Oral microbial communities: Biofilms, interactions, and genetic systems

被引:580
作者
Kolenbrander, PE [1 ]
机构
[1] Natl Inst Dent & Craniofacial Res, Oral Infect & Immun Branch, NIH, Bethesda, MD 20892 USA
关键词
spatial organization; oral bacteria genetic systems; communication; bacterial cell interactions;
D O I
10.1146/annurev.micro.54.1.413
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Oral microbial-plaque communities are biofilms composed of numerous genetically distinct types of bacteria that live in close juxtaposition on host surfaces. These bacteria communicate through physical interactions called coaggregation and coadhesion, as well as other physiological and metabolic interactions. Streptococci and actinomyces are the major initial colonizers of the tooth surface, and the interactions between them and their substrata help establish the early biofilm community. Fusobacteria play a central role as physical bridges that mediate coaggregation of cells and as physiological bridges that promote anaerobic microenvironments which protect coaggregating strict anaerobes in an aerobic atmosphere. New technologies for investigating bacterial populations with 16S rDNA probes have uncovered previously uncultured bacteria and have offered an approach to in situ examination of the spatial arrangement of the participant cells in oral-plaque biofilms. Flow cells with saliva-coated surfaces are particularly useful for studies of biofilm formation and observation. The predicted sequential nature of colonization of the tooth surface by members of different genera can be investigated by using these new technologies and imaging the cells in situ with confocal scanning laser microscopy. Members of at least seven genera now can be subjected to genetic studies owing to the discovery of gene-transfer systems in these genera. Identification of contact-inducible genes in streptococci offers an avenue to explore bacterial responses to their environment and leads the way toward understanding communication among inhabitants of a multispecies biofilm.
引用
收藏
页码:413 / 437
页数:27
相关论文
共 134 条
[51]   Isolation and characterization of a hemin-regulated gene, hemR, from Porphyromonas gingivalis [J].
Karunakaran, T ;
Madden, T ;
Kuramitsu, H .
JOURNAL OF BACTERIOLOGY, 1997, 179 (06) :1898-1908
[52]   INHIBITION OF COAGGREGATION BETWEEN FUSOBACTERIUM-NUCLEATUM AND PORPHYROMONAS (BACTEROIDES) GINGIVALIS BY LACTOSE AND RELATED SUGARS [J].
KOLENBRANDER, PE ;
ANDERSEN, RN .
INFECTION AND IMMUNITY, 1989, 57 (10) :3204-3209
[53]   NUCLEOTIDE-SEQUENCE OF THE STREPTOCOCCUS-GORDONII PK488 COAGGREGATION ADHESIN GENE, SCAA, AND ATP-BINDING CASSETTE [J].
KOLENBRANDER, PE ;
ANDERSEN, RN ;
GANESHKUMAR, N .
INFECTION AND IMMUNITY, 1994, 62 (10) :4469-4480
[54]   INTERGENERIC COAGGREGATION AMONG HUMAN ORAL BACTERIA AND ECOLOGY OF DENTAL PLAQUE [J].
KOLENBRANDER, PE .
ANNUAL REVIEW OF MICROBIOLOGY, 1988, 42 :627-656
[55]   The adhesion-associated sca operon in Streptococcus gordonii encodes an inducible high-affinity ABC transporter for Mn2+ uptake [J].
Kolenbrander, PE ;
Andersen, RN ;
Baker, RA ;
Jenkinson, HF .
JOURNAL OF BACTERIOLOGY, 1998, 180 (02) :290-295
[56]  
Kolenbrander PE, 1999, METHOD ENZYMOL, V310, P322
[57]   COAGGREGATION OF FUSOBACTERIUM-NUCLEATUM, SELENOMONAS-FLUEGGEI, SELENOMONAS-INFELIX, SELENOMONAS-NOXIA, AND SELENOMONAS-SPUTIGENA WITH STRAINS FROM 11 GENERA OF ORAL BACTERIA [J].
KOLENBRANDER, PE ;
ANDERSEN, RN ;
MOORE, LVH .
INFECTION AND IMMUNITY, 1989, 57 (10) :3194-3203
[58]   ADHERE TODAY, HERE TOMORROW - ORAL BACTERIAL ADHERENCE [J].
KOLENBRANDER, PE ;
LONDON, J .
JOURNAL OF BACTERIOLOGY, 1993, 175 (11) :3247-3252
[59]  
KOLENBRANDER PE, 2000, IN PRESS STREPTOCOCC
[60]   TRANSPOSON TN5 MUTAGENESIS OF ACTINOBACILLUS-ACTINOMYCETEMCOMITANS VIA CONJUGATION [J].
KOLODRUBETZ, D ;
KRAIG, E .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1994, 9 (05) :290-296