In vitro method to study antifungal perfusion in Candida Biofilms

Antimycotic perfusion through Candida biofilms was demonstrated by a modification of a simple in vitro diffusion cell bioassay system. Using this model, the perfusion of three commonly used antifungal agents, amphotericin B, fluconazole, and flucytosine, was investigated in biofilms of three different Candida species (i.e., Candida albicans, Candida parapsilosis, and Candida krusei) that were developed on microporous filters. Scanning electron microscopy revealed that C. albicans formed a contiguous biofilm with tightly packed blastospores and occasional hyphae compared with C. parapsilosis and C. krusei, which developed confluent biofilms displaying structural heterogeneity and a lesser cell density, after 48 h of incubation on nutrient agar. Minor structural changes were also perceptible on the superficial layers of the biofilm after antifungal perfusion. The transport of antifungals to the distal biofilm-substratum interface was most impeded by C. albicans biofilms in comparison to C. parapsilosis and C. krusei. Fluconazole and flucytosine demonstrated similar levels of perfusion, while amphotericin B was the least penetrant through all three biofilms, although the latter appeared to cause the most structural damage to the superficial cells of the biofilm compared with the other antifungals. These results suggest that the antifungal perfusion through biofilm mode of growth in Candida is dependent both on the antimycotic and the Candida species in question, and in clinical terms, these phenomena could contribute to the failure of Candida biofilm-associated infections. Finally, the in vitro model we have described should serve as a useful system to investigate the complex interactions that appear to operate in vivo within the biofilm-antifungal interphase.published_or_final_versio

Antibacterial effects of silver diamine fluoride on multi-species cariogenic biofilm on caries

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The interplay of dental pulp stem cells and endothelial cells in an injectable peptide hydrogel on angiogenesis and pulp regeneration in vivo

Securing an adequate blood supply for the survival of cell transplants is critical for a successful outcome in tissue engineering. Interactions between endothelial and progenitor/stem cells are important for vascularization of regenerating tissue. Recently, self-assembling peptide nanofibers were described as a promising environment for pulp regeneration due to their synthetic nature and controlled physicochemical properties. In this study, the peptide hydrogel PuraMatrix™ was used as a scaffold system to investigate the role of dental pulp stem cells (DPSCs) in triggering angiogenesis and the potential for regenerating vascularized pulp in vivo. Human umbilical vein endothelial cells (HUVECs), DPSCs, or cocultures of both cell types were encapsulated in three-dimensional PuraMatrix. The peptide nanofiber microenvironment supported cell survival, cell migration, and capillary network formation in the absence of exogenous growth factors. DPSCs increased early vascular network formation by facilitating the migration of HUVECs and by increasing vascular endothelial growth factor (VEGF) expression. Both the DPSC-monoculture and coculture groups exhibited vascularized pulp-like tissue with patches of osteodentin after transplantation in mice. The cocultured groups exhibited more extracellular matrix, vascularization, and mineralization than the DPSC-monocultures in vivo. The DPSCs play a critical role in initial angiogenesis, whereas coordinated efforts by the HUVECs and DPSCs are required to achieve a balance between extracellular matrix deposition and mineralization. The findings of this study also highlighted the importance of a microenvironment that supports cell-cell interactions and cell migration, which contribute to successful dental pulp regeneration.published_or_final_versio

The role of saliva and serum in Candida albicans biofilm formation on denture acrylic surfaces

The long term effect of either a salivary or a serum pellicle on Candida albicans biofilm formation on denture acrylic surfaces was investigated both by quantifying the ATP (adenosine triphosphate) content of the resultant biofilms and by scanning electron microscopy. When the biofilm formation on saliva-coated acrylic strips was examined, the yeasts initially colonised this surface at a slower rate than the controls although with increasing incubation time, at 72 h, the ATP content was almost ten-fold higher than the protein-free control strips. Ultrastructural studies revealed this to be due to cell aggregation and hyphal emergence, phenomena not observed in the controls. As compared with the control strips, biofilm activity of the serum-coated strips was almost 100-fold greater within 48 h incubation, and scanning electron microscopy revealed multilayer blastospore-blastospore co-adhesion, germ tube, hyphal and pseudohyphal emergence and blastospore-hyphal coadherence. Further immunocytochemical observation revealed that concanavalin-A binding material and fibronectin were involved in biofilm formation on both saliva and serum coated specimens and, in addition, mannan-binding protein and protein-A binding material also contributed to the biofilm formation on serum coated specimens.link_to_OA_fulltex

Motion sensor applications in smart buildings

Among the many kinds of applications of today’s sensor technology, motion detection play a vital role especially for the safety of human being at their day today rituals. In smart buildings, different types of motion sensors are used to monitor parameters which are critical for the safety of its occupants, equipment and also the behavior of any structural changes against environmental changes. Accelerometers which are connected to the structure of those buildings, for example can capture the vibrations caused by vehicles on highways nearby, trains passing by, etc., and can be programmed to take necessary preventive actions to protect the occupants, equipment inside the building and the structure. Vibration free platforms like the one presented in this paper, will be a suitable solution. They can also be used to get a feedback of how the buildings were behaved in the disastrous situations

Phytoforensics: Trees as bioindicators of potential indoor exposure via vapor intrusion

Human exposure to volatile organic compounds (VOCs) via vapor intrusion (VI) is an emerging public health concern with notable detrimental impacts on public health. Phytoforensics, plant sampling to semi-quantitatively delineate subsurface contamination, provides a potential non-invasive screening approach to detect VI potential, and plant sampling is effective and also time- and cost-efficient. Existing VI assessment methods are time- and resourceintensive, invasive, and require access into residential and commercial buildings to drill holes through basement slabs to install sampling ports or require substantial equipment to install groundwater or soil vapor sampling outside the home. Tree-core samples collected in 2 days at the PCE Southeast Contamination Site in York, Nebraska were analyzed for tetrachloroethene (PCE) and results demonstrated positive correlations with groundwater, soil, soil-gas, sub-slab, and indoor-air samples collected over a 2-year period. Because treecore samples were not collocated with other samples, interpolated surfaces of PCE concentrations were estimated so that comparisons could be made between pairs of data. Results indicate moderate to high correlation with average indoor-air and sub-slab PCE concentrations over long periods of time (months to years) to an interpolated tree-core PCE concentration surface, with Spearman\u27s correlation coefficients (ρ) ranging from 0.31 to 0.53 that are comparable to the pairwise correlation between sub-slab and indoor-air PCE concentrations (ρ = 0.55, n = 89). Strong correlations between soil-gas, sub-slab, and indoor-air PCE concentrations and an interpolated tree-core PCE concentration surface indicate that trees are valid indicators of potential VI and human exposure to subsurface environment pollutants. The rapid and non-invasive nature of tree sampling are notable advantages: even with less than 60 trees in the vicinity of the source area, roughly 12 hours of tree-core sampling with minimal equipment at the PCE Southeast Contamination Site was sufficient to delineate vapor intrusion potential in the study area and offered comparable delineation to traditional sub-slab sampling performed at 140 properties over a period of approximately 2 years

Characteristics of community acquired and hospital acquired methicillin resistant Staphylococcus aureus isolates in the National Hospital of Sri Lanka

Introduction and Objectives: Highly virulent community acquired methicillin resistant Staphylococcus aureus (MRSA) strains emerged recently causing infections in healthy young adults without predisposing factors. This descriptive cross-sectional study was conducted to compare socio-demography of patients and microbiology and molecular characteristics of Community acquired (CA) and Hospital acquired (HA) methicillin resistant S. aureus strains isolated at the National Hospital of Sri Lanka.Methods and Results: Antimicrobial susceptibility test and Panton Valentine Leukocidine (PVL) gene detection was carried out on 100 MRSA isolates. CDC epidemiological criteria were used for differentiation of CA and HA MRSA. Of those 100 isolates, 21(21%) were CA-MRSA and 79(79%) were HA-MRSA. Patients did not show any significant difference in acquiring CA MRSA and HA MRSA in relation to their age, sex and gender except ethnicity. The majority of these isolates were from pus samples. CA-MRSA isolates were significantly more sensitive to ciprofloxacin, fusidic acid, tetracycline, cotrimoxazole, and gentamicin compared with HA-MRSA isolates (p&lt;0.001). Inducible, constitutive clindamycin resistance (p&lt;0.001) and multidrug resistant phenotypes were significantly higher (p&lt;0.001) among patients with HA-MRSA infection. All isolates were susceptible to glycopeptides, rifampicin and linezolid. Mupirocin resistance was seen in 6% and all isolates came from patients who harboured HA-MRSA strains (p&lt;0.338). The PVL gene (P&lt;0.001) was present in 20 (95.2%) of CA-MRSA isolates.Conclusion: This study highlights the importance of accurate differentiation of CA and HA MRSA using epidemiological, microbiological and molecular characteristics. Further, awareness of the existence of these types will optimise individual treatment strategies.</p

Candida species exhibit differential in vitro hemolytic activities

A total of 80 Candida isolates representing 14 species were examined for their respective responses to an in vitro hemolytic test. A modification of a previously described plate assay system where the yeasts are incubated on glucose (3%)-enriched sheep blood agar in a carbon dioxide (5%)-rich environment for 48 h was used to evaluate the hemolytic activity. A group of eight Candida species which included Candida albicans (15 isolates), C. dubliniensis (2), C. kefyr (2), C. krusei (4), C. zeylanoides (1), C. glabrata (34), C. tropicalis (5), and C. lusitaniae (2) demonstrated both alpha and beta hemolysis at 48 h postinoculation. Only alpha hemolysis was detectable in four Candida species, viz., C. famata (3), C. guilliermondii (4), C. rugosa (1), and C. utilis (1), while C. parapsilosis (5) and C. pelliculosa (1) failed to demonstrate any hemolytic activity after incubation for 48 h or longer. This is the first study to demonstrate the variable expression profiles of hemolysins by different Candida species.published_or_final_versio