Principales características de las biopelículas relacionadas con procesos patológicos descritos en humanos en los últimos 10 años, revisión sistemática

Principales características de las biopelículas relacionadas con procesos patológicos descritos en humanos en los últimos 10 años, revisión sistemática

Introducción. Uno de los mayores avances en microbiología ha sido el conocimiento del crecimiento de microorganismos sobre diferentes superficies, formando biopelículas, en donde su comportamiento y fisiología es significativamente diferente de aquellos microorganismos que crecen de forma individual o planctónica. En este estudio se describen las principales características de las biopelículas relacionadas con procesos patológicos en humanos.Métodos. Se realizó una revisión sistemática de la literatura relacionada en las bases de datos ScienceDirect, PubMed y el buscador genérico Google Scholar. Se incluyeron en el estudio 35 artículos, los cuales cumplieron con los criterios de inclusión y de exclusión determinados.Resultados. Se describie... Ver más

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Revista Investigaciones Andina

0124-8146

2538-9580

Eraso Cadena, Marcela Patricia

Ríos Osorio, Leonardo Alberto

FUNDACIÓN UNIVERSITARIA DEL AREA ANDINA

10.33132/01248146.556

18

2016-09-21

1491

1506

Colombia

http://purl.org/coar/access_right/c_abf2

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Revista Investigaciones Andina - 2016

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spelling Principales características de las biopelículas relacionadas con procesos patológicos descritos en humanos en los últimos 10 años, revisión sistemática
Nafee N, Husari A, Maurer CK, Lu C, De Rossi C, Steinbach A, et al. Antibiotic-free nanotherapeutics: Ultra-small, mucus-penetrating solid lipid nanoparticles enhance the pulmonary delivery and anti-virulence efficacy of novel quorum sensing inhibitors. J Control Release [Internet]. Elsevier B.V.; 2014;192:131–40. Available from: http://dx.doi.org/10.1016/j.jconrel.2014.06.055
Thenmozhi R, Nithyanand P, Rathna J, Karutha Pandian S. Antibiofilm activity of coral-associated bacteria against different clinical M serotypes of Streptococcus pyogenes. FEMS Immunol Med Microbiol. 2009;57(3):284–94. http://dx.doi.org/10.1111/j.1574-695X.2009.00613.x
Palmer S, Soulsby L, Torgerson PR, Brown DW (eds). Zoonoses Biology, Clinical Practice, and Public Health Control. Oxford University: Oxford; 2011.
Paiva LCF, Vidigal PG, Donatti L, Svidzinski TIE, Consolaro MEL. Assessment of in vitro biofilm formation by Candida species isolates from vulvovaginal candidiasis and ultrastructural characteristics. Micron [Internet]. Elsevier Ltd; 2012;43(2-3):497–502. Available from: http://dx.doi.org/10.1016/j.micron.2011.09.013
Van Der Meer JW, Van De Veerdonk FL, Joosten LA, Kullberg BJ, Netea MG. Severe Candida spp. infections: New insights into natural immunity. Int J Antimicrob Agents [Internet]. Elsevier B.V.; 2010;36(SUPPL. 2):S58–62. Available from: http://dx.doi.org/10.1016/j.ijantimicag.2010.11.013
Ikonomidis A, Vasdeki A, Kristo I, Maniatis AN, Tsakris A, Malizos KN, et al. Association of biofilm formation and methicillin-resistance with accessory gene regulator (agr) loci in Greek Staphylococcus aureus clones. Microb Pathog [Internet]. Elsevier Ltd; 2009;47(6):341–4. Available from: http://dx.doi.org/10.1016/j.micpath.2009.09.011
Frank K, Patel R. Staphylococcus lugdunensis- Not the Average Coagulase-Negative Staphylococcus Species. Clin Microbiol Newsl. 2008;30(8):55–62. http://dx.doi.org/10.1016/j.clinmicnews.2008.03.004
Mikkelsen H, Ball G, Giraud C, Filloux A. Expression of pseudomonas aeruginosa CupD fimbrial genes is antagonistically controlled by RcsB and the EAL-containing PvrR response regulators. PLoS One. 2009;4(6). http://dx.doi.org/10.1371/journal.pone.0006018
Xue T, Ni J, Shang F, Chen X, Zhang M. Autoinducer-2 increases biofilm formation via an ica- and bhp-dependent manner in Staphylococcus epidermidis RP62A. Microbes Infect [Internet]. Elsevier Masson SAS; 2015;17(5):345–52. Available from: http://linkinghub.elsevier.com/retrieve/pii/S1286457915000167
Ioannidis A, Kyratsa A, Ioannidou V, Bersimis S, Chatzipanagiotou S. Detection of biofilm production of Yersinia enterocolitica strains isolated from infected children and comparative antimicrobial susceptibility of biofilm versus planktonic forms. Mol Diagnosis Ther. 2014;18(3):309–14. http://dx.doi.org/10.1007/s40291-013-0080-1
Urrútia G, Bonfill X. Declaración PRISMA: una propuesta para mejorar la publicación de revisiones sistemáticas y metaanálisis. Med Clin (Barc). 2010;135(11):507–11. http://dx.doi.org/10.1016/j.medcli.2010.01.015
Patel I, Patel V, Thakkar A, Kothari V. Microbial Biofilms: Microbes in Social Mode. Int J Agric Food Res. 2014;3(2):34–49.
Meervenne E Van, Weirdt R De, Coillie E Van, Devlieghere F, Herman L, Boon N. Biofilm models for the food industry: Hot spots for plasmid transfer? Pathog Dis. 2014;70(3):332–8. http://dx.doi.org/10.1111/2049-632X.12134
Suntharalingam P, Cvitkovitch DG. Quorum sensing in streptococcal biofilm formation. Trends Microbiol. 2005;13(1):3–6. http://dx.doi.org/10.1016/j.tim.2004.11.009
Schoenfelder SMK, Lange C, Eckart M, Hennig S, Kozytska S, Ziebuhr W. Success through diversity - How Staphylococcus epidermidis establishes as a nosocomial pathogen. Int J Med Microbiol [Internet]. Elsevier GmbH.; 2010;300(6):380–6. Available from: http://dx.doi.org/10.1016/j.ijmm.2010.04.011
Hooshangi S, Bentley WE. From unicellular properties to multicellular behavior: bacteria quorum sensing circuitry and applications. Curr Opin Biotechnol. 2008;19(6):550–5.
Siqueira JF, Rôças IN. Community as the unit of pathogenicity: An emerging concept as to the microbial pathogenesis of apical periodontitis. Oral Surgery, Oral Med Oral Pathol Oral Radiol Endodontology [Internet]. Mosby, Inc.; 2009;107(6):870–8. Available from: http://dx.doi.org/10.1016/j.tripleo.2009.01.044
Rosche B, Li XZ, Hauer B, Schmid A, Buehler K. Microbial biofilms: a concept for industrial catalysis? Trends Biotechnol. 2009;27(11):636–43. http://dx.doi.org/10.1016/j.tibtech.2009.08.001
Azakami H, Akashima HN, Kimichi HA, Oiri YN, Bisu SE, Ato AK. Involvement of N-Acetyl-. Biosci Biotechnol Biochem [Internet]. 2006;70(2):1–6. Available from: papers3://publication/uuid/5BB250C2-D3D3-45CD-81A5-52EDC1CDFA08
El Fertas-Aissani R, Messai Y, Alouache S, Bakour R. Virulence profiles and antibiotic susceptibility patterns of Klebsiella pneumoniae strains isolated from different clinical specimens. Pathol Biol (Paris) [Internet]. Elsevier Masson SAS; 2013;61(5):209–16. Available from: http://www.sciencedirect.com/science/article/pii/S036981141200185X
Srey S, Jahid IK, Ha S Do. Biofilm formation in food industries: A food safety concern. Food Control. Elsevier Ltd; 2013;31(2):572–85. http://dx.doi.org/10.1016/j.foodcont.2012.12.001
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Kaper JB, O'Brien AD. Overview and Historical Perspectives. Microbiol Spectr [Internet]. 2014;2(2). Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=4290666&tool=pmcentrez&rendertype=abstract http://dx.doi.org/10.1128/microbiolspec.ehec-0028-2014
Cusumano CK, Hung CS, Chen SL, Hultgren SJ. Virulence plasmid harbored by uropathogenic Escherichia coli functions in acute stages of pathogenesis. Infect Immun. 2010;78(4):1457–67. http://dx.doi.org/10.1128/IAI.01260-09
Osman KM, Zolnikov TR, Samir A, Orabi A. Prevalence, pathogenic capability, virulence genes, biofilm formation, and antibiotic resistance of Listeria in goat and sheep milk confirms need of hygienic milking conditions. Pathog Glob Health [Internet]. 2014;108(1):21–9. Available from: http://www.maneyonline.com/doi/abs/10.1179/2047773213Y.0000000115 http://dx.doi.org/10.1179/2047773213Y.0000000115
Mikkelsen H, Hui K, Barraud N, Filloux A. The pathogenicity island encoded PvrSR/RcsCB regulatory network controls biofilm formation and dispersal in Pseudomonas aeruginosa PA14. Mol Microbiol. 2013;89(3):450–63. http://dx.doi.org/10.1111/mmi.12287
Ejrnæs K. Bacterial characteristics of importance for recurrent urinary tract infections caused by Escherichia coli. Dan Med Bull [Internet]. 2011;58(4):B4187. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21466767
Modrzewska B, Kurnatowski P. Review articles Selected pathogenic characteristics of fungi from the genus. Ann Parasitol. 2013;59(502):57–66.
Marguerettaz M, Dieppois G, Que YA, Ducret V, Zuchuat S, Perron K. Sputum containing zinc enhances carbapenem resistance, biofilm formation and virulence of Pseudomonas aeruginosa. Microb Pathog [Internet]. 2014;77:36–41. Available from: http://linkinghub.elsevier.com/retrieve/pii/S0882401014001636 http://dx.doi.org/10.1016/j.micpath.2014.10.011
Marrero K, Sánchez A, Rodríguez-Ulloa A, González LJ, Castellanos-Serra L, Paz-Lago D, et al. Anaerobic growth promotes synthesis of colonization factors encoded at the Vibrio pathogenicity island in Vibrio cholerae El Tor. Res Microbiol. 2009;160(1):48–56. http://dx.doi.org/10.1016/j.resmic.2008.10.005
Senadheera D, Cvitkovitch DG. Quorum sensing and biofilm formation by Streptococcus mutans. In: Advances in experimental medicine and biology. 2008. p. 178–88. http://dx.doi.org/10.1007/978-0-387-78885-2_12
Hebbelstrup B, Olsen KEP, Struve C, Krogfelt KA, Petersen AM. Epidemiology and clinical manifestations of enteroaggregative escherichia coli. Clin Microbiol Rev. 2014;27(3):614–30. http://dx.doi.org/10.1128/CMR.00112-13
Arini A, Feurtet-Mazel A, Morin S, Maury-Brachet R, Coste M, Delmas F. Remediation of a watershed contaminated by heavy metals: A 2-year field biomonitoring of periphytic biofilms. Sci Total Environ. 2012;425:242–53. http://dx.doi.org/10.1016/j.scitotenv.2012.02.067
Mizan MFR, Jahid IK, Ha S Do. Microbial biofilms in seafood: A food-hygiene challenge. Food Microbiol [Internet]. Elsevier Ltd; 2015;49:41–55. Available from: http://dx.doi.org/10.1016/j.fm.2015.01.009
Kalia VC. Quorum sensing inhibitors: An overview. Biotechnol Adv [Internet]. Elsevier Inc.; 2013;31(2):224–45. Available from: http://dx.doi.org/10.1016/j.biotechadv.2012.10.004
Seneviratne CJ, Jin L, Samaranayake LP. Biofilm lifestyle of Candida: A mini review. Oral Dis. 2008;14(7):582–90. http://dx.doi.org/10.1111/j.1601-0825.2007.01424.x
Introducción. Uno de los mayores avances en microbiología ha sido el conocimiento del crecimiento de microorganismos sobre diferentes superficies, formando biopelículas, en donde su comportamiento y fisiología es significativamente diferente de aquellos microorganismos que crecen de forma individual o planctónica. En este estudio se describen las principales características de las biopelículas relacionadas con procesos patológicos en humanos.Métodos. Se realizó una revisión sistemática de la literatura relacionada en las bases de datos ScienceDirect, PubMed y el buscador genérico Google Scholar. Se incluyeron en el estudio 35 artículos, los cuales cumplieron con los criterios de inclusión y de exclusión determinados.Resultados. Se describieron los agentes etiológicos involucrados en la formación de biopelículas, así como la caracterización acorde con los sitos orgánicos donde se pueden establecer, y los factores patogénicos relacionados con la formación.Conclusión. En la formación de biopelículas influyen factores animados e inanimados relacionados con características específicas del hospedero.
Eraso Cadena, Marcela Patricia
Ríos Osorio, Leonardo Alberto
18
32
Artículo de revista
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Fundación Universitaria Área Andina
Revista Investigaciones Andina
https://revia.areandina.edu.co/index.php/IA/article/view/556
Español
Revista Investigaciones Andina - 2016
Lazar V. Quorum sensing in biofilms - How to destroy the bacterial citadels or their cohesion/power? Anaerobe [Internet]. Elsevier Ltd; 2011;17(6):280–5. Available from: http://dx.doi.org/10.1016/j.anaerobe.2011.03.023
https://creativecommons.org/licenses/by-nc-sa/4.0/
Silva S, Negri M, Henriques M, Oliveira R, Williams DW, Azeredo J. Adherence and biofilm formation of non-Candida albicans Candida species. Trends Microbiol. 2011;19(5):241–7. http://dx.doi.org/10.1016/j.tim.2011.02.003
Bjarnsholt T, Alhede M, Alhede M, Eickhardt-Sørensen SR, Moser C, Kühl M, et al. The in vivo biofilm. Trends Microbiol. 2013;21(9):466–74. http://dx.doi.org/10.1016/j.tim.2013.06.002
Kaplan JB. Biofilm Dispersal : Mechanisms , Clinical Implications , and Potential Therapeutic Uses. J Dent Res. 2010;89(3):205–18. http://dx.doi.org/10.1177/0022034509359403
Fazeelath Banu. M., Geetha. R. Evaluation of antimicrobial efficacy of essential oils on streptococcus mutans. Int J Pharm Sci Rev Res [Internet]. 2015;33(1):119–21. Available from: http://www.embase.com/search/results?subaction=viewrecord&from=export&id=L605392610
Lembke C, Podbielski A, Jonas L, Hanski E, Hidalgo-grass C, Kreikemeyer B. Characterization of Biofilm Formation by Clinically Relevant Serotypes of Group A Streptococci Characterization of Biofilm Formation by Clinically Relevant Serotypes of Group A Streptococci †. Appl Environ Microbiol. 2006;72(4):2864–75. http://dx.doi.org/10.1128/AEM.72.4.2864-2875.2006
Brackman G, Coenye T. Inhibition of quorum sensing in Staphylococcus spp . Bentham Sci Publ. 2015;1–8.
Hall-Stoodley L, Stoodley P. Developmental regulation of microbial biofilms. Curr Opin Biotechnol. 2002;13(3):228–33. http://dx.doi.org/10.1016/S0958-1669(02)00318-X
Chaves Simões L, Simões M. Biofilms in drinking water: problems and solutions. RSC Adv. 2013;3(8):2520. http://dx.doi.org/10.1039/C2RA22243D
Rohde H, Frankenberger S, Zähringer U, Mack D. Structure, function and contribution of polysaccharide intercellular adhesin (PIA) to Staphylococcus epidermidis biofilm formation and pathogenesis of biomaterial-associated infections. Eur J Cell Biol. 2010;89(1):103–11. http://dx.doi.org/10.1016/j.ejcb.2009.10.005
Burmølle M, Ren D, Bjarnsholt T, Sørensen SJ. Interactions in multispecies biofilms: Do they actually matter? Trends Microbiol [Internet]. Elsevier Ltd; 2014;22(2):84–91. Available from: http://dx.doi.org/10.1016/j.tim.2013.12.004
O'Gara JP, Humphreys H. Staphylococcus epidermidis biofilms: importance and implications. Med Microbiol. 2001;50(2001):582–7. http://dx.doi.org/10.1099/0022-1317-50-7-582
Publication
Zhang K, Ou M, Wang W, Ling J. Effects of quorum sensing on cell viability in Streptococcus mutans biofilm formation. Biochem Biophys Res Commun [Internet]. Elsevier Inc.; 2009;379(4):933–8. Available from: http://dx.doi.org/10.1016/j.bbrc.2008.12.175
Mishra NN, Prasad T, Sharma N, Payasi A, Prasad R, Gupta DK, et al. Pathogenicity and drug resistance in Candida albicans and other yeast species. A review. Acta Microbiol Immunol Hung. 2007;54(3):201–35. http://dx.doi.org/10.1556/AMicr.54.2007.3.1
Cortés ME, Bonilla JC, Sinisterra RD. Biofilm formation, control and novel strategies for eradication. In: Science against microbial pathogens: communicating current research and technological advances. 2011. p. 896–905.
Danne C, Dramsi S. Pili of Gram-positive bacteria: Roles in host colonization. Res Microbiol [Internet]. Elsevier Masson SAS; 2012;163(9-10):645–58. Available from: http://dx.doi.org/10.1016/j.resmic.2012.10.012
Introduction: One of the greatest advances in microbiology has been the knowledge of growth and development of microorganisms on surfaces forming biofilms, and its behavior and physiology are significantly different from those microorganisms that have an individual or planktonic growth. In this study, we describe the main characteristics of biofilms related to pathological processes in humans.Methods: A systematic literature review was conducted in the databases ScienceDirect, PubMed and the generic search engine Google Scholar. In the study were included 35 articles, which met the specific inclusion and exclusion criteria.Results: We describe the etiologic agents involved in the formation of biofilms, the characterization of these organic sites where these can be formed and the pathogenic factors related to the formation of biofilms.Conclusion: Biofilm formation is influenced by animate and inanimate factors involved in the host.
Main characteristics of biofilms related with pathological processes described in humans in the last ten years: systematic review
Journal article
2016-09-21T00:00:00Z
0124-8146
https://revia.areandina.edu.co/index.php/IA/article/download/556/558
2016-09-21T00:00:00Z
2016-09-21
1491
1506
https://doi.org/10.33132/01248146.556
10.33132/01248146.556
2538-9580
institution FUNDACIÓN UNIVERSITARIA DEL AREA ANDINA
thumbnail https://nuevo.metarevistas.org/FUNDACIONUNIVERSITARIADELAREAANDINA/logo.png
country_str Colombia
collection Revista Investigaciones Andina
title Principales características de las biopelículas relacionadas con procesos patológicos descritos en humanos en los últimos 10 años, revisión sistemática
spellingShingle Principales características de las biopelículas relacionadas con procesos patológicos descritos en humanos en los últimos 10 años, revisión sistemática
Eraso Cadena, Marcela Patricia
Ríos Osorio, Leonardo Alberto
title_short Principales características de las biopelículas relacionadas con procesos patológicos descritos en humanos en los últimos 10 años, revisión sistemática
title_full Principales características de las biopelículas relacionadas con procesos patológicos descritos en humanos en los últimos 10 años, revisión sistemática
title_fullStr Principales características de las biopelículas relacionadas con procesos patológicos descritos en humanos en los últimos 10 años, revisión sistemática
title_full_unstemmed Principales características de las biopelículas relacionadas con procesos patológicos descritos en humanos en los últimos 10 años, revisión sistemática
title_sort principales características de las biopelículas relacionadas con procesos patológicos descritos en humanos en los últimos 10 años, revisión sistemática
title_eng Main characteristics of biofilms related with pathological processes described in humans in the last ten years: systematic review
description Introducción. Uno de los mayores avances en microbiología ha sido el conocimiento del crecimiento de microorganismos sobre diferentes superficies, formando biopelículas, en donde su comportamiento y fisiología es significativamente diferente de aquellos microorganismos que crecen de forma individual o planctónica. En este estudio se describen las principales características de las biopelículas relacionadas con procesos patológicos en humanos.Métodos. Se realizó una revisión sistemática de la literatura relacionada en las bases de datos ScienceDirect, PubMed y el buscador genérico Google Scholar. Se incluyeron en el estudio 35 artículos, los cuales cumplieron con los criterios de inclusión y de exclusión determinados.Resultados. Se describieron los agentes etiológicos involucrados en la formación de biopelículas, así como la caracterización acorde con los sitos orgánicos donde se pueden establecer, y los factores patogénicos relacionados con la formación.Conclusión. En la formación de biopelículas influyen factores animados e inanimados relacionados con características específicas del hospedero.
description_eng Introduction: One of the greatest advances in microbiology has been the knowledge of growth and development of microorganisms on surfaces forming biofilms, and its behavior and physiology are significantly different from those microorganisms that have an individual or planktonic growth. In this study, we describe the main characteristics of biofilms related to pathological processes in humans.Methods: A systematic literature review was conducted in the databases ScienceDirect, PubMed and the generic search engine Google Scholar. In the study were included 35 articles, which met the specific inclusion and exclusion criteria.Results: We describe the etiologic agents involved in the formation of biofilms, the characterization of these organic sites where these can be formed and the pathogenic factors related to the formation of biofilms.Conclusion: Biofilm formation is influenced by animate and inanimate factors involved in the host.
author Eraso Cadena, Marcela Patricia
Ríos Osorio, Leonardo Alberto
author_facet Eraso Cadena, Marcela Patricia
Ríos Osorio, Leonardo Alberto
citationvolume 18
citationissue 32
publisher Fundación Universitaria Área Andina
ispartofjournal Revista Investigaciones Andina
source https://revia.areandina.edu.co/index.php/IA/article/view/556
language Español
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Revista Investigaciones Andina - 2016
https://creativecommons.org/licenses/by-nc-sa/4.0/
references Nafee N, Husari A, Maurer CK, Lu C, De Rossi C, Steinbach A, et al. Antibiotic-free nanotherapeutics: Ultra-small, mucus-penetrating solid lipid nanoparticles enhance the pulmonary delivery and anti-virulence efficacy of novel quorum sensing inhibitors. J Control Release [Internet]. Elsevier B.V.; 2014;192:131–40. Available from: http://dx.doi.org/10.1016/j.jconrel.2014.06.055
Thenmozhi R, Nithyanand P, Rathna J, Karutha Pandian S. Antibiofilm activity of coral-associated bacteria against different clinical M serotypes of Streptococcus pyogenes. FEMS Immunol Med Microbiol. 2009;57(3):284–94. http://dx.doi.org/10.1111/j.1574-695X.2009.00613.x
Palmer S, Soulsby L, Torgerson PR, Brown DW (eds). Zoonoses Biology, Clinical Practice, and Public Health Control. Oxford University: Oxford; 2011.
Paiva LCF, Vidigal PG, Donatti L, Svidzinski TIE, Consolaro MEL. Assessment of in vitro biofilm formation by Candida species isolates from vulvovaginal candidiasis and ultrastructural characteristics. Micron [Internet]. Elsevier Ltd; 2012;43(2-3):497–502. Available from: http://dx.doi.org/10.1016/j.micron.2011.09.013
Van Der Meer JW, Van De Veerdonk FL, Joosten LA, Kullberg BJ, Netea MG. Severe Candida spp. infections: New insights into natural immunity. Int J Antimicrob Agents [Internet]. Elsevier B.V.; 2010;36(SUPPL. 2):S58–62. Available from: http://dx.doi.org/10.1016/j.ijantimicag.2010.11.013
Ikonomidis A, Vasdeki A, Kristo I, Maniatis AN, Tsakris A, Malizos KN, et al. Association of biofilm formation and methicillin-resistance with accessory gene regulator (agr) loci in Greek Staphylococcus aureus clones. Microb Pathog [Internet]. Elsevier Ltd; 2009;47(6):341–4. Available from: http://dx.doi.org/10.1016/j.micpath.2009.09.011
Frank K, Patel R. Staphylococcus lugdunensis- Not the Average Coagulase-Negative Staphylococcus Species. Clin Microbiol Newsl. 2008;30(8):55–62. http://dx.doi.org/10.1016/j.clinmicnews.2008.03.004
Mikkelsen H, Ball G, Giraud C, Filloux A. Expression of pseudomonas aeruginosa CupD fimbrial genes is antagonistically controlled by RcsB and the EAL-containing PvrR response regulators. PLoS One. 2009;4(6). http://dx.doi.org/10.1371/journal.pone.0006018
Xue T, Ni J, Shang F, Chen X, Zhang M. Autoinducer-2 increases biofilm formation via an ica- and bhp-dependent manner in Staphylococcus epidermidis RP62A. Microbes Infect [Internet]. Elsevier Masson SAS; 2015;17(5):345–52. Available from: http://linkinghub.elsevier.com/retrieve/pii/S1286457915000167
Ioannidis A, Kyratsa A, Ioannidou V, Bersimis S, Chatzipanagiotou S. Detection of biofilm production of Yersinia enterocolitica strains isolated from infected children and comparative antimicrobial susceptibility of biofilm versus planktonic forms. Mol Diagnosis Ther. 2014;18(3):309–14. http://dx.doi.org/10.1007/s40291-013-0080-1
Urrútia G, Bonfill X. Declaración PRISMA: una propuesta para mejorar la publicación de revisiones sistemáticas y metaanálisis. Med Clin (Barc). 2010;135(11):507–11. http://dx.doi.org/10.1016/j.medcli.2010.01.015
Patel I, Patel V, Thakkar A, Kothari V. Microbial Biofilms: Microbes in Social Mode. Int J Agric Food Res. 2014;3(2):34–49.
Meervenne E Van, Weirdt R De, Coillie E Van, Devlieghere F, Herman L, Boon N. Biofilm models for the food industry: Hot spots for plasmid transfer? Pathog Dis. 2014;70(3):332–8. http://dx.doi.org/10.1111/2049-632X.12134
Suntharalingam P, Cvitkovitch DG. Quorum sensing in streptococcal biofilm formation. Trends Microbiol. 2005;13(1):3–6. http://dx.doi.org/10.1016/j.tim.2004.11.009
Schoenfelder SMK, Lange C, Eckart M, Hennig S, Kozytska S, Ziebuhr W. Success through diversity - How Staphylococcus epidermidis establishes as a nosocomial pathogen. Int J Med Microbiol [Internet]. Elsevier GmbH.; 2010;300(6):380–6. Available from: http://dx.doi.org/10.1016/j.ijmm.2010.04.011
Hooshangi S, Bentley WE. From unicellular properties to multicellular behavior: bacteria quorum sensing circuitry and applications. Curr Opin Biotechnol. 2008;19(6):550–5.
Siqueira JF, Rôças IN. Community as the unit of pathogenicity: An emerging concept as to the microbial pathogenesis of apical periodontitis. Oral Surgery, Oral Med Oral Pathol Oral Radiol Endodontology [Internet]. Mosby, Inc.; 2009;107(6):870–8. Available from: http://dx.doi.org/10.1016/j.tripleo.2009.01.044
Rosche B, Li XZ, Hauer B, Schmid A, Buehler K. Microbial biofilms: a concept for industrial catalysis? Trends Biotechnol. 2009;27(11):636–43. http://dx.doi.org/10.1016/j.tibtech.2009.08.001
Azakami H, Akashima HN, Kimichi HA, Oiri YN, Bisu SE, Ato AK. Involvement of N-Acetyl-. Biosci Biotechnol Biochem [Internet]. 2006;70(2):1–6. Available from: papers3://publication/uuid/5BB250C2-D3D3-45CD-81A5-52EDC1CDFA08
El Fertas-Aissani R, Messai Y, Alouache S, Bakour R. Virulence profiles and antibiotic susceptibility patterns of Klebsiella pneumoniae strains isolated from different clinical specimens. Pathol Biol (Paris) [Internet]. Elsevier Masson SAS; 2013;61(5):209–16. Available from: http://www.sciencedirect.com/science/article/pii/S036981141200185X
Srey S, Jahid IK, Ha S Do. Biofilm formation in food industries: A food safety concern. Food Control. Elsevier Ltd; 2013;31(2):572–85. http://dx.doi.org/10.1016/j.foodcont.2012.12.001
Kaper JB, O'Brien AD. Overview and Historical Perspectives. Microbiol Spectr [Internet]. 2014;2(2). Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=4290666&tool=pmcentrez&rendertype=abstract http://dx.doi.org/10.1128/microbiolspec.ehec-0028-2014
Cusumano CK, Hung CS, Chen SL, Hultgren SJ. Virulence plasmid harbored by uropathogenic Escherichia coli functions in acute stages of pathogenesis. Infect Immun. 2010;78(4):1457–67. http://dx.doi.org/10.1128/IAI.01260-09
Osman KM, Zolnikov TR, Samir A, Orabi A. Prevalence, pathogenic capability, virulence genes, biofilm formation, and antibiotic resistance of Listeria in goat and sheep milk confirms need of hygienic milking conditions. Pathog Glob Health [Internet]. 2014;108(1):21–9. Available from: http://www.maneyonline.com/doi/abs/10.1179/2047773213Y.0000000115 http://dx.doi.org/10.1179/2047773213Y.0000000115
Mikkelsen H, Hui K, Barraud N, Filloux A. The pathogenicity island encoded PvrSR/RcsCB regulatory network controls biofilm formation and dispersal in Pseudomonas aeruginosa PA14. Mol Microbiol. 2013;89(3):450–63. http://dx.doi.org/10.1111/mmi.12287
Ejrnæs K. Bacterial characteristics of importance for recurrent urinary tract infections caused by Escherichia coli. Dan Med Bull [Internet]. 2011;58(4):B4187. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21466767
Modrzewska B, Kurnatowski P. Review articles Selected pathogenic characteristics of fungi from the genus. Ann Parasitol. 2013;59(502):57–66.
Marguerettaz M, Dieppois G, Que YA, Ducret V, Zuchuat S, Perron K. Sputum containing zinc enhances carbapenem resistance, biofilm formation and virulence of Pseudomonas aeruginosa. Microb Pathog [Internet]. 2014;77:36–41. Available from: http://linkinghub.elsevier.com/retrieve/pii/S0882401014001636 http://dx.doi.org/10.1016/j.micpath.2014.10.011
Marrero K, Sánchez A, Rodríguez-Ulloa A, González LJ, Castellanos-Serra L, Paz-Lago D, et al. Anaerobic growth promotes synthesis of colonization factors encoded at the Vibrio pathogenicity island in Vibrio cholerae El Tor. Res Microbiol. 2009;160(1):48–56. http://dx.doi.org/10.1016/j.resmic.2008.10.005
Senadheera D, Cvitkovitch DG. Quorum sensing and biofilm formation by Streptococcus mutans. In: Advances in experimental medicine and biology. 2008. p. 178–88. http://dx.doi.org/10.1007/978-0-387-78885-2_12
Hebbelstrup B, Olsen KEP, Struve C, Krogfelt KA, Petersen AM. Epidemiology and clinical manifestations of enteroaggregative escherichia coli. Clin Microbiol Rev. 2014;27(3):614–30. http://dx.doi.org/10.1128/CMR.00112-13
Arini A, Feurtet-Mazel A, Morin S, Maury-Brachet R, Coste M, Delmas F. Remediation of a watershed contaminated by heavy metals: A 2-year field biomonitoring of periphytic biofilms. Sci Total Environ. 2012;425:242–53. http://dx.doi.org/10.1016/j.scitotenv.2012.02.067
Mizan MFR, Jahid IK, Ha S Do. Microbial biofilms in seafood: A food-hygiene challenge. Food Microbiol [Internet]. Elsevier Ltd; 2015;49:41–55. Available from: http://dx.doi.org/10.1016/j.fm.2015.01.009
Kalia VC. Quorum sensing inhibitors: An overview. Biotechnol Adv [Internet]. Elsevier Inc.; 2013;31(2):224–45. Available from: http://dx.doi.org/10.1016/j.biotechadv.2012.10.004
Seneviratne CJ, Jin L, Samaranayake LP. Biofilm lifestyle of Candida: A mini review. Oral Dis. 2008;14(7):582–90. http://dx.doi.org/10.1111/j.1601-0825.2007.01424.x
Lazar V. Quorum sensing in biofilms - How to destroy the bacterial citadels or their cohesion/power? Anaerobe [Internet]. Elsevier Ltd; 2011;17(6):280–5. Available from: http://dx.doi.org/10.1016/j.anaerobe.2011.03.023
Silva S, Negri M, Henriques M, Oliveira R, Williams DW, Azeredo J. Adherence and biofilm formation of non-Candida albicans Candida species. Trends Microbiol. 2011;19(5):241–7. http://dx.doi.org/10.1016/j.tim.2011.02.003
Bjarnsholt T, Alhede M, Alhede M, Eickhardt-Sørensen SR, Moser C, Kühl M, et al. The in vivo biofilm. Trends Microbiol. 2013;21(9):466–74. http://dx.doi.org/10.1016/j.tim.2013.06.002
Kaplan JB. Biofilm Dispersal : Mechanisms , Clinical Implications , and Potential Therapeutic Uses. J Dent Res. 2010;89(3):205–18. http://dx.doi.org/10.1177/0022034509359403
Fazeelath Banu. M., Geetha. R. Evaluation of antimicrobial efficacy of essential oils on streptococcus mutans. Int J Pharm Sci Rev Res [Internet]. 2015;33(1):119–21. Available from: http://www.embase.com/search/results?subaction=viewrecord&from=export&id=L605392610
Lembke C, Podbielski A, Jonas L, Hanski E, Hidalgo-grass C, Kreikemeyer B. Characterization of Biofilm Formation by Clinically Relevant Serotypes of Group A Streptococci Characterization of Biofilm Formation by Clinically Relevant Serotypes of Group A Streptococci †. Appl Environ Microbiol. 2006;72(4):2864–75. http://dx.doi.org/10.1128/AEM.72.4.2864-2875.2006
Brackman G, Coenye T. Inhibition of quorum sensing in Staphylococcus spp . Bentham Sci Publ. 2015;1–8.
Hall-Stoodley L, Stoodley P. Developmental regulation of microbial biofilms. Curr Opin Biotechnol. 2002;13(3):228–33. http://dx.doi.org/10.1016/S0958-1669(02)00318-X
Chaves Simões L, Simões M. Biofilms in drinking water: problems and solutions. RSC Adv. 2013;3(8):2520. http://dx.doi.org/10.1039/C2RA22243D
Rohde H, Frankenberger S, Zähringer U, Mack D. Structure, function and contribution of polysaccharide intercellular adhesin (PIA) to Staphylococcus epidermidis biofilm formation and pathogenesis of biomaterial-associated infections. Eur J Cell Biol. 2010;89(1):103–11. http://dx.doi.org/10.1016/j.ejcb.2009.10.005
Burmølle M, Ren D, Bjarnsholt T, Sørensen SJ. Interactions in multispecies biofilms: Do they actually matter? Trends Microbiol [Internet]. Elsevier Ltd; 2014;22(2):84–91. Available from: http://dx.doi.org/10.1016/j.tim.2013.12.004
O'Gara JP, Humphreys H. Staphylococcus epidermidis biofilms: importance and implications. Med Microbiol. 2001;50(2001):582–7. http://dx.doi.org/10.1099/0022-1317-50-7-582
Zhang K, Ou M, Wang W, Ling J. Effects of quorum sensing on cell viability in Streptococcus mutans biofilm formation. Biochem Biophys Res Commun [Internet]. Elsevier Inc.; 2009;379(4):933–8. Available from: http://dx.doi.org/10.1016/j.bbrc.2008.12.175
Mishra NN, Prasad T, Sharma N, Payasi A, Prasad R, Gupta DK, et al. Pathogenicity and drug resistance in Candida albicans and other yeast species. A review. Acta Microbiol Immunol Hung. 2007;54(3):201–35. http://dx.doi.org/10.1556/AMicr.54.2007.3.1
Cortés ME, Bonilla JC, Sinisterra RD. Biofilm formation, control and novel strategies for eradication. In: Science against microbial pathogens: communicating current research and technological advances. 2011. p. 896–905.
Danne C, Dramsi S. Pili of Gram-positive bacteria: Roles in host colonization. Res Microbiol [Internet]. Elsevier Masson SAS; 2012;163(9-10):645–58. Available from: http://dx.doi.org/10.1016/j.resmic.2012.10.012
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