Evidence map›Paper›PMID 39835898›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Dispersal of influenza virus populations within the respiratory tract shapes their evolutionary potential.

Lucas M Ferreri, Brittany Seibert, C Joaquin Caceres, Kayle Patatanian, Katie E Holmes, L Claire Gay, Flavio Cargnin Faccin, Matias Cardenas, Silvia Carnaccini, Nishit Shetty and 5 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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  11. Dispersal of influenza virus populations within the respiratory tract shapes their evolutionary potential.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Lucas M FerreriDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.ORCID 0000-0002-1069-9500
Brittany Seibert *Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602.
C Joaquin Caceres *Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602.ORCID 0000-0001-8508-6592
Kayle Patatanian *Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.
Katie E HolmesDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.
L Claire GayDepartment of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602.
Flavio Cargnin FaccinDepartment of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602.ORCID 0000-0002-5006-5182
Matias CardenasDepartment of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602.ORCID 0000-0001-8247-3669
Silvia CarnacciniDepartment of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602.
Nishit ShettyDepartment of Civil and Environmental Engineering, Virginia Tech, Blacksburg, VA 24061.
Daniela RajaoDepartment of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602.ORCID 0000-0002-0772-0065
Katia KoelleDepartment of Biology, College of Arts and Sciences, Emory University, Atlanta, GA 30322.ORCID 0000-0002-0254-6141
Linsey C MarrDepartment of Civil and Environmental Engineering, Virginia Tech, Blacksburg, VA 24061.ORCID 0000-0003-3628-6891
Daniel R PerezDepartment of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602.ORCID 0000-0002-6569-5689
Anice C LowenDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.ORCID 0000-0002-9829-112X

Funding

NIAID Centers of Excellence for Influenza Research and Response: Universal Influenza Vaccine Research Activities75N93021C00014 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GARCIA-SASTRE, ADOLFO · 2021 to 2025
$62.6M
NIAID Centers of Excellence for Influenza Research and Response: Universal Influenza Vaccine Research Activities75N93021C00017 · NIAID · EMORY UNIVERSITY · PI LOWEN, ANICE · 2021 to 2025
$27.3M
Role of spatial structure in shaping viral population diversity and evolutionR01AI154894 · NIAID · EMORY UNIVERSITY · PI KOELLE, KATHARINA V, LOWEN, ANICE C · 2020 to 2024
$2.8M
NIAID NIH HHS 75N93021C00014NIAID NIH HHS 75N93021C00017NIAID NIH HHS R01 AI154894
6 · The paper itself

Abstract

Viral infections are characterized by dispersal from an initial site to secondary locations within the host. How the resultant spatial heterogeneity shapes within-host genetic diversity and viral evolutionary pathways is poorly understood. Here, we show that virus dispersal within and between the nasal cavity and trachea maintains diversity and is therefore conducive to adaptive evolution, whereas dispersal to the lungs gives rise to population heterogeneity. We infected ferrets either intranasally or by aerosol with a barcoded influenza A/California/07/2009 (H1N1) virus. At 1, 2, or 4 days postinfection, dispersal was assessed by collecting 52 samples from throughout the respiratory tract of each animal. Irrespective of inoculation route, barcode compositions across the nasal turbinates and trachea were similar and highly diverse, revealing little constraint on the establishment of infection in the nasal cavity and descent through the trachea. Conversely, infection of the lungs produced genetically distinct viral populations. Lung populations were pauci-clonal, suggesting that each seeded location received relatively few viral genotypes. While aerosol inoculation gave distinct populations at every lung site sampled, within-host dispersal after intranasal inoculation produced larger patches, indicative of local expansion following seeding of the lungs. Throughout the respiratory tract, barcode diversity declined over time, but new diversity was generated through mutation. De novo variants were often unique to a given location, indicating that localized replication following dispersal resulted in population divergence. In summary, dispersal within the respiratory tract operates differently between regions and contributes to the potential for viral evolution to proceed independently in multiple within-host subpopulations.

Indexed as

Influenza A Virus, H1N1 SubtypeOrthomyxoviridae InfectionsRespiratory SystemAnimalsBiological EvolutionEvolution, MolecularFerretsGenetic VariationLungNasal CavityTracheadispersalevolutioninfluenza virus

Identifiers

PMID39835898
PMCPMC11789087

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.