scholarly journals A ?cradle? for support of roller-bottle-cell cultures during microscopic examination

1972 ◽  
Vol 14 (3) ◽  
pp. 505-507
Author(s):  
Peter G. Probst ◽  
Joseph L. Rogers ◽  
Henry C. Orr
Keyword(s):  
Cell Cultures ◽  
Microscopic Examination ◽  
Roller Bottle

Behavior of BAS-9052 OH in Soybean (Glycine max) and Johnsongrass (Sorghum halepense) Plant and Cell Cultures

Weed Science ◽  
1982 ◽  
Vol 30 (6) ◽  
pp. 640-650 ◽  
Author(s):  
Beth A. Swisher ◽  
Frederick T. Corbin
Keyword(s):  
Glycine Max ◽  
Cell Cultures ◽  
Microscopic Examination ◽  
Leaf Primordia ◽  
Sorghum Halepense ◽  
Leaf Stage ◽  
Intact Plants ◽  
Treated Leaf ◽  
Soybean Plants ◽  
Root Apices

Research involved the behavior of BAS-9052 OH {2[1-(ethoxyimino)butyl]-5-[2(ethylthio)propyl]-3-hydroxy-2-cyclohexen-1-one} in soybean [Glycine max(L.) Merr.] and johnsongrass [Sorghum halepense(L.) Pers.] plants, and the fate of14C-BAS-9052 OH in intact plants and cell cultures of both species. Microscopic examination of seedling johnsongrass plants (two- to three-leaf stage) treated with foliar applications of 0.48 μg/plant revealed disorganized apical regions and necrotic cells within the apex and leaf primordia of the shoot. Necrotic zones were also evident at the base of expanding leaves and in root apices 1 day after treatment. Following application of14C-BAS-9052 OH, the same radioactive products were isolated from cell cultures and intact plants. Products included BAS-9052 OH and three unidentified metabolites. Greater proportions of unchanged BAS-9052 OH were extracted from the apical leaves, roots, and cell cultures of johnsongrass than of soybean. BAS-9052 OH was thermal and photo-labile, and a large portion of14C may not have entered the plant as BAS-9052 OH. However, tolerant soybean plants and cell cultures appeared to have metabolized the herbicide more rapidly than susceptible johnsongrass plants and cell cultures. An average of 64% of the14C remained in the treated leaf of johnsongrass compared with 48% in soybean. About one-half as much14C was translocated to the apical leaves of susceptible johnsongrass than tolerant soybean. Therefore, differential uptake and translocation cannot account for the selectivity of BAS-9052 OH.

Detection of latent murine nosematosis and growth of Nosema cuniculi in cell cultures

1970 ◽  
Vol 16 (4) ◽  
pp. 237-242 ◽  
Author(s):  
J. E. Bismanis
Keyword(s):  
Cell Culture ◽  
Infected Cell ◽  
Cell Cultures ◽  
Mouse Embryo ◽  
Microscopic Examination ◽  
Embryo Cell ◽  
Internal Organs ◽  
Persistently Infected ◽  
Mouse Embryo Cell ◽  
Direct Microscopic Examination

Administration of hydrocortisone to mice caused activation of latent nosematosis in at least 25% of the animals. The sporozoan parasite Nosema cuniculi could be demonstrated in the tissues of the internal organs and circulating blood by direct microscopic examination. Growth and multiplication of the parasite could be achieved in mouse embryo cell cultures, where the parasite infected and destroyed only about 2% of the cells, thus establishing a state of persistently infected cell culture. The parasite grown in cell culture retained its mouse pathogenicity.

scholarly journals COMPARATIVE STUDIES OF FELINE VIRAL RHINOTRACHEITIS VIRUS FOR ITS REPLICATION PROPERTIES IN DIFFERENT CELL CULTURES

2018 ◽  
pp. 69-72 ◽  
Author(s):  
Ye. G. Kokorina ◽  
E. I. Elizbarashvili
Keyword(s):  
Virus Replication ◽  
Cell Cultures ◽  
Comparative Studies ◽  
Cytopathic Effect ◽  
Culture Technique ◽  
Virus Titre ◽  
Roller Bottle ◽  
Monolayer Cell ◽  
Susceptible Cell ◽  
Route Of Infection

The results of comparative studies of feline viral rhinotracheitis virus for its culture properties in primary and continuous cell cultures of feline origin (FK, FK (subculture), CrFK, FS, CC-81, FC/Tg) are presented. It was found that viral rhinotracheitis virus replication, irrespective of the route of infection and the culture technique, was consistent and practically equal in susceptible cell cultures. The most pronounced cytopathic effect (more than 75% monolayer degeneration) was observed in all types of cell cultures in 48–72 hours of cultivation. However, the accumulation of feline viral rhinotracheitis virus Grand strain was highest when preliminary adsorption occurred within the specified period of time, monolayer cell cultures were infected with the virus at a dose of 5.5 lg TCID50/ml and roller bottle cultivated, and the рН of the medium was maintained at 7.0–7.4. Single freezing of the virus at a temperature of minus 60 degrees Celsius upon the completion of the cultivation cycle (during 60–72 hours) and its thawing were found to significantly increase the virus titre by 0.5 lg TCID50/ml.

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.

Bacteriophages Associated with Turkey Coecums in Bluecomb-Infected and Healthy Birds

1969 ◽  
Vol 27 ◽  
pp. 226-227
Author(s):  
A. E. Ritchie
Keyword(s):  
Host Cell ◽  
Causal Relationship ◽  
Cell Cultures ◽  
Cell Interaction ◽  
Etiologic Agent ◽  
Viral Origin ◽  
Intestinal Contents ◽  
Host Cell Interaction

The cause of bluecomb disease in turkeys is unknown. Filtration of infective intestinal contents suggests a viral origin. To date, it has not been possible to isolate the etiologic agent in various cell cultures. The purpose of this work was to characterize as many virus-like entities as were recognizable in intestines of both healthy and bluecomb-infected turkeys. By a comparison of the viral populations it was hoped that some insight might be gained into the cause of this disease. Studies of turkey hemorraghic enteritis by Gross and Moore (Avian Dis. 11: 296-307, 1967) have suggested that a bacteriophage-host cell interaction may bear some causal relationship to that disease.

The Fine Structure of Rat Granulosa Cell Cultures Correlated with Progestin Secretion

1973 ◽  
Vol 31 ◽  
pp. 552-553
Author(s):  
T. M. Crisp ◽  
F.R. Denys
Keyword(s):  
Fine Structure ◽  
Granulosa Cell ◽  
Cell Cultures ◽  
Single Injection ◽  
Surrounding Medium ◽  
Petri Dish ◽  
Female Rats ◽  
Vaginal Smear ◽  
Immature Female ◽  
Serum Gonadotropin

The purpose of this paper is to present observations on the fine structure of rat granulosa cell cultures grown in the presence of an adenohypophyseal explant and to correlate the morphology of these cells with progestin secretion. Twenty-six day old immature female rats were given a single injection of 5 IU pregnant mares serum gonadotropin (PMS) in order to obtain ovaries with large vesicular follicles. At 66 hrs. post-PMS administration (estrus indicated by vaginal smear cytology), the ovaries were removed and placed in a petri dish containing medium 199 and 100 U penicillin/streptomycin (P/S)/ml. Under a 20X magnification dissecting microscope, some 5-8 vesicular follicles/ovary were punctured and the granulosa cells were expressed into the surrounding medium. The cells were transferred to centrifuge tubes and spun down at 1000 rpm for 5 mins.

Properties of Isolated Mitochondria of Agaricus Bisporus: Their Relationship to Dormancy and the Germination of Spores

1973 ◽  
Vol 31 ◽  
pp. 458-459
Author(s):  
K. S. McCarty ◽  
R. F. Weave ◽  
L. Kemper ◽  
F. S. Vogel
Keyword(s):  
Mitochondrial Dna ◽  
Ethidium Bromide ◽  
Microscopic Examination ◽  
Agaricus Bisporus ◽  
Osmotic Shock ◽  
Electron Microscopic Examination ◽  
Electron Microscopic ◽  
Isolated Mitochondria ◽  
Dna Strands ◽  
Cytoplasmic Ribosomes

During the prodromal stages of sporulation in the Basidiomycete, Agaricus bisporus, mitochondria accumulate in the basidial cells, zygotes, in the gill tissues prior to entry of these mitochondria, together with two haploid nuclei and cytoplasmic ribosomes, into the exospores. The mitochondria contain prominent loci of DNA [Fig. 1]. A modified Kleinschmidt spread technique1 has been used to evaluate the DNA strands from purified whole mitochondria released by osmotic shock, mitochondrial DNA purified on CsCl gradients [density = 1.698 gms/cc], and DNA purified on ethidium bromide CsCl gradients. The DNA appeared as linear strands up to 25 u in length and circular forms 2.2-5.2 u in circumference. In specimens prepared by osmotic shock, many strands of DNA are apparently attached to membrane fragments [Fig. 2]. When mitochondria were ruptured in hypotonic sucrose and then fixed in glutaraldehyde, the ribosomes were released for electron microscopic examination.

Morphological Examination of a Herpes-type Virus Indigenous for Tree Shrews

1970 ◽  
Vol 28 ◽  
pp. 160-161
Author(s):  
J. P. Brunschwig ◽  
R. M. McCombs ◽  
R. Mirkovic ◽  
M. Benyesh-Melnick
Keyword(s):  
Electron Microscopy ◽  
Soft Tissue ◽  
Chick Embryo ◽  
Soft Tissue Sarcoma ◽  
Cell Cultures ◽  
Tree Shrew ◽  
Type Virus ◽  
Morphological Examination ◽  
Tree Shrews ◽  
Embryo Cells

A new virus, established as a member of the herpesvirus group by electron microscopy, was isolated from spontaneously degenerating cell cultures derived from the kidneys and lungs of two normal tree shrews. The virus was found to replicate best in cells derived from the homologous species. The cells used were a tree shrew cell line, T-23, which was derived from a spontaneous soft tissue sarcoma. The virus did not multiply or did so poorly for a limited number of passages in human, monkey, rodent, rabbit or chick embryo cells. In the T-23 cells, the virus behaved as members of the subgroup B of herpesvirus, in that the virus remained primarily cell associated.

Scanning Electron Microscopy and Electron Microprobe Analysis of Malignant Cell Cultures

1968 ◽  
Vol 26 ◽  
pp. 164-165
Author(s):  
R. I. Johnsson-Hegyeli ◽  
A. F. Hegyeli ◽  
D. K. Landstrom ◽  
W. C. Lane
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Cell Cultures ◽  
Electron Microprobe ◽  
Microprobe Analysis ◽  
Electron Microprobe Analysis ◽  
Three Dimensional ◽  
Malignant Cell ◽  
Interference Microscopy ◽  
Scanning Electron

Last year we reported on the use of reflected light interference microscopy (RLIM) for the direct color photography of the surfaces of living normal and malignant cell cultures without the use of replicas, fixatives, or stains. The surface topography of living cells was found to follow underlying cellular structures such as nuceloli, nuclear membranes, and cytoplasmic organelles, making possible the study of their three-dimensional relationships in time. The technique makes possible the direct examination of cells grown on opaque as well as transparent surfaces. The successful in situ electron microprobe analysis of the elemental composition and distribution within single tissue culture cells was also reported.This paper deals with the parallel and combined use of scanning electron microscopy (SEM) and the two previous techniques in a study of living and fixed cancer cells. All three studies can be carried out consecutively on the same experimental specimens without disturbing the cells or their structural relationships to each other and the surface on which they are grown. KB carcinoma cells were grown on glass coverslips in closed Leighto tubes as previously described. The cultures were photographed alive by means of RLIM, then fixed with a fixative modified from Sabatini, et al (1963).

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