Bacterial Adsorption Research Articles

Development and In-Depth Characterization of Bacteria Repellent and Bacteria Adhesive Antibody-Coated Surfaces Using Optical Waveguide Biosensing.

Bacteria repellent surfaces and antibody-based coatings for bacterial assays have shown a growing demand in the field of biosensors, and have crucial importance in the design of biomedical devices. However, in-depth investigations and comparisons of possible solutions are still missing. The optical waveguide lightmode spectroscopy (OWLS) technique offers label-free, non-invasive, in situ characterization of protein and bacterial adsorption. Moreover, it has excellent flexibility for testing various surface coatings. Here, we describe an OWLS-based method supporting the development of bacteria repellent surfaces and characterize the layer structures and affinities of different antibody-based coatings for bacterial assays. In order to test nonspecific binding blocking agents against bacteria, OWLS chips were coated with bovine serum albumin (BSA), I-block, PAcrAM-g-(PMOXA, NH2, Si), (PAcrAM-P) and PLL-g-PEG (PP) (with different coating temperatures), and subsequent Escherichia coli adhesion was monitored. We found that the best performing blocking agents could inhibit bacterial adhesion from samples with bacteria concentrations of up to 107 cells/mL. Various immobilization methods were applied to graft a wide range of selected antibodies onto the biosensor’s surface. Simple physisorption, Mix&Go (AnteoBind) (MG) films, covalently immobilized protein A and avidin–biotin based surface chemistries were all fabricated and tested. The surface adsorbed mass densities of deposited antibodies were determined, and the biosensor;s kinetic data were evaluated to divine the possible orientations of the bacteria-capturing antibodies and determine the rate constants and footprints of the binding events. The development of affinity layers was supported by enzyme-linked immunosorbent assay (ELISA) measurements in order to test the bacteria binding capabilities of the antibodies. The best performance in the biosensor measurements was achieved by employing a polyclonal antibody in combination with protein A-based immobilization and PAcrAM-P blocking of nonspecific binding. Using this setting, a surface sensitivity of 70 cells/mm2 was demonstrated.

Co-exchanged montmorillonite: a potential antibacterial agent with good antibacterial activity and cytocompatibility.

As a biocompatible material with rich resources and economic benefits, montmorillonite (MMT) has been widely used in the antibacterial field as a drug carrier and toxin adsorbent. In addition, the distinctive structure of MMT provides a possibility to tune its property in a wide range through ion-exchange. In this study, Co-montmorillonite (CoMMT) was prepared by the ion-exchanging method in a Co(NO3)2 solution and its antibacterial activity and cytocompatibility were investigated. The results showed that Co was introduced into MMT successfully and led to an increase in the interlayer spacing of MMT. Also, CoMMT showed a morphology of irregular aggregates consisting of stacked and intertwined lamellae with a uniform cobalt distribution. Besides, CoMMT had better dispersity and higher specific surface area than unmodified MMT. The antibacterial test results showed that CoMMT had good antibacterial activity against S. aureus and E. coli when the CoMMT concentration was higher than 0.2 mg mL-1 and 0.4 mg mL-1, respectively. The possible antibacterial mechanism of CoMMT was speculated and verified by a combination of SEM and EDS results. In addition, CoMMT showed no obvious cytotoxicity to MC3TC-E1 at the observed antibacterial concentration. These findings demonstrated that CoMMT with good biocompatibility and antibacterial activity could be used as a novel antibacterial agent for tissue engineering.

Improved removal performance of Gram-negative and Gram-positive bacteria in sand filtration system with arginine modified biochar amendment

Bacterial removal by sand filtration system is commonly inefficient due to the low bacterial adsorption capacity of sand. To improve the bacterial removal performance, biochar fabricated at different temperatures (400 °C, 550 °C and 700 °C) and arginine modified biochar were added into sand filtration columns as filter layers (0.5 and 1 wt%). Addition of biochar into sand columns could improve the removal efficiency for both Escherichia coli and Bacillus subtilis under both slow (4 m/day) and fast (240 m/day) filtration conditions. Bacterial removal efficiency in sand columns with the addition of biochar fabricated at 700 °C were higher than those fabricated at 400 °C and 550 °C due to its best bacterial adsorption capacity. Modification of biochar with arginine could further improve the bacterial removal performance. Specifically, complete bacterial removal (1.35 × 107 ± 10% cells/mL) could be achieved under both slow and fast filtration conditions in sand columns with 1 wt% arginine functionalized biochar amendment. The enhanced bacterial adsorption capacity mainly contributed to the increased bacterial capture performance in columns with addition of arginine-modified biochar. Bacteria more tightly bounded with arginine-modified biochar than bulk biochar. Moreover, complete bacterial removal with the copresence of 5 mg/L humic acid in suspensions was acquired in columns with addition of 1 wt% arginine-modified biochar. Efficient bacterial removal in actual river water, multiple filtration cycles as well as longtime injection duration (100 pore volumes injection) was also obtained. The results of this study demonstrated that arginine-modified biochar had great potential to treat water contaminated by pathogenic bacteria.

Evaluating Phage Tail Fiber Receptor-Binding Proteins Using a Luminescent Flow-Through 96-Well Plate Assay.

Phages have demonstrated significant potential as therapeutics in bacterial disease control and as diagnostics due to their targeted bacterial host range. Host range has typically been defined by plaque assays; an important technique for therapeutic development that relies on the ability of a phage to form a plaque upon a lawn of monoculture bacteria. Plaque assays cannot be used to evaluate a phage’s ability to recognize and adsorb to a bacterial strain of interest if the infection process is thwarted post-adsorption or is temporally delayed, and it cannot highlight which phages have the strongest adsorption characteristics. Other techniques, such as classic adsorption assays, are required to define a phage’s “adsorptive host range.” The issue shared amongst all adsorption assays, however, is that they rely on the use of a complete bacteriophage and thus inherently describe when all adsorption-specific machinery is working together to facilitate bacterial surface adsorption. These techniques cannot be used to examine individual interactions between a singular set of a phage’s adsorptive machinery (like long tail fibers, short tail fibers, tail spikes, etc.) and that protein’s targeted bacterial surface receptor. To address this gap in knowledge we have developed a high-throughput, filtration-based, bacterial binding assay that can evaluate the adsorptive capability of an individual set of a phage’s adsorption machinery. In this manuscript, we used a fusion protein comprised of an N-terminal bioluminescent tag translationally fused to T4’s long tail fiber binding tip (gp37) to evaluate and quantify gp37’s relative adsorptive strength against the Escherichia coli reference collection (ECOR) panel of 72 Escherichia coli isolates. Gp37 could adsorb to 61 of the 72 ECOR strains (85%) but coliphage T4 only formed plaques on 8 of the 72 strains (11%). Overlaying these two datasets, we were able to identify ECOR strains incompatible with T4 due to failed adsorption, and strains T4 can adsorb to but is thwarted in replication at a step post-adsorption. While this manuscript only demonstrates our assay’s ability to characterize adsorptive capabilities of phage tail fibers, our assay could feasibly be modified to evaluate other adsorption-specific phage proteins.

Silver nanoparticles decorated polyhedral oligomeric silsesquioxane nanocages as an effective nanoadditive for improved structural and biological properties of poly(vinylidene fluoride-co-hexafluoropropylene) nanofiltration membrane

Incorporation of a well-defined functionalized polyhedral oligomeric silsesquioxane (POSS) into a polymer matrix represents a new chemical advancement for applied membrane technology. Herein, POSS nanocages densely decorated with silver (Ag) nanoparticles (NPs) were used as effective hydrophilic and antibacterial additive. In this work, first, a facile and simple chemical reduction strategy is employed to prepare the organic–inorganic hybrid nanocages of Ag@POSS by in situ reduction of the Ag NPs with octa-ammonium molecules of POSS. These Ag@POSS nanocages were added as nanofiller for the fabrication of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) nanohybrid membrane. Ag@POSS nanocages added PVDF-HFP membrane exhibited formation of homogeneous and stable films compared to the unmodified polymeric membranes due to van der Waals and hydrogen bonding interactions of Ag@POSS with –CH2 groups and F atoms of polymer matrix. Pure water flux measurement of nanohybrid membrane showed that Ag@POSS PVDF membrane displays dramatic increase in the permeability (1,554.6 L/m2/h) and hydrophilicity (67°) properties. Furthermore, antibacterial activity and protein adsorption capacity of Ag@POSS PVDF membrane were evaluated by quantitative analysis of living bacterial cells and protein mass adsorption using Escherichia coli and bovine serum albumin (BSA) protein, respectively. The E. coli colonies (108 CFU/mL) on the Ag@POSS PVDF membrane samples tended to decline with 0.5 × 106 CFU/mL compared to neat PVDF-HFP membrane sample (1.3 × 108 CFU/mL). The improvement in biological properties of Ag@POSS PVDF membrane is due to the formation of Ag-octamine on the surface of POSS which lead to the formation of a boundary protection film. The surface–modified POSS with Ag NPs can be used as a nanofiller in polymeric membrane for developing high-performance permeable nanofiltration and antibacterial/antifouling polymeric membranes.

UV-aging of microplastics increases proximal ARG donor-recipient adsorption and leaching of chemicals that synergistically enhance antibiotic resistance propagation

Despite growing attention to environmental pollution by microplastics (MP), the effects of MP aging on bacterial horizontal gene transfer (HGT) have not been systematically investigated. Here, we used UV-aged polystyrene microplastics (PS-MPs) to investigate how aging affects antibiotic resistance genes (ARGs) transfer efficiency from various ARG vectors to recipient bacteria. The adsorption capacity of MP20 (20-day UV-aged PS-MPs) towards E. coli (harboring plasmid-borne blaTEM-1), plasmid pET29 (harboring blaNDM-1) and phage lambda (carrying the aphA1 ARG) increased by 6.6-, 5.2- and 8.3-fold, respectively, relative to pristine PS-MPs (MP0), due to increased specific surface area and affinity for these ARG vectors. Moreover, MP20 released more organic compounds (TOC 1.6 mg/g-MP20, versus 0.2 mg/g-MP0 in 4 h) –possibly depolymerization byproducts (verified by GC-MS), which induced intracellular ROS generation, increased cell permeability and upregulated HGT associated genes. Accordingly, MP20 enhanced ARG transfer frequency from E. coli, plasmid pET29 and phage lambda (relative to MP0) by 1.3-, 4.7- and 3.5-fold, respectively. The Bliss independence model infers that higher bacterial adsorption and exposure to chemicals released during MP aging synergistically enhanced ARG transfer. This underscores the need to assess the significance of this overlooked phenomenon to the environmental dissemination of antibiotic resistance and other HGT processes.

Contamination-resistant, rapid emulsion-based isothermal nucleic acid amplification with Mie-scatter inspired light scatter analysis for bacterial identification

An emulsion loop-mediated isothermal amplification (eLAMP) platform was developed to reduce the impact that contamination has on assay performance. Ongoing LAMP reactions within the emulsion droplets cause a decrease in interfacial tension, causing a decrease in droplet size, which results in decreased light scatter intensity due to Mie theory. Light scatter intensity was monitored via spectrophotometers and fiber optic cables placed at 30° and 60°. Light scatter intensities collected at 3 min, 30° were able to statistically differentiate 103 and 106 CFU/µL initial Escherichia coli O157:H7 concentrations compared to NTC (0 CFU/µL), while the intensity at 60° were able to statistically differentiate 106 CFU/µL initial concentrations and NTC. Control experiments were conducted to validate nucleic acid detection versus bacterial adsorption, finding that the light scatter intensities change is due specifically to ongoing LAMP amplification. After inducing contamination of bulk LAMP reagents, specificity lowered to 0% with conventional LAMP, while the eLAMP platform showed 87.5% specificity. We have demonstrated the use of angle-dependent light scatter intensity as a means of real-time monitoring of an emulsion LAMP platform and fabricated a smartphone-based monitoring system that showed similar trends as spectrophotometer light scatter data, validating the technology for a field deployable platform.

Designing a MOF-based slippery lubricant-infused porous surface with dual functional anti-fouling strategy

Material that resists biofouling adhesion is needed in a complex marine environment, but few of them can combine ultra-low fouling and environmental friendliness. Slippery lubricant-infused porous surface (SLIPS) is such a material, but it lacks the contact-killing ability, which limits its stability and anti-fouling efficiency. Here, we report a metal organic framework (MOF-based) Slippery ionic liquid-infused surface with excellent antifouling performance via synergistic release and contact-killing defense strategy. The dense needle-like MIL-110 array, grown in situ on the aluminum surface, is conducive to the stable storage of quaternary ammonium salt (QAS) ionic liquid. Compared to the control group with mature biofilm formed on the surface, SLIPS showed non-fouling performance in a 10-day test and another 21-day test under more challenging conditions. The adsorption amount of lipopolysaccharide (LPS) on SLIPS was 50% lower than that on the aluminum sheet and the aluminum sheet with MIL-110 grown on the surface as the control groups within three hours. The relationship between bacterial adhesion and LPS adsorption indicated that the anti-adhesion performance of SLIPS was mediated by the weak adhesion and easy release property of its surface to extracellular fouling molecules. This study provides the possibility to systematically reveal the antifouling mechanism of SLIPS on bacterial adhesion.

Developing a Virus-Binding Bacterium Expressing Mx Protein on the Bacterial Surface to Prevent Grouper Nervous Necrosis Virus Infection.

Grouper nervous necrosis virus (GNNV) infection causes mass grouper mortality, leading to substantial economic loss in Taiwan. Traditional methods of controlling GNNV infections involve the challenge of controlling disinfectant doses; low doses are ineffective, whereas high doses may cause environmental damage. Identifying potential methods to safely control GNNV infection to prevent viral outbreaks is essential. We engineered a virus-binding bacterium expressing a myxovirus resistance (Mx) protein on its surface for GNNV removal from phosphate-buffered saline (PBS), thus increasing the survival of grouper fin (GF-1) cells. We fused the grouper Mx protein (which recognizes and binds to the coat protein of GNNV) to the C-terminus of outer membrane lipoprotein A (lpp-Mx) and to the N-terminus of a bacterial autotransporter adhesin (Mx-AIDA); these constructs were expressed on the surfaces of Escherichia coli BL21 (BL21/lpp-Mx and BL21/Mx-AIDA). We examined bacterial surface expression capacity and GNNV binding activity through enzyme-linked immunosorbent assay; we also evaluated the GNNV removal efficacy of the bacteria and viral cytotoxicity after bacterial adsorption treatment. Although both constructs were successfully expressed, only BL21/lpp-Mx exhibited GNNV binding activity; BL21/lpp-Mx cells removed GNNV and protected GF-1 cells from GNNV infection more efficiently. Moreover, salinity affected the GNNV removal efficacy of BL21/lpp-Mx. Thus, our GNNV-binding bacterium is an efficient microparticle for removing GNNV from 10‰ brackish water and for preventing GNNV infection in groupers.

New Insights into Ion Adsorption Type Rare-Earths Mining—Bacterial Adsorption of Yttrium Integrated with Ammonia Nitrogen Removal by a Fungus

Ion adsorption-type heavy rare earths found in southern China are important ore resources, whose yttrium(Y)-group rare-earth elements account for 90% of the total mass of rare earths known on the planet. At present, ammonia-nitrogen wastewater from extraction of rare earths pose threats to the environment. A bacterial strain (Bacillus sp. ZD 1) isolated from the “Foot Cave” mining area was used for adsorption of Y3+. Its adsorption capacity reached 428 μmol/g when the initial concentration of Y3+ was 1.13 mM. Moreover, 50 mg of Bacillus sp. ZD 1 (converted to dry mass) could completely adsorb Y3+ in the mother solution of mixed rare earths from the rare-earth mining area. Ammonia nitrogen in the remaining solution after adsorption was removed through denitrification using a fungus named Galactomyces sp. ZD 27. The final concentration of ammonia nitrogen in wastewater was lower than Indirect Emission Standard of Pollutants for Rare-earth Industry (GB 26451-2011). Furthermore, the resulting fungal cells of Galactomyces sp. ZD 27 could be used to produce single cell proteins, whose content accounted for 70.75% of the dry mass of cells. This study offers a new idea for integrated environmentally-friendly extraction and ecological restoration of the mining area in southern China.

Interactions of Microorganisms with Lipid Langmuir Layers.

Preventing microbial contamination of aquatic environments is crucial for the proper supply of drinking water. Hence, understanding the interactions that govern bacterial and virus adsorption to surfaces is crucial to prevent infection transmittance. Here, we describe a new approach for studying the organization and interactions of various microorganisms, namely, Escherichia coli (E. coli) bacteria, E. coli-specific bacteriophage T4, and plant cucumber green mottle mosaic viruses (CGMMV), at the air/water interface using the Langmuir-Blodgett (LB) technique. CGMMV were found as applicable candidates for further studying their interactions with Langmuir lipid monolayers. The zwitterionic, positively, and negatively charged LB lipid monolayers with adsorbed viruses were deposited onto solid supports and characterized by atomic force microscopy. Using polymerase chain reaction, we indicated that the adsorption of CGMMV onto the LB monolayer is a result of electrostatic interactions. These insights are useful in engineering membrane filters that prevent biofouling for efficient purification systems.

Individual and combined applications of biochar and pyroligneous acid mitigate dissemination of antibiotic resistance genes in agricultural soil

Remediation of agricultural soils polluted with antibiotic resistance genes (ARGs) is important for protecting food safety and human health. However, the feasibility of co-application of biochar and pyroligneous acid, two multifunctional soil amendments, for mitigating dissemination of soil ARGs is unknown. Thus, a woody biochar (BC450) and its by-product, pyroligneous acid (PA450) simultaneously produced at 450 °C from blended wood wastes, were used to compare their individual and combined effects on soil ARG abundance using a 65-day pot experiment planted with leafy vegetable Brassica chinensis L. The individual and combined applications of PA450 and BC450 significantly reduced the absolute abundance of ARGs by 65.7–81.4% and 47.5–72.9% in the corresponding rhizosphere and bulk soil. However, the co-application showed little synergistic effect, probably due to the counteractive effect of BC450 on the PA450-mitigated soil ARG proliferation, resulted from the promoted soil bacterial growth and/or adsorption of antimicrobial components of PA450 by BC450. The decreased abundances of mobile genetic element intI1 and Tn916/1545 in the PA450 treatments demonstrated the potential of PA450 for weakening horizontal gene transfer (HGT). Furthermore, weakened HGT by individual PA450, lowered availability of heavy metals by individual BC450, and different bacterial community (e.g., reduced ARGs bacterial host) together with improved soil properties from co-application of PA450 and BC450 all contributed to the reduced ARG level. This study highlighted the feasibility of co-applications of biochar and pyroligneous acid amendment for mitigating soil ARG pollution. These findings provide important information for developing eco-friendly technologies using biochar and pyroligneous acid in remediating ARG-contaminated soils.

Reduction and bacterial adsorption of dissolved mercuric ion by indigenous bacteria at the Oak Ridge Reservation site

Mercury exists in various forms in the environment and the indigenous bacteria mediated processes have the potential to be used for mercury remediation. In this study, two mixed cultures of indigenous bacteria at the Oak Ridge Reservation site (i.e., ORR soil culture and ORR sediment culture) were selected to study the microbial mediated mercuric reduction under an aerobic condition as well as mercury adsorption onto bacterial surfaces. PCR analysis was performed to provide insights into the microbial community. The mercuric volatilizing experiment demonstrated the mercuric reducing capacity for both ORR cultures, in which the Pseudomonas genus was the dominating Hg0 producer. The investigation of the impact of the sole carbon source revealed the energy-dependent characteristics of the mercuric reduction in this study. Namely, the mercuric reduction was nearly not impacted by the type of carbon source but positively related to the energy that a unit amount of substrate could provide. The study also indicated that the mercury adsorption competed with the reduction. According to the fitting of the Langmuir isotherm, the ORR soil culture was found to have a higher mercury adsorption capacity (i.e., 67.5 mg Hg/g dry biomass) than the ORR sediment culture (i.e., 53.1 mg Hg/g dry biomass). The negative correlation between the reduced mercury mass and adsorbed mercury mass was identified for both ORR cultures.

Biodegradable Anti-Biofilm Fiber-Membrane Ureteral Stent Constructed with a Robust Biomimetic Superhydrophilic Polycationic Hydration Surface Exhibiting Synergetic Antibacterial and Antiprotein Properties.

The biofouling of ureteral stents and subsequent urinary tract infections mainly come from the adsorption and adhesion of proteins and microorganisms and their ensuing proliferation. Although general polycationic surfaces in implants have good antibacterial activities, they suffer from limited durability due to severe protein and bacterial adsorption. Here, a biodegradable and anti-biofilm fiber-membrane structured ureteral stent (FMBUS) with synergetic contact-killing antibacterial activity and antiprotein adsorption is described. The stent is prepared by generating hyperbranched poly(amide-amine)-grafted polydopamine microparticles (≈300nm) on the surface of fibers by in situ polymerization and Schiff base reactions. The biomimetic surface endows the FMBUS with a positive charge (+21.36mV) and superhydrophilicity (water contact angle: 0°). As a result, the stents fulfilled the following functions: i) reduced attachment of host protein due to superhydrophilicity (Lysozyme: 92.1%; human serum albumin: 39.4%); ii) high bactericidal activities against contact pathogenic bacteria (contact-killing rate: 99.9999% for both E. coli and S. aureus; antiadhesion rate: 99.2% for E. coli and 99.9999% for S. aureus); iii) biocompatibility in vitro (relative growth rate of L929: >90% on day 3) and in vivo; and iv) gradient biodegradability to avoid a second surgery of stent extraction 1-2 weeks after implantation.

The control of red water occurrence and opportunistic pathogens risks in drinking water distribution systems: A review

Many problems in drinking water distribution systems (DWDSs) are caused by microbe, such as biofilm formation, biocorrosion and opportunistic pathogens growth. More iron release from corrosion scales may induce red water. Biofilm played great roles on the corrosion. The iron-oxidizing bacteria (IOB) promoted corrosion. However, when iron-reducing bacteria (IRB) and nitrate-reducing bacteria (NRB) became the main bacteria in biofilm, they could induce iron redox cycling in corrosion process. This process enhanced the precipitation of iron oxides and formation of more Fe3O4 in corrosion scales, which inhibited corrosion effectively. Therefore, the IRB and NRB in the biofilm can reduce iron release and red water occurrence. Moreover, there are many opportunistic pathogens in biofilm of DWDSs. The opportunistic pathogens growth in DWDSs related to the bacterial community changes due to the effects of micropollutants. Micropollutants increased the number of bacteria with antibiotic resistance genes (ARGs). Furthermore, extracellular polymeric substances (EPS) production was increased by the antibiotic resistant bacteria, leading to greater bacterial aggregation and adsorption, increasing the chlorine-resistance capability, which was responsible for the enhancement of the particle-associated opportunistic pathogens in DWDSs. Moreover, O3-biological activated carbon filtration-UV-Cl2 treatment could be used to control the iron release, red water occurrence and opportunistic pathogens growth in DWDSs.

A physiological model of the inflammatory-thermal-pain-cardiovascular interactions during an endotoxin challenge.

Inflammation in response to bacterial endotoxin challenge impacts physiological functions, including cardiovascular, thermal and pain dynamics, although the mechanisms are poorly understood. We develop an innovative mathematical model incorporating interaction pathways between inflammation and physiological processes observed in response to an endotoxin challenge. We calibrate the model to individual data from 20subjects in an experimental study of the human inflammatory and physiological responses to endotoxin, and we validate the model against human data from an independent study. Using the model to simulate patient responses to different treatment modalities reveals that a multimodal treatment combining several therapeutic strategies gives the best recovery outcome. Uncontrolled, excessive production of pro-inflammatory mediators from immune cells and traumatized tissues can cause systemic inflammatory conditions such as sepsis, one of the ten leading causes of death in the USA, and one of the three leading causes of death in the intensive care unit. Understanding how inflammation affects physiological processes, including cardiovascular, thermal and pain dynamics, can improve a patient's chance of recovery after an inflammatory event caused by surgery or a severe infection. Although the effects of the autonomic response on the inflammatory system are well-known, knowledge about the reverse interaction is lacking. The present study develops a mathematical model analyzing the inflammatory system's interactions with thermal, pain and cardiovascular dynamics in response to a bacterial endotoxin challenge. We calibrate the model with individual data from an experimental study of the inflammatory and physiological responses to a one-time administration of endotoxin in 20healthy young men and validate it against data from an independent endotoxin study. We use simulation to explore how various treatments help patients exposed to a sustained pathological input. The treatments explored include bacterial endotoxin adsorption, antipyretics and vasopressors, as well as combinations of these. Our findings suggest that the most favourable recovery outcome is achieved by a multimodal strategy, combining all three interventions to simultaneously remove endotoxin from the body and alleviate symptoms caused by the immune system as it fights the infection.

Optimization of oxygen plasma treatment of silicone implant surface for inhibition of capsular contracture

Silicone is the primary implant material used in plastic surgery; however, it exhibits some inherent disadvantages. For instance, it can cause delayed seroma, breast implant-associated anaplastic large cell lymphoma, and capsular contracture, which are closely related to the type of implant surface. Biomaterial surface modification techniques are continuously being improved for application in many fields. Herein, conditions for oxygen (O2) plasma treatment on various surface types of peri-silicone implants were optimized. Following optimal treatment, surface hydrophilicity, protein adsorption, bacterial adhesion, cell viability and proliferation, changes in implant shell mechanical properties, and in vivo tissue response were examined. Hydrophobicity decreased following O2 plasma treatment. Bacterial adhesion and protein adsorption were significantly inhibited, and mechanical properties were improved. There was no topographic change on the implant surface. In vitro cells were evenly distributed on the O2 plasma-treated surface, and in vivo analysis confirmed a decrease in capsule thickness, collagen fiber composition, number of inflammatory cells, and TGF-β1 and α-SMA expression. Additionally, reduced activation of cytokines related to macrophage and T-cell responses was observed. O2 plasma surface treatment, under optimal conditions, is a simple and effective method with potential clinical applications for attenuating excessive capsule formation and the immune response.

Recycling of rural abandoned constructed wetlands: mariculture wastewater treatment

AbstractThis study aimed to investigate the behavioral shifts of constructed wetland (CW) when the treated water was changed from domestic wastewater to mariculture wastewater. The results showed that the average removal efficiencies of ammonium nitrogen (), total nitrogen and chemical oxygen demand (COD) were 29.54, 46.07 and 57.15% in mariculture wastewater, respectively, which were significantly lower than those in domestic wastewater (71.35, 66.34 and 74.98%, respectively). While there was no significant difference in the removal efficiency of nitrate and phosphate (P > 0.05) between the two systems. Based on the analysis of bacterial community and adsorption properties, the results further indicated that the removal mechanism of between both systems was mainly due to substrate adsorption: the maximum adsorption capacity of on the substrate in mariculture wastewater was 5,432 mg kg−1, whereas that in domestic wastewater was 18,033 mg kg−1. In terms of bacterial communities, the dominant bacteria at the family level were Victivallaceae (18.63%) in domestic wastewater and Porphyromonadaceae (18.37%) in mariculture wastewater, which showed the significant alteration to the bacterial community. In conclusion, this study showed that conventional CW could be used for treating wastewater from land-based marine aquaculture, while the operating conditions needed to be optimized in the process of application.

Hydrophobic N-halamine based POSS block copolymer porous films with antibacterial and resistance of bacterial adsorption performances

Functional films with antimicrobial efficacies and resistance of bacterial adhesion have great potential applications. In this paper, polyhedral oligomeric silsesquioxanes-(poly(trifluoroethyl methacrylate))8 (POSS-(PTFEMA)8) block copolymer and olefinic N-halamine monomer precursor containing quaternary ammonium groups (HQS) were used to prepare antibacterial porous films. The HQS compound was chlorinated (HQS-Cl) with tert-butylhypochlorite to achieve antibacterial functionality, and the stability and regenerability of HQS-Cl were examined. The porous film was prepared from POSS-(PTFEMA)8 by the breath figure approach and the stability of the porous films was examined. The surface morphology, stability and mechanical property of the porous films were studied. Moreover, the adding and spraying methods were carried out with HQS-Cl on the pincushion porous films to obtain hydrophobic antibacterial films. The static and dynamic hydrophobic properties were investigated by water contact angle and water droplet impact behavior. In addition, the bacterial adsorption of S. aureus and E. coli O157:H7 on the flat, porous and pincushion structure films were studied. The antibacterial testing results showed that the HQS-Cl modified pincushion films had great antibacterial activity and could completely inactivate 2.38 × 106 CFU/sample of S.aureus and 3.07 × 106 CFU/sample of E. coli O157:H7 within 30 min of contact time.

A Multifunctional Nanosystem Based on Bacterial Cell-Penetrating Photosensitizer for Fighting Periodontitis Via Combining Photodynamic and Antibiotic Therapies.

Photodynamic therapy (PDT), an emerging approach that involves photosensitizers, light, and molecular oxygen, has shown promise for fighting periodontitis. However, PDT does not always acquire the desired therapeutic outcomes since some photosensitizers have strong hydrophobic properties and are difficult to absorb efficiently by periodontal pathogenic bacteria. Here, a hydrophobic photosensitizer chlorin e6 (Ce6) was hydrophilically modified via conjugation with TAT peptide, a cationic cell-penetrating peptide, to improve its solubility and enhance its bacterial adsorption by promoting its interaction with the negatively charged cell walls and penetration through the cell membranes. The obtained TAT-Ce6 conjugate (TAT-Ce6) was used to prepare self-assembled nanoparticles (NPs) for loading tinidazole (TDZ), a clinically used antibiotic agent, thus hoping to achieve synergistic antiperiodontitis effects through combining PDT and antibiotic therapy. Compared to free Ce6, TAT-Ce6 nanoparticles (TAT-Ce6 NPs) had greatly enhanced adsorption and penetration abilities for periodontal pathogen bacteria and also exhibited significantly increased PDT efficiencies in both periodontal pathogen bacteria and monocyte macrophages. Upon 635 nm laser irradiation, TDZ-loaded TAT-Ce6 (TAT-Ce6/TDZ) NPs exerted remarkable synergistic antiperiodontitis effects of PDT and antibiotic therapy, reflecting in the effective killing of periodontal pathogenic bacteria in vitro and the reduced adsorption of alveolar bone in the Sprague-Dawley rat model of periodontitis. Altogether, this study develops a novel photosensitizer that can be efficiently absorbed by the periodontal pathogenic bacteria and also provides a potent combination strategy of PDT with antibiotic therapy for clinical periodontitis treatment.