded DNA that encodes more than 200 proteins, 23 microRNAs and a variety of additional non-coding RNAs. We study molecular mechanisms underlying HCMV replication and pathogenesis. 

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