Identification of NLR-associated amyloid signaling motifs in filamentous bacteria

NLRs (Nod-like receptors) are intracellular receptors regulating immunity, symbiosis, non-self recognition and programmed cell death in animals, plants and fungi. Several fungal NLRs employ amyloid signaling motifs to activate downstream cell-death inducing proteins. Herein, we identify in Archaea and Bacteria, short sequence motifs that occur in the same genomic context as fungal amyloid signaling motifs. We identify 10 families of bacterial amyloid signaling sequences (we term BASS), one of which (BASS3) is related to mammalian RHIM and fungal PP amyloid motifs. We find that BASS motifs occur specifically in bacteria forming multicellular structures (mainly in Actinobacteria and Cyanobacteria). We analyze experimentally a subset of these motifs and find that they behave as prion forming domains when expressed in a fungal model. All tested bacterial motifs also formed fibrils in vitro. We analyze by solid-state NMR and X-ray diffraction, the amyloid state of a protein from Streptomyces coelicolor bearing the most common BASS1 motif and find that it forms highly ordered non-polymorphic amyloid fibrils. This work expands the paradigm of amyloid signaling to prokaryotes and underlies its relation to multicellularity.

[1]  U. Baxa,et al.  Prion and non-prion amyloids of the HET-s prion forming domain. , 2007, Journal of molecular biology.

[2]  S. Saupe,et al.  Genesis of a Fungal Non-Self Recognition Repertoire , 2007, PloS one.

[3]  R. Riek,et al.  High-resolution solid-state NMR spectroscopy of the prion protein HET-s in its amyloid conformation. , 2005, Angewandte Chemie.

[4]  Christiane Ritter,et al.  The mechanism of prion inhibition by HET-S. , 2010, Molecular cell.

[5]  D. Higgins,et al.  Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega , 2011, Molecular systems biology.

[6]  M. Maddelein,et al.  In vivo aggregation of the HET‐s prion protein of the fungus Podospora anserina , 2001, Molecular microbiology.

[7]  P. Rosteck,et al.  Homology between proteins controlling Streptomyces fradiae tylosin resistance and ATP-binding transport. , 1991, Gene.

[8]  H. Remaut,et al.  The Role of Functional Amyloids in Bacterial Virulence , 2018, Journal of molecular biology.

[9]  Yang Wang,et al.  Prokaryotic and Highly-Repetitive WD40 Proteins: A Systematic Study , 2017, Scientific Reports.

[10]  Roland Riek,et al.  The activities of amyloids from a structural perspective , 2016, Nature.

[11]  Raimon Sabaté,et al.  Structural similarity between the prion domain of HET-s and a homologue can explain amyloid cross-seeding in spite of limited sequence identity. , 2010, Journal of molecular biology.

[12]  E. Koonin,et al.  Virus-host arms race at the joint origin of multicellularity and programmed cell death , 2014, Cell cycle.

[13]  N. Keller Fungal secondary metabolism: regulation, function and drug discovery , 2018, Nature Reviews Microbiology.

[14]  F. Ausubel,et al.  The NBS-LRR architectures of plant R-proteins and metazoan NLRs evolved in independent events , 2017, Proceedings of the National Academy of Sciences.

[15]  Oleg Jardetzky,et al.  Probability‐based protein secondary structure identification using combined NMR chemical‐shift data , 2002, Protein science : a publication of the Protein Society.

[16]  A. Loquet,et al.  Functional Amyloids in Health and Disease. , 2018, Journal of molecular biology.

[17]  Philippe Silar,et al.  Bistability and hysteresis of the 'Secteur' differentiation are controlled by a two-gene locus in Nectria haematococca , 2004, BMC Biology.

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

[19]  Pierre M. Durand,et al.  Programmed Cell Death and Complexity in Microbial Systems , 2016, Current Biology.

[20]  L. Serpell,et al.  Common core structure of amyloid fibrils by synchrotron X-ray diffraction. , 1997, Journal of molecular biology.

[21]  E. Koonin,et al.  Origin and evolution of eukaryotic apoptosis: the bacterial connection , 2002, Cell Death and Differentiation.

[22]  G. Choi,et al.  Molecular Characterization of Vegetative Incompatibility Genes That Restrict Hypovirus Transmission in the Chestnut Blight Fungus Cryphonectria parasitica , 2012, Genetics.

[23]  T. N. Bhat,et al.  The Protein Data Bank , 2000, Nucleic Acids Res..

[24]  J. Tschopp,et al.  DAI/ZBP1 recruits RIP1 and RIP3 through RIP homotypic interaction motifs to activate NF‐κB , 2009, EMBO reports.

[25]  Jian-Qun Chen,et al.  A Primary Survey on Bryophyte Species Reveals Two Novel Classes of Nucleotide-Binding Site (NBS) Genes , 2012, PloS one.

[26]  B. Turcq,et al.  HET-E and HET-D belong to a new subfamily of WD40 proteins involved in vegetative incompatibility specificity in the fungus Podospora anserina. , 2002, Genetics.

[27]  A. Murzin Structural principles for the propeller assembly of β‐sheets: The preference for seven‐fold symmetry , 1992, Proteins.

[28]  Andrey V Kajava,et al.  Structure, function, and amyloidogenesis of fungal prions: filament polymorphism and prion variants. , 2006, Advances in protein chemistry.

[29]  Beat H. Meier,et al.  Amyloid Fibrils of the HET-s(218–289) Prion Form a β Solenoid with a Triangular Hydrophobic Core , 2008, Science.

[30]  Christiane Ritter,et al.  Domain organization and structure–function relationship of the HET‐s prion protein of Podospora anserina , 2003, The EMBO journal.

[31]  P. Hieter,et al.  Tetratrico peptide repeat interactions: to TPR or not to TPR? , 1995, Trends in biochemical sciences.

[32]  B. Turcq,et al.  A gene responsible for vegetative incompatibility in the fungus Podospora anserina encodes a protein with a GTP-binding motif and G beta homologous domain. , 1995, Gene.

[33]  Hao Wu,et al.  The Structure of the Necrosome RIPK1-RIPK3 Core, a Human Hetero-Amyloid Signaling Complex , 2018, Cell.

[34]  M. Waterman,et al.  A new algorithm for best subsequence alignments with application to tRNA-rRNA comparisons. , 1987, Journal of molecular biology.

[35]  M. Maddelein,et al.  Methods for the in vivo and in vitro analysis of [Het-s] prion infectivity. , 2006, Methods.

[36]  W. Miller,et al.  A time-efficient, linear-space local similarity algorithm , 1991 .

[37]  B. Habenstein,et al.  Identification of a novel cell death-inducing domain reveals that fungal amyloid-controlled programmed cell death is related to necroptosis , 2016, Proceedings of the National Academy of Sciences.

[38]  C. Soto,et al.  Prion-like characteristics of the bacterial protein Microcin E492 , 2017, Scientific Reports.

[39]  Brian C. Thomas,et al.  A new view of the tree of life , 2016, Nature Microbiology.

[40]  D. Manallack,et al.  IRAK3 modulates downstream innate immune signalling through its guanylate cyclase activity , 2019, Scientific Reports.

[41]  Y. Qi,et al.  Reconstitution and structure of a plant NLR resistosome conferring immunity , 2019, Science.

[42]  R. Riek,et al.  Functional Amyloids. , 2019, Cold Spring Harbor perspectives in biology.

[43]  Sean R. Eddy,et al.  A Probabilistic Model of Local Sequence Alignment That Simplifies Statistical Significance Estimation , 2008, PLoS Comput. Biol..

[44]  Thorsten Lührs,et al.  Correlation of structural elements and infectivity of the HET-s prion , 2005, Nature.

[45]  B. Habenstein,et al.  Signal Transduction by a Fungal NOD-Like Receptor Based on Propagation of a Prion Amyloid Fold , 2015, PLoS biology.

[46]  W. Dyrka,et al.  Theme and variations: evolutionary diversification of the HET-s functional amyloid motif , 2015, Scientific Reports.

[47]  E. Koonin,et al.  Unexpected sequence similarity between nucleosidases and phosphoribosyltransferases of different specificity , 1994, Protein Science.

[48]  B. Habenstein,et al.  3D structure determination of amyloid fibrils using solid-state NMR spectroscopy. , 2018, Methods.

[49]  E. Koonin,et al.  Origin of programmed cell death from antiviral defense? , 2019, Proceedings of the National Academy of Sciences.

[50]  A. Loquet,et al.  Diversity of Amyloid Motifs in NLR Signaling in Fungi , 2017, Biomolecules.

[51]  Sean R. Eddy,et al.  Accelerated Profile HMM Searches , 2011, PLoS Comput. Biol..

[52]  Johanna Napetschnig,et al.  Peptidoglycan‐Sensing Receptors Trigger the Formation of Functional Amyloids of the Adaptor Protein Imd to Initiate Drosophila NF‐&kgr;B Signaling , 2017, Immunity.

[53]  S. Saupe,et al.  Genomic Clustering and Homology between HET-S and the NWD2 STAND Protein in Various Fungal Genomes , 2012, PloS one.

[54]  R. Riek,et al.  The Mechanism of Toxicity in HET-S/HET-s Prion Incompatibility , 2012, PLoS biology.

[55]  K. Hofmann,et al.  Evolutionary link between metazoan RHIM motif and prion-forming domain of fungal heterokaryon incompatibility factor HET-s/HET-s , 2014, Scientific Reports.

[56]  Doug Barrick,et al.  A Naturally Occurring Repeat Protein with High Internal Sequence Identity Defines a New Class of TPR-like Proteins. , 2015, Structure.

[57]  An N-terminal motif in NLR immune receptors is functionally conserved across distantly related plant species , 2019, eLife.

[58]  A. Deveau,et al.  Do fungi have an innate immune response? An NLR-based comparison to plant and animal immune systems , 2017, PLoS pathogens.

[59]  Andrey V. Kajava,et al.  A structure-based approach to predict predisposition to amyloidosis , 2015, Alzheimer's & Dementia.

[60]  A. Debets,et al.  Identification of the het-r vegetative incompatibility gene of Podospora anserina as a member of the fast evolving HNWD gene family , 2009, Current Genetics.

[61]  R. Giraldo,et al.  RepA-WH1 prionoid , 2011, Prion.

[62]  J. Testa,et al.  The cloning and characterization of human MyD88: a member of an IL‐1 receptor related family 1 , 1997, FEBS letters.

[63]  Zhijian J. Chen,et al.  Prion-like Polymerization Underlies Signal Transduction in Antiviral Immune Defense and Inflammasome Activation , 2014, Cell.

[64]  G. Crooks,et al.  WebLogo: a sequence logo generator. , 2004, Genome research.

[65]  Fabian Sievers,et al.  Clustal Omega for making accurate alignments of many protein sequences , 2018, Protein science : a publication of the Protein Society.

[66]  Eugene V Koonin,et al.  Classification of the caspase–hemoglobinase fold: Detection of new families and implications for the origin of the eukaryotic separins , 2002, Proteins.

[67]  Mikael Bodén,et al.  MEME Suite: tools for motif discovery and searching , 2009, Nucleic Acids Res..

[68]  V. Dixit,et al.  Identification of a Novel Homotypic Interaction Motif Required for the Phosphorylation of Receptor-interacting Protein (RIP) by RIP3* , 2002, The Journal of Biological Chemistry.

[69]  Ning Ma,et al.  BLAST+: architecture and applications , 2009, BMC Bioinformatics.

[70]  Adam Godzik,et al.  Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences , 2006, Bioinform..

[71]  Donovan H. Parks,et al.  A standardized bacterial taxonomy based on genome phylogeny substantially revises the tree of life , 2018, Nature Biotechnology.

[72]  Elaina D. Graham,et al.  The reconstruction of 2,631 draft metagenome-assembled genomes from the global oceans , 2017, Scientific Data.

[73]  Bogumil Konopka,et al.  Quantiprot - a Python package for quantitative analysis of protein sequences , 2017, BMC Bioinformatics.

[74]  Zhijian J. Chen,et al.  Prion-Like Polymerization in Immunity and Inflammation. , 2017, Cold Spring Harbor perspectives in biology.

[75]  Matt Nolan,et al.  Improving the coverage of the cyanobacterial phylum using diversity-driven genome sequencing , 2012, Proceedings of the National Academy of Sciences.

[76]  R. Sabaté,et al.  Two structurally similar fungal prions efficiently cross‐seed in vivo but form distinct polymers when coexpressed , 2011, Molecular microbiology.

[77]  Yan-jing Li,et al.  Pharmacokinetics of the prototype and hydrolyzed carboxylic forms of ginkgolides A, B, and K administered as a ginkgo diterpene lactones meglumine injection in beagle dogs. , 2017, Chinese journal of natural medicines.

[78]  Zhengwei Zhu,et al.  CD-HIT: accelerated for clustering the next-generation sequencing data , 2012, Bioinform..

[79]  Robert D. Finn,et al.  HMMER web server: 2018 update , 2018, Nucleic Acids Res..

[80]  C. Kuske,et al.  Polysaccharide Degradation Capability of Actinomycetales Soil Isolates from a Semiarid Grassland of the Colorado Plateau , 2017, Applied and Environmental Microbiology.

[81]  R. Wickner,et al.  Yeast and Fungal Prions: Amyloid-Handling Systems, Amyloid Structure, and Prion Biology. , 2016, Advances in genetics.

[82]  Masaru Tomita,et al.  On dynamics of overlapping genes in bacterial genomes. , 2003, Gene.

[83]  P. Sansonetti [Bacterial virulence]. , 1990, La Revue du praticien.

[84]  B. Bergman,et al.  Prokaryotic Caspase Homologs: Phylogenetic Patterns and Functional Characteristics Reveal Considerable Diversity , 2012, PloS one.

[85]  Evan Bolton,et al.  Database resources of the National Center for Biotechnology Information , 2017, Nucleic Acids Res..

[86]  Bostjan Kobe,et al.  Diversity and Variability of NOD-Like Receptors in Fungi , 2014, Genome biology and evolution.

[87]  I. Longden,et al.  EMBOSS: the European Molecular Biology Open Software Suite. , 2000, Trends in genetics : TIG.

[88]  S. Matthews,et al.  Ecology and Biogenesis of Functional Amyloids in Pseudomonas , 2018, Journal of molecular biology.

[89]  Simon C. Potter,et al.  The EMBL-EBI search and sequence analysis tools APIs in 2019 , 2019, Nucleic Acids Res..

[90]  Z. Khachaturian Alzheimer's & Dementia: The Journal of the Alzheimer's Association , 2008, Alzheimer's & Dementia.

[91]  B. Kobe,et al.  Towards the structure of the TIR-domain signalosome. , 2017, Current opinion in structural biology.

[92]  The UniProt Consortium,et al.  UniProt: a worldwide hub of protein knowledge , 2018, Nucleic Acids Res..

[93]  P. F. Sarris,et al.  Plant and Animal Innate Immunity Complexes: Fighting Different Enemies with Similar Weapons. , 2019, Trends in plant science.

[94]  E. Koonin,et al.  The NACHT family - a new group of predicted NTPases implicated in apoptosis and MHC transcription activation. , 2000, Trends in biochemical sciences.

[95]  Toru Okamoto,et al.  The pseudokinase MLKL mediates necroptosis via a molecular switch mechanism. , 2013, Immunity.

[96]  Kenta Moriwaki,et al.  The RIP1/RIP3 Necrosome Forms a Functional Amyloid Signaling Complex Required for Programmed Necrosis , 2012, Cell.

[97]  Wen-Tso Liu,et al.  Thermodynamically diverse syntrophic aromatic compound catabolism , 2017, Environmental microbiology.

[98]  Jonathan D. G. Jones,et al.  Intracellular innate immune surveillance devices in plants and animals , 2016, Science.

[99]  P. Gladieux,et al.  NLR surveillance of essential SEC-9 SNARE proteins induces programmed cell death upon allorecognition in filamentous fungi , 2018, Proceedings of the National Academy of Sciences.

[100]  Silvio C. E. Tosatto,et al.  The Pfam protein families database in 2019 , 2018, Nucleic Acids Res..

[101]  Malgorzata Kotulska,et al.  AmyLoad: website dedicated to amyloidogenic protein fragments , 2015, Bioinform..

[102]  A. Kajava,et al.  Breaking the amyloidogenicity code: Methods to predict amyloids from amino acid sequence , 2013, FEBS letters.

[103]  A. Bowie,et al.  The family of five: TIR-domain-containing adaptors in Toll-like receptor signalling , 2007, Nature Reviews Immunology.

[104]  M. Sunde,et al.  Viral M45 and necroptosis‐associated proteins form heteromeric amyloid assemblies , 2018, EMBO reports.

[105]  Charles Elkan,et al.  Fitting a Mixture Model By Expectation Maximization To Discover Motifs In Biopolymer , 1994, ISMB.

[106]  Andrea Scrima,et al.  The invasin D protein from Yersinia pseudotuberculosis selectively binds the Fab region of host antibodies and affects colonization of the intestine , 2018, The Journal of Biological Chemistry.

[107]  Beat Meier,et al.  Prions , 2010 .

[108]  S. Henikoff,et al.  Amino acid substitution matrices from protein blocks. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[109]  G. Stubbs,et al.  Fungal prion HET-s as a model for structural complexity and self-propagation in prions , 2014, Proceedings of the National Academy of Sciences.

[110]  G. V. van Wezel,et al.  Chemical ecology of antibiotic production by actinomycetes. , 2017, FEMS microbiology reviews.

[111]  Gregory D. Schuler,et al.  Database resources of the National Center for Biotechnology Information: update , 2004, Nucleic acids research.

[112]  C. MacPhee,et al.  Functional Amyloid and Other Protein Fibers in the Biofilm Matrix☆ , 2018, Journal of molecular biology.