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Implications of the expression of Enterococcus faecalis citrate fermentation genes during infection
Citrate is an ubiquitous compound in nature. However, citrate fermentation is present only in a few pathogenic or nonpathogenic microorganisms. The citrate fermentation pathway includes a citrate transporter, a citrate lyase complex, an oxaloacetate decarboxylase and a regulatory system. Enterococcu...
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Published in: | PloS one 2018-10, Vol.13 (10), p.e0205787-e0205787 |
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description | Citrate is an ubiquitous compound in nature. However, citrate fermentation is present only in a few pathogenic or nonpathogenic microorganisms. The citrate fermentation pathway includes a citrate transporter, a citrate lyase complex, an oxaloacetate decarboxylase and a regulatory system. Enterococcus faecalis is commonly present in the gastro-intestinal microbiota of warm-blooded animals and insect guts. These bacteria can also cause infection and disease in immunocompromised individuals. In the present study, we performed whole genome analysis in Enterococcus strains finding that the complete citrate pathway is present in all of the E. faecalis strains isolated from such diverse habitats as animals, hospitals, water, milk, plants, insects, cheese, etc. These results indicate the importance of this metabolic preservation for persistence and growth of E. faecalis in different niches. We also analyzed the role of citrate metabolism in the E. faecalis pathogenicity. We found that an E. faecalis citrate fermentation-deficient strain was less pathogenic for Galleria mellonella larvae than the wild type. Furthermore, strains with deletions in the oxaloacetate decarboxylase subunits or in the α-acetolactate synthase resulted also less virulent than the wild type strain. We also observed that citrate promoters are induced in blood, urine and also in the hemolymph of G. mellonella. In addition, we showed that citrate fermentation allows E. faecalis to grow better in blood, urine and G. mellonella. The results presented here clearly indicate that citrate fermentation plays an important role in E. faecalis opportunistic pathogenic behavior. |
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However, citrate fermentation is present only in a few pathogenic or nonpathogenic microorganisms. The citrate fermentation pathway includes a citrate transporter, a citrate lyase complex, an oxaloacetate decarboxylase and a regulatory system. Enterococcus faecalis is commonly present in the gastro-intestinal microbiota of warm-blooded animals and insect guts. These bacteria can also cause infection and disease in immunocompromised individuals. In the present study, we performed whole genome analysis in Enterococcus strains finding that the complete citrate pathway is present in all of the E. faecalis strains isolated from such diverse habitats as animals, hospitals, water, milk, plants, insects, cheese, etc. These results indicate the importance of this metabolic preservation for persistence and growth of E. faecalis in different niches. We also analyzed the role of citrate metabolism in the E. faecalis pathogenicity. We found that an E. faecalis citrate fermentation-deficient strain was less pathogenic for Galleria mellonella larvae than the wild type. Furthermore, strains with deletions in the oxaloacetate decarboxylase subunits or in the α-acetolactate synthase resulted also less virulent than the wild type strain. We also observed that citrate promoters are induced in blood, urine and also in the hemolymph of G. mellonella. In addition, we showed that citrate fermentation allows E. faecalis to grow better in blood, urine and G. mellonella. The results presented here clearly indicate that citrate fermentation plays an important role in E. faecalis opportunistic pathogenic behavior.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0205787</identifier><identifier>PMID: 30335810</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acetolactate synthase ; Animals ; Bacteria ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biology and Life Sciences ; Blood ; Carboxy-Lyases - genetics ; Carboxy-Lyases - metabolism ; Care and treatment ; Carrier Proteins - genetics ; Carrier Proteins - metabolism ; Cheese ; Chemical properties ; Citric acid ; Citric Acid - metabolism ; Dairy products ; Dehydrogenases ; Disease Models, Animal ; Enterococcal infections ; Enterococcus faecalis ; Enterococcus faecalis - genetics ; Enterococcus faecalis - immunology ; Enterococcus faecalis - metabolism ; Enterococcus faecalis - pathogenicity ; Enzymes ; Fermentation ; Fermentation - genetics ; Fermentation - immunology ; Food ; Gene expression ; Gene Expression Regulation, Bacterial ; Genes ; Genetic aspects ; Genome, Bacterial - genetics ; Genomes ; Gram-Positive Bacterial Infections - immunology ; Gram-Positive Bacterial Infections - microbiology ; Hemolymph ; Homeotherms ; Humans ; Infections ; Insects ; Intestinal microflora ; Intestine ; Larvae ; Medicine and Health Sciences ; Metabolic Networks and Pathways - genetics ; Metabolism ; Microbiota ; Microorganisms ; Moths - immunology ; Moths - microbiology ; Multigene Family - genetics ; Opportunistic Infections - immunology ; Opportunistic Infections - microbiology ; Otolaryngology ; Oxaloacetate decarboxylase ; Pathogenicity ; Pathogens ; Physical Sciences ; Preservation ; Promoter Regions, Genetic - genetics ; Research and analysis methods ; Signal transduction ; Strains (organisms) ; Urine ; Whole Genome Sequencing</subject><ispartof>PloS one, 2018-10, Vol.13 (10), p.e0205787-e0205787</ispartof><rights>COPYRIGHT 2018 Public Library of Science</rights><rights>2018 Martino et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2018 Martino et al 2018 Martino et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-f539f049667aacebbfd05322693bce42b00ce34073a22b53ef7a6aac5595c2293</citedby><cites>FETCH-LOGICAL-c692t-f539f049667aacebbfd05322693bce42b00ce34073a22b53ef7a6aac5595c2293</cites><orcidid>0000-0003-3945-2859 ; 0000-0003-0508-260X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2122527753/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2122527753?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30335810$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Chaves, Alex V.</contributor><creatorcontrib>Martino, Gabriela P</creatorcontrib><creatorcontrib>Perez, Cristian E</creatorcontrib><creatorcontrib>Magni, Christian</creatorcontrib><creatorcontrib>Blancato, Víctor S</creatorcontrib><title>Implications of the expression of Enterococcus faecalis citrate fermentation genes during infection</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Citrate is an ubiquitous compound in nature. However, citrate fermentation is present only in a few pathogenic or nonpathogenic microorganisms. The citrate fermentation pathway includes a citrate transporter, a citrate lyase complex, an oxaloacetate decarboxylase and a regulatory system. Enterococcus faecalis is commonly present in the gastro-intestinal microbiota of warm-blooded animals and insect guts. These bacteria can also cause infection and disease in immunocompromised individuals. In the present study, we performed whole genome analysis in Enterococcus strains finding that the complete citrate pathway is present in all of the E. faecalis strains isolated from such diverse habitats as animals, hospitals, water, milk, plants, insects, cheese, etc. These results indicate the importance of this metabolic preservation for persistence and growth of E. faecalis in different niches. We also analyzed the role of citrate metabolism in the E. faecalis pathogenicity. 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immunology</subject><subject>Enterococcus faecalis - metabolism</subject><subject>Enterococcus faecalis - pathogenicity</subject><subject>Enzymes</subject><subject>Fermentation</subject><subject>Fermentation - genetics</subject><subject>Fermentation - immunology</subject><subject>Food</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genome, Bacterial - genetics</subject><subject>Genomes</subject><subject>Gram-Positive Bacterial Infections - immunology</subject><subject>Gram-Positive Bacterial Infections - microbiology</subject><subject>Hemolymph</subject><subject>Homeotherms</subject><subject>Humans</subject><subject>Infections</subject><subject>Insects</subject><subject>Intestinal microflora</subject><subject>Intestine</subject><subject>Larvae</subject><subject>Medicine and Health Sciences</subject><subject>Metabolic Networks and Pathways - genetics</subject><subject>Metabolism</subject><subject>Microbiota</subject><subject>Microorganisms</subject><subject>Moths - immunology</subject><subject>Moths - microbiology</subject><subject>Multigene Family - genetics</subject><subject>Opportunistic Infections - immunology</subject><subject>Opportunistic Infections - microbiology</subject><subject>Otolaryngology</subject><subject>Oxaloacetate decarboxylase</subject><subject>Pathogenicity</subject><subject>Pathogens</subject><subject>Physical Sciences</subject><subject>Preservation</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Research and analysis methods</subject><subject>Signal transduction</subject><subject>Strains (organisms)</subject><subject>Urine</subject><subject>Whole Genome Sequencing</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk12L1DAUhoso7of-A9GCIHoxY5o0yfRGWJZVBxYW_LoNaXrSyZA2Y5LK-u83nekuU9kLyUXD6XPenLw5J8teFWhZEF583LrB99Iud66HJcKI8hV_kp0WFcELhhF5erQ_yc5C2CJEyYqx59kJQYTQVYFOM7XudtYoGY3rQ-50HjeQw-3OQwgpNEau-gjeKafUEHItQUlrQq5M9DJCrsF30Me9QN5CDyFvBm_6Nje9BjWGX2TPtLQBXk7f8-zn56sfl18X1zdf1pcX1wvFKhwXmpJKo7JijEupoK51kwrGmFWkVlDiGiEFpEScSIxrSkBzyRJJaUUVxhU5z94cdHfWBTH5EwQuMKaYc0oSsT4QjZNbsfOmk_6vcNKIfcD5VkgfjbIgUiVQl7hhuC7LRtcr4BR0USoCWBGkk9an6bSh7qBRyQQv7Ux0_qc3G9G6P4KlZ2F8LOb9JODd7wFCFJ0JCqyVPbhhXzfhuCpKnNC3_6CP326iWpkukOx36Vw1ioqLZBIreLniiVo-QqXVQGdUaiZtUnyW8GGWkJgIt7GVQwhi_f3b_7M3v-bsuyN2A9LGTXB22LfiHCwPoPIuBA_6weQCiXEW7t0Q4yyIaRZS2uvjB3pIum9-cgeFigXa</recordid><startdate>20181018</startdate><enddate>20181018</enddate><creator>Martino, Gabriela P</creator><creator>Perez, Cristian E</creator><creator>Magni, Christian</creator><creator>Blancato, Víctor S</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-3945-2859</orcidid><orcidid>https://orcid.org/0000-0003-0508-260X</orcidid></search><sort><creationdate>20181018</creationdate><title>Implications of the expression of Enterococcus faecalis citrate fermentation genes during infection</title><author>Martino, Gabriela P ; Perez, Cristian E ; Magni, Christian ; Blancato, Víctor S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-f539f049667aacebbfd05322693bce42b00ce34073a22b53ef7a6aac5595c2293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acetolactate synthase</topic><topic>Animals</topic><topic>Bacteria</topic><topic>Bacterial Proteins - 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However, citrate fermentation is present only in a few pathogenic or nonpathogenic microorganisms. The citrate fermentation pathway includes a citrate transporter, a citrate lyase complex, an oxaloacetate decarboxylase and a regulatory system. Enterococcus faecalis is commonly present in the gastro-intestinal microbiota of warm-blooded animals and insect guts. These bacteria can also cause infection and disease in immunocompromised individuals. In the present study, we performed whole genome analysis in Enterococcus strains finding that the complete citrate pathway is present in all of the E. faecalis strains isolated from such diverse habitats as animals, hospitals, water, milk, plants, insects, cheese, etc. These results indicate the importance of this metabolic preservation for persistence and growth of E. faecalis in different niches. We also analyzed the role of citrate metabolism in the E. faecalis pathogenicity. We found that an E. faecalis citrate fermentation-deficient strain was less pathogenic for Galleria mellonella larvae than the wild type. Furthermore, strains with deletions in the oxaloacetate decarboxylase subunits or in the α-acetolactate synthase resulted also less virulent than the wild type strain. We also observed that citrate promoters are induced in blood, urine and also in the hemolymph of G. mellonella. In addition, we showed that citrate fermentation allows E. faecalis to grow better in blood, urine and G. mellonella. The results presented here clearly indicate that citrate fermentation plays an important role in E. faecalis opportunistic pathogenic behavior.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>30335810</pmid><doi>10.1371/journal.pone.0205787</doi><tpages>e0205787</tpages><orcidid>https://orcid.org/0000-0003-3945-2859</orcidid><orcidid>https://orcid.org/0000-0003-0508-260X</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_plos_journals_2122527753 |
source | Open Access: PubMed Central; Publicly Available Content (ProQuest) |
subjects | Acetolactate synthase Animals Bacteria Bacterial Proteins - genetics Bacterial Proteins - metabolism Biology and Life Sciences Blood Carboxy-Lyases - genetics Carboxy-Lyases - metabolism Care and treatment Carrier Proteins - genetics Carrier Proteins - metabolism Cheese Chemical properties Citric acid Citric Acid - metabolism Dairy products Dehydrogenases Disease Models, Animal Enterococcal infections Enterococcus faecalis Enterococcus faecalis - genetics Enterococcus faecalis - immunology Enterococcus faecalis - metabolism Enterococcus faecalis - pathogenicity Enzymes Fermentation Fermentation - genetics Fermentation - immunology Food Gene expression Gene Expression Regulation, Bacterial Genes Genetic aspects Genome, Bacterial - genetics Genomes Gram-Positive Bacterial Infections - immunology Gram-Positive Bacterial Infections - microbiology Hemolymph Homeotherms Humans Infections Insects Intestinal microflora Intestine Larvae Medicine and Health Sciences Metabolic Networks and Pathways - genetics Metabolism Microbiota Microorganisms Moths - immunology Moths - microbiology Multigene Family - genetics Opportunistic Infections - immunology Opportunistic Infections - microbiology Otolaryngology Oxaloacetate decarboxylase Pathogenicity Pathogens Physical Sciences Preservation Promoter Regions, Genetic - genetics Research and analysis methods Signal transduction Strains (organisms) Urine Whole Genome Sequencing |
title | Implications of the expression of Enterococcus faecalis citrate fermentation genes during infection |
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