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Rapid Inflammasome Activation following Mucosal SIV Infection of Rhesus Monkeys
Author(s) -
Dan H. Barouch,
Khader Ghneim,
William J. Bosche,
Yuan Li,
Brian Berkemeier,
Michael Hull,
Sanghamitra Bhattacharyya,
Mark J. Cameron,
Jinyan Liu,
Kaitlin M. Smith,
Erica N. Borducchi,
Crystal Cabral,
Lauren Peter,
Amanda Brinkman,
Mayuri Shetty,
Hualin Li,
Courtney Gittens,
Chantelle Baker,
Wendeline Wagner,
Mark G. Lewis,
Arnaud D. Colantonio,
Hyung-joo Kang,
Wenjun Li,
Jeffrey D. Lifson,
Michael Piatak,
RafickPierre Sékaly
Publication year - 2016
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.2016.03.021
Subject(s) - biology , simian immunodeficiency virus , inflammasome , virology , immunology , haplorhini , mucosal immunity , immunity , immune system , human immunodeficiency virus (hiv) , inflammation , virus
The earliest events following mucosal HIV-1 infection, prior to measurable viremia, remain poorly understood. Here, by detailed necropsy studies, we show that the virus can rapidly disseminate following mucosal SIV infection of rhesus monkeys and trigger components of the inflammasome, both at the site of inoculation and at early sites of distal virus spread. By 24 hr following inoculation, a proinflammatory signature that lacked antiviral restriction factors was observed in viral RNA-positive tissues. The early innate response included expression of NLRX1, which inhibits antiviral responses, and activation of the TGF-β pathway, which negatively regulates adaptive immune responses. These data suggest a model in which the virus triggers specific host mechanisms that suppress the generation of antiviral innate and adaptive immune responses in the first few days of infection, thus facilitating its own replication. These findings have important implications for the development of vaccines and other strategies to prevent infection.

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