Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 149 (2003), 3473-3484; DOI  10.1099/mic.0.26541-0
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tomaras, A. P.
Right arrow Articles by Actis, L. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tomaras, A. P.
Right arrow Articles by Actis, L. A.
Agricola
Right arrow Articles by Tomaras, A. P.
Right arrow Articles by Actis, L. A.
Microbiology 149 (2003), 3473-3484; DOI  10.1099/mic.0.26541-0
© 2003 Society for General Microbiology

Attachment to and biofilm formation on abiotic surfaces by Acinetobacter baumannii: involvement of a novel chaperone-usher pili assembly system

Andrew P. Tomaras1, Caleb W. Dorsey1,{dagger}, Richard E. Edelmann2 and Luis A. Actis1

1 Departments of Microbiology, Miami University, 40 Pearson Hall, Oxford, OH 45056, USA
2 Departments of Botany, Miami University, 40 Pearson Hall, Oxford, OH 45056, USA

Correspondence
Luis A. Actis
actisla{at}muohio.edu

Acinetobacter baumannii causes severe infections in compromised patients, survives on abiotic surfaces in hospital environments and colonizes different medical devices. In this study the analysis of the processes involved in surface attachment and biofilm formation by the prototype strain 19606 was initiated. This strain attaches to and forms biofilm structures on plastic and glass surfaces, particularly at the liquid–air interface of cultures incubated stagnantly. The cell aggregates, which contain cell stacks separated by water channels, formed under different culture conditions and were significantly enhanced under iron limitation. Electron and fluorescence microscopy showed that pili and exopolysaccharides are part of the cell aggregates formed by this strain. Electron microscopy of two insertion derivatives deficient in attachment and biofilm formation revealed the disappearance of pili-like structures and DNA sequencing analysis showed that the transposon insertions interrupted genes with the highest similarity to hypothetical genes found in Pseudomonas aeruginosa, Pseudomonas putida and Vibrio parahaemolyticus. Although the products of these genes, which have been named csuC and csuE, have no known functions, they are located within a polycistronic operon that includes four other genes, two of which encode proteins related to chaperones and ushers involved in pili assembly in other bacteria. Introduction of a copy of the csuE parental gene restored the adherence phenotype and the presence of pili on the cell surface of the csuE mutant, but not that of the csuC derivative. These results demonstrate that the expression of a chaperone-usher secretion system, some of whose components appear to be acquired from unrelated sources, is required for pili formation and the concomitant attachment to plastic surfaces and the ensuing formation of biofilms by A. baumannii cells.


Abbreviations: DIP, 2,2'-dipyridyl; EDDHA, ethylenediamine-di-(o-hydroxyphenyl) acetic acid; GFP, green fluorescent protein; SEM, scanning electron microscopy; TEM, transmission electron microscopy

The GenBank accession number for the sequence reported in this paper is AY241696.

{dagger}Present address: Department of Medical Microbiology and Immunology, Texas A&M University Health Science Center, College Station, TX, USA.




This article has been cited by other articles:


Home page
Clin. Microbiol. Rev.Home page
A. Y. Peleg, H. Seifert, and D. L. Paterson
Acinetobacter baumannii: Emergence of a Successful Pathogen
Clin. Microbiol. Rev., July 1, 2008; 21(3): 538 - 582.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
C. Niu, K. M. Clemmer, R. A. Bonomo, and P. N. Rather
Isolation and Characterization of an Autoinducer Synthase from Acinetobacter baumannii
J. Bacteriol., May 1, 2008; 190(9): 3386 - 3392.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
T. W. Loehfelm, N. R. Luke, and A. A. Campagnari
Identification and Characterization of an Acinetobacter baumannii Biofilm-Associated Protein
J. Bacteriol., February 1, 2008; 190(3): 1036 - 1044.
[Abstract] [Full Text] [PDF]


Home page
Microbiol. Mol. Biol. Rev.Home page
S.-P. Nuccio and A. J. Baumler
Evolution of the Chaperone/Usher Assembly Pathway: Fimbrial Classification Goes Greek
Microbiol. Mol. Biol. Rev., December 1, 2007; 71(4): 551 - 575.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
T.-L. Chen, C.-L. Chuang, L.-K. Siu, C.-P. Fung, and W.-L. Cho
Genomic species identification is important to delineate the pathological characteristics of Acinetobacter in tunnelled, cuffed haemodialysis catheter-related bacteraemia
Nephrol. Dial. Transplant., March 1, 2007; 22(3): 936 - 938.
[Full Text] [PDF]


Home page
Genes Dev.Home page
M. G. Smith, T. A. Gianoulis, S. Pukatzki, J. J. Mekalanos, L. N. Ornston, M. Gerstein, and M. Snyder
New insights into Acinetobacter baumannii pathogenesis revealed by high-density pyrosequencing and transposon mutagenesis
Genes & Dev., March 1, 2007; 21(5): 601 - 614.
[Abstract] [Full Text] [PDF]


Home page
J Med MicrobiolHome page
E. R. Rhodes, C. J. Shoemaker, S. M. Menke, R. E. Edelmann, and L. A. Actis
Evaluation of different iron sources and their influence in biofilm formation by the dental pathogen Actinobacillus actinomycetemcomitans
J. Med. Microbiol., January 1, 2007; 56(1): 119 - 128.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
D. M. Russo, A. Williams, A. Edwards, D. M. Posadas, C. Finnie, M. Dankert, J. A. Downie, and A. Zorreguieta
Proteins Exported via the PrsD-PrsE Type I Secretion System and the Acidic Exopolysaccharide Are Involved in Biofilm Formation by Rhizobium leguminosarum.
J. Bacteriol., June 1, 2006; 188(12): 4474 - 4486.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
O. Gohl, A. Friedrich, M. Hoppert, and B. Averhoff
The Thin Pili of Acinetobacter sp. Strain BD413 Mediate Adhesion to Biotic and Abiotic Surfaces
Appl. Envir. Microbiol., February 1, 2006; 72(2): 1394 - 1401.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
I. Vallet, S. P. Diggle, R. E. Stacey, M. Camara, I. Ventre, S. Lory, A. Lazdunski, P. Williams, and A. Filloux
Biofilm Formation in Pseudomonas aeruginosa: Fimbrial cup Gene Clusters Are Controlled by the Transcriptional Regulator MvaT
J. Bacteriol., May 1, 2004; 186(9): 2880 - 2890.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2003 Society for General Microbiology.