Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017 Oct 11;22(4):437-441.
doi: 10.1016/j.chom.2017.09.012.

Sociovirology: Conflict, Cooperation, and Communication among Viruses

Affiliations

Sociovirology: Conflict, Cooperation, and Communication among Viruses

Samuel L Díaz-Muñoz et al. Cell Host Microbe. .

Abstract

Viruses are involved in various interactions both within and between infected cells. Social evolution theory offers a conceptual framework for how virus-virus interactions, ranging from conflict to cooperation, have evolved. A critical examination of these interactions could expand our understanding of viruses and be exploited for epidemiological and medical interventions.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Virus-Virus Interactions Are Diverse and Provide Multiple Opportunities for Social Evolution (A–F) Indicated by gray shadows and depicting social interactions, where the action of a viral genome changes the fitness of other viral genomes. Cells are ovals with black borders. (A) A viral genome (thick curved segment) enters the cell and performs transcription (mRNAs, thin curved segments +) and translation, leading to generation of shared intracellular viral proteins (open hexagons). Transcription-translation is a social and potentially cooperative trait because it benefits the other viral genomes in the cell. (B–F) Viral genomes can prevent or promote reproduction of other genomes by changing the probability that they can infect a cell or host by: (B) blocking the entry of other viral genomes into the cell; (C) producing host-level immune changes (dark red outline) that favor the transmission of all infecting viral genomes; (D) inducing the cell to produce molecules essential for transmission to neighboring cells, benefiting all viral genomes in the cell; (E) producing viral proteins that communicate cell infection status, signaling to other viral genomes the abundance of cells available for reproduction; and (F) manipulating host immune signals to induce distant cells to differentially expose receptors favoring entry of some viral genomes over others.
Figure 2
Figure 2
The Problem of Cooperation and Testing Virus-Virus Interactions Using Social Evolution Theory (A) Imagine a population of viruses that perform a costly cooperative action such as transcription (indicated by C). A selfish cheater that does not perform the cooperative action (indicated by S) arises in this population through mutation or coinfection. This selfish cheater is able to benefit from the cooperative behavior of the cooperators without paying the cost. Consequently, the selfish cheater will increase in frequency, even though this leads to a reduction in mean fitness. (B) Testing for evolved social interactions, such as cheating and cooperation. Left: Strains are competed in isolation and in combination to quantify fitness and confirm social traits. Middle: When grown as single infections, a population of cooperators (blue) achieves higher growth than a cheater population (red). Right: In coinfection (purple), the population has lower growth than a population composed solely of cooperators. The social composition of the population reveals why: cheaters (dotted red) initially increase population growth by exploiting cooperators (dotted blue), but growth stalls as the population becomes dominated by cheaters.

References

    1. Andino R., Domingo E. Virology. 2015;479-480:46–51. - PMC - PubMed
    1. Boots M., Mealor M. Science. 2007;315:1284–1286. - PubMed
    1. Bordería A.V., Isakov O., Moratorio G., Henningsson R., Agüera-González S., Organtini L., Gnädig N.F., Blanc H., Alcover A., Hafenstein S. PLoS Pathog. 2015;11 e1004838–e20. - PMC - PubMed
    1. Chao L., Elena S.F. Proc. Biol. Sci. 2017;284:20170228–20170229. - PMC - PubMed
    1. DaPalma T., Doonan B.P., Trager N.M., Kasman L.M. Virus Res. 2010;149:1–9. - PMC - PubMed