Author Topic: (AAN) Increased Archaea species & changes w/therapy in gut microbiome in MS  (Read 111 times)

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Offline agate

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Presented at the annual AAN conference in Philadelphia, April 30, 2014:

Quote
[S24.001] Increased Archaea Species and Changes with Therapy in Gut Microbiome of Multiple Sclerosis Subjects

Sushrut Jhangi,1Roopali Gandhi,1,1Bonnie Glanz,2Sandra Cook,2Parham Nejad,3Doyle Ward,4Ning Li,1Georg Gerber,1Lynn Bry,1Howard Weiner1

1Boston, MA, USA, 2Brookline, MA, USA, 34Cambridge, MA, USA

OBJECTIVE:

To determine if there are differences in the gut microbiome in MS and if changes occur with treatment.

BACKGROUND:

 The gut microbiome plays a key role in shaping the immune repertoire and plays an important role in disease susceptibility in the EAE model. The gut microbiome has been described in other diseases but not yet in MS.

DESIGNS/METHOD:

MS patients from the Partners MS Center [untreated (n=22), glatiramer acetate treated (n=13), and IFN-b treated (n=18)] and healthy controls from the BWH PhenoGenetic project (n=44) were studied. Samples were profiled using two high throughput platforms (454 and Illumina 16s sequencing) to determine community structure and taxonomic composition of the gut microbome.

RESULTS:

We found an increase in Archaea (Methanobrevibacteriaceae) in MS vs. controls (p <0.00001 by 454 sequencing). Archaea are in a kingdom separate from bacteria and eukaryotes and in the human gut are dominated by Methanobrevibacter smithii, which make up 10% of colonic anaerobes in the gut. The cell wall and lipid membranes of M smithii make them strongly immunogenic consistent with a role in the induction of local and systemic inflammatory processes in the host.

We also found two organisms with anti-inflammatory properties that were lower in MS vs. controls and which were increased with treatment.

Specifically: 1) The Butyricimonas genus from Bacteroidetes phylum was lower in the untreated MS vs. controls. Butyricimonas are butyrate producers with anti-inflammatory effects; and 2) The Lachnospiraceae family from the Firmicutes phylum (which are also butyrate producers) was lower in untreated vs. treated MS irrespective of whether they were treated with IFN-β or glatiramer acetate.

CONCLUSION:

Our results identify changes in both pro-and anti-inflammatory epigenetic factors in the gut microbiome of MS subjects that may contribute to disease pathogenesis.

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Study supported by: NIH R21 and NMSS pilot grant.
Category - MS and CNS Inflammatory Disease: Basic Science



S24: Platform Session: Diet and Hormonal Influences in Multiple Sclerosis (2:00 PM-3:45 PM)
MS Speaks--online for 17 years

SPMS, diagnosed 1980. Avonex 2001-2004. Copaxone 2007-2010. Glatopa (glatiramer acetate 40mg 3 times/week) since 12/16/20.

Offline agate

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Could MS begin in the gut? (Scientific American link)
« Reply #1 on: October 11, 2014, 11:16:41 am »
More on this idea in the Scientific American, October 6, 2014, "Could multiple sclerosis begin in the gut?".
MS Speaks--online for 17 years

SPMS, diagnosed 1980. Avonex 2001-2004. Copaxone 2007-2010. Glatopa (glatiramer acetate 40mg 3 times/week) since 12/16/20.