VIRUS DETECTION BY ELECTRON MICROSCOPY

1983 ◽  
pp. 407-412
Author(s):  
R.M. Cole
Keyword(s):  
Electron Microscopy ◽  
Virus Detection

scholarly journals Virus detection by transmission electron microscopy: Still useful for diagnosis and a plus for biosafety

2018 ◽  
Vol 29 (1) ◽  
pp. e2019 ◽  
Author(s):  
Philippe Roingeard ◽  
Pierre-Ivan Raynal ◽  
Sébastien Eymieux ◽  
Emmanuelle Blanchard
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Virus Detection ◽  
Transmission Electron

scholarly journals Multisystemic cellular tropism of SARS-CoV-2 in autopsies of COVID-19 patients

2021 ◽  
Author(s):  
Dickson W.L. Wong ◽  
Barbara M. Klinkhammer ◽  
Sonja Djudjaj ◽  
Sophia Villwock ◽  
M. Cherelle Timm ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
In Situ Hybridization ◽  
Virus Detection ◽  
Viral Rna ◽  
Transmission Electron ◽  
Formalin Fixed Paraffin ◽  
Organ Systems ◽  
Formalin Fixed Paraffin Embedded ◽  
Ffpe Tissues

Background: Multiorgan tropism of SARS-CoV-2 has previously been shown for several major organs. Methods: We have comprehensively analyzed 25 different formalin-fixed paraffin-embedded (FFPE) tissues/organs from autopsies of fatal COVID-19 cases (n=8), using detailed histopathological assessment, detection of SARS-CoV-2 RNA using polymerase chain reaction and RNA in situ hybridization, viral protein using immunohistochemistry, and virus particles using transmission electron microscopy. Finally, we confirmed these findings in an independent external autopsy cohort (n=9). Findings: SARS-CoV-2 RNA was mainly localized in epithelial cells, endothelial and mesenchymal cells across all organs. Next to lung, trachea, kidney, heart, or liver, viral RNA was also found in tonsils, salivary glands, oropharynx, thyroid, adrenal gland, testicles, prostate, ovaries, small bowel, lymph nodes, skin and skeletal muscle. Viral RNA was predominantly found in cells expressing ACE2, TMPRSS2, or both. The SARS-CoV-2 replicating RNA was also detected in these organs. Immunohistochemistry and electron microscopy were not suitable for reliable and specific SARS-CoV-2 detection in autopsies. The findings were validated using in situ hybridization on external COVID-19 autopsy samples. Finally, apart from the lung, correlation of virus detection and histopathological assessment did not reveal any specific alterations that could be attributed to SARS-CoV-2. Conclusion: SARS-CoV-2 could be observed in virtually all organs, colocalizing with ACE2 and TMPRSS2 mainly in epithelial but also in mesenchymal and endothelial cells, and viral replication was found across all organ systems. Apart from the respiratory tract, no specific (histo-)morphologic alterations could be assigned to the SARS-CoV-2 infection.

scholarly journals Synthesis of Gold Nanoparticles Conjugated with Protein A: Towards the Application in Biosensors for Virus Detection

2011 ◽  
Vol 21 (4) ◽  
pp. 333
Author(s):  
Tran Quang Huy ◽  
Mai Anh Tuan
Keyword(s):  
Electron Microscopy ◽  
Gold Nanoparticles ◽  
Influenza A Virus ◽  
Influenza A ◽  
Protein A ◽  
Virus Detection ◽  
Sodium Ascorbate ◽  
Virus Particles ◽  
Transmission Electron ◽  
Vis Spectroscopy

In this article, a facile and effective technique is described to prepare a complex of gold nanoparticles (GNPs)/protein A (PrA) for biosensors in virus detection. GNPs were synthesized by the reduction of tetrachloroauric (III) acid trihydrate using sodium ascorbate, and then coated with PrA via ultracentrifugation. The complex of GNPs/PrA was characterized using UV-vis spectroscopy and transmission electron microscopy. The immunogold labeling method of scanning electron microscopy was also used to verify the capacity for the detection and binding of GNPs/PrA to H$_{1}$N$_{1}$ influenza A virus particles. The results showed that GNPs were spherical, uniform shape, and approximately 10 nm in size. Noticeably, the complex of GNPs/PrA could detect and bind effectively to H$_{1}$N$_{1}$ influenza A virus particles by a large number of GNPs surrounded. The advantage of the complex of GNPs/PrA showed a highly potential application in biosensors with the improvement of the sensitivity and transducing signal for virus detection.

Platinum Compounds as Stains for Electron Microscopy

1974 ◽  
Vol 32 ◽  
pp. 230-231
Author(s):  
S. K. Aggarwal ◽  
P. McAllister ◽  
R. W. Wagner ◽  
B. Rosenberg
Keyword(s):  
Electron Microscopy ◽  
Hela Cells ◽  
Uranyl Acetate ◽  
Sarcoma 180 ◽  
Platinum Compounds ◽  
Kb Cells ◽  
En Bloc ◽  
Human Lymphoma ◽  
Ultrathin Sections ◽  
Blue Coloration

Uranyl acetate has been used as an electron stain for en bloc staining as well as for staining ultrathin sections in conjunction with various lead stains (Fig. 1). Present studies reveal that various platinum compounds also show promise as electron stains. Certain platinum compounds have been shown to be effective anti-tumor agents. Of particular interest are the compounds with either uracil or thymine as one of the ligands (cis-Pt(II)-uracil; cis-Pt(II)-thymine). These compounds are amorphous, highly soluble in water and often exhibit an intense blue coloration. These compounds show enough electron density to be used as stains for electron microscopy. Most of the studies are based on various cell lines (human AV, cells, human lymphoma cells, KB cells, Sarcoma-180 ascites cells, chick fibroblasts and HeLa cells) while studies on tissue blocks are in progress.

Immune Electron Microscopy (IEM) of a Canine Adeno-Associated Virus

1974 ◽  
Vol 32 ◽  
pp. 256-257
Author(s):  
Gunter F. Thomas ◽  
M. David Hoggan
Keyword(s):  
Electron Microscopy ◽  
Cell Cultures ◽  
Complement Fixation ◽  
Hepatitis Virus ◽  
Wide Distribution ◽  
Immune Electron Microscopy ◽  
Adeno Associated Virus ◽  
Virus Like Particle ◽  
Dog Kidney ◽  
Green Monkeys

In 1968, Sugimura and Yanagawa described a small 25 nm virus like particle in association with the Matsuda strain of infectious canine hepatitis virus (ICHV). Domoto and Yanagawa showed that this particle was dependent on ICHV for its replication in primary dog kidney cell cultures (PDK) and was resistant to heating at 70°C for 10 min, and concluded that it was a canine adeno-associated virus (CAAV). Later studies by Onuma and Yanagawa compared CAAV with the known human serotypes (AAV 1, 2, 3) and AAV-4, known to be associated with African Green Monkeys. Using the complement fixation (CF) test, they found that CAAV was serologically related to AAV-3 and had wide distribution in the dog population of Japan.

High Voltage Electron Microscopy of Ion-Milled Dental Enamel

1974 ◽  
Vol 32 ◽  
pp. 60-61
Author(s):  
L. D. Ackerman ◽  
S. H. Y. Wei
Keyword(s):  
Electron Microscopy ◽  
High Voltage ◽  
Third Molar ◽  
Polarized Light ◽  
Dental Enamel ◽  
Longitudinal Section ◽  
Ion Milling ◽  
High Voltage Electron Microscopy ◽  
Voltage Electron ◽  
High Voltage Electron

Mature human dental enamel has presented investigators with several difficulties in ultramicrotomy of specimens for electron microscopy due to its high degree of mineralization. This study explores the possibility of combining ion-milling and high voltage electron microscopy as a means of circumventing the problems of ultramicrotomy.A longitudinal section of an extracted human third molar was ground to a thickness of about 30 um and polarized light micrographs were taken. The specimen was attached to a single hole grid and thinned by argon-ion bombardment at 15° incidence while rotating at 15 rpm. The beam current in each of two guns was 50 μA with an accelerating voltage of 4 kV. A 20 nm carbon coating was evaporated onto the specimen to prevent an electron charge from building up during electron microscopy.

Pathogenesis of Human Hair Defects

1974 ◽  
Vol 32 ◽  
pp. 12-13
Author(s):  
P.S. Porter ◽  
T. Aoyagi ◽  
R. Matta
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Human Hair ◽  
Standard Techniques ◽  
Scanning Electron

Using standard techniques of scanning electron microscopy (SEM), over 1000 human hair defects have been studied. In several of the defects, the pathogenesis of the abnormality has been clarified using these techniques. It is the purpose of this paper to present several distinct morphologic abnormalities of hair and to discuss their pathogenesis as elucidated through techniques of scanning electron microscopy.

Sign in / Sign up

Export Citation Format

Share Document