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Topic:Cell Culture

Cell culture in horses involves the in vitro cultivation of equine cells under controlled conditions. This technique is employed to study various cellular processes, including growth, differentiation, and response to external stimuli, in an isolated environment. Equine cell cultures can be derived from various tissues, such as skin, muscle, or bone, and are used in a range of research applications, including genetic studies, drug testing, and disease modeling. These cultures provide a valuable platform for understanding cellular mechanisms and developing therapeutic strategies. This page compiles peer-reviewed research studies and scholarly articles that explore the methodologies, applications, and findings related to cell culture in equine research.
Antigenic relatedness of equine herpes virus types 1 and 3.
Archives of virology    January 1, 1978   Volume 56, Issue 1-2 33-45 doi: 10.1007/BF01317281
Gutekunst DE, Malmquist WA, Becvar CS.Antiserums prepared in specific pathogen free (SPF) ponies were used in direct and indirect immunofluorescence, immunodiffusion, complement fixation and serum neutralization procedures to study the interrelationships of the three types of equine herpes viruses (EHV-1, EHV-2, and EHV-3). Equine cell cultures infected with each type virus fluoresced when stained with homologous conjugated antiserum. In reciprocal tests EHV-1 and EHV-3 cross-fluoresced, but EHV-2 did not cross-fluoresce. Non-infected cell cultures did not fluoresce when stained with the 3 conjugates. EHV-1 and EHV-3 cross-fluores...
Replication of equine herpesvirus type 1 and type 3: resistance to hydroxyurea and thymidine.
Intervirology    January 1, 1978   Volume 9, Issue 5 276-285 doi: 10.1159/000148945
Allen GP, Cohen JC, Randall CC, O'Callaghan DJ.The replication of equine herpesvirus type 1 (EHV-1) and type 3 (EHV-3) was unimpeded in three different cell types-equine epithelial cells, equine fibroblasts, and mouse fibroblasts-which had been blocked in their capacity to synthesize host DNA by 2.5 mM hydroxyurea (HU) or 2 mM thymidine (TdR). The rate of DNA synthesis in uninfected or equine herpesvirus-infected cells in the presence of HU or TdR was measured by pulse-labeling cell samples with a labeled DNA precursor at different times after infection. DNA synthesis in uninfected cultures was completely inhibited by both compounds. Howev...
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...
Lactoperoxidase-catalyzed iodination of horse cytochrome c:monoiodotyrosyl 74 cytochrome c.
The Journal of biological chemistry    November 10, 1977   Volume 252, Issue 21 7743-7751 
Osheroff N, Feinberg BA, Margoliash E, Morrison M.Iodination of horse cytochrome c with the lactoperoxidase-hydrogen peroxide-iodide system results initially in the formation of the monoiodotyrosyl 74 derivative. This singly modified protein was obtained in pure form by ion exchange chromatography and preparative column electrophoresis. It shows an intact 695 nm absorption band, the midpoint potential of the native protein, a nuclear magnetic resonance spectrum which indicates an undisturbed heme crevice structure, a normal reaction with antibodies directed against native horse cytochrome c, and circular dichroic spectra in which the only cha...
Chromatographic separations of alphavirus strains by hydroxylapatite.
Journal of clinical microbiology    September 1, 1977   Volume 6, Issue 3 238-243 doi: 10.1128/jcm.6.3.238-243.1977
Jahrling PB, Beall JL.Hydroxylapatite column chromatography methods were developed to characterize selected alphavirus populations. Different conditions of pH and phosphate molarity were required to obtain satisfactory elution profiles and separations for Western equine encephalomyelitis virus strains, compared with Eastern equine encephalomyelitis virus and Semliki Forest virus strains. Raising the pH of the buffers effected earlier elutions of all viruses. Selection of phosphate gradients with more gentle slopes and adjustment to the proper pH effected better separations of virus subpopulations. Elution profiles ...
Electron-microscopic study of the development of an equine adenovirus in cultured fetal equine kidney cells.
Canadian journal of microbiology    May 1, 1977   Volume 23, Issue 5 497-509 doi: 10.1139/m77-074
Shahrabadi MS, Marusyk RG, Crawford TB.Sequential changes induced by an equine adenovirus in cultured fetal equine kidney cells were studied by electron microscopy. The first morphological change was the appearance of type I inclusions. These inclusions developed to type II inclusions which appeared as ring forms. Type III inclusions were formed within the central part of type II inclusions and finally filled up most of the nuclear space. As the infection proceeded, type IV inclusions which appeared as dense dark-staining spheres were formed at the center of the type III inclusions and also inside the cytoplasm. These dark-staining...
Apparent propagation of the equine infectious anemia virus in a mosquito (Culex pipiens quinquefasciatus Say) ovarian cell line.
American journal of veterinary research    September 1, 1976   Volume 37, Issue 9 1069-1070 
Breaud TP, Steelman CD, Roth EE, Adams WV.A tissue culture of Culex pipiens quinquefasciatus Say ovarian cells appeared to support the growth of equine infectious anemia (EIA) virus. Shetland ponies inoculated with 2nd, 7th, 9th, and 11th passages of mediums harvested from infected tissue culture had clinical signs of the disease and became EIA positive on 11, 19, 23, and 43 days after inoculation, respectively.
[Infection of HeLa cells by herpes virus of horses type 1 in different temperature and dose of the virus (author’s transl)].
Ceskoslovenska epidemiologie, mikrobiologie, imunologie    May 1, 1976   Volume 25, Issue 3 137-143 
Sláviková K, Blaśkovic D.No abstract available
[Persistent infection of stable cell cultures by herpes virus of horses type 1 (author’s transl)].
Ceskoslovenska epidemiologie, mikrobiologie, imunologie    May 1, 1976   Volume 25, Issue 3 144-150 
Sláviková K, Blaskovic D, Slávik I, Lesso J.No abstract available
Cell-free synthesis of equine herpesvirus type 3 nucleocapsid polypeptides.
Virology    February 1, 1976   Volume 69, Issue 2 751-762 doi: 10.1016/0042-6822(76)90503-1
Allen GP, Bryans JT.No abstract available
Viral antigen production in horse kidney cell cultures infected persistently with equine infectious anemia virus.
National Institute of Animal Health quarterly    January 1, 1976   Volume 16, Issue 1 31-32 
Kono Y.No abstract available
Digitoxin metabolism by rat liver microsomes.
Biochemical pharmacology    September 1, 1975   Volume 24, Issue 17 1639-1641 doi: 10.1016/0006-291x(75)90200-4
Schmoldt A, Benthe HF, Haberland G, Jallon JM, Risler Y, Iwatsubo M, Karuzina II, Bachmanova GI, Kuznetsova GP, Izotov MV, Archakov AI, Kröger H....It has been found that NADPH-dependent hydroxylation of dimethylaniline, aniline, p- and o-nitroanisol and lipid peroxidation is inhibited by the tyrosine-copper (II) complex (low molecular weight analog of superoxide dismutase), which is indicative of a possibility of superoxide radicals formation in these reactions. The inhibition of the above-mentioned reactions with Tyr2-Cu2+ is less pronounced or absent, if cumole hydroperoxide is used as cosubstrate instead of NADPH. Differences in the Tyr2-Cu2+ complex effects on the cumule hydroperoxide-dependent xenobiotics hydroxylation and lipid per...
Isolation and characterization of an adenovirus and isolation of its adenovirus-associated virus in cell culture from foals with respiratory tract disease.
American journal of veterinary research    March 1, 1975   Volume 36, Issue 3 247-250 
Dutta SK.An adenovirus was isolated from a foal with respiratory tract disease. The virus produced cytopathic effects (CPE) in equine embryo kidney (EEK) cell culture, contained deoxyribonucleic acid (DNA), was resistant to chloroform and pH 3, and was moderately resistant to heat. The virus caused hemagglutination of human (type O) erythrocytes. Viral density was 1.34 g/cm,3 and diameter was 75 nm. An adenovirus-associated virus (AAV) isolated from the infected cell culture was 22 nm in diameter. These viruses are classified as equine adenovirus and equine AAV.
Rapid diagnosis of Venezuelan equine encephalomyelitis by fluorescence microscopy.
American journal of veterinary research    February 1, 1975   Volume 36, Issue 2 167-170 
Erickson GA, Maré CJ.Goat Venezuelan equine encephalomyelitis (VEE) antiserum and normal serum were conjugated and evaluated for staining sensitivity and specificity. Cross-staining with either eastern or western equine encephalomyelitis virus-infected cells did not occur. The baby hamster kidney (BHK-21) cell line when combined with highly specific VEE conjugate detected 100 medium suckling mouse intracerebral lethal doses (suckling mouse LD-50/IC) of the 1B subtype of VEE virus per milliliter of equine tissue suspension. Conjugated goat antiserum was assayed for sensitivity for detection of VEE virus-infected eq...
Viral respiratory infections of horses: structure and function of lungs in relation to viral infection.
Journal of the American Veterinary Medical Association    January 1, 1975   Volume 166, Issue 1 76-77 
McChesney AE.Since the advent of cell culture techniques, numerous viruses have been shown to be related to respiratory diseases in horses. Although the viruses differ in many ways, they cause disease with some common characteristics. This report is a summary of some of the available material from written sources and from personal observations. It is intended to help explain some of the changes observed in viral-induced respiratory disease.
Sodium and chloride transport across the equine cecal mucosa.
American journal of veterinary research    December 1, 1974   Volume 35, Issue 12 1511-1514 
Giddings RF, Argenzio RA, Stevens CE.No abstract available
Studies on cell lines derived from a horse with lymphosarcoma.
Cancer    September 1, 1974   Volume 34, Issue 3 696-704 doi: 10.1002/1097-0142(197409)34:3<696::aid-cncr2820340328>3.0.co;2-f
Zachariasewycz E, Baliga V.No abstract available
Detection of tumor-specific antigens in an equine sarcoid cell line.
Infection and immunity    April 1, 1974   Volume 9, Issue 4 714-718 doi: 10.1128/iai.9.4.714-718.1974
Watson RE, Larson KA.Indirect immunofluorescence and lymphocyte cytotoxicity experiments demonstrated the presence of a tumor-specific antigen(s) on the surface of cells from an equine sarcoid cell line (Mc1). Autologous serum (taken from the horse from which the Mc1 cells were derived) and sera from three other sarcoid-bearing horses revealed a similar membrane immunofluorescence when reacted with Mc1 cells, indicating the existence of cross-reacting antibodies. Results of serum colony inhibition experiments indicate that these antibodies are not cytotoxic. Incubation of Mc1 cells with autologous lymphocytes resu...
Propagation of equine infectious anemia virus in horse kidney cell cultures.
National Institute of Animal Health quarterly    January 1, 1974   Volume 14, Issue 4 155-162 
Kono Y, Yoshino T.No abstract available
[Interstitial cells of the testis of cryptorchid horse cultivated in vitro].
Rivista di istochimica, normale e patologica    January 1, 1974   Volume 18, Issue 1-4 132 
Lauria A, Monti T.No abstract available
Virus-like particles in an equine sarcoid cell line.
American journal of veterinary research    December 1, 1973   Volume 34, Issue 12 1601-1603 
England JJ, Watson RE, Larson KA.On electron microscopic examination of a cell line derived from an equine sarcoid, intracytoplasmic oncornavirus-like particles were seen. Cells treated with idoxuridine-dimethyl sulfoxide (idu-dmso) had a two- to four-fold increase in the number of particles as compared with nontreated cells or cells treated with dmso alone. The intracytoplasmic virus-like particles were double membrane structures measuring 80 to 100 nm. in diameter. Particles were seen extracelluarly or budding from the cell membrane into the extracellular space. These extracellular particles were 100 nm. in diameter and con...
Cultural characteristics of a cell line derived from an equine sarcoid.
Applied microbiology    November 1, 1972   Volume 24, Issue 5 727-731 doi: 10.1128/am.24.5.727-731.1972
Watson RE, England JJ, Larson KA.A cell line, derived from a spontaneous equine connective tissue tumor (equine sarcoid), has been established. The morphological and growth characteristics indicative of malignant transformation of the cells include a disoriented, rapid growth and loss of contact inhibition. Further evidence of transformation is the agglutination of these cells by concanavalin A and their ability to divide in semisolid media.
Generalized Equine Cutaneous Mastocytosis.
Veterinary pathology    November 1, 1972   Volume 9, Issue 6 394-407 doi: 10.1177/030098587200900601
Cheville NF, Prasse K, van der Maaten M, Boothe AD.A newborn foal developed generalized cutaneous mastocytosis characterized by multiple elevated nodules of mast cells in skin and basophil hyperplasia in bone marrow. Skin lesions began as small aggregates of mast cells that progressively enlarged, ulcerated, and regressed spontaneously. Eosinophil infiltration, collagen necrosis, and fibroplasia were characteristic of advanced lesions. Many new lesions developed during the first month of life but numbers progressively diminished. Large numbers of mast cells were present in biopsies of lymph node, spleen and bone marrow. Discrete aggregates of ...
Development of an equine herpesvirus in two cell culture systems: light and electron microscopy.
Infection and immunity    November 1, 1972   Volume 6, Issue 5 865-876 doi: 10.1128/iai.6.5.865-876.1972
Fong CK, Hsiung GD.Development of equine herpesvirus strain 82A was studied in cells from primary horse kidney (HOK) cultures and an equine dermis (ED) cell strain. HOK and ED cells are equally susceptible to the 82A virus infection and yield about the same amount of infectious virus. Intranuclear inclusions were present in both cell systems, but a ring-shaped syncytial formation was observed only in infected ED cells. Ultrastructural studies revealed the presence of dense granules 30 nm in diameter and characteristic star-like clusters of granules in the infected HOK cells, but these granules were rarely seen i...
Comparative effects of mare, stallion, gelding horse, and fetal bovine sera on neoplastic transformation in vitro.
Journal of the National Cancer Institute    August 1, 1972   Volume 49, Issue 2 505-511 
Evans VJ, Price FM, Sanford KK, Kerr HA, Handleman SL.No abstract available
Study of the one-step growth curve of equine infectious anemia virus by immunofluorescence.
Infection and immunity    June 1, 1972   Volume 5, Issue 6 890-895 doi: 10.1128/iai.5.6.890-895.1972
Ushimi C, Henson JB, Gorham JR.Primary horse leukocyte cultures were inoculated with 2 or 10 50% tissue culture infective doses (TCID(50)) of equine infectious anemia (EIA) virus per cell, and the titer of cell-associated and fluid-phase virus was determined from 1 to 72 hr postinoculation (PI). Cover slips were collected from 4 to 72 hr PI and stained for EIA viral antigen by the indirect immunofluorescent (FA) technique. Viral replication was detected after a latent period of approximately 18 to 24 hr and reached peak titers of approximately 10(4.5) to 10(6) TCID(50)/0.5 ml from 48 to 72 hr PI. The fluid phase contained 1...
[Low temperature thresholds of reproduction of group A arboviruses in tissue culture].
Voprosy virusologii    May 1, 1972   Volume 17, Issue 3 283-287 
L'vov DK, Cheban DS, Tsilinskiĭ IaIa.No abstract available
[Effect of fusidin on reproduction of Venezuelan equine encephalomyelitis virus in tissue culture].
Antibiotiki    May 1, 1972   Volume 17, Issue 5 457-461 
Gerasimova SS, Novokhatskii AS.No abstract available
Production of high titer eastern equine encephalomyelitis virus and viral antigens in chick embryo suspension cultures.
Archiv fur die gesamte Virusforschung    January 1, 1972   Volume 36, Issue 1 13-17 doi: 10.1007/BF01250290
White A, Rourke S, Berman S, Lowenthal JP.No abstract available
[Structural components of the erythrocyte membrane].
Postepy biochemii    January 1, 1972   Volume 18, Issue 3 351-373 
Gondko R, Slomiany B, Slaska K.No abstract available