The polymicrobial nature of biofilm infection

被引:224
作者
Wolcott, R. [1 ]
Costerton, J. W. [2 ]
Raoult, D. [3 ]
Cutler, S. J. [4 ]
机构
[1] Wound Care Ctr, Lubbock, TX USA
[2] Allegheny Gen Hosp, Ctr Genom Sci, Pittsburgh, PA 15212 USA
[3] Fac Med Marseille, Unite Rickettsies, F-13385 Marseille, France
[4] Univ E London, Sch Hlth & Biosci, London E15 4LZ, England
关键词
Biofilm; co-aggregation; horizontal gene transfer; metabolic cooperation; passive resistance; PCR; polymicrobial; sequencing; synergies; III SECRETION SYSTEM; PSEUDOMONAS-AERUGINOSA; PORPHYROMONAS-GINGIVALIS; STAPHYLOCOCCUS-AUREUS; CHRONIC WOUNDS; STREPTOCOCCUS-PNEUMONIAE; FUSOBACTERIUM-NUCLEATUM; HAEMOPHILUS-INFLUENZAE; ANTIBIOTIC TOLERANCE; HELICOBACTER-PYLORI;
D O I
10.1111/j.1469-0691.2012.04001.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The model of biofilm infection was first proposed over a decade ago. Recent scientific advances have added much to our understanding of biofilms, usually polymicrobial communities, which are commonly associated with chronic infection. Metagenomics has demonstrated that bacteria pursuing a biofilm strategy possess many mechanisms for encouraging diversity. By including multiple bacterial and/or fungal species in a single community, biofilms obtain numerous advantages, such as passive resistance, metabolic cooperation, byproduct influence, quorum sensing systems, an enlarged gene pool with more efficient DNA sharing, and many other synergies, which give them a competitive advantage. Routine clinical cultures are ill-suited for evaluating polymicrobial infections. DNA methods utilizing PCR methods, PCR/mass spectroscopy and sequencing have demonstrated their ability to identify microorganisms and quantitate their contribution to biofilms in clinical infections. A more robust model of biofilm infection along with more accurate diagnosis is rapidly translating into improved clinical outcomes.
引用
收藏
页码:107 / 112
页数:6
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