ArticlePoultry science2026
MicroRNA expression profiling in fowl adenovirus serotype 4-infected Leghorn male hepatoma cells using small RNA deep sequencing.
Article in Poultry science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
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
Fowl adenovirus serotype 4 (FAdV-4) is the causative agent of hydropericardium-hepatitis syndrome (HHS), a disease that causes severe economic losses to the global poultry industry. MicroRNAs (miRNAs) are key regulators of host-pathogen interactions; yet, their temporal expression dynamics and functional roles during FAdV-4 replication in chicken-derived cells remain poorly defined. This study characterized the temporal expression profile of host miRNAs during FAdV-4 infection in Leghorn male hepatoma (LMH) cells to elucidate their regulatory roles in viral replication through small RNA deep sequencing and functional validation. We identified 63 and 126 differentially expressed (DE) miRNAs at 12 hpi and 24 hpi, respectively. These DE miRNAs exhibited time-dependent regulatory functions throughout FAdV-4 infection, and KEGG enrichment confirmed persistent enrichment of their potential target genes within the MAPK signaling and metabolic pathways at both 12 hpi and 24 hpi. Moreover, we also revealed that gga-miR-184-5p could inhibit FAdV-4 replication, while gga-miR-7447-3p could promote FAdV-4 replication. Dual-luciferase reporter assays demonstrated that Family with Sequence Similarity 135 Member B (FAM135B) is directly targeted by gga-miR-184-5p. Overexpression of FAM135B suppressed FAdV-4 replication, an effect that was partially reversed by the introduction of gga-miR-184-5p. These findings deepen our understanding of host-FAdV-4 interaction mechanisms and provide valuable candidate targets for future development of antiviral strategies against FAdV-4 infection in poultry.
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.