Abstract
Soil and aquatic multicellular microorganisms play a critical role in the nutrient-cycling and organismal ecology of soil and aquatic ecosystems. These organisms live and behave in a complex three-dimensional environment. Most studies of microorganismal behavior, in contrast, have been conducted using microscope-based approaches, which limit the movement and behavior to a narrow, nearly two-dimensional focal field. We report on a novel analytical approach that provides real-time analysis of freely swimming C. elegans without dependence on microscope-based equipment. This approach consists of tracking the temporal periodicity of diffraction patterns generated by directing laser light onto nematodes in a cuvette. We measured oscillation frequencies for freely swimming nematodes in cuvettes of different sizes to provide different physical constraints on their swimming. We compared these frequencies with those obtained for nematodes swimming within a small droplet of water on a microscope slide, a strategy used by microscope-based locomotion analysis systems. We collected data from diffraction patterns using two methods: video analysis and real time data acquisition using a fast photodiode. Swimming frequencies of nematodes in a droplet of ionic solution on a microscope slide was confirmed to be 2.00 Hz with a variance of 0.05 Hz for the video analysis method and 0.03 Hz for the real time data acquisition using a photodiode; this result agrees with previously published estimates using microscope-based analytical techniques. We find the swimming frequency of unconstrained worms within larger cuvettes to be 2.37 Hz with a variance of 0.02 Hz. As the cuvette size decreased, so did the oscillation frequency, indicating a change in locomotion when physical constraints are introduced.
Highlights
C. elegans are free-living soil-dwelling nematodes that navigate in three dimensions
We report on a novel analytical approach that provides real-time analysis of freely swimming C. elegans without dependence on microscope-based equipment
We demonstrated that swimming behavior of freely swimming microorganisms can be quantitatively determined using diffraction analysis without relying on a microscope or multiple cameras
Summary
C. elegans are free-living soil-dwelling nematodes that navigate in three dimensions They move both on a solid matrix like soil or agar in a sinusoidal locomotory pattern called “crawling” and in liquid in a different pattern called “swimming” [1]. The speed of locomotion is equal to the body length (about 1 mm) times the oscillation frequency of the head (about 0.8 Hz) [101] Genetic analysis of this rather restricted movement has led to the elucidation of the neuromuscular circuitry and the cellular mechanisms of the generation of the movement [5]. Studies of C. elegans locomotion in liquid, usually within small drops on a microscope slide, have revealed aspects of the plasticity of locomotion in the nematode, in particular the ability to switch locomotory styles upon encountering a different medium [1].
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