Investigating unsaturated fat, monensin, or bromoethanesulfonate in continuous cultures retaining ruminal protozoa. II. Interaction of treatment and presence of protozoa on prokaryotic communities
Increasing the consistency of responses to reduce emissions of ruminal methane and nitrogenous wastes into the environment using microbial inhibitors requires an accurate assessment of microbial community profiles. In addition to direct inhibition of methanogens by feed additives, protozoa are often...
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description | Increasing the consistency of responses to reduce emissions of ruminal methane and nitrogenous wastes into the environment using microbial inhibitors requires an accurate assessment of microbial community profiles. In addition to direct inhibition of methanogens by feed additives, protozoa are often targeted for inhibition because their close physical association with endo- and ectosymbionts stimulates methanogenesis in the rumen. In this study, we first modified a continuous culture system to maintain a diverse protozoal population (faunated subperiod) and then selectively effluxed them without using any chemical agents (defaunated subperiod). In both subperiods, unsaturated fat (potentially inhibitory to ciliate protozoa, methanogens, and gram-positive bacteria), monensin (assumed to inhibit gram-positive bacteria), and bromoethanesulfonate (BES; a potent inhibitor of methanogens) were used to suppress the respective functional groups of microorganisms. Changes in microbial populations were determined using denaturing gradient gel electrophoresis, followed by cloning and DNA sequencing of the excised bands . Neither monensin nor unsaturated fat consistently affected methanogen populations under our conditions in either the faunated or defaunated subperiods. When BES was administered, bands presumptively linked to protozoa-associated methanogens in the faunated subperiod disappeared in the defaunated subperiod. However, there was no noticeable adaptation of the sensitive methanogens to BES. The effect of dietary treatments on bacterial populations in the fermenters was harder to ascertain because of the overriding period effect caused by a different inoculum in each period. Defaunation selectively decreased the intensity of bands associated with ruminococci and clostridia but seemed to increase some Butyrivibrio and related populations. Presence of protozoa influenced both bacterial and archaeal populations, probably by selective predation, competition for substrate, or through symbiotic interactions. |
doi_str_mv | 10.3168/jds.2008-1437 |
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II. Interaction of treatment and presence of protozoa on prokaryotic communities</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Karnati, S.K.R ; Yu, Z ; Firkins, J.L</creator><creatorcontrib>Karnati, S.K.R ; Yu, Z ; Firkins, J.L</creatorcontrib><description>Increasing the consistency of responses to reduce emissions of ruminal methane and nitrogenous wastes into the environment using microbial inhibitors requires an accurate assessment of microbial community profiles. In addition to direct inhibition of methanogens by feed additives, protozoa are often targeted for inhibition because their close physical association with endo- and ectosymbionts stimulates methanogenesis in the rumen. In this study, we first modified a continuous culture system to maintain a diverse protozoal population (faunated subperiod) and then selectively effluxed them without using any chemical agents (defaunated subperiod). In both subperiods, unsaturated fat (potentially inhibitory to ciliate protozoa, methanogens, and gram-positive bacteria), monensin (assumed to inhibit gram-positive bacteria), and bromoethanesulfonate (BES; a potent inhibitor of methanogens) were used to suppress the respective functional groups of microorganisms. Changes in microbial populations were determined using denaturing gradient gel electrophoresis, followed by cloning and DNA sequencing of the excised bands . Neither monensin nor unsaturated fat consistently affected methanogen populations under our conditions in either the faunated or defaunated subperiods. When BES was administered, bands presumptively linked to protozoa-associated methanogens in the faunated subperiod disappeared in the defaunated subperiod. However, there was no noticeable adaptation of the sensitive methanogens to BES. The effect of dietary treatments on bacterial populations in the fermenters was harder to ascertain because of the overriding period effect caused by a different inoculum in each period. Defaunation selectively decreased the intensity of bands associated with ruminococci and clostridia but seemed to increase some Butyrivibrio and related populations. Presence of protozoa influenced both bacterial and archaeal populations, probably by selective predation, competition for substrate, or through symbiotic interactions.</description><identifier>ISSN: 0022-0302</identifier><identifier>EISSN: 1525-3198</identifier><identifier>DOI: 10.3168/jds.2008-1437</identifier><identifier>PMID: 19620670</identifier><language>eng</language><publisher>United States: American Dairy Science Association</publisher><subject>adaptation ; Alkanesulfonates - pharmacology ; Ammonia - analysis ; Animals ; Anti-Infective Agents - pharmacology ; Antiprotozoal Agents - pharmacology ; Bacteria - classification ; Bacteria - drug effects ; Bacteria - metabolism ; bromoethanesulfonate ; Cattle ; continuous systems ; Dietary Fats, Unsaturated - metabolism ; Eukaryota - drug effects ; Eukaryota - metabolism ; Eukaryota - physiology ; Fatty Acids, Volatile - analysis ; Female ; functional diversity ; Gastrointestinal Contents - chemistry ; Gastrointestinal Contents - microbiology ; Gram-positive bacteria ; Hydrocarbons, Brominated - pharmacology ; in vitro studies ; Methane - metabolism ; methane production ; methanogens ; microbial activity ; microbial competition ; microbial ecology ; microbial genetics ; molecular sequence data ; monensin ; Monensin - pharmacology ; Nitrogen - analysis ; Nitrogen - metabolism ; nucleotide sequences ; Phylogeny ; population dynamics ; predation ; Rumen - metabolism ; Rumen - parasitology ; rumen fluids ; rumen microorganisms ; rumen protozoa ; species diversity ; unsaturated fatty acids</subject><ispartof>Journal of dairy science, 2009-08, Vol.92 (8), p.3861-3873</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-840b634f1d47cece912b1524482f1bcf3b0c5e4465aa26bb77e65df9d571bbe63</citedby><cites>FETCH-LOGICAL-c385t-840b634f1d47cece912b1524482f1bcf3b0c5e4465aa26bb77e65df9d571bbe63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19620670$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karnati, S.K.R</creatorcontrib><creatorcontrib>Yu, Z</creatorcontrib><creatorcontrib>Firkins, J.L</creatorcontrib><title>Investigating unsaturated fat, monensin, or bromoethanesulfonate in continuous cultures retaining ruminal protozoa. II. Interaction of treatment and presence of protozoa on prokaryotic communities</title><title>Journal of dairy science</title><addtitle>J Dairy Sci</addtitle><description>Increasing the consistency of responses to reduce emissions of ruminal methane and nitrogenous wastes into the environment using microbial inhibitors requires an accurate assessment of microbial community profiles. In addition to direct inhibition of methanogens by feed additives, protozoa are often targeted for inhibition because their close physical association with endo- and ectosymbionts stimulates methanogenesis in the rumen. In this study, we first modified a continuous culture system to maintain a diverse protozoal population (faunated subperiod) and then selectively effluxed them without using any chemical agents (defaunated subperiod). In both subperiods, unsaturated fat (potentially inhibitory to ciliate protozoa, methanogens, and gram-positive bacteria), monensin (assumed to inhibit gram-positive bacteria), and bromoethanesulfonate (BES; a potent inhibitor of methanogens) were used to suppress the respective functional groups of microorganisms. Changes in microbial populations were determined using denaturing gradient gel electrophoresis, followed by cloning and DNA sequencing of the excised bands . Neither monensin nor unsaturated fat consistently affected methanogen populations under our conditions in either the faunated or defaunated subperiods. When BES was administered, bands presumptively linked to protozoa-associated methanogens in the faunated subperiod disappeared in the defaunated subperiod. However, there was no noticeable adaptation of the sensitive methanogens to BES. The effect of dietary treatments on bacterial populations in the fermenters was harder to ascertain because of the overriding period effect caused by a different inoculum in each period. Defaunation selectively decreased the intensity of bands associated with ruminococci and clostridia but seemed to increase some Butyrivibrio and related populations. Presence of protozoa influenced both bacterial and archaeal populations, probably by selective predation, competition for substrate, or through symbiotic interactions.</description><subject>adaptation</subject><subject>Alkanesulfonates - pharmacology</subject><subject>Ammonia - analysis</subject><subject>Animals</subject><subject>Anti-Infective Agents - pharmacology</subject><subject>Antiprotozoal Agents - pharmacology</subject><subject>Bacteria - classification</subject><subject>Bacteria - drug effects</subject><subject>Bacteria - metabolism</subject><subject>bromoethanesulfonate</subject><subject>Cattle</subject><subject>continuous systems</subject><subject>Dietary Fats, Unsaturated - metabolism</subject><subject>Eukaryota - drug effects</subject><subject>Eukaryota - metabolism</subject><subject>Eukaryota - physiology</subject><subject>Fatty Acids, Volatile - analysis</subject><subject>Female</subject><subject>functional diversity</subject><subject>Gastrointestinal Contents - chemistry</subject><subject>Gastrointestinal Contents - microbiology</subject><subject>Gram-positive bacteria</subject><subject>Hydrocarbons, Brominated - pharmacology</subject><subject>in vitro studies</subject><subject>Methane - metabolism</subject><subject>methane production</subject><subject>methanogens</subject><subject>microbial activity</subject><subject>microbial competition</subject><subject>microbial ecology</subject><subject>microbial genetics</subject><subject>molecular sequence data</subject><subject>monensin</subject><subject>Monensin - pharmacology</subject><subject>Nitrogen - analysis</subject><subject>Nitrogen - metabolism</subject><subject>nucleotide sequences</subject><subject>Phylogeny</subject><subject>population dynamics</subject><subject>predation</subject><subject>Rumen - metabolism</subject><subject>Rumen - parasitology</subject><subject>rumen fluids</subject><subject>rumen microorganisms</subject><subject>rumen protozoa</subject><subject>species diversity</subject><subject>unsaturated fatty acids</subject><issn>0022-0302</issn><issn>1525-3198</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkUtv1DAUhS0EokNhyRa8YtUMfsSOs0QV0JEqsWi7thznZsYlsYsfreD38cNwNIO6sGzL3z33-hyE3lOy5VSqz_dj2jJCVENb3r1AGyqYaDjt1Uu0IYSxhnDCztCblO7rlTIiXqMz2ktGZEc26O_OP0LKbm-y83tcfDK5RJNhxJPJF3gJHnxy_gKHiIcYlgD5YDykMk_BVw47j23wtbqEkrAtc62HhCNk4_yqGcvivJnxQww5_Almi3e7unyGaGx2weMw4RzB5AV8xsaPFYUE3sL68r8MV7Cef5r4O2Rna9NlKd5lB-ktejWZOcG7036O7r59vb28aq5_fN9dfrluLFciN6olg-TtRMe2s2Chp2yodrWtYhMd7MQHYgW0rRTGMDkMXQdSjFM_io4OA0h-jj4ddescv0q1TS8uWZjnakj9vJadIJ1ifQWbI2hjSCnCpB-iW-rkmhK9xqZrbHqNTa-xVf7DSbgMC4zP9Cmn584Htz88uQg6LWaeK05XqZ5ppbmStIIfj-Bkgjb76JK-u2GEckKlUJwo_g_QNrDZ</recordid><startdate>20090801</startdate><enddate>20090801</enddate><creator>Karnati, S.K.R</creator><creator>Yu, Z</creator><creator>Firkins, J.L</creator><general>American Dairy Science Association</general><general>Am Dairy Sci Assoc</general><scope>FBQ</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>7X8</scope></search><sort><creationdate>20090801</creationdate><title>Investigating unsaturated fat, monensin, or bromoethanesulfonate in continuous cultures retaining ruminal protozoa. II. Interaction of treatment and presence of protozoa on prokaryotic communities</title><author>Karnati, S.K.R ; Yu, Z ; Firkins, J.L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-840b634f1d47cece912b1524482f1bcf3b0c5e4465aa26bb77e65df9d571bbe63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>adaptation</topic><topic>Alkanesulfonates - pharmacology</topic><topic>Ammonia - analysis</topic><topic>Animals</topic><topic>Anti-Infective Agents - pharmacology</topic><topic>Antiprotozoal Agents - pharmacology</topic><topic>Bacteria - classification</topic><topic>Bacteria - drug effects</topic><topic>Bacteria - metabolism</topic><topic>bromoethanesulfonate</topic><topic>Cattle</topic><topic>continuous systems</topic><topic>Dietary Fats, Unsaturated - metabolism</topic><topic>Eukaryota - drug effects</topic><topic>Eukaryota - metabolism</topic><topic>Eukaryota - physiology</topic><topic>Fatty Acids, Volatile - analysis</topic><topic>Female</topic><topic>functional diversity</topic><topic>Gastrointestinal Contents - chemistry</topic><topic>Gastrointestinal Contents - microbiology</topic><topic>Gram-positive bacteria</topic><topic>Hydrocarbons, Brominated - pharmacology</topic><topic>in vitro studies</topic><topic>Methane - metabolism</topic><topic>methane production</topic><topic>methanogens</topic><topic>microbial activity</topic><topic>microbial competition</topic><topic>microbial ecology</topic><topic>microbial genetics</topic><topic>molecular sequence data</topic><topic>monensin</topic><topic>Monensin - pharmacology</topic><topic>Nitrogen - analysis</topic><topic>Nitrogen - metabolism</topic><topic>nucleotide sequences</topic><topic>Phylogeny</topic><topic>population dynamics</topic><topic>predation</topic><topic>Rumen - metabolism</topic><topic>Rumen - parasitology</topic><topic>rumen fluids</topic><topic>rumen microorganisms</topic><topic>rumen protozoa</topic><topic>species diversity</topic><topic>unsaturated fatty acids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karnati, S.K.R</creatorcontrib><creatorcontrib>Yu, Z</creatorcontrib><creatorcontrib>Firkins, J.L</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of dairy science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karnati, S.K.R</au><au>Yu, Z</au><au>Firkins, J.L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigating unsaturated fat, monensin, or bromoethanesulfonate in continuous cultures retaining ruminal protozoa. II. Interaction of treatment and presence of protozoa on prokaryotic communities</atitle><jtitle>Journal of dairy science</jtitle><addtitle>J Dairy Sci</addtitle><date>2009-08-01</date><risdate>2009</risdate><volume>92</volume><issue>8</issue><spage>3861</spage><epage>3873</epage><pages>3861-3873</pages><issn>0022-0302</issn><eissn>1525-3198</eissn><abstract>Increasing the consistency of responses to reduce emissions of ruminal methane and nitrogenous wastes into the environment using microbial inhibitors requires an accurate assessment of microbial community profiles. In addition to direct inhibition of methanogens by feed additives, protozoa are often targeted for inhibition because their close physical association with endo- and ectosymbionts stimulates methanogenesis in the rumen. In this study, we first modified a continuous culture system to maintain a diverse protozoal population (faunated subperiod) and then selectively effluxed them without using any chemical agents (defaunated subperiod). In both subperiods, unsaturated fat (potentially inhibitory to ciliate protozoa, methanogens, and gram-positive bacteria), monensin (assumed to inhibit gram-positive bacteria), and bromoethanesulfonate (BES; a potent inhibitor of methanogens) were used to suppress the respective functional groups of microorganisms. Changes in microbial populations were determined using denaturing gradient gel electrophoresis, followed by cloning and DNA sequencing of the excised bands . Neither monensin nor unsaturated fat consistently affected methanogen populations under our conditions in either the faunated or defaunated subperiods. When BES was administered, bands presumptively linked to protozoa-associated methanogens in the faunated subperiod disappeared in the defaunated subperiod. However, there was no noticeable adaptation of the sensitive methanogens to BES. The effect of dietary treatments on bacterial populations in the fermenters was harder to ascertain because of the overriding period effect caused by a different inoculum in each period. Defaunation selectively decreased the intensity of bands associated with ruminococci and clostridia but seemed to increase some Butyrivibrio and related populations. Presence of protozoa influenced both bacterial and archaeal populations, probably by selective predation, competition for substrate, or through symbiotic interactions.</abstract><cop>United States</cop><pub>American Dairy Science Association</pub><pmid>19620670</pmid><doi>10.3168/jds.2008-1437</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | adaptation Alkanesulfonates - pharmacology Ammonia - analysis Animals Anti-Infective Agents - pharmacology Antiprotozoal Agents - pharmacology Bacteria - classification Bacteria - drug effects Bacteria - metabolism bromoethanesulfonate Cattle continuous systems Dietary Fats, Unsaturated - metabolism Eukaryota - drug effects Eukaryota - metabolism Eukaryota - physiology Fatty Acids, Volatile - analysis Female functional diversity Gastrointestinal Contents - chemistry Gastrointestinal Contents - microbiology Gram-positive bacteria Hydrocarbons, Brominated - pharmacology in vitro studies Methane - metabolism methane production methanogens microbial activity microbial competition microbial ecology microbial genetics molecular sequence data monensin Monensin - pharmacology Nitrogen - analysis Nitrogen - metabolism nucleotide sequences Phylogeny population dynamics predation Rumen - metabolism Rumen - parasitology rumen fluids rumen microorganisms rumen protozoa species diversity unsaturated fatty acids |
title | Investigating unsaturated fat, monensin, or bromoethanesulfonate in continuous cultures retaining ruminal protozoa. II. Interaction of treatment and presence of protozoa on prokaryotic communities |
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