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Swarming bacteria respond to increasing barriers to motility by increasing cell length and modifying colony structure

https://doi.org/10.1101/398321
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/meth.2001.1153openalex-snapshot
Protein Recruitment Systems for the Analysis of Protein-Protein Interactions
inferredcites →https://doi.org/10.1007/s00285-005-0345-3openalex-snapshot
A structured-population model of Proteus mirabilis swarm-colony development
inferredcites →https://doi.org/10.1016/0378-1119(91)90599-7openalex-snapshot
A wide-host-range suicide vector for improving reverse genetics in Gram-negative bacteria: inactivation of the blaA gene of Yersinia enterocolitica
inferredcites →https://doi.org/10.1016/j.bpj.2014.05.052openalex-snapshot
Osmotic Pressure in a Bacterial Swarm
inferredcites →https://doi.org/10.1016/j.cell.2015.05.005openalex-snapshot
The Mechanical World of Bacteria
inferredcites →https://doi.org/10.1016/j.jmb.2015.07.025openalex-snapshot
Shelter in a Swarm
inferredcites →https://doi.org/10.1016/j.mib.2016.02.004openalex-snapshot
Sensational biofilms: surface sensing in bacteria
inferredcites →https://doi.org/10.1016/j.mib.2016.12.002openalex-snapshot
Bacterial mechanotransduction
inferredcites →https://doi.org/10.1016/j.tim.2014.05.002openalex-snapshot
Biofilms, flagella, and mechanosensing of surfaces by bacteria
inferredcites →https://doi.org/10.1016/s0076-6879(01)36575-8openalex-snapshot
[3] Surface sensing, swarmer cell differentiation, and biofilm development
inferredcites →https://doi.org/10.1016/s0378-1119(97)00619-7openalex-snapshot
Improved allelic exchange vectors and their use to analyze 987P fimbria gene expression
inferredcites →https://doi.org/10.1021/bm070115wopenalex-snapshot
Does Water Activity Rule P. mirabilis Periodic Swarming? II. Viscoelasticity and Water Balance during Swarming
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nmeth.4509openalex-snapshot
Systematic characterization of maturation time of fluorescent proteins in living cells
inferredcites →https://doi.org/10.1038/nrmicro1820openalex-snapshot
Morphological plasticity as a bacterial survival strategy
inferredcites →https://doi.org/10.1038/nrmicro2405openalex-snapshot
A field guide to bacterial swarming motility
inferredcites →https://doi.org/10.1038/s41598-017-05521-8openalex-snapshot
Torque, but not FliL, regulates mechanosensitive flagellar motor-function
inferredcites →https://doi.org/10.1038/sj.emboj.7600668openalex-snapshot
Sensing wetness: a new role for the bacterial flagellum
inferredcites →https://doi.org/10.1038/srep26005openalex-snapshot
Stigmergy co-ordinates multicellular collective behaviours during Myxococcus xanthus surface migration
inferredcites →https://doi.org/10.1046/j.1365-2958.1998.01060.xopenalex-snapshot
The Myxococcus xanthus lipopolysaccharide O‐antigen is required for social motility and multicellular development
inferredcites →https://doi.org/10.1073/pnas.1016693108openalex-snapshot
Microbubbles reveal chiral fluid flows in bacterial swarms
inferredcites →https://doi.org/10.1073/pnas.1118238109openalex-snapshot
Water reservoir maintained by cell growth fuels the spreading of a bacterial swarm
inferredcites →https://doi.org/10.1073/pnas.1218898110openalex-snapshot
Self-organization of bacterial biofilms is facilitated by extracellular DNA
inferredcites →https://doi.org/10.1073/pnas.1503553112openalex-snapshot
Cell rejuvenation and social behaviors promoted by LPS exchange in myxobacteria
inferredcites →https://doi.org/10.1093/nar/gkh131openalex-snapshot
UniProt: the Universal Protein knowledgebase
inferredcites →https://doi.org/10.1093/nar/gkw1099openalex-snapshot
UniProt: the universal protein knowledgebase
inferredcites →https://doi.org/10.1099/00221287-40-1-29openalex-snapshot
Development of Flagella by Proteus mirabilis
inferredcites →https://doi.org/10.1101/pdb.prot4861openalex-snapshot
PCR Mutagenesis by Overlap Extension and Gene SOE
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07445.xopenalex-snapshot
Surface sensing in Vibrio parahaemolyticus triggers a programme of gene expression that promotes colonization and virulence
inferredcites →https://doi.org/10.1126/science.1160033openalex-snapshot
Genetic Determinants of Self Identity and Social Recognition in Bacteria
inferredcites →https://doi.org/10.1126/science.aan5353openalex-snapshot
Second messenger–mediated tactile response by a bacterial rotary motor
inferredcites →https://doi.org/10.1128/aac.01219-09openalex-snapshot
Proteus mirabilis pmrI , an RppA-Regulated Gene Necessary for Polymyxin B Resistance, Biofilm Formation, and Urothelial Cell Invasion
inferredcites →https://doi.org/10.1128/aac.01384-09openalex-snapshot
Characterization of UDP-Glucose Dehydrogenase and UDP-Glucose Pyrophosphorylase Mutants ofProteus mirabilis: Defectiveness in Polymyxin B Resistance, Swarming, and Virulence
inferredcites →https://doi.org/10.1128/aac.45.7.2030-2037.2001openalex-snapshot
Identification of Proteus mirabilis Mutants with Increased Sensitivity to Antimicrobial Peptides
inferredcites →https://doi.org/10.1128/aem.02946-09openalex-snapshot
Molecular and Genetic Analyses of the Putative Proteus O Antigen Gene Locus
inferredcites →https://doi.org/10.1128/iai.01222-09openalex-snapshot
Transcriptome of Swarming Proteus mirabilis
inferredcites →https://doi.org/10.1128/iai.02232-14openalex-snapshot
New Aspects of RpoE in Uropathogenic Proteus mirabilis
inferredcites →https://doi.org/10.1128/iai.72.7.3941-3950.2004openalex-snapshot
Ultrastructure of Proteus mirabilis Swarmer Cell Rafts and Role of Swarming in Catheter-Associated Urinary Tract Infection
inferredcites →https://doi.org/10.1128/jb.00196-10openalex-snapshot
Loss of the WaaL O-Antigen Ligase Prevents Surface Activation of the Flagellar Gene Cascade in Proteus mirabilis
inferredcites →https://doi.org/10.1128/jb.00230-18openalex-snapshot
Swarmer Cell Development of the Bacterium Proteus mirabilis Requires the Conserved Enterobacterial Common Antigen Biosynthesis Gene rffG
inferredcites →https://doi.org/10.1128/jb.00402-16openalex-snapshot
The Self-Identity Protein IdsD Is Communicated between Cells in Swarming Proteus mirabilis Colonies
inferredcites →https://doi.org/10.1128/jb.01109-07openalex-snapshot
The Wetting Agent Required for Swarming in Salmonella enterica Serovar Typhimurium Is Not a Surfactant
inferredcites →https://doi.org/10.1128/jb.01294-06openalex-snapshot
Genome-Wide Screening of Genes Required for Swarming Motility inEscherichia coliK-12
inferredcites →https://doi.org/10.1128/jb.02063-12openalex-snapshot
Swarming: Flexible Roaming Plans
inferredcites →https://doi.org/10.1128/jb.02235-14openalex-snapshot
Loss of FliL Alters Proteus mirabilis Surface Sensing and Temperature-Dependent Swarming
inferredcites →https://doi.org/10.1128/jb.06047-11openalex-snapshot
Role of the Umo Proteins and the Rcs Phosphorelay in the Swarming Motility of the Wild Type and an O-Antigen ( waaL ) Mutant of Proteus mirabilis
inferredcites →https://doi.org/10.1128/jb.154.2.930-937.1983openalex-snapshot
Extracellular slime associated with Proteus mirabilis during swarming
inferredcites →https://doi.org/10.1128/jb.172.7.4106-4108.1990openalex-snapshot
Regulation of Escherichia coli sigma F RNA polymerase by flhD and flhC flagellar regulatory genes
inferredcites →https://doi.org/10.1128/jb.173.19.6289-6293.1991openalex-snapshot
Transposon mutagenesis in Proteus mirabilis
inferredcites →https://doi.org/10.1128/jb.178.22.6525-6538.1996openalex-snapshot
Periodic phenomena in Proteus mirabilis swarm colony development
inferredcites →https://doi.org/10.1128/jb.182.22.6308-6321.2000openalex-snapshot
Genetics of Swarming Motility inSalmonella entericaSerovar Typhimurium: Critical Role for Lipopolysaccharide
inferredcites →https://doi.org/10.1128/jcm.28.12.2627-2631.1990openalex-snapshot
Modification of the silver staining technique to detect lipopolysaccharide in polyacrylamide gels
inferredcites →https://doi.org/10.1128/mbio.00374-13openalex-snapshot
Two Independent Pathways for Self-Recognition in Proteus mirabilis Are Linked by Type VI-Dependent Export
inferredcites →https://doi.org/10.1159/000077866openalex-snapshot
Dual Flagellar Systems Enable Motility under Different Circumstances
inferredcites →https://doi.org/10.4161/cib.27331openalex-snapshot
Stigmergy

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s00253-019-09846-4openalex-snapshot
Structural changes of bacterial nanocellulose pellicles induced by genetic modification of Komagataeibacter hansenii ATCC 23769
inferred← citeshttps://doi.org/10.1128/jb.00118-19openalex-snapshot
Biofilms 2018: a Diversity of Microbes and Mechanisms
inferred← citeshttps://doi.org/10.33899/rjs.2024.182824openalex-snapshot
Effect of Chitosan Nanoparticles on Growth, Swarming Motility, and Biofilm Formation in Proteus Mirabilis Isolated from Urinary Tract Infections
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