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. 2019 Oct 23;9:15246. doi: 10.1038/s41598-019-51608-9

Figure 1.

Figure 1

Basic principle of Pluronic (PF-127) gel-based burrowing assay. (a) The burrowing assay is conducted in a 12-well plate; in each well, animals are stimulated to move through a gel towards a food source placed at the top. The inset shows the nematodes that have successfully burrowed and reached the food source (E. coli) at the top of the gel (See also supplementary video S1). (b) Burrowing performance of day 1 wild-type adults in the presence and absence of E. coli bacteria in 26% w/w PF-F127. Gel thickness, H = 0.9 cm. N = 39 and 35 animals in the presence and absence of bacteria, respectively. (c) Calcium imaging shows the muscle contractions as the nematode is burrowing in the PF-127 gel. Strain is HBR4: goeIs3 HBR4: goeIs3[Pmyo-3::GCaMP3.35::unc-54-3′utr, unc-119] expressing the calcium indicator GCaMP3 in body wall muscles. Images are taken with 5 s intervals. Arrow heads point to the tail that appears faded in i and ii due to the 3D locomotion. In all three images, the head is on the left. (d) Dynamic quantification of calcium signaling activity from an animal during a 10 second burrowing episode. Each pixel is 1 second apart on the x-axis.