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Of particular significance is the capacity of HCMV to reactivate within solid tissue and bone marrow transplant recipients. While it is known that HCMV latency resides within a fraction of HPCs and monocytes, the exact subset of cells that harbor latent viral genomes during natural infections remain uncharacterized. The capacity to identify changes within the host transcriptome during latent infections is critical for developing approaches that therapeutically or physically eliminate latent viral genome containing cells and will represent a major breakthrough for reducing complications due to HCMV reactivation posttransplant. In this report, we describe the generation and use of a recombinant HCMV that allows specific and distinct labeling of RNA species that are produced within virally infected cells. This is a critical first step in identifying how HCMV affects the host cell during latency and more importantly, allows one to characterize cells that harbor latent HCMV.<\/jats:p>","DOI":"10.1128\/jvi.00880-18","type":"journal-article","created":{"date-parts":[[2018,8,8]],"date-time":"2018-08-08T11:11:42Z","timestamp":1533726702000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":16,"title":["Selective 4-Thiouracil Labeling of RNA Transcripts within Latently Infected Cells after Infection with Human Cytomegalovirus Expressing Functional Uracil Phosphoribosyltransferase"],"prefix":"10.1128","volume":"92","author":[{"given":"Kathryn L.","family":"Roche","sequence":"first","affiliation":[{"name":"FORGE Life Science, Pennsylvania Biotechnology Center, Doylestown, Pennsylvania, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masatoshi","family":"Nukui","sequence":"additional","affiliation":[{"name":"Department of Translational Medicine, Baruch S. 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