Pathogens hijack the epigenome: A new twist on host-pathogen interactions

Natalie C. Silmon De Monerri, Kami Kim

Research output: Contribution to journalArticle

43 Citations (Scopus)

Abstract

Pathogens have evolved strategies to promote their survival by dramatically modifying the transcriptional profile and protein content of the host cells they infect. Modifications of the host transcriptome and proteome are mediated by pathogen-encoded effector molecules that modulate host cells through a variety of different mechanisms. Recent studies highlight the importance of the host chromatin and other epigenetic regulators as targets of pathogens. Host gene regulatory mechanisms may be targeted through cytoplasmic signaling, directly by pathogen effector proteins, and possibly by pathogen RNA. Although many of these changes are short-lived and persist only during the course of infection, several studies indicate that pathogens are able to induce long-term, heritable changes that are essential to pathogenesis of infectious diseases and persistence of pathogens within their hosts. In this review, we discuss how pathogens modulate the epigenome of host cells, a new and flourishing avenue of host-pathogen interaction studies.

Original languageEnglish (US)
Pages (from-to)897-911
Number of pages15
JournalAmerican Journal of Pathology
Volume184
Issue number4
DOIs
StatePublished - 2014

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Host-Pathogen Interactions
Proteome
Regulator Genes
Transcriptome
Epigenomics
Chromatin
Communicable Diseases
Proteins
RNA
Infection

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Medicine(all)

Cite this

Pathogens hijack the epigenome : A new twist on host-pathogen interactions. / Silmon De Monerri, Natalie C.; Kim, Kami.

In: American Journal of Pathology, Vol. 184, No. 4, 2014, p. 897-911.

Research output: Contribution to journalArticle

Silmon De Monerri, Natalie C. ; Kim, Kami. / Pathogens hijack the epigenome : A new twist on host-pathogen interactions. In: American Journal of Pathology. 2014 ; Vol. 184, No. 4. pp. 897-911.
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