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The antifungal caspofungin increases fluoroquinolone activity against Staphylococcus aureus biofilms by inhibiting N-acetylglucosamine transferase

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  1. Vuong Cuong, Kocianova Stanislava, Voyich Jovanka M., Yao Yufeng, Fischer Elizabeth R., DeLeo Frank R., Otto Michael, A Crucial Role for Exopolysaccharide Modification in Bacterial Biofilm Formation, Immune Evasion, and Virulence, 10.1074/jbc.m411374200
  2. Brady Rebecca A., Leid Jeff G., Calhoun Jason H., Costerton J. William, Shirtliff Mark E., Osteomyelitis and the role of biofilms in chronic infection, 10.1111/j.1574-695x.2007.00357.x
  3. Fernandes A., J. Clin. Diagn. Res, 7, 219 (2013)
  4. Falagas Matthew E., Kapaskelis Anastasios M., Kouranos Vasilios D., Kakisi Ourania K., Athanassa Zoe, Karageorgopoulos Drosos E., Outcome of Antimicrobial Therapy in Documented Biofilm-Associated Infections : A Review of the Available Clinical Evidence, 10.2165/00003495-200969100-00005
  5. O'Gara James P., icaand beyond: biofilm mechanisms and regulation inStaphylococcus epidermidisandStaphylococcus aureus, 10.1111/j.1574-6968.2007.00688.x
  6. Hall-Stoodley Luanne, Stoodley Paul, Evolving concepts in biofilm infections, 10.1111/j.1462-5822.2009.01323.x
  7. Otto M., Curr. Top. Microbiol. Immunol., 322, 207 (2008)
  8. Lewis K., Curr. Top. Microbiol. Immunol., 322, 107 (2008)
  9. Saginur R., StDenis M., Ferris W., Aaron S. D., Chan F., Lee C., Ramotar K., Multiple Combination Bactericidal Testing of Staphylococcal Biofilms from Implant-Associated Infections, 10.1128/aac.50.1.55-61.2006
  10. Field D., Front Microbiol., 7, 508 (2016)
  11. Arciola Carla Renata, Campoccia Davide, Ravaioli Stefano, Montanaro Lucio, Polysaccharide intercellular adhesin in biofilm: structural and regulatory aspects, 10.3389/fcimb.2015.00007
  12. Rohde Holger, Frankenberger Stephanie, Zähringer Ulrich, Mack Dietrich, Structure, function and contribution of polysaccharide intercellular adhesin (PIA) to Staphylococcus epidermidis biofilm formation and pathogenesis of biomaterial-associated infections, 10.1016/j.ejcb.2009.10.005
  13. Gerke Christiane, Kraft Angelika, Süßmuth Roderich, Schweitzer Oliver, Götz Friedrich, Characterization of theN-Acetylglucosaminyltransferase Activity Involved in the Biosynthesis of theStaphylococcus epidermidisPolysaccharide Intercellular Adhesin, 10.1074/jbc.273.29.18586
  14. Little Dustin J., Bamford Natalie C., Pokrovskaya Varvara, Robinson Howard, Nitz Mark, Howell P. Lynne, Structural Basis for the De-N-acetylation of Poly-β-1,6-N-acetyl-d-glucosamine in Gram-positive Bacteria, 10.1074/jbc.m114.611400
  15. Atkin Kate E., MacDonald Sandy J., Brentnall Andrew S., Potts Jennifer R., Thomas Gavin H., A different path: Revealing the function of staphylococcal proteins in biofilm formation, 10.1016/j.febslet.2014.04.002
  16. Gad G. F. M., J. Infect. Dev. Ctries., 3, 342 (2009)
  17. Cramton S. E., Infect. Immun., 67, 5427 (1999)
  18. Khoramian Babak, Jabalameli Fereshteh, Niasari-Naslaji Amir, Taherikalani Morovat, Emaneini Mohammad, Comparison of virulence factors and biofilm formation among Staphylococcus aureus strains isolated from human and bovine infections, 10.1016/j.micpath.2015.08.007
  19. Fluckiger U., Ulrich M., Steinhuber A., Doring G., Mack D., Landmann R., Goerke C., Wolz C., Biofilm Formation, icaADBC Transcription, and Polysaccharide Intercellular Adhesin Synthesis by Staphylococci in a Device-Related Infection Model, 10.1128/iai.73.3.1811-1819.2005
  20. Itoh Y., Wang X., Hinnebusch B. J., Preston J. F., Romeo T., Depolymerization of  -1,6-N-Acetyl-D-Glucosamine Disrupts the Integrity of Diverse Bacterial Biofilms, 10.1128/jb.187.1.382-387.2005
  21. Sadovskaya Irina, Chaignon Philippe, Kogan Grigorij, Chokr Ali, Vinogradov Evgeny, Jabbouri Saïd, Carbohydrate-containing components of biofilms producedin vitroby some staphylococcal strains related to orthopaedic prosthesis infections, 10.1111/j.1574-695x.2006.00068.x
  22. Donelli G., Francolini I., Romoli D., Guaglianone E., Piozzi A., Ragunath C., Kaplan J. B., Synergistic Activity of Dispersin B and Cefamandole Nafate in Inhibition of Staphylococcal Biofilm Growth on Polyurethanes, 10.1128/aac.01249-06
  23. Gawande Purushottam V., Leung Kai P., Madhyastha Srinivasa, Antibiofilm and Antimicrobial Efficacy of DispersinB®-KSL-W Peptide-Based Wound Gel Against Chronic Wound Infection Associated Bacteria, 10.1007/s00284-014-0519-6
  24. Chung Pooi Y., Toh Yien S., Anti-biofilm agents: recent breakthrough against multi-drug resistantStaphylococcus aureus, 10.1111/2049-632x.12141
  25. Abouelhassan Yasmeen, Garrison Aaron T., Burch Gena M., Wong Wilson, Norwood Verrill M., Huigens Robert W., Discovery of quinoline small molecules with potent dispersal activity against methicillin-resistant Staphylococcus aureus and Staphylococcus epidermidis biofilms using a scaffold hopping strategy, 10.1016/j.bmcl.2014.09.009
  26. Rogers Steven A., Huigens III Robert W., Melander Christian, A 2-Aminobenzimidazole That Inhibits and Disperses Gram-Positive Biofilms through a Zinc-Dependent Mechanism, 10.1021/ja9024676
  27. Böttcher Thomas, Kolodkin-Gal Ilana, Kolter Roberto, Losick Richard, Clardy Jon, Synthesis and Activity of Biomimetic Biofilm Disruptors, 10.1021/ja3120955
  28. Bouffard F. Aileen, Zambias Robert A., Dropinski James F., Balkovec James M., Hammond Milton L., Abruzzo George K., Bartizal Kenneth F., Marrinan Jean A., Kurtz Myra B., Synthesis and Antifungal Activity of Novel Cationic Pneumocandin Bo Derivatives, 10.1021/jm00028a003
  29. Douglas C. M., Fungal ß(1,3)-D-glucan synthesis, 10.1080/mmy.39.1.55.66
  30. Siala W., Mingeot-Leclercq M.-P., Tulkens P. M., Hallin M., Denis O., Van Bambeke F., Comparison of the Antibiotic Activities of Daptomycin, Vancomycin, and the Investigational Fluoroquinolone Delafloxacin against Biofilms from Staphylococcus aureus Clinical Isolates, 10.1128/aac.03482-14
  31. Van Bambeke F., Michot J.-M., Van Eldere J., Tulkens P.M., Quinolones in 2005: an update, 10.1111/j.1469-0691.2005.01131.x
  32. Bauer J., Siala W., Tulkens P. M., Van Bambeke F., A Combined Pharmacodynamic Quantitative and Qualitative Model Reveals the Potent Activity of Daptomycin and Delafloxacin against Staphylococcus aureus Biofilms, 10.1128/aac.00181-13
  33. Van Bambeke Françoise, Delafloxacin, a non-zwitterionic fluoroquinolone in Phase III of clinical development: evaluation of its pharmacology, pharmacokinetics, pharmacodynamics and clinical efficacy, 10.2217/fmb.15.39
  34. Andes D., Diekema D. J., Pfaller M. A., Bohrmuller J., Marchillo K., Lepak A., In Vivo Comparison of the Pharmacodynamic Targets for Echinocandin Drugs against Candida Species, 10.1128/aac.01584-09
  35. Wiederhold Nathan P., Kontoyiannis Dimitrios P., Chi Jingduan, Prince Randall A., Tam Vincent H., Lewis Russell E., Pharmacodynamics of Caspofungin in a Murine Model of Invasive Pulmonary Aspergillosis: Evidence of Concentration‐Dependent Activity, 10.1086/424465
  36. Grayo S., Lott-Desroches M.-C., Dussurget O., Respaud R., Fontanet A., Join-Lambert O., Singlas E., Le Monnier A., Rapid Eradication of Listeria monocytogenes by Moxifloxacin in a Murine Model of Central Nervous System Listeriosis, 10.1128/aac.00177-08
  37. Patel M. V., De Souza N. J., Gupte S. V., Jafri M. A., Bhagwat S. S., Chugh Y., Khorakiwala H. F., Jacobs M. R., Appelbaum P. C., Antistaphylococcal Activity of WCK 771, a Tricyclic Fluoroquinolone, in Animal Infection Models, 10.1128/aac.48.12.4754-4761.2004
  38. Singh R., Ray P., Das A., Sharma M., Penetration of antibiotics through Staphylococcus aureus and Staphylococcus epidermidis biofilms, 10.1093/jac/dkq257
  39. Stewart P. S., Davison W. M., Steenbergen J. N., Daptomycin Rapidly Penetrates a Staphylococcus epidermidis Biofilm, 10.1128/aac.01728-08
  40. Ikemura T., Mol. Biol. Evol., 2, 13 (1985)
  41. Kane James F, Effects of rare codon clusters on high-level expression of heterologous proteins in Escherichia coli, 10.1016/0958-1669(95)80082-4
  42. Kim Seonghun, Lee Sun Bok, Rare codon clusters at 5′-end influence heterologous expression of archaeal gene in Escherichia coli, 10.1016/j.pep.2006.07.014
  43. Outchkourov Nikolay S., Stiekema Willem J., Jongsma Maarten A., Optimization of the Expression of Equistatin in Pichia pastoris, 10.1006/prep.2001.1523
  44. Stewart Philip, Prospects for Anti-Biofilm Pharmaceuticals, 10.3390/ph8030504
  45. Hogan S., Stevens N.T., Humphreys H., O'Gara J.P., O'Neill E., Current and Future Approaches to the Prevention and Treatment of Staphylococcal Medical Device-Related Infections, 10.2174/1381612820666140905123900
  46. Webb J. S., Thompson L. S., James S., Charlton T., Tolker-Nielsen T., Koch B., Givskov M., Kjelleberg S., Cell Death in Pseudomonas aeruginosa Biofilm Development, 10.1128/jb.185.15.4585-4592.2003
  47. Kostakioti M., Hadjifrangiskou M., Hultgren S. J., Bacterial Biofilms: Development, Dispersal, and Therapeutic Strategies in the Dawn of the Postantibiotic Era, 10.1101/cshperspect.a010306
  48. Flemming H. C., Nat. Rev. Microbiol., 8, 623 (2010)
  49. Peterson Brandon W., He Yan, Ren Yijin, Zerdoum Aidan, Libera Matthew R., Sharma Prashant K., van Winkelhoff Arie-Jan, Neut Danielle, Stoodley Paul, van der Mei Henny C., Busscher Henk J., Viscoelasticity of biofilms and their recalcitrance to mechanical and chemical challenges, 10.1093/femsre/fuu008
  50. Haaber Jakob, Cohn Marianne Thorup, Frees Dorte, Andersen Thorbjørn Joest, Ingmer Hanne, Planktonic Aggregates of Staphylococcus aureus Protect against Common Antibiotics, 10.1371/journal.pone.0041075
  51. Lauderdale K. J., J. Orthop. Res., 28, 55 (2010)
  52. Kaplan Jeffrey B, LoVetri Karen, Cardona Silvia T, Madhyastha Srinivasa, Sadovskaya Irina, Jabbouri Saïd, Izano Era A, Recombinant human DNase I decreases biofilm and increases antimicrobial susceptibility in staphylococci, 10.1038/ja.2011.113
  53. Arciola Carla Renata, Gamberini Simonetta, Campoccia Davide, Visai Livia, Speziale Pietro, Baldassarri Lucilla, Montanaro Lucio, A multiplex PCR method for the detection of all five individual genes ofica locus inStaphylococcus epidermidis. A survey on 400 clinical isolates from prosthesis-associated infections, 10.1002/jbm.a.30445
  54. Buttner H., Front. Cell. Infect. Microbiol., 5, 14 (2015)
  55. Schneider Nils, Bramesfeld Anke, Burruano Larissa, Palliative care in public health: a formal and content-related analysis of European journals, 10.1007/s10389-006-0085-x
  56. Esteban Jaime, Molina-Manso Diana, Spiliopoulou Iris, Cordero-Ampuero José, Fernández-Roblas Ricardo, Foka Antigoni, Gómez-Barrena Enrique, Biofilm development by clinical isolates ofStaphylococcusspp. from retrieved orthopedic prostheses, 10.3109/17453674.2010.537810
  57. Pribaz Jonathan R., Bernthal Nicholas M., Billi Fabrizio, Cho John S., Ramos Romela Irene, Guo Yi, Cheung Ambrose L., Francis Kevin P., Miller Lloyd S., Mouse model of chronic post-arthroplasty infection: Noninvasive in vivo bioluminescence imaging to monitor bacterial burden for long-term study, 10.1002/jor.21519
  58. Francis K. P., Joh D., Bellinger-Kawahara C., Hawkinson M. J., Purchio T. F., Contag P. R., Monitoring Bioluminescent Staphylococcus aureus Infections in Living Mice Using a Novel luxABCDE Construct, 10.1128/iai.68.6.3594-3600.2000
  59. Ricicova M., Kucharikova S., Tournu H., Hendrix J., Bujdakova H., Van Eldere J., Lagrou K., Van Dijck P., Candida albicans biofilm formation in a new in vivo rat model, 10.1099/mic.0.033530-0
  60. Kucharikova S., J. Vis. Exp., 95, 52239 (2015)
  61. Kim J., Pitts B., Stewart P. S., Camper A., Yoon J., Comparison of the Antimicrobial Effects of Chlorine, Silver Ion, and Tobramycin on Biofilm, 10.1128/aac.00054-07
  62. Vuong Cuong, Voyich Jovanka M., Fischer Elizabeth R., Braughton Kevin R., Whitney Adeline R., DeLeo Frank R., Otto Michael, Polysaccharide intercellular adhesin (PIA) protects Staphylococcus epidermidis against major components of the human innate immune system, 10.1046/j.1462-5822.2004.00367.x
  63. Maira-Litran T., Kropec A., Abeygunawardana C., Joyce J., Mark III G., Goldmann D. A., Pier G. B., Immunochemical Properties of the Staphylococcal Poly-N-Acetylglucosamine Surface Polysaccharide, 10.1128/iai.70.8.4433-4440.2002
  64. Elson Leslie Alderman, Morgan Walter Thomas James, A colorimetric method for the determination of glucosamine and chondrosamine, 10.1042/bj0271824
  65. Reissig J. L., J. Biol. Chem., 217, 959 (1955)
  66. Takahashi Tomoko, Ikegami-Kawai Mayumi, Okuda Ryozou, Suzuki Kaori, A fluorimetric Morgan–Elson assay method for hyaluronidase activity, 10.1016/j.ab.2003.08.005
  67. Mann Ethan E., Rice Kelly C., Boles Blaise R., Endres Jennifer L., Ranjit Dev, Chandramohan Lakshmi, Tsang Laura H., Smeltzer Mark S., Horswill Alexander R., Bayles Kenneth W., Modulation of eDNA Release and Degradation Affects Staphylococcus aureus Biofilm Maturation, 10.1371/journal.pone.0005822
  68. Foulston L., Elsholz A. K. W., DeFrancesco A. S., Losick R., The Extracellular Matrix of Staphylococcus aureus Biofilms Comprises Cytoplasmic Proteins That Associate with the Cell Surface in Response to Decreasing pH, 10.1128/mbio.01667-14
  69. Eleaume Heïdy, Jabbouri Saïd, Comparison of two standardisation methods in real-time quantitative RT-PCR to follow Staphylococcus aureus genes expression during in vitro growth, 10.1016/j.mimet.2004.07.015
Bibliographic reference Siala, Wafi ; Kucharíková, Soňa ; Braem, Annabel ; Vleugels, Jef ; Tulkens, Paul M. ; et. al. The antifungal caspofungin increases fluoroquinolone activity against Staphylococcus aureus biofilms by inhibiting N-acetylglucosamine transferase. In: Nature Communications, Vol. 7, no.Nov.3, p. 13286 (2016)
Permanent URL http://hdl.handle.net/2078.1/177860