Quantifying the fractal complexity of nutrient transport channels in Escherichia coli biofilms under varying cell shape and growth environment.

IF 2.6 4区 生物学 Q3 MICROBIOLOGY
Beatrice Bottura, Liam Rooney, Morgan Feeney, Paul A Hoskisson, Gail McConnell
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引用次数: 0

Abstract

Recent mesoscopic characterization of nutrient-transporting channels in Escherichia coli has allowed the identification and measurement of individual channels in whole mature colony biofilms. However, their complexity under different physiological and environmental conditions remains unknown. Analysis of confocal micrographs of colony biofilms formed by cell shape mutants of E. coli shows that channels have high fractal complexity, regardless of cell phenotype or growth medium. In particular, colony biofilms formed by the mutant strain ΔompR, which has a wide-cell phenotype, have a higher fractal dimension when grown on rich medium than when grown on minimal medium, with channel complexity affected by glucose and agar concentrations in the medium. Osmotic stress leads to a dramatic reduction in the ΔompR cell size but has a limited effect on channel morphology. This work shows that fractal image analysis is a powerful tool to quantify the effect of phenotypic mutations and growth environment on the morphological complexity of internal E. coli biofilm structures. If applied to a wider range of mutant strains, this approach could help elucidate the genetic determinants of channel formation in E. coli colony biofilms.

量化不同细胞形状和生长环境下大肠埃希菌生物膜中营养物质运输通道的分形复杂性。
最近对大肠埃希菌营养物质运输通道的中观特征进行了分析,从而能够识别和测量整个成熟菌落生物膜中的单个通道。然而,它们在不同生理和环境条件下的复杂性仍然未知。对大肠杆菌细胞形状突变体形成的菌落生物膜的共聚焦显微照片分析表明,无论细胞表型或生长介质如何,通道都具有很高的分形复杂性。特别是具有宽细胞表型的突变株ΔompR 形成的菌落生物膜,在富培养基上生长时的分形维度高于在最小培养基上生长时的分形维度,而培养基中葡萄糖和琼脂的浓度会影响通道的复杂性。渗透压导致ΔompR 细胞体积急剧缩小,但对通道形态的影响有限。这项工作表明,分形图像分析是量化表型突变和生长环境对大肠杆菌生物膜内部结构形态复杂性影响的有力工具。如果将这种方法应用于更广泛的突变菌株,将有助于阐明大肠杆菌菌落生物膜中通道形成的遗传决定因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbiology-Sgm
Microbiology-Sgm 生物-微生物学
CiteScore
4.60
自引率
7.10%
发文量
132
审稿时长
3.0 months
期刊介绍: We publish high-quality original research on bacteria, fungi, protists, archaea, algae, parasites and other microscopic life forms. Topics include but are not limited to: Antimicrobials and antimicrobial resistance Bacteriology and parasitology Biochemistry and biophysics Biofilms and biological systems Biotechnology and bioremediation Cell biology and signalling Chemical biology Cross-disciplinary work Ecology and environmental microbiology Food microbiology Genetics Host–microbe interactions Microbial methods and techniques Microscopy and imaging Omics, including genomics, proteomics and metabolomics Physiology and metabolism Systems biology and synthetic biology The microbiome.
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