The LysR-Type Transcriptional Regulator BsrA (PA2121) Controls Vital Metabolic Pathways in Pseudomonas aeruginosa

This study shows that BsrA, a LysR-type transcriptional regulator from Pseudomonas aeruginosa, previously identified as a repressor of biofilm synthesis, is part of an intricate global regulatory network. BsrA acts directly and/or indirectly as the repressor and/or activator of genes from vital metabolic pathways (e.g., pyruvate, acetate, and tricarboxylic acid cycle) and is involved in control of transport functions and the formation of surface appendages. ABSTRACT Pseudomonas aeruginosa, a facultative human pathogen causing nosocomial infections, has complex regulatory systems involving many transcriptional regulators. LTTR (LysR-Type Transcriptional Regulator) family proteins are involved in the regulation of various processes, including stress responses, motility, virulence, and amino acid metabolism. The aim of this study was to characterize the LysR-type protein BsrA (PA2121), previously described as a negative regulator of biofilm formation in P. aeruginosa. Genome wide identification of BsrA binding sites using chromatin immunoprecipitation and sequencing analysis revealed 765 BsrA-bound regions in the P. aeruginosa PAO1161 genome, including 367 sites in intergenic regions. The motif T-N11-A was identified within sequences bound by BsrA. Transcriptomic analysis showed altered expression of 157 genes in response to BsrA excess; of these, 35 had a BsrA binding site within their promoter regions, suggesting a direct influence of BsrA on the transcription of these genes. BsrA-repressed loci included genes encoding proteins engaged in key metabolic pathways such as the tricarboxylic acid cycle. The panel of loci possibly directly activated by BsrA included genes involved in pilus/fimbria assembly, as well as secretion and transport systems. In addition, DNA pull-down and regulatory analyses showed the involvement of PA2551, PA3398, and PA5189 in regulation of bsrA expression, indicating that this gene is part of an intricate regulatory network. Taken together, these findings reveal the existence of a BsrA regulon, which performs important functions in P. aeruginosa. IMPORTANCE This study shows that BsrA, a LysR-type transcriptional regulator from Pseudomonas aeruginosa, previously identified as a repressor of biofilm synthesis, is part of an intricate global regulatory network. BsrA acts directly and/or indirectly as the repressor and/or activator of genes from vital metabolic pathways (e.g., pyruvate, acetate, and tricarboxylic acid cycle) and is involved in control of transport functions and the formation of surface appendages. Expression of the bsrA gene is increased in the presence of antibiotics, which suggests its induction in response to stress, possibly reflecting the need to redirect metabolism under stressful conditions. This is particularly relevant for the treatment of infections caused by P. aeruginosa. In summary, the findings of this study demonstrate that the BsrA regulator performs important roles in carbon metabolism, biofilm formation, and antibiotic resistance in P. aeruginosa.

[1]  Jian Yan,et al.  An atlas of the binding specificities of transcription factors in Pseudomonas aeruginosa directs prediction of novel regulators in virulence , 2021, eLife.

[2]  G. Soberón-Chávez,et al.  The third quorum-sensing system of Pseudomonas aeruginosa: Pseudomonas quinolone signal and the enigmatic PqsE protein. , 2019, Journal of medical microbiology.

[3]  Pedro P. Vallejo Ramirez,et al.  Contextual Flexibility in Pseudomonas aeruginosa Central Carbon Metabolism during Growth in Single Carbon Sources , 2019, mBio.

[4]  A. Steinbüchel,et al.  Sulfate Ester Detergent Degradation in Pseudomonas aeruginosa Is Subject to both Positive and Negative Regulation , 2019, Applied and Environmental Microbiology.

[5]  B. Zieniuk,et al.  Interaction of ArmZ with the DNA-Binding Domain of MexZ Induces Expression of mexXY Multidrug Efflux Pump Genes and Antimicrobial Resistance in Pseudomonas aeruginosa , 2019, Antimicrobial Agents and Chemotherapy.

[6]  Xin Wang,et al.  An integrated genomic regulatory network of virulence-related transcriptional factors in Pseudomonas aeruginosa , 2019, Nature Communications.

[7]  Xiaojing Yang,et al.  A putative LysR-type transcriptional regulator inhibits biofilm synthesis in Pseudomonas aeruginosa , 2019, Biofouling.

[8]  J. Coon,et al.  Metabolic Remodeling during Biofilm Development of Bacillus subtilis , 2019, mBio.

[9]  R. Gothalwal,et al.  Emergence of antibiotic resistance Pseudomonas aeruginosa in intensive care unit; a critical review , 2019, Genes & diseases.

[10]  J. Mobley,et al.  Oxylipins mediate cell-to-cell communication in Pseudomonas aeruginosa , 2019, Communications Biology.

[11]  J. Gawor,et al.  Genome sequence of Pseudomonas aeruginosa PAO1161, a PAO1 derivative with the ICEFP2 integrative and conjugative element , 2018, bioRxiv.

[12]  V. Waters,et al.  Epidemiology, Biology, and Impact of Clonal Pseudomonas aeruginosa Infections in Cystic Fibrosis , 2018, Clinical Microbiology Reviews.

[13]  T. Hoang,et al.  Novel dual regulators of Pseudomonas aeruginosa essential for productive biofilms and virulence , 2018, Molecular microbiology.

[14]  G. Phan,et al.  Functional Mechanism of the Efflux Pumps Transcription Regulators From Pseudomonas aeruginosa Based on 3D Structures , 2018, Front. Mol. Biosci..

[15]  Xiaojing Yang,et al.  Regulatory protein SrpA controls phage infection and core cellular processes in Pseudomonas aeruginosa , 2018, Nature Communications.

[16]  B. Görke,et al.  Carbohydrate Utilization in Bacteria: Making the Most Out of Sugars with the Help of Small Regulatory RNAs , 2018, Microbiology spectrum.

[17]  G. Jagura-Burdzy,et al.  Pseudomonas aeruginosa partitioning protein ParB acts as a nucleoid-associated protein binding to multiple copies of a parS-related motif , 2018, bioRxiv.

[18]  Jia-xin Zhu,et al.  Pyruvate cycle increases aminoglycoside efficacy and provides respiratory energy in bacteria , 2018, Proceedings of the National Academy of Sciences.

[19]  L. A. Teixeira,et al.  Prevalence, Antimicrobial Susceptibility, and Clonal Diversity of Pseudomonas aeruginosa in Chronic Wounds , 2017, Journal of wound, ostomy, and continence nursing : official publication of The Wound, Ostomy and Continence Nurses Society.

[20]  Y. Yau,et al.  MexXY efflux pump overexpression and aminoglycoside resistance in cystic fibrosis isolates of Pseudomonas aeruginosa from chronic infections. , 2017, Canadian journal of microbiology.

[21]  A. Fogtman,et al.  Increased ParB level affects expression of stress response, adaptation and virulence operons and potentiates repression of promoters adjacent to the high affinity binding sites parS3 and parS4 in Pseudomonas aeruginosa , 2017, bioRxiv.

[22]  T. Mah,et al.  PA3225 Is a Transcriptional Repressor of Antibiotic Resistance Mechanisms in Pseudomonas aeruginosa , 2017, Antimicrobial Agents and Chemotherapy.

[23]  Kristin M. Jacob,et al.  Regulation of acetyl-CoA synthetase transcription by the CrbS/R two-component system is conserved in genetically diverse environmental pathogens , 2017, PloS one.

[24]  N. Moran,et al.  Convergent evolution of a modified, acetate-driven TCA cycle in bacteria , 2017, Nature Microbiology.

[25]  Joel S. Freundlich,et al.  Enhanced respiration prevents drug tolerance and drug resistance in Mycobacterium tuberculosis , 2017, Proceedings of the National Academy of Sciences.

[26]  Jason H. Yang,et al.  Carbon Sources Tune Antibiotic Susceptibility in Pseudomonas aeruginosa via Tricarboxylic Acid Cycle Control. , 2017, Cell chemical biology.

[27]  L. Rahme,et al.  Evidence for Direct Control of Virulence and Defense Gene Circuits by the Pseudomonas aeruginosa Quorum Sensing Regulator, MvfR , 2016, Scientific Reports.

[28]  Y. Ting,et al.  Streptomycin favors biofilm formation by altering cell surface properties , 2016, Applied Microbiology and Biotechnology.

[29]  G. Leonard,et al.  The solution configurations of inactive and activated DntR have implications for the sliding dimer mechanism of LysR transcription factors , 2016, Scientific Reports.

[30]  Raymond Lo,et al.  Enhanced annotations and features for comparing thousands of Pseudomonas genomes in the Pseudomonas genome database , 2015, Nucleic Acids Res..

[31]  M. Wargo,et al.  Sarcosine Catabolism in Pseudomonas aeruginosa Is Transcriptionally Regulated by SouR , 2015, Journal of bacteriology.

[32]  A. P. Souza,et al.  Characterization of the LysR-type transcriptional regulator YcjZ-like from Xylella fastidiosa overexpressed in Escherichia coli. , 2015, Protein expression and purification.

[33]  U. Römling Small molecules with big effects: Cyclic di-GMP–mediated stimulation of cellulose production by the amino acid ʟ-arginine , 2015, Science Signaling.

[34]  D. Charlier,et al.  Pseudomonas aeruginosa LysR PA4203 Regulator NmoR Acts as a Repressor of the PA4202 nmoA Gene, Encoding a Nitronate Monooxygenase , 2014, Journal of bacteriology.

[35]  Christopher M Thomas,et al.  Dissection of the region of Pseudomonas aeruginosa ParA that is important for dimerization and interactions with its partner ParB , 2014, Microbiology.

[36]  K. Mathee,et al.  Pseudomonas aeruginosa AmpR: an acute-chronic switch regulator. , 2014, Pathogens and disease.

[37]  E. Sonnleitner,et al.  Regulation of Hfq by the RNA CrcZ in Pseudomonas aeruginosa Carbon Catabolite Repression , 2014, PLoS genetics.

[38]  E. Neidle,et al.  The DNA-binding domain of BenM reveals the structural basis for the recognition of a T-N11-A sequence motif by LysR-type transcriptional regulators. , 2013, Acta crystallographica. Section D, Biological crystallography.

[39]  F. O'Gara,et al.  Molecular evolution of LysR-type transcriptional regulation in Pseudomonas aeruginosa. , 2013, Molecular phylogenetics and evolution.

[40]  F. O'Gara,et al.  A Non-Classical LysR-Type Transcriptional Regulator PA2206 Is Required for an Effective Oxidative Stress Response in Pseudomonas aeruginosa , 2013, PloS one.

[41]  Y. Kawamura,et al.  MexXY multidrug efflux system of Pseudomonas aeruginosa , 2012, Front. Microbio..

[42]  L. Burrows Pseudomonas aeruginosa twitching motility: type IV pili in action. , 2012, Annual review of microbiology.

[43]  E. Neidle,et al.  Defying stereotypes: the elusive search for a universal model of LysR‐type regulation , 2012, Molecular microbiology.

[44]  F. Hildebrand,et al.  Global regulation of gene expression by OxyR in an important human opportunistic pathogen , 2012, Nucleic acids research.

[45]  F. Lépine,et al.  Active Starvation Responses Mediate Antibiotic Tolerance in Biofilms and Nutrient-Limited Bacteria , 2011, Science.

[46]  E. Nudler,et al.  H2S: A Universal Defense Against Antibiotics in Bacteria , 2011, Science.

[47]  James J. Collins,et al.  Metabolite-Enabled Eradication of Bacterial Persisters by Aminoglycosides , 2011, Nature.

[48]  G. Fichant,et al.  The PprA-PprB two-component system activates CupE, the first non-archetypal Pseudomonas aeruginosa chaperone-usher pathway system assembling fimbriae. , 2011, Environmental microbiology.

[49]  William Stafford Noble,et al.  FIMO: scanning for occurrences of a given motif , 2011, Bioinform..

[50]  G. Döring Prevention of Pseudomonas aeruginosa infection in cystic fibrosis patients. , 2010, International journal of medical microbiology : IJMM.

[51]  J. Collins,et al.  Bacterial charity work leads to population-wide resistance , 2010, Nature.

[52]  P. Cornelis,et al.  The Pseudomonas aeruginosa oxidative stress regulator OxyR influences production of pyocyanin and rhamnolipids: protective role of pyocyanin. , 2010, Microbiology.

[53]  M. Solà,et al.  Structural studies on the full‐length LysR‐type regulator TsaR from Comamonas testosteroni T‐2 reveal a novel open conformation of the tetrameric LTTR fold , 2010, Molecular microbiology.

[54]  E. Sonnleitner,et al.  Small RNA as global regulator of carbon catabolite repression in Pseudomonas aeruginosa , 2009, Proceedings of the National Academy of Sciences.

[55]  K. Turner,et al.  Epigenetic Control of Virulence Gene Expression in Pseudomonas aeruginosa by a LysR-Type Transcription Regulator , 2009, PLoS genetics.

[56]  D. Hassett,et al.  The Major Catalase Gene (katA) of Pseudomonas aeruginosa PA14 Is under both Positive and Negative Control of the Global Transactivator OxyR in Response to Hydrogen Peroxide , 2009, Journal of bacteriology.

[57]  E. Nudler,et al.  Endogenous Nitric Oxide Protects Bacteria Against a Wide Spectrum of Antibiotics , 2009, Science.

[58]  R. Hancock,et al.  Swarming of Pseudomonas aeruginosa Is Controlled by a Broad Spectrum of Transcriptional Regulators, Including MetR , 2009, Journal of bacteriology.

[59]  D. Hogan,et al.  Identification of genes required for Pseudomonas aeruginosa carnitine catabolism. , 2009, Microbiology.

[60]  F. Rojo,et al.  The Pseudomonas putida Crc global regulator controls the hierarchical assimilation of amino acids in a complete medium: Evidence from proteomic and genomic analyses , 2009, Proteomics.

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

[62]  S. Maddocks,et al.  Structure and function of the LysR-type transcriptional regulator (LTTR) family proteins. , 2008, Microbiology.

[63]  P. Cornelis,et al.  Loss of the oxidative stress regulator OxyR in Pseudomonas aeruginosa PAO1 impairs growth under iron-limited conditions. , 2008, FEMS microbiology letters.

[64]  I. Kukavica-Ibrulj,et al.  Functional genomics of PycR, a LysR family transcriptional regulator essential for maintenance of Pseudomonas aeruginosa in the rat lung. , 2008, Microbiology.

[65]  E. A. Mullins,et al.  A Specialized Citric Acid Cycle Requiring Succinyl-Coenzyme A (CoA):Acetate CoA-Transferase (AarC) Confers Acetic Acid Resistance on the Acidophile Acetobacter aceti , 2008, Journal of bacteriology.

[66]  S. Heeb,et al.  Genome-wide search reveals a novel GacA-regulated small RNA in Pseudomonas species , 2008, BMC Genomics.

[67]  B. Tümmler,et al.  Fitness of Isogenic Colony Morphology Variants of Pseudomonas aeruginosa in Murine Airway Infection , 2008, PloS one.

[68]  F. Govantes,et al.  The LysR‐type regulator AtzR binding site: DNA sequences involved in activation, repression and cyanuric acid‐dependent repositioning , 2007, Molecular microbiology.

[69]  Christopher M Thomas,et al.  Deletion of the parA (soj) Homologue in Pseudomonas aeruginosa Causes ParB Instability and Affects Growth Rate, Chromosome Segregation, and Motility , 2007, Journal of bacteriology.

[70]  A. Sonenshein,et al.  Molecular mechanism of the regulation of Bacillus subtilis gltAB expression by GltC. , 2007, Journal of molecular biology.

[71]  J. Colmer-Hamood,et al.  PtxR modulates the expression of QS‐controlled virulence factors in the Pseudomonas aeruginosa strain PAO1 , 2006, Molecular microbiology.

[72]  L. Rahme,et al.  Mutation analysis of the Pseudomonas aeruginosa mvfR and pqsABCDE gene promoters demonstrates complex quorum-sensing circuitry. , 2006, Microbiology.

[73]  David A. D'Argenio,et al.  Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patients. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[74]  M. Fujisawa,et al.  Complicated urinary tract infection caused by Pseudomonas aeruginosa in a single institution (1999–2003) , 2006, International journal of urology : official journal of the Japanese Urological Association.

[75]  K. Poole,et al.  Mutations in PA2491 (mexS) Promote MexT-Dependent mexEF-oprN Expression and Multidrug Resistance in a Clinical Strain of Pseudomonas aeruginosa , 2005, Journal of bacteriology.

[76]  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.

[77]  T. Nonaka,et al.  Crystal structure of a full-length LysR-type transcriptional regulator, CbnR: unusual combination of two subunit forms and molecular bases for causing and changing DNA bend. , 2003, Journal of molecular biology.

[78]  L. Dijkhuizen,et al.  Analysis of DNA Binding and Transcriptional Activation by the LysR-Type Transcriptional Regulator CbbR of Xanthobacter flavus , 2003, Journal of bacteriology.

[79]  H. Görisch,et al.  Malate:quinone oxidoreductase is essential for growth on ethanol or acetate in Pseudomonas aeruginosa. , 2002, Microbiology.

[80]  Y. Itoh,et al.  Characterization and Regulation of the gbuA Gene, Encoding Guanidinobutyrase in the Arginine Dehydrogenase Pathway of Pseudomonas aeruginosa PAO1 , 2002, Journal of bacteriology.

[81]  L. Rahme,et al.  A quorum sensing-associated virulence gene of Pseudomonas aeruginosa encodes a LysR-like transcription regulator with a unique self-regulatory mechanism , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[82]  Christopher M Thomas,et al.  Quorum-sensing-dependent regulation of biosynthesis of the polyketide antibiotic mupirocin in Pseudomonas fluorescens NCIMB 10586. , 2001, Microbiology.

[83]  D. Haas,et al.  The CbrA–CbrB two‐component regulatory system controls the utilization of multiple carbon and nitrogen sources in Pseudomonas aeruginosa , 2001, Molecular microbiology.

[84]  R. Iwanicka-Nowicka,et al.  Functional Dissection of the LysR-type CysB Transcriptional Regulator , 2001, The Journal of Biological Chemistry.

[85]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[86]  Douwe Molenaar,et al.  Functions of the Membrane-Associated and Cytoplasmic Malate Dehydrogenases in the Citric Acid Cycle ofEscherichia coli , 2000, Journal of bacteriology.

[87]  C. van Delden,et al.  Swarming of Pseudomonas aeruginosa Is Dependent on Cell-to-Cell Signaling and Requires Flagella and Pili , 2000, Journal of bacteriology.

[88]  S. Lory,et al.  Complete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogen , 2000, Nature.

[89]  D. Hassett,et al.  Role of the Pseudomonas aeruginosa oxyR-recG Operon in Oxidative Stress Defense and DNA Repair: OxyR-Dependent Regulation of katB-ankB, ahpB, andahpC-ahpF , 2000, Journal of bacteriology.

[90]  A. Kornberg,et al.  Inorganic polyphosphate is needed for swimming, swarming, and twitching motilities of Pseudomonas aeruginosa. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[91]  T. Köhler,et al.  Characterization of MexT, the Regulator of the MexE-MexF-OprN Multidrug Efflux System of Pseudomonas aeruginosa , 1999, Journal of bacteriology.

[92]  M. I. Betlloch,et al.  ReviewCutaneous manifestations due to Pseudomonas infection , 1999, International journal of dermatology.

[93]  D. Molenaar,et al.  Biochemical and genetic characterization of the membrane-associated malate dehydrogenase (acceptor) from Corynebacterium glutamicum. , 1998, European journal of biochemistry.

[94]  N. Gotoh,et al.  Characterization of MexE–MexF–OprN, a positively regulated multidrug efflux system of Pseudomonas aeruginosa , 1997, Molecular microbiology.

[95]  N. M. Kredich,et al.  In vitro characterization of constitutive CysB proteins from Salmonella typhimurium , 1996, Molecular microbiology.

[96]  A. Wolfe,et al.  Cloning, characterization, and functional expression of acs, the gene which encodes acetyl coenzyme A synthetase in Escherichia coli , 1995, Journal of bacteriology.

[97]  G. Storz,et al.  Mutational analysis of the redox-sensitive transcriptional regulator OxyR: regions important for DNA binding and multimerization , 1995, Journal of bacteriology.

[98]  N. M. Kredich,et al.  Residue threonine‐149 of the Salmonella typhimurium CysB transcription activator: mutations causing constitutive expression of positively regulated genes of the cysteine regulon , 1994, Molecular microbiology.

[99]  S. Lory,et al.  Nucleotide sequence of the rpoN gene and characterization of two downstream open reading frames in Pseudomonas aeruginosa , 1994, Journal of bacteriology.

[100]  C. Locht,et al.  Common accessory genes for the Bordetella pertussis filamentous hemagglutinin and fimbriae share sequence similarities with the papC and papD gene families. , 1992, The EMBO journal.

[101]  S Henikoff,et al.  A large family of bacterial activator proteins. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[102]  D. Charlier,et al.  Differential protein-DNA contacts for activation and repression by ArgP, a LysR-type (LTTR) transcriptional regulator in Escherichia coli. , 2018, Microbiological research.

[103]  F. Rojo,et al.  The Crc and Hfq proteins of Pseudomonas putida cooperate in catabolite repression and formation of ribonucleic acid complexes with specific target motifs. , 2015, Environmental microbiology.

[104]  T. Murphy,et al.  Differential adaptation of microbial pathogens to airways of patients with cystic fibrosis and chronic obstructive pulmonary disease. , 2011, FEMS microbiology reviews.

[105]  E. Pesci,et al.  Dueling quorum sensing systems in Pseudomonas aeruginosa control the production of the Pseudomonas quinolone signal (PQS). , 2004, FEMS microbiology letters.

[106]  J. Rowe,et al.  Enhancement of transformation in Pseudomonas aeruginosa PAO1 by Mg2+ and heat. , 1997, BioTechniques.

[107]  M. Schell Molecular biology of the LysR family of transcriptional regulators. , 1993, Annual review of microbiology.