# Pathogenesis and Transmission of a Reassorted H1 Influenza A Virus Detected in North American Swine

**Authors:** Débora B. Goulart, Carine K. Souza, Giovana C. Zanella, Celeste A. Snyder, Janice C. Zanella, Alexey Markin, Bailey Arruda, Tavis K. Anderson, Amy L. Baker

PMC · DOI: 10.1111/irv.70228 · Influenza and Other Respiratory Viruses · 2026-02-19

## TL;DR

A study found that a reassorted H1 influenza A virus in swine in North America did not spread more efficiently, suggesting other factors may explain its increased detection.

## Contribution

The study provides new insights into why a specific H1 influenza A virus clade became more prevalent in swine, despite no change in transmission efficiency.

## Key findings

- Different NA gene pairings with the 1A.1.1.3 HA clade did not affect viral shedding or transmission in swine.
- All tested IAV strains, regardless of genetic background, transmitted to naïve pigs.
- The increased detection of the H1 1A.1.1.3 clade is likely due to factors like immunity changes or ecological conditions.

## Abstract

The USDA influenza A virus in swine national surveillance plan identified an increase in the detection frequency of a group of swine 1A.1.1.3 hemagglutinin (HA) clade viruses. This change was associated with reassortment events that resulted in new neuraminidase (NA) gene pairings. We hypothesized that the new N1 genes improved the transmission efficiency of the virus.

We assessed the pathogenesis and transmission of four H1 1A.1.1.3 swine strains paired with different NA subtypes and lineages, all of which shared similar internal gene constellations.

There was little variation in the titers of viral nasal shedding across the groups, and the different surface protein pairings had no effect on transmission efficiency. All IAV strains, reflecting both pre‐ and post‐reassortment genetic patterns, were transmitted to naïve indirect contact pigs.

These data indicate that the combinations of 1A.1.1.3 HA with NA subtypes had little impact on transmission. These findings suggest that the increased detection of the H1 1A.1.1.3 clade in the United States was unlikely directly due to altered replication, transmission, or antigenic drift, but perhaps due to changes in population immunity resulting from differential vaccine use or prior exposure, variations in production practices, or ecological conditions.

## Linked entities

- **Genes:** ha (hair bristles) [NCBI Gene 251217], XK (X-linked Kx blood group antigen, Kell and VPS13A binding protein) [NCBI Gene 7504]

## Full-text entities

- **Genes:** PBRM1 (polybromo 1) [NCBI Gene 100525781] {aka PB1}, AHSG (alpha 2-HS glycoprotein) [NCBI Gene 397585] {aka FETUA, FETUIN}
- **Diseases:** Infection (MESH:D007239), death (MESH:D003643), Allergy and Infectious Diseases (MESH:D003141), tracheal lesion (MESH:D014133), bacterial infections (MESH:D001424), lung (MESH:D008171), influenza (MESH:D007251), Disease (MESH:D004194), inflammation (MESH:D007249), bacterial pneumonia (MESH:D018410), pneumonia (MESH:D011014)
- **Chemicals:** o-phenylenediamine dihydrochloride (MESH:C034193), hematoxylin (MESH:D006416), Casmin (-), H&amp;E (MESH:D006371), formalin (MESH:D005557), H2SO4 (MESH:C033158), eosin (MESH:D004801), NAD (MESH:D009243), sialic acids (MESH:D012794), Telazol (MESH:C006131), sialic acid (MESH:D019158), TPCK (MESH:D014108), pentobarbital (MESH:D010424), ceftiofur (MESH:C053503), xylazine (MESH:D014991), Kaolin (MESH:D007616), Baytril (MESH:D000077422)
- **Species:** Mustela putorius furo (black ferret, subspecies) [taxon 9669], Homo sapiens (human, species) [taxon 9606], Hepatovirus A (no rank) [taxon 12092], Orthomyxoviridae (family) [taxon 11308], Influenza A virus (no rank) [taxon 11320], Porcine circovirus 2 (no rank) [taxon 85708], H1N2 subtype (serotype) [taxon 114728], H3N2 subtype (serotype) [taxon 119210], Qubevirus faecium (species) [taxon 39804], Porcine reproductive and respiratory syndrome virus (no rank) [taxon 28344], H1N1 subtype (serotype) [taxon 114727], Meleagris gallopavo (common turkey, species) [taxon 9103], Sus scrofa (pig, species) [taxon 9823], Mesomycoplasma hyopneumoniae (species) [taxon 2099]
- **Mutations:** R292K
- **Cell lines:** MDCK — Canis lupus familiaris (Dog), Spontaneously immortalized cell line (CVCL_0422)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12920019/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12920019/full.md

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Source: https://tomesphere.com/paper/PMC12920019