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

被引:462
作者
Tomaras, AP
Dorsey, CW
Edelmann, RE
Actis, LA
机构
[1] Miami Univ, Dept Microbiol, Oxford, OH 45056 USA
[2] Miami Univ, Dept Bot, Oxford, OH 45056 USA
来源
MICROBIOLOGY-SGM | 2003年 / 149卷
关键词
D O I
10.1099/mic.0.26541-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:3473 / 3484
页数:12
相关论文
共 43 条
[1]  
BARCAK GJ, 1991, METHOD ENZYMOL, V204, P321
[2]   A STUDY OF MORAXELLA GROUP .2. OXIDATIVE-NEGATIVE SPECIES (GENUS ACINETOBACTER) [J].
BAUMANN, P ;
DOUDOROFF, M ;
STANIER, RY .
JOURNAL OF BACTERIOLOGY, 1968, 95 (05) :1520-+
[3]  
BERGOGNEBERENZI.E, 1996, ACINETOBACTER MICROB, P2
[4]   OPPORTUNISTIC NOSOCOMIAL MULTIPLY RESISTANT BACTERIAL-INFECTIONS - THEIR TREATMENT AND PREVENTION [J].
BERGOGNEBEREZIN, E ;
DECRE, D ;
JOLYGUILLOU, ML .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1993, 32 :39-47
[5]   Acinetobacter spp, as nosocomial pathogens: Microbiological, clinical, and epidemiological features [J].
BergogneBerezin, E ;
Towner, KJ .
CLINICAL MICROBIOLOGY REVIEWS, 1996, 9 (02) :148-+
[6]   TAXONOMY OF THE GENUS ACINETOBACTER WITH THE RECOGNITION OF ACINETOBACTER-BAUMANNII SP-NOV, ACINETOBACTER-HAEMOLYTICUS SP-NOV, ACINETOBACTER-JOHNSONII SP-NOV, AND ACINETOBACTER-JUNII SP-NOV AND EMENDED DESCRIPTIONS OF ACINETOBACTER-CALCOACETICUS AND ACINETOBACTER-LWOFFII [J].
BOUVET, PJM ;
GRIMONT, PAD .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1986, 36 (02) :228-240
[7]   CONFIRMATION OF THE FUR OPERATOR SITE BY INSERTION OF A SYNTHETIC OLIGONUCLEOTIDE INTO AN OPERON FUSION PLASMID [J].
CALDERWOOD, SB ;
MEKALANOS, JJ .
JOURNAL OF BACTERIOLOGY, 1988, 170 (02) :1015-1017
[8]   Biofilms: Survival mechanisms of clinically relevant microorganisms [J].
Donlan, RM ;
Costerton, JW .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (02) :167-+
[9]   Genetic and phenotypic analysis of Acinetobacter baumannii insertion derivatives generated with a transposome system [J].
Dorsey, CW ;
Tomaras, AP ;
Actis, LA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (12) :6353-6360
[10]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13