This study found that bio-Pd nanoparticles could launch proton motive force (PMF)-mediated antibiotics efflux pump (AEP) to confer the detoxification capability on Citrobacter freundii, as evidenced by the highest sulfamethoxazole (SMX) specific degradation rate (81.7 μg L mg protein d) at high PMF (pH 6). The batch experiment and RT-qPCR results indicated that bio-Pd activated the AcrB efflux pump through upregulating the AEP transcriptional regulation factor ramA (2.7-3.1 times), which benefited the intra/extracellular respiration and ATP production/utilization. Path analysis revealed that the prosperity of metabolic activity and extracellular electron output capacity enabled SMX biodegradation, mainly through the electron redistribution and energy optimization with the formate dehydrogenase/hydrogenase based Short-chain (FDH/Hase-S-chain). The upregulation of hypE (2.7-8.6 times) and atpD (1.9-2.3 times) genes encoding the Hase respiratory chain and the F-type ATP synthase, respectively, further supports this mechanism. These novel findings provided a new strategy to improve the biodegradation efficiency of antibiotics wastewater.
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http://dx.doi.org/10.1016/j.biortech.2025.132300 | DOI Listing |
BMC Microbiol
March 2025
Department of Nosocomial Infection Control, The Clinical Laboratory, Clinical Microbiology Laboratory, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Background: The investigation into virulence factors, clinical and molecular characteristics, and resistance mechanisms of carbapenem-resistant Pseudomonas aeruginosa (CRPA) in pediatric populations is currently inadequate.
Purpose: This study aimed to investigate the virulence factors, clinical and molecular characteristics, and resistance mechanisms of 135 CRPA isolates in Shanghai, China.
Methods: Analysis of virulence-associated genes and multilocus sequence typing (MLST) provided epidemiological and molecular insights into the isolates.
J Hazard Mater
March 2025
The Key Lab of Pollution Control and Ecosystem Restoration in Industry Clusters, Ministry of Education, School of Environment and Energy, South China University of Technology, Guangzhou Higher Education Mega Centre, Guangzhou 510006, PR China. Electronic address:
Microbial remediation presents a promising approach for combating Cr(VI) pollutants, but the high toxicity of Cr(VI) bottlenecked its practical application. In this study, two-compartmental toxicokinetic (TK) model was constructed to analyze the dynamic Cr(VI) transformation/detoxifying inside Gram-negative/positive bacteria. Phosphomolybdic acid (PMo) could markedly promote the pumping rate (k) and distribution fraction f to accelerate the clearance of toxic substances in compartment two.
View Article and Find Full Text PDFAdv Healthc Mater
March 2025
Aix Marseille Université, INSERM, SSA, MCT, Marseille, 13385, France.
Efflux-mediated antibiotic resistance poses a significant global threat, affecting diverse bacterial species. Clinicians recognize the danger of efflux mechanisms during antibiotic treatment, yet precise diagnostic tools remain unavailable. The antibiogram currently infers abnormal efflux pump activity in clinical isolates, which is subsequently confirmed through transcriptomic or genomic analysis.
View Article and Find Full Text PDFPLoS One
March 2025
Departament de Genètica i de Microbiologia, Facultat de Biociènces, Universitat Autònoma de Barcelona (UAB) Campus Bellaterra, Barcelona, Spain.
Acinetobacter baumannii and Enterobacter cloacae are phylogenetically distant Gram-negative bacterial pathogens that represent significant challenges in healthcare settings due to their remarkable ability to acquire antimicrobial resistance. This study investigates one of the most important efflux pump systems in A. baumannii, AdeABC-AdeRS, and identifies homologous components in E.
View Article and Find Full Text PDFThe sodium efflux pump ATP4 is a leading antimalarial target, but suffers from a lack of high-resolution structural information needed to identify functionally important features in conserved regions and guide rational design of next generation inhibitors. Here, we determine a 3.7Å cryoEM structure of ATP4 purified from CRISPR-engineered parasites, revealing a previously unknown, apicomplexan-specific binding partner, ABP, which forms a conserved, likely modulatory interaction with ATP4.
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