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铜绿假单胞菌生物膜中单个细胞簇水平的积累和位移测量。

Measurements of accumulation and displacement at the single cell cluster level in Pseudomonas aeruginosa biofilms.

作者信息

Klayman Benjamin J, Klapper Isaac, Stewart Philip S, Camper Anne K

机构信息

Center for Biofilm Engineering, 366 EPS Building, Montana State University, Bozeman, MT 59717, USA.

出版信息

Environ Microbiol. 2008 Sep;10(9):2344-54. doi: 10.1111/j.1462-2920.2008.01660.x. Epub 2008 Jun 28.

Abstract

Quantitative descriptions of biofilm growth and dynamics at the individual cell level are largely missing from the literature. To fill this gap, research was done to describe growth, accumulation and displacement patterns in developing Pseudomonas aeruginosa biofilms. A parent strain of PAO1 was labelled with either a cyan or yellow fluorescent protein. These were then grown in a flow cell biofilm together so that pockets of dividing cells could be identified and their accumulation and displacement tracked. This analysis revealed a pattern of exponential accumulation for all clusters followed by a stationary accumulation phase. A background 'carpet' layer of cells uniformly colonizing the surface exhibited zero net accumulation of bio-volume. The individual clusters were found to have a mean accumulation rate of 0.34 h(-1) with a range of 0.28-0.41 h(-1). Cluster accumulation rates were negatively correlated with cluster size; larger clusters accumulated volume at a slower rate (P < 0.001). Pockets of cells on the inside of clusters initially accumulated at a comparable rate to the cluster within which they resided, but later invariably exhibited zero to slightly negative accumulation despite continued exponential (positive) accumulation of the cluster. Expanding clusters were able to displace neighbouring cells from the surface, and larger clusters displaced smaller clusters. This work provides a more detailed quantitative experimental observation of biofilm behaviour than has been described previously.

摘要

关于生物膜在单个细胞水平上的生长和动态的定量描述在文献中基本缺失。为了填补这一空白,开展了相关研究来描述铜绿假单胞菌生物膜发育过程中的生长、聚集和位移模式。PAO1的一个亲本菌株用青色或黄色荧光蛋白进行标记。然后将它们共同培养在流动细胞生物膜中,以便能够识别正在分裂的细胞群,并追踪它们的聚集和位移情况。该分析揭示了所有细胞群的指数聚集模式,随后是稳定聚集阶段。均匀定殖在表面的细胞的背景“地毯”层生物体积的净积累为零。发现单个细胞群的平均积累速率为0.34 h⁻¹,范围在0.28 - 0.41 h⁻¹之间。细胞群的积累速率与细胞群大小呈负相关;较大的细胞群积累体积的速率较慢(P < 0.001)。细胞群内部的细胞最初的积累速率与其所在的细胞群相当,但尽管细胞群持续呈指数(正)积累,这些细胞后来总是表现出零积累到轻微的负积累。不断扩大的细胞群能够将相邻细胞从表面排挤开,较大的细胞群排挤较小的细胞群。这项工作提供了比以前所描述的更详细的生物膜行为的定量实验观察结果。

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