Literature DB >> 35377166

Nonmotile Subpopulations of Pseudomonas aeruginosa Repress Flagellar Motility in Motile Cells through a Type IV Pilus- and Pel-Dependent Mechanism.

Kimberley A Lewis1, Danielle M Vermilyea1, Shanice S Webster1, Christopher J Geiger1, Jaime de Anda2,3,4, Gerard C L Wong2,3,4, George A O'Toole1, Deborah A Hogan1.   

Abstract

The downregulation of Pseudomonas aeruginosa flagellar motility is a key event in biofilm formation, host colonization, and the formation of microbial communities, but the external factors that repress motility are not well understood. Here, we report that on soft agar, swarming motility can be repressed by cells that are nonmotile due to the absence of a flagellum or flagellar rotation. Mutants that lack either flagellum biosynthesis or rotation, when present at as little as 5% of the total population, suppressed swarming of wild-type cells. Non-swarming cells required functional type IV pili and the ability to produce Pel exopolysaccharide to suppress swarming by the flagellated wild type. Flagellated cells required only type IV pili, but not Pel production, for their swarming to be repressed by non-flagellated cells. We hypothesize that interactions between motile and nonmotile cells may enhance the formation of sessile communities, including those involving multiple genotypes, phenotypically diverse cells, and perhaps other species. IMPORTANCE Our study shows that, under the conditions tested, a small population of non-swarming cells can impact the motility behavior of a larger population. The interactions that lead to the suppression of swarming motility require type IV pili and a secreted polysaccharide, two factors with known roles in biofilm formation. These data suggest that interactions between motile and nonmotile cells may enhance the transition to sessile growth in populations and promote interactions between cells with different genotypes.

Entities:  

Keywords:  Pel; Pseudomonas aeruginosa; microbe-microbe interaction; motility; swarming; type IV pili

Mesh:

Substances:

Year:  2022        PMID: 35377166      PMCID: PMC9112919          DOI: 10.1128/jb.00528-21

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.476


  49 in total

1.  Pseudomonas aeruginosa lasR mutant fitness in microoxia is supported by an Anr-regulated oxygen-binding hemerythrin.

Authors:  Michelle E Clay; John H Hammond; Fangfang Zhong; Xiaolei Chen; Caitlin H Kowalski; Alexandra J Lee; Monique S Porter; Thomas H Hampton; Casey S Greene; Ekaterina V Pletneva; Deborah A Hogan
Journal:  Proc Natl Acad Sci U S A       Date:  2020-01-24       Impact factor: 11.205

2.  Structural features of the Pseudomonas fluorescens biofilm adhesin LapA required for LapG-dependent cleavage, biofilm formation, and cell surface localization.

Authors:  Chelsea D Boyd; T Jarrod Smith; Sofiane El-Kirat-Chatel; Peter D Newell; Yves F Dufrêne; George A O'Toole
Journal:  J Bacteriol       Date:  2014-05-16       Impact factor: 3.490

3.  Cyclic-di-GMP-mediated repression of swarming motility by Pseudomonas aeruginosa: the pilY1 gene and its impact on surface-associated behaviors.

Authors:  S L Kuchma; A E Ballok; J H Merritt; J H Hammond; W Lu; J D Rabinowitz; George A O'Toole
Journal:  J Bacteriol       Date:  2010-03-16       Impact factor: 3.490

4.  Type IV pili interactions promote intercellular association and moderate swarming of Pseudomonas aeruginosa.

Authors:  Morgen E Anyan; Aboutaleb Amiri; Cameron W Harvey; Giordano Tierra; Nydia Morales-Soto; Callan M Driscoll; Mark S Alber; Joshua D Shrout
Journal:  Proc Natl Acad Sci U S A       Date:  2014-12-02       Impact factor: 11.205

5.  Genes involved in matrix formation in Pseudomonas aeruginosa PA14 biofilms.

Authors:  Lisa Friedman; Roberto Kolter
Journal:  Mol Microbiol       Date:  2004-02       Impact factor: 3.501

6.  Controlling the Connections of Cells to the Biofilm Matrix.

Authors:  Matthew R Parsek
Journal:  J Bacteriol       Date:  2015-11-02       Impact factor: 3.490

7.  Plate-based assay for swarming motility in Pseudomonas aeruginosa.

Authors:  Dae-Gon Ha; Sherry L Kuchma; George A O'Toole
Journal:  Methods Mol Biol       Date:  2014

8.  Pseudomonas aeruginosa clinical and environmental isolates constitute a single population with high phenotypic diversity.

Authors:  María-Victoria Grosso-Becerra; Christian Santos-Medellín; Abigail González-Valdez; José-Luis Méndez; Gabriela Delgado; Rosario Morales-Espinosa; Luis Servín-González; Luis-David Alcaraz; Gloria Soberón-Chávez
Journal:  BMC Genomics       Date:  2014-04-28       Impact factor: 3.969

9.  Requirements for Pseudomonas aeruginosa acute burn and chronic surgical wound infection.

Authors:  Keith H Turner; Jake Everett; Urvish Trivedi; Kendra P Rumbaugh; Marvin Whiteley
Journal:  PLoS Genet       Date:  2014-07-24       Impact factor: 5.917

10.  Discovery and characterization of a Gram-positive Pel polysaccharide biosynthetic gene cluster.

Authors:  Gregory B Whitfield; Lindsey S Marmont; Cedoljub Bundalovic-Torma; Erum Razvi; Elyse J Roach; Cezar M Khursigara; John Parkinson; P Lynne Howell
Journal:  PLoS Pathog       Date:  2020-04-01       Impact factor: 6.823

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