The morphology of noninfective pseudorabies virus produced by cells treated with 5-fluorouracil.
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Biomedical subjects
Publications and source records attributed to M REISSIG.
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A sequential study is reported of the cytological changes induced in cultures of monkey kidney epithelial cells by poliovirus. The pattern of cytological changes was followed through a single cycle of virus multiplication. Morphological alterations were correlated with the appearance of new infective virus within the cells and in the culture fluid. Alteration of the chromatin pattern of the nucleus, and Type B acidophilic intranuclear inclusions, were seen as early as 4 hours after virus inoculation. Later wrinkling and shrivelling of the nucleus occurred, and eosinophilic cytoplasmic masses appeared. The rounded, pycnotic cell, customarily used as an index of the cytopathic response, was found only during the last stages of the infective process. On the basis of these changes, infected cells could be classified into six different types. Differential cell counts were made on the stained cultures, and the stage of cytopathic degeneration was correlated with the appearance of virus in the cells and in the culture fluid. Newly formed virus could be detected within the infected cells at about the same time that the first nuclear alterations and intranuclear inclusions were seen. The virus-induced morphological changes exhibited a specificity distinct from the classical pycnosis of autolytic degeneration.
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A sequential study is reported of the morphological changes occurring after herpes B virus infection of cells as revealed in ultrathin sections under the electron microscope. Monolayer cultures of renal epithelial cells prepared from the natural host of the virus, the monkey, were infected, and the cellular alterations were correlated with the appearance of infective virus in the culture fluids. The morphological changes consisted in swelling of the cells and disappearance of the nucleolus, followed by margination and gradual decrease of the nuclear chromatin. The inclusion material corresponded to the clear central areas of the nucleus, where the chromatin had disappeared. In the late stages of infection this inclusion material filled the nucleus and formed a classical type A inclusion body. Characteristic particles appeared in the nucleus and cytoplasm of the infected cells a few hours after inoculation. They had a dense center surrounded by one or two membranes. Those with one membrane ranged in size from 60 to 100 mmicro and those with two from 120 to 180 mmicro. Particles showing the same wide variation in size and structure were seen both in the nucleus and in the cytoplasm. They were first visible on the external surface of the swollen but intact cells at about the same time new infective virus became detectable in the culture fluid. A small number of the extracellular, and cytoplasmic, virus particles appeared "binucleated," containing two central bodies, each having its own membrane, both being surrounded by a single external coat. About 180 mmicro in diameter, they were randomly distributed among the "mononucleated" particles.
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Rabbits were inoculated with the C.P.M. strain of myxoma virus and the resulting subcutaneous tumors were fixed, embedded, and sectioned for observation with the electron microscope. Both round cells and the typical stellate myxomatous cells were observed in addition to changes in the collagen pattern at the intercellular spaces. The cytoplasm of the cells showed a great number of bodies of varying size and density, the largest of them having the size and other characteristics of the elementary bodies of the virus. Some of the bodies showed an internal structure, being formed by the tight clumping of small dense particles. Distribution curves of the diameter of the elementary bodies and of the smaller internal particles are presented. The morphological problems involved in the virus-host cell relationship are discussed in the case of the myxoma virus.