Webb Benjamin A, Arapov Timofey D, Scharf Birgit E
Department of Biological Sciences, Virginia Tech, Blacksburg, VA, USA.
Methods Mol Biol. 2018;1729:33-45. doi: 10.1007/978-1-4939-7577-8_4.
Many chemotaxis assays allow for the assessment of bacterial chemotaxis by determining the number of cells migrating toward a chemoattractant or away from a chemorepellent. Some of these assays use a capillary filled with a chemoeffector/agarose mixture to allow cells to accumulate at the mouth of the capillary. Subsequently, assumptions about the relative strengths of chemotaxis strength are based on visual comparisons. Here, we describe a modification of this assay that uses a hydrogel matrix to enable quantitative time-course measurements by analyzing image pixel intensities. This approach allows a high-throughput method when coupled with the aid of a motorized microscope stage.