All Stories

  1. The Pseudomonas aeruginosa PilSR Two-Component System Regulates Both Twitching and Swimming Motilities
  2. Cyclic AMP-Independent Control of Twitching Motility in Pseudomonas aeruginosa
  3. The Type IVa Pilus Machinery Is Recruited to Sites of Future Cell Division
  4. The Conserved Tetratricopeptide Repeat-Containing C-Terminal Domain of Pseudomonas aeruginosa FimV Is Required for Its Cyclic AMP-Dependent and -Independent Functions
  5. Novel Role for PilNO in Type IV Pilus Retraction Revealed by Alignment Subcomplex Mutations
  6. Truncated minor pilin PilE from Pseudomonas aeruginosa
  7. Pseudomonas aeruginosa Minor Pilins Prime Type IVa Pilus Assembly and Promote Surface Display of the PilY1 Adhesin
  8. DNase I and proteinase K impair Listeria monocytogenes biofilm formation and induce dispersal of pre-existing biofilms
  9. TPR3 of FimV from P. aeruginosa (PAO1)
  10. TPR3 of FimV from P. aeruginosa (PAO1)
  11. Role of PBPD1 in Stimulation of Listeria monocytogenes Biofilm Formation by Subminimal Inhibitory β-Lactam Concentrations
  12. A New Twist in the Assembly of Type IV Pilus-like Fibers
  13. Crystal structure of Pseudomonas aeruginosa (strain: PAO1) type IV minor pilin FimU in space group P21
  14. Crystal structure of Pseudomonas aeruginosa (strain: PAO1) type IV minor pilin FimU in space group P65
  15. The dynamics of peptidoglycan structure and function: Conference report on the 3rd Great Wall Symposium
  16. A new route for polar navigation
  17. Functional Mapping of PilF and PilQ in the Pseudomonas aeruginosa Type IV Pilus System
  18. Changes to Its Peptidoglycan-Remodeling Enzyme Repertoire Modulate β-Lactam Resistance in Pseudomonas aeruginosa
  19. The Efflux Inhibitor Phenylalanine-Arginine Beta-Naphthylamide (PAβN) Permeabilizes the Outer Membrane of Gram-Negative Bacteria
  20. PilMNOPQ from the Pseudomonas aeruginosa Type IV Pilus System Form a Transenvelope Protein Interaction Network That Interacts with PilA
  21. The Platform Protein Is Essential for Type IV Pilus Biogenesis
  22. Type IV Pilin Proteins: Versatile Molecular Modules
  23. Pseudomonas aeruginosaTwitching Motility: Type IV Pili in Action
  24. Prime time for minor subunits of the type II secretion and type IV pilus systems
  25. Inhibition of Bacterial Biofilm Formation and Swarming Motility by a Small Synthetic Cationic Peptide
  26. Small-Molecule Modulators of Listeria monocytogenes Biofilm Development
  27. Decoding the roles of pilotins and accessory proteins in secretin escort services
  28. Characterization of the PilN, PilO and PilP type IVa pilus subcomplex
  29. Palmitoyl-dl-Carnitine is a Multitarget Inhibitor of Pseudomonas aeruginosa Biofilm Development
  30. Intravital Microscopy of the Murine Urinary Bladder Microcirculation
  31. Pseudomonas aeruginosa d-Arabinofuranose Biosynthetic Pathway and Its Role in Type IV Pilus Assembly
  32. Maintaining network security: how macromolecular structures cross the peptidoglycan layer
  33. The Peptidoglycan-Binding Protein FimV Promotes Assembly of the Pseudomonas aeruginosa Type IV Pilus Secretin
  34. Evolutionary and functional diversity of thePseudomonastype IVa pilin island
  35. Architecture of the type II secretion and type IV pilus machineries
  36. Pseudomonas aeruginosa Minor Pilins Are Incorporated into Type IV Pili
  37. AlgK Is a TPR-Containing Protein and the Periplasmic Component of a Novel Exopolysaccharide Secretin
  38. Structural Characterization of Novel Pseudomonas aeruginosa Type IV Pilins
  39. PilM/N/O/P Proteins Form an Inner Membrane Complex That Affects the Stability of the Pseudomonas aeruginosa Type IV Pilus Secretin
  40. Periplasmic Domains of Pseudomonas aeruginosa PilN and PilO Form a Stable Heterodimeric Complex
  41. Single-Residue Changes in the C-Terminal Disulfide-Bonded Loop of the Pseudomonas aeruginosa Type IV Pilin Influence Pilus Assembly and Twitching Motility
  42. Mechanical Properties of Type IV Pili in Pseudomonas Aeruginosa
  43. Hypertonic saline resuscitation from hemorrhagic shock does not impair the neutrophil response to intraabdominal infection
  44. Modification of Pseudomonas aeruginosa Pa5196 Type IV Pilins at Multiple Sites with d-Araf by a Novel GT-C Family Arabinosyltransferase, TfpW
  45. Novel Proteins That Modulate Type IV Pilus Retraction Dynamics in Pseudomonas aeruginosa
  46. PilF Is an Outer Membrane Lipoprotein Required for Multimerization and Localization of the Pseudomonas aeruginosa Type IV Pilus Secretin
  47. A Nice Return on the “Stalk” Exchange
  48. Membrane interactions of designed cationic antimicrobial peptides: The two thresholds
  49. Functional role of conserved residues in the characteristic secretion NTPase motifs of the Pseudomonas aeruginosa type IV pilus motor proteins PilB, PilT and PilU
  50. Hydrophobic Interactions in Complexes of Antimicrobial Peptides with Bacterial Polysaccharides
  51. Expression, purification, crystallization and preliminary X-ray analysis ofPseudomonas fluorescensAlgK
  52. Glycosylation of Pseudomonas aeruginosa Strain Pa5196 Type IV Pilins with Mycobacterium-Like α-1,5-Linked d-Araf Oligosaccharides
  53. Abnormalities in the Pulmonary Innate Immune System in Cystic Fibrosis
  54. Common β-lactamases inhibit bacterial biofilm formation
  55. Mycobacterium neoaurum Contamination
  56. Basis for Selectivity of Cationic Antimicrobial Peptides for Bacterial Versus Mammalian Membranes
  57. Weapons of mass retraction
  58. Alginate as an auxiliary bacterial membrane: binding of membrane-active peptides by polysaccharides*
  59. Disparate Subcellular Localization Patterns of Pseudomonas aeruginosa Type IV Pilus ATPases Involved in Twitching Motility
  60. Helix Induction in Antimicrobial Peptides by Alginate in Biofilms
  61. Rapidly Progressive Dementia Due to Mycobacterium neoaurum Meningoencephalitis
  62. Three-component-mediated serotype conversion in Pseudomonas aeruginosa by bacteriophage D3
  63. Tropheryma whippelii as a cause of afebrile culture-negative endocarditis: the evolving spectrum of Whipple's disease
  64. Contamination of Bone Marrow Products with an Actinomycete Resembling Microbacterium Species and Reinfusion into Autologous Stem Cell and Bone Marrow Transplant Recipients
  65. Use of In-Biofilm Expression Technology To Identify Genes Involved in Pseudomonas aeruginosa Biofilm Development
  66. Biofilm Formation by Hyperpiliated Mutants of Pseudomonas aeruginosa
  67. Invited Commentary
  68. Is Surveillance for Multidrug‐Resistant Enterobacteriaceae an Effective Infection Control Strategy in the Absence of an Outbreak?
  69. Molecular mechanisms of cefoxitin resistance in Escherichia coli from the Toronto area hospitals
  70. Three-component-mediated serotype conversion in Pseudomonas aeruginosa by bacteriophage D3
  71. Pseudomonas aeruginosa B-band lipopolysaccharide genes wbpA and wbpI and their Escherichia coli homologues wecC and wecB are not functionally interchangeable
  72. Pseudomonas aeruginosa B-band lipopolysaccharide genes wbpA and wbpI and their Escherichia coli homologues wecC and wecB are not functionally interchangeable
  73. Functional Conservation of the Polysaccharide Biosynthetic Protein WbpM and Its Homologues in Pseudomonas aeruginosa and Other Medically Significant Bacteria
  74. Lipopolysaccharide core phosphates are required for viability and intrinsic drug resistance in Pseudomonas aeruginosa
  75. Issues surrounding the prevention and management of device-related infections
  76. Genetic and biochemical characterization of an operon involved in the biosynthesis of 3-deoxy-d- manno -octulosonic acid in Pseudomonas aeruginosa
  77. Glycosyltransferases of Pseudomonas aeruginosa that assemble the O antigens of A band and B band lipopolysaccharide
  78. Three rhamnosyltransferases responsible for assembly of the A-band D-rhamnan polysaccharide in Pseudomonas aeruginosa: a fourth transferase, WbpL, is required for the initiation of both A-band and B-band lipopolysaccharide synthesis
  79. Three rhamnosyltransferases responsible for assembly of the A-band D-rhamnan polysaccharide in Pseudomonas aeruginosa: a fourth transferase, WbpL, is required for the initiation of both A-band and B-band lipopolysaccharide synthesis
  80. Molecular characterization of the Pseudomonas aeruginosa serotype O5 (PAO1) B-band lipopolysaccharide gene cluster
  81. Assembly Pathways for Biosynthesis of A-Band and B-Band Lipopolysaccharide in Pseudomonas aeruginosa
  82. The Pseudomonas aeruginosa type IV pilus assembly system in three dimensions.