Biofilm Formation and Immunomodulatory Activity of Proteus mirabilis Clinically Isolated Strains
Urinary tract infections (UTIs) and catheter-associated UTIs (CAUTIs) are the principal hospital-acquired infections. is characterized by several virulence factors able to promote adhesion and biofilm formation and ameliorate the colonization of urinary tract and the formation of crystalline biofilm...
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creator | Fusco, Alessandra Coretti, Lorena Savio, Vittoria Buommino, Elisabetta Lembo, Francesca Donnarumma, Giovanna |
description | Urinary tract infections (UTIs) and catheter-associated UTIs (CAUTIs) are the principal hospital-acquired infections.
is characterized by several virulence factors able to promote adhesion and biofilm formation and ameliorate the colonization of urinary tract and the formation of crystalline biofilms on the abiotic surface of the urinary catheters. Since, to date, the role of
in the etiopathogenesis of different types of urinary tract infections is not well established, in this study we sought to characterize two different clinically isolated strains of
(PM1 and PM2) with distinctive phenotypes and analyzed various virulence factors possibly implicated in the ability to induce UTIs and CAUTIs. In particular, we analyzed motility, biofilm formation both on abiotic and biotic surfaces of PM1 and PM2 and paralleled these parameters with the ability to induce an inflammatory response in an epithelial cell model. Results showed that PM1 displayed major motility and a capacity to form biofilm and was associated with an anti-inflammatory response of host cells. Conversely, PM2 exhibited lack motility and a had slower organization in biofilm but promoted an increase of proinflammatory cytokine expression in infected epithelial cells. Our study provides data useful to start uncovering the pathologic basis of
-associated urinary infections. The evidence of different virulence factors expressed by PM1 and PM2 highlights the possibility to use precise and personalized therapies targeting specific virulence pathways. |
doi_str_mv | 10.3390/ijms18020414 |
format | Article |
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is characterized by several virulence factors able to promote adhesion and biofilm formation and ameliorate the colonization of urinary tract and the formation of crystalline biofilms on the abiotic surface of the urinary catheters. Since, to date, the role of
in the etiopathogenesis of different types of urinary tract infections is not well established, in this study we sought to characterize two different clinically isolated strains of
(PM1 and PM2) with distinctive phenotypes and analyzed various virulence factors possibly implicated in the ability to induce UTIs and CAUTIs. In particular, we analyzed motility, biofilm formation both on abiotic and biotic surfaces of PM1 and PM2 and paralleled these parameters with the ability to induce an inflammatory response in an epithelial cell model. Results showed that PM1 displayed major motility and a capacity to form biofilm and was associated with an anti-inflammatory response of host cells. Conversely, PM2 exhibited lack motility and a had slower organization in biofilm but promoted an increase of proinflammatory cytokine expression in infected epithelial cells. Our study provides data useful to start uncovering the pathologic basis of
-associated urinary infections. The evidence of different virulence factors expressed by PM1 and PM2 highlights the possibility to use precise and personalized therapies targeting specific virulence pathways.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms18020414</identifier><identifier>PMID: 28212280</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Berries ; Biofilms ; Biofilms - growth & development ; Catheters ; Colonization ; Crystal structure ; Epithelial cells ; Gene Expression Regulation, Bacterial ; Genes, Bacterial ; Host-Pathogen Interactions - immunology ; Humans ; Immunomodulation ; Immunomodulators ; Inflammation ; Inflammatory response ; Motility ; Nosocomial infections ; Phenotype ; Proteus Infections - immunology ; Proteus Infections - microbiology ; Proteus mirabilis ; Proteus mirabilis - classification ; Proteus mirabilis - isolation & purification ; Proteus mirabilis - physiology ; Surface chemistry ; Urinary tract ; Urinary tract diseases ; Urinary tract infections ; Urinary Tract Infections - immunology ; Urinary Tract Infections - microbiology ; Urogenital system ; Virulence ; Virulence Factors</subject><ispartof>International journal of molecular sciences, 2017-02, Vol.18 (2), p.414-414</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-c445t-5f604851c26704b97c2ff58af7ab24a5d1585bdcb331b4200c0361d10f53bdfb3</citedby><cites>FETCH-LOGICAL-c445t-5f604851c26704b97c2ff58af7ab24a5d1585bdcb331b4200c0361d10f53bdfb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343948/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343948/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28212280$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fusco, Alessandra</creatorcontrib><creatorcontrib>Coretti, Lorena</creatorcontrib><creatorcontrib>Savio, Vittoria</creatorcontrib><creatorcontrib>Buommino, Elisabetta</creatorcontrib><creatorcontrib>Lembo, Francesca</creatorcontrib><creatorcontrib>Donnarumma, Giovanna</creatorcontrib><title>Biofilm Formation and Immunomodulatory Activity of Proteus mirabilis Clinically Isolated Strains</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Urinary tract infections (UTIs) and catheter-associated UTIs (CAUTIs) are the principal hospital-acquired infections.
is characterized by several virulence factors able to promote adhesion and biofilm formation and ameliorate the colonization of urinary tract and the formation of crystalline biofilms on the abiotic surface of the urinary catheters. Since, to date, the role of
in the etiopathogenesis of different types of urinary tract infections is not well established, in this study we sought to characterize two different clinically isolated strains of
(PM1 and PM2) with distinctive phenotypes and analyzed various virulence factors possibly implicated in the ability to induce UTIs and CAUTIs. In particular, we analyzed motility, biofilm formation both on abiotic and biotic surfaces of PM1 and PM2 and paralleled these parameters with the ability to induce an inflammatory response in an epithelial cell model. Results showed that PM1 displayed major motility and a capacity to form biofilm and was associated with an anti-inflammatory response of host cells. Conversely, PM2 exhibited lack motility and a had slower organization in biofilm but promoted an increase of proinflammatory cytokine expression in infected epithelial cells. Our study provides data useful to start uncovering the pathologic basis of
-associated urinary infections. The evidence of different virulence factors expressed by PM1 and PM2 highlights the possibility to use precise and personalized therapies targeting specific virulence pathways.</description><subject>Berries</subject><subject>Biofilms</subject><subject>Biofilms - growth & development</subject><subject>Catheters</subject><subject>Colonization</subject><subject>Crystal structure</subject><subject>Epithelial cells</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genes, Bacterial</subject><subject>Host-Pathogen Interactions - immunology</subject><subject>Humans</subject><subject>Immunomodulation</subject><subject>Immunomodulators</subject><subject>Inflammation</subject><subject>Inflammatory response</subject><subject>Motility</subject><subject>Nosocomial infections</subject><subject>Phenotype</subject><subject>Proteus Infections - immunology</subject><subject>Proteus Infections - microbiology</subject><subject>Proteus mirabilis</subject><subject>Proteus mirabilis - classification</subject><subject>Proteus mirabilis - isolation & purification</subject><subject>Proteus mirabilis - physiology</subject><subject>Surface chemistry</subject><subject>Urinary tract</subject><subject>Urinary tract diseases</subject><subject>Urinary tract infections</subject><subject>Urinary Tract Infections - immunology</subject><subject>Urinary Tract Infections - microbiology</subject><subject>Urogenital system</subject><subject>Virulence</subject><subject>Virulence Factors</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkctLXDEUxkNRqrXuupaAGxedNs97czcFHXwMCBbarmOSm9QMedjkXmH-e-_gOIxduToHzu985_EB8AWjb5R26LtfxooFIohh9gEcYkbIDKGm3dvJD8CnWpcIEUp49xEcEEEwIQIdgvsLn50PEV7lEtXgc4Iq9XAR45hyzP0Y1JDLCp6bwT_5YQWzgz9LHuxYYfRFaR98hfPgkzcqhBVc1Dy12B7-GoryqX4G-06Fao838Qj8ubr8Pb-Z3d5dL-bntzPDGB9m3DWICY4NaVrEdNca4hwXyrVKE6Z4j7ngujeaUqwZQcgg2uAeI8ep7p2mR-DHi-7jqKPtjU3T_CAfi4-qrGRWXr6tJP8g_-YnySmjHROTwNlGoOR_o62DjL4aG4JKNo9VYtFhwWkr3oM2Xddw3K7R0__QZR5Lmj4xUa1glLVkTX19oUzJtRbrtntjJNcuy12XJ_xk99Yt_GorfQasyKRa</recordid><startdate>20170215</startdate><enddate>20170215</enddate><creator>Fusco, Alessandra</creator><creator>Coretti, Lorena</creator><creator>Savio, Vittoria</creator><creator>Buommino, Elisabetta</creator><creator>Lembo, Francesca</creator><creator>Donnarumma, Giovanna</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>8G5</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>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20170215</creationdate><title>Biofilm Formation and Immunomodulatory Activity of Proteus mirabilis Clinically Isolated Strains</title><author>Fusco, Alessandra ; 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is characterized by several virulence factors able to promote adhesion and biofilm formation and ameliorate the colonization of urinary tract and the formation of crystalline biofilms on the abiotic surface of the urinary catheters. Since, to date, the role of
in the etiopathogenesis of different types of urinary tract infections is not well established, in this study we sought to characterize two different clinically isolated strains of
(PM1 and PM2) with distinctive phenotypes and analyzed various virulence factors possibly implicated in the ability to induce UTIs and CAUTIs. In particular, we analyzed motility, biofilm formation both on abiotic and biotic surfaces of PM1 and PM2 and paralleled these parameters with the ability to induce an inflammatory response in an epithelial cell model. Results showed that PM1 displayed major motility and a capacity to form biofilm and was associated with an anti-inflammatory response of host cells. Conversely, PM2 exhibited lack motility and a had slower organization in biofilm but promoted an increase of proinflammatory cytokine expression in infected epithelial cells. Our study provides data useful to start uncovering the pathologic basis of
-associated urinary infections. The evidence of different virulence factors expressed by PM1 and PM2 highlights the possibility to use precise and personalized therapies targeting specific virulence pathways.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>28212280</pmid><doi>10.3390/ijms18020414</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Berries Biofilms Biofilms - growth & development Catheters Colonization Crystal structure Epithelial cells Gene Expression Regulation, Bacterial Genes, Bacterial Host-Pathogen Interactions - immunology Humans Immunomodulation Immunomodulators Inflammation Inflammatory response Motility Nosocomial infections Phenotype Proteus Infections - immunology Proteus Infections - microbiology Proteus mirabilis Proteus mirabilis - classification Proteus mirabilis - isolation & purification Proteus mirabilis - physiology Surface chemistry Urinary tract Urinary tract diseases Urinary tract infections Urinary Tract Infections - immunology Urinary Tract Infections - microbiology Urogenital system Virulence Virulence Factors |
title | Biofilm Formation and Immunomodulatory Activity of Proteus mirabilis Clinically Isolated Strains |
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