2D vs 3D tracking in bacterial motility analysis

被引:4
作者
Acres, Jacqueline [1 ]
Nadeau, Jay [1 ]
机构
[1] Portland State Univ, Dept Phys, 1719 SW 10th Ave, Portland, OR 97201 USA
来源
AIMS BIOPHYSICS | 2021年 / 8卷 / 04期
基金
美国国家航空航天局; 美国国家科学基金会;
关键词
holographic microscopy; microbial motility; Vibrio; reverse and flick; chemotaxis; tracking; DIGITAL HOLOGRAPHIC MICROSCOPY; SHEWANELLA-PUTREFACIENS; CHEMOTAXIS; MOTION; RESOLUTION; ALGORITHM; INFECTION; DYNAMICS; FIELD; FIJI;
D O I
10.3934/biophy.2021030
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Digital holographic microscopy provides the ability to observe throughout a large volume without refocusing. This capability enables simultaneous observations of large numbers of microorganisms swimming in an essentially unconstrained fashion. However, computational tools for tracking large 4D datasets remain lacking. In this paper, we examine the errors introduced by tracking bacterial motion as 2D projections vs. 3D volumes under different circumstances: bacteria free in liquid media and bacteria near a glass surface. We find that while XYZ speeds are generally equal to or larger than XY speeds, they are still within empirical uncertainties. Additionally, when studying dynamic surface behavior, the Z coordinate cannot be neglected.
引用
收藏
页码:385 / 399
页数:15
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