Supramolecular Recognition of Escherichia coli Bacteria by Fluorescent Oligo(Phenyleneethynylene)s with Mannopyranoside Termini Groups
is one the most common bacteria responsible of uropathogenic diseases, which motives the search for rapid and easy methods of detection. By taking advantage of the specific interactions between mannose and type 1 fimbriae, in this work two fluorescent phenyleneethynylene (PE) trimers bearing one or...
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creator | Arias, Enrique Méndez, Maria Teresa Arias, Eduardo Moggio, Ivana Ledezma, Antonio Romero, Jorge Margheri, Giancarlo Giorgetti, Emilia |
description | is one the most common bacteria responsible of uropathogenic diseases, which motives the search for rapid and easy methods of detection. By taking advantage of the specific interactions between mannose and type 1 fimbriae, in this work two fluorescent phenyleneethynylene (PE) trimers bearing one or two 4-aminophenyl-α-D-mannopyranoside termini groups were synthesized for the detection of
Three bacterial strains: ORN 178 (fimbriae I expression), ORN 208 (mutant serotype with no fimbriae expression) and one obtained from a local hospital (SS3) were used. Laser Scanning Confocal Microscopy (LSCM) and Surface Plasmon Resonance (SPR) were applied for the interaction studies following two different approaches: (1) mixing the oligomer solutions with the bacterial suspension, which permitted the observation of stained bacteria and by (2) biosensing as thin films, where bacteria adhered on the surface-functionalized substrate. LSCM allows one to easily visualize that two mannose groups are necessary to have a specific interaction with the fimbriae 1. The sensitivity of SPR assays to
was 10⁴ colony forming unit (CFU)/mL at 50 µL/min flow rate. The combination of PE units with two mannose groups results in a novel molecule that can be used as a specific fluorescent marker as well as a transducer for the detection of
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doi_str_mv | 10.3390/s17051025 |
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Three bacterial strains: ORN 178 (fimbriae I expression), ORN 208 (mutant serotype with no fimbriae expression) and one obtained from a local hospital (SS3) were used. Laser Scanning Confocal Microscopy (LSCM) and Surface Plasmon Resonance (SPR) were applied for the interaction studies following two different approaches: (1) mixing the oligomer solutions with the bacterial suspension, which permitted the observation of stained bacteria and by (2) biosensing as thin films, where bacteria adhered on the surface-functionalized substrate. LSCM allows one to easily visualize that two mannose groups are necessary to have a specific interaction with the fimbriae 1. The sensitivity of SPR assays to
was 10⁴ colony forming unit (CFU)/mL at 50 µL/min flow rate. The combination of PE units with two mannose groups results in a novel molecule that can be used as a specific fluorescent marker as well as a transducer for the detection of
.</description><identifier>ISSN: 1424-8220</identifier><identifier>EISSN: 1424-8220</identifier><identifier>DOI: 10.3390/s17051025</identifier><identifier>PMID: 28471379</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Alkynes ; Assaying ; Bacteria ; Bacterial Adhesion ; Bearing ; E coli ; Escherichia coli ; Ethers ; Flow velocity ; Fluorescence ; Forming ; Lasers ; Mannose ; Microscopy ; Recognition ; Searching ; Sensitivity ; Thin films</subject><ispartof>Sensors (Basel, Switzerland), 2017-05, Vol.17 (5), p.1025</ispartof><rights>Copyright MDPI AG 2017</rights><rights>2017 by the authors. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c403t-8493a3d5ce0e3b047c961bb4626918439196e99dd81c3e9785dc1310b25458b73</citedby><cites>FETCH-LOGICAL-c403t-8493a3d5ce0e3b047c961bb4626918439196e99dd81c3e9785dc1310b25458b73</cites><orcidid>0000-0002-1633-0923</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469630/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469630/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28471379$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arias, Enrique</creatorcontrib><creatorcontrib>Méndez, Maria Teresa</creatorcontrib><creatorcontrib>Arias, Eduardo</creatorcontrib><creatorcontrib>Moggio, Ivana</creatorcontrib><creatorcontrib>Ledezma, Antonio</creatorcontrib><creatorcontrib>Romero, Jorge</creatorcontrib><creatorcontrib>Margheri, Giancarlo</creatorcontrib><creatorcontrib>Giorgetti, Emilia</creatorcontrib><title>Supramolecular Recognition of Escherichia coli Bacteria by Fluorescent Oligo(Phenyleneethynylene)s with Mannopyranoside Termini Groups</title><title>Sensors (Basel, Switzerland)</title><addtitle>Sensors (Basel)</addtitle><description>is one the most common bacteria responsible of uropathogenic diseases, which motives the search for rapid and easy methods of detection. By taking advantage of the specific interactions between mannose and type 1 fimbriae, in this work two fluorescent phenyleneethynylene (PE) trimers bearing one or two 4-aminophenyl-α-D-mannopyranoside termini groups were synthesized for the detection of
Three bacterial strains: ORN 178 (fimbriae I expression), ORN 208 (mutant serotype with no fimbriae expression) and one obtained from a local hospital (SS3) were used. Laser Scanning Confocal Microscopy (LSCM) and Surface Plasmon Resonance (SPR) were applied for the interaction studies following two different approaches: (1) mixing the oligomer solutions with the bacterial suspension, which permitted the observation of stained bacteria and by (2) biosensing as thin films, where bacteria adhered on the surface-functionalized substrate. LSCM allows one to easily visualize that two mannose groups are necessary to have a specific interaction with the fimbriae 1. The sensitivity of SPR assays to
was 10⁴ colony forming unit (CFU)/mL at 50 µL/min flow rate. The combination of PE units with two mannose groups results in a novel molecule that can be used as a specific fluorescent marker as well as a transducer for the detection of
.</description><subject>Alkynes</subject><subject>Assaying</subject><subject>Bacteria</subject><subject>Bacterial Adhesion</subject><subject>Bearing</subject><subject>E coli</subject><subject>Escherichia coli</subject><subject>Ethers</subject><subject>Flow velocity</subject><subject>Fluorescence</subject><subject>Forming</subject><subject>Lasers</subject><subject>Mannose</subject><subject>Microscopy</subject><subject>Recognition</subject><subject>Searching</subject><subject>Sensitivity</subject><subject>Thin films</subject><issn>1424-8220</issn><issn>1424-8220</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdkcFu1DAQhiNERUvhwAsgS1zaw1KP7ST2BQmqtiC1KoJythxnduPKsYOdgPICfe6m2rJqOc1o5tOvf-YvindAP3Ku6EmGmpZAWfmiOADBxEoyRl8-6feL1znfUso45_JVsc-kqIHX6qC4-zkNyfTRo528SeQH2rgJbnQxkLgmZ9l2mJztnCE2eke-GDsuA0OamZz7KSbMFsNIrr3bxKPvHYbZY0Acu3nbHWfy140duTIhxGFOJsTsWiQ3mHoXHLlIcRrym2JvbXzGt4_1sPh1fnZz-nV1eX3x7fTz5coKyseVFIob3pYWKfKGitqqCppGVKxSIAVXoCpUqm0lWI6qlmVrgQNtWClK2dT8sPi01R2mpsf2wXoyXg_J9SbNOhqnn2-C6_Qm_tGlqFTF6SJw9CiQ4u8J86h7t3zAexMwTlmDVCWrJUhY0A__obdxSmE5T4MCWgEwyhfqeEvZFHNOuN6ZAaof0tW7dBf2_VP3O_JfnPwe8U-hvA</recordid><startdate>20170504</startdate><enddate>20170504</enddate><creator>Arias, Enrique</creator><creator>Méndez, Maria Teresa</creator><creator>Arias, Eduardo</creator><creator>Moggio, Ivana</creator><creator>Ledezma, Antonio</creator><creator>Romero, Jorge</creator><creator>Margheri, Giancarlo</creator><creator>Giorgetti, Emilia</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1633-0923</orcidid></search><sort><creationdate>20170504</creationdate><title>Supramolecular Recognition of Escherichia coli Bacteria by Fluorescent Oligo(Phenyleneethynylene)s with Mannopyranoside Termini Groups</title><author>Arias, Enrique ; 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By taking advantage of the specific interactions between mannose and type 1 fimbriae, in this work two fluorescent phenyleneethynylene (PE) trimers bearing one or two 4-aminophenyl-α-D-mannopyranoside termini groups were synthesized for the detection of
Three bacterial strains: ORN 178 (fimbriae I expression), ORN 208 (mutant serotype with no fimbriae expression) and one obtained from a local hospital (SS3) were used. Laser Scanning Confocal Microscopy (LSCM) and Surface Plasmon Resonance (SPR) were applied for the interaction studies following two different approaches: (1) mixing the oligomer solutions with the bacterial suspension, which permitted the observation of stained bacteria and by (2) biosensing as thin films, where bacteria adhered on the surface-functionalized substrate. LSCM allows one to easily visualize that two mannose groups are necessary to have a specific interaction with the fimbriae 1. The sensitivity of SPR assays to
was 10⁴ colony forming unit (CFU)/mL at 50 µL/min flow rate. The combination of PE units with two mannose groups results in a novel molecule that can be used as a specific fluorescent marker as well as a transducer for the detection of
.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>28471379</pmid><doi>10.3390/s17051025</doi><orcidid>https://orcid.org/0000-0002-1633-0923</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alkynes Assaying Bacteria Bacterial Adhesion Bearing E coli Escherichia coli Ethers Flow velocity Fluorescence Forming Lasers Mannose Microscopy Recognition Searching Sensitivity Thin films |
title | Supramolecular Recognition of Escherichia coli Bacteria by Fluorescent Oligo(Phenyleneethynylene)s with Mannopyranoside Termini Groups |
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