Enterotoxigenic Escherichia coli Secretes Active Heat-labile Enterotoxin via Outer Membrane Vesicles
Escherichia coli and other Gram-negative bacteria produce outer membrane vesicles during normal growth. Vesicles may contribute to bacterial pathogenicity by serving as vehicles for toxins to encounter host cells. EnterotoxigenicE. coli (ETEC) vesicles were isolated from culture supernatants and pur...
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Veröffentlicht in: | The Journal of biological chemistry 2000-04, Vol.275 (17), p.12489-12496 |
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description | Escherichia coli and other Gram-negative bacteria produce outer membrane vesicles during normal growth. Vesicles may contribute to bacterial pathogenicity by serving as vehicles for toxins to encounter host cells. EnterotoxigenicE. coli (ETEC) vesicles were isolated from culture supernatants and purified on velocity gradients, thereby removing any soluble proteins and contaminants from the crude preparation. Vesicle protein profiles were similar but not identical to outer membranes and differed between strains. Most vesicle proteins were resistant to dissociation, suggesting they were integral or internal. Thin layer chromatography revealed that major outer membrane lipid components are present in vesicles. Cytoplasmic membranes and cytosol were absent in vesicles; however, alkaline phosphatase and AcrA, periplasmic residents, were localized to vesicles. In addition, physiologically active heat-labile enterotoxin (LT) was associated with ETEC vesicles. LT activity correlated directly with the gradient peak of vesicles, suggesting specific association, but could be removed from vesicles under dissociating conditions. Further analysis revealed that LT is enriched in vesicles and is located both inside and on the exterior of vesicles. The distinct protein composition of ETEC vesicles and their ability to carry toxin may contribute to the pathogenicity of ETEC strains. |
doi_str_mv | 10.1074/jbc.275.17.12489 |
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Vesicles may contribute to bacterial pathogenicity by serving as vehicles for toxins to encounter host cells. EnterotoxigenicE. coli (ETEC) vesicles were isolated from culture supernatants and purified on velocity gradients, thereby removing any soluble proteins and contaminants from the crude preparation. Vesicle protein profiles were similar but not identical to outer membranes and differed between strains. Most vesicle proteins were resistant to dissociation, suggesting they were integral or internal. Thin layer chromatography revealed that major outer membrane lipid components are present in vesicles. Cytoplasmic membranes and cytosol were absent in vesicles; however, alkaline phosphatase and AcrA, periplasmic residents, were localized to vesicles. In addition, physiologically active heat-labile enterotoxin (LT) was associated with ETEC vesicles. LT activity correlated directly with the gradient peak of vesicles, suggesting specific association, but could be removed from vesicles under dissociating conditions. Further analysis revealed that LT is enriched in vesicles and is located both inside and on the exterior of vesicles. The distinct protein composition of ETEC vesicles and their ability to carry toxin may contribute to the pathogenicity of ETEC strains.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.275.17.12489</identifier><identifier>PMID: 10777535</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alkaline Phosphatase - metabolism ; Bacterial Toxins - biosynthesis ; Cell Fractionation ; Cell Membrane - metabolism ; Chromatography, Affinity ; Chromatography, Thin Layer ; Endopeptidases - metabolism ; Enterotoxins - biosynthesis ; Enzyme-Linked Immunosorbent Assay ; Escherichia coli ; Escherichia coli - metabolism ; Escherichia coli Proteins ; Microscopy, Electron ; Temperature</subject><ispartof>The Journal of biological chemistry, 2000-04, Vol.275 (17), p.12489-12496</ispartof><rights>2000 © 2000 ASBMB. 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Vesicles may contribute to bacterial pathogenicity by serving as vehicles for toxins to encounter host cells. EnterotoxigenicE. coli (ETEC) vesicles were isolated from culture supernatants and purified on velocity gradients, thereby removing any soluble proteins and contaminants from the crude preparation. Vesicle protein profiles were similar but not identical to outer membranes and differed between strains. Most vesicle proteins were resistant to dissociation, suggesting they were integral or internal. Thin layer chromatography revealed that major outer membrane lipid components are present in vesicles. Cytoplasmic membranes and cytosol were absent in vesicles; however, alkaline phosphatase and AcrA, periplasmic residents, were localized to vesicles. In addition, physiologically active heat-labile enterotoxin (LT) was associated with ETEC vesicles. LT activity correlated directly with the gradient peak of vesicles, suggesting specific association, but could be removed from vesicles under dissociating conditions. Further analysis revealed that LT is enriched in vesicles and is located both inside and on the exterior of vesicles. The distinct protein composition of ETEC vesicles and their ability to carry toxin may contribute to the pathogenicity of ETEC strains.</description><subject>Alkaline Phosphatase - metabolism</subject><subject>Bacterial Toxins - biosynthesis</subject><subject>Cell Fractionation</subject><subject>Cell Membrane - metabolism</subject><subject>Chromatography, Affinity</subject><subject>Chromatography, Thin Layer</subject><subject>Endopeptidases - metabolism</subject><subject>Enterotoxins - biosynthesis</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Escherichia coli</subject><subject>Escherichia coli - metabolism</subject><subject>Escherichia coli Proteins</subject><subject>Microscopy, Electron</subject><subject>Temperature</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1v1DAQxS0EotvCnRPKAXHLYsdxHHNAqqotRSrqgQ9xs-zx7MZVEhfbu8B_jyEVFCSELyNr3u9pZh4hTxhdMyrbF9cW1o0UaybXrGl7dY-sGO15zQX7dJ-sKG1YrRrRH5HjlK5pea1iD8lRgaUUXKyI28wZY8jhq9_h7KHaJBgwehi8qSCMvnqHEDFjqk4h-wNWF2hyPRrrR6x-w3N1KMDVvvyrtzjZaGasPmLyMGJ6RB5szZjw8W09IR_ON-_PLurLq9dvzk4va-hYl2sDjClpjHJKSNU01jrWS-6k2nKnmHKuAyUUhW1ve-OMMNZICW3bAVe2FfyEvFp8b_Z2Qgc452hGfRP9ZOI3HYzXf3ZmP-hdOOiWt7LnbTF4fmsQw-c9pqwnnwDHsWwT9klLRjvJy4X_J2SyY1wIVoR0EUIMKUXc_pqGUf0jQ10y1CXDguifGRbk6d0t7gBLaEXwbBEMfjd88RG19aGkNv3t83KRYTn5wWPUCTzOgK4gkLUL_t9DfAfCQboE</recordid><startdate>20000428</startdate><enddate>20000428</enddate><creator>Horstman, Amanda L.</creator><creator>Kuehn, Meta J.</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</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>7QL</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20000428</creationdate><title>Enterotoxigenic Escherichia coli Secretes Active Heat-labile Enterotoxin via Outer Membrane Vesicles</title><author>Horstman, Amanda L. ; Kuehn, Meta J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c616t-ac1197aa9d957922bbd1873d79f3d919dd6c9590cf8b8ada5aba77c446c39b453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Alkaline Phosphatase - metabolism</topic><topic>Bacterial Toxins - biosynthesis</topic><topic>Cell Fractionation</topic><topic>Cell Membrane - metabolism</topic><topic>Chromatography, Affinity</topic><topic>Chromatography, Thin Layer</topic><topic>Endopeptidases - metabolism</topic><topic>Enterotoxins - biosynthesis</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Escherichia coli</topic><topic>Escherichia coli - metabolism</topic><topic>Escherichia coli Proteins</topic><topic>Microscopy, Electron</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Horstman, Amanda L.</creatorcontrib><creatorcontrib>Kuehn, Meta J.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Horstman, Amanda L.</au><au>Kuehn, Meta J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enterotoxigenic Escherichia coli Secretes Active Heat-labile Enterotoxin via Outer Membrane Vesicles</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2000-04-28</date><risdate>2000</risdate><volume>275</volume><issue>17</issue><spage>12489</spage><epage>12496</epage><pages>12489-12496</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Escherichia coli and other Gram-negative bacteria produce outer membrane vesicles during normal growth. Vesicles may contribute to bacterial pathogenicity by serving as vehicles for toxins to encounter host cells. EnterotoxigenicE. coli (ETEC) vesicles were isolated from culture supernatants and purified on velocity gradients, thereby removing any soluble proteins and contaminants from the crude preparation. Vesicle protein profiles were similar but not identical to outer membranes and differed between strains. Most vesicle proteins were resistant to dissociation, suggesting they were integral or internal. Thin layer chromatography revealed that major outer membrane lipid components are present in vesicles. Cytoplasmic membranes and cytosol were absent in vesicles; however, alkaline phosphatase and AcrA, periplasmic residents, were localized to vesicles. In addition, physiologically active heat-labile enterotoxin (LT) was associated with ETEC vesicles. LT activity correlated directly with the gradient peak of vesicles, suggesting specific association, but could be removed from vesicles under dissociating conditions. Further analysis revealed that LT is enriched in vesicles and is located both inside and on the exterior of vesicles. The distinct protein composition of ETEC vesicles and their ability to carry toxin may contribute to the pathogenicity of ETEC strains.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>10777535</pmid><doi>10.1074/jbc.275.17.12489</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alkaline Phosphatase - metabolism Bacterial Toxins - biosynthesis Cell Fractionation Cell Membrane - metabolism Chromatography, Affinity Chromatography, Thin Layer Endopeptidases - metabolism Enterotoxins - biosynthesis Enzyme-Linked Immunosorbent Assay Escherichia coli Escherichia coli - metabolism Escherichia coli Proteins Microscopy, Electron Temperature |
title | Enterotoxigenic Escherichia coli Secretes Active Heat-labile Enterotoxin via Outer Membrane Vesicles |
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