Trehalose Biosynthesis Promotes Pseudomonas aeruginosa Pathogenicity in Plants

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.

[1]  F. Ausubel,et al.  Genome-Wide Identification of Pseudomonas aeruginosa Virulence-Related Genes Using a Caenorhabditis elegans Infection Model , 2012, PLoS pathogens.

[2]  C. Kocks,et al.  Pseudomonas aeruginosa RhlR is required to neutralize the cellular immune response in a Drosophila melanogaster oral infection model , 2011, Proceedings of the National Academy of Sciences.

[3]  Mariusz Nowak,et al.  In-Vivo Expression Profiling of Pseudomonas aeruginosa Infections Reveals Niche-Specific and Strain-Independent Transcriptional Programs , 2011, PloS one.

[4]  A. Gravot,et al.  Genetic and physiological analysis of the relationship between partial resistance to clubroot and tolerance to trehalose in Arabidopsis thaliana. , 2011, The New phytologist.

[5]  K. Fahmy,et al.  Trehalose Renders the Dauer Larva of Caenorhabditis elegans Resistant to Extreme Desiccation , 2011, Current Biology.

[6]  A. Rogers,et al.  Inhibition of trehalose breakdown increases new carbon partitioning into cellulosic biomass in Nicotiana tabacum. , 2011, Carbohydrate research.

[7]  W. Frommer,et al.  Sugar transporters for intercellular exchange and nutrition of pathogens , 2010, Nature.

[8]  Masashi Tanaka,et al.  Trehalose extends longevity in the nematode Caenorhabditis elegans , 2010, Aging cell.

[9]  B. Freeman,et al.  Identification of the trehalose biosynthetic loci of Pseudomonas syringae and their contribution to fitness in the phyllosphere. , 2010, Environmental microbiology.

[10]  B. Ryall,et al.  Metabolic profiling of Pseudomonas aeruginosa demonstrates that the anti-sigma factor MucA modulates osmotic stress tolerance. , 2010, Molecular bioSystems.

[11]  C. Dean,et al.  Pseudomonas aeruginosa Increases Formation of Multidrug-Tolerant Persister Cells in Response to Quorum-Sensing Signaling Molecules , 2010, Journal of bacteriology.

[12]  Bárbara Nova-Franco,et al.  Trehalose Metabolism: From Osmoprotection to Signaling , 2009, International journal of molecular sciences.

[13]  J. Vivanco,et al.  Global Gene Expression Profiles Suggest an Important Role for Nutrient Acquisition in Early Pathogenesis in a Plant Model of Pseudomonas aeruginosa Infection , 2008, Applied and Environmental Microbiology.

[14]  I. Burgert,et al.  Disrupting Two Arabidopsis thaliana Xylosyltransferase Genes Results in Plants Deficient in Xyloglucan, a Major Primary Cell Wall Component[W][OA] , 2008, The Plant Cell Online.

[15]  B. Birren,et al.  Dynamics of Pseudomonas aeruginosa genome evolution , 2008, Proceedings of the National Academy of Sciences.

[16]  H. B. Sifton Air-space tissue in plants , 1945, The Botanical Review.

[17]  Frederick M. Ausubel,et al.  Combining Genomic Tools to Dissect Multifactorial Virulence in Pseudomonas aeruginosa , 2008 .

[18]  F. Rolland,et al.  Plant development: introducing trehalose metabolism. , 2007, Trends in plant science.

[19]  M. Pauly,et al.  Interactions between MUR10/CesA7-Dependent Secondary Cellulose Biosynthesis and Primary Cell Wall Structure1[OA] , 2006, Plant Physiology.

[20]  Li Li,et al.  Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial , 2006, Genome Biology.

[21]  A. Paccanaro,et al.  Clustering of Pseudomonas aeruginosa transcriptomes from planktonic cultures, developing and mature biofilms reveals distinct expression profiles , 2006, BMC Genomics.

[22]  G. Martin,et al.  Specific Bacterial Suppressors of MAMP Signaling Upstream of MAPKKK in Arabidopsis Innate Immunity , 2006, Cell.

[23]  S. Baud,et al.  Delayed embryo development in the ARABIDOPSIS TREHALOSE-6-PHOSPHATE SYNTHASE 1 mutant is associated with altered cell wall structure, decreased cell division and starch accumulation. , 2006, The Plant journal : for cell and molecular biology.

[24]  M. Whiteley,et al.  Microarray Analysis of the Osmotic Stress Response in Pseudomonas aeruginosa , 2006, Journal of bacteriology.

[25]  Frederick M Ausubel,et al.  Correction for Liberati et al., An ordered, nonredundant library of Pseudomonas aeruginosa strain PA14 transposon insertion mutants , 2006, Proceedings of the National Academy of Sciences.

[26]  E. Stabb,et al.  New rfp- and pES213-Derived Tools for Analyzing Symbiotic Vibrio fischeri Reveal Patterns of Infection and lux Expression In Situ , 2006, Applied and Environmental Microbiology.

[27]  Xiaoyan Tang,et al.  Flagellin induces innate immunity in nonhost interactions that is suppressed by Pseudomonas syringae effectors. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[28]  R. Sicher,et al.  Exogenous trehalose alters Arabidopsis transcripts involved in cell wall modification, abiotic stress, nitrogen metabolism, and plant defense , 2005 .

[29]  Eric Déziel,et al.  The contribution of MvfR to Pseudomonas aeruginosa pathogenesis and quorum sensing circuitry regulation: multiple quorum sensing‐regulated genes are modulated without affecting lasRI, rhlRI or the production of N‐acyl‐ l‐homoserine lactones , 2004, Molecular microbiology.

[30]  A. V. Van Dijken,et al.  Trehalose Mediated Growth Inhibition of Arabidopsis Seedlings Is Due to Trehalose-6-Phosphate Accumulation1[w] , 2004, Plant Physiology.

[31]  Jonathan D. G. Jones,et al.  Bacterial disease resistance in Arabidopsis through flagellin perception , 2004, Nature.

[32]  C. Dunand,et al.  The MUR3 Gene of Arabidopsis Encodes a Xyloglucan Galactosyltransferase That Is Evolutionarily Related to Animal Exostosins Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.009837. , 2003, The Plant Cell Online.

[33]  Rongchen Wang,et al.  Microarray Analysis of the Nitrate Response in Arabidopsis Roots and Shoots Reveals over 1,000 Rapidly Responding Genes and New Linkages to Glucose, Trehalose-6-Phosphate, Iron, and Sulfate Metabolism1[w] , 2003, Plant Physiology.

[34]  F. Ausubel,et al.  Use of the Galleria mellonella Caterpillar as a Model Host To Study the Role of the Type III Secretion System in Pseudomonas aeruginosa Pathogenesis , 2003, Infection and Immunity.

[35]  A. Elbein,et al.  New insights on trehalose: a multifunctional molecule. , 2003, Glycobiology.

[36]  F. Ausubel,et al.  Hypersusceptibility of cystic fibrosis mice to chronic Pseudomonas aeruginosa oropharyngeal colonization and lung infection , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[37]  A. Goldberg,et al.  Trehalose synthesis is induced upon exposure of Escherichia coli to cold and is essential for viability at low temperatures , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[38]  N. Raikhel,et al.  The mur2 mutant of Arabidopsis thaliana lacks fucosylated xyloglucan because of a lesion in fucosyltransferase AtFUT1 , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[39]  F. Ausubel,et al.  Pathogenesis of the human opportunistic pathogen Pseudomonas aeruginosa PA14 in Arabidopsis. , 2000, Plant physiology.

[40]  J. Argüelles,et al.  Physiological roles of trehalose in bacteria and yeasts: a comparative analysis , 2000, Archives of Microbiology.

[41]  T. Boller,et al.  Trehalose induces the ADP-glucose pyrophosphorylase gene, ApL3, and starch synthesis in Arabidopsis. , 2000, Plant physiology.

[42]  G. Pier,et al.  Acquisition of Expression of the Pseudomonas aeruginosa ExoU Cytotoxin Leads to Increased Bacterial Virulence in a Murine Model of Acute Pneumonia and Systemic Spread , 2000, Infection and Immunity.

[43]  F. Ausubel,et al.  Positive Correlation between Virulence ofPseudomonas aeruginosa Mutants in Mice and Insects , 2000, Journal of bacteriology.

[44]  W. Reiter,et al.  The mur4 mutant of arabidopsis is partially defective in the de novo synthesis of uridine diphospho L-arabinose. , 1999, Plant physiology.

[45]  F. Ausubel,et al.  Killing of Caenorhabditis elegans by Pseudomonas aeruginosa used to model mammalian bacterial pathogenesis. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[46]  Frederick M. Ausubel,et al.  Molecular Mechanisms of Bacterial Virulence Elucidated Using a Pseudomonas Aeruginosa– Caenorhabditis Elegans Pathogenesis Model , 2022 .

[47]  Roberto Kolter,et al.  Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways: a genetic analysis , 1998, Molecular microbiology.

[48]  D. Hassett,et al.  Cloning and Characterization of the Pseudomonas aeruginosa zwf Gene Encoding Glucose-6-Phosphate Dehydrogenase, an Enzyme Important in Resistance to Methyl Viologen (Paraquat) , 1998, Journal of bacteriology.

[49]  F. Ausubel,et al.  Use of model plant hosts to identify Pseudomonas aeruginosa virulence factors. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[50]  R. Kolter,et al.  Green fluorescent protein as a marker for Pseudomonas spp , 1997, Applied and environmental microbiology.

[51]  M. Kurimoto,et al.  Cloning and sequencing of a cluster of genes encoding novel enzymes of trehalose biosynthesis from thermophilic archaebacterium Sulfolobus acidocaldarius. , 1996, Biochimica et biophysica acta.

[52]  M. Kurimoto,et al.  Purification and properties of a novel enzyme, trehalose synthase, from Pimelobacter sp. R48. , 1996, Bioscience, biotechnology and biochemistry.

[53]  F. Ausubel,et al.  Common virulence factors for bacterial pathogenicity in plants and animals. , 1995, Science.

[54]  J. Whitsett,et al.  Correction of lethal intestinal defect in a mouse model of cystic fibrosis by human CFTR. , 1994, Science.

[55]  H. Schweizer,et al.  Construction of improved Escherichia-Pseudomonas shuttle vectors derived from pUC18/19 and sequence of the region required for their replication in Pseudomonas aeruginosa. , 1994, Gene.

[56]  A. Darzins The pilG gene product, required for Pseudomonas aeruginosa pilus production and twitching motility, is homologous to the enteric, single-domain response regulator CheY , 1993, Journal of bacteriology.

[57]  G. M. Smith,et al.  Roles of N-acetylglutaminylglutamine amide and glycine betaine in adaptation of Pseudomonas aeruginosa to osmotic stress , 1993, Applied and environmental microbiology.

[58]  J. Kaper,et al.  Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector , 1991, Infection and immunity.

[59]  A. Bent,et al.  Identification of Pseudomonas syringae pathogens of Arabidopsis and a bacterial locus determining avirulence on both Arabidopsis and soybean. , 1991, The Plant cell.

[60]  N. Panopoulos,et al.  Gene cluster of Pseudomonas syringae pv. "phaseolicola" controls pathogenicity of bean plants and hypersensitivity of nonhost plants , 1986, Journal of bacteriology.

[61]  H. Krisch,et al.  In vitro insertional mutagenesis with a selectable DNA fragment. , 1984, Gene.

[62]  G. Ashwell [12] Colorimetric analysis of sugars , 1957 .

[63]  M. Smogyi,et al.  Notes on sugar determination. , 1952, The Journal of biological chemistry.