Nanopore-based long-read metagenomics uncover the resistome intrusion by antibiotic resistant bacteria from treated wastewater in receiving water body

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Standard

Nanopore-based long-read metagenomics uncover the resistome intrusion by antibiotic resistant bacteria from treated wastewater in receiving water body. / Wu, Ziqi; Che, You; Dang, Chenyuan; Zhang, Miao; Zhang, Xuyang; Sun, Yuhong; Li, Xiang; Zhang, Tong; Xia, Yu.

I: Water Research, Bind 226, 119282, 2022.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Wu, Z, Che, Y, Dang, C, Zhang, M, Zhang, X, Sun, Y, Li, X, Zhang, T & Xia, Y 2022, 'Nanopore-based long-read metagenomics uncover the resistome intrusion by antibiotic resistant bacteria from treated wastewater in receiving water body', Water Research, bind 226, 119282. https://doi.org/10.1016/j.watres.2022.119282

APA

Wu, Z., Che, Y., Dang, C., Zhang, M., Zhang, X., Sun, Y., Li, X., Zhang, T., & Xia, Y. (2022). Nanopore-based long-read metagenomics uncover the resistome intrusion by antibiotic resistant bacteria from treated wastewater in receiving water body. Water Research, 226, [119282]. https://doi.org/10.1016/j.watres.2022.119282

Vancouver

Wu Z, Che Y, Dang C, Zhang M, Zhang X, Sun Y o.a. Nanopore-based long-read metagenomics uncover the resistome intrusion by antibiotic resistant bacteria from treated wastewater in receiving water body. Water Research. 2022;226. 119282. https://doi.org/10.1016/j.watres.2022.119282

Author

Wu, Ziqi ; Che, You ; Dang, Chenyuan ; Zhang, Miao ; Zhang, Xuyang ; Sun, Yuhong ; Li, Xiang ; Zhang, Tong ; Xia, Yu. / Nanopore-based long-read metagenomics uncover the resistome intrusion by antibiotic resistant bacteria from treated wastewater in receiving water body. I: Water Research. 2022 ; Bind 226.

Bibtex

@article{24a818ad7f51488d94439591d7d878b1,
title = "Nanopore-based long-read metagenomics uncover the resistome intrusion by antibiotic resistant bacteria from treated wastewater in receiving water body",
abstract = "Wastewater treatment plant (WWTP) effluent discharge could induce the resistome enrichment in the receiving water environments. However, because of the general lack of a robust antibiotic-resistant bacteria (ARB) identification method, the driving mechanism for resistome accumulation in receiving environment is unclear. Here, we took advantage of the enhanced ARBs recognition by nanopore long reads to distinguish the indigenous ARBs and the accumulation of WWTP-borne ARBs in the receiving water body of a domestic WWTP. A bioinformatic framework (named ARGpore2: https://github.com/sustc-xylab/ARGpore2) was constructed and evaluate to facilitate antibiotic resistance genes (ARGs) and ARBs identification in nanopore reads. ARGs identification by ARGpore2 showed comparable precision and recall to that of the commonly adopt BLASTP-based method, whereas the spectrum of ARBs doubled that of the assembled Illumina dataset. Totally, we identified 33 ARBs genera carrying 65 ARG subtypes in the receiving seawater, whose concentration was in general 10 times higher than clean seawater's. Notably we report a primary resistome intrusion caused by the revival of residual microbes survived from disinfection treatment. These WWTP-borne ARBs, including several animal/human enteric pathogens, contributed up to 85% of the receiving water resistome. Plasmids and class 1 integrons were reckoned as major vehicles facilitating the persistence and dissemination of ARGs. Moreover, our work demonstrated the importance of extensive carrier identification in determining the driving force of multifactor coupled resistome booming in complicated environmental conditions, thereby paving the way for establishing priority for effective ARGs mitigation strategies.",
keywords = "Antibiotic resistance genes, Metagenomic, Nanopore sequencing, Receiving water, WWTP",
author = "Ziqi Wu and You Che and Chenyuan Dang and Miao Zhang and Xuyang Zhang and Yuhong Sun and Xiang Li and Tong Zhang and Yu Xia",
note = "Publisher Copyright: {\textcopyright} 2022",
year = "2022",
doi = "10.1016/j.watres.2022.119282",
language = "English",
volume = "226",
journal = "Water Research",
issn = "0043-1354",
publisher = "I W A Publishing",

}

RIS

TY - JOUR

T1 - Nanopore-based long-read metagenomics uncover the resistome intrusion by antibiotic resistant bacteria from treated wastewater in receiving water body

AU - Wu, Ziqi

AU - Che, You

AU - Dang, Chenyuan

AU - Zhang, Miao

AU - Zhang, Xuyang

AU - Sun, Yuhong

AU - Li, Xiang

AU - Zhang, Tong

AU - Xia, Yu

N1 - Publisher Copyright: © 2022

PY - 2022

Y1 - 2022

N2 - Wastewater treatment plant (WWTP) effluent discharge could induce the resistome enrichment in the receiving water environments. However, because of the general lack of a robust antibiotic-resistant bacteria (ARB) identification method, the driving mechanism for resistome accumulation in receiving environment is unclear. Here, we took advantage of the enhanced ARBs recognition by nanopore long reads to distinguish the indigenous ARBs and the accumulation of WWTP-borne ARBs in the receiving water body of a domestic WWTP. A bioinformatic framework (named ARGpore2: https://github.com/sustc-xylab/ARGpore2) was constructed and evaluate to facilitate antibiotic resistance genes (ARGs) and ARBs identification in nanopore reads. ARGs identification by ARGpore2 showed comparable precision and recall to that of the commonly adopt BLASTP-based method, whereas the spectrum of ARBs doubled that of the assembled Illumina dataset. Totally, we identified 33 ARBs genera carrying 65 ARG subtypes in the receiving seawater, whose concentration was in general 10 times higher than clean seawater's. Notably we report a primary resistome intrusion caused by the revival of residual microbes survived from disinfection treatment. These WWTP-borne ARBs, including several animal/human enteric pathogens, contributed up to 85% of the receiving water resistome. Plasmids and class 1 integrons were reckoned as major vehicles facilitating the persistence and dissemination of ARGs. Moreover, our work demonstrated the importance of extensive carrier identification in determining the driving force of multifactor coupled resistome booming in complicated environmental conditions, thereby paving the way for establishing priority for effective ARGs mitigation strategies.

AB - Wastewater treatment plant (WWTP) effluent discharge could induce the resistome enrichment in the receiving water environments. However, because of the general lack of a robust antibiotic-resistant bacteria (ARB) identification method, the driving mechanism for resistome accumulation in receiving environment is unclear. Here, we took advantage of the enhanced ARBs recognition by nanopore long reads to distinguish the indigenous ARBs and the accumulation of WWTP-borne ARBs in the receiving water body of a domestic WWTP. A bioinformatic framework (named ARGpore2: https://github.com/sustc-xylab/ARGpore2) was constructed and evaluate to facilitate antibiotic resistance genes (ARGs) and ARBs identification in nanopore reads. ARGs identification by ARGpore2 showed comparable precision and recall to that of the commonly adopt BLASTP-based method, whereas the spectrum of ARBs doubled that of the assembled Illumina dataset. Totally, we identified 33 ARBs genera carrying 65 ARG subtypes in the receiving seawater, whose concentration was in general 10 times higher than clean seawater's. Notably we report a primary resistome intrusion caused by the revival of residual microbes survived from disinfection treatment. These WWTP-borne ARBs, including several animal/human enteric pathogens, contributed up to 85% of the receiving water resistome. Plasmids and class 1 integrons were reckoned as major vehicles facilitating the persistence and dissemination of ARGs. Moreover, our work demonstrated the importance of extensive carrier identification in determining the driving force of multifactor coupled resistome booming in complicated environmental conditions, thereby paving the way for establishing priority for effective ARGs mitigation strategies.

KW - Antibiotic resistance genes

KW - Metagenomic

KW - Nanopore sequencing

KW - Receiving water

KW - WWTP

U2 - 10.1016/j.watres.2022.119282

DO - 10.1016/j.watres.2022.119282

M3 - Journal article

C2 - 36332295

AN - SCOPUS:85140990653

VL - 226

JO - Water Research

JF - Water Research

SN - 0043-1354

M1 - 119282

ER -

ID: 345414804