Steinberger R E, Holden P A
Donald Bren School of Environmental Science and Management, University of California-Santa Barbara, Bren Hall, Santa Barbara, CA 93106-5131, USA.
Appl Environ Microbiol. 2005 Sep;71(9):5404-10. doi: 10.1128/AEM.71.9.5404-5410.2005.
The extracellular polymeric substances (EPS) of bacterial biofilms form a hydrated barrier between cells and their external environment. Better characterization of EPS could be useful in understanding biofilm physiology. The EPS are chemically complex, changing with both bacterial strain and culture conditions. Previously, we reported that Pseudomonas aeruginosa unsaturated biofilm EPS contains large amounts of extracellular DNA (eDNA) (R. E. Steinberger, A. R. Allen, H. G. Hansma, and P. A. Holden, Microb. Ecol. 43:416-423, 2002). Here, we investigated the compositional similarity of eDNA to cellular DNA, the relative quantity of eDNA, and the terminal restriction fragment length polymorphism (TRFLP) community profile of eDNA in multiple-species biofilms. By randomly amplified polymorphic DNA analysis, cellular DNA and eDNA appear identical for P. aeruginosa biofilms. Significantly more eDNA was produced in P. aeruginosa and Pseudomonas putida biofilms than in Rhodococcus erythropolis or Variovorax paradoxus biofilms. While the amount of eDNA in dual-species biofilms was of the same order of magnitude as that of of single-species biofilms, the amounts were not predictable from single-strain measurements. By the Shannon diversity index and principle components analysis of TRFLP profiles generated from 16S rRNA genes, eDNA of four-species biofilms differed significantly from either cellular or total DNA of the same biofilm. However, total DNA- and cellular DNA-based TRFLP analyses of this biofilm community yielded identical results. We conclude that extracellular DNA production in unsaturated biofilms is species dependent and that the phylogenetic information contained in this DNA pool is quantifiable and distinct from either total or cellular DNA.
细菌生物膜的胞外聚合物(EPS)在细胞与其外部环境之间形成了一层水合屏障。对EPS进行更深入的表征有助于理解生物膜生理学。EPS的化学组成复杂,会随细菌菌株和培养条件的变化而改变。此前,我们报道过铜绿假单胞菌不饱和生物膜EPS中含有大量胞外DNA(eDNA)(R.E.斯坦伯格、A.R.艾伦、H.G.汉斯马和P.A.霍尔登,《微生物生态学》43:416 - 423,2002年)。在此,我们研究了多物种生物膜中eDNA与细胞DNA的组成相似性、eDNA的相对数量以及eDNA的末端限制性片段长度多态性(TRFLP)群落图谱。通过随机扩增多态性DNA分析,铜绿假单胞菌生物膜的细胞DNA和eDNA看起来是相同的。在铜绿假单胞菌和恶臭假单胞菌生物膜中产生的eDNA明显多于红球菌或奇异贪铜菌生物膜。虽然双物种生物膜中eDNA的量与单物种生物膜中的量处于同一数量级,但无法根据单菌株测量结果预测其数量。通过对16S rRNA基因产生的TRFLP图谱进行香农多样性指数和主成分分析,四物种生物膜的eDNA与同一生物膜的细胞DNA或总DNA有显著差异。然而,基于该生物膜群落的总DNA和细胞DNA的TRFLP分析得出了相同的结果。我们得出结论,不饱和生物膜中胞外DNA的产生具有物种依赖性,并且该DNA库中包含的系统发育信息是可量化的,且与总DNA或细胞DNA不同。