ABSTRACT
Ubiquitous distribution of pharmaceutical contaminants in environment has caused unexpected adverse effects on ecological organisms; however, how microorganisms recover from their toxicities remains largely unknown. In this study, we comprehensively investigated the effect of a representative pollutant, doxylamine (DOX) on a freshwater microalgal species, Chlorella sp. by analyzing the growth patterns, biochemical changes (total chlorophyll, carotenoid, carbohydrate, protein, and antioxidant enzymes), and transcriptomics. We found toxicity of DOX on Chlorella sp. was mainly caused by disrupting synthesis of ribosomes in nucleolus, and r/t RNA binding and processing. Intriguingly, additional bicarbonate enhanced the toxicity of DOX with decreasing the half-maximum effective concentrations from 15.34 mg L-1 to 4.63 mg L-1, which can be caused by inhibiting fatty acid oxidation and amino acid metabolism. Microalgal cells can recover from this stress via upregulating antioxidant enzymatic activities to neutralize oxidative stresses, and photosynthetic pathways and nitrogen metabolism to supply more energies and cellular signaling molecules. This study extended our understanding on how microalgae can recover from chemical toxicity, and also emphasized the effect of environmental factors on the toxicity of these contaminants on aquatic microorganisms.
Subject(s)
Chlorella , Water Pollutants, Chemical , Chlorella/drug effects , Chlorella/metabolism , Chlorella/genetics , Water Pollutants, Chemical/toxicity , Transcriptome/drug effects , Microalgae/drug effects , Microalgae/genetics , Chlorophyll/metabolism , Photosynthesis/drug effects , Oxidative Stress/drug effects , Carotenoids/metabolism , Antioxidants/metabolismABSTRACT
Whether bisphenols, as plasticizers, can influence bacterial uptake of antibiotic resistance genes (ARGs) in natural environment, as well as the underlying mechanism remains largely unknown. Our results showed that four commonly used bisphenols (bisphenol A, S, F, and AF) at their environmental relative concentrations can significantly promote transmission of ARGs by 2.97-3.56 times in Acinetobacter baylyi ADP1. Intriguingly, we observed ADP1 acquired resistance by integrating plasmids uptake and cellular metabolic adaptations other than through reactive oxygen species mediated pathway. Metabolic adaptations including upregulation of capsules polysaccharide biosynthesis and intracellularly metabolic enzymes, which enabled formation of thicker capsules for capturing free plasmids, and degradation of accumulated compounds. Simultaneously, genes encoding DNA uptake and translocation machinery were incorporated to enhance natural transformation of antibiotic resistance carrying plasmids. We further exposed aquatic fish to bisphenols for 120 days to monitor their long-term effects in aquatic environment, which showed that intestinal bacteria communities were dominated by a drug resistant microbiome. Our study provides new insight into the mechanism of enhanced natural transformation of ARGs by bisphenols, and highlights the investigations for unexpectedly-elevated antibiotic-resistant risks by structurally related environmental chemicals.
Subject(s)
Acinetobacter , Benzhydryl Compounds , Phenols , Sulfones , Phenols/toxicity , Phenols/metabolism , Acinetobacter/drug effects , Acinetobacter/genetics , Acinetobacter/metabolism , Benzhydryl Compounds/toxicity , Benzhydryl Compounds/metabolism , Animals , Plasmids , Drug Resistance, Bacterial/genetics , Drug Resistance, Microbial/genetics , Water Pollutants, Chemical/toxicity , Water Pollutants, Chemical/metabolism , Adaptation, Physiological , Plasticizers/toxicity , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/toxicityABSTRACT
Reclaimed water (RW) has been extensively used for irrigation in agriculture, yet the occurrence of antibiotics in real RW, and their toxicity, uptake dynamics and metabolic fate still needs comprehensive exploration. In this study, we investigated the residual concentrations of nineteen antibiotics in the RW from four wastewater treatment plants, and determined their toxicity on plant at environment-relevant concentration. Total found concentrations of these antibiotics ranged from 623.66 ng L-1 to 1536.96 ng L-1, which decreased 10.3 and 19.4 % of roots' length and weight. Uptake dynamics analysis of the most hazardous antibiotic, norfloxacin (NFX) showed increasing amounts in the roots and leaves up to 3087.71 µg g-1. Ryegrass also can remove >80 % of 100 µg L-1 NFX being achieved by biodegradation through ring cleavage, decarboxylation, defluorination, hydrogenation, methylation and oxidation. Toxicity assessment of the identified byproducts showed their more toxic effect on fish, daphnia and algae. This study extended our understanding of the fate of antibiotics in plants during irrigation with reclaimed water, and emphasized its safety and pollutants' biomagnification concerns.
Subject(s)
Anti-Bacterial Agents , Lolium , Anti-Bacterial Agents/toxicity , Anti-Bacterial Agents/metabolism , Lolium/metabolism , Water/metabolism , Agriculture , Biological TransportABSTRACT
The preeminence of sulfonamide drug resistance genes in food waste (FW) and the increased utilization of high-strength organic FW in anaerobic digestion (AD) to enhance methane production have raised severe public health concerns in wastewater treatment plants worldwide. In this regard, the dissemination patterns of different sulfonamide resistance genes (sul1 and sul2) and their impact on the digester core microbiota during AD of FW leachate (FWL) were evaluated. The presence of various sulfonamide antibiotics (SAs) in FWL digesters improved the final methane yield by 37 % during AD compared with FWL digesters without SAs. Microbial population shifts towards hydrolytic, acidogenic, and acetogenic bacteria in the phyla Actinobacteriota, Bacteroidota, Chloroflexi, Firmicutes, Proteobacteria, and Synergistota occurred due to SA induced substrate digestion and absorption through active transport; butanoate, propanoate, and pyruvate metabolism; glycolysis; gluconeogenesis; the citrate cycle; and pentose phosphate pathway. The initial dominance of Methanosaeta (89-96 %) declined to 47-53 % as AD progressed and shifted towards Methanosarcina (40 %) in digesters with the highest SA concentrations at the end of AD. Dissemination of sul1 depended on class 1 integron gene (intl1)-based horizontal gene transfer to pathogenic members of Chloroflexi, Firmicutes, and Patescibacteria, whereas sul2 was transmitted to Synergistota independent of intl1. Low susceptibility and ability to utilize SAs during methanogenesis shielded methanogenic archaea against selection pressure, thus preventing them from interacting with sul or intl1 genes, thereby minimizing the risk of antibiotic resistance development. The observed emergence of cationic antimicrobial peptide, vancomycin, and ß-lactam resistance in the core microbiota during AD of FWL in the presence of SAs suggests that multidrug resistance caused by bacterial transformation could lead to an increase in the environmental resistome through wastewater sludge treatment.
Subject(s)
Chloroflexi , Microbiota , Refuse Disposal , Anaerobiosis , Food , Microbiota/genetics , Sewage/microbiology , Bacteria/metabolism , Sulfanilamide , Anti-Bacterial Agents/metabolism , Firmicutes , Methane/metabolism , BioreactorsABSTRACT
Bisphenols are frequently found in the environment and have been of emerging concern because of their adverse effects on aquatic animals and humans. In this study, we demonstrated that bisphenol A, S, and F (BPA, BPS, BPF) at environmental concentrations induced cardiotoxicity in zebrafish embryos. BPA decreased heart rate at 96 hpf (hours post fertilization) and increased the distance between the sinus venosus (SV) and bulbus arteriosus (BA), in zebrafish. BPF promoted heart pumping and stroke volume, shortened the SV-BAdistance, and increased body weight. Furthermore, we found that BPA increased the expression of the dio3b, thrß, and myh7 genes but decreased the transcription of dio2. In contrast, BPF downregulated the expression of myh7 but upregulated that of thrß. Molecular docking results showed that both BPA and BPF are predicted to bind tightly to the active pockets of zebrafish THRß with affinities of -4.7 and -4.77 kcal/mol, respectively. However, BPS did not significantly affect dio3b, thrß, and myh7 transcription and had a higher affinity for zebrafish THRß (-2.13 kcal/mol). These findings suggest that although BPA, BPS, and BPF have similar structures, they may induce cardiotoxicity through different molecular mechanisms involving thyroid hormone systems. This investigation provides novel insights into the potential mechanism of cardiotoxicity from the perspective of thyroid disruption and offer a cautionary role for the use of BPA substitution.
Subject(s)
Water Pollutants, Chemical , Zebrafish , Animals , Humans , Zebrafish/metabolism , Receptors, Thyroid Hormone/metabolism , Cardiotoxicity , Molecular Docking Simulation , Water Pollutants, Chemical/toxicity , Benzhydryl Compounds/toxicityABSTRACT
Cometabolism has shown great potential in increasing the engineering feasibility of microalgae-based biotechnologies for the aerobic treatment of antibiotics-polluted wastewaters. Yet, the underlying mechanisms involved in improved microalgal performance remain unknown. In this study, we incorporated transcriptomics, gene network analysis, and enzymatic activities with cometabolic pathways of tetracycline (TC) by Chlorella pyrenoidosa to identify the key driving factors. The results demonstrated that cometabolism constructed a metabolic enzymes-photosynthetic machinery to improve the electron transport chain and activities of catalytic enzymes, which resulted in subsequent 100% removal of TC. Coupling formation dynamics of the intermediates with roles of identified metabolic enzymes, degradation of TC can be induced by de/hydroxylation, de/hydrogenation, bond-cleavage, decarboxylation, and deamination. Evaluation of 18 antibiotics' removal in reclaimed water showed cometabolism decreased the total concentrations of these antibiotics from 495.54 ng L-1 to 221.80 ng L-1. Our findings not only highlight the application potential of cometabolism in increasing engineering feasibility of microalgal degradation of antibiotics from wastewaters, but also provide the unique insights into unraveling the "black-box" of cometabolisms in aerobic biodegradation.
Subject(s)
Chlorella , Microalgae , Wastewater , Tetracycline , Anti-Bacterial AgentsABSTRACT
Antibiotic contamination in the environment has significant adverse effects on benthic microorganisms, which causes dysfunction of normal ecological processes. However, in-depth molecular mechanisms underlying the potential ecological impacts of these emerging pollutants are poorly understood. In this study, metabolic perturbations in a freshwater microalga, Desmodesmus quadricauda by sulfacetamide (SFM) were investigated using transcriptomics. The results found 28 genes in the tricarboxylic acid cycle and oxidative phosphorolysis pathways were significantly downregulated by 3.97 to 6.07, and 2.47 to 5.99 folds by 0.1 and 1 mg L-1 SFM, respectively. These results indicated that SFM disrupted the microalgal cellular activities through inhibition of energy metabolism. Whilst, the upregulated genes have been most enriched in porphyrin and chlorophyll metabolism (hemE, hemL, hemY, chlD, chlP, PAO, and CAO), and arachidonic acid metabolism (GGT1_5 and gpx). Expression of these genes was significantly upregulated by up to 3.36 times for tolerance against SFM. Moreover, the genes encoding decarboxylase, oxidoreductases, α-amylase, hydrolases, O-acetyltransferase, and lyase were upregulated by >2 folds, which can induce di/hydroxylation, decarboxylation, bond cleavage and deamination. These findings provide insights into the molecular mechanisms of the ecotoxicological effects of antibiotics on microalgae, and supply useful information for their environmental risk assessment and management.
Subject(s)
Microalgae , Sulfacetamide , Biodegradation, Environmental , Fresh Water , TranscriptomeABSTRACT
Plants are readily exposed to the antibiotics residues in reclaimed water indicating an urgent need to comprehensively analyze their ecotoxicological effects and fate of these emerging contaminants. Here, we unraveled the dissemination of enrofloxacin (ENR) in a pasture grass, Lolium perenne L., and identified multistage defense systems as its adaptation mechanism. Uptaken concentrations of ENR ranged from 1.28 to 246.60 µg g-1 with bioconcentration factors (BCF) upto 15.13, and translocation factors (TF) upto 0.332. The antioxidant enzymatic activities such as superoxide dismutase, peroxidase, and catalase were increased by upto 115%. Further transcriptomics demonstrated that differentially expressed genes (DEGs) involved in glycolysis, tricarboxylic acid (TCA) cycle, oxidative phosphorylation, and glutathione metabolism were significantly up-regulated by 1.56-5.93, 3-7 and 1.04-6.42 times, respectively; whilst, the DEGs in nitrogen and sulfur metabolism pathways were significantly up-regulated by 1.06-5.64 and 2.64-3.54 folds. These processes can supply energy, signaling molecules, and antioxidants for detoxification of ENR in ryegrass. Such results provide understanding into fasting grass adaptability to antibiotics by enhancing the key protective pathways under organic pollutant stresses in environments.
Subject(s)
Lolium , Antioxidants/metabolism , Bioaccumulation , Enrofloxacin , Lolium/genetics , Lolium/metabolism , Oxidative StressABSTRACT
Contamination of fluoroquinolones (FQs) are of emerging concerns because of their adverse effects on environment and humans. This study investigated the ecotoxicological effects, biodegradation, and multiple metabolic pathways of a frequently found FQ, enrofloxacin (ENR) by ryegrass (Lolium perenne L.). Key metabolic genes for driving the metabolism of ENR have been identified using transcriptome profiling of L. perenne and gene network analysis. Toxicity of ENR on ryegrass has been evaluated according to the morphological changes, lipid peroxidation content, and antioxidant enzymatic activities. Moreover, there was 94.33%, 71.58%, 57.22%, and 55.23% removal of 1, 10, 50 and 100 mg L-1 ENR, respectively, which was mainly achieved by biodegradation according to the mass balance. A biodegradation pathway has been proposed by incorporating mass spectrums of extracted ENR intermediates with their formation dynamics. Analysis of differentially expressed genes (DEGs) and their network unraveled that the genes encoding monooxygenase, oxidative carboxylase, methyltransferase, lyase, hydroxylase, dehydrogenase, and peroxidase were the key functional genes. These enzymes can induce di/hydroxylation, decarboxylation, methylation, and bond and ring cleavage of ENR for its effective degradation. This study demonstrated that ryegrass can be used for efficient treatment of ENR polluted water and extended the understanding of the molecular mechanism of antibiotics' biodegradation in plants.
Subject(s)
Lolium , Biodegradation, Environmental , Enrofloxacin , Fluoroquinolones , Humans , Lolium/genetics , Metabolic Networks and PathwaysABSTRACT
The potential of Iris pseudacorus and the associated periphytic biofilm for biodegradation of two common pharmaceutical contaminants (PCs) in urban wastewater was assessed individually and in consortium. An enhanced removal for sulfamethoxazole (SMX) was achieved in consortium (59%) compared to individual sets of I. pseudacorus (50%) and periphytic biofilm (7%) at concentration of 5 mg L-1. Conversely, individual sets of periphytic biofilm (77%) outperformed removal of doxylamine succinate (DOX) compared to individual sets of I. pseudacorus (59%) and consortium (67%) at concentration of 1 mg L-1. Enhanced relative abundance of microflora containing microalgae (Sellaphora, Achnanthidium), rhizobacteria (Acidibacter, Azoarcus, Thioalkalivibrio), and fungi (Serendipita) in periphytic biofilm was observed after treatment. SMX treatment for five days elevated cytochrome P450 enzymes' expressions, including aniline hydroxylase (48%) and aminopyrine N-demethylase (54%) in the periphytic biofilm. Nevertheless, I. pseudacorus showed 175% elevation of aniline hydroxylase along with other biotransformation enzymes, such as peroxidase (629%), glutathione S-transferase (514%), and dichloroindophenol reductase (840%). A floating bed phytoreactor planted with I. pseudacorus and the periphytic biofilm consortium removed 67% SMX and 72% DOX in secondary wastewater effluent. Thus, the implementation of this strategy in constructed wetland-based treatment could be beneficial for managing effluents containing PCs.
Subject(s)
Iris Plant , Pharmaceutical Preparations , Biofilms , Nitrogen/analysis , WastewaterABSTRACT
Bisphenol S (BPS) acts as a xenoestrogen and disturbs the female reproductive system; however, the underlying mechanism has not been elucidated. In this study, the effect of chronic BPS exposure (1 µg/L and 100 µg/L) on ovarian lipid metabolism in zebrafish was investigated to determine its influence on adult reproductive capacity and offspring development. The results showed that long-term (240 days) exposure to BPS induced lipid accumulation in the ovaries by promoting the transport of more lipids from the circulation to the ovaries and by upregulating triacylglycerol synthesis-related genes. Significantly increased expression of cpt2, acadm, acadl, and pparα, which are involved in ß-oxidation in the ovarian mitochondria, indicated that more energy was provided for oocyte maturation in exposed zebrafish ovaries. Thus, the proportion of full-grown stage oocytes in ovaries and egg reproduction were elevated at an accelerated rate, which earlier than normal reproductive cycle (8-10 days posts pawning). Moreover, the maternally BPS-exposed F1 embryos (2 h post-spawning, hpf) showed higher neutral lipid levels, impaired hatching capacity, and increased occurrence of larval deformities. All these findings demonstrated that stimulated lipid synthesis and ß-oxidation in zebrafish ovaries significantly contribute to BPS-induced oocyte precociousness with subsequent effects on the development of unexposed offspring. This study provides new insight into the impact of xenoestrogens on oviparous reproduction in females and offspring development from the perspective of ovarian lipid metabolism.
Subject(s)
Ovary , Zebrafish , Animals , Female , Lipid Metabolism , Oocytes , Phenols , Sulfones , Zebrafish/geneticsABSTRACT
Pharmaceutical contaminants in environment induce unexpected effects on ecological systems and human; thus, development of efficient technologies for their removal is immensely necessary. In this study, biodegradation and metabolic fate of a frequently found pharmaceutical contaminant, doxylamine by Typha angustifolia and Ipomoea aquatica was investigated. Microbial community of the plant rhizosphere has been identified to understand the important roles of the functional microbes. The plants reduced 48-80.5 % of doxylamine through hydrolysis/dehydroxylation and carbonylation/decarbonylation. A constructed phytobed co-planted with T. angustifolia and I. aquatica removed 77.3 %, 100 %, 83.67 %, and 61.13 % of chemical oxygen demand, total nitrogen, total phosphorus, and doxylamine respectively from real wastewater. High-throughput sequencing of soil and rhizosphere indicated that the phyla Proteobacteria, Bacteroidetes, Firmicutes, Planctomycetes, Actinobacteria, and Cyanobacteria dominated the microbial communities of the phytobed. Current study has demonstrated the applicability of the developed phytobeds for the treatment of doxylamine from municipal wastewater and provide a comprehensive understanding of its metabolism through plant and its rhizospheric microbial communities.
Subject(s)
Ipomoea , Microbiota , Typhaceae , Biodegradation, Environmental , Doxylamine , Humans , Rhizosphere , Soil Microbiology , WastewaterABSTRACT
Pharmaceutical contaminants (PCs) have been recognized as emerging contaminants causing unexpected consequences to environment and humans. There is an urgent need for development of efficient technologies to treat these PCs from water. The current study has investigated the removal capacity of a green microalgal species, Scenedesmus obliquus, for doxylamine, chemical oxygen demand (COD), and nutrients from real wastewater. Results have indicated that S. obliquus can grow well in the doxylamine-polluted wastewater with the achievement of 56, 78.5, 100, and 89% removal of doxylamine, COD, total nitrogen (TN), and total phosphorus (TP). Addition of 2 g L-1 bicarbonate enhanced the removal of doxylamine up to 63% and slightly inhibited the removal of COD. Decreased carbohydrate (28-26%) and increased protein content (30-33%) of the harvested biomass have been observed after cultivation in the wastewater. The current study has shown the feasibility of using microalgae-based biotechnologies for PC-contaminated wastewater.
ABSTRACT
Nanoparticles have been commercially used worldwide; however, there is a lack of information of their environmental impacts and ecotoxicity. In this study, the effect of cerium oxide nanoparticle (CeO2NP) on a green microalga Scenedesmus obliquus, and microalgal biodegradation of four sulfonamides (sulfamethazine, sulfamethoxazole, sulfadiazine, and sulfamethoxazole) was investigated. There is insignificant inhibition of microalgal growth induced by CeO2NP; however, it substantially influenced the expression of genes involved in key cellular metabolic activities of S. obliquus. For example, genes involved in photosynthetic activity (psbA) and energy production (ATPF0C) were downregulated with exposure to CeO2NP. The low concentrations of CeO2NP improved microalgal degradation of sulfonamides. This may be because of the upregulated genes encoding hydrogenase and oxidoreductase. The exploration of this study has provided a new understanding of the environmental impacts of CeO2NP on microalgae-based biotechnologies for treatment of wastewater containing emerging organic contaminants.
Subject(s)
Microalgae , Nanoparticles , Scenedesmus , Biomass , Cerium , SulfonamidesABSTRACT
Environmental contamination by benzophenone-3 has gained attention because of its frequent occurrence and adverse environmental impact. Studies investigating the toxicity and removal mechanisms, along with its degradation pathway in microalgae are still rare. In this study, the ecotoxicity of benzophenone-3 on Scenedesmus obliquus was assessed through dose-response test, risk quotient evaluation, and changes of microalgal biochemical characteristics and gene expression. The calculated risk quotients of benzophenone-3 were >1, implying its high environmental risk. Expression of the ATPF0C and Tas genes encoding ATP-synthase and oxidoreductase was significantly increased in S. obliquus after exposure to benzophenone-3, while that of Lhcb1 and HydA genes was reduced. When exposed to 0.1-3â¯mgâ¯L-1 benzophenone-3, 23-29 % removal was achieved by S. obliquus, which was induced by abiotic removal, bioadsorption, bioaccumulation and biodegradation. Metabolic fate analyses showed that biodegradation of benzophenone-3 was induced by hydroxylation, and methylation, forming less toxic intermediates according to the toxicity assessment of the identified products. This study provides a better understanding of the toxicity and metabolic mechanisms of benzophenone-3 in microalgae, demonstrating the potential application of microalgae in the remediation of benzophenone-3 contaminated wastewater.
Subject(s)
Benzophenones/metabolism , Benzophenones/toxicity , Scenedesmus/drug effects , Scenedesmus/metabolism , Water Pollutants, Chemical/metabolism , Water Pollutants, Chemical/toxicity , Benzophenones/chemistry , Gene Expression/drug effects , Hydroxylation , Kinetics , Methylation , Microalgae/drug effects , Microalgae/metabolism , Photosynthesis/drug effects , Risk Assessment , Water Pollutants, Chemical/chemistryABSTRACT
Pharmaceutical contamination in diverse water resources has been recognized as an emerging concern in environment because of its wide distribution and adverse effects on aquatic microorganisms and human health. Plant remediation with augmentation of microorganisms is a cost-effective and environmentally friendly approach toward an efficient treatment of pollutants, which can be easily applied in situ. (Bio)degradation of sulfamethazine (SMZ) by Iris pseudacorus, microalgal consortium, and plant-microalgal consortium was investigated. I. pseudacorus and microalgae could remove 63.5, and 25.8% of 1 mg SMZ L-1, respectively, whereas, the plant-microalgal consortium achieved 74% removal. The identified intermediates extracted after plant remediation indicated (bio)degradation of SMZ was through ring cleavage, hydroxylation, and dehydroxylation. Pigment content (total chlorophyll and carotenoid) of I. pseudacorus was significantly influenced by SMZ stress. A phytoreactor (20 L) constructed with I. pseudacorus achieved 30.0% and 71.3% removal of 1 mg SMZ L-1 from tap water and nutrient medium. This study has provided a better understanding of the metabolic mechanisms of SMZ in plants and showed the potential development of a plant-microalgal consortium as an advanced technology for treatment of these emerging contaminants. Graphical abstract.
Subject(s)
Biodegradation, Environmental , Microalgae/metabolism , Sulfamethazine/metabolism , Water Pollutants, Chemical/metabolism , Chlorophyll/metabolism , Humans , Iris Plant/growth & developmentABSTRACT
Plants serve as appropriate markers of worldwide pollution because they are present in almost every corner of the globe and bioaccumulate xenobiotic chemicals from their environment. The potential of a semi-aquatic plant, Ipomoea aquatica, to uptake and metabolize sulfamethoxazole (SMX) was investigated in this study. I. aquatica exhibited 100% removal of 0.05â¯mgâ¯L-1 SMX from synthetic media within 30â¯h. The I. aquatica achieved 93, 77 and 72% removal of SMX at 0.2, 0.5 and 1â¯mgâ¯L-1, respectively, after 48â¯h. This indicated that removal efficiency of I. aquatica was deteriorating at high concentrations of SMX. The chlorophyll and carotenoid content of I. aquatica was insignificantly influenced by SMX irrespective of its high concentration. Similarly, scanning electron microscopy (SEM) showed that exposure to SMX had an insignificant impact on morphology of the plant organelles. The mechanisms of removal by I. aquatica were explored by evaluating contributions of bioadsorption, bioaccumulation and biodegradation. There was negligible adsorption of SMX to plant roots. Accumulation of SMX within plant roots and stems was not observed; however, I. aquatica accumulated 17% of SMX in leaves. Thus, the major mechanism of elimination of SMX was biodegradation, which accounted for 82% removal of SMX. Gas chromatography-mass spectrometry (GC-MS) confirmed that I. aquatica biodegraded SMX into simpler compounds, and generated 4-aminophenol as its final product. A laboratory scale phytoreactor was used to investigate the application of I. aquatica in a simulated system, where it achieved 49% removal of SMX (0.2â¯mgâ¯L-1) in 10â¯d.
Subject(s)
Biodegradation, Environmental/drug effects , Ipomoea/metabolism , Sulfamethoxazole/metabolism , Water Pollutants, Chemical/chemistry , Water/chemistryABSTRACT
A comprehensive ecotoxicological evaluation of a sulfamethazine (SMZ) and sulfamethoxazole (SMX) mixture was conducted using an indicator microalga, Scenedesmus obliquus. The toxicological effects of this mixture were studied using microalgal growth patterns, biochemical characteristics (total chlorophyll, carotenoid, carbohydrate, fatty acid methyl ester), and elemental and Fourier-transform infrared spectroscopy analyses. The 96-h half maximal effective concentration (EC50) of the SMZ and SMX mixture was calculated to be 0.15â¯mgâ¯L-1 according to the dose-response curves obtained. The chlorophyll content decreased with elevated SMZ and SMX concentrations, while the carotenoid content initially increased and then decreased as concentration raised. The unsaturated fatty acid methyl esters (FAMEs) content was enhanced with higher SMZ and SMX concentrations, while that of saturated FAMEs simultaneously decreased due to SMZ and SMX stress. Elemental analyses showed an improved percentage of nitrogen and sulfur in the microalgal biomass as SMZ and SMX concentrations increased. The microalga S. obliquus was shown to biodegrade the chemicals tested and removed 31.4-62.3% of the 0.025-0.25â¯mg SMZ L-1 and 27.7-46.8% of the 0.025-0.25â¯mg SMX L-1 in the mixture after 12 days of cultivation. The greater biodegradation observed at higher SMZ and SMX concentrations indicates that microalgal degradation of SMZ and SMX could act as an efficient adaptive mechanism to antibiotics.
Subject(s)
Microalgae/drug effects , Scenedesmus/drug effects , Sulfamethazine/toxicity , Sulfamethoxazole/toxicity , Biodegradation, Environmental , Carbohydrates/analysis , Chlorophyll/metabolism , Dose-Response Relationship, Drug , Ecotoxicology/methods , Fatty Acids/metabolism , Microalgae/metabolism , Nitrogen/analysis , Nitrogen/metabolism , Scenedesmus/growth & development , Scenedesmus/metabolism , Sulfamethazine/administration & dosage , Sulfamethoxazole/administration & dosage , Sulfur/metabolism , Water Pollutants, Chemical/toxicityABSTRACT
This study investigated the environmental effects of two common emerging contaminants, sulfamethazine (SMZ) and sulfamethoxazole (SMX), and their mixture using a green microalga, Scenedesmus obliquus. The calculated EC50 values of SMZ, SMX, and their mixture (11:1 wt/wt) after 96 h were 1.23, 0.12, and 0.89 mg L-1, respectively. The toxicity of the mixture could be better predicted using a concentration addition model than an independent action model. The risk quotients of SMZ, SMX, and their mixture were >1 during the experiment, indicating their high potential risks on aquatic microorganisms. Despite their toxicity, S. obliquus exhibited 17.3% and 29.3% removal of 0.1 mg L-1 and 0.2 mg L-1 after 11 days of cultivation. The changes of SMZ and SMX removal were observed when combined, which showed a significantly improved removal of SMZ (up to 3.4 folds) with addition of SMX (0.2 mg L-1). The metabolic pathways of SMZ and SMX were proposed according to mass spectroscopic analysis, which showed six metabolites of SMX and seven intermediates of SMZ, formed as a result of ring cleavage, hydroxylation, methylation, nitrosation, and deamination.