Research for the Environment

Functional metaproteome of the microbiota

Project description

Recent evidence suggests that the composition of the microbial community in the human gut contributes to the development of obesity by increasing the host’s efficacy to harvest energy. Initial reports indicate that bariatric surgery changes the composition of the microbiota. However, neither the underlying mechanisms nor their consequences for the energy homeostasis have been revealed yet.
The aim of this study in a rat model of diet-induced obesity is to investigate the bariatric postoperative effects on the microbial community. The composition of the microbial diversity shall be analyzed at different time points (1 week, 1 month, 6 months postoperatively) by genetic evaluation. At the same time points the metabolic activity of the microbes shall be assessed by measuring the carbon flux within the microbial community. Similarly, the metabolic interaction between host and microbial community shall be observed by tracing the carbon flux into various tissues including visceral and subcutaneous fat, liver and muscle. The long-term goal of these experiments is to reveal, whether and when alterations of the microbial community may contribute to a beneficial postoperative energy homeostasis and whether differences may be found between the bariatric surgery techniques.

workflow

Fig.1 Analysis of the microbiota-proteome and the tissue-proteome using Protein-SIP

Involved researchers

Cooperations

Dr. Manuel Ferrer, CSIC, Institute of Catalysis, Madrid, Spain

Prof. Antonio Suarez, Department of Biochemistry and Molecular Biology, Centro de Investigación Biomédica, University of Granada, Granada, Spain

Publications

Haange SB, Oberbach A, Schlichting N, Hugenholtz F, Smidt H, von Bergen M, Till H, Seifert J. (2012)
Metaproteome analysis and molecular genetics of rat intestinal microbiota reveals section and localization resolved species distribution and enzymatic functionalities.
Journal of Proteome Research 11 (11), 5406-5417

Ferrer M, Ruiz A, Lanza F, Haange SB, Oberbach A, Till H, Campoy C, Segura MT, Richter M, Bargiela R, von Bergen M, Seifert J, Suarez A. (2013)
Microbiota from the distal guts of lean and obese adolescents exhibit partial functional redundancy besides clear differences in community structure.
Environmental Microbiology 15 (1), 211-226.

Pérez-Cobas AE, Gosalbes MJ, Friedrichs A, Knecht H, Artacho A, Eismann K, Otto W, Rojo D, Bargiela R, von Bergen M, Neulinger SC, Däumer C, Heinsen FA, Latorre A, Barbas C, Seifert J, Martins dos Santos V, Ott SJ, Ferrer M, Moya A. (in press)
Gut microbiota disturbance during antibiotic therapy: a multi-omic approach.
Gut (doi: 10.1136/gutjnl-2012-303184)

Funding

IFB Adipositas Erkrankungen, Uniklinkium Leipzig

publications

Kliemt S, Lange C, Otto W, Hintze V, Möller S, von Bergen M, Hempel U, Kalkhof S.
Sulfated hyaluronan containing collagen matrices enhance cell-matrix-interaction, endocytosis, and osteogenic differentiation of human mesenchymal stromal cells.
J Proteome Res. 2012 Nov 21. [Epub ahead of print] PMID:23170904

Haange SB, Oberbach A, Schlichting N, Hugenholtz F, Smidt H, von Bergen M, Till H, Seifert J.
Metaproteome analysis and molecular genetics of rat intestinal microbiota reveals section and localisation resolved species distribution and enzymatic functionalities.
J Proteome Res. 2012 Nov 2;11(11):5406-17. PMID: 23016992

Müller SA, van der Smissen A, von Feilitzsch M, Anderegg U, Kalkhof S, von Bergen M.
Quantitative proteomics reveals altered expression of extracellular matrix related proteins of human primary dermal fibroblasts in response to sulfated hyaluronan and collagen applied as artificial extracellular matrix.
J Mater Sci Mater Med. 2012 Dec;23(12):3053-65. PMID: 22990618

Goettsch C, Kliemt S, Sinningen K, von Bergen M, Hofbauer LC, Kalkhof S.
Quantitative proteomics reveals novel functions of osteoclast-associated receptor in STAT signaling and cell adhesion in human endothelial cells.
J Mol Cell Cardiol. 2012 Dec;53(6):829-37. PMID: 22985931

Salbach J, Kliemt S, Rauner M, Rachner TD, Goettsch C, Kalkhof S, von Bergen M, Möller S, Schnabelrauch M, Hintze V, Scharnweber D, Hofbauer LC.
The effect of the degree of sulfation of glycosaminoglycans on osteoclast function and signaling pathways.
Biomaterials 2012 Nov;33(33):8418-29. PMID: 22954516

Guazzaroni ME, Herbst FA, Lores I, Tamames J, Peláez AI, López-Cortés N, Alcaide M, Del Pozo MV, Vieites JM, von Bergen M, Gallego JL, Bargiela R, López-López A, Pieper DH, Rosselló-Móra R, Sánchez J, Seifert J, Ferrer M.
Metaproteogenomic insights beyond bacterial response to naphthalene exposure and bio-stimulation.
ISME J. 2012 Jul 26. doi: 10.1038/ismej.2012.82.[Epub ahead of print] PMID: 22832345

Taubert M, Vogt C, Wubet T, Kleinsteuber S, Tarkka MT, Harms H, Buscot F, Richnow HH, von Bergen M, Seifert J
Protein-SIP enables time-resolved analysis of the carbon flux in a sulfate-reducing, benzene-degrading microbial consortium.
ISME J. 2012 Jul 12. doi: 10.1038/ismej.2012.68. [Epub ahead of print] PMID: 22791237.


Boll K, Reiche K, Kasack K, Mörbt N, Kretzschmar AK, Tomm JM, Verhaegh G, Schalken J, von Bergen M, Horn F, Hackermüller J.
MiR-130a, miR-203 and miR-205 jointly repress key oncogenic pathways and are downregulated in prostate carcinoma.
Oncogene. 2012 Mar 5. doi: 10.1038/onc.2012.55. [Epub ahead of print] PubMed PMID: 22391564.


Haas S, Jahnke HG, Moerbt N, von Bergen M, Aharinejad S, Andrukhova O, Robitzki AA
DIGE proteome analysis reveals suitability of ischemic cardiac in vitro model for studying cellular response to acute ischemia and regeneration.
PLoS One. 2012;7(2):e31669. Epub 2012 Feb 22. PubMed PMID: 22384053