bioRxivMicrobiologyPreprint
Cell behaviors underlying Myxococcus xanthus aggregate coarsening
P. Murphy, J. Comstock, T. Khan, J. Zhang, R. D. Welch, O. A. Igoshin
Abstract
The soil bacterium Myxococcus xanthus is a model organism with a set of diverse behaviors. These behaviors include the starvation-induced multicellular development program, in which cells move collectively to assemble multicellular aggregates. After initial aggregates have formed, some will disperse, with smaller aggregates having a higher chance of dispersal. Initial aggregation is driven by two changes in cell behavior: cells slow down inside of aggregates and bias their motion by reversing direction less frequently when moving towards aggregates. However, the cell behaviors that drive dispersal are unknown. Here we use fluorescent microscopy to quantify changes in cell behavior after initial aggregates have formed. We observe that after initial aggregate formation, cells adjust the bias in reversal timings by initiating reversals more rapidly when approaching unstable aggregates. Using agent-based modeling, we then show dispersal is predominantly generated by this change in bias, which is strong enough to overcome slowdown inside aggregates. Notably, the change in reversal bias is correlated with the nearest aggregates size, connecting cellular activity to previously observed correlations between aggregate size and fate. To determine if this connection is consistent across strains, we analyze a second M. xanthus strain with reduced levels of dispersal. We find that far fewer cells near smaller aggregates modified their bias. This implies that aggregate dispersal is under genetic control, providing a foundation for further investigations into the role it plays in the life cycle of M. xanthus. ImportanceUnderstanding the processes behind bacterial biofilm formation, maintenance, and dispersal is essential for addressing their effects on health and ecology. Within these multicellular communities, various cues can trigger differentiation into distinct cell types, allowing cells to adapt to their specific local environment. The soil bacterium Myxococcus xanthus forms biofilms in response to starvation, marked by cells aggregating into mounds. Some aggregates persist as spore-filled fruiting bodies, while others disperse after initial formation for unknown reasons. Here, we use a combination of cell tracking analysis and computational simulations to identify behaviors at the cellular level that contribute to aggregate dispersal. Our results suggest that cells in aggregates actively determine whether to disperse or persist and undergo a transition to sporulation based on a self-produced cue related to the aggregates size. Identifying these cues is an important step in understanding and potentially manipulating bacterial cell-fate decisions.
- organism: bacteria (other)
- assay: imaging
- research focus: cell type annotation
- approach: microscopy & imaging analysis
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Agent-Based Modeling Reveals Possible Mechanisms for Observed Aggregation Cell Behaviors in Myxococcus xanthus
Z. Zhang, C. R. Cotter, … O. A. Igoshin·bioRxiv·May 11, 2018
- Data-driven models reveal mutant cell behaviors important for myxobacterial aggregation
Z. Zhang, C. Cotter, … O. A. Igoshin·bioRxiv·Feb 8, 2020
- Unravelling a diversity of cellular structures and aggregation dynamics during the early development of Myxococcus xanthus
Natsuko Rivera‐Yoshida, Alejandro V. Arzola, Mariana Benítez·Biology LettersPeer-reviewed·Oct 1, 2024
- 3D Agent-based modeling without chemical signaling recreatescollective behaviors seen in Myxococcus xanthus colonies
Katherine Copenhagen, Matthew E. Black, Joshua W. Shaevitz·PRX LifePeer-reviewed·Sep 30, 2025
- The mechanism of spatial pattern transition in motile bacterial collectives
Jean-Baptiste Saulnier, Michèle Romanos, … Tâm Mignot·Nature PhysicsPeer-reviewed·Sep 15, 2026
- Formation, collective motion, and merging of macroscopicbacterial aggregates
J. Q. Boedicker, G. Courcoutbetis, … S. Haas·bioRxiv·Jun 9, 2021