Granzyme H destroys the function of critical adenoviral proteins required for viral DNA replication and granzyme B inhibition

Felipe Andrade, Edward Fellows, Dieter E. Jenne, Antony Rosen, C. S.H. Young

Research output: Contribution to journalArticle

Abstract

Granzymes are key components of the immune response that play important roles in eliminating host cells infected by intracellular pathogens. Several granzymes are potent inducers of cell death. However, whether granzymes use additional mechanisms to exert their antipathogen activity remains elusive. Here, we show that in adenovirus-infected cells in which granzyme B (gzmB) and downstream apoptosis pathways are inhibited, granzyme H (gzmH), an orphan granzyme without known function, directly cleaves the adenovirus DNA-binding protein (DBP), a viral component absolutely required for viral DNA replication. We directly addressed the functional consequences of the cleavage of the DBP by gzmH through the generation of a virus that encodes a gzmH-resistant DBP. This virus demonstrated that gzmH directly induces an important decay in viral DNA replication. Interestingly, gzmH also cleaves the adenovirus 100K assembly protein, a major inhibitor of gzmB, and relieves gzmB inhibition. These results provide the first evidence that granzymes can mediate antiviral activity through direct cleavage of viral substrates, and further suggest that different granzymes have synergistic functions to outflank viral defenses that block host antiviral activities.

Original languageEnglish (US)
Pages (from-to)2148-2157
Number of pages10
JournalEMBO Journal
Volume26
Issue number8
DOIs
StatePublished - Apr 18 2007

Keywords

  • Adenovirus
  • Antiviral
  • Cytotoxic
  • Granzyme
  • NK

ASJC Scopus subject areas

  • Neuroscience(all)
  • Molecular Biology
  • Biochemistry, Genetics and Molecular Biology(all)
  • Immunology and Microbiology(all)

Fingerprint Dive into the research topics of 'Granzyme H destroys the function of critical adenoviral proteins required for viral DNA replication and granzyme B inhibition'. Together they form a unique fingerprint.

  • Cite this