Fluoroquinolones(FQs)have the propensity to accumulate in sediments once introduction into aquatic envi-ronments,thereby posing potential threats to benthic organisms,yet the ecotoxicity of sediment-associated FQs rem...Fluoroquinolones(FQs)have the propensity to accumulate in sediments once introduction into aquatic envi-ronments,thereby posing potential threats to benthic organisms,yet the ecotoxicity of sediment-associated FQs remains unclear.In this study,the toxicokinetics and responses of multiple biomarkers in Bellamya aeruginosa,exposed to the three commonly used FQs(norfloxacin,NOR;ciprofloxacin,CIP;levofloxacin,LEVO)at envi-ronmentally relevant concentrations were investigated under sediment exposure scenario.The results revealed that FQs were effectively ingested by B.aeruginosa from sediments,CIP showing the highest bioaccumulation(180.59μg/kg),followed by NOR(74.49μg/kg)and LEVO(36.02μg/kg).CIP exhibiting a highest uptake rate constant(Ks)(4.64 g/(g·day))and the lowest elimination rate constant(K_(e))(0.05 g/(g·day)).The descending order of biological half-life is as follows:CIP(13.62 days),LEVO(8.14 days),and NOR(6.83 days).NOR induced the activity of superoxide dismutase,catalase,and glutathione-S-transferase while CIP and LEVO depressed their activities and increased malondialdehyde content,indicating a more pronounced oxidative damage to B.aerug-inosa caused by CIP and LEVO than NOR.Furthermore,all three FQs were found to induce DNA damage and elevate acetylcholinesterase activity,suggesting distinct genotoxic and neurotoxic effects.Interestingly,despite its low bioaccumulation potential,LEVO exhibited high toxicity towards B.aeruginosa.These findings enhance our understanding of the ecotoxicity of FQs in sediments,providing further evidence of their potential ecological risks.展开更多
Benzalkonium chloride(BAC)is widely employed as a broad-spectrum biocide and has emerged as a significant environmental pollutant.Polymyxin B(PB)serves as the last-line defense for the treatment of Gram-negative patho...Benzalkonium chloride(BAC)is widely employed as a broad-spectrum biocide and has emerged as a significant environmental pollutant.Polymyxin B(PB)serves as the last-line defense for the treatment of Gram-negative pathogens.Previous studies reported that BAC-adapted Pseudomonas aeruginosa increased the tolerance to PB.Herein,we present the novel finding that the combination of BAC and PB exhibited synergistic antibacterial effects against P.aeruginosa.Time-killing assay demonstrated a significant reduction in bacterial cell viability.Scanning electron microscopy,zeta potential analysis,hydrophobicity measurements,and fluorescence probe analyses collectively revealed severe disruption of the cell envelope and membrane potential induced by the combination of BAC and PB.Transcriptomic analysis revealed that the BAC-PB combination notably downreg-ulated the expression of genes involved in lipid A modification and cell envelope production,including phoPQ,pmrAB,bamABCDE,lptABCDEG,lolB,yidC,and murJ.Additionally,the combination group exhibited augmented production of reactive oxygen species and diminished ATP synthesis.The expression of the genes associated with substance metabolism and energy generation was significantly impeded.This study provides significant implica-tions for the interactions of biocides and antibiotics on Gram-negative pathogens,while also addressing antibiotic resistance and developing the external treatment strategy for Pseudomonas-infected wounds and burns.展开更多
Pseudomonas aeruginosa is an opportunistic pathogen responsible for severe nosocomial infections.This multidrug-resistant bacterium can cause pneumonia and cystic fibrosis,both of which are associated with high morbid...Pseudomonas aeruginosa is an opportunistic pathogen responsible for severe nosocomial infections.This multidrug-resistant bacterium can cause pneumonia and cystic fibrosis,both of which are associated with high morbidity and mortality rates.The lipopolysaccharide of P.aeruginosa serves as an attractive target for the development of effective glycoconjugate vaccines.In this article,we report the first chemical synthesis of the highly challenging tetrasaccharide repeating unit of the P.aeruginosa serotype O3 O-antigen using a two-directional[1+(2+1)]glycosylation strategy.The synthesis is particularly challenging due to the poor nucleophilicity of the axial C4 hydroxyl group of l-galactose and the steric hindrance imposed by the 3S-hydroxybutyryl(Hb)chain.Furthermore,the presence of an acetyl group at the ortho position relative to the glycosylation site on l-galactose can lead to undesirable acetyl migration.Additionally,it is noteworthy that the selective removal of a 2-naphthylmethyl ether(Nap)during the late stages of synthesis,particularly in the presence of multiple benzyl groups,can be somewhat challenging to predict.Through the careful selection of synthetic strategies,building blocks,and optimized reaction conditions,we achieved the stereoselective glycosylations,selective oxidation of primary alcohols,remarkable enhancement of acceptor activity,and efficient introduction of the 3S-Hb group.The synthetic methodology presented in this work serves as a valuable reference for the preparation of structurally related oligosaccharides.By incorporating an aminopropyl linker,the target tetrasaccharide facilitates glycan microarray preparation and in vivo immunological assessments,thereby accelerating progress toward a synthetic glycoconjugate vaccine for P.aeruginosa.展开更多
The application of photocatalytic technology in algae killing is limited by the non-floatability and difficulty in recycling of the photocatalysts.Loading photocatalyst on magnetic or floatable carriers is the most po...The application of photocatalytic technology in algae killing is limited by the non-floatability and difficulty in recycling of the photocatalysts.Loading photocatalyst on magnetic or floatable carriers is the most popular method for overcoming the above inadequacies.In this work,a CdZnS/TiO_(2) membrane photocatalyst with adjustable suspended depth(include floating)and flexible assembly is designed,which is less prone to dislodgement due to in situ synthesis and has a wider range of applicability than previously reported photocatalysts.The photocatalytic removal of Microcystis aeruginosa revealed that the suspended depth and distribution format of the CdZnS/TiO_(2) membrane photocatalysts have striking effects on the photocatalytic removal performance of Microcystis aeruginosa,the photocatalytic removal efficiency of CdZnS/TiO_(2)-2 membrane photocatalysts for Microcystis aeruginosa could reach to 98.6%in 60 min when the photocatalysts assembled in the form of 3×3 arrays suspended at a depth of 2 cm from the liquid surface.A tiny amount of TiO_(2) loading allows the formation of Z-Scheme heterojunction,resulting in accelerating the separation efficiency of photogenerated carriers,preserving the photogenerated electrons and holes with stronger reduction and oxidation ability and inhabiting the photo-corrosion of CdZnS.展开更多
We assessed the quorum sensing(QS)inhibitory impact of sesamol against the foodborne bacterium Pseudomonas aeruginosa.At concentrations ranging from 50 to 200μg/mL,sesamol significantly inhibited the production of vi...We assessed the quorum sensing(QS)inhibitory impact of sesamol against the foodborne bacterium Pseudomonas aeruginosa.At concentrations ranging from 50 to 200μg/mL,sesamol significantly inhibited the production of virulence factors such as protease,elastase,pyocyanin,rhamnolipid,and chemotaxis,and improved the susceptibility of bacterial and biofilm cells to colistin.Integrated transcriptomics,metabolomics,and docking analyses indicated that exposure to sesamol destroyed the QS system and down-regulated the expressions of genes encoding virulence and antioxidant enzymes.The down-regulation of genes encoding antioxidant enzymes intensified oxidative stress,as demonstrated by the enhancement of reactive oxygen species and H_(2)O_(2).The enhanced oxidative stress changed the components of the cell membrane,improved its permeability,and ultimately enhanced the susceptibility of bacterial and biofilm cells to colistin.Moreover,exposure to sesamol also led to the disorder of amino acid metabolism and energy metabolism,eventually attenuating the pathogenicity of P.aeruginosa.These findings indicated that sesamol can function as a potent anti-virulence agent to defend against food spoilage caused by P.aeruginosa.展开更多
Objective:To develop chitosan-silver nanoparticles targeting Pseudomonas aeruginosa biofilms and verify their antibacterial performance through animal experiments.Methods:Chitosan,silver nitrate,glacial acetic acid,an...Objective:To develop chitosan-silver nanoparticles targeting Pseudomonas aeruginosa biofilms and verify their antibacterial performance through animal experiments.Methods:Chitosan,silver nitrate,glacial acetic acid,and other chemical reagents were used to synthesize chitosan-silver nanoparticles.The characterization,minimum inhibitory concentration,and biofilm inhibition rate of the chitosan-silver nanoparticles were tested.A total of 40 SD rats were randomly divided into four groups.After routine adaptive feeding,the control group received intraperitoneal injection of normal saline;the model group received intraperitoneal injection of Pseudomonas aeruginosa suspension;the positive group received intraperitoneal injection of Pseudomonas aeruginosa suspension mixed with ampicillin at a volume ratio of 1∶1;the observation group received intraperitoneal injection of Pseudomonas aeruginosa suspension mixed with chitosan-silver nanoparticles(at minimum inhibitory concentration)at a volume ratio of 1∶1.Bacterial load,inflammatory factors,and liver and kidney function indicators in tissues were observed and compared among the four groups on the 3^(rd)day after treatment.Results:When the concentration of chitosansilver nanoparticles reached 8μg/mL or above,the OD value of the experimental wells was close to that of the control wells,indicating that 8μg/mL was the minimum inhibitory concentration of the chitosan-silver nanoparticles;at concentrations of 8μg/mL or above,the biofilm inhibition rate was greater than 80%.The bacterial load in the observation group was significantly lower than that in the model and positive groups(P<0.05).The expression levels of interleukin-6,interferon-γ,and tumor necrosis factor-αin the observation group were significantly lower than those in the model and positive groups(P<0.05).There were no statistically significant differences in alanine aminotransferase,aspartate aminotransferase,blood urea nitrogen,and creatinine levels among the four groups(P>0.05).Conclusion:The chitosan-silver nanoparticles targeting Pseudomonas aeruginosa biofilms constructed in this study exhibit good antibacterial effects against Pseudomonas aeruginosa and have good safety.展开更多
Pseudomonas aeruginosa is an opportunistic pathogen widely distributed in the natural environment,which can cause a variety of infections,especially in people with low immunity and high pathogenicity.In recent years,s...Pseudomonas aeruginosa is an opportunistic pathogen widely distributed in the natural environment,which can cause a variety of infections,especially in people with low immunity and high pathogenicity.In recent years,significant progress has been made in the detection technology of Pseudomonas aeruginosa,covering traditional methods,molecular biology techniques,immunological methods and automated detection systems.Traditional methods such as the national standard method and the filter membrane method are easy to operate,but have the problems of long time consuming and limited sensitivity.Molecular biological techniques(such as PCR,gene cloning)and immunological methods(such as ELISA,colloidal gold immunochromatography)have significantly improved the sensitivity and specificity of detection,but they require high equipment and technology,and are expensive.Automated detection systems,such as VITEK 2 Compact and AutoMS 1000 mass spectrometry identification system,are excellent in improving detection efficiency and accuracy,but their high cost and complex operation process limit their wide application.In addition,the resistance of Pseudomonas aeruginosa to bacteriostatic agents further increases the difficulty of detection.In this paper,the development and application of immunological detection technology,molecular biological technology and immunological technology of Pseudomonas aeruginosa were reviewed,and the principles,advantages,disadvantages and research progress of various detection technologies of Pseudomonas aeruginosa were described,and the future development trend was prospected,in order to provide reference for the optimization and development of detection methods of Pseudomonas aeruginosa.展开更多
Objective Pseudomonas aeruginosa(P.aeruginosa)is a prevalent pathogenic bacterium involved in meningitis;however,the virulence factors contributing to this disease remain poorly understood.Methods The virulence of the...Objective Pseudomonas aeruginosa(P.aeruginosa)is a prevalent pathogenic bacterium involved in meningitis;however,the virulence factors contributing to this disease remain poorly understood.Methods The virulence of the P.aeruginosa A584,isolated from meningitis samples,was evaluated by constructing in vitro blood-brain barrier and in vivo systemic infection models.qPCR,whole-genome sequencing,and drug efflux assays of A584 were performed to analyze the virulence factors.Results Genomic sequencing showed that A584 formed a phylogenetic cluster with the reference strains NY7610,DDRC3,Pa58,and Pa124.Its genome includes abundant virulence factors,such as hemolysin,the Type IV secretion system,and pyoverdine.A584 is a multidrug-resistant strain,and its wide-spectrum resistance is associated with enhanced drug efflux.Moreover,this strain caused significantly more severe damage to the blood-brain barrier than the standard strain,PAO1.qPCR assays further revealed the downregulation of the blood-brain barrier-associated proteins Claudin-5 and Occludin by A584.During systemic infection,A584 exhibited a higher capacity of brain colonization than PAO1(37.1×10^(6) CFU/g brain versus 2.5×10^(6) CFU/g brain),leading to higher levels of the proinflammatory factors IL-1βand TNF-α.Conclusion This study sheds light on the virulence factors of P.aeruginosa involved in meningitis.展开更多
The harmful algal bloom primarily caused by Microcystis aeruginosa(M.aeruginosa)has become one of the serious biological pollution issues in actual water,which has received intense attention worldwide.Over the past ye...The harmful algal bloom primarily caused by Microcystis aeruginosa(M.aeruginosa)has become one of the serious biological pollution issues in actual water,which has received intense attention worldwide.Over the past years,increasing number of publications have reported that metal-organic frameworks(MOFs)based functional materials exhibited significant inhibition against M.aeruginosa via multiple mechanisms,but no review papers systematically presented progresses regarding MOFs-based materials for M.aeruginosa control up to now.With this review paper,we summarized the state-of-the-art studies of MOFsbased materials for M.aeruginosa removal,comparing and discussing the design strategies of MOFs-based materials and their antimicrobial mechanisms.Meanwhile,we discussed methods for evaluating the water purification performances of MOFs-based materials against M.aeruginosa.Finally,the perspectives for design of novel MOFs-based functional materials and application scenarios were proposed to provide an outlook on areas where greater efforts should be made in the future.展开更多
Fournier’s gangrene is a rare urological condition with a poor prognosis and an extremely high mortality rate.Infections caused by pathogenic microorganisms play a critical role in the pathogenesis of Fournier’s gan...Fournier’s gangrene is a rare urological condition with a poor prognosis and an extremely high mortality rate.Infections caused by pathogenic microorganisms play a critical role in the pathogenesis of Fournier’s gangrene.Rapid assessment and thorough debridement are crucial for survival and prognosis of patients with this disease.The present case involved a 62-year-old male patient with poorly controlled diabetes,who presented with unexplained scrotal swelling for 2 days at a local hospital where scrotal surgical debridement was performed.However,the procedure was unsuccessful.This case was characterized by rapid disease progression,widespread wound involvement,and dual infection with multidrug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa.Our team performed early,extensive surgical debridement and,based on the results of antimicrobial susceptibility testing,initiated combination antibiotic therapy.The patient’s condition improved significantly after these interventions.However,the treatment was ultimately discontinued by the patient’s family for personal reasons,and follow-up care was declined.展开更多
Here we report that the presence of MgCO_(3) stimulates the extracellular polymeric substance (EPS) secretion of Microcystis Aeruginosa (M. Aeruginosa). This stimulation led to a significant reduction in the total con...Here we report that the presence of MgCO_(3) stimulates the extracellular polymeric substance (EPS) secretion of Microcystis Aeruginosa (M. Aeruginosa). This stimulation led to a significant reduction in the total concentration of NH_(4)^(+)‒N by more than 86%, and effective recovery of PO_(4)^(3-)‒P within three days from concentrated wastewater (WW), although the secreted EPS inhibited the conversion of MgCO_(3) to specific crystal forms (MgNH4PO4.6H2O or MgHPO4.7H2O). Moreover, with an increase in PO_(4)^(3-) concentration in WW, these crystals appeared, thus the removal of NH_(4)^(+)‒N and PO_(4)^(3-)‒P nutrients can be attributed to the combined effect of M. Aeruginosa and MgCO_(3). We used Surface-Enhanced Raman Spectroscopy (SERS) combined with X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy with Energy-Dispersive X-ray Spectroscopy (FESEM-EDS), and X-ray Photoelectron Spectroscopy (XPS) to investigate the mechanism for competitive interactions between M. Aeruginosa and MgCO_(3) in removing NH_(4)^(+)‒N and PO_(4)^(3-)‒P. We identified that the bound EPS accumulated amorphous Mg–P–O dense particles on M. Aeruginosa, while soluble EPS, containing –COOH groups of humic-like substances decreased the pH of the solution and coordinated with Mg^(2+) ions. Therefore, both secreted bound and soluble EPS play a vital role in hindering the transformation of Mg^(2+) ions or MgCO_(3) to MgNH4PO4.6H2O or MgHPO4.7H2O crystals within WW, and they enhanced M. Aeruginosa 's ability in absorbing nutrients of NH_(4)^(+)‒N and PO_(4)^(3-)‒P. This mechanism plays a crucial role in the efficient recovery of NH_(4)^(+)‒N and PO_(4)^(3-)‒P from concentrated wastewater sources such as aerobically or anaerobically digested effluent from various sources like agriculture, livestock, and domestic wastewaters.展开更多
[Objective] The aim of this study was to investigate the prokaryotic expression of pseudomonas aeruginosa Lipase gene.[Method]Lipase gene was amplified by PCR from the genome DNA of pseudomonas aeruginosa,and its nucl...[Objective] The aim of this study was to investigate the prokaryotic expression of pseudomonas aeruginosa Lipase gene.[Method]Lipase gene was amplified by PCR from the genome DNA of pseudomonas aeruginosa,and its nucleotide sequence was determined.The prokaryotic expression vector of Lipase gene was constructed by the gene recombination technique.The protein expression was induced for 4 hours by IPTG with the final concentration of 1.0 mmol/L,and then SDS-PAGE electrophoresis was analyzed.[Result]The sequence of mature peptides in Lipase gene cloned from pseudomonas aeruginosa had a 99.36% homology with that of pseudomonas aeruginosa lipase submitted in NCBI,so the prokaryotic expression vector of Lipase gene pET32a-Lip was successfully constructed.Furthermore,the results of SDS-PAGE electrophoresis showed that the target gene was expressed highly and effectively.[Conclusion]The cloned pseudomonas aeruginosa lipase with its signal peptide could be normally expressed in E.coli and also used for further study.展开更多
[Objective] The research aimed to analyze the inhibitory mechanism of Sophora japonica n-hexane extract which significantly inhibited Microcystis aeruginosa in the prior research.[Method] S.japonica n-hexane extract w...[Objective] The research aimed to analyze the inhibitory mechanism of Sophora japonica n-hexane extract which significantly inhibited Microcystis aeruginosa in the prior research.[Method] S.japonica n-hexane extract was used to treat M.aeruginosa.By inspecting chlorophyll a content,protein content,cell membrane permeability and superoxide dismutase（SOD） activity,the inhibitory mechanism of S.japonica n-hexane extract on M.aeruginosa was analyzed initially.[Result] S.japonica n-hexane extract destroyed the cell membrane system of M.aeruginosa,and increased the cell membrane permeability.The contents of chlorophyll a and protein respectively declined to 10% and 50% of that in the control group after cultivated for 7 d,which indicated the photosynthetic reaction system of M.aeruginosa was destroyed.In addition,under the effect of S.japonica n-hexane extract,SOD activity of M.aeruginosa increased in the early period and decreased in the latter period.[Conclusion] The possible inhibitory mechanism of S.japonica n-hexane extract on M.aeruginosa was destroying the cell membrane to increase the membrane permeability;destroying the photosynthetic reaction system to decrease the contents of photosynthetic pigment and protein;making SOD activity showing the phased variation.展开更多
基金supported by the Hunan Provincial Natural Science Foundation of China(Nos.2023JJ40518 and 2023JJ30490)the Scientific Research Foundation of Hunan Provincial Education Department(Nos.21B0511 and 22A0384)the Research Funding Project of Jishou University for talent introduction.
文摘Fluoroquinolones(FQs)have the propensity to accumulate in sediments once introduction into aquatic envi-ronments,thereby posing potential threats to benthic organisms,yet the ecotoxicity of sediment-associated FQs remains unclear.In this study,the toxicokinetics and responses of multiple biomarkers in Bellamya aeruginosa,exposed to the three commonly used FQs(norfloxacin,NOR;ciprofloxacin,CIP;levofloxacin,LEVO)at envi-ronmentally relevant concentrations were investigated under sediment exposure scenario.The results revealed that FQs were effectively ingested by B.aeruginosa from sediments,CIP showing the highest bioaccumulation(180.59μg/kg),followed by NOR(74.49μg/kg)and LEVO(36.02μg/kg).CIP exhibiting a highest uptake rate constant(Ks)(4.64 g/(g·day))and the lowest elimination rate constant(K_(e))(0.05 g/(g·day)).The descending order of biological half-life is as follows:CIP(13.62 days),LEVO(8.14 days),and NOR(6.83 days).NOR induced the activity of superoxide dismutase,catalase,and glutathione-S-transferase while CIP and LEVO depressed their activities and increased malondialdehyde content,indicating a more pronounced oxidative damage to B.aerug-inosa caused by CIP and LEVO than NOR.Furthermore,all three FQs were found to induce DNA damage and elevate acetylcholinesterase activity,suggesting distinct genotoxic and neurotoxic effects.Interestingly,despite its low bioaccumulation potential,LEVO exhibited high toxicity towards B.aeruginosa.These findings enhance our understanding of the ecotoxicity of FQs in sediments,providing further evidence of their potential ecological risks.
基金supported by the National Natural Science Foundation of China(No.32170121).
文摘Benzalkonium chloride(BAC)is widely employed as a broad-spectrum biocide and has emerged as a significant environmental pollutant.Polymyxin B(PB)serves as the last-line defense for the treatment of Gram-negative pathogens.Previous studies reported that BAC-adapted Pseudomonas aeruginosa increased the tolerance to PB.Herein,we present the novel finding that the combination of BAC and PB exhibited synergistic antibacterial effects against P.aeruginosa.Time-killing assay demonstrated a significant reduction in bacterial cell viability.Scanning electron microscopy,zeta potential analysis,hydrophobicity measurements,and fluorescence probe analyses collectively revealed severe disruption of the cell envelope and membrane potential induced by the combination of BAC and PB.Transcriptomic analysis revealed that the BAC-PB combination notably downreg-ulated the expression of genes involved in lipid A modification and cell envelope production,including phoPQ,pmrAB,bamABCDE,lptABCDEG,lolB,yidC,and murJ.Additionally,the combination group exhibited augmented production of reactive oxygen species and diminished ATP synthesis.The expression of the genes associated with substance metabolism and energy generation was significantly impeded.This study provides significant implica-tions for the interactions of biocides and antibiotics on Gram-negative pathogens,while also addressing antibiotic resistance and developing the external treatment strategy for Pseudomonas-infected wounds and burns.
基金the National Key R&D Program of China(No.2023YFC2308000)the National Natural Science Foundation of China(Nos.22478153,22477046,22177041)+2 种基金the Max Planck Society International Partner Group Programthe China Scholarship Council(CSC)the Fundamental Research Funds for the Central Universities for funding.
文摘Pseudomonas aeruginosa is an opportunistic pathogen responsible for severe nosocomial infections.This multidrug-resistant bacterium can cause pneumonia and cystic fibrosis,both of which are associated with high morbidity and mortality rates.The lipopolysaccharide of P.aeruginosa serves as an attractive target for the development of effective glycoconjugate vaccines.In this article,we report the first chemical synthesis of the highly challenging tetrasaccharide repeating unit of the P.aeruginosa serotype O3 O-antigen using a two-directional[1+(2+1)]glycosylation strategy.The synthesis is particularly challenging due to the poor nucleophilicity of the axial C4 hydroxyl group of l-galactose and the steric hindrance imposed by the 3S-hydroxybutyryl(Hb)chain.Furthermore,the presence of an acetyl group at the ortho position relative to the glycosylation site on l-galactose can lead to undesirable acetyl migration.Additionally,it is noteworthy that the selective removal of a 2-naphthylmethyl ether(Nap)during the late stages of synthesis,particularly in the presence of multiple benzyl groups,can be somewhat challenging to predict.Through the careful selection of synthetic strategies,building blocks,and optimized reaction conditions,we achieved the stereoselective glycosylations,selective oxidation of primary alcohols,remarkable enhancement of acceptor activity,and efficient introduction of the 3S-Hb group.The synthetic methodology presented in this work serves as a valuable reference for the preparation of structurally related oligosaccharides.By incorporating an aminopropyl linker,the target tetrasaccharide facilitates glycan microarray preparation and in vivo immunological assessments,thereby accelerating progress toward a synthetic glycoconjugate vaccine for P.aeruginosa.
基金financially supported by the Natural Science Foundation of ShanDong(Nos.ZR2023QD152 and ZR2021MD002).
文摘The application of photocatalytic technology in algae killing is limited by the non-floatability and difficulty in recycling of the photocatalysts.Loading photocatalyst on magnetic or floatable carriers is the most popular method for overcoming the above inadequacies.In this work,a CdZnS/TiO_(2) membrane photocatalyst with adjustable suspended depth(include floating)and flexible assembly is designed,which is less prone to dislodgement due to in situ synthesis and has a wider range of applicability than previously reported photocatalysts.The photocatalytic removal of Microcystis aeruginosa revealed that the suspended depth and distribution format of the CdZnS/TiO_(2) membrane photocatalysts have striking effects on the photocatalytic removal performance of Microcystis aeruginosa,the photocatalytic removal efficiency of CdZnS/TiO_(2)-2 membrane photocatalysts for Microcystis aeruginosa could reach to 98.6%in 60 min when the photocatalysts assembled in the form of 3×3 arrays suspended at a depth of 2 cm from the liquid surface.A tiny amount of TiO_(2) loading allows the formation of Z-Scheme heterojunction,resulting in accelerating the separation efficiency of photogenerated carriers,preserving the photogenerated electrons and holes with stronger reduction and oxidation ability and inhabiting the photo-corrosion of CdZnS.
基金supported by grants from the National Natural Science Foundation of China(32000091)General Projects of Natural Science Research in Universities of Jiangsu Province(20KJB180019)Jiangsu Youth Talent Promotion Project(TJ-2021-066)。
文摘We assessed the quorum sensing(QS)inhibitory impact of sesamol against the foodborne bacterium Pseudomonas aeruginosa.At concentrations ranging from 50 to 200μg/mL,sesamol significantly inhibited the production of virulence factors such as protease,elastase,pyocyanin,rhamnolipid,and chemotaxis,and improved the susceptibility of bacterial and biofilm cells to colistin.Integrated transcriptomics,metabolomics,and docking analyses indicated that exposure to sesamol destroyed the QS system and down-regulated the expressions of genes encoding virulence and antioxidant enzymes.The down-regulation of genes encoding antioxidant enzymes intensified oxidative stress,as demonstrated by the enhancement of reactive oxygen species and H_(2)O_(2).The enhanced oxidative stress changed the components of the cell membrane,improved its permeability,and ultimately enhanced the susceptibility of bacterial and biofilm cells to colistin.Moreover,exposure to sesamol also led to the disorder of amino acid metabolism and energy metabolism,eventually attenuating the pathogenicity of P.aeruginosa.These findings indicated that sesamol can function as a potent anti-virulence agent to defend against food spoilage caused by P.aeruginosa.
文摘Objective:To develop chitosan-silver nanoparticles targeting Pseudomonas aeruginosa biofilms and verify their antibacterial performance through animal experiments.Methods:Chitosan,silver nitrate,glacial acetic acid,and other chemical reagents were used to synthesize chitosan-silver nanoparticles.The characterization,minimum inhibitory concentration,and biofilm inhibition rate of the chitosan-silver nanoparticles were tested.A total of 40 SD rats were randomly divided into four groups.After routine adaptive feeding,the control group received intraperitoneal injection of normal saline;the model group received intraperitoneal injection of Pseudomonas aeruginosa suspension;the positive group received intraperitoneal injection of Pseudomonas aeruginosa suspension mixed with ampicillin at a volume ratio of 1∶1;the observation group received intraperitoneal injection of Pseudomonas aeruginosa suspension mixed with chitosan-silver nanoparticles(at minimum inhibitory concentration)at a volume ratio of 1∶1.Bacterial load,inflammatory factors,and liver and kidney function indicators in tissues were observed and compared among the four groups on the 3^(rd)day after treatment.Results:When the concentration of chitosansilver nanoparticles reached 8μg/mL or above,the OD value of the experimental wells was close to that of the control wells,indicating that 8μg/mL was the minimum inhibitory concentration of the chitosan-silver nanoparticles;at concentrations of 8μg/mL or above,the biofilm inhibition rate was greater than 80%.The bacterial load in the observation group was significantly lower than that in the model and positive groups(P<0.05).The expression levels of interleukin-6,interferon-γ,and tumor necrosis factor-αin the observation group were significantly lower than those in the model and positive groups(P<0.05).There were no statistically significant differences in alanine aminotransferase,aspartate aminotransferase,blood urea nitrogen,and creatinine levels among the four groups(P>0.05).Conclusion:The chitosan-silver nanoparticles targeting Pseudomonas aeruginosa biofilms constructed in this study exhibit good antibacterial effects against Pseudomonas aeruginosa and have good safety.
基金College Students’Innovation and Entrepreneurship Training Program Project(X202511049398)College Students’Innovation and Entrepreneurship Training Program Project(X202511049201)+1 种基金College Students’Innovation and Entrepreneurship Training Program Project(D202504071303298456)Hainan Vocational University of Science and Technology University-Level Scientific Research Funding Project(HKKY2024-87).
文摘Pseudomonas aeruginosa is an opportunistic pathogen widely distributed in the natural environment,which can cause a variety of infections,especially in people with low immunity and high pathogenicity.In recent years,significant progress has been made in the detection technology of Pseudomonas aeruginosa,covering traditional methods,molecular biology techniques,immunological methods and automated detection systems.Traditional methods such as the national standard method and the filter membrane method are easy to operate,but have the problems of long time consuming and limited sensitivity.Molecular biological techniques(such as PCR,gene cloning)and immunological methods(such as ELISA,colloidal gold immunochromatography)have significantly improved the sensitivity and specificity of detection,but they require high equipment and technology,and are expensive.Automated detection systems,such as VITEK 2 Compact and AutoMS 1000 mass spectrometry identification system,are excellent in improving detection efficiency and accuracy,but their high cost and complex operation process limit their wide application.In addition,the resistance of Pseudomonas aeruginosa to bacteriostatic agents further increases the difficulty of detection.In this paper,the development and application of immunological detection technology,molecular biological technology and immunological technology of Pseudomonas aeruginosa were reviewed,and the principles,advantages,disadvantages and research progress of various detection technologies of Pseudomonas aeruginosa were described,and the future development trend was prospected,in order to provide reference for the optimization and development of detection methods of Pseudomonas aeruginosa.
基金supported by National Natural Science Foundation of China,China(32170102)Natural Science Foundation of Tianjin(21JCYBJC01420)the Fundamental Research Funds for the Central Universities(63233050)。
文摘Objective Pseudomonas aeruginosa(P.aeruginosa)is a prevalent pathogenic bacterium involved in meningitis;however,the virulence factors contributing to this disease remain poorly understood.Methods The virulence of the P.aeruginosa A584,isolated from meningitis samples,was evaluated by constructing in vitro blood-brain barrier and in vivo systemic infection models.qPCR,whole-genome sequencing,and drug efflux assays of A584 were performed to analyze the virulence factors.Results Genomic sequencing showed that A584 formed a phylogenetic cluster with the reference strains NY7610,DDRC3,Pa58,and Pa124.Its genome includes abundant virulence factors,such as hemolysin,the Type IV secretion system,and pyoverdine.A584 is a multidrug-resistant strain,and its wide-spectrum resistance is associated with enhanced drug efflux.Moreover,this strain caused significantly more severe damage to the blood-brain barrier than the standard strain,PAO1.qPCR assays further revealed the downregulation of the blood-brain barrier-associated proteins Claudin-5 and Occludin by A584.During systemic infection,A584 exhibited a higher capacity of brain colonization than PAO1(37.1×10^(6) CFU/g brain versus 2.5×10^(6) CFU/g brain),leading to higher levels of the proinflammatory factors IL-1βand TNF-α.Conclusion This study sheds light on the virulence factors of P.aeruginosa involved in meningitis.
基金supported by National Natural Science Foundation of China(Nos.22176012,52370025)the Pyramid Talent Training Project of Beijing University of Civil Engineering and Architecture(No.JDLJ20220802)+1 种基金the Doctor Graduate Scientific Research Ability Improvement Project of Beijing University of Civil Engineering and Architecture(No.DG2023014)Guangxi Key Laboratory of Urban Water Environment。
文摘The harmful algal bloom primarily caused by Microcystis aeruginosa(M.aeruginosa)has become one of the serious biological pollution issues in actual water,which has received intense attention worldwide.Over the past years,increasing number of publications have reported that metal-organic frameworks(MOFs)based functional materials exhibited significant inhibition against M.aeruginosa via multiple mechanisms,but no review papers systematically presented progresses regarding MOFs-based materials for M.aeruginosa control up to now.With this review paper,we summarized the state-of-the-art studies of MOFsbased materials for M.aeruginosa removal,comparing and discussing the design strategies of MOFs-based materials and their antimicrobial mechanisms.Meanwhile,we discussed methods for evaluating the water purification performances of MOFs-based materials against M.aeruginosa.Finally,the perspectives for design of novel MOFs-based functional materials and application scenarios were proposed to provide an outlook on areas where greater efforts should be made in the future.
基金supported by the Collaborative Innovation Center of China’s Ministry of Education(grant no.2020-39)Constructive Project of Innovative Talent Platform for Precise Repair of Wounds(grant no.2021-3)+1 种基金Scientific Research and Talent Training Fund of Kweichow Moutai Hospital(grant no.2022-13)Shanghai Wang Zhengguo Trauma Medicine Development Foundation(grant no.SZYZ-TR-05).
文摘Fournier’s gangrene is a rare urological condition with a poor prognosis and an extremely high mortality rate.Infections caused by pathogenic microorganisms play a critical role in the pathogenesis of Fournier’s gangrene.Rapid assessment and thorough debridement are crucial for survival and prognosis of patients with this disease.The present case involved a 62-year-old male patient with poorly controlled diabetes,who presented with unexplained scrotal swelling for 2 days at a local hospital where scrotal surgical debridement was performed.However,the procedure was unsuccessful.This case was characterized by rapid disease progression,widespread wound involvement,and dual infection with multidrug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa.Our team performed early,extensive surgical debridement and,based on the results of antimicrobial susceptibility testing,initiated combination antibiotic therapy.The patient’s condition improved significantly after these interventions.However,the treatment was ultimately discontinued by the patient’s family for personal reasons,and follow-up care was declined.
基金supported by Cultivating Fund Project of Hubei Hongshan Laboratory(2022hspy002).
文摘Here we report that the presence of MgCO_(3) stimulates the extracellular polymeric substance (EPS) secretion of Microcystis Aeruginosa (M. Aeruginosa). This stimulation led to a significant reduction in the total concentration of NH_(4)^(+)‒N by more than 86%, and effective recovery of PO_(4)^(3-)‒P within three days from concentrated wastewater (WW), although the secreted EPS inhibited the conversion of MgCO_(3) to specific crystal forms (MgNH4PO4.6H2O or MgHPO4.7H2O). Moreover, with an increase in PO_(4)^(3-) concentration in WW, these crystals appeared, thus the removal of NH_(4)^(+)‒N and PO_(4)^(3-)‒P nutrients can be attributed to the combined effect of M. Aeruginosa and MgCO_(3). We used Surface-Enhanced Raman Spectroscopy (SERS) combined with X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy with Energy-Dispersive X-ray Spectroscopy (FESEM-EDS), and X-ray Photoelectron Spectroscopy (XPS) to investigate the mechanism for competitive interactions between M. Aeruginosa and MgCO_(3) in removing NH_(4)^(+)‒N and PO_(4)^(3-)‒P. We identified that the bound EPS accumulated amorphous Mg–P–O dense particles on M. Aeruginosa, while soluble EPS, containing –COOH groups of humic-like substances decreased the pH of the solution and coordinated with Mg^(2+) ions. Therefore, both secreted bound and soluble EPS play a vital role in hindering the transformation of Mg^(2+) ions or MgCO_(3) to MgNH4PO4.6H2O or MgHPO4.7H2O crystals within WW, and they enhanced M. Aeruginosa 's ability in absorbing nutrients of NH_(4)^(+)‒N and PO_(4)^(3-)‒P. This mechanism plays a crucial role in the efficient recovery of NH_(4)^(+)‒N and PO_(4)^(3-)‒P from concentrated wastewater sources such as aerobically or anaerobically digested effluent from various sources like agriculture, livestock, and domestic wastewaters.
基金Supported by Subproject of"Development and Utilization of Plant Resources under Special Environment"from the National Project"863"(2007AA021401)Corps Doctoral Foundation of"Study on Transgenic Breeding Technology"(2006JC07)~~
文摘[Objective] The aim of this study was to investigate the prokaryotic expression of pseudomonas aeruginosa Lipase gene.[Method]Lipase gene was amplified by PCR from the genome DNA of pseudomonas aeruginosa,and its nucleotide sequence was determined.The prokaryotic expression vector of Lipase gene was constructed by the gene recombination technique.The protein expression was induced for 4 hours by IPTG with the final concentration of 1.0 mmol/L,and then SDS-PAGE electrophoresis was analyzed.[Result]The sequence of mature peptides in Lipase gene cloned from pseudomonas aeruginosa had a 99.36% homology with that of pseudomonas aeruginosa lipase submitted in NCBI,so the prokaryotic expression vector of Lipase gene pET32a-Lip was successfully constructed.Furthermore,the results of SDS-PAGE electrophoresis showed that the target gene was expressed highly and effectively.[Conclusion]The cloned pseudomonas aeruginosa lipase with its signal peptide could be normally expressed in E.coli and also used for further study.
基金Supported by National Natural Science Foundation of China(41076097,41006097,41106113)Science and Technology Research Key Projectof Chinese Ministry of Education(211065)+2 种基金Natural Science Foundation of Jiangsu Province,China(BK2010322)Open Research of Jiangsu Key Laboratory of Environmental Material and Environmental Engineering(K090027,K090025,K090026,K090028)"New Century"Talent Project of Yangzhou University,China~~
文摘[Objective] The research aimed to analyze the inhibitory mechanism of Sophora japonica n-hexane extract which significantly inhibited Microcystis aeruginosa in the prior research.[Method] S.japonica n-hexane extract was used to treat M.aeruginosa.By inspecting chlorophyll a content,protein content,cell membrane permeability and superoxide dismutase（SOD） activity,the inhibitory mechanism of S.japonica n-hexane extract on M.aeruginosa was analyzed initially.[Result] S.japonica n-hexane extract destroyed the cell membrane system of M.aeruginosa,and increased the cell membrane permeability.The contents of chlorophyll a and protein respectively declined to 10% and 50% of that in the control group after cultivated for 7 d,which indicated the photosynthetic reaction system of M.aeruginosa was destroyed.In addition,under the effect of S.japonica n-hexane extract,SOD activity of M.aeruginosa increased in the early period and decreased in the latter period.[Conclusion] The possible inhibitory mechanism of S.japonica n-hexane extract on M.aeruginosa was destroying the cell membrane to increase the membrane permeability;destroying the photosynthetic reaction system to decrease the contents of photosynthetic pigment and protein;making SOD activity showing the phased variation.
