Influence of batch or fed-batch growth on Staphylococcus epidermidis biofilm formation

被引:32
作者
Cerca, N
Pier, GB
Vilanova, M
Oliveira, R
Azeredo, J
机构
[1] Univ Minho, Ctr Engn Biol, P-4710057 Braga, Portugal
[2] Harvard Univ, Brigham & Womens Hosp, Channing Lab, Med Sch,Dept Med, Boston, MA 02115 USA
[3] Univ Porto, Inst Ciencias Biomed Abel Salazar, P-4100 Oporto, Portugal
关键词
acrylic; haemagglutination; medical devices; nosocomial infections; PNAG; Staphylococcus epidermidis;
D O I
10.1111/j.1472-765X.2004.01601.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
Aims: To make a quantitative evaluation of the differences in biofilm formation by Staphylococcus epidermidis using batch and fed-batch growth systems and to correlate this with production of the major biofilm polysaccharide, poly-N-acetyl glucosamine (PNAG). Methods and Results: Dry weight measurements of biofilms formed in batch and fed-batch conditions were compared with haemagglutination titres, which measure the amount of PNAG produced. Strains grown in batch systems developed less biofilm than when grown in fed-batch systems. A good correlation was found between the amount of biofilm formed in fed-batch systems and the haemagglutination titres. Conclusions: Differences in biofilm formation and PNAG production by S. epidermidis are dependent on the availability of nutrients, with higher availability correlating with more biofilm and PNAG production. Significance of and Impact of the Study: Comparisons of the formation of biofilms by S. epidermidis are dependent on choosing an appropriate biofilm growth system. Comparability or disparity of conclusions among different investigations will be strongly influenced by which mode S. epidermidis biofilms are formed.
引用
收藏
页码:420 / 424
页数:5
相关论文
共 18 条
[1]   Laboratory methods for studies of bacterial adhesion [J].
An, YH ;
Friedman, RJ .
JOURNAL OF MICROBIOLOGICAL METHODS, 1997, 30 (02) :141-152
[2]   The intercellular adhesion (ica) locus is present in Staphylococcus aureus and is required for biofilm formation [J].
Cramton, SE ;
Gerke, C ;
Schnell, NF ;
Nichols, WW ;
Götz, F .
INFECTION AND IMMUNITY, 1999, 67 (10) :5427-5433
[3]   Biofilms: Survival mechanisms of clinically relevant microorganisms [J].
Donlan, RM ;
Costerton, JW .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (02) :167-+
[4]  
EVERAERT EP, 1997, MICROBIOLOGY, V143, P1569
[5]   Screening for Staphylococcus epidermidis markers discriminating between skin-flora strains and those responsible for infections of joint prostheses [J].
Galdbart, JO ;
Allignet, J ;
Tung, HS ;
Rydèn, C ;
El Solh, N .
JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (01) :351-355
[6]   Characterization of Tn917 insertion mutants of Staphylococcus epidermidis affected in biofilm formation [J].
Heilmann, C ;
Gerke, C ;
PerdreauRemington, F ;
Gotz, F .
INFECTION AND IMMUNITY, 1996, 64 (01) :277-282
[7]   The control of Staphylococcus epidermidis biofilm formation and in vivo infection rates by covalently bound furanones [J].
Hume, EBH ;
Baveja, J ;
Muir, BW ;
Schubert, TL ;
Kumar, N ;
Kjelleberg, S ;
Griesser, HJ ;
Thissen, H ;
Read, R ;
Poole-Warren, LA ;
Schindhelm, K ;
Willcox, MDP .
BIOMATERIALS, 2004, 25 (20) :5023-5030
[8]   Isolation, structural characterization, and immunological evaluation of a high-molecular-weight exopolysaccharide from Staphylococcus aureus [J].
Joyce, JG ;
Abeygunawardana, C ;
Xu, QW ;
Cook, JC ;
Hepler, R ;
Przysiecki, CT ;
Grimm, KM ;
Roper, K ;
Ip, CCY ;
Cope, L ;
Montgomery, D ;
Chang, M ;
Campie, S ;
Brown, M ;
McNeely, TB ;
Zorman, J ;
Maira-Litrán, T ;
Pier, GB ;
Keller, PM ;
Jansen, KU ;
Mark, GE .
CARBOHYDRATE RESEARCH, 2003, 338 (09) :903-922
[9]   Association of biofilm production of coagulase-negative staphylococci with expression of a specific polysaccharide intercellular adhesin [J].
Mack, D ;
Haeder, M ;
Siemssen, N ;
Laufs, R .
JOURNAL OF INFECTIOUS DISEASES, 1996, 174 (04) :881-884
[10]   Essential functional role of the polysaccharide intercellular adhesin of Staphylococcus epidermidis in hemagglutination [J].
Mack, D ;
Riedewald, J ;
Rohde, H ;
Magnus, T ;
Feucht, HH ;
Elsner, HA ;
Laufs, R ;
Rupp, ME .
INFECTION AND IMMUNITY, 1999, 67 (02) :1004-1008