Targeting bacterial quorum sensing shows promise in improving intestinal barrier function following burn‑site infection
Burn‑site infections, commonly due to Pseudomonas aeruginosa, have been associated with deranged intestinal integrity, allowing bacteria and their products to translocate from the gut to the circulatory system. The P. aeruginosa quorum sensing (QS) transcription factor MvfR (PqsR) controls the expre...
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description | Burn‑site infections, commonly due to Pseudomonas aeruginosa, have been associated with deranged intestinal integrity, allowing bacteria and their products to translocate from the gut to the circulatory system. The P. aeruginosa quorum sensing (QS) transcription factor MvfR (PqsR) controls the expression of numerous virulence factors, and the synthesis of several toxic products. However, the role of QS in intestinal integrity alterations, to the best of our knowledge, has not been previously investigated. Using a proven anti‑MvfR, anti‑virulence agent, the in vivo results of the present study revealed that inhibition of MvfR function significantly decreased Fluorescein Isothiocyanate‑Dextran (FITC‑Dextran) flow from the intestine to the systemic circulation, diminished bacterial translocation from the intestine to mesenteric lymph nodes (MLNs), and improved tight junction integrity in thermally injured and infected mice. In addition, the MvfR antagonist administration alleviates the intestinal inflammation, as demonstrated by reduced ileal TNF‑α and fecal lipocalin‑2 concentrations. In addition, it is associated with lower levels of circulating endotoxin and decreased P. aeruginosa dissemination from the burn wound to the ileum. Collectively, these results hold great promise that the inhibition of this QS system mitigates gut hyperpermeability by attenuating the derangement of morphological and immune aspects of the intestinal barrier, suggesting that MvfR function is crucial in the deterioration of intestinal integrity following P. aeruginosa burn‑site infection. Therefore, an anti‑virulence approach targeting MvfR, could potentially offer a novel therapeutic approach against multi‑drug resistant P. aeruginosa infections following thermal injuries. Since this approach is targeting virulence pathways that are non‑essential for growth or viability, our strategy is hypothesized to minimize the development of bacterial resistance, and preserve the beneficial enteric microbes, while improving intestinal integrity that is deranged as a result of burn and infection. |
doi_str_mv | 10.3892/mmr.2019.10071 |
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The P. aeruginosa quorum sensing (QS) transcription factor MvfR (PqsR) controls the expression of numerous virulence factors, and the synthesis of several toxic products. However, the role of QS in intestinal integrity alterations, to the best of our knowledge, has not been previously investigated. Using a proven anti‑MvfR, anti‑virulence agent, the in vivo results of the present study revealed that inhibition of MvfR function significantly decreased Fluorescein Isothiocyanate‑Dextran (FITC‑Dextran) flow from the intestine to the systemic circulation, diminished bacterial translocation from the intestine to mesenteric lymph nodes (MLNs), and improved tight junction integrity in thermally injured and infected mice. In addition, the MvfR antagonist administration alleviates the intestinal inflammation, as demonstrated by reduced ileal TNF‑α and fecal lipocalin‑2 concentrations. In addition, it is associated with lower levels of circulating endotoxin and decreased P. aeruginosa dissemination from the burn wound to the ileum. Collectively, these results hold great promise that the inhibition of this QS system mitigates gut hyperpermeability by attenuating the derangement of morphological and immune aspects of the intestinal barrier, suggesting that MvfR function is crucial in the deterioration of intestinal integrity following P. aeruginosa burn‑site infection. Therefore, an anti‑virulence approach targeting MvfR, could potentially offer a novel therapeutic approach against multi‑drug resistant P. aeruginosa infections following thermal injuries. Since this approach is targeting virulence pathways that are non‑essential for growth or viability, our strategy is hypothesized to minimize the development of bacterial resistance, and preserve the beneficial enteric microbes, while improving intestinal integrity that is deranged as a result of burn and infection.</description><identifier>ISSN: 1791-2997</identifier><identifier>EISSN: 1791-3004</identifier><identifier>DOI: 10.3892/mmr.2019.10071</identifier><identifier>PMID: 30896813</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>Antibiotics ; Backup software ; Bacteria ; Burns ; Circulatory system ; Cytokines ; Dextran ; Dextrans ; Digestive system ; Drug resistance ; Fluorescein ; Fluorescein isothiocyanate ; Gastrointestinal tract ; Ileum ; Infection ; Infections ; Intestine ; Laboratories ; Lipocalin ; Lymph nodes ; Lymphocytes ; Microorganisms ; Multidrug resistance ; Novels ; Permeability ; Polysaccharides ; Pseudomonas aeruginosa ; Quorum sensing ; Regulation ; Sepsis ; T cells ; Therapeutics ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α ; Virulence factors</subject><ispartof>Molecular medicine reports, 2019-05, Vol.19 (5), p.4057-4066</ispartof><rights>COPYRIGHT 2019 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2019</rights><rights>Copyright: © Adiliaghdam et al. 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-bfe75d4b8879d3eadeb045934b00065a9ea0b92bfdc866aef24f568586323a943</citedby><cites>FETCH-LOGICAL-c485t-bfe75d4b8879d3eadeb045934b00065a9ea0b92bfdc866aef24f568586323a943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30896813$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Adiliaghdam, Fatemeh</creatorcontrib><creatorcontrib>Almpani, Marianna</creatorcontrib><creatorcontrib>Gharedaghi, Mohammad Hadi</creatorcontrib><creatorcontrib>Najibi, Mehran</creatorcontrib><creatorcontrib>Hodin, Richard A</creatorcontrib><creatorcontrib>Rahme, Laurence G</creatorcontrib><title>Targeting bacterial quorum sensing shows promise in improving intestinal barrier function following burn‑site infection</title><title>Molecular medicine reports</title><addtitle>Mol Med Rep</addtitle><description>Burn‑site infections, commonly due to Pseudomonas aeruginosa, have been associated with deranged intestinal integrity, allowing bacteria and their products to translocate from the gut to the circulatory system. The P. aeruginosa quorum sensing (QS) transcription factor MvfR (PqsR) controls the expression of numerous virulence factors, and the synthesis of several toxic products. However, the role of QS in intestinal integrity alterations, to the best of our knowledge, has not been previously investigated. Using a proven anti‑MvfR, anti‑virulence agent, the in vivo results of the present study revealed that inhibition of MvfR function significantly decreased Fluorescein Isothiocyanate‑Dextran (FITC‑Dextran) flow from the intestine to the systemic circulation, diminished bacterial translocation from the intestine to mesenteric lymph nodes (MLNs), and improved tight junction integrity in thermally injured and infected mice. In addition, the MvfR antagonist administration alleviates the intestinal inflammation, as demonstrated by reduced ileal TNF‑α and fecal lipocalin‑2 concentrations. In addition, it is associated with lower levels of circulating endotoxin and decreased P. aeruginosa dissemination from the burn wound to the ileum. Collectively, these results hold great promise that the inhibition of this QS system mitigates gut hyperpermeability by attenuating the derangement of morphological and immune aspects of the intestinal barrier, suggesting that MvfR function is crucial in the deterioration of intestinal integrity following P. aeruginosa burn‑site infection. Therefore, an anti‑virulence approach targeting MvfR, could potentially offer a novel therapeutic approach against multi‑drug resistant P. aeruginosa infections following thermal injuries. Since this approach is targeting virulence pathways that are non‑essential for growth or viability, our strategy is hypothesized to minimize the development of bacterial resistance, and preserve the beneficial enteric microbes, while improving intestinal integrity that is deranged as a result of burn and infection.</description><subject>Antibiotics</subject><subject>Backup software</subject><subject>Bacteria</subject><subject>Burns</subject><subject>Circulatory system</subject><subject>Cytokines</subject><subject>Dextran</subject><subject>Dextrans</subject><subject>Digestive system</subject><subject>Drug resistance</subject><subject>Fluorescein</subject><subject>Fluorescein isothiocyanate</subject><subject>Gastrointestinal tract</subject><subject>Ileum</subject><subject>Infection</subject><subject>Infections</subject><subject>Intestine</subject><subject>Laboratories</subject><subject>Lipocalin</subject><subject>Lymph nodes</subject><subject>Lymphocytes</subject><subject>Microorganisms</subject><subject>Multidrug resistance</subject><subject>Novels</subject><subject>Permeability</subject><subject>Polysaccharides</subject><subject>Pseudomonas aeruginosa</subject><subject>Quorum sensing</subject><subject>Regulation</subject><subject>Sepsis</subject><subject>T cells</subject><subject>Therapeutics</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><subject>Virulence factors</subject><issn>1791-2997</issn><issn>1791-3004</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptUstqFTEYDqLY2nbrUgZcn9NcZ5KNUIpVoeCmrkOS-XOaMpOcJjMt3fkKvqJP0szxWCuULHL5LuRLPoTeE7xmUtHTccxriolaE4w78godkk6RFcOYv96vqVLdAXpXyg3GraBCvUUHDEvVSsIO0cOVyRuYQtw01rgJcjBDczunPI9NgVgWoFyn-9JscxpDgSbEJox1c7dAIU5QqrqKrMk5QG78HN0UUmx8GoZ0v3Oec_z981cJ0yL3sMOP0RtvhgIn-_kI_bj4fHX-dXX5_cu387PLleNSTCvroRM9t1J2qmdgerCYC8W4xUseo8Bgq6j1vZNta8BT7kUrhWwZZUZxdoQ-_fHdznaE3kGcshn0NofR5AedTND_IzFc60260y3vKCGsGnzcG-R0O9e4-ibVQPXOmlYClbRT9B9rYwbQNWWqZq6-mNNnQgpew7QLa_0Cq44exuBSBB_q-UsCl1MpGfzTxQnWSwN0bYBeGqB3DaiCD8_jPtH_fjl7BMxDsLc</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Adiliaghdam, Fatemeh</creator><creator>Almpani, Marianna</creator><creator>Gharedaghi, Mohammad Hadi</creator><creator>Najibi, Mehran</creator><creator>Hodin, Richard A</creator><creator>Rahme, Laurence G</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. Spandidos</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20190501</creationdate><title>Targeting bacterial quorum sensing shows promise in improving intestinal barrier function following burn‑site infection</title><author>Adiliaghdam, Fatemeh ; Almpani, Marianna ; Gharedaghi, Mohammad Hadi ; Najibi, Mehran ; Hodin, Richard A ; Rahme, Laurence G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c485t-bfe75d4b8879d3eadeb045934b00065a9ea0b92bfdc866aef24f568586323a943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Antibiotics</topic><topic>Backup software</topic><topic>Bacteria</topic><topic>Burns</topic><topic>Circulatory system</topic><topic>Cytokines</topic><topic>Dextran</topic><topic>Dextrans</topic><topic>Digestive system</topic><topic>Drug resistance</topic><topic>Fluorescein</topic><topic>Fluorescein isothiocyanate</topic><topic>Gastrointestinal tract</topic><topic>Ileum</topic><topic>Infection</topic><topic>Infections</topic><topic>Intestine</topic><topic>Laboratories</topic><topic>Lipocalin</topic><topic>Lymph nodes</topic><topic>Lymphocytes</topic><topic>Microorganisms</topic><topic>Multidrug resistance</topic><topic>Novels</topic><topic>Permeability</topic><topic>Polysaccharides</topic><topic>Pseudomonas aeruginosa</topic><topic>Quorum sensing</topic><topic>Regulation</topic><topic>Sepsis</topic><topic>T cells</topic><topic>Therapeutics</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumor necrosis factor-α</topic><topic>Virulence factors</topic><toplevel>online_resources</toplevel><creatorcontrib>Adiliaghdam, Fatemeh</creatorcontrib><creatorcontrib>Almpani, Marianna</creatorcontrib><creatorcontrib>Gharedaghi, Mohammad Hadi</creatorcontrib><creatorcontrib>Najibi, Mehran</creatorcontrib><creatorcontrib>Hodin, Richard A</creatorcontrib><creatorcontrib>Rahme, Laurence G</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular medicine reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Adiliaghdam, Fatemeh</au><au>Almpani, Marianna</au><au>Gharedaghi, Mohammad Hadi</au><au>Najibi, Mehran</au><au>Hodin, Richard A</au><au>Rahme, Laurence G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting bacterial quorum sensing shows promise in improving intestinal barrier function following burn‑site infection</atitle><jtitle>Molecular medicine reports</jtitle><addtitle>Mol Med Rep</addtitle><date>2019-05-01</date><risdate>2019</risdate><volume>19</volume><issue>5</issue><spage>4057</spage><epage>4066</epage><pages>4057-4066</pages><issn>1791-2997</issn><eissn>1791-3004</eissn><abstract>Burn‑site infections, commonly due to Pseudomonas aeruginosa, have been associated with deranged intestinal integrity, allowing bacteria and their products to translocate from the gut to the circulatory system. The P. aeruginosa quorum sensing (QS) transcription factor MvfR (PqsR) controls the expression of numerous virulence factors, and the synthesis of several toxic products. However, the role of QS in intestinal integrity alterations, to the best of our knowledge, has not been previously investigated. Using a proven anti‑MvfR, anti‑virulence agent, the in vivo results of the present study revealed that inhibition of MvfR function significantly decreased Fluorescein Isothiocyanate‑Dextran (FITC‑Dextran) flow from the intestine to the systemic circulation, diminished bacterial translocation from the intestine to mesenteric lymph nodes (MLNs), and improved tight junction integrity in thermally injured and infected mice. In addition, the MvfR antagonist administration alleviates the intestinal inflammation, as demonstrated by reduced ileal TNF‑α and fecal lipocalin‑2 concentrations. In addition, it is associated with lower levels of circulating endotoxin and decreased P. aeruginosa dissemination from the burn wound to the ileum. Collectively, these results hold great promise that the inhibition of this QS system mitigates gut hyperpermeability by attenuating the derangement of morphological and immune aspects of the intestinal barrier, suggesting that MvfR function is crucial in the deterioration of intestinal integrity following P. aeruginosa burn‑site infection. Therefore, an anti‑virulence approach targeting MvfR, could potentially offer a novel therapeutic approach against multi‑drug resistant P. aeruginosa infections following thermal injuries. Since this approach is targeting virulence pathways that are non‑essential for growth or viability, our strategy is hypothesized to minimize the development of bacterial resistance, and preserve the beneficial enteric microbes, while improving intestinal integrity that is deranged as a result of burn and infection.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>30896813</pmid><doi>10.3892/mmr.2019.10071</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibiotics Backup software Bacteria Burns Circulatory system Cytokines Dextran Dextrans Digestive system Drug resistance Fluorescein Fluorescein isothiocyanate Gastrointestinal tract Ileum Infection Infections Intestine Laboratories Lipocalin Lymph nodes Lymphocytes Microorganisms Multidrug resistance Novels Permeability Polysaccharides Pseudomonas aeruginosa Quorum sensing Regulation Sepsis T cells Therapeutics Tumor necrosis factor-TNF Tumor necrosis factor-α Virulence factors |
title | Targeting bacterial quorum sensing shows promise in improving intestinal barrier function following burn‑site infection |
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