Abstract
Multiplex RT-PCR analysis of human cytomegalovirus (HCMV) replication in human fibroblasts showed transcription of the natural killer (NK) cell decoy gene, UL18, from 72 h onwards. Transcription of glycoprotein B (gpUL55; a late gene) occurred from early time-points and peaked at 24 h post-infection. UL18 mRNA was also detected in the peripheral blood mononuclear cells of organ transplant recipients with HCMV viraemia, especially those with HCMV DNA virus loads greater than 10(5) genomes/ml whole blood. Thus, UL18 is produced via a low abundance transcript late during the infectious cycle at a time coincidental with the increased risk of NK cell lysis as a consequence of class I HLA down-regulation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Base Sequence
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Cells, Cultured
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Cytomegalovirus / genetics*
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Cytomegalovirus / immunology
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Cytomegalovirus / physiology
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Cytomegalovirus Infections / immunology
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Cytomegalovirus Infections / virology
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DNA Primers / genetics
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DNA, Viral / genetics
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DNA, Viral / metabolism
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Down-Regulation
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Genes, Viral*
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HLA Antigens / metabolism
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Humans
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Immunocompromised Host
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In Vitro Techniques
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Killer Cells, Natural / immunology*
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Polymerase Chain Reaction
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RNA, Messenger / genetics
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RNA, Messenger / metabolism
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RNA, Viral / genetics
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RNA, Viral / metabolism
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Transcription, Genetic
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Transplantation Immunology
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Viremia / immunology
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Viremia / virology
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Virus Replication
Substances
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DNA Primers
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DNA, Viral
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HLA Antigens
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RNA, Messenger
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RNA, Viral