Difference between revisions of "PMID:19543378"

From OMPwiki
(Table edited by Joncrz via TableEdit)
(Table edited by Joncrz via TableEdit)
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*Taxon: Pseudomonas aeruginosa
 
*Taxon: Pseudomonas aeruginosa
 
*Strain: PA14
 
*Strain: PA14
*Substrain:  
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*Substrain: PA3885
 
*NCBI Taxon ID: 652611
 
*NCBI Taxon ID: 652611
 
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*Taxon: Pseudomonas aeruginosa
 
*Taxon: Pseudomonas aeruginosa
 
*Strain: PA14
 
*Strain: PA14
*Substrain:  
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*Substrain: PA3885
 
*NCBI Taxon ID: 652611
 
*NCBI Taxon ID: 652611
 
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*Taxon: Pseudomonas aeruginosa
 
*Taxon: Pseudomonas aeruginosa
 
*Strain: PA14
 
*Strain: PA14
*Substrain:  
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*Substrain: PA3885
 
*NCBI Taxon ID: 652611
 
*NCBI Taxon ID: 652611
 
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Figure 2B, .3% agar plates
 
Figure 2B, .3% agar plates
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a mutation or genetic difference within a strain
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*Taxon: Pseudomonas aeruginosa
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*Strain: PA14
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*Substrain: PA3885
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*NCBI Taxon ID: 652611
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*Genotype of Reference Strain: tpbA<sup>+</sup>
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*Genotype of Experimental Strain : tpbA<sup>-</sup>
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*Reference Condition: 37C after 24hours
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*Experimental Condition: 37C after 24hours
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increased cell aggregation
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Fig. 4A, LB medium
 
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Revision as of 18:53, 13 August 2014

Citation

Ueda, A and Wood, TK (2009) Connecting quorum sensing, c-di-GMP, pel polysaccharide, and biofilm formation in Pseudomonas aeruginosa through tyrosine phosphatase TpbA (PA3885).PLoS Pathog. 5:e1000483

Abstract

With the opportunistic pathogen Pseudomonas aeruginosa, quorum sensing based on homoserine lactones was found to influence biofilm formation. Here we discern a mechanism by which quorum sensing controls biofilm formation by screening 5850 transposon mutants of P. aeruginosa PA14 for altered biofilm formation. This screen identified the PA3885 mutant, which had 147-fold more biofilm than the wild-type strain. Loss of PA3885 decreased swimming, abolished swarming, and increased attachment, although this did not affect production of rhamnolipids. The PA3885 mutant also had a wrinkly colony phenotype, formed pronounced pellicles, had substantially more aggregation, and had 28-fold more exopolysaccharide production. Expression of PA3885 in trans reduced biofilm formation and abolished aggregation. Whole transcriptome analysis showed that loss of PA3885 activated expression of the pel locus, an operon that encodes for the synthesis of extracellular matrix polysaccharide. Genetic screening identified that loss of PelABDEG and the PA1120 protein (which contains a GGDEF-motif) suppressed the phenotypes of the PA3885 mutant, suggesting that the function of the PA3885 protein is to regulate 3,5-cyclic diguanylic acid (c-di-GMP) concentrations as a phosphatase since c-di-GMP enhances biofilm formation by activating PelD, and c-di-GMP inhibits swarming. Loss of PA3885 protein increased cellular c-di-GMP concentrations; hence, PA3885 protein is a negative regulator of c-di-GMP production. Purified PA3885 protein has phosphatase activity against phosphotyrosine peptides and is translocated to the periplasm. Las-mediated quorum sensing positively regulates expression of the PA3885 gene. These results show that the PA3885 protein responds to AHL signals and likely dephosphorylates PA1120, which leads to reduced c-di-GMP production. This inhibits matrix exopolysaccharide formation, which leads to reduced biofilm formation; hence, we provide a mechanism for quorum sensing control of biofilm formation through the pel locus and suggest PA3885 should be named TpbA for tyrosine phosphatase related to biofilm formation and PA1120 should be TpbB.

Links

PubMed Online version:10.1371/journal.ppat.1000483

Keywords

Adhesins, Bacterial; Bacterial Proteins; Biofilms; Cyclic GMP; Gene Expression Regulation, Bacterial; Glycolipids; Mutation; Periplasm; Phenotype; Polysaccharides, Bacterial; Protein Tyrosine Phosphatases; Pseudomonas aeruginosa; Quorum Sensing; Second Messenger Systems; Tyrosine

Main Points of the Paper

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Materials and Methods Used

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Phenotype Annotations

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Phenotype of Taxon Information Genotype Information (if known) Condition Information OMP ID OMP Term Name ECO ID ECO Term Name Notes Status

a mutation or genetic difference within a strain

  • Taxon: Pseudomonas aeruginosa
  • Strain: PA14
  • Substrain: PA3885
  • NCBI Taxon ID: 652611
  • Genotype of Reference Strain: tpbA+
  • Genotype of Experimental Strain : tpbA-
  • Reference Condition: after 8 hours in LB at 37C
  • Experimental Condition: after 8 hours in LB at 37C
OMP:0007020

increased biofilm formation

ECO:0000182

in vitro culture assay evidence

Figure 1A- by 147-fold, crystal violet staining

complete

a mutation or genetic difference within a strain

  • Taxon: Pseudomonas aeruginosa
  • Strain: PA14
  • Substrain: PA3885
  • NCBI Taxon ID: 652611
  • Genotype of Reference Strain: tpbA+
  • Genotype of Experimental Strain : tpbA-
  • Reference Condition: 37C after 24hours
  • Experimental Condition: 37C after 24hours
OMP:0006167

abolished cell motility by swarming

figure 2A, BM-2 agar

a mutation or genetic difference within a strain

  • Taxon: Pseudomonas aeruginosa
  • Strain: PA14
  • Substrain: PA3885
  • NCBI Taxon ID: 652611
  • Genotype of Reference Strain: tpbA+
  • Genotype of Experimental Strain : tpbA-
  • Reference Condition: 37C after 24hours
  • Experimental Condition: 37C after 24hours
OMP:0007093

decreased cell motility by swimming

Figure 2B, .3% agar plates

a mutation or genetic difference within a strain

  • Taxon: Pseudomonas aeruginosa
  • Strain: PA14
  • Substrain: PA3885
  • NCBI Taxon ID: 652611
  • Genotype of Reference Strain: tpbA+
  • Genotype of Experimental Strain : tpbA-
  • Reference Condition: 37C after 24hours
  • Experimental Condition: 37C after 24hours

increased cell aggregation

Fig. 4A, LB medium


Notes

References

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