Andrea Gloria-Soria, Ricardo B.R. Azevedo  Current Biology 

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npr-1 Regulates Foraging and Dispersal Strategies in Caenorhabditis elegans  Andrea Gloria-Soria, Ricardo B.R. Azevedo  Current Biology  Volume 18, Issue 21, Pages 1694-1699 (November 2008) DOI: 10.1016/j.cub.2008.09.043 Copyright © 2008 Elsevier Ltd Terms and Conditions

Figure 1 Gregarious and Solitary Worms Differ in Their Spatial Pattern of Food Consumption (A–I) The foraging strategies of solitary (N2 strain, [D]–[F]) and gregarious (RC301 strain, [G]–[I]) worms are compared. Images are GFP fluorescence micrographs of each bacterial lawn 12 (D, G), 24 (E, H), and 36 (F, I) hr after 40 48-hr-old worms (postfertilization) were transferred to the plate. Undisturbed control lawns are shown for comparison (A–C). The lawn in (A) has a diameter of 12 mm. (J) Change in mean GFP fluorescence over the entire lawn, rescaled such that the initial value, at time 0, is set at 100%. (K) Change in the ratio of mean GFP fluorescence in the border and center of the lawn, covering 40% and 60% of the total area of the lawn, respectively (dashed circles in [A] mark the two sectors). Values are means and 95% CI (n = 4 replicates per treatment). Time is calculated from the start of the experiment, so worms are 48- to 96-hr-old during the period shown. Current Biology 2008 18, 1694-1699DOI: (10.1016/j.cub.2008.09.043) Copyright © 2008 Elsevier Ltd Terms and Conditions

Figure 2 Gregarious and Solitary Worms Differ in Their Dispersal Propensity in an npr-1-Dependent Manner (A) Assay plate containing 12 lawns with a diameter of ∼12 mm each, arranged in three concentric rings, numbered 1–3, at a distance of approximately 2, 4, and 6 cm from the center. (B) Proportion of individuals found in ring i (xi) after 72 hr in three representative strains. (C) Expected values of xi under a Markov model for a range of individual dispersal probabilities per hour, λ (calculated for α = 1; Supplemental Experimental Procedures). (D) Estimates of λ for three solitary and three gregarious natural isolates, one backcrossed strain, and two npr-1 mutant strains. Values are means and 95% CI from arcsine-transformed estimates based on the number of independent experiments in parentheses. All estimates for DA508 were λ = 0.05, the maximum value allowed in the model. In (B) and (D), values are means and 95% CI based on the numbers of independent experiments in parentheses. See Figure S4 for data on other wild strains. (E) λ in N2 as a function of population density (number of individuals). Lines show a linear regression model and 95% CI (F[1,20] = 22.5, p = 0.0001, r2 = 0.53). Current Biology 2008 18, 1694-1699DOI: (10.1016/j.cub.2008.09.043) Copyright © 2008 Elsevier Ltd Terms and Conditions

Figure 3 Gregarious and Solitary Worms Differ in Individual Dispersal Propensity in an npr-1-Dependent Manner Proportion of hermaphrodites remaining in the bacterial lawn over time in three representative strains. Lines are exponential survival models fitted for each strain: the slope estimates the individual dispersal probability (λ) per hour (Supplemental Experimental Procedures). See Figure S5 for data on other gregarious and solitary strains. Current Biology 2008 18, 1694-1699DOI: (10.1016/j.cub.2008.09.043) Copyright © 2008 Elsevier Ltd Terms and Conditions

Figure 4 Fragmentation of a Food Resource Increases the Relative Fitness of the Gregarious Allele Solitary (N2) and gregarious (DA609) strains were allowed to compete with a reference solitary fluorescent strain (PD4251) in continuous and fragmented food environments. Values show the mean frequency of individuals from the test strain after 5 days of competition (∼2 generations) based on n = 6 replicate experiments (see Supplemental Experimental Procedures). Error bars are 95% CI. The dashed line shows the expected frequencies if the test and reference strains have the same fitness. Current Biology 2008 18, 1694-1699DOI: (10.1016/j.cub.2008.09.043) Copyright © 2008 Elsevier Ltd Terms and Conditions