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Research Article | Therapeutics and Prevention

Combinatorial Approaches to Viral Attenuation

Matthew L. Paff, Benjamin R. Jack, Bartram L. Smith, James J. Bull, Claus O. Wilke
Olga Zhaxybayeva, Editor
Matthew L. Paff
aDepartment of Integrative Biology, The University of Texas at Austin, Austin, Texas, USA
bInstitute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas, USA
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Benjamin R. Jack
aDepartment of Integrative Biology, The University of Texas at Austin, Austin, Texas, USA
bInstitute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas, USA
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Bartram L. Smith
aDepartment of Integrative Biology, The University of Texas at Austin, Austin, Texas, USA
bInstitute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas, USA
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James J. Bull
aDepartment of Integrative Biology, The University of Texas at Austin, Austin, Texas, USA
bInstitute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas, USA
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Claus O. Wilke
aDepartment of Integrative Biology, The University of Texas at Austin, Austin, Texas, USA
bInstitute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas, USA
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  • ORCID record for Claus O. Wilke
Olga Zhaxybayeva
Dartmouth College
Roles: Editor
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DOI: 10.1128/mSystems.00046-18
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ABSTRACT

Attenuated viruses have numerous applications, in particular in the context of live viral vaccines. However, purposefully designing attenuated viruses remains challenging, in particular if the attenuation is meant to be resistant to rapid evolutionary recovery. Here we develop and analyze a new attenuation method, promoter ablation, using an established viral model, bacteriophage T7. Ablation of promoters of the two most highly expressed T7 proteins (scaffold and capsid) led to major reductions in transcript abundance of the affected genes, with the effect of the double knockout approximately additive of the effects of single knockouts. Fitness reduction was moderate and also approximately additive; fitness recovery on extended adaptation was partial and did not restore the promoters. The fitness effect of promoter knockouts combined with a previously tested codon deoptimization of the capsid gene was less than additive, as anticipated from their competing mechanisms of action. In one design, the engineering created an unintended consequence that led to further attenuation, the effect of which was studied and understood in hindsight. Overall, the mechanisms and effects of genome engineering on attenuation behaved in a predictable manner. Therefore, this work suggests that the rational design of viral attenuation methods is becoming feasible.

IMPORTANCE Live viral vaccines rely on attenuated viruses that can successfully infect their host but have reduced fitness or virulence. Such attenuated viruses were originally developed through trial and error, typically by adaptation of the wild-type virus to novel conditions. That method was haphazard, with no way of controlling the degree of attenuation or the number of attenuating mutations or preventing evolutionary reversion. Synthetic biology now enables rational design and engineering of viral attenuation, but rational design must be informed by biological principles to achieve stable, quantitative attenuation. This work shows that in a model system for viral attenuation, bacteriophage T7, attenuation can be obtained from rational design principles, and multiple different attenuation approaches can be combined for enhanced overall effect.

  • Received April 2, 2018.
  • Accepted July 5, 2018.
  • Copyright © 2018 Paff et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

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Combinatorial Approaches to Viral Attenuation
Matthew L. Paff, Benjamin R. Jack, Bartram L. Smith, James J. Bull, Claus O. Wilke
mSystems Jul 2018, 3 (4) e00046-18; DOI: 10.1128/mSystems.00046-18

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Combinatorial Approaches to Viral Attenuation
Matthew L. Paff, Benjamin R. Jack, Bartram L. Smith, James J. Bull, Claus O. Wilke
mSystems Jul 2018, 3 (4) e00046-18; DOI: 10.1128/mSystems.00046-18
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KEYWORDS

bacteriophages
codon deoptimization
promoter knockout
viral attenuation

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