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Antibiotic Pollution in the Environment: From Microbial Ecology to Public Policy
Abstract
The ability to fight bacterial infections with antibiotics has been a longstanding cornerstone of modern medicine. However, wide-spread overuse and misuse of antibiotics has led to unintended consequences, which in turn require large-scale changes of policy for mitigation. In this review, we address two broad classes of corollaries of antibiotics overuse and misuse. Firstly, we discuss the spread of antibiotic resistance from hotspots of resistance evolution to the environment, with special concerns given to potential vectors of resistance transmission. Secondly, we outline the effects of antibiotic pollution independent of resistance evolution on natural microbial populations, as well as invertebrates and vertebrates. We close with an overview of current regional policies tasked with curbing the effects of antibiotics pollution and outline areas in which such policies are still under development.
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“However, the crisis we see today is due in part to the excessive use of antibiotics by humans and for animals (D'Costa et al., 2011; Kraemer et al., 2019).”
From Review of emerging contaminants in green stormwater infrastructure: antibiotic resistance genes, microplastics, tire wear particles, PFAS, and temperature (2024) · cites this paper as Kraemer et al., 2019
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A metagenome-wide association study of gut microbiota in type 2 diabetes
Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762
Global increase and geographic convergence in antibiotic consumption between 2000 and 2015
Klein, E. Y., Van Boeckel, T. P., Martinez, E. M., Pant, S., Gandra, S., Levin, S. A., Goossens, H., & Laxminarayan, R. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1717295115 · Cited by 3,232
The crisis in antibiotic resistance
Neu, H. C. (1992) · Science · doi:10.1126/science.257.5073.1064 · Cited by 2,834 · cited 1×
“This prognostic directed world leaders to call for an immediate reduction in antibiotic use [8,13,14].”
BackgroundAntibiotic resistance is ancient
D’Costa, V. M., King, C. E., Kalan, L., Morar, M., Sung, W. W. L., Schwarz, C., Froese, D., Zazula, G., Calmels, F., Debruyne, R., et al. (2011) · Nature · doi:10.1038/nature10388 · Cited by 2,720
Rizzo, L., Manaia, C., Merlin, C., Schwartz, T., Dagot, C., Ploy, M. C., Michael, I., & Fatta-Kassinos, D. (2013) · Science of The Total Environment · doi:10.1016/j.scitotenv.2013.01.032 · Cited by 2,493
Kong, H. H., Oh, J., Deming, C., Conlan, S., Grice, E. A., Beatson, M. A., Nomicos, E., Polley, E. C., Komarow, H. D., Program, N. C. S., et al. (2012) · Genome Research · doi:10.1101/gr.131029.111 · Cited by 1,808
Microbial Exposure During Early Life Has Persistent Effects on Natural Killer T Cell Function
Olszak, T., An, D., Zeissig, S., Vera, M. P., Richter, J., Franke, A., Glickman, J. N., Siebert, R., Baron, R. M., Kasper, D. L., et al. (2012) · Science · doi:10.1126/science.1219328 · Cited by 1,661
The shared antibiotic resistome of soil bacteria and human pathogens
Forsberg, K. J., Reyes, A., Wang, B., Selleck, E. M., Sommer, M. O. A., & Dantas, G. (2012) · Science · doi:10.1126/science.1220761 · Cited by 1,650
The gut microbiome in atherosclerotic cardiovascular disease
Jie, Z., Xia, H., Zhong, S.-L., Feng, Q., Li, S., Liang, S., Zhong, H., Liu, Z., Gao, Y., Zhao, H., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00900-1 · Cited by 1,638
Sampling the Antibiotic Resistome
D'Costa, V. M., McGrann, K. M., Hughes, D. W., & Wright, G. D. (2006) · Science · doi:10.1126/science.1120800 · Cited by 1,594
Jakobsson, H. E., Jernberg, C., Andersson, A. F., Sjölund-Karlsson, M., Jansson, J. K., & Engstrand, L. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009836 · Cited by 1,160
Gut microbiota induce IGF-1 and promote bone formation and growth
Yan, J., Herzog, J. W., Tsang, K., Brennan, C. A., Bower, M. A., Garrett, W. S., Sartor, B. R., Aliprantis, A. O., & Charles, J. F. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1607235113 · Cited by 750
Antibiotic resistance is prevalent in an isolated cave microbiome
Bhullar, K., Waglechner, N., Pawlowski, A., Koteva, K., Banks, E. D., Johnston, M. D., Barton, H. A., & Wright, G. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034953 · Cited by 736
Levy, S. B., FitzGerald, G. B., & Macone, A. B. (1976) · New England Journal of Medicine · doi:10.1056/nejm197609092951103 · Cited by 352
Research works printed but not linked: 197
- Levy, S.B., and Bergman, M.M. (2003). The Antibiotic Paradox: How the Misuse of Antibiotics Destroys Their Curative Powers. Clinical Infectious Diseases, Perseus Publishing. [2nd ed.]. · doi:10.1086/344466
- Barber, 1961, Hospital infection yeaterday and today, J. Clin. Pathol., 14, 2, 10.1136/jcp.14.1.2 · doi:10.1136/jcp.14.1.2
- Davies, 2006, Where have all the antibiotics gone?, Can. J. Infect. Dis. Med. Microbiol., 17, 287, 10.1155/2006/707296 · DOI · Paper page
- Abraham, 1940, An enzyme from bacteria able to destroy penicillin, Nature, 146, 837, 10.1038/146837a0 · DOI · Paper page
- Barber, 1948, Infection by penicillin-resistant staphylococci, Lancet, 2, 641, 10.1016/S0140-6736(48)92166-7 · DOI · Paper page
- Barber, 1947, Staphylococcal Infection due to Penicillin-resistant Strains, BMJ, 2, 863, 10.1136/bmj.2.4534.863 · DOI
- Smith, 2000, Population structure and evolutionary dynamics of pathogenic bacteria, BioEssays, 22, 1115, 10.1002/1521-1878(200012)22:12<1115::AID-BIES9>3.0.CO;2-R · DOI
- Bush, 2011, Tackling antibiotic resistance, Nat. Rev. Microbiol., 9, 894, 10.1038/nrmicro2693 · DOI · Paper page
- Davies, 2013, Annual Report of the Chief Medical Officer: Infection and the Rise of Antimicrobial esistance, Lancet, 381, 1606, 10.1016/S0140-6736(13)60604-2 · DOI · Paper page
- Livermore, 2011, Discovery research: The scientific challenge of finding new antibiotics, J. Antimicrob. Chemother., 66, 1941, 10.1093/jac/dkr262 · DOI · Paper page
- Cohen, 1992, Epidemiology of drug resistance: Implications for a post-antimicrobial era, Science, 257, 1050, 10.1126/science.257.5073.1050 · DOI · Paper page
- Brower, 2015, Global trends in antimicrobial use in food animals, Proc. Natl. Acad. Sci. USA, 112, 5649, 10.1073/pnas.1503141112 · DOI · Paper page
- Henriksson, 2018, Unpacking factors influencing antimicrobial use in global aquaculture and their implication for management: A review from a systems perspective, Sustain. Sci., 13, 1105, 10.1007/s11625-017-0511-8 · DOI · Paper page
- Petrovic, 2018, Towards the understanding of antibiotic occurrence and transport in groundwater: Findings from the Baix Fluvià alluvial aquifer (NE Catalonia, Spain), Sci. Total Environ., 612, 1387, 10.1016/j.scitotenv.2017.09.012 · DOI
- Andersson, 2012, Evolution of antibiotic resistance at non-lethal drug concentrations, Drug Resist. Updates, 15, 162, 10.1016/j.drup.2012.03.005 · DOI · Paper page
- 2009, Antibiotics in the aquatic environment—A review—Part II, Chemosphere, 75, 435, 10.1016/j.chemosphere.2008.12.006 · DOI · Paper page
- Finland, 1979, Emergence of antibiotic resistance in hospitals, 1935–1975, Rev. Infect. Dis., 1, 4, 10.1093/clinids/1.1.4 · DOI · Paper page
- Spellberg, 2008, Antibiotic resistance and antibiotic development, Lancet Infect. Dis., 8, 211, 10.1016/S1473-3099(08)70048-3 · DOI
- Shoemaker, 2001, Evidence for extensive resistance gene transfer among Bacteroides spp. and among Bacteroides and other genera in the human colon, Appl. Environ. Microbiol., 67, 561, 10.1128/AEM.67.2.561-568.2001 · DOI · Paper page
- Knapp, 2010, Evidence of increasing antibiotic resistance gene abundances in archived soils since 1940, Environ. Sci. Technol., 44, 580, 10.1021/es901221x · DOI · Paper page
- Walsh, 2000, Molecular mechanisms that confer antibacterial drug resistance, Nature, 406, 775, 10.1038/35021219 · DOI · Paper page
- Wright, 2011, Molecular mechanisms of antibiotic resistance, Chem. Commun., 47, 4055, 10.1039/c0cc05111j · DOI · Paper page
- Gullberg, E., Cao, S., Berg, O.G., Ilbäck, C., Sandegren, L., Hughes, D., and Andersson, D.I. (2011). Selection of resistant bacteria at very low antibiotic concentrations. PLoS Pathog., 7. · DOI · Paper page
- Kim, 2014, Alternating antibiotic treatments constrain evolutionary paths to multidrug resistance, Proc. Natl. Acad. Sci. USA, 111, 14494, 10.1073/pnas.1409800111 · DOI · Paper page
- Haas, 2003, Regulation of antibiotic production in root-colonizing Peudomonas spp. and relevance for biological control of plant disease, Ann. Rev. Phytopathol., 41, 117, 10.1146/annurev.phyto.41.052002.095656 · DOI · Paper page
- Long, 2001, Antagonistic Interactions among Marine Pelagic Bacteria, Appl. Environ. Microbiol., 67, 4975, 10.1128/AEM.67.11.4975-4983.2001 · DOI · Paper page
- Davies, 2006, Are antibiotics naturally antibiotics?, J. Ind. Microbiol. Biotechnol., 33, 496, 10.1007/s10295-006-0112-5 · DOI · Paper page
- Goh, 2002, Transcriptional modulation of bacterial gene expression by subinhibitory concentrations of antibiotics, Proc. Natl. Acad. Sci. USA, 99, 17025, 10.1073/pnas.252607699 · DOI · Paper page
- Skindersoe, 2008, Effects of antibiotics on quorum sensing in Pseudomonas aeruginosa, Antimicrob. Agents Chemother., 52, 3648, 10.1128/AAC.01230-07 · DOI · Paper page
- Aminov, 2009, The role of antibiotics and antibiotic resistance in nature, Environ. Microbiol., 11, 2970, 10.1111/j.1462-2920.2009.01972.x · DOI · Paper page
- Evans, 1988, Characterization of the Conjugation System Associated with the Staphylococcus aureus Plasmid pJE1, Microbiology, 134, 1, 10.1099/00221287-134-1-1 · DOI
- Zhang, 2013, Combined treatment with the antibiotics kanamycin and streptomycin promotes the conjugation of Escherichia coli, FEMS Microbiol. Lett., 348, 149, 10.1111/1574-6968.12282 · DOI
- Perron, G.G., Whyte, L., Turnbaugh, P.J., Goordial, J., Hanage, W.P., Dantas, G., and Desai, M.M. (2015). Functional characterization of bacteria isolated from ancient arctic soil exposes diverse resistance mechanisms to modern antibiotics. PLoS ONE, 10. · DOI
- Lee, S.H., and Lee, J.H. (2011). Molecular Characterization of TEM-Type beta-Lactamases Identified in Cold-Seep Sediments of Edison Seamount (South of Lihir Island, Papua New Guinea). Handbook of Molecular Microbial Ecology II: Metagenomics in Different Habitats, Wiley-Blackwell. · DOI
- 2008, Antibiotics and antibiotic resistance genes in natural environments, Science, 321, 365, 10.1126/science.1159483 · DOI · Paper page
- Norman, 2009, Conjugative plasmids: Vessels of the communal gene pool, Philos. Trans. R. Soc. B Boil. Sci., 364, 2275, 10.1098/rstb.2009.0037 · DOI · Paper page
- Palmer, 2011, Horizontal Gene Transfer and the Genomics of Enterococcal Antibiotic Resistance, Curr. Opin. Microbiol., 13, 632, 10.1016/j.mib.2010.08.004 · DOI · Paper page
- Springman, 2009, Selection, recombination, and virulence gene diversity among group B streptococcal genotypes, J. Bacteriol., 191, 5419, 10.1128/JB.00369-09 · DOI
- Fournier, P.E., Vallenet, D., Barbe, V., Audic, S., Ogata, H., Poirel, L., Richet, H., Robert, C., Mangenot, S., and Abergel, C. (2006). Comparative genomics of multidrug resistance in Acinetobacter baumannii. PLoS Genet., 2. · DOI · Paper page
- Barton, 2011, Bacteriophage-mediated transduction of antibiotic resistance in enterococci, Lett. Appl. Microbiol., 52, 559, 10.1111/j.1472-765X.2011.03043.x · DOI
- Colomer-Lluch, M., Jofre, J., and Muniesa, M. (2011). Antibiotic resistance genes in the bacteriophage DNA fraction of environmental samples. PLoS ONE, 6. · DOI · Paper page
- Xu, 2011, Resistance class 1 integron in clinical methicillin-resistant Staphylococcus aureus strains in southern China, 2001–2006, Clin. Microbiol. Infect., 17, 714, 10.1111/j.1469-0691.2010.03379.x · doi:10.1111/j.1469-0691.2010.03379.x
- Machado, 2008, Antibiotic resistance integrons and extended-spectrum β-lactamases among Enterobacteriaceae isolates recovered from chickens and swine in Portugal, J. Antimicrob. Chemother., 62, 296, 10.1093/jac/dkn179 · doi:10.1093/jac/dkn179
- Mazel, 2002, The role of integrons in antibiotic resistance gene capture, Int. J. Med. Microbiol., 292, 115, 10.1078/1438-4221-00197 · DOI · Paper page
- Gillings, 2015, Using the class 1 integron-integrase gene as a proxy for anthropogenic pollution, ISME J., 9, 1269, 10.1038/ismej.2014.226 · DOI · Paper page
- Box, 2002, Evidence of Extensive Interspecies Transfer of Integron-Mediated Antimicrobial Resistance Genes among Multidrug-Resistant Enterobacteriaceae in a Clinical Setting, J. Infect. Dis., 186, 49, 10.1086/341078 · DOI
- Summers, 1993, Mercury released from dental ‘silver’ fillings provokes an increase in mercury- and antibiotic-resistant bacteria in oral and intestinal floras of primates, Antimicrob. Agents Chemother., 37, 825, 10.1128/AAC.37.4.825 · DOI
- Hayashi, 2000, The DsbA-DsbB disulfide bond formation system of Burkholderia cepacia is involved in the production of protease and alkaline phosphatase, motility, metal resistance, and multi-drug resistance, Microbiol. Immunol., 44, 41, 10.1111/j.1348-0421.2000.tb01244.x · DOI
- Wright, 2006, Co-selection of antibiotic and metal resistance, Trends Microbiol., 14, 176, 10.1016/j.tim.2006.02.006 · DOI · Paper page
- Chen, 2013, Differentiating anthropogenic impacts on ARGs in the Pearl River Estuary by using suitable gene indicators, Water Res., 47, 2811, 10.1016/j.watres.2013.02.042 · DOI · Paper page
- Ju, 2019, Wastewater treatment plant resistomes are shaped by bacterial composition, genetic exchange, and upregulated expression in the effluent microbiomes, ISME J., 13, 346, 10.1038/s41396-018-0277-8 · DOI · Paper page
- Graham, 2016, Appearance of β-lactam Resistance Genes in Agricultural Soils and Clinical Isolates over the 20 th Century, Sci. Rep., 6, 21550, 10.1038/srep21550 · DOI
- Pruden, 2012, Correlation between upstream human activities and riverine antibiotic resistance genes, Environ. Sci. Technol., 46, 11541, 10.1021/es302657r · DOI · Paper page
- Baquero, 2008, Antibiotics and antibiotic resistance in water environments, Curr. Opin. Biotechnol., 19, 260, 10.1016/j.copbio.2008.05.006 · DOI · Paper page
- Berendonk, 2015, Tackling antibiotic resistance: The environmental framework, Nat. Rev. Microbiol., 13, 310, 10.1038/nrmicro3439 · DOI · Paper page
- Pitout, 2005, Emergence of Enterobacteriaceae producing extended-spectrum β-lactamases (ESBLs) in the community, J. Antimicrob. Chemother., 56, 52, 10.1093/jac/dki166 · DOI · Paper page
- Breathnach, 2012, Multidrug-resistant Pseudomonas aeruginosa outbreaks in two hospitals: Association with contaminated hospital waste-water systems, J. Hosp. Infect., 82, 19, 10.1016/j.jhin.2012.06.007 · doi:10.1016/j.jhin.2012.06.007
- Wang, 2003, Healthcare-associated outbreak due to pan-drug resistant Acinetobacter baumannii in a surgical intensive care unit, J. Hosp. Infect., 53, 97, 10.1053/jhin.2002.1348 · DOI
- Mathers, 2017, The Hospital Water Environment as a Reservoir for Carbapenem-Resistant Organisms Causing Hospital-Acquired Infections—A Systematic Review of the Literature, Clin. Infect. Dis., 64, 1435, 10.1093/cid/cix132 · DOI · Paper page
- Folkesson, 2012, Adaptation of Pseudomonas aeruginosa to the cystic fibrosis airway: An evolutionary perspective, Nat. Rev. Microbiol., 10, 841, 10.1038/nrmicro2907 · DOI · Paper page
- López-Causapé, C., Rojo-Molinero, E., Mulet, X., Cabot, G., Moyà, B., Figuerola, J., Togores, B., Pérez, J.L., and Oliver, A. (2013). Clonal Dissemination, Emergence of Mutator Lineages and Antibiotic Resistance Evolution in Pseudomonas aeruginosa Cystic Fibrosis Chronic Lung Infection. PLoS ONE, 8. · DOI
- Hocquet, 2016, What happens in hospitals does not stay in hospitals: Antibiotic-resistant bacteria in hospital wastewater systems, J. Hosp. Infect., 93, 395, 10.1016/j.jhin.2016.01.010 · DOI · Paper page
- Reinthaler, 2003, Antibiotic resistance of E. Coli in sewage and sludge, Water Res., 37, 1685, 10.1016/S0043-1354(02)00569-9 · DOI · Paper page
- Szczepanowski, 2009, Detection of 140 clinically relevant antibiotic-resistance genes in the plasmid metagenome of wastewater treatment plant bacteria showing reduced susceptibility to selected antibiotics, Microbiology, 155, 2306, 10.1099/mic.0.028233-0 · DOI · Paper page
- Frigon, 2018, Water and sanitation: An essential battlefront in the war on antimicrobial resistance, FEMS Microbiol. Ecol., 94, fiy101
- Yang, 2014, Fate of antibiotic resistance genes in sewage treatment plant revealed by metagenomic approach, Water Res., 62, 97, 10.1016/j.watres.2014.05.019 · DOI · Paper page
- Chen, 2013, Occurrence and removal of antibiotic resistance genes in municipal wastewater and rural domestic sewage treatment systems in eastern China, Environ. Int., 55, 9, 10.1016/j.envint.2013.01.019 · DOI · Paper page
- Munir, 2011, Release of antibiotic resistant bacteria and genes in the effluent and biosolids of five wastewater utilities in Michigan, Water Res., 45, 681, 10.1016/j.watres.2010.08.033 · DOI · Paper page
- Eamens, 2008, Salmonella uptake in sheep exposed to pastuRes. after biosolids application to agricultural land, Soil Res., 46, 302, 10.1071/SR07152 · DOI
- Diehl, 2010, Effect of temperature on the fate of genes encoding tetracycline resistance and the integrase of class 1 integrons within anaerobic and aerobic digesters treating municipal wastewater solids, Environ. Sci. Technol., 44, 9128, 10.1021/es102765a · DOI · Paper page
- Mackie, 2009, Fate and Transport of Antibiotic Residues and Antibiotic Resistance Genes following Land Application of Manure Waste, J. Environ. Q., 38, 1086, 10.2134/jeq2008.0128 · DOI · Paper page
- Ventola, 2015, The antibiotic resistance crisis: Part 1: Causes and threats, Pharm. Ther. J., 40, 277
- Woolhouse, 2015, Antimicrobial resistance in humans, livestock and the wider environment, Philos. Trans. R. Soc. B Boil. Sci., 370, 20140083, 10.1098/rstb.2014.0083 · DOI · Paper page
- Pruden, 2006, Antibiotic resistance genes as emerging contaminants: Studies in northern Colorado, Environ. Sci. Technol., 40, 7445, 10.1021/es060413l · DOI · Paper page
- Peak, 2007, Abundance of six tetracycline resistance genes in wastewater lagoons at cattle feedlots with different antibiotic use strategies, Environ. Microbiol., 9, 143, 10.1111/j.1462-2920.2006.01123.x · DOI · Paper page
- Cabello, 2016, Aquaculture as yet another environmental gateway to the development and globalisation of antimicrobial resistance, Lancet Infect. Dis., 16, 127, 10.1016/S1473-3099(16)00100-6 · DOI · Paper page
- Shah, 2014, Antimicrobial resistance and antimicrobial resistance genes in marine bacteria from salmon aquaculture and non-aquaculture sites, Environ. Microbiol., 16, 1310, 10.1111/1462-2920.12421 · DOI · Paper page
- Buschmann, A.H., Tomova, A., López, A., Maldonado, M.A., Henríquez, L.A., Ivanova, L., Moy, F., Godfrey, H.P., and Cabello, F.C. (2012). Salmon aquaculture and antimicrobial resistance in the marine environment. PLoS ONE, 7. · DOI
- Watts, J.E.M., Schreier, H.J., Lanska, L., and Hale, M.S. (2017). The rising tide of antimicrobial resistance in aquaculture: Sources, sinks and solutions. Mar. Drugs, 15. · DOI · Paper page
- Larsson, 2014, Pollution from drug manufacturing: Review and perspectives, Philos. Trans. R. Soc. B Boil. Sci., 369, 20130571, 10.1098/rstb.2013.0571 · DOI · Paper page
- Larsson, 2007, Effluent from drug manufactuRes. contains extremely high levels of pharmaceuticals, J. Hazard. Mater., 148, 751, 10.1016/j.jhazmat.2007.07.008 · DOI · Paper page
- Li, 2009, Antibiotic-resistance profile in environmental bacteria isolated from penicillin production wastewater treatment plant and the receiving river, Environ. Microbiol., 11, 1506, 10.1111/j.1462-2920.2009.01878.x · DOI · Paper page
- Johnning, 2013, Acquired genetic mechanisms of a multiresistant bacterium isolated from a treatment plant receiving wastewater from antibiotic production, Appl. Environ. Microbiol., 79, 7256, 10.1128/AEM.02141-13 · DOI
- Storteboom, 2010, Identification of antibiotic-resistance-gene molecular signatuRes. suitable as tracers of pristine River, urban, and agricultural sources, Environ. Sci. Technol., 44, 1947, 10.1021/es902893f · DOI
- Graham, 2011, Antibiotic resistance gene abundances associated with waste discharges to the AlmendaRes. river near Havana, Cuba, Environ. Sci. Technol., 45, 418, 10.1021/es102473z · DOI · Paper page
- Pei, 2006, Effect of River Landscape on the sediment concentrations of antibiotics and corresponding antibiotic resistance genes (ARG), Water Res., 40, 2427, 10.1016/j.watres.2006.04.017 · DOI · Paper page
- Kristiansson, E., Fick, J., Janzon, A., Grabic, R., Rutgersson, C., Weijdegård, B., Söderström, H., and Joakim Larsson, D.G. (2011). Pyrosequencing of antibiotic-contaminated river sediments reveals high levels of resistance and gene transfer elements. PLoS ONE, 6. · DOI · Paper page
- Li, 2018, Global Survey of Antibiotic Resistance Genes in Air, Environ. Sci. Technol., 52, 10975, 10.1021/acs.est.8b02204 · DOI · Paper page
- Hu, 2018, Metagenomic profiling of ARGs in airborne particulate matters during a severe smog event, Sci. Total Environ., 615, 1332, 10.1016/j.scitotenv.2017.09.222 · DOI
- Dueker, M.E., O’Mullan, G.D., Martínez, J.M., Juhl, A.R., and Weathers, K.C. (2017). Onshore wind speed modulates microbial aerosols along an urban waterfront. Atmosphere, 8. · DOI
- Pirnay, J.P., Bilocq, F., Pot, B., Cornelis, P., Zizi, M., Van Eldere, J., Deschaght, P., Vaneechoutte, M., Jennes, S., and Pitt, T. (2009). Pseudomonas aeruginosa population structure revisited. PLoS ONE, 4. · DOI · Paper page
- Hwang, 2005, Phylogenetic characterization of virulence and resistance phenotypes of Pseudomonas syringae, Appl. Environ. Microbiol., 71, 5182, 10.1128/AEM.71.9.5182-5191.2005 · DOI · Paper page
- Christner, 2008, Ubiquity of biological ice nucleators in snowfall, Science, 319, 1214, 10.1126/science.1149757 · DOI · Paper page
- Li, 2016, Bioaerosol emissions and detection of airborne antibiotic resistance genes from a wastewater treatment plant, Atmos. Environ., 124, 404, 10.1016/j.atmosenv.2015.06.030 · DOI · Paper page
- Gao, 2017, Size-related bacterial diversity and tetracycline resistance gene abundance in the air of concentrated poultry feeding operations, Environ. Pollut., 220, 1342, 10.1016/j.envpol.2016.10.101 · DOI
- McEachran, 2015, Antibiotics, bacteria, and antibiotic resistance genes: Aerial transport from cattle feed yards via particulate matter, Environ. Health Perspect., 123, 337, 10.1289/ehp.1408555 · DOI · Paper page
- Gilbert, 2010, Airborne bacteria and antibiotic resistance genes in hospital rooms, Aerobiologia, 26, 185, 10.1007/s10453-010-9155-1 · DOI
- Angelin, 2015, The human gut microbiome as a transporter of antibiotic resistance genes between continents, Antimicrob. Agents Chemother., 59, 6551, 10.1128/AAC.00933-15 · DOI
- Langelier, 2018, Microbiome and Antimicrobial Resistance Gene Dynamics in International Travelers, Emerg. Infect. Dis., 2018, 506394
- Hanselman, 2006, Methicillin-resistant Staphylococcus aureus colonization in veterinary personnel, Emerg. Infect. Dis., 12, 1933, 10.3201/eid1212.060231 · DOI
- Price, 2007, Elevated risk of carrying gentamicin-resistant Escherichia coli among U.S. poultry workers, Environ. Health Perspect., 115, 1738, 10.1289/ehp.10191 · DOI
- Levy, 1978, Emergence of antibiotic-resistant bacteria in the intestinal flora of farm inhabitants, J. Infect. Dis., 137, 688, 10.1093/infdis/137.5.688 · DOI
- Chang, 2015, Antibiotics in agriculture and the risk to human health: How worried should we be?, Evol. Appl., 8, 240, 10.1111/eva.12185 · DOI · Paper page
- Lis, 2009, Methicillin resistance of airborne coagulase-negative staphylococci in homes of persons having contact with a hospital environment, Am, J. Infect. Control, 37, 177, 10.1016/j.ajic.2008.09.013 · doi:10.1016/j.ajic.2008.09.013
- Baran, 2002, Stool Colonization With Vancomycin-Resistant Enterococci in Healthcare Workers and Their Households, Infect. Control Hosp. Epidemiol., 23, 23, 10.1086/501963 · DOI
- Eveillard, 2004, Carriage of Methicillin-Resistant Staphylococcus aureus Among Hospital Employees: Prevalence, Duration, and Transmission to Households, Infect. Control Hosp. Epidemiol., 25, 114, 10.1086/502360 · DOI · Paper page
- Zurek, 2014, Insects represent a link between food animal farms and the urban environment for antibiotic resistance traits, Appl. Environ. Microbiol., 80, 3562, 10.1128/AEM.00600-14 · DOI · Paper page
- Doud, 2014, Role of House Flies in the Ecology of Enterococcus faecalis from Wastewater Treatment Facilities, Microb. Ecol., 67, 380, 10.1007/s00248-013-0337-6 · DOI
- Donkor, 2013, Microbial Carriage of Cockroaches at a Tertiary Care Hospital in Ghana, Environ. Health Insights, 7, 59
- Tilahun, 2012, High load of multi-drug resistant nosocomial neonatal pathogens carried by cockroaches in a neonatal intensive care unit at Tikur Anbessa specialized hospital, AdDis. Ababa, Ethiopia, Antimicrob. Resist. Infect. Control, 1, 12, 10.1186/2047-2994-1-12 · doi:10.1186/2047-2994-1-12
- Joyner, C., Mills, M.K., and Nayduch, D. (2013). Pseudomonas aeruginosa in Musca domestica L.: Temporospatial examination of bacteria population dynamics and house fly antimicrobial responses. PLoS ONE, 8. · doi:10.1371/journal.pone.0079224
- Petridis, 2006, Horizontal transfer of Shiga toxin and antibiotic resistance genes among Escherichia coli strains in house fly (Diptera: Muscidae) gut, J. Med. Entomol., 43, 288, 10.1093/jmedent/43.2.288 · doi:10.1093/jmedent/43.2.288
- Vittecoq, 2016, Antimicrobial resistance in wildlife, J. Appl. Ecol., 53, 519, 10.1111/1365-2664.12596 · DOI · Paper page
- Allen, 2011, Antimicrobial resistance in generic Escherichia coli isolates from wild small mammals living in swine farm, residential, landfill, and natural environments in Southern Ontario, Canada, Appl. Environ. Microbiol., 77, 882, 10.1128/AEM.01111-10 · doi:10.1128/aem.01111-10
- Kozak, 2009, Antimicrobial resistance in Escherichia coli isolates from Swine and wild small mammals in the proximity of swine farms and in natural environments in Ontario, Canada, Appl. Environ. Microbiol., 75, 559, 10.1128/AEM.01821-08 · DOI · Paper page
- Marcelino, 2018, High levels of antibiotic resistance gene expression among birds living in a wastewater treatment plant, BioRxiv, 2018, 462366
- Radhouani, 2011, Molecular characterization of antibiotic resistance in enterococci recovered from seagulls (Larus cachinnans) representing an environmental health problem, J. Environ. Monit., 13, 2227, 10.1039/c0em00682c · DOI
- Poeta, 2008, Seagulls of the Berlengas natural reserve of Portugal as carriers of fecal Escherichia coli harboring CTX-M and TEM extended-spectrum beta-lactamases, Appl. Environ. Microbiol., 74, 7439, 10.1128/AEM.00949-08 · DOI
- Andrews, 2004, Survival of enterococci and Tn 916 -like conjugative transposons in soil, Can. J. Microbiol., 50, 957, 10.1139/w04-090 · doi:10.1139/w04-090
- Jamieson, 2002, Movement and persistence of fecal bacteria in agricultural soils and subsurface drainage water: A review, Can. Biosyst. Eng., 44, 1
- Avery, 2008, Survival of Escherichia coli O157:H7 in waters from lakes, rivers, puddles and animal-drinking troughs, Sci. Total Environ., 389, 378, 10.1016/j.scitotenv.2007.08.049 · doi:10.1016/j.scitotenv.2007.08.049
- Xi, 2009, Prevalence of antibiotic resistance in drinking water treatment and distribution systems, Appl. Environ. Microbiol., 75, 5714, 10.1128/AEM.00382-09 · DOI · Paper page
- Andersson, 1999, The biological cost of antibiotic resistance, Curr. Opin. Microbiol., 2, 489, 10.1016/S1369-5274(99)00005-3 · DOI · Paper page
- Andersson, 2010, Antibiotic resistance and its cost: Is it possible to reverse resistance?, Nat. Rev. Microbiol., 8, 260, 10.1038/nrmicro2319 · DOI · Paper page
- Schmitt, 2006, Tetracyclines and tetracycline resistance in agricultural soils: Microcosm and field studies, Microb. Ecol., 51, 267, 10.1007/s00248-006-9035-y · DOI · Paper page
- Munir, 2011, Levels of Antibiotic Resistance Genes in Manure, Biosolids, and Fertilized Soil, J. Environ. Q., 40, 248, 10.2134/jeq2010.0209 · DOI · Paper page
- Nielsen, 2000, Natural transformation of Acinetobacter sp. strain BD413 with cell lysates of Acinetobacter sp., Pseudomonas fluorescens, and Burkholderia cepacia in soil microcosms, Appl. Environ. Microbiol., 66, 206, 10.1128/AEM.66.1.206-212.2000 · doi:10.1128/aem.66.1.206-212.2000
- Smalla, 1997, Manure enhances plasmid mobilization and survival of Pseudomonas putida introduced into field soil, Appl. Environ. Microbiol., 63, 1980, 10.1128/aem.63.5.1980-1986.1997 · DOI
- Martin, 2003, Organization and Expression of Genes Involved in the Biosynthesis of Antibiotics and other Secondary Metabolites, Ann. Rev. Microbiol., 43, 173, 10.1146/annurev.mi.43.100189.001133 · DOI · Paper page
- Barlow, 2003, Experimental prediction of the natural evolution of antibiotic resistance, Genetics, 163, 1237, 10.1093/genetics/163.4.1237 · DOI
- Davies, 2010, Origins and evolution of antibiotic resistance, Microbiologia, 74, 417
- Yim, 2007, Antibiotics as signalling molecules, Philos. Trans. R. Soc. B Boil. Sci., 362, 1195, 10.1098/rstb.2007.2044 · DOI · Paper page
- Hall, 2004, Evolution of the serine β-lactamases: Past, present and future, Drug Resist. Updates, 7, 111, 10.1016/j.drup.2004.02.003 · DOI · Paper page
- Aminov, 2007, Evolution and ecology of antibiotic resistance genes, FEMS Microbiol. Lett., 271, 147, 10.1111/j.1574-6968.2007.00757.x · DOI · Paper page
- 2017, Effect of antibiotics on bacterial populations: A multi-hierarchical selection process, F1000Research, 6, 51, 10.12688/f1000research.9685.1 · DOI
- Casadesus, 2013, Contribution of phenotypic heterogeneity to adaptive antibiotic resistance, Proc. Natl. Acad. Sci. USA, 111, 355
- Dunlop, 2018, Heterogeneity in efflux pump expression predisposes antibiotic-resistant cells to mutation, Science, 362, 686, 10.1126/science.aar7981 · DOI
- Lee, 2018, Intermediate Levels of Antibiotics May Increase Diversity of Colony Size Phenotype in Bacteria, Comput. Struct. Biotechnol. J., 16, 307, 10.1016/j.csbj.2018.08.004 · DOI
- Saxer, G., Doebeli, M., and Travisano, M. (2010). The repeatability of adaptive radiation during long-term experimental evolution of Escherichia coli in a multiple nutrient environment. PLoS ONE, 5. · DOI
- Justice, 2008, Morphological plasticity as a bacterial survival strategy, Nat. Rev. Microbiol., 6, 162, 10.1038/nrmicro1820 · DOI · Paper page
- Foster, 2007, Stress-induced mutagenesis in bacteria, Crit. Rev. Biochem. Mol. Biol., 42, 373, 10.1080/10409230701648494 · DOI · Paper page
- Andersson, 2014, Microbiological effects of sublethal levels of antibiotics, Nat. Rev. Microbiol., 12, 465, 10.1038/nrmicro3270 · DOI · Paper page
- Maiques, 2006, β-lactam antibiotics induce the SOS response and horizontal transfer of virulence factors in Staphylococcus aureus, J. Bacteriol., 188, 2726, 10.1128/JB.188.7.2726-2729.2006 · DOI · Paper page
- Slager, 2014, Antibiotic-induced replication stress triggers bacterial competence by increasing gene dosage near the origin, Cell, 157, 395, 10.1016/j.cell.2014.01.068 · DOI · Paper page
- Davies, 2006, The world of subinhibitory antibiotic concentrations, Curr. Opin. Microbiol., 9, 445, 10.1016/j.mib.2006.08.006 · DOI · Paper page
- Blount, 2006, Riboswitches as antibacterial drug targets, Nat. Biotechnol., 24, 1558, 10.1038/nbt1268 · DOI · Paper page
- Mion, 2018, Interference in bacterial quorum sensing: A biopharmaceutical perspective, Front. Pharmacol., 9, 203, 10.3389/fphar.2018.00203 · DOI · Paper page
- Lozupone, 2007, Global patterns in bacterial diversity, Proc. Natl. Acad. Sci. USA, 104, 11436, 10.1073/pnas.0611525104 · DOI · Paper page
- Caporaso, 2011, Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample, Proc. Natl. Acad. Sci. USA, 108, 4516, 10.1073/pnas.1000080107 · DOI · Paper page
- Torsvik, 2002, Microbial Diversity and Function in Soil: From Genes to Ecosystems, Curr. Opin. Microbiol., 5, 240, 10.1016/S1369-5274(02)00324-7 · DOI · Paper page
- Gibbons, 2015, Microbial diversity-exploration of natural ecosystems and microbiomes, Curr. Opin. Genet. Dev., 35, 66, 10.1016/j.gde.2015.10.003 · DOI
- Goss, 2019, One Health—Cycling of diverse microbial communities as a connecting force for soil, plant, animal, human and ecosystem health, Sci. Total Environ., 664, 927, 10.1016/j.scitotenv.2019.02.091 · DOI
- Delcour, 2009, Outer membrane permeability and antibiotic resistance, Biochim. Biophys. Acta Proteins Proteom., 1794, 808, 10.1016/j.bbapap.2008.11.005 · DOI · Paper page
- Ding, 2010, Effect of antibiotics in the environment on microbial populations, Appl. Microbiol. Biotechnol., 87, 925, 10.1007/s00253-010-2649-5 · DOI · Paper page
- Eckert, 2019, Antibiotic disturbance affects aquatic microbial community composition and food web interactions but not community resilience, Mol. Ecol., 28, 1170, 10.1111/mec.15033 · DOI
- Grenni, 2018, Ecological effects of antibiotics on natural ecosystems: A review, Microchem. J., 136, 25, 10.1016/j.microc.2017.02.006 · DOI · Paper page
- Westergaard, 2001, Effects of tylosin as a disturbance on the soil microbial community, Soil Biol. Biochem., 33, 2061, 10.1016/S0038-0717(01)00134-1 · DOI · Paper page
- Beck, 2005, Effects of sulfonamide and tetracycline antibiotics on soil microbial activity and microbial biomass, Chemosphere, 59, 457, 10.1016/j.chemosphere.2005.01.023 · DOI · Paper page
- Mrozik, 2019, Antibiotics in the Soil Environment—Degradation and Their Impact on Microbial Activity and Diversity, Front. Microbiol., 10, 338, 10.3389/fmicb.2019.00338 · DOI · Paper page
- Drury, 2013, Triclosan exposure increases triclosan resistance and influences taxonomic composition of benthic bacterial communities, Environ. Sci. Technol., 47, 8923, 10.1021/es401919k · DOI
- Cunha, 2001, Antibiotic side effects, Med. Clin. N. Am., 85, 149, 10.1016/S0025-7125(05)70309-6 · DOI · Paper page
- Mojica, E.-R.E., and Aga, D.S. (2011). Antibiotics Pollution in Soil and Water: Potential Ecological and Human Health Issues. Encyclopedia of Environmental Health, Elsevier. · DOI
- Ye, 2007, Trace analysis of trimethoprim and sulfonamide, macrolide, quinolone, and tetracycline antibiotics in chlorinated drinking water using liquid chromatography electrospray tandem mass spectrometry, Anal. Chem., 79, 1135, 10.1021/ac060972a · DOI · Paper page
- Halden, 2005, Co-occurrence of triclocarban and triclosan in U.S. water resources, Environ. Sci. Technol., 39, 1420, 10.1021/es049071e · DOI · Paper page
- Bever, 2018, Effects of triclosan in breast milk on the infant fecal microbiome, Chemosphere, 203, 467, 10.1016/j.chemosphere.2018.03.186 · doi:10.1016/j.chemosphere.2018.03.186
- Weatherly, 2017, Triclosan exposure, transformation, and human health effects, J. Toxicol. Environ. Health Part B Crit. Rev., 20, 447, 10.1080/10937404.2017.1399306 · DOI · Paper page
- Calafat, 2008, Urinary concentrations of triclosan in the U.S. population: 2003–2004, Environ. Health Perspect., 116, 303, 10.1289/ehp.10768 · DOI · Paper page
- Snow, 2015, A review of ecological effects and environmental fate of illicit drugs in aquatic ecosystems, J. Hazard. Mater., 282, 18, 10.1016/j.jhazmat.2014.06.062 · DOI
- Kelly, 2015, Antibiotic stewardship should consider environmental fate of antibiotics, Environ. Sci. Technol., 49, 5257, 10.1021/acs.est.5b01519 · DOI
- Flaherty, 2005, Effects of pharmaceuticals on Daphnia survival, growth, and reproduction, Chemosphere, 61, 200, 10.1016/j.chemosphere.2005.02.016 · DOI · Paper page
- Migliore, 1997, Toxicity of several important agricultural antibiotics to Artemia, Water Res., 31, 1801, 10.1016/S0043-1354(96)00412-5 · DOI
- Jung, 2008, Environmental levels of ultraviolet light potentiate the toxicity of sulfonamide antibiotics in Daphnia magna, Ecotoxicology, 17, 37, 10.1007/s10646-007-0174-9 · doi:10.1007/s10646-007-0174-9
- Liu, 2018, Progress of research on the toxicology of antibiotic pollution in aquatic organisms, Acta Ecol. Sin., 38, 36, 10.1016/j.chnaes.2018.01.006 · DOI · Paper page
- Wang, 2014, Toxicity evaluation of β-diketone antibiotics on the development of embryo-larval zebrafish (Danio rerio), Environ. Toxicol., 29, 1134, 10.1002/tox.21843 · DOI
- Lin, 2014, Integrated biomarker responses in zebrafish exposed to sulfonamides, Environ. Toxicol. Pharmacol., 38, 444, 10.1016/j.etap.2014.07.020 · DOI
- Wang, 2009, Adverse effects of enrofloxacin when associated with environmental stress in Tra catfish (Pangasianodon hypophthalmus), Chemosphere, 77, 1577, 10.1016/j.chemosphere.2009.09.038 · doi:10.1016/j.chemosphere.2009.09.038
- Zhang, 2015, Effects of tetracycline on developmental toxicity and molecular responses in zebrafish (Danio rerio) embryos, Ecotoxicology, 24, 707, 10.1007/s10646-015-1417-9 · DOI
- Xu, 2006, Residues of enrofloxacin, furazolidone and their metabolites in Nile tilapia (Oreochromis niloticus), Aquaculture, 254, 1, 10.1016/j.aquaculture.2005.10.030 · doi:10.1016/j.aquaculture.2005.10.030
- Zhang, 2016, Toxicity assessment of combined fluoroquinolone and tetracycline exposure in zebrafish (Danio rerio), Environ. Toxicol., 31, 736, 10.1002/tox.22087 · DOI
- Kim, 2017, Multigenerational Effects of the Antibiotic Tetracycline on Transcriptional Responses of Daphnia magna and Its Relationship to Higher Levels of Biological Organizations, Environ. Sci. Technol., 51, 12898, 10.1021/acs.est.7b05050 · DOI
- Raymann, 2018, The role of the gut microbiome in health and disease of adult honey bee workers, Curr. Opin. Insect Sci., 26, 97, 10.1016/j.cois.2018.02.012 · DOI · Paper page
- Turnbaugh, 2011, Human Health and Disease in a Microbial World, Front. Microbiol., 2, 190, 10.3389/fmicb.2011.00190 · DOI
- Langdon, 2016, The effects of antibiotics on the microbiome throughout development and alternative approaches for therapeutic modulation, Genome Med., 8, 39, 10.1186/s13073-016-0294-z · DOI · Paper page
- Ianiro, 2016, Antibiotics as deep modulators of gut microbiota: Between good and evil, Gut, 65, 1906, 10.1136/gutjnl-2016-312297 · DOI · Paper page
- Schmidt, 2016, Influence of Fishmeal-Free Diets on Microbial Communities in Atlantic Salmon (Salmo salar) Recirculation Aquaculture Systems, Appl. Environ. Microbiol., 82, 4470, 10.1128/AEM.00902-16 · DOI
- Schmidt, 2015, Community assembly of a euryhaline fish microbiome during salinity acclimation, Mol. Ecol., 24, 2537, 10.1111/mec.13177 · DOI
- Navarrete, 2008, Oxytetracycline treatment reduces bacterial diversity of intestinal microbiota of Atlantic salmon, J. Aquat. Anim. Health, 20, 177, 10.1577/H07-043.1 · DOI · Paper page
- Schmidt, 2017, Subtle Microbiome Manipulation Using Probiotics Reduces Antibiotic-Associated Mortality in Fish, MSystems, 2, e00133-17, 10.1128/mSystems.00133-17 · DOI
- Bielen, 2017, Negative environmental impacts of antibiotic-contaminated effluents from pharmaceutical industries, Water Res., 126, 79, 10.1016/j.watres.2017.09.019 · DOI · Paper page
- Carlson, 2017, Microbiome disruption and recovery in the fish Gambusia affinis following exposure to broad-spectrum antibiotic, Infect. Drug Resist., 10, 143, 10.2147/IDR.S129055 · DOI
- Pindling, 2018, Dysbiosis and early mortality in zebrafish larvae exposed to subclinical concentrations of streptomycin, FEMS Microbiol. Lett., 365, fny188, 10.1093/femsle/fny188 · DOI
- Yan, 2016, Long-term effects of antibiotics, norfloxacin, and sulfamethoxazole, in a partial life-cycle study with zebrafish (Danio rerio): Effects on growth, development, and reproduction, Environ. Sci. Pollut. Res., 23, 18222, 10.1007/s11356-016-7018-1 · DOI
- Adlard, 2015, The butterfly effect: Parasite diversity, environment, and emerging disease in aquatic wildlife, Trends Parasitol., 31, 160, 10.1016/j.pt.2014.11.001 · DOI
- Holloway, 2017, Antibiotic use in South East Asia and policies to promote appropriate use: Reports from country situational analyses, BMJ, 358, j2291, 10.1136/bmj.j2291 · DOI
- Ghafur, 2013, Chennai Declaration: A solution to the antibiotic resistance in developing countries, Indian J. Cancer, 50, 71, 10.4103/0019-509X.104065 · DOI
- Leonard, 2015, Human recreational exposure to antibiotic resistant bacteria in coastal bathing waters, Environ. Int., 82, 92, 10.1016/j.envint.2015.02.013 · DOI · Paper page
- Ashbolt, 2013, Human health risk assessment (HHRA) for environmental development and transfer of antibiotic resistance, Environ. Health Perspect., 121, 993, 10.1289/ehp.1206316 · DOI · Paper page
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Metadata
- Authors
- Kraemer, S. A., Ramachandran, A., & Perron, G. G.
- Affiliations
- Department of Biology, Concordia University, 7141 Sherbrooke Street W, Montreal, QC H4B1R6, Canada
- Department of Biology, Reem-Kayden Center for Sciences and Computation, Bard College, 31 Campus Road, Annandale-On-Hudson, NY 12504, USA
- ORCID
- Perron, Gabriel G.
- Venue
- Microorganisms
- Publisher
- MDPI AG
- Published
- 2019-06-22
- Volume
- 7
- Issue
- 6
- Pages
- 180
- ISSN
- 2076-2607
- Cited by
- 932
- References
- 14
- Language
- en
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