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Bacterial lipodipeptide, Lipid 654, is a microbiome-associated biomarker for multiple sclerosis
Multiple sclerosis (MS) is an autoimmune disease of unknown etiology. Infectious agents have been suggested to have a role as environmental factors in MS, but this concept remains controversial. Recently, gastrointestinal commensal bacteria have been implicated in the pathogenesis of autoimmune dise...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232052/ https://www.ncbi.nlm.nih.gov/pubmed/25505950 http://dx.doi.org/10.1038/cti.2013.11 |
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author | Farrokhi, Vahid Nemati, Reza Nichols, Frank C Yao, Xudong Anstadt, Emily Fujiwara, Mai Grady, James Wakefield, Daniel Castro, Wanda Donaldson, James Clark, Robert B |
author_facet | Farrokhi, Vahid Nemati, Reza Nichols, Frank C Yao, Xudong Anstadt, Emily Fujiwara, Mai Grady, James Wakefield, Daniel Castro, Wanda Donaldson, James Clark, Robert B |
author_sort | Farrokhi, Vahid |
collection | PubMed |
description | Multiple sclerosis (MS) is an autoimmune disease of unknown etiology. Infectious agents have been suggested to have a role as environmental factors in MS, but this concept remains controversial. Recently, gastrointestinal commensal bacteria have been implicated in the pathogenesis of autoimmune diseases, but mechanisms underlying the relationship of human systemic autoimmunity with the commensal microbiome have yet to be identified. Consistent with the lack of understanding of pathogenic mechanisms and relevant environmental factors in MS, no blood biomarkers have been identified that distinguish MS patients from healthy individuals. We recently identified a unique gastrointestinal and oral bacteria-derived lipodipeptide, Lipid 654, which is produced by commensal bacteria and functions as a human and mouse Toll-like receptor 2 ligand. Using multiple-reaction-monitoring mass spectrometry, a critical approach in targeted lipidomics, we now report that Lipid 654 can be recovered in the serum of healthy individuals. Most interestingly, we find that Lipid 654 is expressed at significantly lower levels in the serum of patients with MS compared with both healthy individuals and patients with Alzheimer's disease. These results thus identify for the first time a potential mechanism relating the gastrointestinal and oral commensal microbiome to a human systemic autoimmune disease. In addition, these results also identify a potential etiologic environmental factor and novel clinically relevant serum biomarker for MS. |
format | Online Article Text |
id | pubmed-4232052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42320522014-12-11 Bacterial lipodipeptide, Lipid 654, is a microbiome-associated biomarker for multiple sclerosis Farrokhi, Vahid Nemati, Reza Nichols, Frank C Yao, Xudong Anstadt, Emily Fujiwara, Mai Grady, James Wakefield, Daniel Castro, Wanda Donaldson, James Clark, Robert B Clin Transl Immunology Original Article Multiple sclerosis (MS) is an autoimmune disease of unknown etiology. Infectious agents have been suggested to have a role as environmental factors in MS, but this concept remains controversial. Recently, gastrointestinal commensal bacteria have been implicated in the pathogenesis of autoimmune diseases, but mechanisms underlying the relationship of human systemic autoimmunity with the commensal microbiome have yet to be identified. Consistent with the lack of understanding of pathogenic mechanisms and relevant environmental factors in MS, no blood biomarkers have been identified that distinguish MS patients from healthy individuals. We recently identified a unique gastrointestinal and oral bacteria-derived lipodipeptide, Lipid 654, which is produced by commensal bacteria and functions as a human and mouse Toll-like receptor 2 ligand. Using multiple-reaction-monitoring mass spectrometry, a critical approach in targeted lipidomics, we now report that Lipid 654 can be recovered in the serum of healthy individuals. Most interestingly, we find that Lipid 654 is expressed at significantly lower levels in the serum of patients with MS compared with both healthy individuals and patients with Alzheimer's disease. These results thus identify for the first time a potential mechanism relating the gastrointestinal and oral commensal microbiome to a human systemic autoimmune disease. In addition, these results also identify a potential etiologic environmental factor and novel clinically relevant serum biomarker for MS. Nature Publishing Group 2013-11-15 /pmc/articles/PMC4232052/ /pubmed/25505950 http://dx.doi.org/10.1038/cti.2013.11 Text en Copyright © 2013 Australasian Society for Immunology Inc. http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Farrokhi, Vahid Nemati, Reza Nichols, Frank C Yao, Xudong Anstadt, Emily Fujiwara, Mai Grady, James Wakefield, Daniel Castro, Wanda Donaldson, James Clark, Robert B Bacterial lipodipeptide, Lipid 654, is a microbiome-associated biomarker for multiple sclerosis |
title | Bacterial lipodipeptide, Lipid 654, is a microbiome-associated biomarker for multiple sclerosis |
title_full | Bacterial lipodipeptide, Lipid 654, is a microbiome-associated biomarker for multiple sclerosis |
title_fullStr | Bacterial lipodipeptide, Lipid 654, is a microbiome-associated biomarker for multiple sclerosis |
title_full_unstemmed | Bacterial lipodipeptide, Lipid 654, is a microbiome-associated biomarker for multiple sclerosis |
title_short | Bacterial lipodipeptide, Lipid 654, is a microbiome-associated biomarker for multiple sclerosis |
title_sort | bacterial lipodipeptide, lipid 654, is a microbiome-associated biomarker for multiple sclerosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232052/ https://www.ncbi.nlm.nih.gov/pubmed/25505950 http://dx.doi.org/10.1038/cti.2013.11 |
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