Gut bacterial aggregates as living gels

  1. Brandon H Schlomann
  2. Raghuveer Parthasarathy  Is a corresponding author
  1. Department of Physics, Institute of Molecular Biology, and Materials Science Institute, University of Oregon, United States
  2. Department of Physics and Department of Molecular and Cell Biology, University of California, Berkeley, United States
4 figures, 4 tables and 2 additional files

Figures

Overview of experimental methods.

Larval zebrafish were derived germ-free and then monoassociated with single bacterial species (left). After 24 hr of colonization, images spanning the entire gut were acquired with light sheet …

Figure 2 with 2 supplements
Different bacterial species exhibit similar cluster size distributions.

Reverse cumulative distributions, the probability that the cluster size is greater than n as a function of n, for eight bacterial strains in larval zebrafish intestines. Small circles connected by …

Figure 2—figure supplement 1
Cluster size distributions as probability densities.

Different bacterial species exhibit similar cluster size distributions. Probability densities for eight bacterial strains monoassociated in larval zebrafish intestines. Small circles connected by …

Figure 2—figure supplement 2
Images of individual z-slices showing mild heterogeneity of fluorescence intensity within aggregates.

Fluorescence intensity is mostly homogeneous within clusters, although small dark regions do occur. Three individual z slices of a fish colonized with Enterobacter are shown. The approximate gut …

A minimal model inspired by evolutionary dynamics generates power law distributions.

(A) Fragmentation is analogous to mutation and we can construct a genealogy that mirrors the physical structure of the clusters. (B) Summary of a growth/fragmentation process that includes the …

Figure 3—source data 1

Results of power-law fits to simulated distributions.

https://cdn.elifesciences.org/articles/71105/elife-71105-fig3-data1-v2.xlsx
Figure 4 with 3 supplements
Size-dependent aggregation introduces a plateau in the size distribution.

(A) Schematic of the generalized model. Parameters summarized in Table 3. (B) Reverse cumulative distributions obtained from simulations for different values of νA (left, middle, right) and α

Figure 4—figure supplement 1
Distributions of growth/fragmentation process at short times.

Mild curvature appears in the minimal growth/fragmentation process distribution at finite time, but the result is inconsistent with experimental data. Circles are the result of stochastic …

Figure 4—figure supplement 2
Distributions for a process with density-dependent growth, fragmentation, and expulsion.

A modified process with carrying capacity and expulsion does not produce a plateau in the stationary size distribution. Reverse cumulative distributions computed from stochastic simulations with …

Figure 4—figure supplement 3
Distributions for a model with only aggregation and νA=1.

Plateaus arise at the gelation transition of purely aggregating systems. Reverse cumulative distributions computed from stochastic simulations are shown. Different curves represent different …

Tables

Table 1
Summary of cluster data by bacterial strain.

Each row corresponds to one of the bacterial strains included in this study. Entries include strain name, total number of fish colonized with that strain, total number of clusters identified across …

Bacterial strainNumber of fishNumber of clustersSource publication
Aeromonas ZOR00016445Schlomann et al., 2018
Aeromonas ZOR000261901Schlomann et al., 2018
Enterobacter ZOR0014183597Schlomann et al., 2018; Schlomann et al., 2019
Plesiomonas ZOR00113223Schlomann et al., 2018
Pseudomonas ZWU00066133Schlomann et al., 2018
Vibrio ZOR003662430Schlomann et al., 2018
Vibrio ZWU0020 Δmot115888Wiles et al., 2020
Vibrio ZWU0020 Δche113551Wiles et al., 2020
Table 2
Analytic results for the minimal growth-fragmentation process.

Distribution exponent, μ, as a function of fragmentation exponent, νF, fragmentation rate, β, and growth rate, r, as plotted in Figure 3D. Results are expected to be valid for long times (t), large …

νF=1νF=2/3νF=0
distribution exponent, μ1+11-β/r53+βr1+β/r1+β/r
Table 3
Summary of model variables and parameters.
Variable/parameterDescription
nCluster size (number of cells)
p(n)Probability of cluster size, n
P(size>n)Cumulative probability; probability of size being larger than n
μExponent of power law; p(n)n-μ, P(size>n)n-μ+1
rCell division rate
KCarrying capacity; maximum number of cells
βFragmentation rate
νFFragmentation exponent; clusters of size n fragment with rate βnνF
αAggregation rate
νAAggregation exponent; clusters of sizes n and m aggregate with rate α(nm)νA
λExpulsion rate
νEExpulsion exponent; clusters of size n are expelled with rate λnνE
Key resources table
Reagent type (species)
or resource
DesignationSource or referenceIdentifiersAdditional
information
Software, algorithmAnalysis codeThis studysee Materials and methods, Simulations
OtherCluster size dataSchlomann and moments, 2018
OtherCluster size dataSchlomann et al., 2019
OtherCluster size dataWiles et al., 2020

Additional files

Supplementary file 1

Cumulative distribution exponents of cluster size distributions by strain, with analysis of sensitivity to single-cell detection.

The small size regime of the cluster size distributions were fit to a power-law model for sizes up to 100 cells using two methods: a linear fit to P(size>n) and maximum likelihood estimation (Materials and methods). The fits were done for each animal and the resulting mean ± std. dev of the exponents (corresponding to μ-1, as defined in the text) are given for each strain. For each method, the fits were done twice, once including single cells, and once considering only cells of size two or greater. As discussed in the main text, the largest uncertainty in cluster size enumeration from the images occurs at small sizes. Ignoring single cells in the fit only mildly changes the average exponent, and all changes are within uncertainties. Most exponents are consistent with μ-1=1.

https://cdn.elifesciences.org/articles/71105/elife-71105-supp1-v2.xlsx
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