Evidence map›Paper›PMID 41720824›Full record

ArticleScientific reports2026

Spatial localization of avian and human influenza A virus receptors in male and female bovine reproductive tissues.

Brette D Poliakiwski, Thainá Minela, Damon J Smith, Zachary K Seekford, Joe W Cain, Odile Polanco, Gregory A Johnson, Lacey J Luense, Pablo J Ross, Kiril M Dimitrov and 2 more

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Brette D PoliakiwskiDepartment of Animal Science, College of Agriculture and Life Sciences, Texas A&M University, College Station, TX, USA.
Thainá MinelaDepartment of Animal Science, College of Agriculture and Life Sciences, Texas A&M University, College Station, TX, USA.
Damon J SmithDepartment of Animal Science, College of Agriculture and Life Sciences, Texas A&M University, College Station, TX, USA.
Zachary K SeekfordDepartment of Animal Science, College of Agriculture and Life Sciences, Texas A&M University, College Station, TX, USA.
Joe W CainDepartment of Veterinary Integrative Biosciences, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
Odile PolancoDepartment of Animal Science, College of Agriculture and Life Sciences, Texas A&M University, College Station, TX, USA.
Gregory A JohnsonDepartment of Veterinary Integrative Biosciences, School of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA.
Lacey J LuenseDepartment of Animal Science, College of Agriculture and Life Sciences, Texas A&M University, College Station, TX, USA.
Pablo J RossST Genetics, Navasota, TX, USA.
Kiril M DimitrovTexas A&M Veterinary Medical Diagnostic Laboratory, College Station, TX, 77843, USA.
G Cliff LambDepartment of Animal Science, College of Agriculture and Life Sciences, Texas A&M University, College Station, TX, USA.
Ky G PohlerDepartment of Animal Science, College of Agriculture and Life Sciences, Texas A&M University, College Station, TX, USA. Ky.Pohler@ag.tamu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Highly pathogenic avian influenza virus (HPAIV) of the H5N1 type has recently emerged as a major concern in livestock, with widespread outbreaks now confirmed in U.S. dairy cattle. This raises critical questions about the susceptibility of bovine reproductive tissues to viral entry, replication, and potential transmission. Influenza A viruses (IAV) initiate infection through hemagglutinin (HA) binding to host cell surface sialic acid residues, avian-adapted strains preferentially bind α2,3-linked sialic acids, while human-adapted strains bind α2,6-linked residues. This study aimed to characterize the spatial distribution of α2,6-linked sialic acids (human-like receptors), α2,3-Galβ1-4, and α2,3-Galβ1-3 (avian-like receptors) in male and female bovine reproductive tissues using lectin-based histochemistry. Post-mortem reproductive tissues were collected from bulls (n = 4) and multiparous cows (n = 3) and stained with biotinylated lectins. Human-like receptors were detected in the luminal epithelium of the penile urethra, vas deferens, epididymis, seminiferous tubules, vagina, cervix, uterus, oviduct, and mammary gland. Avian-like receptors were also detected in the penile urethra, epididymis, vagina, cervix, oviduct, and mammary gland, though α2,3-Galβ1-4 and α2,3-Galβ1-3 localization varied by tissue. These findings represent the first comprehensive spatial mapping of IAV receptors in bovine reproductive tissues and highlight potential sites for viral entry or shedding.

Indexed as

Genitalia, FemaleGenitalia, MaleInfluenza A virusInfluenza A Virus, H5N1 SubtypeReceptors, VirusAnimalsCattleFemaleHumansMaleReceptors, VirusAvian InfluenzaBovineMAA-IMAA-IISialic acid receptorsSNA

Identifiers

PMID41720824
PMCPMC13022054

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LicenceCC BY-NC-ND
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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.