Staphylococcus biofilm components as targets for vaccines and drugs

被引:15
作者
Visai, L.
Arciola, C. R.
Pietrocola, G.
Rindi, S.
Oliver, P.
Speziale, P.
机构
[1] Univ Pavia, Dept Biochem, I-27100 Pavia, Italy
[2] Rizzoli Orthoped Inst, Res Unit Implant Infect, Bologna, Italy
[3] Univ Bologna, Dept Expt Pathol, Bologna, Italy
关键词
staphylococcus; Biofilm; adhesins; vaccine;
D O I
10.1177/039139880703000911
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Staphylococci have become the most common cause of nosocomial infections, especially in patients with predisposing factors such as indwelling or implanted foreign polymer bodies. The pathogenesis of foreign-body associated infections with S.aureus and S. epidermidis is mainly related to the ability of these bacteria to form thick, adherent multilayered biofilms. In a biofilm, staphylococci are protected against antibiotic treatment and attack from the immune system, thus making eradication of the infections problematic. This necessitates the discovery of novel prophylactic and therapeutic strategies to treat these infections. In this review, we provide an overview of staphylococcal biofilm components and discuss new possible approaches to controlling these persistent biofilm-dwelling bacteria.
引用
收藏
页码:813 / 819
页数:7
相关论文
共 46 条
[21]   Enzymatic detachment of Staphylococcus epidermidis biofilms [J].
Kaplan, JB ;
Ragunath, C ;
Velliyagounder, K ;
Fine, DH ;
Ramasubbu, N .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (07) :2633-2636
[22]   Bap:: A family of surface proteins involved in biofilm formation [J].
Lasa, I ;
Penadés, JR .
RESEARCH IN MICROBIOLOGY, 2006, 157 (02) :99-107
[23]   Conversion of Staphylococcus epidermidis strains from commensal to invasive by expression of the ica locus encoding production of biofilm exopolysaccharide [J].
Li, HL ;
Xu, L ;
Wang, JP ;
Wen, YM ;
Voung, C ;
Otto, M ;
Gao, Q .
INFECTION AND IMMUNITY, 2005, 73 (05) :3188-3191
[24]   Biofilm formation in medical device-related infection [J].
Mack, D. ;
Rohde, H. ;
Harris, L. G. ;
Davies, A. P. ;
Horstkotte, M. A. ;
Knobloch, J. K-M. .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 2006, 29 (04) :343-359
[25]   The intercellular adhesin involved in biofilm accumulation of Staphylococcus epidermidis is a linear beta-1,6-linked glucosaminoglycan: Purification and structural analysis [J].
Mack, D ;
Fischer, W ;
Krokotsch, A ;
Leopold, K ;
Hartmann, R ;
Egge, H ;
Laufs, R .
JOURNAL OF BACTERIOLOGY, 1996, 178 (01) :175-183
[26]  
Maira-Litran T, 2004, VACCINE, V22, P872, DOI 10.1016/j.vaccine.2003.11.033
[27]   Quorum-sensing control in Staphylococci - a target for antimicrobial drug therapy? [J].
Otto, M .
FEMS MICROBIOLOGY LETTERS, 2004, 241 (02) :135-141
[28]   The Staphylococcus aureus surface protein SasG and its homologues promote bacterial adherence to human desquamated nasal epithelial cells [J].
Roche, FM ;
Meehan, M ;
Foster, TJ .
MICROBIOLOGY-SGM, 2003, 149 :2759-2767
[29]   Induction of Staphylococcus epidermidis biofilm formation via proteolytic processing of the accumulation-associated protein by staphylococcal and host proteases [J].
Rohde, H ;
Burdelski, C ;
Bartscht, K ;
Hussain, M ;
Buck, F ;
Horstkotte, MA ;
Knobloch, JKM ;
Heilmann, C ;
Herrmann, M ;
Mack, D .
MOLECULAR MICROBIOLOGY, 2005, 55 (06) :1883-1895
[30]   The molecular basis of fibronectin-mediated bacterial adherence to host cells [J].
Schwarz-Linek, U ;
Höök, M ;
Potts, JR .
MOLECULAR MICROBIOLOGY, 2004, 52 (03) :631-641