Endogenous retroviruses promote homeostatic and inflammatory responses to the microbiota
Author(s) -
Djalma S. Lima-Júnior,
Siddharth R. Krishnamurthy,
Nicolas Bouladoux,
Nicholas Collins,
SeongJi Han,
Erin Chen,
Michael G. Constantinides,
Verena M. Link,
Ai Ing Lim,
Michel Enamorado,
Christophe Cataisson,
Louis Gil,
Indira Rao,
Taylor K. Farley,
Galina Koroleva,
Jan Attig,
Stuart H. Yuspa,
Michael A. Fischbach,
George Kassiotis,
Yasmine Belkaid
Publication year - 2021
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2021.05.020
Subject(s) - biology , inflammation , immunity , endogeny , endogenous retrovirus , immune system , immunology , innate immune system , homeostasis , microbiology and biotechnology , transcription factor , interferon , genetics , gene , genome , endocrinology
The microbiota plays a fundamental role in regulating host immunity. However, the processes involved in the initiation and regulation of immunity to the microbiota remain largely unknown. Here, we show that the skin microbiota promotes the discrete expression of defined endogenous retroviruses (ERVs). Keratinocyte-intrinsic responses to ERVs depended on cyclic GMP-AMP synthase (cGAS)/stimulator of interferon genes protein (STING) signaling and promoted the induction of commensal-specific T cells. Inhibition of ERV reverse transcription significantly impacted these responses, resulting in impaired immunity to the microbiota and its associated tissue repair function. Conversely, a lipid-enriched diet primed the skin for heightened ERV- expression in response to commensal colonization, leading to increased immune responses and tissue inflammation. Together, our results support the idea that the host may have co-opted its endogenous virome as a means to communicate with the exogenous microbiota, resulting in a multi-kingdom dialog that controls both tissue homeostasis and inflammation.
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