Drivers of within-host genetic diversity in acute infections of viruses.

Genetic diversity is the fuel of evolution and facilitates adaptation to novel environments. However, our understanding of what drives differences in the genetic diversity during the early stages of viral infection is somewhat limited. Here, we use ultra-deep sequencing to interrogate 43 clinical sa...

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Main Authors: Maoz Gelbart, Sheri Harari, Ya'ara Ben-Ari, Talia Kustin, Dana Wolf, Michal Mandelboim, Orna Mor, Pleuni S Pennings, Adi Stern
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-11-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1009029
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spelling doaj-4ca7fb080cd24f098020e0bb9e2c1de72021-04-21T17:57:08ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742020-11-011611e100902910.1371/journal.ppat.1009029Drivers of within-host genetic diversity in acute infections of viruses.Maoz GelbartSheri HarariYa'ara Ben-AriTalia KustinDana WolfMichal MandelboimOrna MorPleuni S PenningsAdi SternGenetic diversity is the fuel of evolution and facilitates adaptation to novel environments. However, our understanding of what drives differences in the genetic diversity during the early stages of viral infection is somewhat limited. Here, we use ultra-deep sequencing to interrogate 43 clinical samples taken from early infections of the human-infecting viruses HIV, RSV and CMV. Hundreds to thousands of virus templates were sequenced per sample, allowing us to reveal dramatic differences in within-host genetic diversity among virus populations. We found that increased diversity was mostly driven by presence of multiple divergent genotypes in HIV and CMV samples, which we suggest reflect multiple transmitted/founder viruses. Conversely, we detected an abundance of low frequency hyper-edited genomes in RSV samples, presumably reflecting defective virus genomes (DVGs). We suggest that RSV is characterized by higher levels of cellular co-infection, which allow for complementation and hence elevated levels of DVGs.https://doi.org/10.1371/journal.ppat.1009029
collection DOAJ
language English
format Article
sources DOAJ
author Maoz Gelbart
Sheri Harari
Ya'ara Ben-Ari
Talia Kustin
Dana Wolf
Michal Mandelboim
Orna Mor
Pleuni S Pennings
Adi Stern
spellingShingle Maoz Gelbart
Sheri Harari
Ya'ara Ben-Ari
Talia Kustin
Dana Wolf
Michal Mandelboim
Orna Mor
Pleuni S Pennings
Adi Stern
Drivers of within-host genetic diversity in acute infections of viruses.
PLoS Pathogens
author_facet Maoz Gelbart
Sheri Harari
Ya'ara Ben-Ari
Talia Kustin
Dana Wolf
Michal Mandelboim
Orna Mor
Pleuni S Pennings
Adi Stern
author_sort Maoz Gelbart
title Drivers of within-host genetic diversity in acute infections of viruses.
title_short Drivers of within-host genetic diversity in acute infections of viruses.
title_full Drivers of within-host genetic diversity in acute infections of viruses.
title_fullStr Drivers of within-host genetic diversity in acute infections of viruses.
title_full_unstemmed Drivers of within-host genetic diversity in acute infections of viruses.
title_sort drivers of within-host genetic diversity in acute infections of viruses.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2020-11-01
description Genetic diversity is the fuel of evolution and facilitates adaptation to novel environments. However, our understanding of what drives differences in the genetic diversity during the early stages of viral infection is somewhat limited. Here, we use ultra-deep sequencing to interrogate 43 clinical samples taken from early infections of the human-infecting viruses HIV, RSV and CMV. Hundreds to thousands of virus templates were sequenced per sample, allowing us to reveal dramatic differences in within-host genetic diversity among virus populations. We found that increased diversity was mostly driven by presence of multiple divergent genotypes in HIV and CMV samples, which we suggest reflect multiple transmitted/founder viruses. Conversely, we detected an abundance of low frequency hyper-edited genomes in RSV samples, presumably reflecting defective virus genomes (DVGs). We suggest that RSV is characterized by higher levels of cellular co-infection, which allow for complementation and hence elevated levels of DVGs.
url https://doi.org/10.1371/journal.ppat.1009029
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