Cargando…
Viral invasion fitness across a continuum from lysis to latency
The prevailing paradigm in ecological studies of viruses and their microbial hosts is that the reproductive success of viruses depends on the proliferation of the ‘predator’, that is, the virus particle. Yet, viruses are obligate intracellular parasites, and the virus genome—the actual unit of selec...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476163/ https://www.ncbi.nlm.nih.gov/pubmed/31024737 http://dx.doi.org/10.1093/ve/vez006 |
_version_ | 1783412860428222464 |
---|---|
author | Weitz, Joshua S Li, Guanlin Gulbudak, Hayriye Cortez, Michael H Whitaker, Rachel J |
author_facet | Weitz, Joshua S Li, Guanlin Gulbudak, Hayriye Cortez, Michael H Whitaker, Rachel J |
author_sort | Weitz, Joshua S |
collection | PubMed |
description | The prevailing paradigm in ecological studies of viruses and their microbial hosts is that the reproductive success of viruses depends on the proliferation of the ‘predator’, that is, the virus particle. Yet, viruses are obligate intracellular parasites, and the virus genome—the actual unit of selection—can persist and proliferate from one cell generation to the next without lysis or the production of new virus particles. Here, we propose a theoretical framework to quantify the invasion fitness of viruses using an epidemiological cell-centric metric that focuses on the proliferation of viral genomes inside cells instead of virus particles outside cells. This cell-centric metric enables direct comparison of viral strategies characterized by obligate killing of hosts (e.g. via lysis), persistence of viral genomes inside hosts (e.g. via lysogeny), and strategies along a continuum between these extremes (e.g. via chronic infections). As a result, we can identify environmental drivers, life history traits, and key feedbacks that govern variation in viral propagation in nonlinear population models. For example, we identify threshold conditions given relatively low densities of susceptible cells and relatively high growth rates of infected cells in which lysogenic and other chronic strategies have higher potential viral reproduction than lytic strategies. Altogether, the theoretical framework helps unify the ongoing study of eco-evolutionary drivers of viral strategies in natural environments. |
format | Online Article Text |
id | pubmed-6476163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64761632019-04-25 Viral invasion fitness across a continuum from lysis to latency Weitz, Joshua S Li, Guanlin Gulbudak, Hayriye Cortez, Michael H Whitaker, Rachel J Virus Evol Research Article The prevailing paradigm in ecological studies of viruses and their microbial hosts is that the reproductive success of viruses depends on the proliferation of the ‘predator’, that is, the virus particle. Yet, viruses are obligate intracellular parasites, and the virus genome—the actual unit of selection—can persist and proliferate from one cell generation to the next without lysis or the production of new virus particles. Here, we propose a theoretical framework to quantify the invasion fitness of viruses using an epidemiological cell-centric metric that focuses on the proliferation of viral genomes inside cells instead of virus particles outside cells. This cell-centric metric enables direct comparison of viral strategies characterized by obligate killing of hosts (e.g. via lysis), persistence of viral genomes inside hosts (e.g. via lysogeny), and strategies along a continuum between these extremes (e.g. via chronic infections). As a result, we can identify environmental drivers, life history traits, and key feedbacks that govern variation in viral propagation in nonlinear population models. For example, we identify threshold conditions given relatively low densities of susceptible cells and relatively high growth rates of infected cells in which lysogenic and other chronic strategies have higher potential viral reproduction than lytic strategies. Altogether, the theoretical framework helps unify the ongoing study of eco-evolutionary drivers of viral strategies in natural environments. Oxford University Press 2019-04-22 /pmc/articles/PMC6476163/ /pubmed/31024737 http://dx.doi.org/10.1093/ve/vez006 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Weitz, Joshua S Li, Guanlin Gulbudak, Hayriye Cortez, Michael H Whitaker, Rachel J Viral invasion fitness across a continuum from lysis to latency |
title | Viral invasion fitness across a continuum from lysis to latency |
title_full | Viral invasion fitness across a continuum from lysis to latency |
title_fullStr | Viral invasion fitness across a continuum from lysis to latency |
title_full_unstemmed | Viral invasion fitness across a continuum from lysis to latency |
title_short | Viral invasion fitness across a continuum from lysis to latency |
title_sort | viral invasion fitness across a continuum from lysis to latency |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476163/ https://www.ncbi.nlm.nih.gov/pubmed/31024737 http://dx.doi.org/10.1093/ve/vez006 |
work_keys_str_mv | AT weitzjoshuas viralinvasionfitnessacrossacontinuumfromlysistolatency AT liguanlin viralinvasionfitnessacrossacontinuumfromlysistolatency AT gulbudakhayriye viralinvasionfitnessacrossacontinuumfromlysistolatency AT cortezmichaelh viralinvasionfitnessacrossacontinuumfromlysistolatency AT whitakerrachelj viralinvasionfitnessacrossacontinuumfromlysistolatency |