| Literature DB >> 29555018 |
Laurelle Jackson1,2, Jessica Hunter1,2, Sandile Cele1, Isabella Markham Ferreira1,2, Andrew C Young1,3, Farina Karim1, Rajhmun Madansein4,5, Kaylesh J Dullabh4, Chih-Yuan Chen4, Noel J Buckels4, Yashica Ganga1, Khadija Khan1, Mikael Boulle1, Gila Lustig1, Richard A Neher6,7, Alex Sigal1,2,8.
Abstract
HIV has been reported to be cytotoxic in vitro and in lymph node infection models. Using a computational approach, we found that partial inhibition of transmissions of multiple virions per cell could lead to increased numbers of live infected cells. If the number of viral DNA copies remains above one after inhibition, then eliminating the surplus viral copies reduces cell death. Using a cell line, we observed increased numbers of live infected cells when infection was partially inhibited with the antiretroviral efavirenz or neutralizing antibody. We then used efavirenz at concentrations reported in lymph nodes to inhibit lymph node infection by partially resistant HIV mutants. We observed more live infected lymph node cells, but with fewer HIV DNA copies per cell, relative to no drug. Hence, counterintuitively, limited attenuation of HIV transmission per cell may increase live infected cell numbers in environments where the force of infection is high.Entities:
Keywords: HIV induced cell death; Lymph node; cell-to-cell spread; computational biology; human; infectious disease; microbiology; multiple Infections per cell; systems biology; viral fitness; virus
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Year: 2018 PMID: 29555018 PMCID: PMC5896883 DOI: 10.7554/eLife.30134
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140