Biofilm structure and cell vitality in a laboratory model of subgingival plaque

被引:36
作者
Hope, C. K. [1 ]
Wilson, M. [1 ]
机构
[1] UCL, Eastman Dent Inst, Div Microbial Dis, London WC1E 6BT, England
关键词
subgingival plaque; anaerobic biofilm; confocal laser scanning microscopy; viability; constant-depth film fermenter;
D O I
10.1016/j.mimet.2006.01.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The accumulation of dental plaque below the gingival margin (i.e. subgingival plaque) is responsible for the most prevalent microbe-induced diseases of humans - the periodontal diseases. Access to this plaque is difficult, making studies of its structure in vivo very difficult. We have, therefore, used a constant-depth film fennenter to grow microcosm subgingival dental plaques under conditions similar to those existing in vivo to enable us to study certain aspects of its structure. Confocal laser scanning microscopy revealed that the biofilms consisted of pillar-like stacks of bacteria separated by. water channels. In terms of their structure, these microcosm dental plaques reached a pseudo steady-state after 4 days. Individual optical sections generally showed the outer layers of the biofilm stacks to contain a high proportion of nonviable cells surrounding an inner core of predominantly viable cells with 'veins' of nonviable bacteria penetrating from the outer layers through into the inner core. Such a structure differs from that classically described for biofilms growing in an aerobic atmosphere where the arrangement of viable and nonviable bacteria is usually reversed. The reasons for the preponderance of nonviable bacteria in the outer layer of the bacterial stacks remain to be established. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:390 / 398
页数:9
相关论文
共 43 条
[1]   Particulate Bioglass® reduces the viability of bacterial biofilms formed on its surface in an in vitro model [J].
Allan, I ;
Newman, H ;
Wilson, M .
CLINICAL ORAL IMPLANTS RESEARCH, 2002, 13 (01) :53-58
[2]   Individual vitality pattern of in situ dental biofilms at different locations in the oral cavity [J].
Arweiler, NB ;
Hellwig, E ;
Sculean, A ;
Hein, N ;
Auschill, TM .
CARIES RESEARCH, 2004, 38 (05) :442-447
[3]   Spatial distribution of vital and dead microorganisms in dental biofilms [J].
Auschill, TM ;
Artweiler, NB ;
Netuschil, L ;
Brecx, M ;
Reich, E ;
Sculean, A .
ARCHIVES OF ORAL BIOLOGY, 2001, 46 (05) :471-476
[4]   TOTAL PROTEIN IN HUMAN CREVICULAR FLUID [J].
BANG, JS ;
CIMASONI, G .
JOURNAL OF DENTAL RESEARCH, 1971, 50 (06) :1683-&
[5]   ADAPTATION OF STREPTOCOCCUS-MUTANS AND ENTEROCOCCUS-HIRAE TO ACID STRESS IN CONTINUOUS CULTURE [J].
BELLI, WA ;
MARQUIS, RE .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1991, 57 (04) :1134-1138
[6]   Multiparametric flow cytometry and cell sorting for the assessment of viable, injured, and dead bifidobacterium cells during bile salt stress [J].
Ben Amor, K ;
Breeuwer, P ;
Verbaarschot, P ;
Rombouts, FM ;
Akkermans, ADL ;
De Vos, WM ;
Abee, T .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (11) :5209-5216
[7]   An optical microsensor to measure fluorescent light intensity in biofilms [J].
Beyenal, H ;
Yakymyshyn, C ;
Hyungnak, J ;
Davis, CC ;
Lewandowski, Z .
JOURNAL OF MICROBIOLOGICAL METHODS, 2004, 58 (03) :367-374
[8]   A modified chemostat system to study the ecology of oral biofilms [J].
Bradshaw, DJ ;
Marsh, PD ;
Schilling, KM ;
Cummins, D .
JOURNAL OF APPLIED BACTERIOLOGY, 1996, 80 (02) :124-130
[9]   THE RELATIONSHIP OF GINGIVAL FLUID LEUKOCYTE ELASTASE ACTIVITY TO GINGIVAL FLUID-FLOW RATE [J].
DARANY, DG ;
BECK, FM ;
WALTERS, JD .
JOURNAL OF PERIODONTOLOGY, 1992, 63 (09) :743-747
[10]  
EASTOE JE, 1988, BIOCH ORAL BIOL, P475