Pseudomonas biofilm formation and antibiotic resistance are linked to phenotypic variation

被引:739
作者
Drenkard, E
Ausubel, FM [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/416740a
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Colonization of the lungs of cystic fibrosis (CF) patients by the opportunistic bacterial pathogen Pseudomonas aeruginosa is the principal cause of mortality in CF populations(1,2). Pseudomonas aeruginosa infections generally persist despite the use of long-term antibiotic therapy(1,3). This has been explained by postulating that P. aeruginosa forms an antibiotic-resistant biofilm(4,5) consisting of bacterial communities embedded in an exopolysaccharide matrix. Alternatively, it has been proposed that resistant P. aeruginosa variants may be selected in the CF respiratory tract by antimicrobial therapy itself(1,6). Here we report that both explanations are correct, and are interrelated. We found that antibiotic-resistant phenotypic variants of P. aeruginosa with enhanced ability to form biofilms arise at high frequency both in vitro and in the lungs of CF patients. We also identified a regulatory protein (PvrR) that controls the conversion between antibiotic-resistant and antibiotic-susceptible forms. Compounds that affect PvrR function could have an important role in the treatment of CF infections.
引用
收藏
页码:740 / 743
页数:5
相关论文
共 28 条
[1]   Determination of minimum inhibitory concentrations [J].
Andrews, JM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2001, 48 :5-16
[2]  
Ausubel F.M., 1992, SHORT PROTOCOLS MOL, V2nd
[3]   Green fluorescent protein as a marker for Pseudomonas spp. [J].
Bloemberg, GV ;
OToole, GA ;
Lugtenberg, BJJ ;
Kolter, R .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (11) :4543-4551
[4]  
Christensen BB, 1999, METHOD ENZYMOL, V310, P20
[5]   Bacterial biofilms: A common cause of persistent infections [J].
Costerton, JW ;
Stewart, PS ;
Greenberg, EP .
SCIENCE, 1999, 284 (5418) :1318-1322
[6]   CONSTRUCTION OF AN EAE DELETION MUTANT OF ENTEROPATHOGENIC ESCHERICHIA-COLI BY USING A POSITIVE-SELECTION SUICIDE VECTOR [J].
DONNENBERG, MS ;
KAPER, JB .
INFECTION AND IMMUNITY, 1991, 59 (12) :4310-4317
[7]   BACTERIAL-CELL SURFACE HYDROPHOBICITY PROPERTIES IN THE MEDIATION OF INVITRO ADHESION BY THE RABBIT ENTERIC PATHOGEN ESCHERICHIA-COLI STRAIN RDEC-1 [J].
DRUMM, B ;
NEUMANN, AW ;
POLICOVA, Z ;
SHERMAN, PM .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (05) :1588-1594
[8]   REPLICATION OF AN ORIGIN-CONTAINING DERIVATIVE OF PLASMID RK2 DEPENDENT ON A PLASMID FUNCTION PROVIDED IN TRANS [J].
FIGURSKI, DH ;
HELINSKI, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (04) :1648-1652
[9]   Microbial pathogenesis in cystic fibrosis: Mucoid Pseudomonas aeruginosa and Burkholderia cepacia [J].
Govan, JRW ;
Deretic, V .
MICROBIOLOGICAL REVIEWS, 1996, 60 (03) :539-+
[10]   IDENTIFICATION AND CHARACTERIZATION OF A LOCUS WHICH REGULATES MULTIPLE FUNCTIONS IN PSEUDOMONAS-TOLAASII, THE CAUSE OF BROWN BLOTCH DISEASE OF AGARICUS-BISPORUS [J].
GREWAL, SIS ;
HAN, B ;
JOHNSTONE, K .
JOURNAL OF BACTERIOLOGY, 1995, 177 (16) :4658-4668