Mechanisms of total phosphorus removal and reduction of β-lactam antibiotic resistance genes by exogenous fungal combination activated sludge

[Display omitted] •Constructing combined-activated sludge (TAS) using Trichoderma and activated sludge.•Explained the mechanism of TAS to remove TP anomalies.•TAS system enhances antibiotic inactivation mechanism.•TAS reduces the diversity and transmission risk of β-ARGs. This study utilized Trichod...

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Veröffentlicht in:Bioresource technology 2024-02, Vol.393, p.130046-130046, Article 130046
Hauptverfasser: Cai, Yixiang, Liu, Feng, He, Guiyi, Kong, Xiaoliang, Jiang, Yuexi, Liu, Ji, Yan, Binghua, Zhang, Shunan, Zhang, Jiachao, Yan, Zhiyong
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Sprache:eng
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Zusammenfassung:[Display omitted] •Constructing combined-activated sludge (TAS) using Trichoderma and activated sludge.•Explained the mechanism of TAS to remove TP anomalies.•TAS system enhances antibiotic inactivation mechanism.•TAS reduces the diversity and transmission risk of β-ARGs. This study utilized Trichoderma and activated sludge to construct combined activated sludge (TAS). The metagenomic approach was employed to examine the shifts in microbial community structure and function of TAS under amoxicillin stress and investigate the mechanism underlying the reduction of β-lactam antibiotic resistance genes (β-ARGs). The findings demonstrated that the elevated aundance of glpa, glpd, ugpq, glpq, and glpb were primarily responsible for the reduction in total phosphorus (TP) removal by TAS. The increased abundance of Proteobacteria and Verrucomicrobia led to enhanced expression of ugpb, phnd, and phne, thereby improving the TP removal of TAS. Furthermore, antibiotic inactivation has gradually become the primary antibiotic resistance mechanism in TAS. Specifically, an increase in the abundance of OXA-309 in TAS will decrease the probability of amoxicillin accumulation in TAS. A decrease in β-ARGs diversity confirmed this. This study presents a novel approach to reducing antibiotic and ARG accumulation in sludge.
ISSN:0960-8524
1873-2976
DOI:10.1016/j.biortech.2023.130046