4.7 Article

Trehalose Biosynthesis Promotes Pseudomonas aeruginosa Pathogenicity in Plants

Journal

PLOS PATHOGENS
Volume 9, Issue 3, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.ppat.1003217

Keywords

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Funding

  1. MBRC Tosteson Fellowship
  2. Program for Breakthrough Biomedical Research
  3. NIH [DP2 OD007290, R01 HL092515, R37 GM48707, R01 AI085581]
  4. NSF [MCB-0519898]
  5. Division Of Integrative Organismal Systems
  6. Direct For Biological Sciences [929226] Funding Source: National Science Foundation

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Pseudomonas aeruginosa strain PA14 is a multi-host pathogen that infects plants, nematodes, insects, and vertebrates. Many PA14 factors are required for virulence in more than one of these hosts. Noting that plants have a fundamentally different cellular architecture from animals, we sought to identify PA14 factors that are specifically required for plant pathogenesis. We show that synthesis by PA14 of the disaccharide trehalose is required for pathogenesis in Arabidopsis, but not in nematodes, insects, or mice. In-frame deletion of two closely-linked predicted trehalose biosynthetic operons, treYZ and treS, decreased growth in Arabidopsis leaves about 50 fold. Exogenously co-inoculated trehalose, ammonium, or nitrate, but not glucose, sulfate, or phosphate suppressed the phenotype of the double Delta treYZ Delta treS mutant. Exogenous trehalose or ammonium nitrate does not suppress the growth defect of the double Delta treYZ Delta treS mutant by suppressing the plant defense response. Trehalose also does not function intracellularly in P. aeruginosa to ameliorate a variety of stresses, but most likely functions extracellularly, because wild-type PA14 rescued the in vivo growth defect of the Delta treYZ Delta treS in trans. Surprisingly, the growth defect of the double Delta treYZ Delta treS double mutant was suppressed by various Arabidopsis cell wall mutants that affect xyloglucan synthesis, including an xxt1xxt2 double mutant that completely lacks xyloglucan, even though xyloglucan mutants are not more susceptible to pathogens and respond like wild-type plants to immune elicitors. An explanation of our data is that trehalose functions to promote the acquisition of nitrogen-containing nutrients in a process that involves the xyloglucan component of the plant cell wall, thereby allowing P. aeruginosa to replicate in the intercellular spaces in a leaf. This work shows how P. aeruginosa, a multi-host opportunistic pathogen, has repurposed a highly conserved house-keeping anabolic pathway (trehalose biosynthesis) as a potent virulence factor that allows it to replicate in the intercellular environment of a leaf.

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