User menu

Antibacterial Activity of 1-[(2,4-Dichlorophenethyl)amino]-3-Phenoxypropan-2-ol against Antibiotic-Resistant Strains of Diverse Bacterial Pathogens, Biofilms and in Pre-clinical Infection Models

Bibliographic reference Defraine, Valerie ; Verstraete, Laure ; Van Bambeke, Françoise ; Anantharajah, Ahalieyah ; Townsend, Eleanor M. ; et. al. Antibacterial Activity of 1-[(2,4-Dichlorophenethyl)amino]-3-Phenoxypropan-2-ol against Antibiotic-Resistant Strains of Diverse Bacterial Pathogens, Biofilms and in Pre-clinical Infection Models. In: Frontiers in Microbiology, Vol. 8, p. 1-10 (2017)
Permanent URL http://hdl.handle.net/2078.1/191828
  1. Arivett Brock A., Ream David C., Fiester Steven E., Mende Katrin, Murray Clinton K., Thompson Mitchell G., Kanduru Shrinidhi, Summers Amy M., Roth Amanda L., Zurawski Daniel V., Actis Luis A., Draft Genome Sequences of Klebsiella pneumoniae Clinical Type Strain ATCC 13883 and Three Multidrug-Resistant Clinical Isolates, 10.1128/genomea.01385-14
  2. Baba Tomoya, Ara Takeshi, Hasegawa Miki, Takai Yuki, Okumura Yoshiko, Baba Miki, Datsenko Kirill A, Tomita Masaru, Wanner Barry L, Mori Hirotada, Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection, 10.1038/msb4100050
  3. Bassetti Matteo, Merelli Maria, Temperoni Chiara, Astilean Augusta, New antibiotics for bad bugs: where are we?, 10.1186/1476-0711-12-22
  4. Boucher Helen W., Talbot George H., Bradley John S., Edwards John E., Gilbert David, Rice Louis B., Scheld Michael, Spellberg Brad, Bartlett John, Bad Bugs, No Drugs: No ESKAPE! An Update from the Infectious Diseases Society of America, 10.1086/595011
  5. Boyle B., Fernandez L., Laroche J., Kukavica-Ibrulj I., Mendes C. M. F., Hancock R. W., Levesque R. C., Complete Genome Sequences of Three Pseudomonas aeruginosa Isolates with Phenotypes of Polymyxin B Adaptation and Inducible Resistance, 10.1128/jb.06246-11
  6. Briers Y., Walmagh M., Van Puyenbroeck V., Cornelissen A., Cenens W., Aertsen A., Oliveira H., Azeredo J., Verween G., Pirnay J.-P., Miller S., Volckaert G., Lavigne R., Engineered Endolysin-Based "Artilysins" To Combat Multidrug-Resistant Gram-Negative Pathogens, 10.1128/mbio.01379-14
  7. Buyck Julien M., Tulkens Paul M., Van Bambeke Françoise, Pharmacodynamic Evaluation of the Intracellular Activity of Antibiotics towards Pseudomonas aeruginosa PAO1 in a Model of THP-1 Human Monocytes, 10.1128/aac.02609-12
  8. Cohen Nadia R., Lobritz Michael A., Collins James J., Microbial Persistence and the Road to Drug Resistance, 10.1016/j.chom.2013.05.009
  9. Conlon B. P., Nakayasu E. S., Fleck L. E., LaFleur M. D., Isabella V. M., Coleman K., Leonard S. N., Smith R. D., Adkins J. N., Lewis K., Activated ClpP kills persisters and eradicates a chronic biofilm infection, 10.1038/nature12790
  10. Cui Peng, Niu Hongxia, Shi Wanliang, Zhang Shuo, Zhang Hao, Margolick Joseph, Zhang Wenhong, Zhang Ying, Disruption of Membrane by Colistin Kills Uropathogenic Escherichia coli Persisters and Enhances Killing of Other Antibiotics, 10.1128/aac.01481-16
  11. DESCHEEMAEKER P., LAMMENS C., POT B., VANDAMME P., GOOSSENS H., Evaluation of Arbitrarily Primed PCR Analysis and Pulsed-Field Gel Electrophoresis of Large Genomic DNA Fragments for Identification of Enterococci Important in Human Medicine, 10.1099/00207713-47-2-555
  12. The Bacterial Challenge: Time to React. (2009)
  13. Point Prevalence Survey of Healthcare-associated Infections and Antimicrobial Use in European Acute Care Hospitals 2011–2012. (2013)
  14. Breakpoint Tables for Interpretation of MICs and Zone Diameters. Version 7.1 2017. (2017)
  15. Fauvart M., De Groote V. N., Michiels J., Role of persister cells in chronic infections: clinical relevance and perspectives on anti-persister therapies, 10.1099/jmm.0.030932-0
  16. Feng Jie, Shi Wanliang, Zhang Shuo, Sullivan David, Auwaerter Paul G., Zhang Ying, A Drug Combination Screen Identifies Drugs Active against Amoxicillin-Induced Round Bodies of In Vitro Borrelia burgdorferi Persisters from an FDA Drug Library, 10.3389/fmicb.2016.00743
  17. Fischbach M. A., Walsh C. T., Antibiotics for Emerging Pathogens, 10.1126/science.1176667
  18. Gallo Stephanie W., Ferreira Carlos Alexandre S., de Oliveira Sílvia D., Combination of polymyxin B and meropenem eradicates persister cells from Acinetobacter baumannii strains in exponential growth, 10.1099/jmm.0.000542
  19. Garrison Aaron T., Abouelhassan Yasmeen, Kallifidas Dimitris, Bai Fang, Ukhanova Maria, Mai Volker, Jin Shouguang, Luesch Hendrik, Huigens Robert W., Halogenated Phenazines that Potently Eradicate Biofilms, MRSA Persister Cells in Non-Biofilm Cultures, andMycobacterium tuberculosis, 10.1002/anie.201508155
  20. Gill Erin E., Franco Octavio L., Hancock Robert. E. W., Antibiotic Adjuvants: Diverse Strategies for Controlling Drug-Resistant Pathogens, 10.1111/cbdd.12478
  21. Helaine S., Cheverton A. M., Watson K. G., Faure L. M., Matthews S. A., Holden D. W., Internalization of Salmonella by Macrophages Induces Formation of Nonreplicating Persisters, 10.1126/science.1244705
  22. Hermans Kim, Nguyen T.L. Anh, Roberfroid Stefanie, Schoofs Geert, Verhoeven Tine, De Coster David, Vanderleyden Jos, De Keersmaecker Sigrid C.J., Gene expression analysis of monospecies Salmonella Typhimurium biofilms using Differential Fluorescence Induction, 10.1016/j.mimet.2011.01.012
  23. Hunt Piper Reid, TheC. elegansmodel in toxicity testing : TheC. elegansmodel in toxicity testing, 10.1002/jat.3357
  24. Kean Ryan, Rajendran Ranjith, Haggarty Jennifer, Townsend Eleanor M., Short Bryn, Burgess Karl E., Lang Sue, Millington Owain, Mackay William G., Williams Craig, Ramage Gordon, Candida albicans Mycofilms Support Staphylococcus aureus Colonization and Enhances Miconazole Resistance in Dual-Species Interactions, 10.3389/fmicb.2017.00258
  25. Koeva Martina, Gutu Alina D., Hebert Wesley, Wager Jeffrey D., Yonker Lael M., O'Toole George A., Ausubel Frederick M., Moskowitz Samuel M., Joseph-McCarthy Diane, An Antipersister Strategy for Treatment of Chronic Pseudomonas aeruginosa Infections, 10.1128/aac.00987-17
  26. LaFleur M. D., Kumamoto C. A., Lewis K., Candida albicans Biofilms Produce Antifungal-Tolerant Persister Cells, 10.1128/aac.00684-06
  27. Lee Daniel G, Urbach Jonathan M, Wu Gang, Liberati Nicole T, Feinbaum Rhonda L, Miyata Sachiko, Diggins Lenard T, He Jianxin, Saucier Maude, Deziel Eric, Friedman Lisa, Li Li, Grills George, Montgomery Kate, Kucherlapati Raju, Rahme Laurence G, Ausubel Frederick M, 10.1186/gb-2006-7-10-r90
  28. Lee Jin-Hyung, Kim Yong-Guy, Gwon Giyeon, Wood Thomas K., Lee Jintae, Halogenated indoles eradicate bacterial persister cells and biofilms, 10.1186/s13568-016-0297-6
  29. Lewis Kim, Persister cells, dormancy and infectious disease, 10.1038/nrmicro1557
  30. Liebens Veerle, Defraine Valerie, Knapen Wouter, Swings Toon, Beullens Serge, Corbau Romu, Marchand Arnaud, Chaltin Patrick, Fauvart Maarten, Michiels Jan, Identification of 1-((2,4-Dichlorophenethyl)Amino)-3-Phenoxypropan-2-ol, a Novel Antibacterial Compound Active against Persisters of Pseudomonas aeruginosa, 10.1128/aac.00836-17
  31. Livermore D.M., The need for new antibiotics, 10.1111/j.1465-0691.2004.1004.x
  32. Merabishvili Maia, Vandenheuvel Dieter, Kropinski Andrew M., Mast Jan, De Vos Daniel, Verbeken Gilbert, Noben Jean-Paul, Lavigne Rob, Vaneechoutte Mario, Pirnay Jean-Paul, Characterization of Newly Isolated Lytic Bacteriophages Active against Acinetobacter baumannii, 10.1371/journal.pone.0104853
  33. Michiels Joran Elie, Van den Bergh Bram, Verstraeten Natalie, Michiels Jan, Molecular mechanisms and clinical implications of bacterial persistence, 10.1016/j.drup.2016.10.002
  34. Mulcahy L. R., Burns J. L., Lory S., Lewis K., Emergence of Pseudomonas aeruginosa Strains Producing High Levels of Persister Cells in Patients with Cystic Fibrosis, 10.1128/jb.01651-09
  35. O’Neill, Tackling Drug-resistant Infections Globally: Final Report and Recommendations. The Review on Antimicrobial Resistance. (2016)
  36. Pena-Miller Rafael, Laehnemann David, Jansen Gunther, Fuentes-Hernandez Ayari, Rosenstiel Philip, Schulenburg Hinrich, Beardmore Robert, When the Most Potent Combination of Antibiotics Selects for the Greatest Bacterial Load: The Smile-Frown Transition, 10.1371/journal.pbio.1001540
  37. Pendleton Jack N, Gorman Sean P, Gilmore Brendan F, Clinical relevance of the ESKAPE pathogens, 10.1586/eri.13.12
  38. Porta-de-la-Riva Montserrat, Fontrodona Laura, Villanueva Alberto, Cerón Julián, Basic Caenorhabditis elegans Methods: Synchronization and Observation, 10.3791/4019
  39. Rice Louis B., Federal Funding for the Study of Antimicrobial Resistance in Nosocomial Pathogens: No ESKAPE, 10.1086/533452
  40. Shen Qingshan, Zhou Wei, Hu Liangbin, Qi Yonghua, Ning Hongmei, Chen Jian, Mo Haizhen, Bactericidal activity of alpha-bromocinnamaldehyde against persisters in Escherichia coli, 10.1371/journal.pone.0182122
  41. Shin S. H., Kim S., Kim J. Y., Lee S., Um Y., Oh M.-K., Kim Y.-R., Lee J., Yang K.-S., Complete Genome Sequence of Enterobacter aerogenes KCTC 2190, 10.1128/jb.00028-12
  42. Singh R., Manjunatha U., Boshoff H. I. M., Ha Y. H., Niyomrattanakit P., Ledwidge R., Dowd C. S., Lee I. Y., Kim P., Zhang L., Kang S., Keller T. H., Jiricek J., Barry C. E., PA-824 Kills Nonreplicating Mycobacterium tuberculosis by Intracellular NO Release, 10.1126/science.1164571
  43. Smith Karen, Collier Andrew, Townsend Eleanor M., O’Donnell Lindsay E., Bal Abhijit M., Butcher John, Mackay William G., Ramage Gordon, Williams Craig, One step closer to understanding the role of bacteria in diabetic foot ulcers: characterising the microbiome of ulcers, 10.1186/s12866-016-0665-z
  44. Stiernagle, Maintenance of C. elegans. (2006)
  45. Tamma P. D., Cosgrove S. E., Maragakis L. L., Combination Therapy for Treatment of Infections with Gram-Negative Bacteria, 10.1128/cmr.05041-11
  46. Townsend Eleanor M., Sherry Leighann, Rajendran Ranjith, Hansom Donald, Butcher John, Mackay William G., Williams Craig, Ramage Gordon, Development and characterisation of a novel three-dimensional inter-kingdom wound biofilm model, 10.1080/08927014.2016.1252337
  47. Van Acker Heleen, Sass Andrea, Bazzini Silvia, De Roy Karen, Udine Claudia, Messiaen Thomas, Riccardi Giovanna, Boon Nico, Nelis Hans J., Mahenthiralingam Eshwar, Coenye Tom, Biofilm-Grown Burkholderia cepacia Complex Cells Survive Antibiotic Treatment by Avoiding Production of Reactive Oxygen Species, 10.1371/journal.pone.0058943
  48. Van den Bergh Bram, Fauvart Maarten, Michiels Jan, Formation, physiology, ecology, evolution and clinical importance of bacterial persisters, 10.1093/femsre/fux001
  49. Global Priority List of Antibiotic-resistant Bacteria to Guide Research, Discovery, and Development of New Antibiotics. (2017)
  50. Wood Thomas K., Combatting bacterial persister cells : Combatting Persister Cells, 10.1002/bit.25721
  51. Yang Shoufeng, Hay Iain D., Cameron David R., Speir Mary, Cui Bintao, Su Feifei, Peleg Anton Y., Lithgow Trevor, Deighton Margaret A., Qu Yue, Antibiotic regimen based on population analysis of residing persister cells eradicates Staphylococcus epidermidis biofilms, 10.1038/srep18578