Diversity of biofilms produced by quorum-sensing-deficient clinical isolates of Pseudomonas aeruginosa

被引:29
作者
Schaber, J. Andy
Hammond, Adrienne
Carty, Nancy L.
Williams, Simon C.
Colmer-Hamood, Jane A.
Burrowes, Ben H.
Dhevan, Vijian
Griswold, John A.
Hamood, Abdul N. [1 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Dept Microbiol & Immunol, Lubbock, TX 79430 USA
[2] Texas Tech Univ, Hlth Sci Ctr, Dept Surg, Lubbock, TX 79430 USA
[3] Texas Tech Univ, Hlth Sci Ctr, Dept Cell Biol & Biochem, Lubbock, TX 79430 USA
[4] Texas Tech Univ, Hlth Sci Ctr, Sch Med, Lubbock, TX 79430 USA
关键词
D O I
10.1099/jmm.0.47031-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The quorum-sensing (QS) systems control several virulence attributes of Pseudomonas aeruginosa. Five QS-deficient P. aeruginosa clinical isolates (CI) that were obtained from wound (CI-1), tracheal (CI-2, CI-3, CI-4) and urinary tract (CI-5) infections had previously been characterized. In this study, a flow-through continuous-culture system was utilized to examine in detail the biofilms formed by these isolates in comparison with the P. aeruginosa prototrophic strain PAO1. Analysis of the biofilms by confocal laser scanning microscopy and COMSTAT image analysis at 1 and 7 days post-inoculation showed that the isolates produced diverse biofilms. In comparison with PAO1, the CI produced biofilms that scarcely or partially covered the surface at day 1, although CI-1 produced larger microcolonies. At day 7, CI-2 and CI-4 produced mature biofilms denser than that produced by PAO1, while the biofilm formed by CI-1 changed very little from day 1. CI-1 was defective in both swarming and twitching motilities, and immunoblotting analysis confirmed that it produced a reduced level of PiIA protein. The twitching-motility defect of CI-1 was not complemented by a plasmid carrying intact pilA. In the 48 In colony biofilm assay, the Cl varied in susceptibility to imipenem, gentamicin and piperacillin/tazobactam. These results suggest that: (1) the isolates produced biofilms with different structures and densities from that of PAO1; (2) biofilm formation by the isolates was not influenced by either the isolation site or the QS deficiencies of the isolates; (3) the behaviour of CI-1 in the different biofilm systems may be due to its lack of swarming motility and type IV pilus-related twitching motility.
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页码:738 / 748
页数:11
相关论文
共 44 条
[21]   Heterogeneity of biofilms formed by nonmucoid Pseudomonas aeruginosa isolates from patients with cystic fibrosis [J].
Lee, B ;
Haagensen, JAJ ;
Ciofu, O ;
Andersen, JB ;
Hoiby, N ;
Molin, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (10) :5247-5255
[22]   CHARACTERIZATION OF A LOCUS DETERMINING THE MUCOID STATUS OF PSEUDOMONAS-AERUGINOSA - ALGU SHOWS SEQUENCE SIMILARITIES WITH A BACILLUS SIGMA-FACTOR [J].
MARTIN, DW ;
HOLLOWAY, BW ;
DERETIC, V .
JOURNAL OF BACTERIOLOGY, 1993, 175 (04) :1153-1164
[23]   Putative exopolysaccharide synthesis genes influence Pseudomonas aeruginosa biofilm development [J].
Matsukawa, M ;
Greenberg, EP .
JOURNAL OF BACTERIOLOGY, 2004, 186 (14) :4449-4456
[24]   Catheter-related urinary tract infection [J].
Nicolle, LE .
DRUGS & AGING, 2005, 22 (08) :627-639
[25]   Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development [J].
O'Toole, GA ;
Kolter, R .
MOLECULAR MICROBIOLOGY, 1998, 30 (02) :295-304
[26]   Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways:: a genetic analysis [J].
O'Toole, GA ;
Kolter, R .
MOLECULAR MICROBIOLOGY, 1998, 28 (03) :449-461
[27]   F116 - DNA BACTERIOPHAGE SPECIFIC FOR PILI OF PSEUDOMONAS-AERUGINOSA STRAIN PAO [J].
PEMBERTON, JM .
VIROLOGY, 1973, 55 (02) :558-560
[28]  
Pollack M, 2000, PRINCIPLES PRACTICE, V5th ed.
[29]   Clinical implications of basic research: Biofilms, antimicrobial resistance, and airway infection [J].
Prince, AS .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (14) :1110-1111
[30]   Type III protein secretion is associated with death in lower respiratory and systemic Pseudomonas aeruginosa infections [J].
Roy-Burman, A ;
Savel, RH ;
Racine, S ;
Swanson, BL ;
Revadigar, NS ;
Fujimoto, J ;
Sawa, T ;
Frank, DW ;
Wiener-Kronish, JP .
JOURNAL OF INFECTIOUS DISEASES, 2001, 183 (12) :1767-1774