Consecutive ultrafiltration and silica adsorption for recovery of extracellular antibiotic resistance genes from an urban river.


Journal

Environmental pollution (Barking, Essex : 1987)
ISSN: 1873-6424
Titre abrégé: Environ Pollut
Pays: England
ID NLM: 8804476

Informations de publication

Date de publication:
May 2020
Historique:
received: 17 09 2019
revised: 15 01 2020
accepted: 22 01 2020
pubmed: 12 2 2020
medline: 5 6 2020
entrez: 12 2 2020
Statut: ppublish

Résumé

The dissemination of antibiotic resistance (AR) has attracted global attention because of the increasing antibiotic treatment failure it has caused. Through natural transformation, a live bacterium takes up extracellular DNA (exDNA), which facilitates AR dissemination. However, recovery of exDNA from water samples is challenging. In this study, we validated a consecutive ultrafiltration-based protocol to simultaneously recover intracellular DNA (inDNA), dissolved exDNA (Dis_exDNA, dissolved in the bulk water), and adsorbed exDNA (Ads_exDNA, adsorbed to the surfaces of suspended particles). Using hollow fiber ultrafiltration (HFUF), all DNA fractions were concentrated from environmental water samples, after which Dis_exDNA (supernatant) was separated from inDNA and Ads_exDNA (pellets) using centrifugation. Ads_exDNA was washed off from the pellets with proteinase K and sodium phosphate buffer. Dis_exDNA and Ads_exDNA were further concentrated using centrifugal ultrafiltration, from which silica binding was performed. inDNA was extracted from washed pellets with a commercial kit. For inDNA, HFUF showed recovery efficiencies of 96.5 ± 18.5% and 88.0 ± 2.0% for total cells and cultured Escherichia coli, respectively (n = 3). To represent all possible DNA fragments in water environment, exDNA with different lengths (10.0, 4.0, 1.0, and 0.5 kbp) were spiked to test the recovery efficiencies for Dis_exDNA. The whole process achieved 62.2%-62.9% recovery for 10 and 4 kbp exDNA, and 38.8%-44.5% recovery for 1.0 and 0.5 kbp exDNA. Proteinase K treatment enhanced the recovery of Ads_exDNA by 4.0-10.7 times. The protocol was applied to water samples from an urban river in Tokyo, Japan. The abundance of AR genes (ARGs) in inDNA, Dis_exDNA, and Ads_exDNA increased downstream of wastewater treatment plants. ARGs in Ads_exDNA and Dis_exDNA accounted for 1.8%-26.7% and 0.03%-20.9%, respectively, of the total DNA, implying that Ads_exDNA and Dis_exDNA are nonnegligible potential pools for the horizontal transfer of ARGs.

Identifiants

pubmed: 32041028
pii: S0269-7491(19)35335-7
doi: 10.1016/j.envpol.2020.114062
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Waste Water 0
Silicon Dioxide 7631-86-9

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

114062

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no competing financial interests related to the publication of this study.

Auteurs

Miaomiao Liu (M)

Department of Urban Engineering, Graduate School of Engineering, University of Tokyo, 7-3-1, Hongo, Bunkyo, Tokyo, 113-8656, Japan.

Akihiko Hata (A)

Department of Environmental and Civil Engineering, Faculty of Engineering, Toyama Prefectural University, 5180, Kurokawa, Imizu City, Toyama, 939-0398, Japan.

Hiroyuki Katayama (H)

Department of Urban Engineering, Graduate School of Engineering, University of Tokyo, 7-3-1, Hongo, Bunkyo, Tokyo, 113-8656, Japan.

Ikuro Kasuga (I)

Department of Urban Engineering, Graduate School of Engineering, University of Tokyo, 7-3-1, Hongo, Bunkyo, Tokyo, 113-8656, Japan; VNU-Vietnam Japan University, My Dinh Campus, Luu Huu Phuoc Street, My Dinh 1 Ward, Nam Tu Liem District, Hanoi, Viet Nam. Electronic address: kasuga@env.t.u-tokyo.ac.jp.

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Classifications MeSH