Temperature-Dependent Control of Staphylococcus aureus Biofilms and Virulence by Thermoresponsive Oligo(N-vinylcaprolactam)

被引:14
作者
Lee, Jin-Hyung [1 ]
Kim, Yong-Guy [1 ]
Lee, Kayeon [1 ]
Kim, Seong-Cheol [2 ]
Lee, Jintae [1 ]
机构
[1] Yeungnam Univ, Sch Chem Engn, Gyongsan 712749, South Korea
[2] Yeungnam Univ, Dept Nano Med & Polymer Mat, Gyongsan 712749, South Korea
基金
新加坡国家研究基金会;
关键词
biofilm; hydrophilicity; N-vinylcaprolactam; thermoresponsive polymer; Staphylococcus aureus; ESCHERICHIA-COLI; BIOMEDICAL APPLICATIONS; CAENORHABDITIS-ELEGANS; BACTERIAL ADHESION; ALPHA-TOXIN; MECHANISMS; CINNAMALDEHYDE; INFECTIONS; RESISTANCE; CARVACROL;
D O I
10.1002/bit.25496
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
Bacterial biofilms are associated with persistent infections because they are highly tolerant of antimicrobial agents, and in the case of Staphylococcus aureus, which is a leading cause of nosocomial infections because of its resistance to diverse antibiotics, biofilm formation is a known mechanism of drug resistance. In the present study, we investigated the ability of thermoresponsive oligo (N-vinylcaprolactam) (OVCL) to control biofilm formation by and the virulence of S. aureus. One synthetic and four commercial OVCLs (MW240,000) at 50 mu g/mL were found to increase S. aureus biofilm formation 7-fold at 25 degrees C, but to markedly inhibit S. aureus biofilm formation at 37 degrees C. Confocal and scanning electron microscopy confirmed the temperature-dependent effect of OVCL on S. aureus biofilms. It was found that the addition of OVCL to S. aureus culture caused cells to become dramatically more hydrophilic at 37 degrees C, which partially supports the biofilm reduction. Also, transcriptional analysis showed that OVCL temperature-dependently regulated biofilm-related genes (aur, agrA, and icaA) in S. aureus. In addition, it was found surface coatings containing OVCL effectively controlled S. aureus biofilm formation on solid glass surfaces. Furthermore, OVCL inhibited the hemolysis of human red blood cells by S. aureus at 37 degrees C and attenuated S. aureus virulence in the nematode Caenorhabditis elegans. These results suggest that OVCL has potential use for controlling bacterial biofilm formation and virulence. Biotechnol. Bioeng. 2015;112: 716-724. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:716 / 724
页数:9
相关论文
共 32 条
[1]  
An YH, 1998, J BIOMED MATER RES, V43, P338, DOI 10.1002/(SICI)1097-4636(199823)43:3<338::AID-JBM16>3.0.CO
[2]  
2-B
[3]   Staphylococcal biofilm disassembly [J].
Boles, Blaise R. ;
Horswill, Alexander R. .
TRENDS IN MICROBIOLOGY, 2011, 19 (09) :449-455
[4]   Alpha-toxin is required for biofilm formation by Staphylococcus aureus [J].
Caiazza, NC ;
O'Toole, GA .
JOURNAL OF BACTERIOLOGY, 2003, 185 (10) :3214-3217
[5]   Zwitterionic carboxybetaine polymer surfaces and their resistance to long-term biofilm formation [J].
Cheng, Gang ;
Li, Guozhu ;
Xue, Hong ;
Chen, Shengfu ;
Bryers, James D. ;
Jiang, Shaoyi .
BIOMATERIALS, 2009, 30 (28) :5234-5240
[6]   Bacterial biofilms: A common cause of persistent infections [J].
Costerton, JW ;
Stewart, PS ;
Greenberg, EP .
SCIENCE, 1999, 284 (5418) :1318-1322
[7]   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
[8]   Biofilms: Survival mechanisms of clinically relevant microorganisms [J].
Donlan, RM ;
Costerton, JW .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (02) :167-+
[9]   Bacterial adhesion: Seen any good biofilms lately? [J].
Dunne, WM .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (02) :155-+
[10]   Aminoglycoside antibiotics induce bacterial biofilm formation [J].
Hoffman, LR ;
D'Argenio, DA ;
MacCoss, MJ ;
Zhang, ZY ;
Jones, RA ;
Miller, SI .
NATURE, 2005, 436 (7054) :1171-1175