Superinfection promotes replication and diversification of defective HIV-1 proviruses in people with non-suppressible viraemia

During replication of some RNA viruses, defective particles can spontaneously arise and interfere with wild-type (WT) virus replication. However, these defective interfering particles (DIPs) have not been reported in people with HIV-1 (PWH). Here we find DIPs in PWH who have a rare, polyclonal form of non-suppressible viraemia (NSV). We characterized the source of NSV in two PWH who never reached undetectable viral load despite adherence to antiretroviral therapy (ART). Remarkably, in each participant, we found a diverse set of defective viral genomes sharing the same fatal deletions. This paradoxical accumulation of mutations by viruses with fatal defects was driven by superinfection with intact viruses, resulting in mobilization of defective genomes and accumulation of additional mutations during untreated infection. These defective proviruses interfere with WT virus replication, conditionally replicate and, in one case, have an R<sub>0</sub> > 1, enabling in vivo spread. Despite this, clinical outcomes showed no beneficial effect of these DIPs. These findings demonstrate that fatally defective proviruses, traditionally considered evolutionary dead ends, can replicate and diversify upon superinfection without preventing disease progression.

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Publication Details

Journal
Nature Microbiology
Published
2025-10-03
DOI
https://doi.org/10.1038/s41564-025-02135-z
Citations
1
Primary Topic
HIV Research and Treatment
Type
article
Field-Weighted Citation Impact
1.04

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article

Superinfection promotes replication and diversification of defective HIV-1 proviruses in people with non-suppressible viraemia

Eileen P. Scully, Janet D. Siliciano, Vivek Hariharan, Subul Beg et al.
1 citations
Nature Microbiology
HIV Research and Treatment
1.04
article

Superinfection promotes replication and diversification of defective HIV-1 proviruses in people with non-suppressible viraemia

Eileen P. Scully, Janet D. Siliciano, Vivek Hariharan, Subul Beg, Milica Moskovljevic, Francesco R. Simonetti, Emily J. Fray, Nicholas M. Pathoulas, Jun Lai, David S. Block, Anushka Singhal, Filippo Dragoni, Jeanne Keruly, Elizabeth A. Gilliams, Richard D. Moore, Robert F. Siliciano, Jennifer A. White, Hao Zhang
article en
1 citations

Abstract

During replication of some RNA viruses, defective particles can spontaneously arise and interfere with wild-type (WT) virus replication. However, these defective interfering particles (DIPs) have not been reported in people with HIV-1 (PWH). Here we find DIPs in PWH who have a rare, polyclonal form of non-suppressible viraemia (NSV). We characterized the source of NSV in two PWH who never reached undetectable viral load despite adherence to antiretroviral therapy (ART). Remarkably, in each participant, we found a diverse set of defective viral genomes sharing the same fatal deletions. This paradoxical accumulation of mutations by viruses with fatal defects was driven by superinfection with intact viruses, resulting in mobilization of defective genomes and accumulation of additional mutations during untreated infection. These defective proviruses interfere with WT virus replication, conditionally replicate and, in one case, have an R<sub>0</sub> > 1, enabling in vivo spread. Despite this, clinical outcomes showed no beneficial effect of these DIPs. These findings demonstrate that fatally defective proviruses, traditionally considered evolutionary dead ends, can replicate and diversify upon superinfection without preventing disease progression.

Nature MicrobiologyVol. 10(11)
Howard Hughes Medical Institute (US), Johns Hopkins University (US), Johns Hopkins Medicine (US)
Johns Hopkins University, National Institutes of Health, NIH Office of the Director, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 19%
HIV Research and Treatment
1.04
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