Prevention of vascular graft infections after impregnation with pathogen-specific bacteriophages: an in vitro experimental model

被引:0
作者
Bisdas, T. [1 ]
Bagaev, E. [1 ]
Burgwitz, K. [1 ]
Marsch, G. [1 ]
Wilhelmi, M. [1 ]
Haverich, A. [1 ]
Teebken, O. E. [1 ]
机构
[1] Hannover Med Sch, Klin Herz Thorax Transplantat & Gefasschirurg, D-30625 Hannover, Germany
来源
GEFASSCHIRURGIE | 2011年 / 16卷 / 06期
关键词
Vascular graft infection; Impregnation; Antibiotics; Bacteriophages; Prosthesis infection; PSEUDOMONAS-AERUGINOSA; BIOFILMS; SUSCEPTIBILITY;
D O I
10.1007/s00772-011-0950-y
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The in vitro antibacterial effect of bacteriophages (BPH) as impregnation agents was tested for prevention of vascular graft infections. Pathogen-specific BPHs for S. epidermidis, S. aureus, P. aeruginosa and E. coli were tested. In each case 7 segments of prosthesis tissue sized 1 cm(2) were impregnated for each group (15 min), a further 7 segments were used as a positive control and 4 as a negative control and 5 segments were observed under scanning electron microscopy (SEM). After 24 h incubation (37A degrees C) segments were washed 3 times in 20 ml PBS. Viable adherent bacteria were released by sonification and the optical density (OD) of the bacterial solutions was measured. A total of 6 dilution steps of 1:10 of the solution was made and incubated for 24 h (37A degrees C) on agar plates. Colony formed units (CFU) after the 4(th) and 6(th) dilution were counted. Impregnation with BPHs against S. epidermidis and E. coli showed a statistically significant reduction of OD, CFU-4 and CFU-6. For S. aureus and P. aeruginosa, all parameters were comparable to the positive control group. The microbiological findings were confirmed by SEM bio-films. The pathogen-specific BPHs tested were effective in prevention of in vitro graft infections caused by S. epidermidis and E. coli but not by S. aureus and P. aeruginosa.
引用
收藏
页码:387 / 394
页数:8
相关论文
共 29 条
[1]  
Bisdas T, 2010, GEFASSCHIRURGIE, V15, P448, DOI 10.1007/s00772-010-0843-5
[2]   Cryopreserved arterial homografts vs silver-coated Dacron grafts for abdominal aortic infections with intraoperative evidence of microorganisms [J].
Bisdas, Theodosios ;
Wilhelmi, Mathias ;
Haverich, Axel ;
Teebken, Omke E. .
JOURNAL OF VASCULAR SURGERY, 2011, 53 (05) :1274-1281
[3]   Bacteriophage therapy rescues mice bacteremic from a clinical isolate of vancomycin-resistant Enterococcus faecium [J].
Biswas, B ;
Adhya, S ;
Washart, P ;
Paul, B ;
Trostel, AN ;
Powell, B ;
Carlton, R ;
Merril, CR .
INFECTION AND IMMUNITY, 2002, 70 (01) :204-210
[4]   Susceptibility of Staphylococcus epidermidis planktonic cells and biofilms to the lytic action of staphylococcus bacteriophage K [J].
Cerca, N. ;
Oliveira, R. ;
Azeredo, J. .
LETTERS IN APPLIED MICROBIOLOGY, 2007, 45 (03) :313-317
[5]   Daptomycin and Rifampin Alone and in Combination Prevent Vascular Graft Biofilm Formation and Emergence of Antibiotic Resistance in a Subcutaneous Rat Pouch Model of Staphylococcal Infection [J].
Cirioni, O. ;
Mocchegiani, F. ;
Ghiselli, R. ;
Silvestri, C. ;
Gabrielli, E. ;
Marchionni, E. ;
Orlando, F. ;
Nicolini, D. ;
Risaliti, A. ;
Giacometti, A. .
EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY, 2010, 40 (06) :817-822
[6]   Novel approaches to developing new antibiotics for bacterial infections [J].
Coates, A. R. M. ;
Hu, Y. .
BRITISH JOURNAL OF PHARMACOLOGY, 2007, 152 (08) :1147-1154
[7]   New strategies for antibacterial drug design: Targeting non-multiplying latent bacteria [J].
Coates A.R.M. ;
Hu Y. .
Drugs in R & D, 2006, 7 (3) :133-151
[8]   Bacteriophage T4 multiplication in a glucose-limited Escherichia coli biofilm [J].
Corbin, BD ;
McLean, RJC ;
Aron, GM .
CANADIAN JOURNAL OF MICROBIOLOGY, 2001, 47 (07) :680-684
[9]   Using bacteriophages to reduce formation of catheter-associated biofilms by Staphylococcus epidermidis [J].
Curtin, JJ ;
Donlan, RM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (04) :1268-1275
[10]   LYTIC INFECTION OF ESCHERICHIA-COLI BIOFILMS BY BACTERIOPHAGE-T4 [J].
DOOLITTLE, MM ;
COONEY, JJ ;
CALDWELL, DE .
CANADIAN JOURNAL OF MICROBIOLOGY, 1995, 41 (01) :12-18