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Molecular Analysis of Model Gut Microbiotas by Imaging Mass Spectrometry and Nanodesorption Electrospray Ionization Reveals Dietary Metabolite Transformations
The communities constituting our microbiotas are emerging as mediators of the health-disease continuum. However, deciphering the functional impact of microbial communities on host pathophysiology represents a formidable challenge, due to the heterogeneous distribution of chemical and microbial speci...
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Published in: | Analytical chemistry (Washington) 2012-11, Vol.84 (21), p.9259-9267 |
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creator | Rath, Christopher M Alexandrov, Theodore Higginbottom, Steven K Song, Jiao Milla, Marcos E Fischbach, Michael A Sonnenburg, Justin L Dorrestein, Pieter C |
description | The communities constituting our microbiotas are emerging as mediators of the health-disease continuum. However, deciphering the functional impact of microbial communities on host pathophysiology represents a formidable challenge, due to the heterogeneous distribution of chemical and microbial species within the gastrointestinal (GI) tract. Herein, we apply imaging mass spectrometry (IMS) to localize metabolites from the interaction between the host and colonizing microbiota. This approach complements other molecular imaging methodologies in that analytes need not be known a priori, offering the possibility of untargeted analysis. Localized molecules within the GI tract were then identified in situ by surface sampling with nanodesorption electrospray ionization Fourier transform ion cyclotron resonance-mass spectrometry (nanoDESI FTICR-MS). Products from diverse structural classes were identified including cholesterol-derived lipids, glycans, and polar metabolites. Specific chemical transformations performed by the microbiota were validated with bacteria in culture. This study illustrates how untargeted spatial characterization of metabolites can be applied to the molecular dissection of complex biology in situ. |
doi_str_mv | 10.1021/ac302039u |
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However, deciphering the functional impact of microbial communities on host pathophysiology represents a formidable challenge, due to the heterogeneous distribution of chemical and microbial species within the gastrointestinal (GI) tract. Herein, we apply imaging mass spectrometry (IMS) to localize metabolites from the interaction between the host and colonizing microbiota. This approach complements other molecular imaging methodologies in that analytes need not be known a priori, offering the possibility of untargeted analysis. Localized molecules within the GI tract were then identified in situ by surface sampling with nanodesorption electrospray ionization Fourier transform ion cyclotron resonance-mass spectrometry (nanoDESI FTICR-MS). Products from diverse structural classes were identified including cholesterol-derived lipids, glycans, and polar metabolites. Specific chemical transformations performed by the microbiota were validated with bacteria in culture. 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Chem</addtitle><description>The communities constituting our microbiotas are emerging as mediators of the health-disease continuum. However, deciphering the functional impact of microbial communities on host pathophysiology represents a formidable challenge, due to the heterogeneous distribution of chemical and microbial species within the gastrointestinal (GI) tract. Herein, we apply imaging mass spectrometry (IMS) to localize metabolites from the interaction between the host and colonizing microbiota. This approach complements other molecular imaging methodologies in that analytes need not be known a priori, offering the possibility of untargeted analysis. Localized molecules within the GI tract were then identified in situ by surface sampling with nanodesorption electrospray ionization Fourier transform ion cyclotron resonance-mass spectrometry (nanoDESI FTICR-MS). Products from diverse structural classes were identified including cholesterol-derived lipids, glycans, and polar metabolites. Specific chemical transformations performed by the microbiota were validated with bacteria in culture. This study illustrates how untargeted spatial characterization of metabolites can be applied to the molecular dissection of complex biology in situ.</description><subject>Analytical chemistry</subject><subject>Animals</subject><subject>Arachidonic Acid - metabolism</subject><subject>Bacteria</subject><subject>Bacteria - growth & development</subject><subject>Bacteria - metabolism</subject><subject>Bile Acids and Salts - metabolism</subject><subject>Biomarkers - metabolism</subject><subject>Biotransformation</subject><subject>Chemistry</subject><subject>Culture Techniques</subject><subject>Diet</subject><subject>Digestive system</subject><subject>Exact sciences and technology</subject><subject>Fourier transforms</subject><subject>gastrointestinal system</subject><subject>image analysis</subject><subject>intestinal microorganisms</subject><subject>Intestines - microbiology</subject><subject>ionization</subject><subject>lipids</subject><subject>Mass Spectrometry</subject><subject>Metabolites</subject><subject>Metabolomics</subject><subject>Mice</subject><subject>microbial communities</subject><subject>microbial culture</subject><subject>Microbiota</subject><subject>Molecular Imaging - methods</subject><subject>Molecules</subject><subject>Nanotechnology - methods</subject><subject>pathophysiology</subject><subject>polysaccharides</subject><subject>Polysaccharides - metabolism</subject><subject>Spectrometric and optical methods</subject><issn>0003-2700</issn><issn>1520-6882</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpl0cFu1DAQBmALgehSOPACyBJCKofA2Emc7LEqpVRqQIJyjibOpHLlxIsnQVoeps-Ku11aBCdL9jdj-x8hXip4p0Cr92hz0JCvl0dipUoNmalr_VisACDPdAVwIJ4xXwMoBco8FQc6B1ibUq3ETRM82cVjlMcT-i07lmGQTejJy7Nllo2zMXQuzMiy28rzEa_cdCUbZJbfNmTnGEaa41bi1MvPOKVCDnEzuzDJU787503EVBkm9wt3-1_pJ6Fn-cHRjKm0SUsXvJtJXkaceAhx3El-Lp4MSdKL_Xoovn88vTz5lF18OTs_Ob7IsIRqzqp1XfS6I8yNtn0JRGT6oe51r6FQdQFWDdShLVShUOVQlbqnweq1sWVpLOaH4uiu7yaGHwvx3I6OLXmPE4WFW30bpS60Vom-_odehyWm7LhVqiigqCtTJfX2TqX0mCMN7Sa6MX22VdDeDq29H1qyr_Ydl26k_l7-mVICb_YA2aIfUkbW8YMzRoMuqgeHlv961X8X_gboZ62S</recordid><startdate>20121106</startdate><enddate>20121106</enddate><creator>Rath, Christopher M</creator><creator>Alexandrov, Theodore</creator><creator>Higginbottom, Steven K</creator><creator>Song, Jiao</creator><creator>Milla, Marcos E</creator><creator>Fischbach, Michael A</creator><creator>Sonnenburg, Justin L</creator><creator>Dorrestein, Pieter C</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20121106</creationdate><title>Molecular Analysis of Model Gut Microbiotas by Imaging Mass Spectrometry and Nanodesorption Electrospray Ionization Reveals Dietary Metabolite Transformations</title><author>Rath, Christopher M ; 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Chem</addtitle><date>2012-11-06</date><risdate>2012</risdate><volume>84</volume><issue>21</issue><spage>9259</spage><epage>9267</epage><pages>9259-9267</pages><issn>0003-2700</issn><issn>1520-6882</issn><eissn>1520-6882</eissn><coden>ANCHAM</coden><abstract>The communities constituting our microbiotas are emerging as mediators of the health-disease continuum. However, deciphering the functional impact of microbial communities on host pathophysiology represents a formidable challenge, due to the heterogeneous distribution of chemical and microbial species within the gastrointestinal (GI) tract. Herein, we apply imaging mass spectrometry (IMS) to localize metabolites from the interaction between the host and colonizing microbiota. This approach complements other molecular imaging methodologies in that analytes need not be known a priori, offering the possibility of untargeted analysis. Localized molecules within the GI tract were then identified in situ by surface sampling with nanodesorption electrospray ionization Fourier transform ion cyclotron resonance-mass spectrometry (nanoDESI FTICR-MS). Products from diverse structural classes were identified including cholesterol-derived lipids, glycans, and polar metabolites. Specific chemical transformations performed by the microbiota were validated with bacteria in culture. This study illustrates how untargeted spatial characterization of metabolites can be applied to the molecular dissection of complex biology in situ.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>23009651</pmid><doi>10.1021/ac302039u</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analytical chemistry Animals Arachidonic Acid - metabolism Bacteria Bacteria - growth & development Bacteria - metabolism Bile Acids and Salts - metabolism Biomarkers - metabolism Biotransformation Chemistry Culture Techniques Diet Digestive system Exact sciences and technology Fourier transforms gastrointestinal system image analysis intestinal microorganisms Intestines - microbiology ionization lipids Mass Spectrometry Metabolites Metabolomics Mice microbial communities microbial culture Microbiota Molecular Imaging - methods Molecules Nanotechnology - methods pathophysiology polysaccharides Polysaccharides - metabolism Spectrometric and optical methods |
title | Molecular Analysis of Model Gut Microbiotas by Imaging Mass Spectrometry and Nanodesorption Electrospray Ionization Reveals Dietary Metabolite Transformations |
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