Periodic reversal of direction allows Myxobacteria to swarm

Many bacteria can rapidly traverse surfaces from which they are extracting nutrient for growth. They generate flat, spreading colonies, called swarms because they resemble swarms of insects. We seek to understand how members of any dense swarm spread efficiently while being able to perceive and interfere minimally with the motion of others. To this end, we investigate swarms of the myxobacterium, Myxococcus xanthus. Individual M. xanthus cells are elongated; they always move in the direction of their long axis; and they are in constant motion, repeatedly touching each other. Remarkably, they regularly reverse their gliding directions. We have constructed a detailed cell- and behavior-based computational model of M. xanthus swarming that allows the organization of cells to be computed. By using the model, we are able to show that reversals of gliding direction are essential for swarming and that reversals increase the outflow of cells across the edge of the swarm. Cells at the swarm edge gain maximum exposure to nutrient and oxygen. We also find that the reversal period predicted to maximize the outflow of cells is the same (within the errors of measurement) as the period observed in experiments with normal M. xanthus cells. This coincidence suggests that the circuit regulating reversals evolved to its current sensitivity under selection for growth achieved by swarming. Finally, we observe that, with time, reversals increase the cell alignment, and generate clusters of parallel cells.

[1]  D. Kaiser Myxococcus-from single-cell polarity to complex multicellular patterns. , 2008, Annual review of genetics.

[2]  E. Purcell Life at Low Reynolds Number , 2008 .

[3]  M. Borgnia,et al.  Three-Dimensional Imaging of the Highly Bent Architecture of Bdellovibrio bacteriovorus by Using Cryo-Electron Tomography , 2008, Journal of bacteriology.

[4]  Yi Jiang,et al.  Social Interactions in Myxobacterial Swarming , 2007, PLoS Comput. Biol..

[5]  D. Whitworth,et al.  Myxobacteria : multicellularity and differentiation , 2007 .

[6]  L. Søgaard-Andersen,et al.  Coupling of protein localization and cell movements by a dynamically localized response regulator in Myxococcus xanthus , 2007, The EMBO journal.

[7]  Michael J Shelley,et al.  Orientational order and instabilities in suspensions of self-locomoting rods. , 2007, Physical review letters.

[8]  Dale Kaiser,et al.  Bacterial Swarming: A Re-examination of Cell-Movement Patterns , 2007, Current Biology.

[9]  J. Shaevitz,et al.  Evidence That Focal Adhesion Complexes Power Bacterial Gliding Motility , 2007, Science.

[10]  Dale Kaiser,et al.  Gliding motility and polarized slime secretion , 2007, Molecular microbiology.

[11]  P. Youderian,et al.  Transposon Insertions of magellan-4 That Impair Social Gliding Motility in Myxococcus xanthus , 2006, Genetics.

[12]  C. Wolgemuth Force and flexibility of flailing myxobacteria. , 2005, Biophysical journal.

[13]  Albert Goldbeter,et al.  A biochemical oscillator explains several aspects of Myxococcus xanthus behavior during development. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[14]  Ruifeng Yang,et al.  AglZ Is a Filament-Forming Coiled-Coil Protein Required for Adventurous Gliding Motility of Myxococcus xanthus , 2004, Journal of bacteriology.

[15]  H. Vlamakis,et al.  Analysis of the Frz signal transduction system of Myxococcus xanthus shows the importance of the conserved C‐terminal region of the cytoplasmic chemoreceptor FrzCD in sensing signals , 2004, Molecular microbiology.

[16]  M. McBride,et al.  Cytophaga-Flavobacterium Gliding Motility , 2004, Journal of Molecular Microbiology and Biotechnology.

[17]  L. McCarter Dual Flagellar Systems Enable Motility under Different Circumstances , 2004, Journal of Molecular Microbiology and Biotechnology.

[18]  P. Youderian,et al.  Identification of genes required for adventurous gliding motility in Myxococcus xanthus with the transposable element mariner , 2003, Molecular microbiology.

[19]  A. Merz,et al.  Bacterial Surface Motility: Slime Trails, Grappling Hooks and Nozzles , 2002, Current Biology.

[20]  Lotte Søgaard-Andersen,et al.  Pattern formation by a cell surface-associated morphogen in Myxococcus xanthus , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Roy D. Welch,et al.  Cell behavior in traveling wave patterns of myxobacteria , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[22]  I. Vetter,et al.  The Guanine Nucleotide-Binding Switch in Three Dimensions , 2001, Science.

[23]  J. Warren Catheter-associated urinary tract infections. , 2001, International journal of antimicrobial agents.

[24]  D. Helbing Traffic and related self-driven many-particle systems , 2000, cond-mat/0012229.

[25]  L. Jelsbak,et al.  The cell surface-associated intercellular C-signal induces behavioral changes in individual Myxococcus xanthus cells during fruiting body morphogenesis. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[26]  D. Kaiser,et al.  Gliding Mutants of Myxococcus xanthuswith High Reversal Frequencies and Small Displacements , 1999, Journal of bacteriology.

[27]  Gerard T. Barkema,et al.  Monte Carlo Methods in Statistical Physics , 1999 .

[28]  R. Belas,et al.  Characterization of Proteus mirabilisPrecocious Swarming Mutants: Identification of rsbA, Encoding a Regulator of Swarming Behavior , 1998, Journal of bacteriology.

[29]  P. Hartzell Complementation of sporulation and motility defects in a prokaryote by a eukaryotic GTPase. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[30]  R. Harshey,et al.  Bees aren't the only ones: swarming in Gram‐negative bacteria , 1994, Molecular microbiology.

[31]  D. Zusman,et al.  "Frizzy" genes of Myxococcus xanthus are involved in control of frequency of reversal of gliding motility. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[32]  A. Omu,et al.  The contribution of multiple pregnancy to perinatal mortality in Benin City. , 1983, Journal of obstetrics and gynaecology.

[33]  D. Kaiser,et al.  Nutrition of Myxococcus xanthus, a fruiting myxobacterium , 1978, Journal of bacteriology.

[34]  H. Berg,et al.  Physics of chemoreception. , 1977, Biophysical journal.

[35]  J. M. Beebe The Morphology and Cytology of Myxococcus xanthus, N. Sp , 1941, Journal of bacteriology.

[36]  Jonathan Hodgkin,et al.  Genetics of gliding motility in Myxococcus xanthus (Myxobacterales): Two gene systems control movement , 2004, Molecular and General Genetics MGG.

[37]  D. Kaiser,et al.  Genetics of gliding motility in Myxococcus xanthus (Myxobacterales): Genes controlling movement of single cells , 2004, Molecular and General Genetics MGG.

[38]  R. P. Burchard Studies on gliding motility inMyxococcus xanthus , 2004, Archives of Microbiology.

[39]  D. Zusman,et al.  "Frizzy" aggregation genes of the gliding bacterium Myxococcus xanthus show sequence similarities to the chemotaxis genes of enteric bacteria. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[40]  H. Reichenbach,et al.  Myxobacteria: A Most Peculiar Group of Social Prokaryotes , 1984 .

[41]  Dale Kaiser,et al.  Cell movement and its coordination in swarms of myxococcus xanthus , 1983 .

[42]  I. M. Soboĺ,et al.  Die Monte-Carlo-Methode , 1971 .