Prevention of Staphylococcus aureus biofilm formation and reduction in established biofilm density using a combination of phage K and modified derivatives

被引:113
作者
Kelly, D. [1 ]
McAuliffe, O. [2 ]
Ross, R. P. [2 ]
Coffey, A. [1 ]
机构
[1] Cork Inst Technol, Dept Biol Sci, Cork, Ireland
[2] TEAGASC, Moorepark Food Res Ctr, Dept Biotechnol, Fermoy, Cork, Ireland
基金
爱尔兰科学基金会;
关键词
bacteriophage; biocontrol; biofilm; cocktail; modification; Staphylococcus aureus; BACTERIOPHAGE; EPIDERMIDIS; SUSCEPTIBILITY; RESTRICTION; INFECTION; SYSTEM; CELLS;
D O I
10.1111/j.1472-765X.2012.03205.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 investigate the ability of a mixture of phage K and six of its modified derivatives to prevent biofilm formation by Staphylococcus aureus and also to reduce the established biofilm density. Aims: To investigate the ability of a mixture of phage K and six of its modified derivatives to prevent biofilm formation by Staphylococcus aureus and also to reduce the established biofilm density. Methods and Results: The bioluminescence-producing Staph. aureus Xen29 strain was used in the study, and incubation of this strain in static microtitre plates at 37 degrees C for 48 h confirmed its strong biofilm-forming capacity. Subsequently, removal of established biofilms of Staph. aureus Xen29 with the hightitre phage combination was investigated over time periods of 24 h, 48 h and 72 h. Results suggested that these biofilms were eliminated in a time-dependant manner, with biofilm biomass reduction significantly greater after 72 h than after 24-48 h. In addition, initial challenge of Staph. aureus Xen29 with the phage cocktail resulted in the complete inhibition of biofilm formation over a 48-h period with no appearance of phage resistance. Conclusions: In general, our findings demonstrate the potential use of a modified phage combination for the prevention and successful treatment of Staph. aureus biofilms, which are implicated in several antibiotic-resistant infections. Significance and Impact of the Study: This study highlights the first use of phage K for the successful removal and prevention of biofilms of Staph. aureus.
引用
收藏
页码:286 / 291
页数:6
相关论文
共 39 条
[1]   The use of phages for the removal of infectious biofilms [J].
Azeredo, J. ;
Sutherland, I. W. .
CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2008, 9 (04) :261-266
[2]   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
[3]   Comparative assessment of antibiotic susceptibility of coagulase-negative staphylococci in biofilm versus planktonic culture as assessed by bacterial enumeration or rapid XTT colorimetry [J].
Cerca, N ;
Martins, S ;
Cerca, F ;
Jefferson, KK ;
Pier, GB ;
Oliveira, R ;
Azeredo, J .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 56 (02) :331-336
[4]   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
[5]   Biofilms: Survival mechanisms of clinically relevant microorganisms [J].
Donlan, RM ;
Costerton, JW .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (02) :167-+
[6]   Preventing biofilms of clinically relevant organisms using bacteriophage [J].
Donlan, Rodney M. .
TRENDS IN MICROBIOLOGY, 2009, 17 (02) :66-72
[7]   Biofilm formation by persistent and non-persistent isolates of Staphylococcus epidermidis from a neonatal intensive care unit [J].
Eftekhar, F. ;
Speert, D. P. .
JOURNAL OF HOSPITAL INFECTION, 2009, 71 (02) :112-116
[8]   Bacteriophage Cocktail for the Prevention of Biofilm Formation by Pseudomonas aeruginosa on Catheters in an In Vitro Model System [J].
Fu, Weiling ;
Forster, Terri ;
Mayer, Oren ;
Curtin, John J. ;
Lehman, Susan M. ;
Donlan, Rodney M. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (01) :397-404
[9]   Bovine whey proteins inhibit the interaction of Staphylococcus aureus and bacteriophage K [J].
Gill, J. J. ;
Sabour, P. M. ;
Leslie, K. E. ;
Griffiths, M. W. .
JOURNAL OF APPLIED MICROBIOLOGY, 2006, 101 (02) :377-386
[10]  
Górski A, 2009, CURR OPIN INVEST DR, V10, P766