Inhibition of bacterial motility and spreading via release of cranberry derived materials from silicone substrates

Colloids and Surfaces B: Biointerfaces

Volumn 110, Issue , 2013, Pages 275-280

  Chan, Michelle ^a   Hidalgo, Gabriela ^a   Asadishad, Bahareh ^a   Almeida, Sergio ^a   Muja, Naser ^a   Mohammadi, Maziar Shah ^a   Nazhat, Showan N ^a   Tufenkji, Nathalie ^a  

^a MCGILL UNIVERSITY   (Canada)

Author keywords

Bacterial motility; Catheter; Cranberry; Silicone; Swarming

Indexed keywords

BACTERIAL COLONIZATION; BACTERIAL MOTILITY; BACTERIAL PATHOGENS; BROAD APPLICATION; CRANBERRY; DERIVED MATERIALS; SILICONE SUBSTRATES; SWARMING;

BIOMEDICAL EQUIPMENT; CATHETERS; ESCHERICHIA COLI; GENE EXPRESSION; SILICONES; SUBSTRATES;

BACTERIA;

CRANBERRY POWDER; NATURAL PRODUCT; PROANTHOCYANIDIN DERIVATIVE; SILICONE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; AQUEOUS SOLUTION; ARTICLE; BACTERIAL COLONIZATION; BACTERIAL MOTILITY; BACTERIAL PHENOMENA AND FUNCTIONS; BACTERIAL STRAIN; COMPOSITE MATERIAL; CONTROLLED STUDY; CRANBERRY; DOWN REGULATION; DRUG RELEASE; DRUG TARGETING; ESCHERICHIA COLI; FLAGELLIN GENE; GENE; GENE EXPRESSION; NONHUMAN; PRIORITY JOURNAL; PROTEUS MIRABILIS; QUANTITATIVE STUDY;

ANIMALS; DIPTERA; ESCHERICHIA COLI; PARTICLE SIZE; PLANT EXTRACTS; PROTEUS MIRABILIS; SILICONES; SURFACE PROPERTIES;

BACTERIA (MICROORGANISMS); ESCHERICHIA COLI; PROTEUS MIRABILIS; VACCINIUM MACROCARPON;

EID: 84878937998     PISSN: 09277765     EISSN: 18734367     Source Type: Journal    
DOI: 10.1016/j.colsurfb.2013.03.047     Document Type: Article

References (47)

1. Hall-Stoodley L., Stoodley J.W.C.P. Bacterial biofilms: from the natural environment to infectious diseases. Nat. Rev. Microbiol. 2004, 2:95-108.
2. Habash M., Reid G. Microbial biofilms: their development and significance for medical device-related infections. J. Clin. Pharmacol. 1999, 39(9):887-898.
3. Nuzzo R.G. Stable antifouling surfaces. Nat. Mater. 2003, 2:207-208.
4. Flemming H.C. Biofouling in water systems - cases, causes and countermeasures. Appl. Microbiol. Biotechnol. 2002, 59(6):629-640.
5. Harshey R.M. Bacterial motility on a surface: many ways to a common goal. Annu. Rev. Microbiol. 2003, 57:249-273.
6. Wang R., et al. Inhibition of Escherichia coli and Proteus mirabilis adhesion and biofilm formation on medical grade silicone surface. Biotechnol. Bioeng. 2012, 109(2):336-345.
7. Lawrence E.L., Turner I.G. Materials for urinary catheters: a review of their history and development in the UK. Med. Eng. Phys. 2005, 27(6):443-453.
8. Denstedt J.D., Reid T.A.W.G. Biomaterials used in urology: current issues of biocompatibility, infection, and encrustation. J. Endourol. 1998, 12:493-500.
9. Bayston R., Fisher L.E., Weber K. An antimicrobial modified silicone peritoneal catheter with activity against both Gram positive and Gram negative bacteria. Biomaterials 2009, 30(18):3167-3173.
10. Gilbert R.E., Harden M. Effectiveness of impregnated central venous catheters for catheter related blood stream infection: a systematic review. Curr. Opin. Infect. Dis. 2008, 21(3):235-245. 10.1097/QCO.0b013e3282ffd6e0.
11. Gottenbos B., et al. In vitro and in vivo antimicrobial activity of covalently coupled quaternary ammonium silane coatings on silicone rubber. Biomaterials 2002, 23(6):1417-1423.
12. Eydelnant I.A., Tufenkji N. Cranberry derived proanthocyanidins reduce bacterial adhesion to selected biomaterials. Langmuir 2008, 24(18):10273-10281.
13. Pinzón-Arango P.A., Camesano Y.L.T.A. Role of cranberry on bacterial adhesion forces and implications for Escherichia coli-Uroepithelial cell attachment. J. Med. Food 2009, 12:259-270.
14. Camesano T.A., Pinzón-Arango Y.L.P.A. Cranberry prevents the adhesion of bacteria: overview of relevant health benefits. Agro. Food Ind. Hi-Tech 2007, 18:24-27.
15. Burger O., et al. Inhibition of Helicobacter pylori adhesion to human gastric mucus by a high-molecular-weight constituent of cranberry juice. Crit. Rev. Food Sci. Nutr. 2002, 42(Suppl. 3):279-284.
16. Howell A.B., Krueger J.D.R.C.G., Winterbottom R., Cunningham D.G., Leahy M. A-type cranberry proanthocyanidins and uropathogenic bacterial anti-adhesion activity. Phytochemistry 2005, 66:2281-2291.
17. Harmidy K., Tufenkji N., Gruenheid S. Perturbation of host cell cytoskeleton by cranberry proanthocyanidins and their effect on enteric infections. PLoS ONE 2011, 6(11):e27267.
18. Narayansingh R., Hurta R.A.R. Cranberry extract and quercetin modulate the expression of cyclooxygenase-2 (COX-2) and IκBα in human colon cancer cells. J. Sci. Food Agric. 2009, 89(3):542-547.
19. García-Lafuente A., et al. Flavonoids as anti-inflammatory agents: implications in cancer and cardiovascular disease. Inflamm. Res. 2009, 58(9):537-552.
20. Hidalgo G., Chan M., Tufenkji N. Inhibition of Escherichia coli CFT073 fliC expression and motility by cranberry materials. Appl. Environ. Microbiol. 2011, 77(19):6852-6857.
21. O'May C., Tufenkji N. The swarming motility of Pseudomonas aeruginosa is blocked by cranberry proanthocyanidins and other tannin-containing materials. Appl. Environ. Microbiol. 2011, 77(9):3061-3067.
22. O'May C., et al. Tannin derived materials can block swarming motility and enhance biofilm formation in Pseudomonas aeruginosa. Biofouling 2012, 28(10):1063-1076.
23. McCall J., Hidalgo G., Asadishad B., Tufenkji N. Cranberry impairs selected behaviors essential for virulence in Proteus mirabilis HI4320. Canadian J. Microbiol. 2013, in press.
24. Mobley H.L.T., et al. Isogenic P-fimbrial deletion mutants of pyelonephritogenic Escherichia coli: the role of αGal(1-4)βGal binding in virulence of a wild-type strain. Mol. Microbiol. 1993, 10:143-155.
25. Mobley H.L.T., Warren J.W. Urease-positive bacteriuria obstruction of long-term urinary catheters. J. Clin. Microbiol. 1987, 25(11):2216-2217.
26. Cote J., et al. Analyzing cranberry bioactive compounds. Crit. Rev. Food Sci. Nutr. 2010, 50:872-888.
27. Hümmer W., Schreier P. Analysis of proanthocyanidins. Mol. Nutr. Food Res. 2008, 52(12):1381-1398.
28. Livak K., Schmittgen T. Analysis of relative gene expression data using real-time quantitative PCR and the 2(T)(-delta delta C) method. Methods 2001, 25:402-408.
29. Pearson M.M., Mobley H.L.T. Repression of motility during fimbrial expression: identification of 14 mrpJ gene paralogues in Proteus mirabilis. Mol. Microbiol. 2008, 69(2):548-558.
30. Lane M.C., et al. Expression of flagella is coincident with uropathogenic Escherichia coli ascension to the upper urinary tract. Proc. Natl. Acad. Sci. U.S.A. 2007, 104(42):16669-16674.
31. Colo G.D. Controlled drug release from implantable matrices based on hydrophobic polymers. Biomaterials 1992, 13(12):850-856.
32. Tiwary A.K., Rana V. Cross-linked chitosan films: effect of cross-linking density on swelling parameters. J. Pharm. Sci. 2010, 23:443-448.
33. Schwan W.R. Survival of uropathogenic Escherichia coli in the murine urinary tract is dependent on OmpR. Microbiology 2009, 155(6):1832-1839.
34. Wright K.J., Seed P.C., Hultgren S.J. Uropathogenic Escherichia coli flagella aid in efficient urinary tract colonization. Infect. Immun. 2005, 73(11):7657-7668.
35. Kearns D.B. A field guide to bacterial swarming motility. Nat. Rev. Microbiol. 2010, 8:634-644.
36. Stickler D., Hughes G. Ability of Proteus mirabilis to swarm over urethral catheters. Eur. J. Clin. Microbiol. Infect. Dis. 1999, 18(3):206-208.
37. Reddy S.T., et al. Micropatterned surfaces for reducing the risk of catheter-associated urinary tract infection: an in vitro study on the effect of sharklet micropatterned surfaces to inhibit bacterial colonization and migration of uropathogenic Escherichia coli. J. Endourol. 2001, 25(9):1547-1552.
38. Hayward N.J., Incledon G.M., Spragg J.E. Effect of firm agar on the swarming of Proteus and Clostridium species and on the colonies of clinically important bacteria (Plates IX-XI). J. Med. Microbiol. 1978, 11(2):155-164.
39. Harshey R.M. Bees aren't the only ones: swarming in Gram-negative bacteria. Mol. Microbiol. 1994, 13(3):389-394.
40. Harshey R.M., Matsuyama T. Dimorphic transition in Escherichia coli and Salmonella typhimurium: surface-induced differentiation into hyperflagellate swarmer cells. Proc. Natl. Acad. Sci. U.S.A. 1994, 91(18):8631-8635.
41. Jones B.V., et al. Ultrastructure of Proteus mirabilis swarmer cell rafts and role of swarming in catheter-associated urinary tract infection. Infect. Immun. 2004, 72(7):3941-3950.
42. Mobley H.L.T., Belas R. Swarming and pathogenicity of Proteus mirabilis in the urinary tract. Trends Microbiol. 1995, 3:280-284.
43. Tremblay J., Déziel E. Gene expression in Pseudomonas aeruginosa swarming motility. BMC Genomics 2010, 11:587.
44. Rather P.N. Swarmer cell differentiation in Proteus mirabilis. Environ. Microbiol. 2005, 7(8):1065-1073.
45. Pearson M.M., et al. Transcriptome of swarming Proteus mirabilis. Infect. Immun. 2010, 78(6):2834-2845.
46. Pinzon-Arango P.A., Holguin K., Camesano T.A. Impact of cranberry juice and proanthocyanidins on the ability of Escherichia coli to form biofilms. Food Sci. Biotechnol. 2011, 20(5):1315-1321.
47. Zodrow K.R., Schiffman J.D., Elimelech M. Biodegradable polymer (PLGA) coatings featuring cinnamaldehyde and carvacrol mitigate biofilm formation. Langmuir 2012, 28:13993-13999.