Cargando…

Influenza A virus undergoes compartmentalized replication in vivo dominated by stochastic bottlenecks

Transmission of influenza A viruses (IAV) between hosts is subject to numerous physical and biological barriers that impose genetic bottlenecks, constraining viral diversity and adaptation. The bottlenecks within hosts and their potential impacts on evolutionary pathways taken during infection are p...

Descripción completa

Detalles Bibliográficos
Autores principales: Amato, Katherine A., Haddock, Luis A., Braun, Katarina M., Meliopoulos, Victoria, Livingston, Brandi, Honce, Rebekah, Schaack, Grace A., Boehm, Emma, Higgins, Christina A., Barry, Gabrielle L., Koelle, Katia, Schultz-Cherry, Stacey, Friedrich, Thomas C., Mehle, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197827/
https://www.ncbi.nlm.nih.gov/pubmed/35701424
http://dx.doi.org/10.1038/s41467-022-31147-0
_version_ 1784727501152452608
author Amato, Katherine A.
Haddock, Luis A.
Braun, Katarina M.
Meliopoulos, Victoria
Livingston, Brandi
Honce, Rebekah
Schaack, Grace A.
Boehm, Emma
Higgins, Christina A.
Barry, Gabrielle L.
Koelle, Katia
Schultz-Cherry, Stacey
Friedrich, Thomas C.
Mehle, Andrew
author_facet Amato, Katherine A.
Haddock, Luis A.
Braun, Katarina M.
Meliopoulos, Victoria
Livingston, Brandi
Honce, Rebekah
Schaack, Grace A.
Boehm, Emma
Higgins, Christina A.
Barry, Gabrielle L.
Koelle, Katia
Schultz-Cherry, Stacey
Friedrich, Thomas C.
Mehle, Andrew
author_sort Amato, Katherine A.
collection PubMed
description Transmission of influenza A viruses (IAV) between hosts is subject to numerous physical and biological barriers that impose genetic bottlenecks, constraining viral diversity and adaptation. The bottlenecks within hosts and their potential impacts on evolutionary pathways taken during infection are poorly understood. To address this, we created highly diverse IAV libraries bearing molecular barcodes on two gene segments, enabling high-resolution tracking and quantification of unique virus lineages within hosts. Here we show that IAV infection in lungs is characterized by multiple within-host bottlenecks that result in “islands” of infection in lung lobes, each with genetically distinct populations. We perform site-specific inoculation of barcoded IAV in the upper respiratory tract of ferrets and track viral diversity as infection spreads to the trachea and lungs. We detect extensive compartmentalization of discrete populations within lung lobes. Bottleneck events and localized replication stochastically sample individual viruses from the upper respiratory tract or the trachea that become the dominant genotype in a particular lobe. These populations are shaped strongly by founder effects, with limited evidence for positive selection. The segregated sites of replication highlight the jackpot-style events that contribute to within-host influenza virus evolution and may account for low rates of intrahost adaptation.
format Online
Article
Text
id pubmed-9197827
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-91978272022-06-16 Influenza A virus undergoes compartmentalized replication in vivo dominated by stochastic bottlenecks Amato, Katherine A. Haddock, Luis A. Braun, Katarina M. Meliopoulos, Victoria Livingston, Brandi Honce, Rebekah Schaack, Grace A. Boehm, Emma Higgins, Christina A. Barry, Gabrielle L. Koelle, Katia Schultz-Cherry, Stacey Friedrich, Thomas C. Mehle, Andrew Nat Commun Article Transmission of influenza A viruses (IAV) between hosts is subject to numerous physical and biological barriers that impose genetic bottlenecks, constraining viral diversity and adaptation. The bottlenecks within hosts and their potential impacts on evolutionary pathways taken during infection are poorly understood. To address this, we created highly diverse IAV libraries bearing molecular barcodes on two gene segments, enabling high-resolution tracking and quantification of unique virus lineages within hosts. Here we show that IAV infection in lungs is characterized by multiple within-host bottlenecks that result in “islands” of infection in lung lobes, each with genetically distinct populations. We perform site-specific inoculation of barcoded IAV in the upper respiratory tract of ferrets and track viral diversity as infection spreads to the trachea and lungs. We detect extensive compartmentalization of discrete populations within lung lobes. Bottleneck events and localized replication stochastically sample individual viruses from the upper respiratory tract or the trachea that become the dominant genotype in a particular lobe. These populations are shaped strongly by founder effects, with limited evidence for positive selection. The segregated sites of replication highlight the jackpot-style events that contribute to within-host influenza virus evolution and may account for low rates of intrahost adaptation. Nature Publishing Group UK 2022-06-14 /pmc/articles/PMC9197827/ /pubmed/35701424 http://dx.doi.org/10.1038/s41467-022-31147-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Amato, Katherine A.
Haddock, Luis A.
Braun, Katarina M.
Meliopoulos, Victoria
Livingston, Brandi
Honce, Rebekah
Schaack, Grace A.
Boehm, Emma
Higgins, Christina A.
Barry, Gabrielle L.
Koelle, Katia
Schultz-Cherry, Stacey
Friedrich, Thomas C.
Mehle, Andrew
Influenza A virus undergoes compartmentalized replication in vivo dominated by stochastic bottlenecks
title Influenza A virus undergoes compartmentalized replication in vivo dominated by stochastic bottlenecks
title_full Influenza A virus undergoes compartmentalized replication in vivo dominated by stochastic bottlenecks
title_fullStr Influenza A virus undergoes compartmentalized replication in vivo dominated by stochastic bottlenecks
title_full_unstemmed Influenza A virus undergoes compartmentalized replication in vivo dominated by stochastic bottlenecks
title_short Influenza A virus undergoes compartmentalized replication in vivo dominated by stochastic bottlenecks
title_sort influenza a virus undergoes compartmentalized replication in vivo dominated by stochastic bottlenecks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197827/
https://www.ncbi.nlm.nih.gov/pubmed/35701424
http://dx.doi.org/10.1038/s41467-022-31147-0
work_keys_str_mv AT amatokatherinea influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT haddockluisa influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT braunkatarinam influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT meliopoulosvictoria influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT livingstonbrandi influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT honcerebekah influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT schaackgracea influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT boehmemma influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT higginschristinaa influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT barrygabriellel influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT koellekatia influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT schultzcherrystacey influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT friedrichthomasc influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks
AT mehleandrew influenzaavirusundergoescompartmentalizedreplicationinvivodominatedbystochasticbottlenecks