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Coevolution pays off: Herpesviruses have the license to escape the DNA sensing pathway. | LitMetric

Coevolution pays off: Herpesviruses have the license to escape the DNA sensing pathway.

Med Microbiol Immunol

Viral Immune Modulation Research Group, Helmholtz Centre for Infection Research, Brunswick, Germany.

Published: August 2019

AI Article Synopsis

  • Early detection of viral infections by pattern recognition receptors (PRR) is vital for activating a strong immune response, particularly through cytosolic DNA sensors that trigger type I interferon production via the STING protein.
  • Herpesviruses, large DNA viruses, have developed numerous strategies to evade and manipulate host immune responses, specifically targeting the DNA sensing and STING pathways.
  • This review will highlight the mechanisms of DNA sensing and the sophisticated ways herpesviruses adapt to influence crucial aspects of the innate immune response.

Article Abstract

Early detection of viral invasion by pattern recognition receptors (PRR) is crucial for the induction of a rapid and efficient immune response. Cytosolic DNA sensors are the most recently described class of PRR, and induce transcription of type I interferons (IFN) and proinflammatory cytokines via the key adaptor protein stimulator of interferon genes (STING). Herpesviruses are a family of large DNA viruses widely known for their immense arsenal of proteins dedicated to manipulating and evading host immune responses. Tantamount to the significant role played by DNA sensors and STING in innate immune responses, herpesviruses have in turn evolved a range of mechanisms targeting virtually every step of this key signaling pathway. Strikingly, some herpesviruses also take advantage of this pathway to promote their own replication. In this review, we will summarize the current understanding of DNA sensing and subsequent induction of signaling and transcription, and showcase the close adaptation of herpesviruses to their host reflected by the myriad of viral proteins dedicated to modulating this critical innate immune pathway.

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Source
http://dx.doi.org/10.1007/s00430-019-00582-0DOI Listing

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