Assessment of cadexomer iodine against Staphylococcus aureus biofilm in vivo and in vitro using confocal laser scanning microscopy

被引:40
作者
Akiyama, H [1 ]
Oono, T [1 ]
Saito, M [1 ]
Iwatsuki, K [1 ]
机构
[1] Okayama Univ, Grad Sch Med & Dent, Dept Dermatol, Okayama 7008558, Japan
关键词
cadexomer iodine; Staphylococcus aureus; glycocalyx; biofilm; confocal laser scanning microscope;
D O I
10.1111/j.1346-8138.2004.tb00549.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Cadexomer iodine releases iodine (0.9% weight/weight) slowly from beads of dextrin and epichlorhydrin. This preparation is an effective debridement and antiseptic agent for chronic excludative wounds. The purpose of the present study is to examine the influence of cadexomer iodine against glycocalyx production of Staphylococcus aureus isolated from furuncle lesions on cut wounds in mice using confocal laser scanning microscope (CLSM), and the increase in and glycocalyx production of S. aureus in vitro. In the present study, distinct S. aureus cells and glycocalyx were not detected in the dermis around the cadexomer iodine beads or within those beads, while S. aureus cells encircled by glycocalyx were soaked up by the cadexomer beads and were detected within them in vivo and in vitro. We suggest that cadexomer iodine soaks up S. aureus cells encircled by glycocalyx, directly destroys biofilm structures, and collapses glycocalyx during dehydration, and further, that iodine can subsequently kill S. aureus cells within biofilm. Cadexomer iodine is a promising treatment to clear S. aureus cells within biofilm from skin lesions of exudative or infectious wounds and to prevent wound exacerbation.
引用
收藏
页码:529 / 534
页数:6
相关论文
共 11 条
[1]   Confocal laser scanning microscopic observation of glycocalyx production by Staphylococcus aureus in skin lesions of bullous impetigo, atopic dermatitis and pemphigus foliaceus [J].
Akiyama, H ;
Hamada, T ;
Huh, WK ;
Yamasaki, O ;
Oono, T ;
Fujimoto, W ;
Iwatsuki, K .
BRITISH JOURNAL OF DERMATOLOGY, 2003, 148 (03) :526-532
[2]   Changes in Staphylococcus aureus density and lesion severity after topical application of povidone-iodine in cases of atopic dermatitis [J].
Akiyama, H ;
Tada, J ;
Toi, Y ;
Kanzaki, H ;
Arata, J .
JOURNAL OF DERMATOLOGICAL SCIENCE, 1997, 16 (01) :23-30
[3]   Effects of acetic acid on biofilms formed by Staphylococcus aureus [J].
Akiyama, H ;
Yamasaki, O ;
Tada, J ;
Arata, J .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1999, 291 (10) :570-573
[4]   Staphylococcus aureus infection on cut wounds in the mouse skin: Experimental staphylococcal botryomycosis [J].
Akiyama, H ;
Kanzaki, H ;
Tada, J ;
Arata, J .
JOURNAL OF DERMATOLOGICAL SCIENCE, 1996, 11 (03) :234-238
[5]   Confocal laser scanning microscopic observation of glycocalyx production by Staphylococcus aureus in mouse skin:: does S-aureus generally produce a biofilm on damaged skin? [J].
Akiyama, H ;
Huh, WK ;
Yamasaki, O ;
Oono, T ;
Iwatsuki, K .
BRITISH JOURNAL OF DERMATOLOGY, 2002, 147 (05) :879-885
[6]   Confocal laser microscopic observation of glycocalyx production by Staphylococcus aureus in vitro [J].
Akiyama, H ;
Huh, WK ;
Fujii, K ;
Yamasaki, O ;
Oono, T ;
Iwatsuki, K .
JOURNAL OF DERMATOLOGICAL SCIENCE, 2002, 29 (01) :54-61
[7]  
AKIYAMA H, IN PRESS BR J DERMAT
[8]  
Costerton J. W., 1992, ENCY MICROBIOLOGY, V2, P311
[9]  
Hansson C, 1998, INT J DERMATOL, V37, P390
[10]  
Sundberg J, 1997, WOUNDS, V9, P68