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The Dual Roles of Nano Zero-Valent Iron and Zinc Oxide in Antibiotics Resistance Genes (ARGs) Spread in Sediment

Nanoparticles (NPs) are widely used and ubiquitous in the environment, but the consequences of their release into the environment on antibiotics resistance genes (ARGs), microbial abundance, and community, are largely unknown. Therefore, this study examined the effect of nano zero-valent iron (nZVI)...

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Autores principales: Luo, Ling, Deng, Dahang, Zhao, Xin, Hu, Hairong, Li, Xinyi, Gu, Jidong, He, Yan, Yang, Gang, Deng, Ouping, Xiao, Yinlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368363/
https://www.ncbi.nlm.nih.gov/pubmed/35954758
http://dx.doi.org/10.3390/ijerph19159405
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author Luo, Ling
Deng, Dahang
Zhao, Xin
Hu, Hairong
Li, Xinyi
Gu, Jidong
He, Yan
Yang, Gang
Deng, Ouping
Xiao, Yinlong
author_facet Luo, Ling
Deng, Dahang
Zhao, Xin
Hu, Hairong
Li, Xinyi
Gu, Jidong
He, Yan
Yang, Gang
Deng, Ouping
Xiao, Yinlong
author_sort Luo, Ling
collection PubMed
description Nanoparticles (NPs) are widely used and ubiquitous in the environment, but the consequences of their release into the environment on antibiotics resistance genes (ARGs), microbial abundance, and community, are largely unknown. Therefore, this study examined the effect of nano zero-valent iron (nZVI) and zinc oxide (nZnO) on tetracycline resistance genes (tet-ARGs) and class 1 integron (intI1) in sediment under laboratory incubation. The coexistence of NPs and tetracycline (TC) on tet-ARGs/intI1 was also investigated. It was found that nZVI and nZnO promoted tet-ARGs/intI1 abundance in sediment without TC but reduced the inducing effect of TC on tet-ARGs/intI1 in sediment overlaid with TC solution. Without TC, nZVI, intI1, and the bacterial community could directly promote tet-ARGs spread in nZVI sediment, while intI1 and bacterial abundance were the most directly important reasons for tet-ARGs spread in nZnO sediment. With TC, nZVI and bacterial community could reduce tet-ARGs abundance in nZVI sediment, while nZnO and bacterial community could directly promote tet-ARGs in nZnO sediment. Finally, these findings provided valuable information for understanding the role of NPs in promoting and reducing ARGs in the environment.
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spelling pubmed-93683632022-08-12 The Dual Roles of Nano Zero-Valent Iron and Zinc Oxide in Antibiotics Resistance Genes (ARGs) Spread in Sediment Luo, Ling Deng, Dahang Zhao, Xin Hu, Hairong Li, Xinyi Gu, Jidong He, Yan Yang, Gang Deng, Ouping Xiao, Yinlong Int J Environ Res Public Health Article Nanoparticles (NPs) are widely used and ubiquitous in the environment, but the consequences of their release into the environment on antibiotics resistance genes (ARGs), microbial abundance, and community, are largely unknown. Therefore, this study examined the effect of nano zero-valent iron (nZVI) and zinc oxide (nZnO) on tetracycline resistance genes (tet-ARGs) and class 1 integron (intI1) in sediment under laboratory incubation. The coexistence of NPs and tetracycline (TC) on tet-ARGs/intI1 was also investigated. It was found that nZVI and nZnO promoted tet-ARGs/intI1 abundance in sediment without TC but reduced the inducing effect of TC on tet-ARGs/intI1 in sediment overlaid with TC solution. Without TC, nZVI, intI1, and the bacterial community could directly promote tet-ARGs spread in nZVI sediment, while intI1 and bacterial abundance were the most directly important reasons for tet-ARGs spread in nZnO sediment. With TC, nZVI and bacterial community could reduce tet-ARGs abundance in nZVI sediment, while nZnO and bacterial community could directly promote tet-ARGs in nZnO sediment. Finally, these findings provided valuable information for understanding the role of NPs in promoting and reducing ARGs in the environment. MDPI 2022-07-31 /pmc/articles/PMC9368363/ /pubmed/35954758 http://dx.doi.org/10.3390/ijerph19159405 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Luo, Ling
Deng, Dahang
Zhao, Xin
Hu, Hairong
Li, Xinyi
Gu, Jidong
He, Yan
Yang, Gang
Deng, Ouping
Xiao, Yinlong
The Dual Roles of Nano Zero-Valent Iron and Zinc Oxide in Antibiotics Resistance Genes (ARGs) Spread in Sediment
title The Dual Roles of Nano Zero-Valent Iron and Zinc Oxide in Antibiotics Resistance Genes (ARGs) Spread in Sediment
title_full The Dual Roles of Nano Zero-Valent Iron and Zinc Oxide in Antibiotics Resistance Genes (ARGs) Spread in Sediment
title_fullStr The Dual Roles of Nano Zero-Valent Iron and Zinc Oxide in Antibiotics Resistance Genes (ARGs) Spread in Sediment
title_full_unstemmed The Dual Roles of Nano Zero-Valent Iron and Zinc Oxide in Antibiotics Resistance Genes (ARGs) Spread in Sediment
title_short The Dual Roles of Nano Zero-Valent Iron and Zinc Oxide in Antibiotics Resistance Genes (ARGs) Spread in Sediment
title_sort dual roles of nano zero-valent iron and zinc oxide in antibiotics resistance genes (args) spread in sediment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368363/
https://www.ncbi.nlm.nih.gov/pubmed/35954758
http://dx.doi.org/10.3390/ijerph19159405
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