详细信息
Removal of sulfonamide antibiotic resistant bacterial and intracellular antibiotic resistance genes by UVC-activated peroxymonosulfate ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Removal of sulfonamide antibiotic resistant bacterial and intracellular antibiotic resistance genes by UVC-activated peroxymonosulfate
作者:Hu, Yaru[1];Zhang, Tianyang[1,2];Jiang, Lei[3];Yao, Shijie[1];Ye, Hui[3];Lin, Kuangfei[1];Cui, Changzheng[1,2]
机构:[1]East China Univ Sci & Technol, State Environm Protect Key Lab Environm Risk Asse, Sch Resources & Environm Engn, Shanghai 200237, Peoples R China;[2]Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China;[3]Natl Engn Res Ctr Urban Water Resources, Shanghai 200082, Peoples R China
年份:2019
卷号:368
起止页码:888
外文期刊名:CHEMICAL ENGINEERING JOURNAL
收录:;EI(收录号:20191006604404);WOS:【SCI-EXPANDED(收录号:WOS:000462769600082)】;
基金:This work was supported by the National Water Pollution Control and Management Technology Major Projects (No. 2017ZX07402003), Shanghai Municipal Science and Technology Commission (No. 16XD1420500) and Open Project of State Key Laboratory of Urban Water Resource and Environment (No. QA201612), Shanghai Sailing Program (No. 18YF1406000), China Postdoctoral Science Foundation (No. 2017M621391) and the Fundamental Research Funds for the Central Universities (No. 222201814055).
语种:英文
外文关键词:UVC-activated peroxymonosulfate; Antibiotic resistant bacteria; Intracellular antibiotic resistance genes; Sulfate radical; Water treatment
摘要:The inactivation of an isolated sulfonamide antibiotic resistant bacteria (ARB) HLS-6 and reduction of intracellular sul1 and intI1 in its genome by UVC irradiation, PMS oxidation and UVC-activated peroxymonosulfate (UVC/PMS) treatments were investigated in this study. The UVC/PMS treatment was superior to the other two methods in the inactivation of ARB and reduction of qPCR-sul1 and qPCR-intI1. The HLS-6 ARB (10(8) CFU/mL) could be effectively inactivated 5.3 log by UVC (100 mu W/cm(2))/PMS (1 mg/L), and the reduction rates of qPCR-sul1 and qPCR-intI1 by UVC (100 mu W/cm(2))/PMS (20 mg/L), reached up to 2.9 log and 3.4 log, respectively within 30 min. qPCR-intI1 reacted faster than qPCR-sul1 in all methods. Sulfate radical was responsible for the reduction of target genes, while hydroxyl radical had negligible effect on that. The dosage of PMS positively affected the reduction of both genes during UVC/PMS, while the initial concentration of ARB could negatively influence the reduction of target genes. The pH 5 of reaction solution was most beneficial to the reduction of ARGs. The reduction rates at pH 5 reached up to 3.1 log (sul1) and 3.3 log (intI1). The reduction of target genes was slightly facilitated in the initial 5 min and suppressed after 5 min with the co-existence of sulfamethoxazole. This study will provide a potential alternative method for controlling the antibiotic resistance in aquatic environment.
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