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Published on: November 1, 2011
Region between the canine distemper virus M and F genes modulates virulence by controlling fusion protein expression
Danielle E Anderson1, Veronika von Messling
1INRS-Institut Armand-Frappier, University of Quebec, Laval, Quebec, Canada.
Abstract:
Morbilliviruses, including measles and canine distemper virus (CDV), are nonsegmented, negative-stranded RNA viruses that cause severe diseases in humans and animals. The transcriptional units in their genomes are separated by untranslated regions (UTRs), which contain essential transcription and translation signals. Due to its increased length, the region between the matrix (M) protein and fusion (F) protein open reading frames is of particular interest. In measles virus, the entire F 5' region is untranslated, while several start codons are found in most other morbilliviruses, resulting in a long F protein signal peptide (Fsp). To characterize the role of this region in morbillivirus pathogenesis, we constructed recombinant CDVs, in which either the M-F UTR was replaced with that between the nucleocapsid (N) and phosphoprotein (P) genes, or 106 Fsp residues were deleted. The Fsp deletion alone had no effect in vitro and in vivo. In contrast, substitution of the UTR was associated with a slight increase in F gene and protein expression. Animals infected with this virus either recovered completely or experienced prolonged disease and death due to neuroinvasion. The combination of both changes resulted in a virus with strongly increased F gene and protein expression and complete attenuation. Taken together, our results provide evidence that the region between the morbillivirus M and F genes modulates virulence through transcriptional control of the F gene expression.
Insights
The region between morbillivirus matrix (M) and fusion (F) genes influences viral disease. Modifying this region affects F gene expression, impacting canine distemper virus (CDV) virulence and neuroinvasion.
Area of Science:
- Virology
- Molecular Biology
- Pathogenesis
Background:
- Morbilliviruses are nonsegmented, negative-stranded RNA viruses causing severe diseases.
- Untranslated regions (UTRs) separate transcriptional units and contain regulatory signals.
- The M-F UTR and F protein signal peptide (Fsp) are critical for morbillivirus pathogenesis.
Purpose of the Study:
- To investigate the role of the M-F UTR and Fsp in morbillivirus pathogenesis.
- To characterize how modifications in these regions affect viral gene expression and virulence.
Main Methods:
- Construction of recombinant canine distemper viruses (CDVs).
- Engineered viruses with altered M-F UTRs or deleted Fsp residues.
- In vitro and in vivo analyses of viral gene expression, pathogenesis, and neuroinvasion.
Main Results:
- Fsp deletion alone had no significant effect on viral replication or virulence.
- M-F UTR substitution increased F gene and protein expression, leading to varied disease outcomes, including neuroinvasion.
- Combined modifications resulted in high F gene expression and complete viral attenuation.
Conclusions:
- The region between the M and F genes modulates morbillivirus virulence.
- Transcriptional control of F gene expression is a key mechanism for virulence modulation.
- Findings provide insights into morbillivirus pathogenesis and potential therapeutic targets.
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