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J. Virol., Mar 1995, 1678-1686, Vol 69, No. 3
A Zurbriggen, HU Graber, A Wagner and M Vandevelde
Canine distemper virus (CDV), a negative-strand RNA morbillivirus, causes a
progressive demyelinating disease in which virus persistence plays an
essential role. The antiviral immune response leads to virus clearance in
the inflammatory lesions. However, CDV can replicate and persist outside
these inflammatory lesions within the brain. How CDV is capable of
persisting in the presence of an effective antiviral immune response is
poorly understood. In the present investigation, we studied several aspects
of virus replication in primary dog brain cell cultures (DBCC), comparing
an attenuated CDV strain and a virulent CDV strain. Confluent DBCC were
infected with either virulent A75/17-CDV or attenuated Onderstepoort-CDV
and monitored for 60 days. Persistence was not associated with defective
virus production, because all mRNAs and corresponding proteins were
continuously expressed in the noncytolytic infection. Quantitative
measurements did not detect a difference between the two types of infection
in the rate of virus transcription and protein synthesis at the level of
the single cell. However, electron microscopy and virus titration
experiments showed that in the persistent CDV infection virus budding is
strongly limited compared with that of the attenuated virus. Morphometry
and immunocytochemistry showed profound differences in the way the two
viruses spread in the culture. The attenuated CDV spread randomly to
immediately adjacent cells, whereas persistent CDV spread selectively to
more-distant cells by way of cell processes. In conclusion, the present
study supports a mechanism of CDV persistence through selective spread by
way of cell processes, enabling virulent CDV to invade the central nervous
system without the need of releasing much virus into the extracellular
space.
Copyright © 1995, American Society for Microbiology
Canine distemper virus persistence in the nervous system is associated with noncytolytic selective virus spread
Institute of Animal Neurology, University of Bern, Switzerland.
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