Comparative genomics support reduced-genome Paraburkholderia symbionts of Dictyostelium discoideum amoebas are ancestrally adapted professional symbionts

The social amoeba Dictyostelium discoideum is a predatory soil protist frequently used for studying host-pathogen interactions. A subset of D. discoideum strains isolated from soil persistently carry symbiotic Paraburkholderia, recently formally described as P. agricolaris, P. bonniea, and P. hayleyella. The three facultative symbiont species of D. discoideum present a unique opportunity to study a naturally occurring symbiosis in a laboratory model protist. In addition, there is a large difference in genome size between P. agricolaris (8.7 million base pairs) vs. P. hayleyella and P. bonniea (4.1 Mbp) and in GC content (62% vs. 59%). We took a comparative genomics approach and compared the three genomes of D. discoideum-symbionts to 12 additional Paraburkholderia genomes to test for genome evolution patterns that frequently accompany host adaptation. Overall, P. agricolaris is difficult to distinguish from other Paraburkholderia based on its genome size and content, but the two reduced genomes of P. bonniea and P. hayleyella display characteristics that support evolution in a host environment. In addition, all three D. discoideum-symbiont genomes have increased secretion system and motility genes that may mediate interactions with their host. Specifically, adjacent BurBor-like type 3 and T6SS-5-like type 6 secretion system operons shared among all three D. discoideum-symbiont genomes may be important for host interaction. Ultimately, our combined evidence supports that the reduced-genome D. discoideum-symbionts have evolved to be professional symbionts ancestrally adapted to their protist hosts.

[1]  J. Strassmann,et al.  Context dependence in the symbiosis between Dictyostelium discoideum and Paraburkholderia , 2022, bioRxiv.

[2]  L. Moulin,et al.  Genetic Diversity of Type 3 Secretion System in Burkholderia s.l. and Links With Plant Host Adaptation , 2021, Frontiers in Microbiology.

[3]  J. McCutcheon,et al.  Pseudofinder: Detection of Pseudogenes in Prokaryotic Genomes , 2021, bioRxiv.

[4]  U. Hentschel Harnessing the power of host–microbe symbioses to address grand challenges , 2021, Nature Reviews Microbiology.

[5]  P. Keeling,et al.  Bacterial and archaeal symbioses with protists , 2021, Current Biology.

[6]  K. King,et al.  Microbial evolution and transitions along the parasite–mutualist continuum , 2021, Nature Reviews Microbiology.

[7]  Jiangning Song,et al.  BastionHub: a universal platform for integrating and analyzing substrates secreted by Gram-negative bacteria , 2020, Nucleic Acids Res..

[8]  J. Kamanova,et al.  Bordetella Type III Secretion Injectosome and Effector Proteins , 2020, Frontiers in Cellular and Infection Microbiology.

[9]  Susanne DiSalvo,et al.  Paraburkholderia Symbionts Display Variable Infection Patterns That Are Not Predictive of Amoeba Host Outcomes , 2020, Genes.

[10]  J. Strassmann,et al.  Endosymbiotic adaptations in three new bacterial species associated with Dictyostelium discoideum: Paraburkholderia agricolaris sp. nov., Paraburkholderia hayleyella sp. nov., and Paraburkholderia bonniea sp. nov , 2020, PeerJ.

[11]  M. Schaefers Regulation of Virulence by Two-Component Systems in Pathogenic Burkholderia , 2020, Infection and Immunity.

[12]  A. Arkin,et al.  GapMind: Automated Annotation of Amino Acid Biosynthesis , 2019, mSystems.

[13]  Yoko Sato,et al.  KEGG Mapper for inferring cellular functions from protein sequences , 2019, Protein science : a publication of the Protein Society.

[14]  T. Richards,et al.  The Ecology and Evolution of Pangenomes , 2019, Current Biology.

[15]  J. Strassmann,et al.  Fitness costs and benefits vary for two facultative Burkholderia symbionts of the social amoeba, Dictyostelium discoideum , 2019, Ecology and evolution.

[16]  J. McCutcheon,et al.  The Life of an Insect Endosymbiont from the Cradle to the Grave , 2019, Current Biology.

[17]  C. Buchrieser,et al.  Intracellular parasitism, the driving force of evolution of Legionella pneumophila and the genus Legionella , 2019, Genes & Immunity.

[18]  Nicole A. Hynson,et al.  A Developing Symbiosis: Enabling Cross-Talk Between Ecologists and Microbiome Scientists , 2019, Front. Microbiol..

[19]  J. Strassmann,et al.  The specificity of Burkholderia symbionts in the social amoeba farming symbiosis: Prevalence, species, genetic and phenotypic diversity , 2019, Molecular ecology.

[20]  T. West,et al.  The Burkholderia Type VI Secretion System 5: Composition, Regulation and Role in Virulence , 2019, Front. Microbiol..

[21]  Claire Bertelli,et al.  Microbial genomic island discovery, visualization and analysis , 2018, Briefings Bioinform..

[22]  J. Strassmann,et al.  Symbiont location, host fitness, and possible coadaptation in a symbiosis between social amoebae and bacteria , 2018, eLife.

[23]  I. Park,et al.  Genomic Features and Insights into the Taxonomy, Virulence, and Benevolence of Plant-Associated Burkholderia Species , 2018, International journal of molecular sciences.

[24]  J. Strassmann,et al.  Burkholderia bacteria use chemotaxis to find social amoeba Dictyostelium discoideum hosts , 2018, The ISME Journal.

[25]  Chao Zhang,et al.  ASTRAL-III: polynomial time species tree reconstruction from partially resolved gene trees , 2018, BMC Bioinformatics.

[26]  J. Strassmann,et al.  Endosymbiotic adaptations in three new bacterial species associated with Dictyostelium discoideum: Burkholderia agricolaris sp. nov., Burkholderia hayleyella sp. nov., and Burkholderia bonniea sp. nov , 2018, bioRxiv.

[27]  J. Dunn,et al.  Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses , 2018, Front. Immunol..

[28]  J. Wernegreen In it for the long haul: evolutionary consequences of persistent endosymbiosis. , 2017, Current opinion in genetics & development.

[29]  Martin Wu,et al.  Comparative Genomic Analysis of Acanthamoeba Endosymbionts Highlights the Role of Amoebae as a “Melting Pot” Shaping the Rickettsiales Evolution , 2017, Genome biology and evolution.

[30]  Yejun Wang,et al.  A global survey of bacterial type III secretion systems and their effectors , 2017, Environmental microbiology.

[31]  A. Arkin,et al.  Filling gaps in bacterial amino acid biosynthesis pathways with high-throughput genetics , 2017, bioRxiv.

[32]  Mihnea R. Mangalea,et al.  Nitrate Sensing and Metabolism Inhibit Biofilm Formation in the Opportunistic Pathogen Burkholderia pseudomallei by Reducing the Intracellular Concentration of c-di-GMP , 2017, Front. Microbiol..

[33]  Matthew R. Laird,et al.  IslandViewer 4: expanded prediction of genomic islands for larger-scale datasets , 2017, Nucleic Acids Res..

[34]  M. Fares,et al.  Chance and necessity in the genome evolution of endosymbiotic bacteria of insects , 2017, The ISME Journal.

[35]  Minoru Kanehisa,et al.  KEGG: new perspectives on genomes, pathways, diseases and drugs , 2016, Nucleic Acids Res..

[36]  Thijs J. G. Ettema,et al.  A Rickettsiales symbiont of amoebae with ancient features. , 2016, Environmental microbiology.

[37]  A. Latorre,et al.  Snapshots of a shrinking partner: Genome reduction in Serratia symbiotica , 2016, Scientific Reports.

[38]  Suzanna E Lewis,et al.  JBrowse: a dynamic web platform for genome visualization and analysis , 2016, Genome Biology.

[39]  M. Kanehisa,et al.  BlastKOALA and GhostKOALA: KEGG Tools for Functional Characterization of Genome and Metagenome Sequences. , 2016, Journal of molecular biology.

[40]  Thomas Nussbaumer,et al.  EffectiveDB—updates and novel features for a better annotation of bacterial secreted proteins and Type III, IV, VI secretion systems , 2015, Nucleic Acids Res..

[41]  Minoru Kanehisa,et al.  KEGG as a reference resource for gene and protein annotation , 2015, Nucleic Acids Res..

[42]  Wen-Sui Lo,et al.  Winding paths to simplicity: genome evolution in facultative insect symbionts. , 2016, FEMS microbiology reviews.

[43]  M. Touchon,et al.  Identification of protein secretion systems in bacterial genomes , 2015, Scientific Reports.

[44]  J. Strassmann,et al.  Burkholderia bacteria infectiously induce the proto-farming symbiosis of Dictyostelium amoebae and food bacteria , 2015, Proceedings of the National Academy of Sciences.

[45]  Jacqueline A. Keane,et al.  Circlator: automated circularization of genome assemblies using long sequencing reads , 2015, Genome Biology.

[46]  Tandy Warnow,et al.  ASTRID: Accurate Species TRees from Internode Distances , 2015, bioRxiv.

[47]  Yufeng Yao,et al.  SecReT6: a web-based resource for type VI secretion systems found in bacteria. , 2015, Environmental microbiology.

[48]  Andrew J. Page,et al.  Roary: rapid large-scale prokaryote pan genome analysis , 2015, bioRxiv.

[49]  Christophe Dessimoz,et al.  Inferring Horizontal Gene Transfer , 2015, PLoS Comput. Biol..

[50]  Michael Y. Galperin,et al.  Expanded microbial genome coverage and improved protein family annotation in the COG database , 2014, Nucleic Acids Res..

[51]  Chao Xie,et al.  Fast and sensitive protein alignment using DIAMOND , 2014, Nature Methods.

[52]  Torsten Seemann,et al.  Prokka: rapid prokaryotic genome annotation , 2014, Bioinform..

[53]  Matthew Fraser,et al.  InterProScan 5: genome-scale protein function classification , 2014, Bioinform..

[54]  D. Goodlett,et al.  VgrG-5 Is a Burkholderia Type VI Secretion System-Exported Protein Required for Multinucleated Giant Cell Formation and Virulence , 2014, Infection and Immunity.

[55]  R Core Team,et al.  R: A language and environment for statistical computing. , 2014 .

[56]  P. Vandamme,et al.  Burkholderia sprentiae sp. nov., isolated from Lebeckia ambigua root nodules. , 2013, International journal of systematic and evolutionary microbiology.

[57]  J. Strassmann,et al.  Social amoeba farmers carry defensive symbionts to protect and privatize their crops , 2013, Nature Communications.

[58]  Didier Raoult,et al.  Postgenomic analysis of bacterial pathogens repertoire reveals genome reduction rather than virulence factors. , 2013, Briefings in functional genomics.

[59]  Aaron A. Klammer,et al.  Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data , 2013, Nature Methods.

[60]  Qiangde Duan,et al.  Flagella and bacterial pathogenicity , 2013, Journal of basic microbiology.

[61]  A. Maurelli,et al.  Antivirulence Genes: Insights into Pathogen Evolution through Gene Loss , 2012, Infection and Immunity.

[62]  Inanç Birol,et al.  Hive plots - rational approach to visualizing networks , 2012, Briefings Bioinform..

[63]  N. Moran,et al.  Extreme genome reduction in symbiotic bacteria , 2011, Nature Reviews Microbiology.

[64]  Ting-Hsiang Wu,et al.  Dissection of the Burkholderia intracellular life cycle using a photothermal nanoblade , 2011, Proceedings of the National Academy of Sciences.

[65]  Yahua Chen,et al.  Regulation of Type VI Secretion System during Burkholderia pseudomallei Infection , 2011, Infection and Immunity.

[66]  S. Bozzaro,et al.  The Professional Phagocyte Dictyostelium discoideum as a Model Host for Bacterial Pathogens , 2011, Current drug targets.

[67]  D. DeShazer,et al.  The Cluster 1 Type VI Secretion System Is a Major Virulence Determinant in Burkholderia pseudomallei , 2011, Infection and Immunity.

[68]  Thomas Rattei,et al.  Effective—a database of predicted secreted bacterial proteins , 2010, Nucleic Acids Res..

[69]  M. Horn,et al.  The genome of the amoeba symbiont "Candidatus Amoebophilus asiaticus" encodes an afp-like prophage possibly used for protein secretion. , 2010, Virulence.

[70]  T. West,et al.  Burkholderia Type VI Secretion Systems Have Distinct Roles in Eukaryotic and Bacterial Cell Interactions , 2010, PLoS pathogens.

[71]  Christina Toft,et al.  Evolutionary microbial genomics: insights into bacterial host adaptation , 2010, Nature Reviews Genetics.

[72]  N. Perna,et al.  progressiveMauve: Multiple Genome Alignment with Gene Gain, Loss and Rearrangement , 2010, PloS one.

[73]  P. Tan,et al.  Identification of a regulatory cascade controlling Type III Secretion System 3 gene expression in Burkholderia pseudomallei , 2010, Molecular microbiology.

[74]  Fiona S. L. Brinkman,et al.  Detecting genomic islands using bioinformatics approaches , 2010, Nature Reviews Microbiology.

[75]  Paramvir S. Dehal,et al.  FastTree 2 – Approximately Maximum-Likelihood Trees for Large Alignments , 2010, PloS one.

[76]  J. Badger,et al.  Continuing Evolution of Burkholderia mallei Through Genome Reduction and Large-Scale Rearrangements , 2010, Genome biology and evolution.

[77]  M. Wagner,et al.  The Genome of the Amoeba Symbiont “Candidatus Amoebophilus asiaticus” Reveals Common Mechanisms for Host Cell Interaction among Amoeba-Associated Bacteria , 2009, Journal of bacteriology.

[78]  Mark D. Robinson,et al.  edgeR: a Bioconductor package for differential expression analysis of digital gene expression data , 2009, Bioinform..

[79]  D. Raoult,et al.  Massive comparative genomic analysis reveals convergent evolution of specialized bacteria , 2009, Biology Direct.

[80]  João C Setubal,et al.  Protein secretion systems in bacterial-host associations, and their description in the Gene Ontology , 2009, BMC Microbiology.

[81]  N. Moran,et al.  Genomics and evolution of heritable bacterial symbionts. , 2008, Annual review of genetics.

[82]  Raymond Lo,et al.  The Burkholderia Genome Database: facilitating flexible queries and comparative analyses , 2008, Bioinform..

[83]  T. Soldati,et al.  Eat, kill or die: when amoeba meets bacteria. , 2008, Current opinion in microbiology.

[84]  N. Garçon Chance and necessity , 2008, Human vaccines.

[85]  P. Vandamme,et al.  Burkholderia sartisoli sp. nov., isolated from a polycyclic aromatic hydrocarbon-contaminated soil. , 2008, International journal of systematic and evolutionary microbiology.

[86]  P. Vandamme,et al.  Burkholderia bryophila sp. nov. and Burkholderia megapolitana sp. nov., moss-associated species with antifungal and plant-growth-promoting properties. , 2007, International journal of systematic and evolutionary microbiology.

[87]  Ziheng Yang PAML 4: phylogenetic analysis by maximum likelihood. , 2007, Molecular biology and evolution.

[88]  V. Daubin,et al.  Comparative genomics and the evolution of prokaryotes. , 2007, Trends in microbiology.

[89]  A. Maurelli Black holes, antivirulence genes, and gene inactivation in the evolution of bacterial pathogens. , 2007, FEMS microbiology letters.

[90]  K. Brown,et al.  ATP-binding cassette systems in Burkholderia pseudomallei and Burkholderia mallei , 2007, BMC Genomics.

[91]  Terry Gaasterland,et al.  DarkHorse: a method for genome-wide prediction of horizontal gene transfer , 2007, Genome Biology.

[92]  Peer Bork,et al.  PAL2NAL: robust conversion of protein sequence alignments into the corresponding codon alignments , 2006, Nucleic Acids Res..

[93]  H. Ochman,et al.  The Nature and Dynamics of Bacterial Genomes , 2006, Science.

[94]  sung-taik lee,et al.  Burkholderia terrae sp. nov., isolated from a forest soil. , 2006, International journal of systematic and evolutionary microbiology.

[95]  Patricia Siguier,et al.  ISfinder: the reference centre for bacterial insertion sequences , 2005, Nucleic Acids Res..

[96]  P. Vandamme,et al.  Burkholderia phytofirmans sp. nov., a novel plant-associated bacterium with plant-beneficial properties. , 2005, International journal of systematic and evolutionary microbiology.

[97]  Jun Yu,et al.  VFDB: a reference database for bacterial virulence factors , 2004, Nucleic Acids Res..

[98]  N. Moran,et al.  Genomic changes following host restriction in bacteria. , 2004, Current opinion in genetics & development.

[99]  R. Titball,et al.  ATP-Binding Cassette Transporters Are Targets for the Development of Antibacterial Vaccines and Therapies , 2004, Infection and Immunity.

[100]  O. White,et al.  Structural flexibility in the Burkholderia mallei genome. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[101]  P. de Vos,et al.  Classification of the biphenyl- and polychlorinated biphenyl-degrading strain LB400T and relatives as Burkholderia xenovorans sp. nov. , 2004, International journal of systematic and evolutionary microbiology.

[102]  M. Gerstein,et al.  Comprehensive analysis of pseudogenes in prokaryotes: widespread gene decay and failure of putative horizontally transferred genes , 2004, Genome Biology.

[103]  Ulrich Dobrindt,et al.  Genomic islands in pathogenic and environmental microorganisms , 2004, Nature Reviews Microbiology.

[104]  Robert C. Edgar,et al.  MUSCLE: multiple sequence alignment with high accuracy and high throughput. , 2004, Nucleic acids research.

[105]  N. Moran,et al.  Consequences of reductive evolution for gene expression in an obligate endosymbiont , 2003, Molecular microbiology.

[106]  Y. Gan,et al.  Flagella Are Virulence Determinants of Burkholderia pseudomallei , 2003, Infection and Immunity.

[107]  E. Murphy,et al.  BhuR, a Virulence-Associated Outer Membrane Protein of Bordetella avium, Is Required for the Acquisition of Iron from Heme and Hemoproteins , 2002, Infection and Immunity.

[108]  N. Moran,et al.  Microbial Minimalism Genome Reduction in Bacterial Pathogens , 2002, Cell.

[109]  P. de Vos,et al.  Diversity of transconjugants that acquired plasmid pJP4 or pEMT1 after inoculation of a donor strain in the A- and B-horizon of an agricultural soil and description of Burkholderia hospita sp. nov. and Burkholderia terricola sp. nov. , 2002, Systematic and applied microbiology.

[110]  P. de Vos,et al.  Burkholderia tuberum sp. nov. and Burkholderia phymatum sp. nov., nodulate the roots of tropical legumes. , 2002, Systematic and applied microbiology.

[111]  C. K. Vanderpool,et al.  The Bordetella bhu Locus Is Required for Heme Iron Utilization , 2001, Journal of bacteriology.

[112]  P. Vandamme,et al.  Burkholderia fungorum sp. nov. and Burkholderia caledonica sp. nov., two new species isolated from the environment, animals and human clinical samples. , 2001, International journal of systematic and evolutionary microbiology.

[113]  J. Hacker,et al.  Ecological fitness, genomic islands and bacterial pathogenicity , 2001, EMBO reports.

[114]  Michael Y. Galperin,et al.  The COG database: a tool for genome-scale analysis of protein functions and evolution , 2000, Nucleic Acids Res..

[115]  C. Kurland,et al.  Reductive evolution of resident genomes. , 1998, Trends in microbiology.

[116]  J. Haurat,et al.  Burkholderia graminis sp. nov., a rhizospheric Burkholderia species, and reassessment of [Pseudomonas] phenazinium, [Pseudomonas] pyrrocinia and [Pseudomonas] glathei as Burkholderia. , 1998, International journal of systematic bacteriology.

[117]  Thomas L. Madden,et al.  Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. , 1997, Nucleic acids research.

[118]  Jeff F. Miller,et al.  Roles for motility in bacterial–host interactions , 1997, Molecular microbiology.

[119]  S Falkow,et al.  Copyright © 1997, American Society for Microbiology Common Themes in Microbial Pathogenicity Revisited , 2022 .

[120]  H. Ochman,et al.  Amelioration of Bacterial Genomes: Rates of Change and Exchange , 1997, Journal of Molecular Evolution.

[121]  E. Falsen,et al.  Bacteria Are Omnipresent on Phanerochaete chrysosporium Burdsall , 1996, Applied and environmental microbiology.