Virus wars: using one virus to block the spread of another

Author:

Paff Matthew L.12,Nuismer Scott L.3,Ellington Andrew425,Molineux Ian J.42,Bull James J.126

Affiliation:

1. Department of Integrative Biology, University of Texas, Austin, TX, United States

2. The Institute for Cellular and Molecular Biology, University of Texas, Austin, TX, United States

3. Department of Biological Sciences, University of Idaho, Moscow, ID, United States

4. Department of Molecular Biosciences, University of Texas at Austin, Austin, TX, United States

5. Center for Systems, Biology, University of Texas at Austin, Austin, TX, United States

6. Center for Computational Biology and Bioinformatics, University of Texas, Austin, TX, United States

Abstract

The failure of traditional interventions to block and cure HIV infections has led to novel proposals that involve treating infections with therapeutic viruses–infectious viruses that specifically inhibit HIV propagation in the host. Early efforts in evaluating these proposals have been limited chiefly to mathematical models of dynamics, for lack of suitable empirical systems. Here we propose, develop and analyze an empirical system of a therapeutic virus that protects a host cell population against a lethal virus. The empirical system usesE. colibacteria as the host cell population, an RNA phage as the lethal virus and a filamentous phage as the therapeutic virus. Basic dynamic properties are established for each virus alone and then together. Observed dynamics broadly agree with those predicted by a computer simulation model, although some differences are noted. Two cases of dynamics are contrasted, differing in whether the therapeutic virus is introduced before the lethal virus or after the lethal virus. The therapeutic virus increases in both cases but by different mechanisms. With the therapeutic virus introduced first, it spreads infectiously without any appreciable change in host dynamics. With the therapeutic virus introduced second, host abundance is depressed at the time therapy is applied; following an initial period of therapeutic virus spread by infection, the subsequent rise of protection is through reproduction by hosts already protected. This latter outcome is due to inheritance of the therapeutic virus state when the protected cell divides. Overall, the work establishes the feasibility and robustness to details of a viral interference using a therapeutic virus.

Funder

National Science Foundation

NIH GM

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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