44,371 research outputs found
Levorotatory carbohydrates and xylitol subdue Streptococcus mutans and Candida albicans adhesion and biofilm formation
Dietary carbohydrates and polyols affect the microbial colonization of oral surfaces by modulating adhesion and biofilm formation. The aim of this study was to evaluate the influence of a select group of l-carbohydrates and polyols on either Streptococcus mutans or Candida albicans adhesion and biofilm formation in vitro. S. mutans or C. albicans suspensions were inoculated on polystyrene substrata in the presence of Tryptic soy broth containing 5% of the following compounds: d-glucose, d-mannose, l-glucose, l-mannose, d- and l-glucose (raceme), d- and l-mannose (raceme), l-glucose and l-mannose, sorbitol, mannitol, and xylitol. Microbial adhesion (2h) and biofilm formation (24h) were evaluated using MTT-test and Scanning Electron Microscopy (SEM). Xylitol and l-carbohydrates induced the lowest adhesion and biofilm formation in both the tested species, while sorbitol and mannitol did not promote C. albicans biofilm formation. Higher adhesion and biofilm formation was noted in both organisms in the presence of d-carbohydrates relative to their l-carbohydrate counterparts. These results elucidate, hitherto undescribed, interactions of the individually tested strains with l- and d-carbohydrates, and how they impact fungal and bacterial colonization. In translational terms, our data raise the possibility of using l-form of carbohydrates and xylitol for dietary control of oral plaque biofilms
The L-p-to-L-q boundedness of commutators with applications to the Jacobian operator
Supplying the missing necessary conditions, we complete the characterisation of the L-p -> L-q boundedness of commutators [b, T] of pointwise multiplication and Calderon-Zygmund operators, for arbitrary pairs of 1 q, our results are new even for special classical operators with smooth kernels. As an application, we show that every f is an element of L-p(R-d) can be represented as a convergent series of normalised Jacobians J(u) = det del uof u is an element of (over dot(W))(1,dp)(R-d)(d). This extends, from p = 1 to p > 1, a result of Coifman, Lions, Meyer and Semmes about J:. (over dot(W))(1,d)(R-d)(d) -> H-1(R-d), and supports a conjecture of Iwaniec about the solvability of the equation Ju = f is an element of L-p(R-d). (C) 2021 The Author(s). Published by Elsevier Masson SAS.Peer reviewe
De Maiestate / Praeside M. Jacobo Thomasio, Moralis Philosoph. P. P., publice disputabit Johannes Dunte, R. L. Author & Respon: ad diem 9. Septembr. H L. Q. C.
DE MAIESTATE / PRAESIDE M. JACOBO THOMASIO, MORALIS PHILOSOPH. P. P., PUBLICE DISPUTABIT JOHANNES DUNTE, R. L. AUTHOR & RESPON: AD DIEM 9. SEPTEMBR. H L. Q. C.
De Maiestate / Praeside M. Jacobo Thomasio, Moralis Philosoph. P. P., publice disputabit Johannes Dunte, R. L. Author & Respon: ad diem 9. Septembr. H L. Q. C. (1)
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Beiträge (21
Supplementary_file_1 – Supplemental material for Assessment of Nutritional Status in Sri Lankan Children: Validity of Current Anthropometry Cutoffs?
Supplemental material, Supplementary_file_1 for Assessment of Nutritional Status in Sri Lankan Children: Validity of Current Anthropometry Cutoffs? by Loretta S. Warnakulasuriya, Manel A. M. Fernando, A. V. Nihal Adikaram, A. R. M. Thawfeek, W. M. L. Anurasiri, R. Elisabet, Peter Bergsten, K. D. Renuka Ruchira Silva, Dulani L. Samaranayake and Vithanage Pujitha Wickramasinghe in Asia Pacific Journal of Public Health</p
Fungal species in endodontic infections : A systematic review and meta-analysis
Fungal infections are common on oral mucosae, but their role in other oral sites is ill defined. Over the last few decades, numerous studies have reported the presence of fungi, particularly Candida species in endodontic infections, albeit in relatively small numbers in comparison to its predominant anaerobic bacteriome. Here, we review the fungal biome of primary and secondary endodontic infections, with particular reference to the prevalence and behavior of Candida species. Meta-analysis of the available data from a total of 39 studies fitting the inclusion criteria, indicate the overall weighted mean prevalence (WMP) of fungal species in endodontic infections to be 9.11% (from a cumulative total of 2003 samples), with 9.0% in primary (n = 1341), and 9.3% in secondary infections (n = 662). Nevertheless, WMP for fungi in primary and secondary infections which were 6.3% and 7.5% for culture-based studies, increased to 12.5% and 16.0% in molecular studies, respectively. The most prevalent fungal species was Candida spp. The high heterogeneity in the reported fungal prevalence suggests the need for standardized sampling, and speciation methods. The advent of the new molecular biological analytical platforms, such as the next generation sequencing (NGS), and matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF), that enables identification and quantitation of a broad spectrum of hitherto unknown organisms in endodontic infections should radically alter our understanding of the endodontic mycobiome in the future. Candida spp. appear to be co-pathogens with bacteria in approximately one in ten patients with endodontic infections. Hence, clinicians should comprehend the importance and the role of fungi in endodontic infections and be cognizant of the need to eradicate both bacteria and fungi for successful therapy
Supplementary_File_2-17th_July – Supplemental material for Assessment of Nutritional Status in Sri Lankan Children: Validity of Current Anthropometry Cutoffs?
Supplemental material, Supplementary_File_2-17th_July for Assessment of Nutritional Status in Sri Lankan Children: Validity of Current Anthropometry Cutoffs? by Loretta S. Warnakulasuriya, Manel A. M. Fernando, A. V. Nihal Adikaram, A. R. M. Thawfeek, W. M. L. Anurasiri, R. Elisabet, Peter Bergsten, K. D. Renuka Ruchira Silva, Dulani L. Samaranayake and Vithanage Pujitha Wickramasinghe in Asia Pacific Journal of Public Health</p
Going Beyond Counting First Authors in Author Co-citation Analysis
The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Appropriate Similarity Measures for Author Cocitation Analysis
We provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
Exopolysaccharide Matrix Of Developed Candida Albicans Biofilms After Exposure To Antifungal Agents
This study aimed to evaluate the effects of fluconazole or nystatin exposure on developed Candida albicans biofilms regarding their exopolysaccharide matrix. The minimal inhibitory concentration (MIC) against fluconazole or nystatin was determined for C. albicans reference strain (ATCC 90028). Poly(methlymethacrylate) resin (PMMA) specimens were fabricated according to the manufacturer's instructions and had their surface roughness measured. Biofilms were developed on specimens surfaces for 48 h and after that were exposed during 24 h to fluconazole or nystatin prepared in a medium at MIC, 10 x MIC or 100 x MIC. Metabolic activity was evaluated using an XTT assay. Production of soluble and insoluble exopolysaccharide and intracellular polysaccharides was evaluated by the phenol-sulfuric method. Confocal laser scanning microscope was used to evaluate biofilm architecture and percentage of dead/live cells. Data were analyzed statistically by ANOVA and Tukey's test at 5% significance level. The presence of fluconazole or nystatin at concentrations higher than MIC results in a great reduction of metabolic activity (p0.05). The exposure to nystatin also did not alter the exopolysaccharide matrix at all the tested concentrations (p>0.05). Biofilm architecture was not affected by either of the antifungal agents (p>0.05). Nystatin promoted higher proportion of dead cells (p<0.05). It may be concluded that fluconazole and nystatin above the MIC concentration reduced the metabolic activity of C. albicans biofilms; however, they were not able to alter the exopolysaccharide matrix and biofilm architecture.236716722Gendreau, L., Loewy, Z.G., Epidemiology and etiology of denture stomatitis (2011) J Prosthodont, 20, pp. 251-260Tobudic, S., Kratzer, C., Lassnigg, A., Presterl, E., Antifungal susceptibility of Candida albicans in biofilms (2012) Mycoses, 55, pp. 199-204Chaffin, W.L., Candida albicans cell wall proteins (2008) Microbiol Mol Biol Rev, 72, pp. 495-544Seneviratne, C.J., Jin, L., Samaranayake, L.P., Biofilm lifestyle of Candida: A mini review (2008) Oral Dis, 14, pp. 582-590Ramage, G., Rajendran, R., Sherry, L., Williams, C., Fungal biofilm resistance (2012) Int J Microbiol, , 528-521Chandra, J., Kuhn, D.M., Mukherjee, P.K., Hoyer, L.L., McCormick, T., Ghannoum, M.A., Biofilm formation by the fungal pathogen Candida albicans: Development, architecture, and drug resistance (2001) J Bacteriol, 183, pp. 5385-5394Konopka, K., Dorocka-Bobkowska, B., Gebremedhin, S., Duzgunes, N., Susceptibility of Candida biofilms to histatin 5 and fluconazole (2010) Antonie Van Leeuwenhoek, 97, pp. 413-417Baillie, G.S., Douglas, L.J., Effect of growth rate on resistance of Candida albicans biofilms to antifungal agents (1998) Antimicrob Agents Chemother, 42, pp. 1900-1905Niimi, M., Firth, N.A., Cannon, R.D., Antifungal drug resistance of oral fungi (2010) Odontology, 98, pp. 15-25Ramage, G., Mowat, E., Jones, B., Williams, C., Lopez-Ribot, J., Our current understanding of fungal biofilms (2009) Crit Rev Microbiol, 35, pp. 340-355Baillie, G.S., Douglas, L.J., Matrix polymers of Candida biofilms and their possible role in biofilm resistance to antifungal agents (2000) J Antimicrob Chemother, 46, pp. 397-403Seneviratne, C.J., Jin, L.J., Samaranayake, Y.H., Samaranayake, L.P., Cell density and cell aging as factors modulating antifungal resistance of Candida albicans biofilms (2008) Antimicrob Agents Chemother, 52, pp. 3259-3266da Silva, W.J., Seneviratne, J., Samaranayake, L.P., Del Bel Cury, A.A., Bioactivity and architecture of Candida albicans biofilms developed on poly (methyl methacrylate) resin surface (2010) J Biomed Mater Res B Appl Biomater, 94, pp. 149-156(2008) Reference Method For Broth Dilution Antifungal Susceptibility Testing of Yeasts, Approved Standard, , CLSI, CLSI Document M27-A3, Wayne, PA:CLSIda Silva, W.J., Seneviratne, J., Parahitiyawa, N., Rosa, E.A., Samaranayake, L.P., Del Bel Cury, A.A., Improvement of XTT assay performance for studies involving Candida albicans biofilms (2008) Braz Dent J, 19, pp. 364-369Tenuta, L.M., Ricomini, F.A.P., Del Bel Cury, A.A., Cury, J.A., Effect of sucrose on the selection of mutans streptococci and lactobacilli in dental biofilm formed in situ (2006) Caries Res, 40, pp. 546-549Dubois, M., Gilles, K., Hamilton, J.K., Rebers, P.A., Smith, F., A colorimetric method for the determination of sugars (1951) Nature, 28, p. 167. , 168Heydorn, A., Nielsen, A.T., Hentzer, M., Sternberg, C., Givskov, M., Ersboll, B.K., Quantification of biofilm structures by the novel computer program COMSTAT (2000) Microbiology, 146, pp. 2395-2407Force, R.W., Nahata, M.C., Salivary concentrations of ketoconazole and fluconazole: Implications for drug efficacy in oropharyngeal and esophageal candidiasis (1995) Ann Pharmacother, 29, pp. 10-15Gomes, P.N., da Silva, W.J., Pousa, C.C., Narvaes, E.A., Del Bel Cury, A.A., Bioactivity and cellular structure of Candida albicans and Candida glabrata biofilms grown in the presence of fluconazole (2011) Arch Oral Biol, 56, pp. 1274-1281Ellepola, A.N., Samaranayake, L.P., Oral candidal infections and antimycotics (2000) Crit Rev Oral Biol Med, 11, pp. 172-198Ellepola, A.N., Samaranayake, L.P., The postantifungal effect (PAFE) of antimycotics on oral C. albicans isolates and its impact on candidal adhesion (1998) Oral Dis, 4, pp. 260-267Nett, J.E., Sanchez, H., Cain, M.T., Andes, D.R., Genetic basis of Candida biofilm resistance due to drug-sequestering matrix glucan (2010) J Infect Dis, 202, pp. 171-175Mores, A.U., Souza, R.D., Cavalca, L., de Paula e Carvalho, A., Gursky, L.C., Rosa, R.T., Enhancement of secretory aspartyl protease production in biofilms of Candida albicans exposed to subinhibitory concentrations of fluconazole (2011) Mycoses, 54, pp. 195-201Goncalves, L.M., Del Bel Cury, A.A., Sartoratto, A., Garcia, R.V.L., Silva, W.J., Effects of undecylenic acid released from denture liner on Candida biofilms (2012) J Dent Res, 91, pp. 985-98
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Raul Morin, author of 'Among the Valiant' shakes hands with Dr. Hector P. Garcia (photograph)
(L. to R.): Raul Morin, author of 'Among the Valiant' shakes hands with Dr. Hector P. Garcia
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