Biofilm formation in Streptococcus pneumoniae

被引:66
作者
Domenech, Mirian
Garcia, Ernesto
Moscoso, Miriam [1 ]
机构
[1] CSIC, Ctr Invest Biol, Dept Microbiol Mol & Biol Infecc, Madrid, Spain
关键词
OTITIS-MEDIA; IN-VITRO; CAPSULAR POLYSACCHARIDE; HAEMOPHILUS-INFLUENZAE; BACTERIAL PATHOGENS; EPITHELIAL-CELLS; ADHERENCE; CHILDREN; VARIANTS; SYSTEM;
D O I
10.1111/j.1751-7915.2011.00294.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Biofilm-grown bacteria are refractory to antimicrobial agents and show an increased capacity to evade the host immune system. In recent years, studies have begun on biofilm formation by Streptococcus pneumoniae, an important human pathogen, using a variety of in vitro model systems. The bacterial cells in these biofilms are held together by an extracellular matrix composed of DNA, proteins and, possibly, polysaccharide(s). Although neither the precise nature of these proteins nor the composition of the putative polysaccharide(s) is clear, it is known that choline-binding proteins are required for successful biofilm formation. Further, many genes appear to be involved, although the role of each appears to vary when biofilms are produced in batch or continuous culture. Prophylactic and therapeutic measures need to be developed to fight S. pneumoniae biofilm formation. However, much care needs to be taken when choosing strains for such studies because different S. pneumoniae isolates can show remarkable genomic differences. Multispecies and in vivo biofilm models must also be developed to provide a more complete understanding of biofilm formation and maintenance.
引用
收藏
页码:455 / 465
页数:11
相关论文
共 76 条
[1]   Phenotypic characterization of Streptococcus pneumoniae biofilm development [J].
Allegrucci, M ;
Hu, FZ ;
Shen, K ;
Hayes, J ;
Ehrlich, GD ;
Post, JC ;
Sauer, K .
JOURNAL OF BACTERIOLOGY, 2006, 188 (07) :2325-2335
[2]   Formation of Streptococcus pneumoniae non-phase-variable colony variants is due to increased mutation frequency present under biofilm growth conditions [J].
Allegrucci, Magee ;
Sauer, Karin .
JOURNAL OF BACTERIOLOGY, 2008, 190 (19) :6330-6339
[3]   Characterization of colony morphology variants isolated from Streptococcus pneumoniae biofilms [J].
Allegrucci, Magee ;
Sauer, Karin .
JOURNAL OF BACTERIOLOGY, 2007, 189 (05) :2030-2038
[4]   The use of phages for the removal of infectious biofilms [J].
Azeredo, J. ;
Sutherland, I. W. .
CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2008, 9 (04) :261-266
[5]   The pneumococcal response to oxidative stress includes a role for Rgg [J].
Bortoni, Magda E. ;
Terra, Vanessa S. ;
Hinds, Jason ;
Andrew, Peter W. ;
Yesilkaya, Hasan .
MICROBIOLOGY-SGM, 2009, 155 :4123-4134
[6]   Biofilms:: the matrix revisited [J].
Branda, SS ;
Vik, Å ;
Friedman, L ;
Kolter, R .
TRENDS IN MICROBIOLOGY, 2005, 13 (01) :20-26
[7]   Medical Biofilms [J].
Bryers, James D. .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 100 (01) :1-18
[8]   The use of Sorbarod biofilms to study the antimicrobial susceptibility of a strain of Streptococcus pneumoniae [J].
Budhani, RK ;
Struthers, JK .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 40 (04) :601-602
[9]   Interaction of Streptococcus pneumoniae and Moraxella catarrhalis:: Investigation of the indirect pathogenic role of β-lactamase-producing moraxellae by use of a continuous-culture biofilm system [J].
Budhani, RK ;
Struthers, JK .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (10) :2521-2526
[10]   Contribution of serotype and genetic background to biofilm formation by Streptococcus pneumoniae [J].
Camilli, R. ;
Pantosti, A. ;
Baldassarri, L. .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2011, 30 (01) :97-102