No abstract

No abstract

Antibiotic resistance is a serious global threat for public health. Considering the high abundance of cell-free DNA encoding antibiotic resistance genes (ARGs) in both clinical and environmental settings, natural transformation is an important horizontal gene transfer pathway to transmit antibiotic resistance. It is acknowledged that antibiotics are key drivers for disseminating antibiotic resistance, yet the contributions of non-antibiotic pharmaceuticals on transformation of ARGs are overlooked. In this study, we report that some commonly consumed non-antibiotic pharmaceuticals, at clinically and environmentally relevant concentrations, significantly facilitated the spread of antibiotic resistance through the uptake of exogenous ARGs. This included nonsteroidal anti-inflammatories, ibuprofen, naproxen, diclofenac, the lipid-lowering drug, gemfibrozil, and the β-blocker propranolol. Based on the results of flow cytometry, whole-genome RNA sequencing and proteomic analysis, the enhanced transformation of ARGs was affiliated with promoted bacterial competence, enhanced stress levels, over-produced reactive oxygen species and increased cell membrane permeability. In addition, a mathematical model was proposed and calibrated to predict the dynamics of transformation during exposure to non-antibiotic pharmaceuticals. Given the high consumption of non-antibiotic pharmaceuticals, these findings reveal new concerns regarding antibiotic resistance dissemination exacerbated by non-antibiotic pharmaceuticals.

Antibiotic resistance is a global threat to public health. The use of antibiotics at sub-inhibitory concentrations has been recognized as an important factor in disseminating antibiotic resistance via horizontal gene transfer. Although non-antibiotic, human-targeted pharmaceuticals are widely used by society (95% of the pharmaceuticals market), the potential contribution to the spread of antibiotic resistance is not clear. Here, we report that commonly consumed, non-antibiotic pharmaceuticals, including nonsteroidal anti-inflammatories (ibuprofen, naproxen, diclofenac), a lipid-lowering drug (gemfibrozil), and a β-blocker (propranolol), at clinically and environmentally relevant concentrations, significantly accelerated the dissemination of antibiotic resistance via plasmid-borne bacterial conjugation. Various indicators were used to study the bacterial response to these drugs, including monitoring reactive oxygen species (ROS) and cell membrane permeability by flow cytometry, cell arrangement, and whole-genome RNA and protein sequencing. Enhanced conjugation correlated well with increased production of ROS and cell membrane permeability. Additionally, these non-antibiotic pharmaceuticals induced responses similar to those detected when bacteria are exposed to antibiotics, such as inducing the SOS response and enhancing efflux pumps. The findings advance understanding of the transfer of antibiotic resistance genes, emphasizing the concern that non-antibiotic, human-targeted pharmaceuticals enhance the spread of antibiotic resistance among bacterial populations.

A pressurized chemical-looping combustion combined cycle (PCLC) system is proposed for solid fuels combustion with potential high system efficiency, improving the fuel conversion and lowering the cost for CO 2 sequestration. In this study, pressurized CLC of coal with Companhia Valedo Rio Doce (CVRD) iron ore was investigated in a laboratory fixed bed reactor focusing on cyclic performance. CVRD iron ore particles were exposed alternately for 20 cycles to reduction by 0.4 g of Chinese Xuzhou bituminous coal gasified with 87% steam/N 2 mixture and oxidation with 5% O 2 in N 2 at 970 °C at atmospheric pressure (0.1 MPa) and a typical elevated pressure of 0.5 MPa. With increasing number of redox cycles, more pyrolysis gases are oxidized by the oxygen carrier. At elevated pressure, the char gasification is intensified with negligible gasification intermediate products released. The CO 2 fraction increases from 80% to approximate 90% after 10 cycles at atmospheric pressure. At elevated pressures, the average CO 2 fraction stabilizes at 95.75%, approximate to the equilibrium value. The carbon conversion at 0.1 MPa and 0.5 MPa is 76.48 and 84.65%, respectively, and maintains approximately the same during the cycles because excessive steam gasification agent used in this study. The oxygen carrier conversion determined from the oxygen mass balance verifies that reduction level increases with the cycle number. The physical and chemical properties of oxygen carrier particles were characterized. X-ray diffraction (XRD) analysis verifies the extent of reduction level increases with cycles. No detectable formation of compound of iron oxide and coal ash was observed. Scanning electron microscope (SEM) analyses show that the iron ore particles become porous and that more pores formed with cycles. Agglomeration of particles was not observed in all experiments at both pressures. Energy-dispersive X-ray spectroscopy (EDX) analysis show an increasing amount of coal ash on the oxygen carrier particles with increasing numbers of cycles. Pore size analyses show that the oxygen carrier particles maintained mesopores for both atmospheric and elevated pressure. The increase of both surface area and pore volume illustrates that the particles become more porous with redox cycles. This study show that pressurized CLC of coal is promising and a low-cost iron ore-based oxygen carrier may be suitable for pressurized CLC of coal.