Publication:
Pseudomonas aeruginosa: A model for biofilm formation

dc.contributor.author McDougald, Diane en_US
dc.contributor.author Klebensberger, Janosch en_US
dc.contributor.author Tolker-Nielsen, Tim en_US
dc.contributor.author Webb, Jeremy S. en_US
dc.contributor.author Conibear, Tim en_US
dc.contributor.author Rice, Scott A. en_US
dc.contributor.author Kirov, Sylvia M. en_US
dc.contributor.author Matz, Carsten en_US
dc.contributor.author Kjelleberg, Staffan en_US
dc.contributor.other Rhem, B. en_US
dc.date.accessioned 2021-11-25T13:07:07Z
dc.date.available 2021-11-25T13:07:07Z
dc.date.issued 2008 en_US
dc.description.abstract Much of the fundamental understanding of microbial physiology is based on laboratory studies of freely suspended cells. While these studies have been essential for our foundational understanding of the genetics, physiology and behavior of microbes, it is now recognized that a majority of bacterial cells in nature exist in biofilms [1] associated with surfaces or as floating cell aggregates. In fact, it has recently been proposed that microbial communities originally developed on surfaces, including the first bacterial and archael cells, and that the planktonic cell phenotype evolved as a dispersal mechanism [2]. Hallmarks of cells residing in biofilm communities are increased metabolic efficiency [3] as well as increased resistance to environmental stresses such as desiccation, ultraviolet radiation and oxidative stress [4–6]. This correlation has dramatic consequences as residing in aggregates has been shown to confer increased resistance of bacterial cells also to biocides such as antibiotics, disinfectants and detergents [7–9]. In addition, once established, these biofilms are able to resist invasion by other organisms and predation by protozoans in nature or host immune cells in the human body [5,6,10]. This is especially problematic as it is also recognized that the majority of bacterial infections involve biofilms [11]. The recent explosion of research in the field of biofilm biology has led to an enhanced appreciation for the multicellular aspects of microbiology and has resulted in the general acceptance of a model of the biofilm mode of life. Pseudomonas aeruginosa has become a model organism for the study of biofilms due to its metabolic versatility and variability in its response to environmental signals, which promotes successful colonization of different habitats and growth under varying environmental conditions [12,13]. This ability is likely a reflection of its large genome, allowing for metabolic plasticity and quick responses to varying stimuli. P. aeruginosa is also a human pathogen that causes infection in burn patients, and is the predominant cause of lung infections and mortality in patients with cystic fibrosis (CF) [14,15]. This chapter will address various aspects of biofilm development, dispersal and resistance, and its role in the infection process. en_US
dc.identifier.isbn 978-3-527-31914-5 en_US
dc.identifier.uri http://hdl.handle.net/1959.4/11409
dc.language English
dc.language.iso EN en_US
dc.publisher Wiley-VCH Verlag GmbH and Co. en_US
dc.rights CC BY-NC-ND 3.0 en_US
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/3.0/au/ en_US
dc.source Legacy MARC en_US
dc.subject.other cystic fibrosis en_US
dc.subject.other Pseudomonas en_US
dc.subject.other biofilm en_US
dc.subject.other Pseudomonas aeruginosa en_US
dc.title Pseudomonas aeruginosa: A model for biofilm formation en_US
dc.type Book Chapter en
dcterms.accessRights metadata only access
dspace.entity.type Publication en_US
unsw.accessRights.uri http://purl.org/coar/access_right/c_14cb
unsw.publisher.place Weinheim en_US
unsw.relation.faculty Science
unsw.relation.ispartofpagefrompageto 215-253 en_US
unsw.relation.ispartoftitle Pseudomonas. Model Organism, Pathogen, Workhorse en_US
unsw.relation.originalPublicationAffiliation McDougald, Diane, Centre for Marine Biofouling & Bioinnovation, UNSW en_US
unsw.relation.originalPublicationAffiliation Klebensberger, Janosch, Centre for Marine Biofouling & Bioinnovation, UNSW en_US
unsw.relation.originalPublicationAffiliation Tolker-Nielsen, Tim, Centre for Biomedical Microbiology, BioCentrum-DTU, Technical University of Denmark, Lyngby, Denmark en_US
unsw.relation.originalPublicationAffiliation Webb, Jeremy S., School of Biological Sciences, University of Southampton, Southampton, UK en_US
unsw.relation.originalPublicationAffiliation Conibear, Tim, School of Biological Sciences, University of Southampton, Southampton, UK en_US
unsw.relation.originalPublicationAffiliation Rice, Scott A., Centre for Marine Biofouling & Bioinnovation, UNSW en_US
unsw.relation.originalPublicationAffiliation Kirov, Sylvia M., School of Medicine (Pathology), University of Tasmania, Hobart, Australia en_US
unsw.relation.originalPublicationAffiliation Matz, Carsten, GBF - National Research Centre for Biotechnology, Center for Biomedical Microbiology en_US
unsw.relation.originalPublicationAffiliation Kjelleberg, Staffan, Centre for Marine Biofouling & Bioinnovation, UNSW en_US
unsw.relation.school School of Biological, Earth & Environmental Sciences *
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