Erratum: Magnetic nanoparticle targeted hyperthermia of cutaneous staphylococcus aureus infection (Annals of Biomedical Engineering (2012) DOI: 10.1007/s10439-012-0698-x);Magnetic nanoparticle targeted hyperthermia of cutaneous staphylococcus aureus infection

Annals of Biomedical Engineering

Volumn 41, Issue 3, 2013, Pages 598-609

  Kim, Min Ho ^a,b   Yamayoshi, Itsukyo ^a   Mathew, Steven ^a   Lin, Hubert ^a   Nayfach, Joseph ^c   Simon, Scott I ^a  

^a University of California   (United States)

^b KENT STATE UNIVERSITY   (United States)

^c Qteris Inc   (United States)

Author keywords

Alternating magnetic field; Antimicrobial thermotherapy; Magnetic nanoparticle; S. aureus biofilm

Indexed keywords

BACTERIA; BIOFILMS; ENZYME INHIBITION; MAGNETIC FIELDS; NANOPARTICLES; PHYSICAL THERAPY;

ALTERNATING MAGNETIC FIELD; ANTIBODY-TARGETED; HIGH FREQUENCY HF; MAGNETIC NANO-PARTICLES; S. AUREUS; STANDARD OF CARES; STAPHYLOCOCCUS AUREUS; THERMOTHERAPIES;

NANOMAGNETICS;

BACTERIUM ANTIBODY; IMMOBILIZED ANTIBODY; MAGNETITE NANOPARTICLE; STAPHYLOCOCCUS PROTEIN A;

ANIMAL; ARTICLE; BIOFILM; BIOMEDICAL ENGINEERING; C57BL MOUSE; FEMALE; GROWTH, DEVELOPMENT AND AGING; HYPERTHERMIC THERAPY; IMMUNOLOGY; MAGNETOTHERAPY; METHODOLOGY; MICROBIOLOGY; MOUSE; PHYSIOLOGY; STAPHYLOCOCCAL SKIN INFECTION; STAPHYLOCOCCUS AUREUS; TRANSGENIC MOUSE; WOUND INFECTION;

ANIMALS; ANTIBODIES, BACTERIAL; ANTIBODIES, IMMOBILIZED; BIOFILMS; BIOMEDICAL ENGINEERING; FEMALE; HYPERTHERMIA, INDUCED; MAGNETIC FIELD THERAPY; MAGNETITE NANOPARTICLES; MICE; MICE, INBRED C57BL; MICE, TRANSGENIC; STAPHYLOCOCCAL PROTEIN A; STAPHYLOCOCCAL SKIN INFECTIONS; STAPHYLOCOCCUS AUREUS; WOUND INFECTION;

EID: 84876164103     PISSN: 00906964     EISSN: 15739686     Source Type: Journal    
DOI: 10.1007/s10439-012-0709-y     Document Type: Erratum

References (54)

1. American Diabetes Association. Consensus development conference on diabetic foot wound care: 7-8, April 1999, Boston, Massachusetts. Diabetes Care 22(1354):1360, 1999.
2. Amorena, B., E. Gracia, M. Monzon, J. Leiva, C. Oteiza, M. Perez, et al. Antibiotic susceptibility assay for Staphylococcus aureus in biofilms developed in vitro. J. Antimicrob. Chemother. 44:43-55, 1999.
3. Anon. Editorial: Antibiotic resistance and topical treatment. Br. Med. J. 2:649-650, 1978.
4. Bernthal, N. M., A. I. Stavrakis, F. Billi, J. S. Cho, T. J. Kremen, S. I. Simon, et al. A mouse model of post-arthroplasty Staphylococcus aureus joint infection to evaluate in vivo the efficacy of antimicrobial implant coatings. PLoS ONE 5:e12580, 2010.
5. Bjarnsholt, T., K. Kirketerp-Moller, P. O. Jensen, K. G. Madsen, R. Phipps, K. Krogfelt, et al. Why chronic wounds will not heal: a novel hypothesis. Wound Repair Regen. 16:2-10, 2008.
6. Bucci, O. M. Electromagnetism, nanotechnologies and biology: New challenges and opportunities. Electromagnetic Theory (EMTS) on 2010 URSI International Symposium, pp. 77-80, 2010.
7. Caubet, R., F. Pedarros-Caubet, M. Chu, and E. Freye. de Belem Rodrigues M, Moreau JM, et al. A radio frequency electric current enhances antibiotic efficacy against bacterial biofilms. Antimicrob. Agents Chemother. 48:4662-4664, 2004.
8. Cebrian, G., J. Raso, S. Condon, and P. Manas. Acquisition of pulsed electric fields resistance in Staphylococcus aureus after exposure to heat and alkaline shocks. Food Control 25:407-414, 2012.
9. Celli, J., and B. B. Finlay. Bacterial avoidance of phagocytosis. Trends Microbiol. 10:232-237, 2002.
10. Cho, J. S., E. M. Pietras, N. C. Garcia, R. I. Ramos, D. M. Farzam, H. R. Monroe, et al. IL-17 is essential for host defense against cutaneous Staphylococcus aureus infection in mice. J. Clin. Invest. 120:1762-1773, 2010.
11. Cho, J. S., J. Zussman, N. P. Donegan, R. I. Ramos, N. C. Garcia, D. Z. Uslan, et al. Noninvasive in vivo imaging to evaluate immune responses and antimicrobial therapy against Staphylococcus aureus and USA300 MRSA skin infections. J. Invest. Dermatol. 131:907-915, 2011.
12. Dana, B., and Gannot, I. An analytic analysis of the diffusive-heat-flow equation for different magnetic field profiles for a single magnetic nanoparticle. J. Atomic Mol. Opt. Phys., 2012. DOI: 10.1155/2012/135708.
13. Daum, R. S., and B. Spellberg. Progress toward a Staphylococcus aureus vaccine. Clin. Infect. Dis. 54:560-567, 2012.
14. Davies, D. Understanding biofilm resistance to antibacterial agents. Nat. Rev. Drug Discov. 2:114-122, 2003.
15. Di Poto, A., M. S. Sbarra, G. Provenza, L. Visai, and P. Speziale. The effect of photodynamic treatment combined with antibiotic action or host defence mechanisms on Staphylococcus aureus biofilms. Biomaterials 30:3158-3166, 2009.
16. Donlan, R. M., and J. W. Costerton. Biofilms: survival mechanisms of clinically relevant microorganisms. Clin. Microbiol. Rev. 15:167-193, 2002.
17. Dowd, S. E., R. D. Wolcott, Y. Sun, T. McKeehan, E. Smith, and D. Rhoads. Polymicrobial nature of chronic diabetic foot ulcer biofilm infections determined using bacterial tag encoded FLX amplicon pyrosequencing (bTEFAP). PLoS ONE 3:e3326, 2008.
18. Dudeck, O., K. Bogusiewicz, J. Pinkernelle, G. Gaffke, M. Pech, G. Wieners, et al. Local arterial infusion of superparamagnetic iron oxide particles in hepatocellular carcinoma: a feasibility and 3.0 T MRI study. Invest. Radiol. 41:527-535, 2006.
19. Edwards, R., and K. G. Harding. Bacteria and wound healing. Curr. Opin. Infect. Dis. 17:91-96, 2004.
20. Ensing, G. T., B. L. Roeder, J. L. Nelson, J. R. van Horn, H. C. van der Mei, H. J. Busscher, et al. Effect of pulsed ultrasound in combination with gentamicin on bacterial viability in biofilms on bone cements in vivo. J. Appl. Microbiol. 99:443-448, 2005.
21. Faust, N., F. Varas, L. M. Kelly, S. Heck, and T. Graf. Insertion of enhanced green fluorescent protein into the lysozyme gene creates mice with green fluorescent granulocytes and macrophages. Blood 96:719-726, 2000.
22. Fonder, M. A., G. S. Lazarus, D. A. Cowan, B. Aronson-Cook, A. R. Kohli, and A. J. Mamelak. Treating the chronic wound: a practical approach to the care of nonhealing wounds and wound care dressings. J. Am. Acad. Dermatol. 58:185-206, 2008.
23. Foster, T. J. Immune evasion by staphylococci. Nat. Rev. Microbiol. 3:948-958, 2005.
24. Giladi, M., Y. Porat, A. Blatt, E. Shmueli, Y. Wasserman, E. D. Kirson, et al. Microbial growth inhibition by alternating electric fields in mice with Pseudomonas aeruginosa lung infection. Antimicrob. Agents Chemother. 54:3212-3218, 2010.
25. Han, A., J. M. Zenilman, J. H. Melendez, M. E. Shirtliff, A. Agostinho, G. James, et al. The importance of a multifaceted approach to characterizing the microbial flora of chronic wounds. Wound Repair Regen. 19:532-541, 2011.
26. Hassani, M., G. Cebrian, P. Mannas, S. Condon, and R. Pagan. Induced thermotolerance under nonisothermal treatments of a heat sensitive and a resistant strain of Staphylococcus aureus in media of different pH. Lett. Appl. Microbiol. 43:619-624, 2006.
27. Ivkov, R., D. E. Bordelon, C. Cornejo, C. Gruttner, F. Westphal, and T. L. DeWeese. Magnetic nanoparticle heating efficiency reveals magneto-structural differences when characterized with wide ranging and high amplitude alternating magnetic fields. J. Appl. Phys. 109:124904, 2011.
28. Ivkov, R., S. J. DeNardo, W. Daum, A. R. Foreman, R. C. Goldstein, V. S. Nemkov, et al. Application of high amplitude alternating magnetic fields for heat induction of nanoparticles localized in cancer. Clin. Cancer Res. 11:7093s-7103s, 2005.
29. Jain, T. K., M. K. Reddy, M. A. Morales, D. L. Leslie-Pelecky, and V. Labhasetwar. Biodistribution, clearance, and biocompatibility of iron oxide magnetic nanoparticles in rats. Mol. Pharm. 5:316-327, 2008.
30. Jordan, A., R. Scholz, K. Maier-Hauff, F. K. van Landeghem, N. Waldoefner, U. Teichgraeber, et al. The effect of thermotherapy using magnetic nanoparticles on rat malignant glioma. J. Neurooncol. 78:7-14, 2006.
31. Keblinski, P., D. G. Cahill, A. Bodapati, C. R. Sullivan, and T. A. Taton. Limits of localized heating by electromagnetically excited nanoparticles. J. Appl. Phys. 100:054305, 2006.
32. Kennedy, J., I. S. Blair, D. A. McDowell, and D. J. Bolton. An investigation of the thermal inactivation of Staphylococcus aureus and the potential for increased thermotolerance as a result of chilled storage. J. Appl. Microbiol. 99:1229-1235, 2005.
33. Kennedy, C. A., and J. P. O'Gara. Contribution of culture media and chemical properties of polystyrene tissue culture plates to biofilm development by Staphylococcus aureus. J. Med. Microbiol. 53:1171-1173, 2004.
34. Kim, M. H., J. L. Granick, C. Kwok, N. J. Walker, D. L. Borjesson, F. R. Curry, et al. Neutrophil survival and c-kit(+)-progenitor proliferation in Staphylococcus aureus-infected skin wounds promote resolution. Blood 117:3343-3352, 2011.
35. Kim, M. H., W. Liu, D. L. Borjesson, F. R. Curry, L. S. Miller, A. L. Cheung, et al. Dynamics of neutrophil infiltration during cutaneous wound healing and infection using fluorescence imaging. J. Invest. Dermatol. 128:1812-1820, 2008.
36. Lambrechts, S. A., T. N. Demidova, M. C. Aalders, T. Hasan, and M. R. Hamblin. Photodynamic therapy for Staphylococcus aureus infected burn wounds in mice. Photochem. Photobiol. Sci. 4:503-509, 2005.
37. Lee, J. H., J. T. Jang, J. S. Choi, S. H. Moon, S. H. Noh, J. W. Kim, et al. Exchange-coupled magnetic nanoparticles for efficient heat induction. Nat. Nanotechnol. 6:418-422, 2011.
38. Liu, C., A. Bayer, S. E. Cosgrove, R. S. Daum, S. K. Fridkin, R. J. Gorwitz, et al. Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children. Clin. Infect. Dis. 52:e18-e55, 2011.
39. Luciani, N., C. Wilhelm, and F. Gazeau. The role of cell-released microvesicles in the intercellular transfer of magnetic nanoparticles in the monocyte/macrophage system. Biomaterials 31:7061-7069, 2010.
40. Maier-Hauff, K., R. Rothe, R. Scholz, U. Gneveckow, P. Wust, B. Thiesen, et al. Intracranial thermotherapy using magnetic nanoparticles combined with external beam radiotherapy: results of a feasibility study on patients with glioblastoma multiforme. J. Neurooncol. 81:53-60, 2007.
41. Miller, L. S., R. M. O'Connell, M. A. Gutierrez, E. M. Pietras, A. Shahangian, C. E. Gross, et al. MyD88 mediates neutrophil recruitment initiated by IL-1R but not TLR2 activation in immunity against Staphylococcus aureus. Immunity 24:79-91, 2006.
42. Monroe, D. Looking for chinks in the armor of bacterial biofilms. PLoS Biol. 5:e307, 2007.
43. Pankhurst, Q. A., J. Connolly, S. K. Jones, and J. Dobson. Applications of magnetic nanoparticles in biomedicine. J. Phys. D Appl. Phys. 36:R167-R181, 2003.
44. Parsek, M. R., and P. K. Singh. Bacterial biofilms: an emerging link to disease pathogenesis. Annu. Rev. Microbiol. 57:677-701, 2003.
45. Pitt, W. G., M. O. McBride, J. K. Lunceford, R. J. Roper, and R. D. Sagers. Ultrasonic enhancement of antibiotic action on gram-negative bacteria. Antimicrob. Agents Chemother. 38:2577-2582, 1994.
46. Ray, P. C., S. A. Khan, A. K. Singh, D. Senapati, and Z. Fan. Nanomaterials for targeted detection and photothermal killing of bacteria. Chem. Soc. Rev. 41:3193-3209, 2012.
47. Rooijakkers, S. H., K. P. van Kessel, and J. A. van Strijp. Staphylococcal innate immune evasion. Trends Microbiol. 13:596-601, 2005.
48. Smith, J. A., and J. J. O'Connor. Nasal carriage of Staphylococcus aureus in diabetes mellitus. Lancet 2:776-777, 1966.
49. Spinowitz, B. S., M. H. Schwenk, P. M. Jacobs, W. K. Bolton, M. R. Kaplan, C. Charytan, et al. The safety and efficacy of ferumoxytol therapy in anemic chronic kidney disease patients. Kidney Int. 68:1801-1807, 2005.
50. Thomas, L., L. Dekker, M. Kallumadil, P. Southern, M. Wilson, S. Nair, et al. Carboxylic acid-stabilised iron oxide nanoparticles for use in magnetic hyperthermia. J. Mater. Chem. 19:6529-6535, 2009.
51. Tuazon, C. U., A. Perez, T. Kishaba, and J. N. Sheagren. Staphylococcus aureus among insulin-injecting diabetic patients. An increased carrier rate. JAMA. 231:1272, 1975.
52. van der Borden, A. J., P. G. Maathuis, E. Engels, G. Rakhorst, H. C. van der Mei, H. J. Busscher, et al. Prevention of pin tract infection in external stainless steel fixator frames using electric current in a goat model. Biomaterials 28:2122-2126, 2007.
53. Wintermute, E. H., and P. A. Silver. Dynamics in the mixed microbial concourse. Genes Dev. 24:2603-2614, 2010.
54. Zolfaghari, P. S., S. Packer, M. Singer, S. P. Nair, J. Bennett, C. Street, et al. In vivo killing of Staphylococcus aureus using a light-activated antimicrobial agent. BMC Microbiol. 9:27, 2009.