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...
Main Authors: | , , , , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
eLife Sciences Publications Ltd
2019-07-01
|
Series: | eLife |
Subjects: | |
Online Access: | https://elifesciences.org/articles/47117 |
id |
doaj-8f9c877ea32349559ba7e12f43882bd9 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT dgarrettbrown themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT raymondsoto themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT soumyayandamuri themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT colleenstone themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT lauradickey themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT joaocarlosgomesneto themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT elissadpastuzyn themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT rickeshabell themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT charissepetersen themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT kaitlinbuhrke themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT robertsfujinami themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT ryanmoconnell themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT wzacstephens themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT jasondshepherd themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT thomaselane themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT junelround themicrobiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT dgarrettbrown microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT raymondsoto microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT soumyayandamuri microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT colleenstone microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT lauradickey microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT joaocarlosgomesneto microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT elissadpastuzyn microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT rickeshabell microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT charissepetersen microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT kaitlinbuhrke microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT robertsfujinami microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT ryanmoconnell microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT wzacstephens microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT jasondshepherd microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT thomaselane microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling AT junelround microbiotaprotectsfromviralinducedneurologicdamagethroughmicrogliaintrinsictlrsignaling |
_version_ |
1721459002531905536 |