Evidence map›Paper›PMID 41728991›Full record

ArticleMicrobiology spectrum2026

Primary bovine embryonic fibroblasts demonstrate variable fitness following infection with highly pathogenic avian influenza H5N1 strains and are susceptible to a recently circulating human 2009 pandemic lineage H1N1 strain.

Grace K Wenger, Deann T Snyder, Justin R Prigge, Allyson H Turner, Sara A Jaffrani, Edward E Schmidt, Emily A Bruce, Emma K Loveday

Abstract read
In one paragraph

Article in Microbiology spectrum, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Grace K WengerMicrobiology and Cell Biology Department, Montana State University, Bozeman, Montana, USA.ORCID 0009-0000-6616-2502
Deann T SnyderMicrobiology and Cell Biology Department, Montana State University, Bozeman, Montana, USA.ORCID 0000-0003-3087-7260
Justin R PriggeMicrobiology and Cell Biology Department, Montana State University, Bozeman, Montana, USA.
Allyson H TurnerDepartment of Microbiology and Molecular Genetics, University of Vermont, Burlington, Vermont, USA.ORCID 0009-0009-9576-6095
Sara A JaffraniDepartment of Microbiology and Molecular Genetics, University of Vermont, Burlington, Vermont, USA.ORCID 0009-0007-3684-0756
Edward E SchmidtMicrobiology and Cell Biology Department, Montana State University, Bozeman, Montana, USA.ORCID 0000-0002-9959-4990
Emily A BruceDepartment of Microbiology and Molecular Genetics, University of Vermont, Burlington, Vermont, USA.ORCID 0000-0001-8391-370X
Emma K LovedayMicrobiology and Cell Biology Department, Montana State University, Bozeman, Montana, USA.ORCID 0000-0002-1154-7728

Funding

Using Dengue Controlled Human Infection Model to Identify Adaptive Immune Correlates of ProtectionP20GM125498 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Kristen Pierce · 2018 to 2026
$24.9M
Single cell heterogeneity of influenza A virus genetic diversity and host adaptation using drop-based microfluidicsR21AI178432 · NIAID · MONTANA STATE UNIVERSITY - BOZEMAN · PI LOVEDAY, EMMA KATE · 2023 to 2024
$421k
Montana Agricultural Experiment Station MONB00443National Institutes of Health, National Institute of Allergy and Infectious Diseases N7593021C00045National Institutes of Health, National Institute of Allergy and Infectious Diseases R21AI178432-01National Institutes of Health, National Institute of General Medical Sciences P20GM125498NIAID NIH HHS R21 AI178432NIGMS NIH HHS P20 GM125498U.S. Department of Agriculture 35208-11567
6 · The paper itself

Abstract

The recent emergence of highly pathogenic avian influenza (HPAI) H5N1 (clade 2.3.4.4b, genotype B3.13) in dairy cattle presents substantial challenges to the agricultural sector and public health. Mechanistic studies of infection and transmission in cattle have proven difficult due to animal handling restrictions and the limited availability of established cell culture models. Primary bovine embryonic fibroblasts (BeEFs) were isolated and investigated here as a model to study influenza A virus (IAV) infection dynamics. We compared sialylation profiles, infectious virus production, viral replication, and plaque morphology in BeEFs following infection with the bovine HPAI H5N1 and an earlier 2.3.4.4b genotype (B1.1) isolated in 2022. The data presented here demonstrate increased expression of α-2,3 sialic acids compared to α-2,6 sialic acids in BeEFs, similar to sialylation profiles previously reported in bovine mammary tissue. These data also display increased viral fitness of the bovine origin HPAI H5N1 strains across bovine and avian cell lines, consistent with previous characterization in bovine mammary tissue. Furthermore, BeEFs were fully susceptible to a 2022 H1N1pdm09-like IAV strain while maintaining resistance to the 2009 H1N1pdm09 IAV as previously characterized in mammary cells. This study highlights the ongoing zoonotic adaptation of HPAI H5N1 in mammals and the potential for coinfection with select human H1N1 2009 pandemic lineage strains, enabling the potential development of reassortant strains. These data support the ability of BeEFs to serve as a complementary IMPORTANCE: Zoonotic spillover to humans with avian influenza A subtypes, such as H5N1, can have extraordinarily high mortality rates. Recently, highly pathogenic avian influenza (HPAI) H5N1 has spread to dairy cattle and caused widespread disease in over a thousand herds across the United States. This widespread infection not only poses notable economic challenges to agricultural industries but also represents a notable concern to human public health. While studies of infection dynamics of HPAI H5N1 in cattle remain crucial, animal handling restrictions and a lack of well-characterized cell culture models make this work challenging. The significance of our research lies in identifying an

Indexed as

FibroblastsInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H5N1 SubtypeInfluenza, HumanOrthomyxoviridae InfectionsAnimalsCattleCells, CulturedHumansInfluenza in BirdsSialic AcidsVirus ReplicationSialic Acidsavian virusescattleinfluenzaviral pathogenesisvirulence

Identifiers

PMID41728991
PMCPMC13055317

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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.