| Literature DB >> 31761718 |
Jason M Hataye1, Joseph P Casazza2, Katharine Best3, C Jason Liang4, Taina T Immonen5, David R Ambrozak2, Samuel Darko6, Amy R Henry6, Farida Laboune6, Frank Maldarelli7, Daniel C Douek6, Nicolas W Hengartner3, Takuya Yamamoto8, Brandon F Keele5, Alan S Perelson3, Richard A Koup9.
Abstract
A population at low census might go extinct or instead transition into exponential growth to become firmly established. Whether this pivotal event occurs for a within-host pathogen can be the difference between health and illness. Here, we define the principles governing whether HIV-1 spread among cells fails or becomes established by coupling stochastic modeling with laboratory experiments. Following ex vivo activation of latently infected CD4 T cells without de novo infection, stochastic cell division and death contributes to high variability in the magnitude of initial virus release. Transition to exponential HIV-1 spread often fails due to release of an insufficient amount of replication-competent virus. Establishment of exponential growth occurs when virus produced from multiple infected cells exceeds a critical population size. We quantitatively define the crucial transition to exponential viral spread. Thwarting this process would prevent HIV transmission or rebound from the latent reservoir. Published by Elsevier Inc.Entities:
Keywords: Allee effect; HIV; critical threshold; exponential growth; latency; latent reservoir; mathematical modeling; population dynamics; rebound; viral dynamics
Mesh:
Year: 2019 PMID: 31761718 PMCID: PMC6948011 DOI: 10.1016/j.chom.2019.10.006
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023