• 1.

  Mijnendonckx, K., Leys, N., Mahillon, J., Silver, S. & Van Houdt, R. Antimicrobial silver: uses, toxicity and potential for resistance. BioMetals 26, 609–621 (2013).

  CAS  Article  Google Scholar

• 2.

  Molling, J. W., Seezink, J. W., Teunissen, B. E., Muijrers-Chen, I. & Borm, P. J. Comparative performance of a panel of commercially available antimicrobial nanocoatings in Europe. Nanotechnol. Sci. Appl. 7, 97–104 (2014).

  Article  Google Scholar

• 3.

  Silver nanoparticles market by application (electronics & electrical, healthcare, food & beverages, textiles) and segment forecasts to 2022. GrandView Research (2015); https://www.grandviewresearch.com/industry-analysis/silver-nanoparticles-market

• 4.

  Panacek, A. et al. Silver colloid nanoparticles: synthesis, characterization, and their antibacterial activity. J. Phys. Chem. B 110, 16248–16253 (2006).

  CAS  Article  Google Scholar

• 5.

  Franci, G. et al. Silver nanoparticles as potential antibacterial agents. Molecules 20, 8856–8874 (2015).

  CAS  Article  Google Scholar

• 6.

  Duran, N. et al. Silver nanoparticles: a new view on mechanistic aspects on antimicrobial activity. Nanomedicine 12, 789–799 (2016).

  CAS  Article  Google Scholar

• 7.

  Lara, H. H., Ayala-Nunez, N. V., Turrent, L. & Padilla, C. R. Bactericidal effect of silver nanoparticles against multidrug-resistant bacteria. World J. Microbiol. Biotechnol. 26, 615–621 (2010).

  CAS  Article  Google Scholar

• 8.

  Graves, J. L. et al. Rapid evolution of silver nanoparticle resistance in Escherichia coli. Front. Genet. 6, 42 (2015).

  Article  CAS  Google Scholar

• 9.

  Gunawan, C., Teoh, W. Y., Marquis, C. P. & Amal, R. Induced adaptation of Bacillus sp. to antimicrobial nanosilver. Small 9, 3554–3560 (2013).

  CAS  Article  Google Scholar

• 10.

  Panacek, A. et al. Bacterial resistance to silver nanoparticles and how to overcome it. Nat. Nano. 13, 65–71 (2018).

  CAS  Article  Google Scholar

• 11.

  Losasso, C. et al. Antibacterial activity of silver nanoparticles: sensitivity of different Salmonella serovars. Front. Microbiol. 5, 227 (2014).

  Article  Google Scholar

• 12.

  Valentin, E. et al. Heritable nanosilver resistance in priority pathogen: a unique genetic adaptation and comparison with ionic silver and antibiotics. Nanoscale 12, 2384–2392 (2020).

  CAS  Article  Google Scholar

• 13.

  Gunawan, C. et al. Widespread and indiscriminate nanosilver use: genuine potential for microbial resistance. ACS Nano 11, 3438–3445 (2017).

  CAS  Article  Google Scholar

• 14.

  Haefeli, C., Franklin, C. & Hardy, K. Plasmid-determined silver resistance in Pseudomonas stutzeri isolated from a silver mine. J. Bacteriol. 158, 389–392 (1984).

  CAS  Article  Google Scholar

• 15.

  Li, X. Z., Nikaido, H. & Williams, K. E. Silver-resistant mutants of Escherichia coli display active efflux of Ag⁺ and are deficient in porins. J. Bacteriol. 179, 6127–6132 (1997).

  CAS  Article  Google Scholar

• 16.

  Gupta, A., Matsui, K., Lo, J. F. & Silver, S. Molecular basis for resistance to silver cations in Salmonella. Nat. Med. 5, 183–188 (1999).

  CAS  Article  Google Scholar

• 17.

  Silver, S. Bacterial silver resistance: molecular biology and uses and misuses of silver compounds. FEMS Microbiol. Rev. 27, 341–353 (2003).

  CAS  Article  Google Scholar

• 18.

  Pelgrift, R. Y. & Friedman, A. J. Nanotechnology as a therapeutic tool to combat microbial resistance. Adv. Drug Deliv. Rev. 65, 1803–1815 (2013).

  CAS  Article  Google Scholar

• 19.

  Wang, L., Hu, C. & Shao, L. The antimicrobial activity of nanoparticles: present situation and prospects for the future. Int J. Nanomed. 12, 1227–1249 (2017).

  CAS  Article  Google Scholar

• 20.

  Johnston, K. A. et al. Impacts of broth chemistry on silver ion release, surface chemistry composition, and bacterial cytotoxicity of silver nanoparticles. ES: Nano 5, 304–312 (2018).

  CAS  Google Scholar

• 21.

  Johnston, K. A., Smith, A. M., Marbella, L. E. & Millstone, J. E. Impact of as-synthesized ligands and low-oxygen conditions on silver nanoparticle surface functionalized. Langmuir 32, 3820–3826 (2016).

  CAS  Article  Google Scholar

• 22.

  Bastus, N. G., Merkoci, F., Piella, J. & Puntes, V. Synthesis of highly monodisperse citrate-stabilized silver nanoparticles of up to 200 nm: kinetic control and catalytic properties. Chem. Mater. 26, 2836–2846 (2014).

  CAS  Article  Google Scholar

• 23.

  Ivanova, E. P., Bazaka, K. & Crawford, R. J. in New Functional Biomaterials for Medicine and Healthcare Ch. 3, 71–99 (Woodhead, 2014).

• 24.

  Olofsson, S. K. & Cars, O. Optimizing drug exposure to minimize selection of antibiotic resistance. Clin. Infect. Dis. 45, S129–S136 (2007).

  CAS  Article  Google Scholar

• 25.

  Gullberg, E. et al. Selection of resistant bacteria at very low antibiotic concentrations. PLoS Pathog. 7, e1002158 (2011).

  CAS  Article  Google Scholar

• 26.

  Adam, M., Murali, B., Glenn, N. O. & Potter, S. S. Epigenetic inheritance based evolution of antibiotic resistance in bacteria. BMC Evol. Biol. 8, 52 (2008).

  Article  CAS  Google Scholar

• 27.

  George, A. M. & Levy, S. B. Amplifiable resistance to tetracycline, chloramphenicol, and other antibiotics in Escherichia coli: involvement of a non-plasmid-determined efflux of tetracycline. J. Bacteriol. 155, 531–540 (1983).

  CAS  Article  Google Scholar

• 28.

  Zhao, Y. et al. Small molecule-capped gold nanoparticles as potent antibacterial agents that target Gram-negative bacteria. J. Am. Chem. Soc. 132, 12349–12356 (2010).

  CAS  Article  Google Scholar

• 29.

  Ji, F. et al. Tetrabromobisphenol A (TBBPA) exhibits specific antimicrobial activity against Gram-positive bacteria without detectable resistance. Chem. Commun. 53, 3512–3515 (2017).

  CAS  Article  Google Scholar

• 30.

  Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing: Twentieth Informational Supplement Vol. 30(1) (Approved Standard M100-S20, Clinical and Laboratory Standards Institute, 2010).

• 31.

  Silver, S. in Molecular Biology, Pathogenicity, and Ecology of Bacterial Plasmids (eds Levy, S. B. et al.) 179–189 (Plenum, 1981).

• 32.

  Flynn, K. M., Cooper, T. F., Moore, F. B. G. & Cooper, V. S. The environment affects epistatic interactions to alter the topology of an empirical fitness landscape. PLoS Genet. 9, e1003426 (2013).

  CAS  Article  Google Scholar

• 33.

  Hall, A. E. et al. Environment changes epistasis to alter trade-offs along alternative evolutionary paths. Evolution 73, 2094–2105 (2019).

  Article  Google Scholar

• 34.

  Stabryla, L. M., Johnston, K. A., Millstone, J. E. & Gilbertson, L. M. Emerging investigator series: it’s not all about the ion: support for particle-specific contributions to silver nanoparticle antimicrobial activity. ES: Nano 5, 2047–2068 (2018).

  CAS  Google Scholar

• 35.

  Sandoval-Motta, S. & Aldana, M. Adaptive resistance to antibiotics in bacteria: a systems biology perspective. WIREs Syst. Biol. Med 8, 253–267 (2016).

  Article  Google Scholar

• 36.

  Normark, B. H. & Normark, S. Evolution and spread of antibiotic resistance. J. Intern. Med. 252, 91–106 (2002).

  CAS  Article  Google Scholar

• 37.

  Lok, C.-N. et al. Proteomic identification of the cus system as a major determinant of constitutive Escherichia coli silver resistance of chromosomal origin. J. Proteome Res. 7, 2351–2356 (2008).

  Article  Google Scholar

• 38.

  Knetsch, M. L. & Koole, L. H. New strategies in the development of antimicrobial coatings: the example of increasing usage of silver and silver nanoparticles. Polymers 3, 340–366 (2011).

  CAS  Article  Google Scholar

• 39.

  Chopra, I. The increasing use of silver-based products as antimicrobial agents: a useful development or a cause for concern? J. Antimicrob. Chemother. 59, 587–590 (2007).

  CAS  Article  Google Scholar

• 40.

  Bridges, K., Kidson, A., Lowbury, E. J. L. & Wilkins, M. D. Gentamicin- and silver-resistant Pseudomonas in a burns unit. Brit. Med. J. 1, 446–449 (1979).

  CAS  Article  Google Scholar

• 41.

  Gudipaty, S. A. & McEvoy, M. M. The histidine kinase CusS senses silver ions through direct binding by its sensor domain. Chem. Biochem. 1844, 1656–1661 (2014).

  CAS  Google Scholar

• 42.

  Affandi, T. & McEvoy, M. M. Mechanism of metal ion-induced activation of a two-component sensor kinase. Biochem. J. 476, 115–135 (2019).

  CAS  Article  Google Scholar

• 43.

  Cooper, V. S. Experimental evolution as a high-throughput screen for genetic adaptations. mSphere 3, e00121–18 (2018).

  Article  Google Scholar

• 44.

  Tajkarimi, M. et al. Selection for ionic- confers silver nanoparticle resistance in Escherichia coli. JSM Nanotechnol. Nanomed. 5, 1047 (2017).

  Google Scholar

• 45.

  Randall, C. P., Gupta, A., Jackson, N., Busse, D. & O’Neill, A. J. Silver resistance in Gram-negative bacteria: a dissection of endogenous and exogenous mechanisms. J. Antimicrob. Chemother. 70, 1037–1046 (2015).

  CAS  Google Scholar

• 46.

  Koskella, B., Taylor, T. B., Bates, J. & Buckling, A. Using experimental evolution to explore natural patterns between bacterial motility and resistance to bacteriophages. ISME J. 5, 1809–1817 (2011).

  Article  Google Scholar

• 47.

  Samad, T. et al. Swimming bacteria promote dispersal of non-motile Staphylococcal species. ISME J. 11, 1933–1937 (2017).

  Article  Google Scholar

• 48.

  Gauger, E. J. et al. Role of motility and the flhDC operon in Escherichia coli MG1655 colonization of the mouse intestine. Infect. Immun. 75, 3315–3324 (2007).

  CAS  Article  Google Scholar

• 49.

  Barker, C. S., Prub, B. M. & Matsumura, P. Increased motility of Escherichia coli by insertion sequence element integration into the regulatory region of the flhD operon. J. Bacteriol. 186, 7529–7537 (2004).

  CAS  Article  Google Scholar

• 50.

  Sanchez-Torres, V., Hu, H. & Wood, T. K. GGDEF proteins YeaI, YedQ, and YfiN reduce early biofilm formation and swimming motility in Escherichia coli. Appl. Microbiol. Biotechnol. 90, 651–658 (2011).

  CAS  Article  Google Scholar

• 51.

  Butler, M. T., Wang, Q. & Harshey, R. M. Cell density and mobility protect swarming bacteria against antibiotics. Proc. Natl Acad. Sci. USA 107, 3776–3781 (2010).

  CAS  Article  Google Scholar

• 52.

  Lai, S., Tremblay, J. & Deziel, E. Swarming motility: a multicellular behaviour conferring antimicrobial resistance. Environ. Microbiol. 11, 126–136 (2009).

  CAS  Article  Google Scholar

• 53.

  Sun, E. et al. Broad-spectrum adaptive antibiotic resistance associated with Pseudomonas aeruginosa mucin-dependent surfing motility. Antimicrob. Agents Chemother. 62, e00848–18 (2018).

  CAS  Google Scholar

• 54.

  Zhang, H. et al. Stress resistance, motility and biofilm formation mediated by a 25kb plasmid pLMSZ08 in Listeria monocytogenes. Food Control 94, 345–352 (2018).

  CAS  Article  Google Scholar

• 55.

  Asadishad, B., Hidalgo, G. & Tufenkji, N. Pomegranate materials inhibit flagellin gene expression and flagellar-propelled motility of uropathogenic Escherichia coli strain CFT073. FEMS Microbiol. Lett. 334, 87–94 (2012).

  CAS  Article  Google Scholar

• 56.

  Paramelle, D. et al. A rapid method to estimate the concentration of citrate capped silver nanoparticles from UV-visible light spectra. Analyst 139, 4855–4861 (2014).

  CAS  Article  Google Scholar

• 57.

  Zhang, W., Crittenden, J., Li, K. & Chen, Y. Attachment efficiency of nanoparticle aggregation in aqueous dispersions: modeling and experimental validation. Environ. Sci. Technol. 46, 7054–7062 (2012).

  CAS  Article  Google Scholar

• 58.

  Li, X., Lenhart, J. J. & Walker, H. W. Dissolution-accompanied aggregation kinetics of silver nanoparticles. Langmuir 26, 16690–16698 (2010).

  CAS  Article  Google Scholar

• 59.

  Ma, R. et al. Size-controlled dissolution of organic-coated silver nanoparticles. Environ. Sci. Technol. 46, 752–759 (2012).

  CAS  Article  Google Scholar

• 60.

  Biggest Threats and Data (Centers for Disease Control and Prevention, 2020); https://www.cdc.gov/drugresistance/biggest-threats.html

• 61.

  Demirdjian, S. et al. Phosphatidylinositol-(3,4,5)-trisphosphate induces phagocytosis of nonmotile Pseudomonas aeruginosa. Infect. Immun. 86, 215–218 (2018).

  Article  Google Scholar

• 62.

  Deatherage, D. E. & Barrick, J. E. Identification of mutations in laboratory-evolved microbes from next-generation sequencing data using breseq. Methods Mol. Biol. 1151, 165–188 (2014).

  CAS  Article  Google Scholar

• 63.

  Narayanaswamy, V. P. et al. In vitro activity of novel glycopolymer against clinical isolates of multidrug-resistant Staphylococcus aureus. PLoS One 13, e0191522 (2018).

  Article  CAS  Google Scholar

• 64.

  Li, X. et al. Functional gold nanoparticles as potent antimicrobial agents against multi-drug-resistant bacteria. ACS Nano 8, 10682–10686 (2014).

  CAS  Article  Google Scholar

• 65.

  Landman, D., Salamera, J. & Quale, J. Irreproducible and uninterpretable polymyxin B MICs for Enterobacter cloacae and Enterobacter aerogenes. J. Clin. Microbiol. 51, 4106–4111 (2013).

  Article  CAS  Google Scholar

• 66.

  El-Halfawy, O. M. & Valvano, M. A. Antimicrobial heteroresistance: an emerging field in need of clarity. Clin. Microbiol. Rev. 28, 191–207 (2015).

  CAS  Article  Google Scholar

• 67.

  Baalousha, M. et al. The concentration-dependent behavior of nanoparticles. Environ. Chem. 13, 1–3 (2015).

  Article  CAS  Google Scholar

• 68.

  Lecture 11: Antimicrobial Susceptibility Testing—Broth Dilution. Online video clip. Technical Univ. Denmark (n.d); https://www.coursera.org/lecture/antimicrobial-resistance/lecture-11-antimicrobial-susceptibility-testing-broth-dilution-VeNw0

• 69.

  Clinical and Laboratory Standards Institute. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically 9th edn, Vol. 32(2) (Approved Standard M7-A9, Clinical and Laboratory Standards Institute, 2012).

• 70.

  Riley, M. et al. Escherichia coli K-12: a cooperatively developed annotation snapshot—2005. Nucleic Acids Res. 34, 1–9 (2006).

  CAS  Article  Google Scholar

Coinsmart. Beste Bitcoin-Börse in Europa
Source: https://www.nature.com/articles/s41565-021-00929-w