Cargando…
Mechanism for Collective Cell Alignment in Myxococcus xanthus Bacteria
Myxococcus xanthus cells self-organize into aligned groups, clusters, at various stages of their lifecycle. Formation of these clusters is crucial for the complex dynamic multi-cellular behavior of these bacteria. However, the mechanism underlying the cell alignment and clustering is not fully under...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550276/ https://www.ncbi.nlm.nih.gov/pubmed/26308508 http://dx.doi.org/10.1371/journal.pcbi.1004474 |
_version_ | 1782387431488618496 |
---|---|
author | Balagam, Rajesh Igoshin, Oleg A. |
author_facet | Balagam, Rajesh Igoshin, Oleg A. |
author_sort | Balagam, Rajesh |
collection | PubMed |
description | Myxococcus xanthus cells self-organize into aligned groups, clusters, at various stages of their lifecycle. Formation of these clusters is crucial for the complex dynamic multi-cellular behavior of these bacteria. However, the mechanism underlying the cell alignment and clustering is not fully understood. Motivated by studies of clustering in self-propelled rods, we hypothesized that M. xanthus cells can align and form clusters through pure mechanical interactions among cells and between cells and substrate. We test this hypothesis using an agent-based simulation framework in which each agent is based on the biophysical model of an individual M. xanthus cell. We show that model agents, under realistic cell flexibility values, can align and form cell clusters but only when periodic reversals of cell directions are suppressed. However, by extending our model to introduce the observed ability of cells to deposit and follow slime trails, we show that effective trail-following leads to clusters in reversing cells. Furthermore, we conclude that mechanical cell alignment combined with slime-trail-following is sufficient to explain the distinct clustering behaviors observed for wild-type and non-reversing M. xanthus mutants in recent experiments. Our results are robust to variation in model parameters, match the experimentally observed trends and can be applied to understand surface motility patterns of other bacterial species. |
format | Online Article Text |
id | pubmed-4550276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45502762015-09-01 Mechanism for Collective Cell Alignment in Myxococcus xanthus Bacteria Balagam, Rajesh Igoshin, Oleg A. PLoS Comput Biol Research Article Myxococcus xanthus cells self-organize into aligned groups, clusters, at various stages of their lifecycle. Formation of these clusters is crucial for the complex dynamic multi-cellular behavior of these bacteria. However, the mechanism underlying the cell alignment and clustering is not fully understood. Motivated by studies of clustering in self-propelled rods, we hypothesized that M. xanthus cells can align and form clusters through pure mechanical interactions among cells and between cells and substrate. We test this hypothesis using an agent-based simulation framework in which each agent is based on the biophysical model of an individual M. xanthus cell. We show that model agents, under realistic cell flexibility values, can align and form cell clusters but only when periodic reversals of cell directions are suppressed. However, by extending our model to introduce the observed ability of cells to deposit and follow slime trails, we show that effective trail-following leads to clusters in reversing cells. Furthermore, we conclude that mechanical cell alignment combined with slime-trail-following is sufficient to explain the distinct clustering behaviors observed for wild-type and non-reversing M. xanthus mutants in recent experiments. Our results are robust to variation in model parameters, match the experimentally observed trends and can be applied to understand surface motility patterns of other bacterial species. Public Library of Science 2015-08-26 /pmc/articles/PMC4550276/ /pubmed/26308508 http://dx.doi.org/10.1371/journal.pcbi.1004474 Text en © 2015 Balagam, Igoshin http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Balagam, Rajesh Igoshin, Oleg A. Mechanism for Collective Cell Alignment in Myxococcus xanthus Bacteria |
title | Mechanism for Collective Cell Alignment in Myxococcus xanthus Bacteria |
title_full | Mechanism for Collective Cell Alignment in Myxococcus xanthus Bacteria |
title_fullStr | Mechanism for Collective Cell Alignment in Myxococcus xanthus Bacteria |
title_full_unstemmed | Mechanism for Collective Cell Alignment in Myxococcus xanthus Bacteria |
title_short | Mechanism for Collective Cell Alignment in Myxococcus xanthus Bacteria |
title_sort | mechanism for collective cell alignment in myxococcus xanthus bacteria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550276/ https://www.ncbi.nlm.nih.gov/pubmed/26308508 http://dx.doi.org/10.1371/journal.pcbi.1004474 |
work_keys_str_mv | AT balagamrajesh mechanismforcollectivecellalignmentinmyxococcusxanthusbacteria AT igoshinolega mechanismforcollectivecellalignmentinmyxococcusxanthusbacteria |