Reduction Of Viable Bacteria Research Articles

Curcumin-loaded silk fibroin e-gel scaffolds for wound healing applications

Recently, silk fibroin gel systems (e-gel), formed with weak electric fields have been prepared for various tissue-engineering applications such as neural, cartilage and bone. Here, we demonstrated the effectiveness of an electroresponsive silk fibroin (SF) hydrogel, which is a 3-D scaffold formed and used as a wound dressing material. SEM studies revealed that the curcumin (CUR)-loaded SF (CUR-SF) consisted of a 3-D porous structure with a porosity percent of 80% and a swelling ratio over 100%. Colony forming unit assay confirmed that CUR-SF e-gel scaffolds produced a reduction in viable bacteria compared to bare SF scaffolds. In vitro studies performed with immortalized human keratinocyte (HaCaT) indicated no toxicity of CUR-loaded SF e-gel scaffolds to healthy cells. Taking all the results together, it was suggested that the CUR-SF e-gel scaffolds could improve the wound healing activity in comparison to SF without curcumin and be potentially used as a wound dressing material.

One-step coagulation to construct durable anti-fouling and antibacterial cellulose film exploiting Ag@AgCl nanoparticle- triggered photo-catalytic degradation

An anti-fouling and antibacterial surface of cellulose film was obtained by one-step coagulation of the cellulose-LiCl/Dimethyl acetamide (DMAc) solution with AgNO3 and polyvinyl pyrrolidone (PVP). The AgCl nanocrystals were embedded on the surface of cellulose film with the assistance of PVP, and the Ag@AgCl was formed due to the partly decomposition of AgCl under the visible-light irradiation. Morphology and size of the Ag@AgCl in cellulose matrix could be regulated by changing the concentration of PVP. From a series of comparative tests, Ag@AgCl could be stably embedded on cellulose film at the concentration of 1wt% PVP, and its photo-degradation efficiency could be still retained 89% after 5-cycle testing. Meanwhile, a dramatic reduction in viable bacteria was also observed within 120min of exposure on this film, and when exposure time was 180min, no active bacteria was observed.This work provided a simple pathway to construct the functional cellulose film which could be applied as packaging materials.

Effects of photodynamic laser and violet-blue led irradiation on Staphylococcus aureus biofilm and Escherichia coli lipopolysaccharide attached to moderately rough titanium surface: in vitro study.

Effective decontamination of biofilm and bacterial toxins from the surface of dental implants is a yet unresolved issue. This study investigates the in vitro efficacy of photodynamic treatment (PDT) with methylene blue (MB) photoactivated with λ 635nm diode laser and of λ 405nm violet-blue LED phototreatment for the reduction of bacterial biofilm and lipopolysaccharide (LPS) adherent to titanium surface mimicking the bone-implant interface. Staphylococcus aureus biofilm grown on titanium discs with a moderately rough surface was subjected to either PDT (0.1% MB and λ 635nm diode laser) or λ 405nm LED phototreatment for 1 and 5min. Bactericidal effect was evaluated by vital staining and residual colony-forming unit count. Biofilm and titanium surface morphology were analyzed by scanning electron microscopy (SEM). In parallel experiments, discs coated with Escherichia coli LPS were treated as above before seeding with RAW 264.7 macrophages to quantify LPS-driven inflammatory cell activation by measuring the enhanced generation of nitric oxide (NO). Both PDT and LED phototreatment induced a statistically significant (p < 0.05 or higher) reduction of viable bacteria, up to -99 and -98% (5min), respectively. Moreover, besides bactericidal effect, PDT and LED phototreatment also inhibited LPS bioactivity, assayed as nitrite formation, up to -42%, thereby blunting host inflammatory response. Non-invasive phototherapy emerges as an attractive alternative in the treatment of peri-implantitis to reduce bacteria and LPS adherent to titanium implant surface without causing damage of surface microstructure. Its efficacy in the clinical setting remains to be investigated.

Effectiveness of a pre-procedural mouthwash in reducing bacteria in dental aerosols: randomized clinical trial

The aim of this randomized, single blinded clinical trial was to evaluate the effect of a pre-procedural mouthwash containing cetylpyridinium chloride (CPC), zinc lactate (Zn) and sodium fluoride (F) in the reduction of viable bacteria in oral aerosol after a dental prophylaxis with ultrasonic scaler. Sixty systemically healthy volunteers receiving dental prophylaxis were randomly assigned to one of the following experimental groups (15 per group): (i) rinsing with 0.075% CPC, 0.28% Zn and 0.05% F (CPC+Zn+F), (ii) water or (iii) 0.12% chlorhexidine digluconate (CHX), and (iv) no rinsing. Viable bacteria were collected from different locations in the dental office on enriched TSA plates and anaerobically incubated for 72 hours. The colonies were counted and species were then identified by Checkerboard DNA-DNA Hybridization. The total number of colony-forming units (CFUs) detected in the aerosols from volunteers who rinsed with CPC+Zn+F or CHX was statistically significantly (p<0.05) lower than of those subjects who did not rinse or who rinsed with water. When all locations were considered together, the aerosols from the CPC+Zn+F and CHX groups showed, respectively, 70% and 77% fewer CFUs than those from the No Rinsing group and 61% and 70% than those from the Water group. The mean proportions of bacterial species from the orange complex were statistically significantly (p<0.05) lower in aerosols from the CPC+Zn+F and CHX groups compared with the others two groups. In conclusion, the mouthwash containing CPC+Zn+F, is effective in reducing viable bacteria in oral aerosol after a dental prophylaxis with ultrasonic scaler.

'Artilysation' of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci.

Endolysins constitute a promising class of antibacterials against Gram-positive bacteria. Recently, endolysins have been engineered with selected peptides to obtain a new generation of lytic proteins, Artilysins, with specific activity against Gram-negative bacteria. Here, we demonstrate that artilysation can also be used to enhance the antibacterial activity of endolysins against Gram-positive bacteria and to reduce the dependence on external conditions. Art-240, a chimeric protein of the anti-streptococcal endolysin λSa2lys and the polycationic peptide PCNP, shows a similar species specificity as the parental endolysin, but the bactericidal activity against streptococci increases and is less affected by elevated NaCl concentrations and pH variations. Time-kill experiments and time-lapse microscopy demonstrate that the killing rate of Art-240 is approximately two-fold higher compared to wildtype endolysin λSa2lys, with a reduction in viable bacteria of 3 log units after 10 min. In addition, lower doses of Art-240 are required to achieve the same bactericidal effect.

A new buildup biofilm model that mimics accumulation of material in flexible endoscope channels

The objective of this study was to develop a new build up biofilm (BBF) model that was based on repeated exposure to test soil containing Enterococcus faecalis and Pseudomonas aeruginosa and repeated rounds of fixation to mimic the accumulation of patient material in endoscope channels during reprocessing. The new BBF model is a novel adaptation of the minimum biofilm effective concentration (MBEC) 96-well model where biofilm is formed on plastic pegs. The new MBEC-BBF model was developed over eight days and included four rounds of partial fixation using glutaraldehyde. There was 6.14Log10cfu/cm2 of E. faecalis and 7.71Log10cfu/cm2 of P. aeruginosa in the final BBF. Four detergents (two enzymatic and two non-enzymatic) were tested alone or in combination with orthophthalaldehyde, glutaraldehyde or accelerated hydrogen peroxide to determine if BBF could be either removed or the bacteria within the BBF killed. None of the detergents alone could remove the biofilm or reduce the bacterial level in the BBF as determined by viable count and scanning electron microscopy. The combination of detergents and disinfectants tested provided a 3 to 5Log10 reduction in viable bacteria but no combination could provide the expected 6Log10 reduction. Our data indicated that once formed BBF was extremely difficult to eliminate. Future research using the BBF model may help develop new cleaning and disinfection methods that can prevent or eliminate BBF within endoscope channels.

Electrochemical scaffold generates localized, low concentration of hydrogen peroxide that inhibits bacterial pathogens and biofilms.

We hypothesized that low concentrations of H2O2 could be generated through the electrochemical conversion of oxygen by applying an electric potential to a conductive scaffold and produce a low, but constant, concentration of H2O2 that would be sufficient to destroy biofilms. To test our hypothesis we used a multidrug-resistant Acinetobacter baumannii strain, because this species is often implicated in difficult-to-treat biofilm infections. We used conductive carbon fabric as the scaffold material (“e-scaffold”). In vitro experiments demonstrated the production of a maximum constant concentration of ~25 μM H2O2 near the e-scaffold surface. An e-scaffold was overlaid onto an existing A. baumannii biofilm, and within 24 h there was a ~4-log reduction in viable bacteria with an ~80% decrease in biofilm surface coverage. A similar procedure was used to overlay an e-scaffold onto an existing A. baumannii biofilm that was grown on a porcine explant. After 24 h, there was a ~3-log reduction in viable bacteria from the infected porcine explants with no observable damage to the underlying mammalian tissue based on a viability assay and histology. This research establishes a novel foundation for an alternative antibiotic-free wound dressing to eliminate biofilms.

Graphene–CdS nanocomposite inactivation performance toward Escherichia coli in the presence of humic acid under visible light irradiation

Graphene–CdS (G–CdS) nanocomposite was prepared successfully via a two-step solvothermal process, with CdS uniformly dispersed on the graphene nanosheets. The photocatalytic disinfection activity of G–CdS was evaluated, and the result shows that G–CdS exhibited higher inactivation efficiency toward the gram-negative bacterium, Escherichia coli, than pure CdS nanoparticles under visible light irradiation. Exposure to 10mg of pure CdS resulted in a 1.1-log inactivation after 60min, but resulted in 5.3-log reduction of viable bacteria when exposure to 10mg G–CdS under the same illumination conditions. In addition, the impacts of humic acid (HA), a kind of natural organic matter (NOM), on its bactericidal properties have also been determined. G–CdS in the presence of HA (10mg/L) significantly decreased its toxicity, causing less than 0.4-log inactivation after 60min. Lipid peroxidation, intercellular ROS generation and antioxidant enzyme activities assays indicate that excess oxidative stress induced by G–CdS suppressed the antioxidant defense system, subsequently affected the normal function of lipid, protein and nucleic acid, and thus resulted in cell death. However, the decreased toxicity of G–CdS in the presence of HA may be attributed to that (1) HA presents a barrier to prevent the physical contact between bacteria cells and G–CdS, which was the first step of toxicity mechanisms; (2) HA acts as an antioxidant to react with any ROS and reduce the toxicity.

Highly enhanced bactericidal effects of medium chain fatty acids (caprylic, capric, and lauric acid) combined with edible plant essential oils (carvacrol, eugenol, β-resorcylic acid, trans-cinnamaldehyde, thymol, and vanillin) against Escherichia coli O157:H7

Medium chain fatty acids (MCFAs) and essential oils (EOs) are known to be natural antimicrobials, but their combined effects have not been fully investigated. The objective of the present study was to examine the bactericidal effects of various combined treatments of MCFAs [caprylic (CA), capric (CPA), and lauric acid (LRA)] and EOs [carvacrol (CAR), eugenol (EUG), β-resorcylic acid (RA), trans-cinnamaldehyde (TC), thymol (TM), and vanillin (VNL)]. Escherichia coli O157:H7, was treated with 1) control (2% ethanol), 2) MCFA alone, 3) EO alone, and 4) different combinations of MCFAs and EOs at 37 °C for 5 and 10 min. Synergistic bactericidal effects were observed with combined treatments; the log reduction in viable bacteria in response to the combined treatments was much greater than the sum of the effects of the two compounds applied individually. For example, individual treatment with 0.2 mM CPA (0.004%) and 0.4 mM RA (0.006%) for 5 min resulted in a negligible reduction in bacterial load (0.25 and 0.21 log reduction, respectively), whereas combined treatment at the same concentrations and for the same time reduced the bacterial population in the test sample to an undetectable level (initial population: 7.51 log CFU/ml; detection limit: 1 CFU/ml). The ranking of EOs showing the highest bacterial killing activities when combined with MCFAs was generally RA, CAR, TM > EUG > TC > VNL. All the antimicrobials used in this study are natural compounds that have been widely used in industry, so they are both consumer- and user-friendly. Combined treatment can overcome the disadvantages of MCFAs and EOs such as unpleasant odor and high cost because the required concentrations can be reduced. Our results indicate that the combined treatments used here could be successfully used to eliminate foodborne pathogens, significantly improving the microbiological safety of foods.

Inactivation of Bacteria on Explanted Dialysis Catheter Lumens with Fiber Optically Delivered Ultraviolet Light

PurposeTo evaluate the germicidal effect of fiber optically delivered ultraviolet (UV) light on colonized explanted dialysis catheters. Materials and MethodsExplanted dialysis catheters were screened for intraluminal colonization by culturing 1 mL of a saline flush. Catheters growing >10 colony-forming units were treated with doses of fiber optically delivered UV light (range, 40–1,300 mJ/cm2). For each UV-treated catheter, an unexposed segment was first cut and set aside as a control sample. A sterile optical fiber was inserted into the catheter hub and advanced to the catheter tip. The fiber was slowly withdrawn at a constant rate while exposing the inner lumen to UV light. A second UV-exposed segment was then removed. The UV-exposed and control segments were split and sonicated to remove the adherent bacteria. The bacteria were counted and identified. ResultsThere were 14 colonized catheters treated with UV light. The catheters were primarily colonized with coagulase-negative staphylococci (60%) and Staphylococcus aureus (33%). There was a significant reduction in viable bacteria between the UV-treated versus untreated segments of each infected catheter (P = .04). In the seven treated catheters with >100,000 colony-forming units per cm2 of luminal surface area, there was a >99.5% reduction of viable bacteria in all UV-exposed samples, with no residual viable bacteria in four of seven (57%) of the samples. ConclusionsThis study demonstrates the technical feasibility and benchtop efficacy of using fiber optics to deliver UV light into the lumen of a colonized dialysis catheter and inactivating bacteria on the intraluminal surface.

Swirl Flow Bioreactor coupled with Cu-alginate beads: A system for the eradication of Coliform and Escherichia coli from biological effluents.

It is estimated that approximately 1.1 billion people globally drink unsafe water. We previously reported both a novel copper-alginate bead, which quickly reduces pathogen loading in waste streams and the incorporation of these beads into a novel swirl flow bioreactor (SFB), of low capital and running costs and of simple construction from commercially available plumbing pipes and fittings. The purpose of the present study was to trial this system for pathogen reduction in waste streams from an operating Dewats system in Hinjewadi, Pune, India and in both simulated and real waste streams in Seattle, Washington, USA. The trials in India, showed a complete inactivation of coliforms in the discharged effluent (Mean Log removal Value (MLRV) = 3.51), accompanied by a total inactivation of E. coli with a MLRV of 1.95. The secondary clarifier effluent also showed a 4.38 MLRV in viable coliforms during treatment. However, the system was slightly less effective in reducing E. coli viability, with a MLRV of 1.80. The trials in Seattle also demonstrated the efficacy of the system in the reduction of viable bacteria, with a LRV of 5.67 observed of viable Raoultella terrigena cells (100%).

SUSCEPTIBILIDADE DE AMOSTRAS CLÍNICAS DE PSEUDOMONAS AERUGINOSA A ANTIBIÓTICOS E A CLOREXIDINA

Backgound and Objectives: Aimed to investigate whether there is a possible association between antibiotic resistance and susceptibility to chlorhexidine of 65 clinical strains of Pseudomonas aeruginosa isolated from patients in a Brazilian hospital. Methods: The samples were identified by the MicroScan system and the sensitivity to antibiotics was performed by the disk diffusion technique. The minimum inhibitory concentration (MIC) of chlorhexidine was evaluated by broth dilution method and bactericidal activity at concentrations of 0.2% and 2%, was evaluated by the test suspension, according to the European Standard 1040. Results: All strains tested showed sensitivity to polymyxin, followed by piperacillin / tazobactam (75.4%), ceftazidime and cefepime (41.5%), tobramycin (36.9%), aztreonam and amikacin (33.8%), levofloxacin (30.8%), ciprofloxacin (29.2%), ofloxacin (27.3%), gentamicin (26.2%) and ceftriaxone (7.7%). The MIC of chlorhexidine ranged from 2.5 to 40 micrograms / ml, with MIC50 and MIC90 of 10 and 20 mg / ml. In a suspension test, the concentration of chlorhexidine in 2% destroy any bacterial cell inoculum of 65 samples. At the concentration of 0.2% chlorhexidine removed 24.2% (15/65) of samples. A sample showed reduced susceptibility chlorhexidine, ie, in the test suspension, the reduction of viable bacteria in the inoculum was less than 5 log10. Three other samples were very close to a logarithmic reduction of 5. Conclusion: In our study, the results of in vitro tests with chlorhexidine were homogeneous, seeming to indicate an association of biocide with multiple antibiotic resistance of P aeruginosa samples tested. Noteworthy is the finding of a sample of P. aeruginosa with reduced susceptibility to chlorhexidine use in dilution of 0.2%. KEYWORDS: Pseudomonas aeruginosa. Chlorhexidine. Resistance.

Construction of cellulose based ZnO nanocomposite films with antibacterial properties through one-step coagulation.

Cellulose based ZnO nanocomposite (RCZ) films were prepared from cellulose carbamate-NaOH/ZnO solutions through one-step coagulation in Na2SO4 aqueous solutions. The structure and properties of RCZ films were characterized using XRD, FTIR, XPS, SEM, TEM, TG, tensile testing, and antibacterial activity tests. The content of ZnO in RCZ films was obtained in the range of 2.7-15.1 wt %. ZnO nanoparticles with a hexagonal wurtzite structure agglomerated into large particles, which firmly embedded in the cellulose matrix. RCZ films displayed good mechanical properties and high thermal stability. Moreover, the films exhibited excellent UV-blocking properties and antibacterial activities against Staphylococcus aureus and Escherichia coli. A dramatic reduction in viable bacteria was observed within 3 h of exposure, while all of the bacteria were killed within 6 h. This work provided a novel and simple pathway for the preparation of regenerated cellulose films with ZnO nanoparticles for application as functional biomaterials.

Development of an Antibacterial Root Canal Filling System Containing MDPB

An antibacterial monomer 12-methacryloyloxydodecylpyridinum bromide (MDPB)-containing experimental, chemically cured primer was prepared to develop a new resin-based root canal filling system. This study investigated the antibacterial effects of the MDPB-containing primer (experimental primer [EP]) against Enterococcus faecalis and assessed the in vitro bonding and sealing abilities of the filling system, consisting of EP and a Bis-GMA-based sealer resin. Antibacterial effects of EP were evaluated by contact with planktonic or adherent bacteria for 30 or 60 sec, and the viable bacterial number was counted. The antibacterial effects against E. faecalis in dentinal tubules were also assessed, according to a root canal infection model. Bonding and sealing abilities of the experimental filling system were examined by microtensile bond strength tests and leakage tests based on fluid filtration methods. Significantly greater reduction in viable bacteria in planktonic and adherent form was obtained by short-period contact with EP compared with the control primer (without MDPB) or with the proprietary (Epiphany) primer (p < .05). Significantly greater bactericidal effects of the EP inside the dentinal tubule of root, as opposed to the control primer or Epiphany primer, were confirmed according to a root canal infection model (p < .05), and 100% killing of E. faecalis could be obtained by the application of EP after irrigation with a 5% sodium hypochlorite solution. The experimental endodontic filling system demonstrated significantly greater bond strength to root dentin than Epiphany sealer system (Epiphany primer and Epiphany Root Canal Sealant; p < .05), showing formation of resin tags and a hybridized layer. Leakage tests clarified that the experimental system provided excellent sealing. This study confirmed that the MDPB-containing experimental antibacterial primer has the ability to effectively disinfect the root canal. Additionally, the experimental root canal filling system employing this primer and the Bis-GMA-based sealer resin is useful for achieving good sealing, suggesting its possible benefit for successful endodontic treatments.

Antibiofilm Efficacy of Photosensitizer-functionalized Bioactive Nanoparticles on Multispecies Biofilm

IntroductionNewer disinfection strategies based on antibacterial nanoparticles and photodynamic therapy (PDT) aim to eliminate residual biofilm bacteria during root canal treatment. The aim of the current study was to test the newly developed rose bengal–functionalized chitosan nanoparticles (CSRBnps) for their interaction/uptake with monospecies bacteria/biofilm and assess their antibiofilm efficacy on a multispecies biofilm model in vitro. MethodsThe interaction of CSRBnps with bacterial cells was conducted using atomic force microscopy. Their membrane-damaging effect was determined by measuring the absorbance at 260 nm (OD260nm) using Enterococcus faecalis. The penetration of CSRBnps into E. faecalis biofilms was evaluated using confocal laser scanning microscopy (CLSM). Multispecies biofilms of Streptococcus oralis, Prevotella intermedia, and Actinomyces naeslundii were grown on dentin sections for 21 days to assess the antibiofilm efficacy. The biofilms were subjected to PDT (60 J/cm2) using CSRBnps and rose bengal. The treated/untreated biofilms were examined under scanning electron microscopy and CLSM. ResultsThe CSRBnps synthesized were 60 ± 20 nm and showed absorption spectra similar to rose bengal. Atomic force microscopy showed adherence of CSRBnps to bacteria, roughening of cell surface, and cell disruption after PDT. CSRBnp treatment resulted in significantly increased bacterial membrane damage (P < .05). CSRBnps exhibited deeper penetration into the biofilm structure. Scanning electron microscopy and CLSM confirmed the complete disruption of multispecies biofilm with a reduction in viable bacteria and biofilm thickness (P < .05). ConclusionsThese novel photosensitizer functionalized bioactive nanoparticles with increased affinity to bacterial cell membrane, higher penetration into biofilm structure, and enhanced ability to eliminate clinically relevant multispecies bacterial biofilm present a potential antibiofilm agent for root canal disinfection.

The effectiveness of enzymic irrigation in removing a nutrient‐stressed endodontic multispecies biofilm

To establish a nutrient-stressed multispecies model biofilm and investigate the dynamics of biofilm killing and disruption by 1% trypsin and 1% proteinase K with or without ultrasonic activation. Nutrient-stressed biofilms (Propionibacterium acnes, Staphylococcus epidermidis, Actinomyces radicidentis, Streptococcus mitis and Enterococcus faecalis OMGS 3202) were grown on hydroxyapatite discs and in prepared root canals of single-rooted teeth in modified fluid universal medium. The treatment groups included trypsin, proteinase K, 0.2% chlorhexidine gluconate and 1% sodium hypochlorite (NaOCl) (with and without ultrasonics). NaOCl and chlorhexidine were the positive controls and untreated group, and sterile saline was the negative control. The biofilms were investigated using confocal laser scanning microscopy (CLSM) with live/dead staining and quantitative microbial culture. Nutrient stress in the multispecies biofilm was apparent as the medium pH became alkaline, glucose was absent, and serum proteins were degraded in the supernatant. The CLSM showed the percentage reduction in viable bacteria at the biofilm surface level due to nutrient starvation. On the disc model, trypsin and proteinase K were effective in killing bacteria; their aerobic viable counts were significantly lower (P<0.01) than the negative control and chlorhexidine. NaOCl was the most effective agent (P<0.001). In the tooth model, when compared to saline, trypsin with ultrasonics caused significant killing both aerobically and anaerobically (P<0.05). Chlorhexidine (1.46±0.42), trypsin (3.56±1.18) and proteinase K (4.2±1.01) with ultrasonics were significantly effective (P<0.05) in reducing the substratum coverage as compared to saline with ultrasonics (12%±4.9). Trypsin with ultrasonic activation has a biofilm killing and disrupting potential.

Assessment of viable periodontal pathogens by reverse transcription quantitative polymerase chain reaction

Molecular biological methods for the detection of periodontitis-associated bacteria based on DNA amplification have many advantages over classical culture techniques. However, when it comes to assessing immediate therapeutic success, e.g. reduction of viable bacteria, DNA-based polymerase chain reaction is unsuitable because it does not distinguish between live and dead bacteria. Our objective was to establish a simple RNA-based method that is easily set up and allows reliable assessment of the live bacterial load. We compared conventional quantitative real-time PCR (qPCR), propidium monoazide-qPCR and reverse transcription qPCR (RT-qPCR) for the detection of periodontal pathogens after antibiotic treatment in vitro. Applicability was tested using clinical samples of subgingival plaque obtained from patients at different treatment stages. The bacterial load was remarkably stable over prolonged periods when assessed by conventional qPCR, while both propidium monoazide intercalation as well as cDNA quantitation showed a decline according to decreasing numbers of viable bacteria after antibiotic treatment. Clinical samples of subgingival plaque were directly subjected to DNase I treatment and RT without previous extraction or purification steps. While the results of the DNA- and RNA-based methods are comparable in untreated patients, the classical qPCR frequently detected substantial bacterial load in treated patients where RT-qPCR no longer indicates the presence of those pathogens. The disagreement rates ranged between 4 and 20% in first visit patients and 8-50% in the group of currently treated patients. We propose to use RNA-based detection methods to verify the successful eradication of periodontal pathogens.

In VitroAntibacterial and Antibiofilm Activities of Chlorogenic Acid against Clinical Isolates ofStenotrophomonas maltophiliaincluding the Trimethoprim/Sulfamethoxazole Resistant Strain

The in vitro antibacterial and antibiofilm activity of chlorogenic acid against clinical isolates of Stenotrophomonas maltophilia was investigated through disk diffusion, minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), time-kill and biofilm assays. A total of 9 clinical S. maltophilia isolates including one isolate resistant to trimethoprim/sulfamethoxazole (TMP/SMX) were tested. The inhibition zone sizes for the isolates ranged from 17 to 29 mm, while the MIC and MBC values ranged from 8 to 16 μg mL−1 and 16 to 32 μg mL−1. Chlorogenic acid appeared to be strongly bactericidal at 4x MIC, with a 2-log reduction in viable bacteria at 10 h. In vitro antibiofilm testing showed a 4-fold reduction in biofilm viability at 4x MIC compared to 1x MIC values (0.085 < 0.397 A 490 nm) of chlorogenic acid. The data from this study support the notion that the chlorogenic acid has promising in vitro antibacterial and antibiofilm activities against S. maltophilia.

The Role of Lipid Raft Aggregation in the Infection of Type II Pneumocytes by Mycobacterium tuberculosis

Dynamic, cholesterol-dense regions of the plasma membrane, known as lipid rafts (LR), have been observed to develop during and may be directly involved in infection of host cells by various pathogens. This study focuses on LR aggregation induced in alveolar epithelial cells during infection with Mycobacterium tuberculosis (Mtb) bacilli. We report dose- and time-dependent increases in LR aggregation after infection with three different strains at multiplicities of infection of 1, 10 and 100 from 2–24 hr post infection (hpi). Specific strain-dependent variations were noted among H37Rv, HN878 and CDC1551 with H37Rv producing the most significant increase from 15 aggregates per cell (APC) to 27 APC at MOI 100 during the 24 hour infection period. Treatment of epithelial cells with Culture Filtrate Protein, Total Lipids and gamma-irradiated whole cells from each strain failed to induce the level of LR aggregation observed during infection with any of the live strains. However, filtered supernatants from infected epithelial cells did produce comparable LR aggregation, suggesting a secreted mycobacterial product produced during infection of host cells is responsible for LR aggregation. Disruption of lipid raft formation prior to infection indicates that Mtb bacilli utilize LR aggregates for internalization and survival in epithelial cells. Treatment of host cells with the LR-disruption agent Filipin III produced a nearly 22% reduction in viable bacteria for strains H37Rv and HN878, and a 7% reduction for strain CDC1551 after 6 hpi. This study provides evidence for significant mycobacterial-induced changes in the plasma membrane of alveolar epithelial cells and that Mtb strains vary in their ability to facilitate aggregation and utilization of LR.

Photocatalytic and antimicrobial properties of surgical implant coatings of titanium dioxide deposited though cathodic arc evaporation

Nanostructured crystalline titanium dioxide coatings deposited by cathodic arc evaporated on titanium grade five medical implant substrates were demonstrated to exhibit UV-induced photocatalytic activity that can be utilized to provide bactericidal effects against Staphylococcus epidermidis. The photocatalytic activity of the coatings was confirmed via degradation of Rhodamine B under UV illumination. A 90 % reduction of viable bacteria was achieved in a clinically suitable time of only 2 min with a UV dose of 2.4 J delivered at 365 nm. These results are encouraging for the development of antimicrobial surfaces in orthopedics and dentistry in order to prevent or treat post-surgical infections. To assess the possibility of employing photocatalysis for elimination of S. epidermidis, known to cause medical device related infections, under short enough times to be clinically useful on an implant surface produced with a technique that is suitable for mass production.