Fate Of Antibiotics Research Articles

Degradation of norfloxacin by the synergistic effect of micro-nano bubbles and sodium hypochlorite: kinetics, influencing factors and pathways.

This study thoroughly investigated the degradation of norfloxacin (NOR) under the influence of micro-nanobubbles (MNBs) and sodium hypochlorite (NaClO), focusing on their synergistic effects. The impact of various environmental factors, including NaClO concentration, pH, inorganic anions, and surfactants, on NOR degradation efficiency within the MNBs/NaClO system was systematically assessed. The basic properties of the MNBs/NaClO system and the degradation kinetics of NOR were explored. The degradation products and pathways of NOR were explored to reveal the degradation mechanism of antibiotics in the MNBs/NaClO system by employing density functional theory (DFT) and high-performance liquid chromatography-mass spectrometry (HPLC-MS). The redox potential of the MNBs/NaClO system exhibited significantly superior properties than the single system, with bubble sizes predominantly in the nanoscale. The degradation kinetics of NOR adhered to a pseudo-first-order reaction model, with optimal degradation occurring at a 0.025% NaClO volume concentration. Acidic conditions promoted the degradation of NOR, and alkaline conditions inhibited the degradation of NOR. Inorganic anions PO43-, HCO3-, and CO32- in the water matrix led to strong inhibition of NOR degradation. Cationic surfactants accelerated the degradation process of NOR, while anionic and nonionic surfactants had a consistent inhibitory effect on the degradation of NOR. Based on the degradation behavior, three potential pathways for NOR degradation were proposed: quinolone group transformation, defluorination reaction, piperazine ring cracking and quinolone ring decomposition. This research contributes a novel technical approach for addressing antibiotic pollution and offers a theoretical framework for understanding the fate of antibiotics in the environment.

Optical characteristic of dissolved organic matter polar fractions by spectrum technologies and the relationship with indirect photodegradation of ofloxacin

Ofloxacin (OFL) is a commonly used antibiotic and is widely present in various water bodies. Indirect photodegradation is crucial for the transformation and fate of antibiotics in surface water, which largely depends on the structure and composition of dissolved organic matter (DOM). Nevertheless, knowledge about the optical characteristics of diverse DOM polar fractions as well as the relationship with indirect photodegradation of antibiotics is still scarce. In this study, XAD-8 in combination with anion and cation exchange resins was used to separate DOM into six polar fractions: hydrophilic acid (HIA), hydrophilic basic (HIB), hydrophilic neutral (HIN), hydrophobic acid (HOA), hydrophobic basic (HOB) and hydrophobic neutral (HON). UV–vis and fluorescence spectroscopy were applied to analyze DOM polar fractions and explore their impact on OFL indirect photodegradation. The results showed that indirect photodegradation was the primary photodegradation route of OFL when the irradiation wavelength was greater than 320 nm, triple-state excited DOM (3DOM*) was the main reactive intermediates (RIs) that affected the indirect photodegradation of OFL. Excitation-emission matrix spectroscopy combined with parallel factor analysis (EEMs-PARAFAC) and correlation analysis demonstrated that terrestrial humic-like substances could yield generous RIs to facilitate OFL indirect photodegradation. The HIB and HOA fractions of SRNOM contained large aromaticity and humification degree and more terrestrial humic-like substances, thus exhibiting greater OFL indirect photodegradation rates. The HOA and HOB fractions of FA had abundant terrestrial humic-like substances and contributed more to OFL indirect photodegradation. This study helped us understand the effect of DOM structural characteristics on the OFL indirect photodegradation.

Swine wastewater co-exposed with veterinary antibiotics enhanced the antibiotic resistance of endophytes in radish (Raphanus sativus L.)

The widespread utilization of antibiotics in livestock has promoted the accumulation and diffusion of antibiotics and antibiotic resistance in agricultural soils and crops. Here we investigated the mechanisms of antibiotic uptake and accumulation in swine wastewater (SW)-treated radish (Raphanus sativus L.) and subsequent impacts on endophyte antibiotic resistance. Under SW treatments, exposure to 500 μg/L sulfamethazine (SMZ) and enrofloxacin (EFX) significantly affected radish biomass, with SMZ causing 63.0% increases and EFX causing 36.3% decreases relative to the untreated control. EFX uptake by radish were from 5 to 100-folds over SMZ. Passive diffusion through anion channel proteins on cell membranes was an important route for SMZ uptake, while both passive diffusion and energy-dependent processes contributed to the uptake of EFX. Bacterial community was time-dependent as a function of both antibiotics and SW, the bacterial alpha diversity in liquid solution co-treated with antibiotics and SW increased over time. The abundance of antibiotic resistance genes (ARGs) in the roots was positively correlated with ARGs in the Hoagland's solution under antibiotic-alone treatments. EFX co-exposure with SW enhanced the dissemination of ARGs from swine wastewater into plant roots, and significant correlations existed between ARGs and integrons in both Hoagland's solution and roots. These findings increased our understanding of the fate of antibiotics in crops and their subsequent impacts on antibiotic resistance of endophytic bacteria.

Unraveling phytoremediation mechanisms of the common reed (Phragmites australis) suspension cells towards ciprofloxacin: Xenobiotic transformation and metabolic reprogramming

Phytoremediation is an effective solution to treat pollution with antibiotic compounds in aquatic environments; however, the underlying mechanisms for plants to cope with antibiotic pollutants are obscure. Here we used cell suspension culture to investigate the distribution and transformation of ciprofloxacin (CIP) in common reed (Phragmites australis) plants, as well as the accompanying phenotypic and metabolic responses of plants. By means of radioactive isotope labelling, we found that in total 68 % of CIP was transformed via intracellular Phase I transformation (reduction and methylation), Phase Ⅱ conjugation (glycosylation), and Phase Ⅲ compartmentalization (cell-bound residue formation mainly in cell walls, 23 %). The reduction and glycosylation products were secreted by the cells. To mitigate stress induced by CIP and its transformation products, the cells activated the defense system by up-regulating both intra- and extra-cellular antioxidant metabolites (e.g., catechin, l-cystine, and dehydroascorbic acid), anti-C/N metabolism disorder metabolites (e.g., succinic acid), secreting signaling (e.g., nicotinic acid), and anti-stress (e.g., allantoin) metabolites. Notably, the metabolic reprogramming could be involved in the CIP transformation process (e.g., glycosylation). Our findings reveal the strategy of wetland plants to cope with the stress from CIP by transforming the xenobiotic compound and reprogramming metabolism, and provide novel insights into the fate of antibiotics and plant defense mechanisms during phytoremediation.

The fate of antibiotics and antibiotic resistance genes in Large-Scale chicken farm Environments: Preliminary view of the performance of National veterinary Antimicrobial use reduction Action in Guangdong, China

In 2018, China implemented the Veterinary Antimicrobial Use Reduction Action to curb the rapid development of antibiotic resistance (AR). However, the AR-related pollutions in animal farms after the reduction policy has been poorly investigated. Here, we performed a comprehensive investigation combining UPLC-MS/MS, metagenomic, and bacterial genomic analyses in eight representative large-scale chicken farms in Guangdong, China. Our results showed that antibiotics and ARGs contaminations were more severe in broiler farms than in layer farms. Notably, diverse tet(X) variants were prevalent in the chicken farms. These tet(X)s was carried by diverse E. coli lineages and obviously correlated with ISCR2 and IS1B transposases. The resistomes in chicken farms was significantly correlated with microbial community, and multiple factor analyses indicated that the joint effect of antibiotics-microbial community-MGEs was the most dominant driver of ARGs. Host tracking identified a variety of ARG bacterial hosts and the co-occurrence of ARGs-MRGs-MGEs. Source tracking indicated that the inherent component represented the main feature of resistomes in different hosts, while ARG transfer between the chicken gut and farm environments were frequent. A multiperspective evaluation of AR risk revealed that the early effect of antibiotic reduction was exhibited by the mitigation of maximum level of risky ARGs, prevalence of environmental AR pathogens, and HGT potential of ARGs mediated by phage structures. Overall, our findings provide insights into the antibiotic and ARG profiles in large-scale chicken farms with different rearing strategies and demonstrate a preliminary view of the performance of antibiotic reduction actions in China.

Fate of micropollutants in struvite production from swine wastewater with sacrificial magnesium anode

Struvite recovery shows significant potential for simultaneously recovering nitrogen (N) and phosphorus (P) from swine wastewater but is challenged by the occurrence and transformation of antibiotic residuals. Electrochemically mediated struvite precipitation with sacrificial magnesium anode (EMSP-Mg) is promising due to its automation and chemical-free merits. However, the fate of antibiotics remains underexplored. We investigated the behavior of sulfadiazine (SD), an antibiotic frequently detected but less studied than others within the EMSP-Mg system. Significantly less SD (≤ 5%) was co-precipitated with recovered struvite in EMSP-Mg than conventional chemical struvite precipitation (CSP) processes (15.0 to 50.0%). The reduced SD accumulation in struvite recovered via EMSP was associated with increased pH and electric potential differences, which likely enhanced the electrostatic repulsion between SD and struvite. In contrast, the typical strategies used in enhancing P removal in the EMSP-Mg system, including increasing the Mg/P ratio or the Mg-release rates, have shown negligible effects on SD adsorption. Furthermore, typical coexisting ions (Ca2+, Cl−, and HCO3−) inhibited SD adsorption onto recovered products. These results provide new insights into the interactions between antibiotics and struvite within the EMSP-Mg system, enhancing our understanding of antibiotic migration pathways and aiding the development of novel EMSP processes for cleaner struvite recovery.

Characteristics of chemical aged biochars and their adsorption behaviors for norfloxacin

The biochar after long-term application will inevitably undergo ageing, thus promoting or inhibiting its remediation efficiency for antibiotics due to the differences in feedstocks and ageing process. To elucidate the adsorption performance and mechanisms of norfloxacin (NOR) by the different aged biochars, a batch of fresh biochars (BCs) prepared from Platanus orientalis Linn. leaf at 400 and 700 ℃ were aged by H2O2 (HBCs) and KMnO4 (MBCs) to simulate the natural ageing process. Compared with BCs, HBCs and MBCs showed larger specific surface area, richer micropores and O-containing functional groups. The maximum adsorption capacities of MBCs (43.96–49.32 mg g−1) and HBCs (18.38–19.79 mg g−1) were generally greater than those of BCs (16.44–20.01 mg g−1), which was resulted from the enhanced pore filling and hydrogen bonds. Furthermore, MBCs introduced with MnOx showed higher adsorption performances than those of HBCs, mainly due to the surface complexation. Na+ and Ca2+ inhibited the NOR adsorption by all the aged biochars. Humic acid and citric acid enhanced NOR adsorption at pH 3.0 but weakened the adsorption at pH 7.0. Furthermore, the NOR removal efficiency of BCs and aged biochars in the natural waters were reduced by 20–25 % and 6–17 %, respectively, showing the excellent sorption performance of the aged biochars. Our findings clarified the enhanced adsorption capacities of NOR by the aged biochar and the potential adsorption mechanism, providing the evidence for predicting the environmental fate of antibiotics in water environment and designing the functional biochars for controlling antibiotic pollution.

Land use and spatial contiguity are key driven factors of antibiotic multimedia patterns in the megacity river network

The widespread spread of antibiotics in the environment poses a growing threat to human health. This study investigated the distribution and fate of antibiotics concerning land use characteristics, hydrological conditions, and spatial contiguity within a megacity river network. Temporally, the average concentrations of twenty antibiotics in water (354 ng/L), suspended particulate matter (SPM) (46 ng/L), and sediment (151 ng/g) during dry season were notably higher than that in the corresponding environment media (water: 127 ng/L, SPM: 2 ng/L, and sediment: 49 ng/g) during the wet season. Moreover, the inter-annual variation of antibiotics in water showed a decreasing trend. Spatially, substantial antibiotic contamination was observed in a human-intensive watershed, particularly in the upstream and central city sections. The macrolides in water were most affected by land use types and hydrological processes. Antibiotic contamination in water exhibited a stronger spatial autocorrelation compared to other media. Nevertheless, the interconnectedness of antibiotic contamination in sediments during the wet season warrants attention, and relevant authorities should enhance environmental monitoring in watersheds with pollution hotspots. Certain antibiotics, such as sulfamethoxazole, enrofloxacin, and florfenicol, were transported via urban rivers to the ocean, potentially posing environmental risks to coastal water quality. Local sources accounted for the predominant portion (>50 %) of most antibiotics in various media. The correlation distances of antibiotics in waters during the wet season could screen ecological risk prioritization in aquatic environments.

Sulfate radical-dominated colorimetric sensing platform for ultrafast and portable monitoring of tetracycline in environment

Tetracycline (TC) is one of the most frequently detected antibiotics in environmental. Monitoring the concentration of TC is essential for understanding environmental fate of antibiotics. In this work, bimetallic N-doped carbon catalysts of M/Co@NC (M= Ni, Mn, Cu, Zn, Fe) were rationally synthesized via molten salt-assisted pyrolysis. The distinctive synergistic interplay between Cu and Co endowed Cu/Co@NC superior activation capacity for peroxymonosulphate (PMS). Inspired by the advantages of sulfate radical (SO4•−), an original colorimetric sensing platform was developed by using PMS as oxidant and rhodamine B (RhB) as chromogenic agents. Notably, this platform achieved an ultrafast visual reaction within 60 s and exhibited broad pH applicability under pH 2–9. Then, leveraging a competitive inhibition mechanism, dual-mode colorimetric and fluorescent sensing platforms were established for TC detection under neutral conditions. The fluorescent platform exhibited a reliable liner range from 0.001 to 15 μg/mL with limit of detection of 2 ng/mL. Excellent selectivity was found for TC even among different antibiotics. Theoretical calculations elucidated that the superior selectivity arises from a higher electrophilic attack (f-) of TC. Based on these finding, a smartphone-assisted test strip was developed and successfully deployed for the rapid monitoring of TC in practical water samples. This work not only synthesized an efficient PMS activator, but also proposed a novel visual sensing mode with ultrafast detection times, wide pH applicability and portable operation.

Indirect Impact of Eutrophication on Occurrence, Air-Water Exchange, and Vertical Sinking Fluxes of Antibiotics in a Subtropical River.

A significant challenge that warrants attention is the influence of eutrophication on the biogeochemical cycle of emerging contaminants (ECs) in aquatic environments. Antibiotics pollution in the eutrophic Pearl River in South China was examined to offer new insights into the effects of eutrophication on the occurrence, air-water exchange fluxes (Fair-water), and vertical sinking fluxes (Fsinking) of antibiotics. Antibiotics transferred to the atmosphere primarily through aerosolization controlled by phytoplankton biomass and significant spatiotemporal variations were observed in the Fair-water of individual antibiotics throughout all sites and seasons. The Fsinking of ∑AB14 (defined as a summary of 14 antibiotics) was 750.46 ± 283.19, 242.71 ± 122.87, and 346.74 ± 249.52 ng of m-2 d-1 in spring, summer, and winter seasons. Eutrophication indirectly led to an elevated pH, which reduced seasonal Fair-water of antibiotics, sediment aromaticity, and phytoplankton hydrophobicity, thereby decreasing antibiotic accumulation in sediments and phytoplankton. Negative correlations were further found between Fsinking and the water column daily loss of antibiotics with phytoplankton biomass. The novelty of this study is to provide new complementary knowledge for the regulation mechanisms of antibiotics by phytoplankton biological pump, offering novel perspectives and approaches to understanding the coupling between eutrophication and migration and fate of antibiotics in a subtropical eutrophic river.

Antibiotics Uptake from Soil and Translocation in the Plants - Meta-analysis.

Antibiotics reach agricultural soils via fertilization with manure and biosolids as well as irrigation withwastewater and have the potential to be taken up by growing crops. The fate of antibiotics in terms of uptakefrom soil to plants, as well as translocation from root to leaves, is determined by a combination of antibiotic'sphysio-chemical (e.g. speciation, lipophilicity), soil (e.g. organic carbon content, pH) and plant (e.g.transpiration rates) characteristics. In this meta-analysis, a literature search was executed to obtain an overview of antibiotic uptake to plants, with an aim to identify uptake and translocation patterns of different antibiotic classes. Overall, we found that higher uptake of tetracyclines to plant leaves was observed compared to sulfonamides. Differences were also observed in translocation within the plants, where tetracyclines were found in roots and leaves with close to equal concentrations, while the sulfonamides represented a tendency to accumulate to the root fraction. The antibiotic's characteristics have a high influence on their fate, for example, the high water-solubility and uncharged speciation in typical agricultural soil pH ranges likely induces tetracycline uptake from soil and translocation in plant. Despite the advances in knowledge over the past decade, our meta-analysis indicated that the available research is focused on a limited number of analytes and antibiotic classes. Furthermore, fastgrowing plant species (e.g. spinach, lettuce, and radish) are overly represented in studies compared to crop species with higher significance for human food sources (e.g. corn, wheat, and potato), requiring more attention in future research.

Goethite-Bound Copper Controls the Fate of Antibiotics in Aquatic Environments

Goethite-Bound Copper Controls the Fate of Antibiotics in Aquatic Environments

Microbial phylogenetic divergence between surface-water and sedimentary ecosystems drove the resistome profiles

Antibiotic pollution and the evolution of antibiotic resistance genes (ARGs) are increasingly viewed as major threats to both ecosystem security and human health, and have drawn attention. This study investigated the fate of antibiotics in aqueous and sedimentary substrates and the impact of ecosystem shifts between water and sedimentary phases on resistome profiles. The findings indicated notable variations in the concentration and distribution patterns of antibiotics across various environmental phases. Based on the partition coefficient (Kd), the total antibiotic concentration was significantly greater in the surface water (1405.45 ng/L; 49.5 %) compared to the suspended particulate matter (Kd = 0.64; 892.59 ng/g; 31.4 %) and sediment (Kd = 0.4; 542.64 ng/g; 19.1 %). However, the relative abundance of ARGs in surface water and sediment was disproportionate to the abundance of antibiotics concentration, and sediments were the predominant ARGs reservoirs. Phylogenetic divergence of the microbial communities between the surface water and the sedimentary ecosystems potentially played important roles in driving the ARGs profiles between the two distinctive ecosystems. ARGs of Clinical importance; including blaGES, MCR-7.1, ermB, tet(34), tet36, tetG-01, and sul2 were significantly increased in the surface water, while blaCTX-M-01, blaTEM, blaOXA10-01, blaVIM, tet(W/N/W), tetM02, and ermX were amplified in the sediments. cfxA was an endemic ARG in surface-water ecosystems while the endemic ARGs of the sedimentary ecosystems included aacC4, aadA9-02, blaCTX-M-04, blaIMP-01, blaIMP-02, bla-L1, penA, erm(36), ermC, ermT-01, msrA-01, pikR2, vgb-01, mexA, oprD, ttgB, and aac. These findings offer a valuable information for the identification of ARGs-specific high-risk reservoirs.

Fate of antibiotics and hormones during hydrothermal carbonization of poultry litter: degradation kinetics and toxicity assessment of filtrates and hydrochars

This study investigated degradation kinetics of five selected organic micropollutants (OMPs) present in poultry litter (namely: sulfadiazine, tetracycline, and doxycycline hyclate (antibiotics); estrone and 17-β-estradiol (hormones)) during hydrothermal carbonization (HTC) treatment as the temperature stepwise increased to 250 °C. All five pure OMPs were completely degraded before 250 °C was reached during the HTC process. Nevertheless, presence of poultry litter slowed down the degradation of OMPs. Through elemental mass balance calculation, it is noted that after 15 min (temperature less than 137 °C), 69–82% of organic carbon and 50–66% of organic nitrogen initially consisting part of the target antibiotics were fully mineralized. Both HTC filtrates and hydrochars obtained from poultry litter inhibited Escherichia coli and Bacillus subtilis growth. A combination of high salinity, high nutrients, dissolved organic carbon, and other ions in the filtrate as well as the adsorption of OMPs on hydrochars were probably the reason for the high toxicity.

Unraveling how Fe-Mn modified biochar mitigates sulfamonomethoxine in soil water: The activated biodegradation and hydroxyl radicals formation

This study indicated that the application of a novel Fe-Mn modified rice straw biochar (Fe/Mn-RS) as soil amendment facilitated the removal of sulfamonomethoxine (SMM) in soil water microcosms, primarily via activating degradation mechanism rather than adsorption. The similar enhancement on SMM removal did not occur using rice straw biochar (RS). Comparison of Fe/Mn-RS with RS showed that Fe/Mn-RS gains new physic-chemical properties such as abundant oxygenated C-centered persistent free radicals (PFRs). In the Fe/Mn-RS microcosms, the degradation contributed 79.5–83.8% of the total SMM removal, which was 1.28–1.70 times higher than that in the RS microcosms. Incubation experiments using sterilized and non-sterilized microcosms further revealed that Fe/Mn-RS triggered both the biodegradation and abiotic degradation of SMM. For abiotic degradation of SMM, the abundant •OH generation, induced by Fe/Mn-RS, was demonstrated to be the major contributor, according to EPR spectroscopy and free radical quenching experiments. Fenton-like bio-reaction occurred in this process where Fe (Ⅲ), Mn (Ⅲ) and Mn (Ⅳ) gained electrons, resulting in oxidative hydroxylation of SMM. This work provides new insights into the impacts of biochar on the fates of antibiotics in soil water and a potential solution for preventing antibiotic residues in agricultural soil becoming a non-point source pollutant.

Cu(II) inhibited the transport of tetracycline in porous media: role of complexation.

Tetracycline (TC) and Cu(II) coexist commonly in various waters, which may infiltrate into the subterranean environment through runoff and leaching, resulting in substantial ecological risks. However, the underlying mechanisms why Cu(II) affects the transport of TC in porous media remain to be further explored and supported by more evidence, especially the role of complexation. In this study, the transport of TC with coexisting Cu(II) was comprehensively explored with column experiments and density functional theory (DFT) calculation. At natural environmental concentrations, Cu(II) significantly inhibited the transport of TC in the quartz sand column. Cu(II) augmented the retention of TC in the column mainly via electrostatic force and complexation. The interaction between TC and TC-Cu complexes on the surface of SiO2 was investigated with first-principles calculations for the first time. There were strong van der Waals forces and coordination bonds on the surface of complexes and SiO2, leading to higher adsorption energy than that of TC and inhibiting its penetration. This study offers novel insights and theoretical framework for the transport of antibiotics in the presence of metal ions to better understand the fate of antibiotics in nature.

Enhanced photolysis of tetracycline by Zn(II): Role of complexation

Zn(II) is a necessary additive during antibiotic production and aquaculture, leading to the coexistence of Zn(II) and antibiotics in aquatic environment, especially in receiving waters of pharmaceutical and aquaculture wastewater. However, the roles of Zn(II) in the photochemical behavior of antibiotics are still not clear, which limits the understanding of the fate of antibiotic in nature. In this study, tetracycline (TC) was selected as typical antibiotic to evaluate the effect of Zn(II) on antibiotic photolysis. The removal of TC was accelerated by 22.75 % with TC:Zn(II) molar ratio at 1:5. The mechanism of Zn(II)-induced TC photolysis was explored via reactive oxygen species (ROS) analysis and density functional theory (DFT) calculation for the first time. Zn(II) could enhance the formation of TC excited states and further produce more singlet oxygen (12.54 % higher than control group) to promote indirect photolysis. Besides, Zn(II) could react with TC via complexation, and the complex was more vulnerable to attack by reactive oxygen species due to more active sites. Furthermore, the structure and toxicity of intermediates were identified with mass spectrometer, T.E.S.T. and ECOSAR software. Zn(II) hardly changed the degradation path of TC, and TC was mainly degraded via ring opening, demethylation, deamidation, and hydrogen abstraction with more toxic intermediates than the parent molecule. This work is significant to better understand the environmental fate of antibiotics, and also provides new insight into wastewater treatment in the pharmaceutical and aquaculture industry.

Occurrence and fate of antibiotics and ARGs in a wastewater treatment plant with JHB process in Guangzhou, South China: Removal performance, interaction and host analysis

Wastewater treatment plants (WWTPs) are recognized as sinks for antibiotics and sources of antibiotic resistance genes (ARGs). Thus, it is crucial to understand the occurrence and fate of antibiotics and ARGs in each treatment unit to propose an optimal regulation strategy for pollution control. In this study, the occurrence and fate of antibiotics and ARGs in a WWTP from Guangzhou, southern China with Johannesburg (JHB) process, a common WWTP treatment technique in China, were investigated. Occurrence and fate of a total of 17 common antibiotics and 14 ARGs types were determined in each treatment unit in the WWTP. The contribution of each treatment unit to the total removal efficiency of antibiotics and ARGs in the WWTP were investigated. Although a high removal rate (95.32 %) was observed for total antibiotics, risk quotient (RQ) analysis showed that chloramphenicol in effluent still presented notable ecological risk. We further found that disinfection dramatically increased ARGs abundance and risk of horizontal gene transfer (HGT). Contribution of various environmental factors to microbial community structure and ARGs variation were also quantified with variation partitioning analysis (VPA). Co-occurrence network analysis further revealed the potential hosts of ARGs. This study contributed to a specific understanding of the fate of antibiotics and ARGs within the WWTP with JHB process and provided insight into the removal of antibiotics and ARGs in the wastewater.

Highly porous NiFe-mixed metal oxides derived from calcinated layered double hydroxide for efficient antibiotics removal

Tetracycline (TC), a widely employed broad-spectrum antibiotic with global prevalence, possesses the ability to infiltrate soil matrices and potentially reach groundwater systems, thereby posing a consequential human health risk. To address this concern, a novel NiFe-mixed metal oxides (MMO) composite was synthesized and employed within quartz sand as a strategic measure to regulate the downward migration of TC. In-depth investigations of TC transport behavior in quartz sand, complemented by NiFe-MMO, were conducted via a series of rigorous batch and saturation-filled column experiments. The impacts of NiFe-MMO dosage, ionic strength, cationic types, solution pH, and flow rates on TC transport were systematically and comprehensively scrutinized. Our findings reveal that even minute quantities of NiFe-MMO prompt substantial TC adsorption, facilitated by electrostatic interactions and surface complexation, notably in low-concentration background solutions. Additionally, the presence of Ca2+ engenders a bridging effect, further enhancing TC adsorption onto the sand. These significant observations bear far-reaching implications in elucidating the fate of antibiotics within the intricate interplay of soil and groundwater domains. The strategic amalgamation of NiFe-MMO and quartz sand offers innovative prospects for managing TC dissemination, thereby augmenting endeavors toward sustainable environmental protection.

Simultaneous adsorption and biodegradation of oxytetracycline in wastewater by Mycolicibacterium sp. immobilized on magnetic biochar

Due to the adverse effects of long-term oxytetracycline (OTC) residues in aquatic environments, an effective treatment is urgently needed. Immobilized microbial technology has been widely explored in the treatment of various organic pollutants in aquatic environments with its excellent environmental adaptability. Nevertheless, studies on its application in the removal of antibiotics are relatively scarce and not in sufficient depth. Only a few studies have further investigated the final fate of antibiotics in the immobilized bacteria system. In this study, a novel kind of OTC-degrading bacteria Mycolicibacterium sp. was immobilized on straw biochar and magnetic biochar, respectively. Magnetic biochar was proved to be a more satisfactory immobilization carrier due to its superior property and the advantage of easy recycling. Compared with free bacteria, immobilized bacteria had stronger environmental adaptability under different OTC concentrations, pH, and heavy metal ions. After 5 cycles, immobilized bacteria could still remove 71.8% of OTC, indicating that it had a stable recyclability. Besides, OTC in real swine wastewater was completely removed by immobilized bacteria within 2 days. The results of FTIR showed that bacteria were successfully immobilized on biochar and O–H, N–H, and C–N groups might be involved in the removal of OTC. The fate analysis indicated that OTC was removed by simultaneous adsorption and biodegradation, while biodegradation (92.8%) played a dominant role in the immobilized bacteria system. Meanwhile, the amount of adsorbed OTC (7.20%) was rather small, which could effectively decrease the secondary pollution of OTC. At last, new degradation pathways of OTC were proposed. This study provides an eco-friendly and effective approach to remedy OTC pollution in wastewater.