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   Trehalose Biosynthesis Promotes Pseudomonas aeruginosa Pathogenicity in Plants  
   
نویسنده djonović s. ,urbach j.m. ,drenkard e. ,bush j. ,feinbaum r. ,ausubel j.l. ,traficante d. ,risech m. ,kocks c. ,fischbach m.a. ,priebe g.p. ,ausubel f.m.
منبع plos pathogens - 2013 - دوره : 9 - شماره : 3
چکیده    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 δtreyzδtres mutant. exogenous trehalose or ammonium nitrate does not suppress the growth defect of the double δtreyzδtres 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 δtreyzδtres in trans. surprisingly,the growth defect of the double δtreyzδtres 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. © 2013 djonović et al.
آدرس department of molecular biology,massachusetts general hospital,boston,ma,united states,department of genetics,harvard medical school,boston,ma, United States, department of molecular biology,massachusetts general hospital,boston,ma, United States, department of molecular biology,massachusetts general hospital,boston,ma,united states,department of genetics,harvard medical school,boston,ma, United States, department of molecular biology,massachusetts general hospital,boston,ma, United States, department of molecular biology,massachusetts general hospital,boston,ma,united states,department of genetics,harvard medical school,boston,ma, United States, department of molecular biology,massachusetts general hospital,boston,ma,united states,skidmore college,saratoga springs,ny, United States, division of infectious diseases,department of medicine,brigham and women's hospital,boston,ma,united states,lake erie college of osteopathic medicine,greensburg,pa, United States, division of infectious diseases,department of medicine,brigham and women's hospital,boston,ma, United States, department of molecular biology,massachusetts general hospital,boston,ma,united states,department of genetics,harvard medical school,boston,ma,united states,max delbrück center for molecular medicine,berlin, Germany, department of bioengineering and therapeutic sciences,university of california,san francisco,san francisco,ca, United States, division of infectious diseases,department of medicine,brigham and women's hospital,boston,ma,united states,division of critical care medicine,department of anesthesiology,perioperative and pain medicine,boston children's hospital,boston,ma, United States, department of molecular biology,massachusetts general hospital,boston,ma,united states,department of genetics,harvard medical school,boston,ma, United States
 
     
   
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