Effect of Farnesol on Planktonic and Biofilm Cells of Staphylococcus epidermidis

被引:68
作者
Gomes, Fernanda I. A. [1 ]
Teixeira, Pilar [1 ]
Azeredo, Joana [1 ]
Oliveira, Rosario [1 ]
机构
[1] Univ Minho, Ctr Biol Engn, Inst Biotechnol & Bioengn, P-4710057 Braga, Portugal
关键词
COAGULASE-NEGATIVE STAPHYLOCOCCI; PERSISTER CELLS; AUREUS; SUSCEPTIBILITY;
D O I
10.1007/s00284-009-9408-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Staphylococcus epidermidis is now amongst the most important pathogenic agents responsible for bloodstream nosocomial infections and for biofilm formation on indwelling medical devices. Its increasing resistance to common antibiotics is a challenge for the development of new antimicrobial agents. Accordingly, the goal of this study was to evaluate the effect of farnesol, a natural sesquiterpenoid, on Staphylococcus epidermidis planktonic and biofilm cells. Farnesol displayed a significant inhibitory effect on planktonic cells. Small concentrations (100 mu M) were sufficient to exhibit antibacterial effect on these cells. In biofilm cells the effect of farnesol was not so pronounced and it seems to be strongly dependent on the cells metabolic activity and amount of matrix. Interestingly, the effect of farnesol at 200 mu M was similar to the effect of vancomycin at peak serum concentration either in planktonic or biofilm cells. Overall, the results indicate a potential antibacterial effect of farnesol against S. epidermidis, and therefore the possible action of this molecule on the prevention of S. epidermidis related infections.
引用
收藏
页码:118 / 122
页数:5
相关论文
共 16 条
[1]   Sensitization of Staphylococcus aureus and Escherichi coli to antibiotics by the sesquiterpenoid nerolidol, farnesol, bisabolol, and apritone [J].
Brehm-Stecher, BF ;
Johnson, EA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (10) :3357-3360
[2]   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
[3]   Comparative evaluation of coagulase-negative staphylococci (CoNS) adherence to acrylic by a static method and a parallel-plate flow dynamic method [J].
Cerca, N ;
Pier, GB ;
Oliveira, R ;
Azeredo, J .
RESEARCH IN MICROBIOLOGY, 2004, 155 (09) :755-760
[4]   The antibacterial effects of terpene alcohols on Staphylococcus aureus and their mode of action [J].
Inoue, Y ;
Shiraishi, A ;
Hada, T ;
Hirose, K ;
Hamashima, H ;
Shimada, J .
FEMS MICROBIOLOGY LETTERS, 2004, 237 (02) :325-331
[5]   Poly-N-acetylglucosamine mediates biofilm formation and antibiotic resistance in Actinobacillus pleuropneumoniae [J].
Izano, Era A. ;
Sadovskaya, Irina ;
Vinogradov, Evgeny ;
Mulks, Martha H. ;
Velllyagounder, Kabilan ;
Ragunath, Chandran ;
Kher, William B. ;
Ramasubbu, Narayanan ;
Jabbouri, Said ;
Perry, Malcolm B. ;
Kaplan, Jeffrey B. .
MICROBIAL PATHOGENESIS, 2007, 43 (01) :1-9
[6]   Effect of farnesol on Staphylococcus aureus biofilm formation and antimicrobial susceptibility [J].
Jabra-Rizk, MA ;
Meiller, TF ;
James, CE ;
Shirtliff, ME .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (04) :1463-1469
[7]   Persister cells and tolerance to antimicrobials [J].
Keren, I ;
Kaldalu, N ;
Spoering, A ;
Wang, YP ;
Lewis, K .
FEMS MICROBIOLOGY LETTERS, 2004, 230 (01) :13-18
[8]   Uses and limitations of the XTT assay in studies of Candida growth and metabolism [J].
Kuhn, DM ;
Balkis, M ;
Chandra, J ;
Mukherjee, PK ;
Ghannoum, MA .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (01) :506-508
[9]   Persister cells, dormancy and infectious disease [J].
Lewis, Kim .
NATURE REVIEWS MICROBIOLOGY, 2007, 5 (01) :48-56
[10]   Time course of biofilm formation by Staphylococcus aureus and Staphylococcus epidermidis mastitis isolates [J].
Oliveira, M. ;
Nunes, S. F. ;
Carneiro, C. ;
Bexiga, R. ;
Bernardo, F. ;
Vilela, C. L. .
VETERINARY MICROBIOLOGY, 2007, 124 (1-2) :187-191