ArticleTransboundary and emerging diseases2026
Genetic Characterization and Pathogenicity of a Triple-Reassortant H1N1 Swine Influenza Virus Isolated in Guangdong.
Article in Transboundary and emerging diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Genetic Characterization and Pathogenicity of a Triple-Reassortant H1N1 Swine Influenza Virus Isolated in Guangdong.Transboundary and emerging diseases · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
An H1N1 subtype swine influenza virus (SIV) was isolated from nasal swabs collected from pigs with suspected swine influenza (SI) on a farm in Guangdong, China. The virus, designated A/Swine/Guangdong/JJK/2025(H1N1) (abbreviated as JJK), underwent whole-genome sequencing and phylogenetic analysis, which confirmed that it is a triple-reassortant strain. The hemagglutination (HA) and neuraminidase (NA) genes originated from the Eurasian avian-like (EA) H1N1 lineage, the internal genes (PB2, PB1, PA, NP, and M) originated from the 2009 pandemic H1N1 lineage, and the NS gene originated from the triple-reassortant H1N2 lineage. Each of the eight gene segments showed the highest homology to a different reference virus. Analysis of key amino acid substitutions identified multiple mutations in proteins, such as HA, PB2, and PB1, that are associated with enhanced mammalian adaptation, increased virulence, and modulation of host immune responses. Animal pathogenicity testing demonstrated that JJK was significantly pathogenic in female BALB/c mice, with an MLD
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.