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肺炎克雷伯菌菌落和生物膜内生长速率的空间变化。

Spatial variations in growth rate within Klebsiella pneumoniae colonies and biofilm.

作者信息

Wentland E J, Stewart P S, Huang C T, McFeters G A

机构信息

Center for Biofilm Engineering, Montana State University, Bozeman 59717, USA.

出版信息

Biotechnol Prog. 1996 May-Jun;12(3):316-21. doi: 10.1021/bp9600243.

Abstract

The use of acridine orange to visualize and quantify spatial variations in growth rate within Klebsiella pneumoniae colonies and biofilm was investigated. Bacterial colonies supported on polycarbonate filter membranes were grown on R2A agar plates. Some colonies were sampled for cell enumeration, while others were cryoembedded, sectioned, and stained with the fluorescent nucleic acid stain acridine orange. Spatial patterns of fluorescent color and intensity with depth in the colony were quantified using confocal microscopy and image analysis of stained cross sections. Colonies sampled in the midexponential phase were thin (20 microns), had high average specific growth rates (> 1 h-1), and had all the cells stained bright orange. Colonies sampled after more than 24 h of growth were thick (> 200 microns) and were growing slowly (mu < 0.15 h-1). These older colonies were characterized by distinct bands of orange at the colony edges and a dark green center. Stained biofilm cross sections displayed a similar orange band at the biofilm-bulk fluid interface and a green interior. Colony-average specific growth rates, determined by calculating the local slope of the cell accumulation versus time data, were correlated with colony-average fluorescence intensities. There was no correlation between average specific growth rate and orange or green intensity individually, but growth rate did correlate with the orange:green intensity ratio (r2 = 0.57). The resulting regression was used to predict specific growth rate profiles within colonies. These profiles indicated that bacteria were growing rapidly near the air and agar interfaces and more slowly in the center of the colonies when thicker than about 30 microns. The dimension of the orange bands ranged from 10 to 30 microns, which may indicate the thickness of growing regions. The inherent variability associated with this technique suggests that it is best applied in single species systems and that the results should be regarded as qualitative in nature.

摘要

研究了使用吖啶橙来可视化和量化肺炎克雷伯菌菌落及生物膜内生长速率的空间变化。支撑在聚碳酸酯滤膜上的细菌菌落在R2A琼脂平板上生长。一些菌落用于细胞计数,而其他菌落则进行冷冻包埋、切片,并用荧光核酸染料吖啶橙染色。使用共聚焦显微镜和染色横截面的图像分析来量化菌落中荧光颜色和强度随深度的空间模式。在指数中期采样的菌落较薄(20微米),平均比生长速率较高(>1 h-1),所有细胞均染成亮橙色。生长超过24小时后采样的菌落较厚(>200微米),生长缓慢(μ<0.15 h-1)。这些较老的菌落的特征是在菌落边缘有明显的橙色带和深绿色中心。染色的生物膜横截面在生物膜-主体流体界面处显示出类似的橙色带和绿色内部。通过计算细胞积累与时间数据的局部斜率确定的菌落平均比生长速率与菌落平均荧光强度相关。平均比生长速率与橙色或绿色强度单独之间没有相关性,但生长速率确实与橙色:绿色强度比相关(r2 = 0.57)。所得回归用于预测菌落内的比生长速率分布。这些分布表明,当菌落厚度超过约30微米时,细菌在空气和琼脂界面附近生长迅速,而在菌落中心生长较慢。橙色带的尺寸范围为10至30微米,这可能表明生长区域的厚度。与该技术相关的固有变异性表明,它最适用于单一物种系统,并且结果在本质上应被视为定性的。

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