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Updated: Oct 23, 2026

Purification and Visualization of Influenza A Viral Ribonucleoprotein Complexes
Published on: February 8, 2009
Electron microscopic evidence for parainfluenza type III/retrovirus phenotypically mixed particles
Abstract:
Sublines of malignant permanent human fibroblast cell lines were shown to be infected by a type-D retrovirus (PMFV) and by a parainfluenza virus type III in an earlier study (2, 6). Careful electron microscopical investigations of these sublines have proved "viral structural elements" of both viruses in the same cell. We obtained electron microscopic evidence--though rarely--for parainfluenza type III/PMFV mixed-particles.
Insights
This study found evidence of both a type-D retrovirus (PMFV) and parainfluenza virus type III within the same human fibroblast cells. Researchers also observed rare instances of mixed viral particles, suggesting co-infection.
Area of Science:
- Virology
- Cell Biology
- Electron Microscopy
Background:
- Previous studies identified type-D retrovirus (PMFV) and parainfluenza virus type III infections in human fibroblast cell lines.
- Malignant permanent human fibroblast sublines were utilized for investigation.
Purpose of the Study:
- To investigate the co-existence of PMFV and parainfluenza virus type III within infected human fibroblast cells.
- To identify viral structural elements of both viruses in the same cell using electron microscopy.
Main Methods:
- Utilized electron microscopy for high-resolution imaging of infected human fibroblast sublines.
- Performed detailed ultrastructural analysis to identify viral components.
Main Results:
- Confirmed the presence of "viral structural elements" of both PMFV and parainfluenza virus type III within the same cells.
- Observed rare instances of mixed parainfluenza type III/PMFV particles via electron microscopy.
Conclusions:
- Provides electron microscopic evidence for the co-infection of human fibroblast cells by PMFV and parainfluenza virus type III.
- Suggests the potential for the formation of mixed viral particles during co-infection.
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