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Molecular Hydrogen as an Energy Source for Helicobacter pylori
The gastric pathogen Helicobacter pylori is known to be able to use molecular hydrogen as a respiratory substrate when grown in the laboratory. We found that hydrogen is available in the gastric mucosa of mice and that its use greatly increased the stomach colonization by H. pylori. Hydrogenase acti...
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Published in: | Science (American Association for the Advancement of Science) 2002-11, Vol.298 (5599), p.1788-1790 |
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description | The gastric pathogen Helicobacter pylori is known to be able to use molecular hydrogen as a respiratory substrate when grown in the laboratory. We found that hydrogen is available in the gastric mucosa of mice and that its use greatly increased the stomach colonization by H. pylori. Hydrogenase activity in H. pylori is constitutive but increased fivefold upon incubation with hydrogen. Hydrogen concentrations measured in the stomachs of live mice were found to be 10 to 50 times as high as the H. pylori affinity for hydrogen. A hydrogenase mutant strain is much less efficient in its colonization of mice. Therefore, hydrogen present in animals as a consequence of normal colonic flora is an energy-yielding substrate that can facilitate the maintenance of a pathogenic bacterium. |
doi_str_mv | 10.1126/science.1077123 |
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Psychology ; Gastric Mucosa - metabolism ; Gastric Mucosa - microbiology ; Gene Expression Regulation, Bacterial ; Genes ; Genes, Reporter ; Helicobacter pylori ; Helicobacter pylori - growth & development ; Helicobacter pylori - metabolism ; Hydrogen ; Hydrogen - metabolism ; Hydrogenase - genetics ; Hydrogenase - metabolism ; Kinetics ; Land Settlement ; Mice ; Microbial colonization ; Microbiology ; Mutation ; Oxidation ; Oxidation-Reduction ; Oxygenases - genetics ; Oxygenases - metabolism ; Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains ; Pathogens ; Plasmids ; Stomach ; Transcription, Genetic</subject><ispartof>Science (American Association for the Advancement of Science), 2002-11, Vol.298 (5599), p.1788-1790</ispartof><rights>Copyright 2002 American Association for the Advancement of Science</rights><rights>2003 INIST-CNRS</rights><rights>COPYRIGHT 2002 American Association for the Advancement of Science</rights><rights>COPYRIGHT 2002 American Association for the Advancement of Science</rights><rights>Copyright American Association for the Advancement of Science Nov 29, 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c709t-eb2371de0dbe3df26b0b6f5ab21d65d72a5fa8db635e5d1a84243917841109693</citedby><cites>FETCH-LOGICAL-c709t-eb2371de0dbe3df26b0b6f5ab21d65d72a5fa8db635e5d1a84243917841109693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/213608217/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/213608217?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,2884,2885,21378,21394,27924,27925,33611,33612,33877,33878,43733,43880,58238,58471,74221,74397</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14399176$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12459589$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Olson, Jonathan W.</creatorcontrib><creatorcontrib>Maier, Robert J.</creatorcontrib><title>Molecular Hydrogen as an Energy Source for Helicobacter pylori</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><description>The gastric pathogen Helicobacter pylori is known to be able to use molecular hydrogen as a respiratory substrate when grown in the laboratory. We found that hydrogen is available in the gastric mucosa of mice and that its use greatly increased the stomach colonization by H. pylori. Hydrogenase activity in H. pylori is constitutive but increased fivefold upon incubation with hydrogen. Hydrogen concentrations measured in the stomachs of live mice were found to be 10 to 50 times as high as the H. pylori affinity for hydrogen. A hydrogenase mutant strain is much less efficient in its colonization of mice. Therefore, hydrogen present in animals as a consequence of normal colonic flora is an energy-yielding substrate that can facilitate the maintenance of a pathogenic bacterium.</description><subject>Animals</subject><subject>Bacteria</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Catechol 2,3-Dioxygenase</subject><subject>Colon - metabolism</subject><subject>Colon - microbiology</subject><subject>Dioxygenases</subject><subject>Energy</subject><subject>Energy Metabolism</subject><subject>Energy sources</subject><subject>Fermentation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastric Mucosa - metabolism</subject><subject>Gastric Mucosa - microbiology</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genes</subject><subject>Genes, Reporter</subject><subject>Helicobacter pylori</subject><subject>Helicobacter pylori - growth & development</subject><subject>Helicobacter pylori - metabolism</subject><subject>Hydrogen</subject><subject>Hydrogen - metabolism</subject><subject>Hydrogenase - genetics</subject><subject>Hydrogenase - metabolism</subject><subject>Kinetics</subject><subject>Land Settlement</subject><subject>Mice</subject><subject>Microbial colonization</subject><subject>Microbiology</subject><subject>Mutation</subject><subject>Oxidation</subject><subject>Oxidation-Reduction</subject><subject>Oxygenases - genetics</subject><subject>Oxygenases - metabolism</subject><subject>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</subject><subject>Pathogens</subject><subject>Plasmids</subject><subject>Stomach</subject><subject>Transcription, Genetic</subject><issn>0036-8075</issn><issn>1095-9203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>ALSLI</sourceid><sourceid>CJNVE</sourceid><sourceid>M0P</sourceid><recordid>eNqN0s-LEzEUB_BBFLeunr2IDII_Dju7-TH5dRHWsnYXqj2seg2ZzJsyJZ3UZAbsf29KB5dK0ZJDIO-TwHv5ZtlLjC4xJvwq2hY6C5cYCYEJfZRNMFKsUATRx9kEIcoLiQQ7y57FuEIo1RR9mp1hUjLFpJpkH794B3ZwJuS32zr4JXS5ibnp8psOwnKb3_shWMgbnwC41vrK2B5Cvtk6H9rn2ZPGuAgvxv08-_755tv0tpgvZnfT63lhBVJ9ARWhAteA6gpo3RBeoYo3zFQE15zVghjWGFlXnDJgNTayJCVVWMgSp364oufZ-_27m-B_DhB7vW6jBedMB36IWpSUSEXVTr77tySCUC7RfyGWjEmCcIJv_oKrNJMutasJphxJgkVCF3u0NA502zW-D8amaUIwznfQtOn4WrGylALv3iyO8LRqWKcZH_EfDnwiPfzql2aIUd_dfz2ZLn6cTD_NTqVyNj-gF8eo9c7BEnTKxXRxwK_23AYfY4BGb0K7NmGrMdK7kOsx5HoMebrxevyQoVpD_eDHVCfwdgQmWuOaYDrbxgeXspXCxZN7tXer2Pvwp04lpSih3yJHCB4</recordid><startdate>20021129</startdate><enddate>20021129</enddate><creator>Olson, Jonathan W.</creator><creator>Maier, Robert J.</creator><general>American Association for the Advancement of Science</general><general>The American Association for the Advancement of Science</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>8GL</scope><scope>IBG</scope><scope>IOV</scope><scope>ISN</scope><scope>0-V</scope><scope>3V.</scope><scope>7QF</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QQ</scope><scope>7QR</scope><scope>7SC</scope><scope>7SE</scope><scope>7SN</scope><scope>7SP</scope><scope>7SR</scope><scope>7SS</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7TK</scope><scope>7TM</scope><scope>7U5</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>D1I</scope><scope>DWQXO</scope><scope>F28</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9-</scope><scope>K9.</scope><scope>KB.</scope><scope>KR7</scope><scope>L6V</scope><scope>L7M</scope><scope>LK8</scope><scope>L~C</scope><scope>L~D</scope><scope>M0K</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>R05</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20021129</creationdate><title>Molecular Hydrogen as an Energy Source for Helicobacter pylori</title><author>Olson, Jonathan W. ; Maier, Robert J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c709t-eb2371de0dbe3df26b0b6f5ab21d65d72a5fa8db635e5d1a84243917841109693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Bacteria</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Catechol 2,3-Dioxygenase</topic><topic>Colon - metabolism</topic><topic>Colon - microbiology</topic><topic>Dioxygenases</topic><topic>Energy</topic><topic>Energy Metabolism</topic><topic>Energy sources</topic><topic>Fermentation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastric Mucosa - metabolism</topic><topic>Gastric Mucosa - microbiology</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genes</topic><topic>Genes, Reporter</topic><topic>Helicobacter pylori</topic><topic>Helicobacter pylori - growth & development</topic><topic>Helicobacter pylori - metabolism</topic><topic>Hydrogen</topic><topic>Hydrogen - metabolism</topic><topic>Hydrogenase - genetics</topic><topic>Hydrogenase - metabolism</topic><topic>Kinetics</topic><topic>Land Settlement</topic><topic>Mice</topic><topic>Microbial colonization</topic><topic>Microbiology</topic><topic>Mutation</topic><topic>Oxidation</topic><topic>Oxidation-Reduction</topic><topic>Oxygenases - genetics</topic><topic>Oxygenases - metabolism</topic><topic>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</topic><topic>Pathogens</topic><topic>Plasmids</topic><topic>Stomach</topic><topic>Transcription, 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J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Hydrogen as an Energy Source for Helicobacter pylori</atitle><jtitle>Science (American Association for the Advancement of Science)</jtitle><addtitle>Science</addtitle><date>2002-11-29</date><risdate>2002</risdate><volume>298</volume><issue>5599</issue><spage>1788</spage><epage>1790</epage><pages>1788-1790</pages><issn>0036-8075</issn><eissn>1095-9203</eissn><coden>SCIEAS</coden><abstract>The gastric pathogen Helicobacter pylori is known to be able to use molecular hydrogen as a respiratory substrate when grown in the laboratory. We found that hydrogen is available in the gastric mucosa of mice and that its use greatly increased the stomach colonization by H. pylori. Hydrogenase activity in H. pylori is constitutive but increased fivefold upon incubation with hydrogen. Hydrogen concentrations measured in the stomachs of live mice were found to be 10 to 50 times as high as the H. pylori affinity for hydrogen. A hydrogenase mutant strain is much less efficient in its colonization of mice. Therefore, hydrogen present in animals as a consequence of normal colonic flora is an energy-yielding substrate that can facilitate the maintenance of a pathogenic bacterium.</abstract><cop>Washington, DC</cop><pub>American Association for the Advancement of Science</pub><pmid>12459589</pmid><doi>10.1126/science.1077123</doi><tpages>3</tpages></addata></record> |
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subjects | Animals Bacteria Bacteriology Biological and medical sciences Catechol 2,3-Dioxygenase Colon - metabolism Colon - microbiology Dioxygenases Energy Energy Metabolism Energy sources Fermentation Fundamental and applied biological sciences. Psychology Gastric Mucosa - metabolism Gastric Mucosa - microbiology Gene Expression Regulation, Bacterial Genes Genes, Reporter Helicobacter pylori Helicobacter pylori - growth & development Helicobacter pylori - metabolism Hydrogen Hydrogen - metabolism Hydrogenase - genetics Hydrogenase - metabolism Kinetics Land Settlement Mice Microbial colonization Microbiology Mutation Oxidation Oxidation-Reduction Oxygenases - genetics Oxygenases - metabolism Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains Pathogens Plasmids Stomach Transcription, Genetic |
title | Molecular Hydrogen as an Energy Source for Helicobacter pylori |
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