Community proteogenomics reveals insights into the physiology of phyllosphere bacteria

Aerial plant surfaces represent the largest biological interface on Earth and provide essential services as sites of carbon dioxide fixation, molecular oxygen release, and primary biomass production. Rather than existing as axenic organisms, plants are colonized by microorganisms that affect both their health and growth. To gain insight into the physiology of phyllosphere bacteria under in situ conditions, we performed a culture-independent analysis of the microbiota associated with leaves of soybean, clover, and Arabidopsis thaliana plants using a metaproteogenomic approach. We found a high consistency of the communities on the 3 different plant species, both with respect to the predominant community members (including the alphaproteobacterial genera Sphingomonas and Methylo bacterium) and with respect to their proteomes. Observed known proteins of Methylobacterium were to a large extent related to the ability of these bacteria to use methanol as a source of carbon and energy. A remarkably high expression of various TonB-dependent receptors was observed for Sphingomonas. Because these outer membrane proteins are involved in transport processes of various carbohydrates, a particularly large substrate utilization pattern for Sphingomonads can be assumed to occur in the phyllosphere. These adaptations at the genus level can be expected to contribute to the success and coexistence of these 2 taxa on plant leaves. We anticipate that our results will form the basis for the identification of unique traits of phyllosphere bacteria, and for uncovering previously unrecorded mechanisms of bacteria-plant and bacteria-bacteria relationships.

[1]  L. Holm,et al.  The Pfam protein families database , 2005, Nucleic Acids Res..

[2]  Ludmila Chistoserdova,et al.  The expanding world of methylotrophic metabolism. , 2009, Annual review of microbiology.

[3]  T. Boller,et al.  Innate Immunity in Plants: An Arms Race Between Pattern Recognition Receptors in Plants and Effectors in Microbial Pathogens , 2009, Science.

[4]  J. Vorholt,et al.  Sigma factor mimicry involved in regulation of general stress response , 2009, Proceedings of the National Academy of Sciences.

[5]  Vincent J. Denef,et al.  Systems Biology: Functional analysis of natural microbial consortia using community proteomics , 2009, Nature Reviews Microbiology.

[6]  N. Fierer,et al.  Bacterial Succession on the Leaf Surface: A Novel System for Studying Successional Dynamics , 2009, Microbial Ecology.

[7]  M. Lidstrom,et al.  Comprehensive proteomics of Methylobacterium extorquens AM1 metabolism under single carbon and nonmethylotrophic conditions , 2008, Proteomics.

[8]  Dmitry A Rodionov,et al.  New Substrates for Tonb-dependent Transport: Do We Only See the 'tip of the Iceberg'? , 2022 .

[9]  J. Vorholt,et al.  Cultivation-Independent Characterization of Methylobacterium Populations in the Plant Phyllosphere by Automated Ribosomal Intergenic Spacer Analysis , 2008, Applied and Environmental Microbiology.

[10]  J. Vorholt,et al.  PhyR Is Involved in the General Stress Response of Methylobacterium extorquens AM1 , 2007, Journal of bacteriology.

[11]  S. Tringe,et al.  Quantitative Phylogenetic Assessment of Microbial Communities in Diverse Environments , 2007, Science.

[12]  D. Meyer,et al.  Plant Carbohydrate Scavenging through TonB-Dependent Receptors: A Feature Shared by Phytopathogenic and Aquatic Bacteria , 2007, PloS one.

[13]  J. Leveau Microbial communities in the phyllosphere , 2007 .

[14]  M. Bailey,et al.  Microbial Ecology of Aerial Plant Surfaces , 2006 .

[15]  J. Vorholt,et al.  A proteomic study of Methylobacterium extorquens reveals a response regulator essential for epiphytic growth , 2006, Proceedings of the National Academy of Sciences.

[16]  D. Crowley,et al.  Bacterial Diversity in Tree Canopies of the Atlantic Forest , 2006, Science.

[17]  T. Kudo,et al.  Intra- and Interspecific Comparisons of Bacterial Diversity and Community Structure Support Coevolution of Gut Microbiota and Termite Host , 2005, Applied and Environmental Microbiology.

[18]  J. Vorholt,et al.  Methylotrophic Metabolism Is Advantageous for Methylobacterium extorquens during Colonization of Medicago truncatula under Competitive Conditions , 2005, Applied and Environmental Microbiology.

[19]  S. Lindow,et al.  Pseudomonas syringae genes induced during colonization of leaf surfaces. , 2005, Environmental microbiology.

[20]  S. Lindow,et al.  Quorum sensing regulates exopolysaccharide production, motility, and virulence in Pseudomonas syringae. , 2005, Molecular plant-microbe interactions : MPMI.

[21]  E. Purdom,et al.  Diversity of the Human Intestinal Microbial Flora , 2005, Science.

[22]  J. Handelsman,et al.  Introducing DOTUR, a Computer Program for Defining Operational Taxonomic Units and Estimating Species Richness , 2005, Applied and Environmental Microbiology.

[23]  S. Tringe,et al.  Comparative Metagenomics of Microbial Communities , 2004, Science.

[24]  Shihui Yang,et al.  Genome-wide identification of plant-upregulated genes of Erwinia chrysanthemi 3937 using a GFP-based IVET leaf array. , 2004, Molecular plant-microbe interactions : MPMI.

[25]  S. Acinas,et al.  Fine-scale phylogenetic architecture of a complex bacterial community , 2004, Nature.

[26]  J. Yates,et al.  A model for random sampling and estimation of relative protein abundance in shotgun proteomics. , 2004, Analytical chemistry.

[27]  Robert D. Finn,et al.  The Pfam protein families database , 2007, Nucleic Acids Res..

[28]  S. Giovannoni,et al.  The uncultured microbial majority. , 2003, Annual review of microbiology.

[29]  S. Gordon,et al.  Solution Structure of the Mycobacterium tuberculosis Complex Protein MPB70 , 2003, Journal of Biological Chemistry.

[30]  A. Lapidus,et al.  Methylotrophy in Methylobacterium extorquens AM1 from a Genomic Point of View , 2003, Journal of bacteriology.

[31]  S. Lindow,et al.  Microbiology of the Phyllosphere , 2003, Applied and Environmental Microbiology.

[32]  I. Galbally,et al.  The Production of Methanol by Flowering Plants and the Global Cycle of Methanol , 2002 .

[33]  Julia A. Vorholt,et al.  Cofactor-dependent pathways of formaldehyde oxidation in methylotrophic bacteria , 2002, Archives of Microbiology.

[34]  P. Lindblad,et al.  Fasciclin Domain Proteins Are Present in Nostoc Symbionts of Lichens , 2002, Applied and Environmental Microbiology.

[35]  J. Boch,et al.  Identification of Pseudomonas syringae pv. tomato genes induced during infection of Arabidopsis thaliana , 2002, Molecular microbiology.

[36]  H. Rennenberg,et al.  Chemolithoautotrophic Nitrifiers in the Phyllosphere of a Spruce Ecosystem Receiving High Atmospheric Nitrogen Input , 2002, Current Microbiology.

[37]  D. Crowley,et al.  Microbial phyllosphere populations are more complex than previously realized , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[38]  S. S. Hirano,et al.  Bacteria in the Leaf Ecosystem with Emphasis onPseudomonas syringae—a Pathogen, Ice Nucleus, and Epiphyte , 2000, Microbiology and Molecular Biology Reviews.

[39]  A. Chakrabarty,et al.  Involvement of the exopolysaccharide alginate in the virulence and epiphytic fitness of Pseudomonas syringae pv. syringae , 1999, Molecular microbiology.

[40]  S. Long,et al.  Bacterial genes induced within the nodule during the Rhizobium–legume symbiosis , 1999, Molecular microbiology.

[41]  M. Bailey,et al.  Temporal fluctuations in the pseudomonad population associated with sugar beet leaves , 1999 .

[42]  K. Senoo,et al.  High population of Sphingomonas species on plant surface , 1998 .

[43]  M. Lidstrom,et al.  Molecular and mutational analysis of a DNA region separating two methylotrophy gene clusters in Methylobacterium extorquens AM1. , 1997, Microbiology.

[44]  L. Kinkel Microbial population dynamics on leaves. , 1997, Annual review of phytopathology.

[45]  W. A. Corpe,et al.  Ecology of the methylotrophic bacteria on living leaf surfaces , 1989 .

[46]  S. Lindow,et al.  Flagellar Motility Confers Epiphytic Fitness Advantages upon Pseudomonas syringae , 1987, Applied and environmental microbiology.