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RESEARCH REFERENCES

  • Abicht, H.K., Gonskikh, Y., Gerber, S.D. and Solioz, M. (2013) Non-enzymic copper reduction by menaquinone enhances copper toxicity in Lactococcus lactis IL1403. Microbiology 159, 1190– 1197.
  • Adaikkalam, V. and Swarup, S. (2002) Molecular characterization of an operon, cueAR, encoding a putative P1-type ATPase and a MerR-type regulatory protein involved in copper homeostasis in Pseudomonas putida. Microbiology 148, 2857– 2867.
  • Amachawadi, R.G., Scott, H.M., Alvarado, C.A., Mainini, T.R., Vinasco, J., Drouillard, J.S. and Nagaraja, T.G. (2013) Occurrence of the transferable copper resistance gene tcrB among fecal enterococci of U.S. feedlot cattle fed copper-supplemented diets. Appl Environ Microbiol 79, 4369– 4375.
  • Amachawadi, R.G., Scott, H.M., Vinasco, J., Tokach, M.D., Dritz, S.S., Nelssen, J.L. and Nagaraja, T.G. (2015) Effects of in-feed copper, chlortetracycline, and tylosin on the prevalence of transferable copper resistance gene, tcrB, among fecal enterococci of weaned piglets. Foodborne Pathog Dis 12, 670– 678.
  • Antsotegi-Uskola, M., Markina-Iñarrairaegui, A. and Ugalde, U. (2017) Copper Resistance in Aspergillus nidulans Relies on the PI-Type ATPase CrpA, Regulated by the Transcription Factor AceA. Front Microbiol 8, 912.
  • Applerot, G., Lellouche, J., Lipovsky, A., Nitzan, Y., Lubart, R., Gedanken, A. and Banin, E. (2012) Understanding the antibacterial mechanism of CuO nanoparticles: revealing the route of induced oxidative stress. Small 8, 3326– 3337.
  • Azam, A., Ahmed, A.S., Oves, M., Khan, M.S. and Memic, A. (2012) Size-dependent antimicrobial properties of CuO nanoparticles against Gram-positive and -negative bacterial strains. Int J Nanomedicine 7, 3527– 3535.
  • Besaury, L., Bodilis, J., Delgas, F., Andrade, S., De la Iglesia, R., Ouddane, B. and Quillet, L. (2013) Abundance and diversity of copper resistance genes cusA and copA in microbial communities in relation to the impact of copper on Chilean marine sediments. Mar Pollut Bull 67, 16– 25.
  • Besold, A.N., Culbertson, E.M. and Culotta, V.C. (2016) The Yin and Yang of copper during infection. J Biol Inorg Chem 21, 137– 144.
  • Bleichert, P., Espírito Santo, C., Hanczaruk, M., Meyer, H. and Grass, G. (2014) Inactivation of bacterial and viral biothreat agents on metallic copper surfaces. Biometals 27, 1179– 1189.
  • Bogdanović, U., Vodnik, V., Mitrić, M., Dimitrijević, S., Škapin, S.D., Žunič, V., Budimir, M. and Stoiljković, M. (2015) Nanomaterial with high antimicrobial efficacy–copper/polyaniline nanocomposite. ACS Appl Mater Interfaces 7, 1955– 1966.
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  • Chaturvedi, K.S., Hung, C.S., Crowley, J.R., Stapleton, A.E. and Henderson, J.P. (2012) The siderophore yersiniabactin binds copper to protect pathogens during infection. Nat Chem Biol 8, 731– 736.
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  • Cui, Z., Ibrahim, M., Yang, C., Fang, Y., Annam, H., Li, B., Wang, Y., Xie, G.L. et al. (2014) Susceptibility of opportunistic Burkholderia glumae to copper surfaces following wet or dry surface contact. Molecules 19, 9975– 9985.
  • Dalecki, A.G., Crawford, C.L. and Wolschendorf, F. (2017) Copper and antibiotics: discovery, modes of action, and opportunities for medicinal applications. Adv Microb Physiol 70, 193– 260.
  • Dietl, A.M., Amich, J., Leal, S., Beckmann, N., Binder, U., Beilhack, A., Pearlman, E. and Haas, H. (2016) Histidine biosynthesis plays a crucial role in metal homeostasis and virulence of Aspergillus fumigatus. Virulence 7, 465– 476.
  • Ding, C., Festa, R.A., Chen, Y.L., Espart, A., Palacios, Ò., Espín, J., Capdevila, M., Atrian, S. et al. (2013) Cryptococcus neoformans copper detoxification machinery is critical for fungal virulence. Cell Host Microbe 13, 265– 276.
  • Djoko, K.Y., Ong, C.Y., Walker, M.J. and McEwan, A.G. (2015) The role of copper and zinc toxicity in innate immune defense against bacterial pathogens. J Biol Chem 290, 18954– 18961.
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  • Elguindi, J., Wagner, J. and Rensing, C. (2009) Genes involved in copper resistance influence survival of Pseudomonas aeruginosa on copper surfaces. J Appl Microbiol 106, 1448– 1455.
  • Emam, H.E., Ahmed, H.B. and Bechtold, T. (2017) In-situ deposition of Cu2O micro-needles for biologically active textiles and their release properties. Carbohydr Polym 165, 255– 265.
  • Espírito Santo, C., Taudte, N., Nies, D.H. and Grass, G. (2008) Contribution of copper ion resistance to survival of Escherichia coli on metallic copper surfaces. Appl Environ Microbiol 74, 977– 986.
  • Espírito Santo, C., Lam, E.W., Elowsky, C.G., Quaranta, D., Domaille, D.W., Chang, C.J. and Grass, G. (2011) Bacterial killing by dry metallic copper surfaces. Appl Environ Microbiol 77, 794– 802.
  • Espírito Santo, C., Quaranta, D. and Grass, G. (2012) Antimicrobial metallic copper surfaces kill Staphylococcus haemolyticus via membrane damage. MicrobiologyOpen 1, 46– 52.
  • Faúndez, G., Troncoso, M., Navarrete, P. and Figueroa, G. (2004) Antimicrobial activity of copper surfaces against suspensions of Salmonella enterica and Campylobacter jejuni. BMC Microbiol 4, 19.
  • Festa, R.A. and Thiele, D.J. (2011) Copper: an essential metal in biology. Curr Biol 21, R877– R883.
  • Festa, R.A., Jones, M.B., Butler-Wu, S., Sinsimer, D., Gerads, R., Bishai, W.R., Peterson, S.N. and Darwin, K.H. (2011) A novel copper-responsive regulon in Mycobacterium tuberculosis. Mol Microbiol 79, 133– 148.
  • Fujimori, Y., Sato, T., Hayata, T., Nagao, T., Nakayama, M., Nakayama, T., Sugamata, R. and Suzuki, K. (2012) Novel antiviral characteristics of nanosized copper(I) iodide particles showing inactivation activity against 2009 pandemic H1N1 influenza virus. Appl Environ Microbiol 78, 951– 955.
  • Georgatsou, E., Mavrogiannis, L.A., Fragiadakis, G.S. and Alexandraki, D. (1997) The yeast Fre1p/Fre2p cupric reductases facilitate copper uptake and are regulated by the copper-modulated Mac1p activator. J Biol Chem 272, 13786– 137892.
  • German, N., Lüthje, F., Hao, X., Rønn, R. and Rensing, C. (2016) Microbial virulence and interactions with metals. Prog Mol Biol Transl Sci 142, 27– 49.
  • Ghasemian, E., Naghoni, A., Tabaraie, B. and Tabaraie, T. (2012) In vitro susceptibility of filamentous fungi to copper nanoparticles assessed by rapid XTT colorimetry and agar dilution method. J Mycol Med 22, 322– 328.
  • Giannousi, K., Lafazanis, K., Arvanitidis, J., Pantazaki, A. and Dendrinou-Samara, C. (2014) Hydrothermal synthesis of copper based nanoparticles: antimicrobial screening and interaction with DNA. J Inorg Biochem 133, 24– 32.
  • Giner-Lamia, J., López-Maury, L., Reyes, J.C. and Florencio, F.J. (2012) The CopRS two-component system is responsible for resistance to copper in the cyanobacterium Synechocystis sp. PCC 6803. Plant Physiol 159, 1806– 1818.
  • Giner-Lamia, J., López-Maury, L. and Florencio, F.J. (2015) CopM is a novel copper-binding protein involved in copper resistance in Synechocystis sp. PCC 6803. MicrobiologyOpen 4, 167– 185.
  • Giner-Lamia, J., Pereira, S.B., Bovea-Marco, M., Futschik, M.E., Tamagnini, P. and Oliveira, P. (2016) Extracellular proteins: novel key components of metal resistance in cyanobacteria? Front Microbiol 7, 878.
  • Gold, B., Deng, H., Bryk, R., Vargas, D., Eliezer, D., Roberts, J., Jiang, X. and Nathan, C. (2008) Identification of a copper-binding metallothionein in pathogenic mycobacteria. Nat Chem Biol 4, 609– 616.
  • Goudarzi, M., Saviz, S., Ghoranneviss, M. and Salar Elahi, A. (2017) Medical equipment antiseptic processes using the atmospheric plasma sprayed copper coatings. J X-Ray Sci Technol 25, 479– 485.
  • Grass, G., Rensing, C. and Solioz, M. (2011) Metallic copper as an antimicrobial surface. Appl Environ Microbiol 77, 1541– 1547.
  • Grossoehme, N., Kehl-Fie, T.E., Ma, Z., Adams, K.W., Cowart, D.M., Scott, R.A., Skaar, E.P. and Giedroc, D.P. (2011) Control of copper resistance and inorganic sulfur metabolism by paralogous regulators in Staphylococcus aureus. J Biol Chem 286, 13522– 13531.
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  • Gutiérrez, M.F., Malaquias, P., Hass, V., Matos, T.P., Lourenço, L., Reis, A., Loguercio, A.D. and Farago, P.V. (2017) The role of copper nanoparticles in an etch-and-rinse adhesive on antimicrobial activity, mechanical properties and the durability of resin-dentine interfaces. J Dent 61, 12– 20.
  • Halbus, A.F., Horozov, T.S. and Paunov, V.N. (2017) Colloid particle formulations for antimicrobial applications. Adv Colloid Interface Sci 249, 134– 148.
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