scholarly journals Scanning Electron Microscopy (SEM) and Environmental SEM: Suitable Tools for Study of Adhesion Stage and Biofilm Formation

10.5772/34990 ◽  
2012 ◽  
Author(s):  
Soumya El ◽  
Saad Koraichi ◽  
Hassan Latrache ◽  
Fatima Hamadi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Biofilm Formation ◽  
Environmental Sem ◽  
Scanning Electron

Biological Evaluation of Selected 1,2,3-triazole Derivatives as Antibacterial and Antibiofilm Agents

2020 ◽  
Vol 20 (24) ◽  
pp. 2186-2191
Author(s):  
Lialyz Soares Pereira André ◽  
Renata Freire Alves Pereira ◽  
Felipe Ramos Pinheiro ◽  
Aislan Cristina Rheder Fagundes Pascoal ◽  
Vitor Francisco Ferreira ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Staphylococcus Aureus ◽  
Biofilm Formation ◽  
Antimicrobial Agents ◽  
Public Health Problem ◽  
Biological Evaluation ◽  
Major Public Health Problem ◽  
Community Environments ◽  
Scanning Electron

Background: Resistance to antimicrobial agents is a major public health problem, being Staphylococcus aureus prevalent in infections in hospital and community environments and, admittedly, related to biofilm formation in biotic and abiotic surfaces. Biofilms form a complex and structured community of microorganisms surrounded by an extracellular matrix adhering to each other and to a surface that gives them even more protection from and resistance against the action of antimicrobial agents, as well as against host defenses. Methods: Aiming to control and solve these problems, our study sought to evaluate the action of 1,2,3- triazoles against a Staphylococcus aureus isolate in planktonic and in the biofilm form, evaluating the activity of this triazole through Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) tests. We have also performed cytotoxic evaluation and Scanning Electron Microscopy (SEM) of the biofilms under the treatment of the compound. The 1,2,3-triazole DAN 49 showed bacteriostatic and bactericidal activity (MIC and MBC 128 μg/mL). In addition, its presence interfered with the biofilm formation stage (1/2 MIC, p <0.000001) and demonstrated an effect on young preformed biofilm (2 MICs, p <0.05). Results: Scanning Electron Microscopy images showed a reduction in the cell population and the appearance of deformations on the surface of some bacteria in the biofilm under treatment with the compound. Conclusion: Therefore, it was possible to conclude the promising anti-biofilm potential of 1,2,3-triazole, demonstrating the importance of the synthesis of new compounds with biological activity.

scholarly journals Intraocular lens biofilm formation supported by scanning electron microscopy imaging

2019 ◽  
Vol 67 (10) ◽  
pp. 1708
Author(s):  
Dipankar Das ◽  
Harsha Bhattacharjee ◽  
Krishna Gogoi ◽  
JayantaK Das ◽  
Puneet Misra ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Intraocular Lens ◽  
Biofilm Formation ◽  
Microscopy Imaging ◽  
Scanning Electron

scholarly journals Suppressive Effects of Hainosan (Painongsan) against Biofilm Production by Streptococcus mutans

2020 ◽  
Vol 8 (3) ◽  
pp. 71
Author(s):  
Masaaki Minami ◽  
Hiroshi Takase ◽  
Masayo Taira ◽  
Toshiaki Makino
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Streptococcus Mutans ◽  
Biofilm Formation ◽  
Confocal Laser Microscopy ◽  
Confocal Laser ◽  
Transmission Electron Microscopy Analysis ◽  
Laser Microscopy ◽  
Dental Plaques ◽  
Scanning Electron

Streptococcus mutans, a bacterium that causes dental plaques, forms a biofilm on tooth surfaces. This biofilm can cause gingivitis by stimulating the gingival margin. However, there is no established treatment for biofilm removal. Hainosan (Painongsan), a traditional Japanese Kampo formula, has been used to treat gingivitis. Therefore, we investigated the biofilm suppressive effects of the hainosan extract (HNS) and its components on S. mutans. We conducted scanning electron microscopy and confocal laser microscopy analyses to clarify the anti-biofilm activities of HNS and its crude drugs. We also performed a quantitative RT-PCR assay to assess the biofilm-related gene expression. HNS showed a significant dose-dependent suppressive effect on biofilm formation. Both the scanning electron microscopy and confocal laser microscopy analyses also revealed the significant inhibitory effects of the extract on biofilm formation. Transmission electron microscopy analysis showed that HNS disrupted the surface of the bacterial wall. Furthermore, HNS reduced the hydrophobicity of the bacteria, and suppressed the mRNA expression of β-glucosyltransferase (gtfB), glucosyltransferase-SI (gtfC), and fructosyltransferase (ftf). Among the constituents of hainosan, the extract of the root of Platycodon grandiflorum (PG) showed the strongest biofilm suppression effect. Platycodin D, one of the constituent natural compounds of PG, inhibited S. mutans-associated biofilm. These findings indicate that hainosan eliminates dental plaques by suppressing biofilm formation by S. mutans.

Environmental SEM in a Multi-User Biological Sciences E.M. Unit

1999 ◽  
Vol 5 (S2) ◽  
pp. 286-287
Author(s):  
Christopher J. Gilpin ◽  
Mohamed S. Baguneid
Keyword(s):  
Biological Sciences ◽  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
High Vacuum ◽  
Environmental Scanning Electron Microscopy ◽  
Environmental Scanning ◽  
Environmental Sem ◽  
Imaging Mechanisms ◽  
Scanning Electron ◽  
The Ideal

Environmental scanning electron microscopy (ESEM) has matured into a mainstream technique in many areas of microscopy. Instrumentation has evolved and our understanding of some of the imaging mechanisms has progressed. However the majority of laboratories where ESEMs are located are based around the materials sciences. Despite the fact that ESEM is the only SEM instrument that permits liquid water to be present whilst imaging, the housing of such a microscope in biological EM units has been relatively rare. This authors laboratory is a multi-user EM unit based in a School of Biological Sciences. There exists the opportunity for basic biological scientists, clinical and pre-clinical medical and dental researchers to make use of such a resource. Indeed as the ESEM is housed alongside a conventional high vacuum instrument and a cryo high vacuum instrument there exists the ideal opportunity to carry out comparative studies.This study will examine a range of biological samples using ESEM, cryo SEM and dry high vacuum SEM.

APPLICATION OF SCANNING ELECTRONIC MICROSCOPY FOR THE PURPOSE OF STUDYING CANDIDA ALBICANS BIOFILM ON THE SURFACE OF BASIC PLASTICS OF REMOVABLE ORTHOPEDIC DESIGNS

2019 ◽  
Vol 64 (5) ◽  
pp. 308-313 ◽  
Author(s):  
M. G. Chesnokova ◽  
V. A. Chesnokov ◽  
A. Yu. Mironov
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Candida Albicans ◽  
Electron Microscope ◽  
Biofilm Formation ◽  
Scanning Electronic Microscopy ◽  
Electronic Microscopy ◽  
Orthopedic Rehabilitation ◽  
Candida Albicans Biofilms ◽  
Scanning Electron

The most common pathology in the clinic of orthopedic dentistry is the presence of partial adentia in patients, manifested in the form of defects of dentition of various localization and length. Removable orthopedic structures in the oral cavity are a potential place for adhesion and colonization of microorganisms. The aim of the research was to study Candida albicans biofilms on the surface of base plastics of removable orthopedic structures using scanning electron microscopy. 175 cultures of C. albicans were isolated and identified from the oral mucosa of patients at various stages of orthopedic rehabilitation. When studying the surface of samples of plastics of hot and cold type polymerization and Candida biofilms using a JEOL JCM 5700 scanning electron microscope (JEOL, Japan), features of biofilm formation were established. An assessment of the nature of the manifestation of the hemagglutinating activity of clinical strains of Candida fungi in the hemagglutination test with human erythrocytes I (O), II (A) of the human and guinea pig blood groups was carried out. The total number of hemagglutinating strains was 37.14%, with the prevalence of the proportion of manna-resistant (MRHA) cultures - 23.43% of cases. Micrographs of the C. albicans yeast-like biofilm biofilm were obtained on the surface of hot and cold-type plastics in incubation dynamics. Scanning electron microscopy revealed the most pronounced changes in the surface of hot plastics of polymerization compared to cold plastics with long incubation of C. albicans, which characterize the loosening of plastics and the appearance of cracks on the surface, and the cracking of a yeast-like fungus biofilm was noted.

scholarly journals Cajuputs candy impairs Candida albicans and Streptococcus mutans mixed biofilm formation in vitro

F1000Research ◽  
2020 ◽  
Vol 8 ◽  
pp. 1923
Author(s):  
Siska Septiana ◽  
Boy Muchlis Bachtiar ◽  
Nancy Dewi Yuliana ◽  
Christofora Hanny Wijaya
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Candida Albicans ◽  
Streptococcus Mutans ◽  
Biofilm Formation ◽  
Microscopy Imaging ◽  
Biofilm Inhibition ◽  
Yeast Form ◽  
Melaleuca Cajuputi ◽  
Scanning Electron

Background: Cajuputs candy (CC), an Indonesian functional food, utilizes the bioactivity of Melaleuca cajuputi essential oil (MCEO) to maintain oral cavity health. Synergistic interaction between Candida albicans and Streptococcus mutans is a crucial step in the pathogenesis of early childhood caries. Our recent study revealed several alternative MCEOs as the main flavors in CC. The capacity of CC to interfere with the fungus-bacterium relationship remains unknown. This study aimed to evaluate CC efficacy to impair biofilm formation by these dual cariogenic microbes. Methods: The inhibition capacity of CC against mixed-biofilm comprising C. albicans and S. mutans was assessed by quantitative (crystal violet assay, tetrazolium salt [MTT] assay, colony forming unit/mL counting, biofilm-related gene expression) and qualitative analysis (light microscopy and scanning electron microscopy). Result: Both biofilm-biomass and viable cells were significantly reduced in the presence of CC. Scanning electron microscopy imaging confirmed this inhibition capacity, demonstrating morphology alteration of C. albicans, along with reduced microcolonies of S. mutans in the biofilm mass. This finding was related to the transcription level of selected biofilm-associated genes, expressed either by C. albicans or S. mutans. Based on qPCR results, CC could interfere with the transition of C. albicans yeast form to the hyphal form, while it suppressed insoluble glucan production by S. mutans. G2 derived from Mojokerto MCEO showed the greatest inhibition activity on the relationship between these cross-kingdom oral microorganisms (p < 0.05). Conclusion: In general, all CC formulas showed biofilm inhibition capacity. Candy derived from Mojokerto MCEO showed the greatest capacity to maintain the yeast form of C. albicans and to inhibit extracellular polysaccharide production by S. mutans. Therefore, the development of dual-species biofilms can be impaired effectively by the CC tested.

Scanning Electron Microscopy image analysis of fiber glass insulation

1992 ◽  
Vol 50 (2) ◽  
pp. 994-995
Author(s):  
H. Talbot ◽  
D. Jeulin ◽  
L.W. Hobbs
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Image Analysis ◽  
Glass Fibers ◽  
Insulation Material ◽  
Glass Insulation ◽  
Microscopy Image ◽  
Microscopy Image Analysis ◽  
Environmental Sem ◽  
Scanning Electron

Glass wool, made of chemically bound glass fibers which trap stagnant air, has been used in a variety of applications as phonic and thermic insulation material. Mechanical and insulating qualities of the material depend heavily on the characteristics of the fibers themselves. Aside from the composition of the glass, the length and diameter distributions of the fibers within the material can be related to these characteristics. A fast and reliable means for obtaining these size distributions is therefore a crucial issue for quality control.Scanning electron microscopy (SEM) imaging was used to access sub-micron dimensions of the fibers; and image analysis, as opposed to manual procedures, was used for obtaining measurements.Samples of clean raw fibers (free of binder) were dispersed with ultrasound into a pH 9 aqueous solution and later deposited on a track-etched polycarbonate filter with 0.2 μm pore size. The filter was then dried, coated, and observed in BSE mode in a standard SEM, or left uncoated and observed in an environmental SEM (ESEM).

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