β-lactams resistance gene quantification in an antibiotic resistant Escherichia coli water suspension treated by advanced oxidation with UV/H2O2

Journal of Hazardous Materials

Volumn 323, Issue , 2017, Pages 426-433

  Ferro, Giovanna ^a   Guarino, Francesco ^a   Cicatelli, Angela ^a   Rizzo, Luigi ^a  

^a UNIVERSITY OF SALERNO   (Italy)

Author keywords

Antibiotic resistance; DNA; Water disinfection; lactams resistance gene

Indexed keywords

AMIDES; ANTIBIOTICS; CELL CULTURE; DISINFECTION; DNA; ESCHERICHIA COLI; GENES; WATER TREATMENT;

ADVANCED OXIDATION; ANTIBIOTIC RESISTANCE; ANTIBIOTIC RESISTANCE GENES; ANTIBIOTIC-RESISTANT ESCHERICHIA COLI; DISINFECTION PROCESS; POTENTIAL TRANSFER; RESISTANCE GENES; WATER DISINFECTIONS;

POLYMERASE CHAIN REACTION;

BACTERIAL DNA; BACTERIAL RNA; BETA LACTAMASE; HYDROGEN PEROXIDE; RNA 16S; WATER; ANTIINFECTIVE AGENT; BETA LACTAM;

ANTIBIOTIC RESISTANCE; ANTIBIOTICS; CELLS AND CELL COMPONENTS; COLIFORM BACTERIUM; DISINFECTION; DNA; GENE EXPRESSION; HYDROGEN PEROXIDE; OXIDATION; POLYMERASE CHAIN REACTION; ULTRAVIOLET RADIATION;

ANTIBIOTIC RESISTANCE; ARTICLE; BACTERIAL CELL; BACTERIAL GENE; BACTERIAL STRAIN; BACTERIAL SURVIVAL; BACTERIUM COLONY; CELL SURVIVAL; COLONY FORMING UNIT; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DISINFECTION; DNA EXTRACTION; ESCHERICHIA COLI; EXPERIMENTAL DESIGN; LIMIT OF DETECTION; NONHUMAN; OXIDATION; POLYMERASE CHAIN REACTION; QUALITATIVE ANALYSIS; SUSPENSION; ULTRAVIOLET RADIATION; BACTERIAL COUNT; BETA-LACTAM RESISTANCE; CHEMISTRY; DRUG EFFECT; GENETICS; OXIDATION REDUCTION REACTION; RADIATION RESPONSE;

ESCHERICHIA COLI;

ANTI-BACTERIAL AGENTS; BETA-LACTAM RESISTANCE; BETA-LACTAMS; COLONY COUNT, MICROBIAL; DISINFECTION; DNA, BACTERIAL; ESCHERICHIA COLI; HYDROGEN PEROXIDE; OXIDATION-REDUCTION; POLYMERASE CHAIN REACTION; ULTRAVIOLET RAYS;

EID: 84960152998     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2016.03.014     Document Type: Article

References (51)

1. [1] W.H.O. WHO, ANTIMICROBIAL RESISTANCE Global Report on Surveillance in 2014.
2. [2] Martinez, J.L., Environmental pollution by antibiotics and by antibiotic resistance determinants. Environ. Pollut. 157 (2009), 2893–2902.
3. [3] Rizzo, L., Manaia, C., Merlin, C., Schwartz, T., Dagot, C., Ploy, M.C., Michael, I., Fatta-Kassinos, D., Urban wastewater treatment plants as hotspots for antibiotic resistant bacteria and genes spread into the environment: a review. Sci. Total Environ. 447 (2013), 345–360.
4. [4] Vaz-Moreira, I., Nunes, O.C., Manaia, C.M., Bacterial diversity and antibiotic resistance in water habitats: searching the links with the human microbiome. FEMS Microbiol. Rev. 38 (2014), 761–778.
5. [5] Czekalski, N., Gascon Diez, E., Burgmann, H., Wastewater as a point source of antibiotic-resistance genes in the sediment of a freshwater lake. ISME J. 8 (2014), 1381–1390.
6. [6] Di Cesare, A., Eckert, E.M., Teruggi, A., Fontaneto, D., Bertoni, R., Callieri, C., Corno, G., Constitutive presence of antibiotic resistance genes within the bacterial community of a large subalpine lake. Mol. Ecol. 24 (2015), 3888–3900.
7. [7] Manaia, C.M., Macedo, G., Fatta-Kassinos, D., Nunes, O.C., Antibiotic resistance in urban aquatic environments: can it becontrolled?. Appl. Microbiol. Biotechnol. 100 (2015), 1543–1557.
8. [8] Varela, A.R., Manageiro, V., Ferreira, E., Guimarães, M.A., da Costa, P.M., Caniça, M., Manaia, C.M., Molecular evidence of the close relatedness of clinical, gull and wastewater isolates of quinolone-resistant Escherichia coli. J. Glob. Antimicrob. Resist. 3 (2015), 286–289.
9. [9] Narciso-da-Rocha, C., Varela, A.R., Schwartz, T., Nunes, O.C., Manaia, C.M., blaTEM and vanA as indicator genes of antibiotic resistance contamination in a hospital—urban wastewater treatment plant system. J. Glob. Antimicrob. Resist. 2 (2014), 309–315.
10. [10] Rodriguez-Mozaz, S., Chamorro, S., Marti, E., Huerta, B., Gros, M., Sànchez-Melsiò, A., Borrego, C.M., Barcelò, D., Balcàzar, J.L., Occurrence of antibiotics and antibiotic resistance genes in hospital and urban wastewaters and their impact on the receiving river. Water Res. 69 (2015), 234–242.
11. [11] Kümmerer, K., Antibiotics in the aquatic environment – a review – part II. Chemosphere 75 (2009), 435–441.
12. [12] Watkinson, A.J., Murby, E.J., Costanzo, S.D., Removal of antibiotics in conventional and advanced wastewater treatment: implications for environmental discharge and wastewater recycling. Water Res. 41 (2007), 4164–4176.
13. [13] Schwartz, T., Kohnen, W., Jansen, B., Obst, U., Detection of antibiotic-resistant bacteria and their resistance genes in wastewater, surface water, and drinking water bioelms. FEMS Microbiol. Ecol. 43 (2003), 325–335.
14. [14] Pruden, A., Pei, R., Storteboom, H., Carlson, K.H., Antibiotic resistance genes as emerging contaminants: studies in Northern Colorado. Environ. Sci. Technol. 40 (2006), 7445–7450.
15. [15] Xi, C., Zhang, Y., Marrs, C.F., Ye, W., Simon, C., Foxman, B., Nriagu, J., Prevalence of antibiotic resistance in drinking water treatment and distribution systems. Appl. Environ. Microbiol. 75 (2009), 5714–5718.
16. [16] Berendonk, T.U., Manaia, C.M., Merlin, C., Fatta-Kassinos, D., Cytryn, E., Walsh, F., Burgmann, H., Sorum, H., Norstrom, M., Pons, M.N., Kreuzinger, N., Huovinen, P., Stefani, S., Schwartz, T., Kisand, V., Baquero, F., Martinez, J.L., Tackling antibiotic resistance: the environmental framework. Nat. Rev. Microbiol. 13 (2015), 310–317.
17. [17] NEREUS COST Action in 2015.
18. [18] Auerbach, E.A., Seyfried, E.E., McMahon, K.D., Tetracycline resistance genes in activated sludge wastewater treatment plants. Water Res. 41 (2007), 1143–1151.
19. [19] Guo, M.T., Yuan, Q.B., Yang, J., Ultraviolet reduction of erythromycin and tetracycline resistant heterotrophic bacteria and their resistance genes in municipal wastewater. Chemosphere 93 (2013), 2864–2868.
20. [20] Huang, J.J., Hu, H.Y., Wu, Y.H., Wei, B., Lu, Y., Effect of chlorination and ultraviolet disinfection on tetA-mediated tetracycline resistance of Escherichia coli. Chemosphere 90 (2013), 2247–2253.
21. [21] De Luca, A., Dantas, R.F., Simões, A.S.M., Toscano, I.A.S., Lofrano, G., Cruz, A., Esplugas, S., Atrazine removal in municipal secondary effluents by fenton and photo-Fenton treatments. Chem. Eng. Technol. 36 (2013), 2155–2162.
22. [22] Malato, S., Fernández-Ibáñez, P., Maldonado, M.I., Blanco, J., Gernjak, W., Decontamination and disinfection of water by solar photocatalysis: recent overview and trends. Catal. Today 147 (2009), 1–59.
23. [23] Miralles-Cuevas, S., Oller, I., Ruiz Aguirre, A., Sánchez Pérez, J.A., Malato Rodríguez, S., Removal of pharmaceuticals at microg L-1 by combined nanofiltration and mild solar photo-Fenton. Chem. Eng. J. 239 (2014), 68–74.
24. [24] Rizzo, L., Bioassays as a tool for evaluating advanced oxidation processes in water and wastewater treatment. Water Res. 45 (2011), 4311–4340.
25. [25] Agulló-Barceló, M., Polo-López, M.I., Lucena, F., Jofre, J., Fernández-Ibáñez, P., Solar advanced oxidation processes as disinfection tertiary treatments for real wastewater: implications for water reclamation. Appl. Catal. B: Environ. 136–137 (2013), 341–350.
26. 2 and neutral photo-Fenton at pilot scale in a domestic wastewater treatment plant. Water Res. 47 (2013), 5836–5845.
27. 2 powders. Photochem. Photobiol. 88 (2012), 728–735.
28. [28] Karaolia, P., Michael, I., Garcia-Fernandez, I., Aguera, A., Malato, S., Fernandez-Ibanez, P., Fatta-Kassinos, D., Reduction of clarithromycin and sulfamethoxazole-resistant Enterococcus by pilot-scale solar-driven Fenton oxidation. Sci. Total Environ. 468–469 (2014), 19–27.
29. 2 photocatalysis: effect on a multi drug resistant Escherichia coli strain. Water Res. 53 (2014), 145–152.
30. 2 on antibiotic-resistant and antibiotic-sensitive bacteria. Chem. Technol. Biotechnol. 85 (2010), 1642–1653.
31. [31] Fiorentino, A., Ferro, G., Alferez Castro, M., Polo-López, M.I., Fernández-Ibañez, P., Rizzo, L., Inactivation and regrowth of multidrug resistant bacteria in urban wastewater after disinfection by solar-driven and chlorination processes. J. Photochem. Photobiol. B: Biol. 148 (2015), 43–50.
32. [32] McKinney, C.W., Pruden, A., Ultraviolet disinfection of antibiotic resistant bacteria and their antibiotic resistance genes in water and wastewater. Environ. Sci. Technol. 46 (2012), 13393–13400.
33. [33] Munir, M., Wong, K., Xagoraraki, I., Release of antibiotic resistant bacteria and genes in the effluent and biosolids of five wastewater utilities in Michigan. Water Res. 45 (2011), 681–693.
34. [34] Yuan, Q.B., Guo, M.T., Yang, J., Fate ofantibiotic resistant bacteria and genes during wastewater chlorination: implication for antibiotic resistance control. PLoS One 4 (2015), 1–11.
35. [35] Dunlop, P.S.M., Ciavola, M., Rizzo, L., McDowell, D.A., Byrne, J.A., Effect of photocatalysis on the transfer of antibiotic resistance genesin urban wastewater. Catal. Today 240 (2015), 55–60.
36. [36] Zhuang, Y., Geng, R.H.J., Zhang, Y., Zhang, Y., Ding, L., Xu, K., Inactivation of antibiotic resistance genes inmunicipal wastewater by chlorination, ultraviolet, and ozonation disinfection. Environ. Sci. Pollut. Res. 22 (2015), 7037–7044.
37. [37] Rizzo, L., Ferro, G., Manaia, C.M., Wastewater disinfection by solar heterogeneous photocatalysis: effect on tetracycline resistant/sensitive Enterococcus strains. Glob. NEST J. 16 (2014), 455–462.
38. [38] EUCAST, European Committee on Antimicrobial Susceptibility Testing in 2015.
39. [39] Bichai, F., Polo-Lopez, M.I., Fernandez Ibanez, P., Solar disinfection of wastewater to reduce contamination of lettuce crops by Escherichia coli in reclaimed water irrigation. Water Res. 46 (2012), 6040–6050.
40. [41] Bustin, S.A., Benes, V., Garson, J.A., Hellemans, J., Huggett, J., Kubista, M., Mueller, R., Nolan, T., Pfaffl, M.W., Shipley, G., Vandesompele, J., Wittwer, C.T., The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. Clin. Chem. 55 (2009), 611–622.
41. [42] Blattner, F.R., Plunkett, I.G., Bloch, C.A., Perna, N.T., Burland, V., Riley, M., Collado, -V.J., Glasner, J.D., Rode, C.K., Mayhew, G.F., Gregor, J., Wayne Davis, N., Kirkpatrick, H.A., Goeden, M.A., Rose, D.J., Mau, B., Shao, Y., The complete genome sequence of Escherichia coli K-12. Science 277 (1997), 1453–1462.
42. [43] Grenier, F., Matteau, D., Baby, V., Rodrigue, S., Complete genome sequence of Escherichia coli BW25113. Genome Announc. 2 (2014), e01038–01014.
43. [44] A. Biosystems Creating Standard Curves with Genomic DNA or Plasmid DNA Templates for Use in Quantitative PCR in 2003.
44. [45] Liu, Y., He, X., Fu, Y., Dionysiou, D.D., Degradation kinetics and mechanism of oxytetracycline by hydroxyl radical-based advanced oxidation processes. Chem. Eng. J. 284 (2016), 1317–1327.
45. 2 photocatalytic disinfection. Water Res. 38 (2004), 1069–1077.
46. [47] McGuigan, K.G., Conroy, R.M., Mosler, H.J., du Preez, M., Ubomba-Jaswa, E., Fernandez-Ibanez, P., Solar water disinfection (SODIS): a review from bench-top to roof-top. J. Hazard. Mater. 235–236 (2012), 29–46.
47. [48] Cengiz, M., Uslu, M.O., Balcioglu, I., Treatment of E. coli HB101 and the tetM gene by Fenton's reagent and ozone in cow manure. J. Environ. Manage. 91 (2010), 2590–2593.
48. [49] Öncü, N.B., Menceloğlu, Y.Z., Balcıoğlu, I.A., Comparison of the effectiveness of chlorine, ozone, and photocatalytic disinfection in reducing the risk of antibiotic resistance pollution. J. Adv. Oxid. Technol. 14 (2011), 196–203.
49. [50] Shi, P., Jia, S., Zhang, X.X., Zhang, T., Cheng, S., Li, A., Metagenomic insights into chlorination effects on microbial antibiotic resistance in drinking water. Water Res. 47 (2013), 111–120.
50. 2 on wild Fusarium solani spores in distilled and natural well water. Water Res. 43 (2009), 1841–1850.
51. [52] Polo-López, M.I., García-Fernández, I., Oller, I., Fernández-Ibáñez, P., Solar disinfection of fungal spores in water aided by low concentrations of hydrogen peroxide. Photochem. Photobiol. Sci. 10 (2011), 381–388.