The microbiota protects from viral-induced neurologic damage through microglia-intrinsic TLR signaling

Symbiotic microbes impact the function and development of the central nervous system (CNS); however, little is known about the contribution of the microbiota during viral-induced neurologic damage. We identify that commensals aid in host defense following infection with a neurotropic virus through e...

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Main Authors: D Garrett Brown, Raymond Soto, Soumya Yandamuri, Colleen Stone, Laura Dickey, Joao Carlos Gomes-Neto, Elissa D Pastuzyn, Rickesha Bell, Charisse Petersen, Kaitlin Buhrke, Robert S Fujinami, Ryan M O'Connell, W Zac Stephens, Jason D Shepherd, Thomas E Lane, June L Round
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2019-07-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/47117
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spelling doaj-8f9c877ea32349559ba7e12f43882bd92021-05-05T17:46:36ZengeLife Sciences Publications LtdeLife2050-084X2019-07-01810.7554/eLife.47117The microbiota protects from viral-induced neurologic damage through microglia-intrinsic TLR signalingD Garrett Brown0https://orcid.org/0000-0001-8779-7048Raymond Soto1https://orcid.org/0000-0002-8483-6459Soumya Yandamuri2Colleen Stone3Laura Dickey4Joao Carlos Gomes-Neto5Elissa D Pastuzyn6Rickesha Bell7https://orcid.org/0000-0002-0554-0730Charisse Petersen8Kaitlin Buhrke9Robert S Fujinami10Ryan M O'Connell11W Zac Stephens12Jason D Shepherd13https://orcid.org/0000-0001-7384-8289Thomas E Lane14https://orcid.org/0000-0003-0392-0825June L Round15https://orcid.org/0000-0002-7158-9874Department of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Neurobiology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Neurobiology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, United StatesSymbiotic microbes impact the function and development of the central nervous system (CNS); however, little is known about the contribution of the microbiota during viral-induced neurologic damage. We identify that commensals aid in host defense following infection with a neurotropic virus through enhancing microglia function. Germfree mice or animals that receive antibiotics are unable to control viral replication within the brain leading to increased paralysis. Microglia derived from germfree or antibiotic-treated animals cannot stimulate viral-specific immunity and microglia depletion leads to worsened demyelination. Oral administration of toll-like receptor (TLR) ligands to virally infected germfree mice limits neurologic damage. Homeostatic activation of microglia is dependent on intrinsic signaling through TLR4, as disruption of TLR4 within microglia, but not the entire CNS (excluding microglia), leads to increased viral-induced clinical disease. This work demonstrates that gut immune-stimulatory products can influence microglia function to prevent CNS damage following viral infection.https://elifesciences.org/articles/47117microbiotaTLR 4Neurological damagemicrogliaJHMV
collection DOAJ
language English
format Article
sources DOAJ
author D Garrett Brown
Raymond Soto
Soumya Yandamuri
Colleen Stone
Laura Dickey
Joao Carlos Gomes-Neto
Elissa D Pastuzyn
Rickesha Bell
Charisse Petersen
Kaitlin Buhrke
Robert S Fujinami
Ryan M O'Connell
W Zac Stephens
Jason D Shepherd
Thomas E Lane
June L Round
spellingShingle D Garrett Brown
Raymond Soto
Soumya Yandamuri
Colleen Stone
Laura Dickey
Joao Carlos Gomes-Neto
Elissa D Pastuzyn
Rickesha Bell
Charisse Petersen
Kaitlin Buhrke
Robert S Fujinami
Ryan M O'Connell
W Zac Stephens
Jason D Shepherd
Thomas E Lane
June L Round
The microbiota protects from viral-induced neurologic damage through microglia-intrinsic TLR signaling
eLife
microbiota
TLR 4
Neurological damage
microglia
JHMV
author_facet D Garrett Brown
Raymond Soto
Soumya Yandamuri
Colleen Stone
Laura Dickey
Joao Carlos Gomes-Neto
Elissa D Pastuzyn
Rickesha Bell
Charisse Petersen
Kaitlin Buhrke
Robert S Fujinami
Ryan M O'Connell
W Zac Stephens
Jason D Shepherd
Thomas E Lane
June L Round
author_sort D Garrett Brown
title The microbiota protects from viral-induced neurologic damage through microglia-intrinsic TLR signaling
title_short The microbiota protects from viral-induced neurologic damage through microglia-intrinsic TLR signaling
title_full The microbiota protects from viral-induced neurologic damage through microglia-intrinsic TLR signaling
title_fullStr The microbiota protects from viral-induced neurologic damage through microglia-intrinsic TLR signaling
title_full_unstemmed The microbiota protects from viral-induced neurologic damage through microglia-intrinsic TLR signaling
title_sort microbiota protects from viral-induced neurologic damage through microglia-intrinsic tlr signaling
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2019-07-01
description Symbiotic microbes impact the function and development of the central nervous system (CNS); however, little is known about the contribution of the microbiota during viral-induced neurologic damage. We identify that commensals aid in host defense following infection with a neurotropic virus through enhancing microglia function. Germfree mice or animals that receive antibiotics are unable to control viral replication within the brain leading to increased paralysis. Microglia derived from germfree or antibiotic-treated animals cannot stimulate viral-specific immunity and microglia depletion leads to worsened demyelination. Oral administration of toll-like receptor (TLR) ligands to virally infected germfree mice limits neurologic damage. Homeostatic activation of microglia is dependent on intrinsic signaling through TLR4, as disruption of TLR4 within microglia, but not the entire CNS (excluding microglia), leads to increased viral-induced clinical disease. This work demonstrates that gut immune-stimulatory products can influence microglia function to prevent CNS damage following viral infection.
topic microbiota
TLR 4
Neurological damage
microglia
JHMV
url https://elifesciences.org/articles/47117
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