Literature DB >> 22121301

Comparison of the Transport of Tetracycline-Resistant and Tetracycline-Susceptible Escherichia coli Isolated from Lake Michigan.

Jacob J Walczak1, Sonia L Bardy, Lucia Feriancikova, Shangping Xu.   

Abstract

It was recently reported that tetracycline could enhance the mobility of manure-derived Escherichia coli within saturated porous media (Walczak et al. (Water Research 45:1681-1690, 2011)). It was also shown, however, that E. coli from various sources could display marked variation in their mobility (Bolster et al. (Journal of Environmental Quality 35:1018-1025, 2009)). The focus of this research was to examine if the observed difference in the mobility of manure-derived tetracycline-resistant (tet(R)) and tetracycline-susceptible (tet(S)) E. coli strains was source-dependent. Specifically, E. coli were isolated from Lake Michigan, and the influence of tetracycline resistance on Lake Michigan-derived E. coli was investigated through column transport experiments. Additionally, a variety of cell morphology and surface properties were determined and related to the observed bacterial transport behavior. Our experimental results showed that, consistent with previous observations, the deposition rate coefficients of the tet(R)E. coli strain was ~20-100% higher than those of the tet(S)E. coli strain. The zeta potential of the tet(R)E. coli cells was ~25 mV more negative than the tet(S)E. coli cells. Because the surfaces of the E. coli cells and the quartz sands were negatively charged, the repulsive electrostatic double-layer interaction between the tet(R)E. coli cells and the quartz sands was stronger, and the mobility of the tet(R)E. coli cells in the sand packs was thus higher. The tet(R)E. coli cells were also more hydrophilic than the tet(S)E. coli cells. Results from migration to hydrocarbon phase (MATH) tests showed that about ~35% more tet(S)E. coli cells partitioned to the hydrocarbon phase. As it was previously shown that cell hydrophobicity could enhance the attachment of bacterial cells to quartz sand, the difference in cell hydrophobicity could also have contributed to the observed higher mobility of the tet(R)E. coli cells. The size of the tet(R) and tet(S)E. coli cells were similar, suggesting that the observed difference in their mobility was not size-related. Characterization of cell surface properties also showed that tet(R) and tetS E. coli cells differed slightly in cell-bound lipopolysaccharide contents and had distinct outer membrane protein profiles. Such difference could alter cell surface properties which in turn led to changes in cell mobility.

Entities:  

Year:  2011        PMID: 22121301      PMCID: PMC3223934          DOI: 10.1007/s11270-011-0825-6

Source DB:  PubMed          Journal:  Water Air Soil Pollut        ISSN: 0049-6979            Impact factor:   2.520


  35 in total

Review 1.  Structure of bacterial lipopolysaccharides.

Authors:  Martine Caroff; Doris Karibian
Journal:  Carbohydr Res       Date:  2003-11-14       Impact factor: 2.104

2.  Influence of growth phase on bacterial deposition: interaction mechanisms in packed-bed column and radial stagnation point flow systems.

Authors:  Sharon L Walker; Jeremy A Redman; Menachem Elimelech
Journal:  Environ Sci Technol       Date:  2005-09-01       Impact factor: 9.028

3.  Analysis of outer membrane proteome of Escherichia coli related to resistance to ampicillin and tetracycline.

Authors:  Changxin Xu; Xiangmin Lin; Haixia Ren; Yueling Zhang; Sanying Wang; Xuanxian Peng
Journal:  Proteomics       Date:  2006-01       Impact factor: 3.984

4.  Cell surface analysis techniques: What do cell preparation protocols do to cell surface properties?

Authors:  R S Pembrey; K C Marshall; R P Schneider
Journal:  Appl Environ Microbiol       Date:  1999-07       Impact factor: 4.792

5.  Influence of tetracycline resistance on the transport of manure-derived Escherichia coli in saturated porous media.

Authors:  Jacob J Walczak; Sonia L Bardy; Lucia Feriancikova; Shangping Xu
Journal:  Water Res       Date:  2010-12-21       Impact factor: 11.236

6.  Geographical variation in antibiotic resistance profiles of Escherichia coli isolated from swine, poultry, beef and dairy cattle farm water retention ponds in Florida.

Authors:  S Parveen; J Lukasik; T M Scott; M L Tamplin; K M Portier; S Sheperd; K Braun; S R Farrah
Journal:  J Appl Microbiol       Date:  2006       Impact factor: 3.772

7.  Growth-condition dependent expression of Pasteurella haemolytica A1 outer membrane proteins, capsule, and leukotoxin.

Authors:  D M Gatewood; B W Fenwick; M M Chengappa
Journal:  Vet Microbiol       Date:  1994-08-01       Impact factor: 3.293

8.  Changes in antibiotic resistance patterns of Escherichia coli during domestic wastewater treatment.

Authors:  Jamie R Lefkowitz; Metin Duran
Journal:  Water Environ Res       Date:  2009 Sep-Oct       Impact factor: 1.946

9.  Phenotyping and genotyping of antibiotic-resistant Escherichia coli isolated from a natural river basin.

Authors:  Jianying Hu; Jiachen Shi; Hong Chang; Dong Li; Min Yang; Yoichi Kamagata
Journal:  Environ Sci Technol       Date:  2008-05-01       Impact factor: 9.028

Review 10.  Lipopolysaccharide: Biosynthetic pathway and structure modification.

Authors:  Xiaoyuan Wang; Peter J Quinn
Journal:  Prog Lipid Res       Date:  2009-10-06       Impact factor: 16.195

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  2 in total

1.  The effects of starvation on the transport of Escherichia coli in saturated porous media are dependent on pH and ionic strength.

Authors:  Jacob J Walczak; Lixia Wang; Sonia L Bardy; Lucia Feriancikova; Jin Li; Shangping Xu
Journal:  Colloids Surf B Biointerfaces       Date:  2011-10-13       Impact factor: 5.268

2.  Effects of outer membrane protein TolC on the transport of Escherichia coli within saturated quartz sands.

Authors:  Lucia Feriancikova; Sonia L Bardy; Lixia Wang; Jin Li; Shangping Xu
Journal:  Environ Sci Technol       Date:  2013-05-16       Impact factor: 9.028

  2 in total

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