Transport of antibiotic resistance plasmids in porous media and the influence of surfactants

Peipei Chen, Chaoqi Chen, Xiqing Li

Front. Environ. Sci. Eng. ›› 2018, Vol. 12 ›› Issue (2) : 5.

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Front. Environ. Sci. Eng. ›› 2018, Vol. 12 ›› Issue (2) : 5. DOI: 10.1007/s11783-017-0986-7
RESEARCH ARTICLE
RESEARCH ARTICLE

Transport of antibiotic resistance plasmids in porous media and the influence of surfactants

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Highlights

Indigenous and engineered plasmids have similar transport behavior in porous media.

Indigenous plasmid pK5 transports similarly in quartz sand and soil.

Anionic surfactant SDS has negligible effect on plasmid transport in porous media.

Cationic surfactant CTAB affects plasmid transport at high concentrations.

Indigenous plasmids may transport over significant distances in environment.

Abstract

Transport of engineered antibiotic resistance plasmids in porous media has been reported to potentially cause significant spreading of antibiotic resistance in the environment. In this work, transport of an indigenous resistance plasmid pK5 in porous media was investigated through packed column experiments. At identical ionic strengths in CaCl2 solutions, the breakthroughs of pK5 from soil columns were very close to those from quartz sand columns, indicating that transport of pK5 in quartz sand and soil was similar. A similarity in transport behavior was also found between pK5 and an engineered plasmid pBR322 that has approximately the same number of base pairs as pK5. The influence of surfactants, a major group of constituents in soil solutions, was examined using an engineered plasmid pcDNA3.1(+)/myc-His A. The impact of an anionic surfactant, sodium dodecyl sulfate (SDS), was negligible at concentrations up to 200 mg·L1. Cetyltrimethyl ammonium bromide (CTAB), a cationic surfactant, was found to significantly enhance plasmid adsorption at high concentrations. However, at environmentally relevant concentrations (<1 mg·L1), the effect of this surfactant was also minimal. The negligible impact of surfactants and the similarity between the transport of engineered and indigenous plasmids indicate that under environmentally relevant conditions, indigenous plasmids in soil also have the potential to transport over long distances and lead to the spreading of antibiotic resistance.

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Keywords

Indigenous plasmid / Transport / Porous media / Surfactants

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Peipei Chen, Chaoqi Chen, Xiqing Li. Transport of antibiotic resistance plasmids in porous media and the influence of surfactants. Front. Environ. Sci. Eng., 2018, 12(2): 5 https://doi.org/10.1007/s11783-017-0986-7

References

[1]
Chee-Sanford J C, Mackie R I, Koike S, Krapac I G, Lin Y F, Yannarell A C, Maxwell S, Aminov R I. Fate and transport of antibiotic residues and antibiotic resistance genes following land application of manure waste. Journal of Environmental Quality, 2009, 38(3): 1086–1108
CrossRef Pubmed Google scholar
[2]
Gielen G J H P, Heuvel M R, Clinton P W, Greenfield L G. Factors impacting on pharmaceutical leaching following sewage application to land. Chemosphere, 2009, 74(4): 537–542
CrossRef Pubmed Google scholar
[3]
Gatica J, Cytryn E. Impact of treated wastewater irrigation on antibiotic resistance in the soil microbiome. Environmental Science and Pollution Research International, 2013, 20(6): 3529–3538
CrossRef Pubmed Google scholar
[4]
Marti R, Scott A, Tien Y C, Murray R, Sabourin L, Zhang Y, Topp E. Impact of manure fertilization on the abundance of antibiotic-resistant bacteria and frequency of detection of antibiotic resistance genes in soil and on vegetables at harvest. Applied and Environmental Microbiology, 2013, 79(18): 5701–5709
CrossRef Pubmed Google scholar
[5]
Finley R L, Collignon P, Larsson D G, McEwen S A, Li X Z, Gaze W H, Reid-Smith R, Timinouni M, Graham D W, Topp E. The scourge of antibiotic resistance: the important role of the environment. Clinical infectious diseases: an official publication of the Infectious Diseases Society of America, 2013, 57(5): 704–710
CrossRef Pubmed Google scholar
[6]
Davies J. Inactivation of antibiotics and the dissemination of resistance genes. Science, 1994, 264(5157): 375–382
CrossRef Pubmed Google scholar
[7]
Heuer H, Smalla K. Plasmids foster diversification and adaptation of bacterial populations in soil. FEMS Microbiology Reviews, 2012, 36(6): 1083–1104
CrossRef Pubmed Google scholar
[8]
Davison J. Genetic exchange between bacteria in the environment. Plasmid, 1999, 42(2): 73–91
CrossRef Pubmed Google scholar
[9]
Backert S, Meyer T F. Type IV secretion systems and their effectors in bacterial pathogenesis. Current Opinion in Microbiology, 2006, 9(2): 207–217
CrossRef Pubmed Google scholar
[10]
Levy-Booth D J, Campbell R G, Gulden R H, Hart M M, Powell J R, Klironomos J N, Pauls K P, Swanton C J, Trevors J T, Dunfield K E. Cycling of extracellular DNA in the soil environment. Soil Biology & Biochemistry, 2007, 39(12): 2977–2991
CrossRef Google scholar
[11]
Cai P, Huang Q Y, Zhang X W. Interactions of DNA with clay minerals and soil colloidal particles and protection against degradation by DNase. Environmental Science & Technology, 2006, 40(9): 2971–2976
CrossRef Pubmed Google scholar
[12]
Ogram A, Sayler G S, Gustin D, Lewis R J. DNA adsorption to soils and sediments. Environmental Science & Technology, 1988, 22(8): 982–984
CrossRef Pubmed Google scholar
[13]
Pietramellara G, Franchi M, Gallori E, Nannipieri P. Effect of molecular characteristics of DNA on its adsorption and binding on homoionic montmorillonite and kaolinite. Biology and Fertility of Soils, 2001, 33(5): 402–409
CrossRef Google scholar
[14]
Poté J, Ceccherini M T, Van V T, Rosselli W, Wildi W, Simonet P, Vogel T M. Fate and transport of antibiotic resistance genes in saturated soil columns. European Journal of Soil Biology, 2003, 39(2): 65–71
CrossRef Google scholar
[15]
Poté J, Teresa Ceccherini M, Rosselli W, Wildi W, Simonet P, Vogel T M. Leaching and transformability of transgenic DNA in unsaturated soil columns. Ecotoxicology and Environmental Safety, 2010, 73(1): 67–72
CrossRef Pubmed Google scholar
[16]
Rysz M, Alvarez P J J. Transport of antibiotic-resistant bacteria and resistance-carrying plasmids through porous media. Water Science and Technology: A Journal of the International Association on Water Pollution Research, 2006, 54(11): 363–370
CrossRef Pubmed Google scholar
[17]
Chen C, Li J, DeVries S L, Zhang P, Li X. Transport of antibiotic resistance plasmids in porous media. Vadose Zone Journal, 2015, 14(3): 
CrossRef Google scholar
[18]
del Valle M, Alonso J, Bartrolí J, Martí I. Spectrophotometric determination of low levels of anionic surfactants in water by solvent extraction in a flow injection system. Analyst (London), 1988, 113(11): 1677–1681
CrossRef Google scholar
[19]
Corada-Fernández C, Jiménez-Martínez J, Candela L, González-Mazo E, Lara-Martín P A. Occurrence and spatial distribution of emerging contaminants in the unsaturated zone. Case study: Guadalete River Basin (Cadiz, Spain). Chemosphere, 2015, 119(S): S131–S137
[20]
Mungray A K, Kumar P. Anionic surfactants in treated sewage and sludges: risk assessment to aquatic and terrestrial environments. Bioresource Technology, 2008, 99(8): 2919–2929
CrossRef Pubmed Google scholar
[21]
Cantarero S, Prieto C A, López I. Occurrence of high-tonnage anionic surfactants in Spanish sewage sludge. Journal of Environmental Management, 2012, 95(S): S149–S153
[22]
Eskilsson K, Leal C, Lindman B, Miguel M, Nylander T. DNA-surfactant complexes at solid surfaces. Langmuir, 2001, 17(5): 1666–1669
CrossRef Google scholar
[23]
Braem A D, Campos-Terán J, Lindman B. Influence of DNA adsorption and DNA/cationic surfactant coadsorption on the interaction forces between hydrophobic surfaces. Langmuir, 2004, 20(15): 6407–6413
CrossRef Pubmed Google scholar
[24]
Cárdenas M, Braem A, Nylander T, Lindman B. DNA compaction at hydrophobic surfaces induced by a cationic amphiphile. Langmuir, 2003, 19(19): 7712–7718
CrossRef Google scholar
[25]
Cárdenas M, Wacklin H, Campbell R A, Nylander T. Structure of DNA-cationic surfactant complexes at hydrophobically modified and hydrophilic silica surfaces as revealed by neutron reflectometry. Langmuir, 2011, 27(20): 12506–12514
CrossRef Pubmed Google scholar
[26]
Adamczyk Z, Siwek B, Zembala M, Weronski P. Kinetics of localized adsorption of colloid particles. Langmuir, 1992, 8(11): 2605–2610
CrossRef Google scholar
[27]
Adamczyk Z, Barbasz J, Cieśla M. Mechanisms of fibrinogen adsorption at solid substrates. Langmuir, 2011, 27(11): 6868–6878
CrossRef Pubmed Google scholar
[28]
Xie Y, Li S, Wu K, Wang J, Liu G. A hybrid adsorption/ultrafiltration process for perchlorate removal. Journal of Membrane Science, 2011, 366(1–2): 237–244
CrossRef Google scholar
[29]
Elimelech M, O’Melia C R. Kinetics of deposition of colloidal particles in porous media. Environmental Science & Technology, 1990, 24(10): 1528–1536
CrossRef Google scholar
[30]
Yee N, Fein J B, Daughney C J. Experimental study of the pH, ionic strength, and reversibility behavior of bacteria–mineral adsorption. Geochimica et Cosmochimica Acta, 2000, 64(4): 609–617
CrossRef Google scholar
[31]
Edmeades D C, Wheeler D M, Clinton O E. The chemical-composition and ionic-strength of soil solutions from New Zealand topsoils. Australian Journal of Soil Research, 1985, 23(2): 151–165
[32]
Olkowska E, Ruman M, Kowalska A, Polkowska Ż. Determination of surfactants in environmental samples. Part I. Cationic compounds. Ecological Chemistry and Engineering S-Chemia I Inzynieria Ekologiczna S, 2013, 20(1): 69–77
CrossRef Google scholar
[33]
Samardžić M, Galović O, Petrušić S, Sak-Bosnar M. The analysis of anionic surfactants in effluents using a DDA-TPB potentiometric sensor. International Journal of Electrochemical Science, 2014, 9(11): 6166–6181
[34]
Lara-Martín P A, Gómez-Parra A, González-Mazo E. Simultaneous extraction and determination of anionic surfactants in waters and sediments. Journal of Chromatography. A, 2006, 1114(2): 205–210
CrossRef Pubmed Google scholar
[35]
Olkowska E, Ruman M, Kowalska A, Polkowska Ż. Determination of surfactants in environmental samples. Part II. Anionic compounds. Ecological Chemistry and Engineering S-Chemia I Inzynieria Ekologiczna S, 2013, 20(2): 331–342
CrossRef Google scholar

Acknowledgements

This study was supported by the National Natural Science Foundation of China (Grant No. 41171362) and by the Undergraduate Student Research Training Program of the Ministry of Education of China. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of the funding agency.

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2017 Higher Education Press and Springer-Verlag Berlin Heidelberg
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