Human papillomavirus type 16 antagonizes IRF6 regulation of IL-1β.

Bibliographic Details
Title: Human papillomavirus type 16 antagonizes IRF6 regulation of IL-1β.
Authors: Michelle Ainouze, Pauline Rochefort, Peggy Parroche, Guillaume Roblot, Issam Tout, François Briat, Claudia Zannetti, Marie Marotel, Nadege Goutagny, Philip Auron, Alexandra Traverse-Glehen, Aude Lunel-Potencier, Francois Golfier, Murielle Masson, Alexis Robitaille, Massimo Tommasino, Christine Carreira, Thierry Walzer, Thomas Henry, Katia Zanier, Gilles Trave, Uzma Ayesha Hasan
Source: PLoS Pathogens, Vol 14, Iss 8, p e1007158 (2018)
Publisher Information: Public Library of Science (PLoS), 2018.
Publication Year: 2018
Collection: LCC:Immunologic diseases. Allergy
LCC:Biology (General)
Subject Terms: Immunologic diseases. Allergy, RC581-607, Biology (General), QH301-705.5
More Details: Human papillomavirus type 16 (HPV16) and other oncoviruses have been shown to block innate immune responses and to persist in the host. However, to avoid viral persistence, the immune response attempts to clear the infection. IL-1β is a powerful cytokine produced when viral motifs are sensed by innate receptors that are members of the inflammasome family. Whether oncoviruses such as HPV16 can activate the inflammasome pathway remains unknown. Here, we show that infection of human keratinocytes with HPV16 induced the secretion of IL-1β. Yet, upon expression of the viral early genes, IL-1β transcription was blocked. We went on to show that expression of the viral oncoprotein E6 in human keratinocytes inhibited IRF6 transcription which we revealed regulated IL-1β promoter activity. Preventing E6 expression using siRNA, or using E6 mutants that prevented degradation of p53, showed that p53 regulated IRF6 transcription. HPV16 abrogation of p53 binding to the IRF6 promoter was shown by ChIP in tissues from patients with cervical cancer. Thus E6 inhibition of IRF6 is an escape strategy used by HPV16 to block the production IL-1β. Our findings reveal a struggle between oncoviral persistence and host immunity; which is centered on IL-1β regulation.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1553-7366
1553-7374
Relation: https://doaj.org/toc/1553-7366; https://doaj.org/toc/1553-7374
DOI: 10.1371/journal.ppat.1007158
Access URL: https://doaj.org/article/13c5c32805e54812a1ed1b3f489a9f19
Accession Number: edsdoj.13c5c32805e54812a1ed1b3f489a9f19
Database: Directory of Open Access Journals
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More Details
ISSN:15537366
15537374
DOI:10.1371/journal.ppat.1007158
Published in:PLoS Pathogens
Language:English