Viral G Protein-Coupled Receptors Encoded by β- and γ-Herpesviruses

Mette M. Rosenkilde, Naotaka Tsutsumi, Julius M. Knerr, Dagmar F. Kildedal, K. Christopher Garcia

Research output: Contribution to journalReview articlepeer-review

6 Citations (Scopus)


Herpesviruses are ancient large DNA viruses that have exploited gene capture as part of their strategy to escape immune surveillance, promote virus spreading, or reprogram host cells to benefit their survival. Most acquired genes are transmembrane proteins and cytokines, such as viral G protein-coupled receptors (vGPCRs), chemokines, and chemokine-binding proteins. This review focuses on the vGPCRs encoded by the human β- and γ-herpesviruses. These include receptors from human cytomegalovirus, which encodes four vGPCRs: US27, US28, UL33, and UL78; human herpesvirus 6 and 7 with two receptors: U12 and U51; Epstein-Barr virus with one: BILF1; and Kaposi's sarcoma-associated herpesvirus with one: open reading frame 74, ORF74. We discuss ligand binding, signaling, and structures of the vGPCRs in light of robust differences from endogenous receptors. Finally, we briefly discuss the therapeutic targeting of vGPCRs as future treatment of acute and chronic herpesvirus infections.

Original languageEnglish
Pages (from-to)329-351
Number of pages23
JournalAnnual Review of Virology
Issue number1
Publication statusPublished - Sept 29 2022


  • broad-spectrum ligand binding
  • chemokine receptor
  • G protein signaling
  • GPCR structure
  • herpesvirus

ASJC Scopus subject areas

  • Virology


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