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Biomedical subjects

E F Lascano

Publications and source records attributed to E F Lascano.

At least 37 records · Page 2Linked to original sources
PubMed1980

Histological study of the progression of herpes simplex virus in mice.

The progress of an experimental infection with Herpesvirus hominis type 1 was studied in newborn mice inoculated into the foot pad of the hind leg. To trace the viral antigen, the unlabeled antibody enzyme PAP (peroxidase/antiperoxidase) method was employed. The virus antigen appeared first in the epidermal and connective tissue cells of the inoculation site, and then progressed along the sciatic nerve. This nerve was studied by electron microscopy and showed active multiplication within the Schwann cells, with the production of virions, some of which were found in the intercellular spaces. No intra-axonal particles were observed. The infection then spread to the spinal ganglia and to the spinal cord. In this progression, the pia mater appeared to play an important role. From the spinal cord, the infection spread to the encephalon. The present study supports a mixed route for the neural transport of herpes simplex virus: a) by cell-to-cell transmission (Schwann and connective tissue cells in the sciatic nerve; meningeal cells, neurons and glial cells in the CNS); b) by a passive motion of the virions along the intercellular spaces. The inoculated virus also gave rise to viremia with viral multiplication in several viscera.

Animals↗
PubMed1975

Fine structure of the germinal membrane of Echinococcus granulosus cysts.

The ultrastructure of the hydatid cyst germinal membrane was studied. It was divided into 3 regions, the tegument, the tegumental cell region, and the innermost area bordering the cyst cavity. The morphology of tegumental, muscular, flame, duct, and glycogen-containing cells and cells containing lysosomal-like bodies is described. The significance of these findings is discussed in terms of the possible function of these structures and present knowledge on the penetration of macromolecules into hydatid cysts.

Animals↗
PubMed1974

Ultrastructure of Junín virus in mouse whole brain and mouse brain tissue cultures.

Comparative ultrastructural studies were performed on the development of Junín virus in mouse brain and in cerebellum explants and brain monolayers of the same animal. In mouse brain, neurons and astrocytes released virus particles by a budding mechanism identical to that previously described for this virus. In the neurons, the viral multiplication took place in the perikarion as well as in the cytoplasmic processes, including areas near synapses. Viral particles were observed emerging from pericapillary neurons and astrocytes. In the explants, the budding also occurred in neurons and astrocytes. In the monolayers, however, the virus originated in astrocytes and cells of fibroblastic appearance, which were the two cell types that developed in this substrate. These results indicate that the characteristics of the development of Junín virus in mouse brain are faithfully reproduced in cerebellum explants from the same animal, thus allowing some extrapolation of data from one system to the other. The explant proved to be a better model than the monolayer, not only because it reproduced the structural complexity of nervous tissue better, but also because it contains neurons and astrocytes, i.e., the two cell types that release the virus in the in vivo system.

Animals↗
PubMed1969

Morphogenesis of aura virus.

Aura virus, a member of the Western equine-encephalitis-Whataroa subgroup of group A arboviruses, was studied by electron microscopy in suckling mouse brain and chick embryo cultured cells. Virus precursors, budding particles, and complete virus particles were first detected 10 hr after infection in chick embryo cells and 24 hr after inoculation in mouse brain. Virus precursors were generally seen aligned along cytomembranes, and were less frequently seen closely associated with viroplasm-like foci, tubular aggregates, or scattered in the cytoplasmic matrix without an apparent connection to any other structure. The assembly of mature virus was observed to take place by a budding process of the virus precursor from the plasma membrane into the extracellular space, and from the cytoplasmic membranes into the lumina of vacuoles and cisternae. It was demonstrated that the endoplasmic reticulum participates in the assembly of intracellular virions. Indirect evidence was found to indicate that the Golgi complex may also form mature virus. Aura virions had a size, shape, and structure similar to those of the previously described group A arboviruses.

Journal Article↗