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Topic:Electron Microscopy

Electron microscopy is a technique that uses a beam of electrons to create an image of a specimen at a much higher resolution than is possible with light microscopy. In equine research, electron microscopy is employed to examine the ultrastructural details of horse tissues and cells. This technique allows researchers to investigate cellular and subcellular structures, providing insights into various physiological and pathological conditions in horses. By utilizing electron microscopy, scientists can study the morphology of tissues affected by diseases, understand the structural integrity of cellular components, and observe the interactions between pathogens and host cells. This page compiles peer-reviewed research studies and scholarly articles that explore the application, methodology, and findings of electron microscopy in the study of equine biology and health.
A rapid and simple method for the isolation of pure eosinophilic leukocytes from horse blood.
Experientia    December 15, 1978   Volume 34, Issue 12 1654-1656 doi: 10.1007/BF02034734
Jörg A, Portmann P, Fellay G, Dreyer JL, Meyer J.An improved and short method is described for the isolation of intact eosinophilic leukocytes from horse blood with high yield (1--1.5 g/20 l). Viability and purity of the preparations were verified by light and electron microscopy and by the trypan blue exclusion test. Isolated eosinophils were 98--100% pure, intact and viable, and they could be shown to phagocytise immune-complexes.
Malignant medulloepithelioma of the optic nerve in a horse.
Veterinary pathology    July 1, 1978   Volume 15, Issue 4 488-494 doi: 10.1177/030098587801500406
Eagle RC, Font RL, Swerczek TW.An 18-month-old Standardbred filly had a large intraocular tumor involving the optic nerve. The tumor was a malignant medulloepithelioma, a rare intraocular neoplasm derived from the primitive medullary epithelium. By light microscopy the tumor had cords and lobules of primitive neuroepithelial cells that formed clefts and true rosettes. Electron microscopy of the rosettes showed a girdle of zonulae adherentes joining the apices of the cells as well as several basal bodies. This is the sixth report of equine intraocular medulloepithelioma, and, to the best of our knowledge, the first intraocul...
Demonstration of equine infectious anemia virus in primary leukocyte cultures by electron microscopy.
American journal of veterinary research    December 1, 1977   Volume 38, Issue 12 2067-2069 
McConnel MB, Katada M, McConnell S, Moore R.Electron microscopy was used to demonstrate the presence of viral particles in primary cultures of leukocytes taken from a horse after SC inoculation with the Wyoming strain of equine infectious anemia virus. Unlike previous studies, the exposure virus was not passaged through cell culture prior to horse inoculation. Cultures were begun approximately 1 week before and 1 week after the 1st pyrexic period after inoculation. In both samples, viral particles and cytoplasmic alterations were observed resembling those previously reported in equine infectious anemia virus and other retravirus-infecte...
Isolation of mycoplasmas from the respiratory tract of horses in Australia.
The Veterinary record    March 20, 1976   Volume 98, Issue 12 235-237 doi: 10.1136/vr.98.12.235
Moorthy AR, Spradbrow PB.Mycoplasmas were isolated from two of 43 nasal swabs taken from live horses, and from one of 28 tracheal swabs taken from slaughtered horses. The slaughtered horse that yielded mycoplasmas had no gross pathological changes in the respiratory tract, but the nasal isolations were made from horses with rhinitis. The three mycoplasmas could be distinguished by cultural characteristics, and probably they represent three different species.
Purification and characterization of equine infectious anemia virus.
Archives of virology    January 1, 1976   Volume 51, Issue 1-2 107-114 doi: 10.1007/BF01317839
Matheka HD, Coggins L, Shively JN, Norcross NL.EIA virus was purified from equine fetal kidney cell cultures by PEG-precipitation, two sucrose-gradient sedimentations (5-30 per cent) and (25 to 60 per cent) centrifugation, using the immunodiffusion test to follow the procedure. Purified EIA virus had a density (20 degrees C) of 1.162 and a sedimentation constant of S20w=656. electron microscopy revealed a particle of about 100 nm in diameter with a very flexible but usually spherical shape. The dense core may be at various locations inside the membrane bound particle.
[Comparative study of tracheal epithelium of different mammals].
Acta anatomica    January 1, 1976   Volume 94, Issue 2 262-282 
Pavelka M, Ronge HR, Stockinger G.Tracheal epithelia of ten different mammals were investigated with the light and the electron microscope. Characteristic differences were found concerning the thickness of the epithelia, the length of the cilia, the density of the cells in the epithelia, the numerical distribution of the different cells and their ultrastructure. Special attention was paid to the morphology of the kinetosomes. Brush cells and chromaffin cells, which are sparsely distributed in the different tracheal epithelia, were discussed.
Ultrastructure of the synovial membrane.
Annals of clinical and laboratory science    November 1, 1975   Volume 5, Issue 6 489-498 
Schumacher HR.The normal synovial membrane as seen by electron microscopy is bordered by one to three layers of lining cells that include some with phagocytic function, others rich in endoplasmic reticulum for protein synthesis and additional cells with mixed properties. Lining cells with prominent Golgi apparatus probably produce the synovial hyaluronic acid. The synovial matrix contains collagen and mucopolysaccharide. It offers little barrier to diffusion of most materials. Superficial capillaries and venules are fenestrated and presumably allow rapid exchange of fluid and electrolytes. Deeper venules ha...
The fine structure of the glycocalyx of equine spermatozoa: a high-resolution cytochemical study.
Journal of reproduction and fertility. Supplement    October 1, 1975   Issue 23 91-94 
Hernández-Jáuregui P, Sosa A, González-Angulo A.Equine spermatozoa were obtained from ejaculates of young stallions. The seminal plasma was removed and the sperm pellets washed three times with 0-15 M-NaCl solution before final centrifugation at 4500 g for 15 min. The pellets were fixed in a mixture of 2-5% glutaraldehyde in 0-1 M-cacodylate buffer, pH 7-4, with 0-5% Alcian blue and post-fixed in 1% osmium tetroxide with 1% lanthanum nitrate; other samples were treated with ruthenium red. All samples were dehydrated in ascending concentrations of ethanol, embedded in araldite and thin sections examined in an electron microscope. Electron de...
Leucocyte myosin and its location in the cell.
Biochimica et biophysica acta    August 19, 1975   Volume 400, Issue 2 222-243 doi: 10.1016/0005-2795(75)90177-4
Shibata N, Tatsumi N, Tanaka K, Okamura Y, Senda N.The intracellular location of the binding site of antibody against purified myosin prepared from equine leucocytes was investigated in neutrophils and lymphocytes by electron microscopy using peroxidase-labelled antibody method. The myosin extracted from equine leucocytes could bind skeletal muscle F-actin and the formed complex showed the biophysical and biochemical properties and electron microscopic appearance of actomyosin. On immunodiffusion, the leucocyte myosin formed a single precipitin line with its antibody prepared in rabbits. The antibody also formed single precipitin lines with my...
Equine infectious anemia virus from infected horse serum.
Infection and immunity    September 1, 1974   Volume 10, Issue 3 667-668 doi: 10.1128/iai.10.3.667-668.1974
Nakajima H, Yoshino T, Ushimi C.Equine infectious anemia virus was purified from infected horse serum samples. Electron microscope observation on negatively stained preparations of purified virus showed roughly spherical particles sized between 100 and 200 nm in diameter. In disrupted particles, an envelope was visible but no internal structure could be resolved. Since the purified virus fraction had a strong antigenic activity to antiserum in immunodiffusion reaction, these particles are thought to be the causative virus of equine infectious anemia.
The origin of equine endometrial cups. 3. Light and electron microscopic study of fully developed equine endometrial cups.
The Anatomical record    December 1, 1973   Volume 177, Issue 4 503-517 doi: 10.1002/ar.1091770404
Hamilton DW, Allen WR, Moor RM.No abstract available
Electron microscopy of equine infectious anemia virus.
Journal of virology    October 1, 1969   Volume 4, Issue 4 521-527 doi: 10.1128/JVI.4.4.521-527.1969
Tajima M, Nakajima H, Ito Y.Equine infectious anemia (EIA) virus was observed in thin sections of infected cultured horse leukocytes by electron microscopy. The virus particles had a spherical shape and were between 80 and 120 nm in diameter. Most of them contained an electron-dense nucleoid 40 to 60 nm in diameter. They were observed to form by a process of budding from the plasma membrane and appeared to have thin surface projections. The particles described were not detected in uninfected cultured cells, and their appearance could be prevented by adding EIA immune serum to the inoculum. The implications of these findi...
Morphogenesis of Venezuelan equine encephalomyelitis virus.
Journal of virology    October 1, 1969   Volume 4, Issue 4 496-504 doi: 10.1128/JVI.4.4.496-504.1969
Bykovsky AF, Yershov FI, Zhdanov VM.Morphogenesis of Venezuelan equine encephalomyelitis virus was studied by means of electron microscopy. Virus-specific structures (factories, viroplasts) were found at early stages of infection; these structures were composed of fibrillar and cylindrical formations, aggregates of ribosomes, and viral nucleoids. The latter emerged from fibrillar and cylindrical structures. Aggregates of viral nucleoids were found in the cytoplasm and occasionally in the nuclei of virus-infected cells. Viral envelopes and mature virions were formed on the cell membranes and on the membranes of intracellular vacu...
Electron microscopic observations on the blood of the horse. I. Neutrophils in the peripheral blood of clinically healthy horses.
The Japanese journal of veterinary research    June 1, 1966   Volume 14, Issue 1 71-78 
Sonoda M, Kobayashi K.Recently, in the field of the human hematology, electron microscopic methods have been becoming more and more important as one of the most useful methods for differentiating the blood cells in the states of health and various diseases, and several research publications have been pres en ted. On the other hand, in the field of veterinary hematology, some reports on the blood cells of several domestic animals using electron microscopy have been presented, but in these publications 1,3.5,7,9,13.17,19), only a few of the blood cells were described and there is no systematic observation usin...
Electron microscopy of equine abortion virus.
American journal of veterinary research    March 1, 1961   Volume 22 250-265 
TAJIMA M, SHIMIZU T, ISHIZAKI R.No abstract available
Polysaccharide storage myopathy in the M. longissimus lumborum of showjumpers and dressage horses with back pain.
   April 5, 2026  
This study was designed to investigate whether horses with clinical signs of back pain due to suspected soft tissue injuries were affected by polysaccharide storage myopathy (PSSM). Diagnosis of PSSM in muscle biopsies obtained from the M. longissimus lumborum of 5 showjumpers and 4 dressage horses with a history of back pain is reported. M. longissimus lumborum biopsies of these horses were characterised histopathologically and in 3/9 cases also by electron microscopy. Observations were compared with M. gluteus biopsies of the same horses, and with M. gluteus biopsies obtained from 6 Standard...