PubMed Health⌕ Search

Biomedical subjects

J D ALMEIDA

Publications and source records attributed to J D ALMEIDA.

14 recordsLinked to original sources

POWASSAN VIRUS: MORPHOLOGY AND CYTOPATHOLOGY.

Powassan virus, a North American tickborne group B arbovirus, multiplied after simultaneous inoculation into bottles or tubes of virus and trypsinized suspension of continuous-line cultures of rhesus monkey kidney cells, strain LLC-MK2. Cytopathic effects comprising cell rounding and cytoplasmic vacuolation were first observed five days after inoculation. Mixture of Powassan antiserum with virus before inoculation into tissue cultures inhibited the appearance of cytopathic effects. Hemagglutinins for rooster erythrocytes, optimally at pH 6.4 and 22 degrees C., first appeared in tissue culture supernatant fluids four days after inoculation.Electron microscopic observation of thin sections of infected tissue culture cells showed virus particles 360-380 A.U. along outer cell membranes and edges of cytoplasmic vacuoles. In phosphotungstic acid negatively stained preparations, intact virus particles, 400-450 A.U. total diameter, were observed inside infected cells. In particles in which the peripheral layer became discontinuous, geometrically arranged subunits compatible with cubic symmetry were observed.

Animals↗

VIRUS-LIKE PARTICLES IN BLOOD OF TWO ACUTE LEUKEMIA PATIENTS.

A modified negative staining technique suited to demonstrating fragile virus particles in the electron microscope revealed particles having a surrounding membranous sac and an internal filamentous component of a consistent diameter of 75 A in the blood of two patients with acute leukemia. No particles of this type were seen in the blood of four other patients with acute leukemia or in the blood of six normal individuals.

Acute Disease↗

A CLASSIFICATION OF VIRUS PARTICLES BASED ON MORPHOLOGY.

Recent improvements in electron microscope techniques which allow the study of virus fine structure have permitted the grouping of many viruses on a purely morphological basis. Briefly the techniques used in electron microscopy for the study of viruses are reviewed and the symmetry properties of virus particles as revealed by negative staining are discussed somewhat more fully.Finally, virus particles are grouped on two bases, firstly the site of formation of the virus within the cell as seen by thin sectioning techniques, and secondly the symmetry property of the virus as seen by negative staining. Consideration of the groupings obtained in this way reveals that the biochemical and physical properties of a virus can be deduced from the readily established morphological characteristics.

Classification↗

An electron microscope study of polyoma virus in hamster kidney.

Electron microscope studies were made of hamster kidneys taken at daily intervals after injection of a variant of polyoma virus into newborn animals. Particular attention was paid to the period 5 to 6 days after injection at which time the necrotizing response was at its peak and virus particles were seen in greatest numbers. The most numerous particles were about 28 mmicro in diameter. They were observed mainly within nuclei of stromal cells and are similar to the particles seen in large numbers in polyoma-infected mouse cells growing in vitro. They were not observed in cells of fully developed tumors. Filamentous or tubular structures closely associated with the 28 mmicro particles and probably concerned in their formation are described. Considerable quantities of viral material were contained within cytoplasmic inclusions. In some of the inclusions larger particles of diameter 60 mmicro were observed. The origin of these particles and their relation to the 28 mmicro particles is discussed.

Animals↗