ArticleBMC genomics2025
Time-series transcriptomic analysis of Nile tilapia reveals the crucial roles of long non-coding RNA and transcription factor in response to Aeromonas veronii infection.
Article in BMC genomics, 2025. 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
9 authors.
Funding
Abstract
Nile tilapia (Oreochromis niloticus) is a vital aquaculture species worldwide, prized for its rapid growth and high productivity. However, the increasing prevalence of Aeromonas veronii infections has led to significant economic losses in the Nile tilapia industry. To elucidate the molecular mechanisms underlying the host immune response, we performed transcriptome sequencing of Nile tilapia spleen tissues at 3, 7, and 10 days post-infection. Furthermore, weighted gene co-expression network analysis was employed to identify key genes and pathways, and a regulatory network was subsequently constructed to elucidate regulatory relationships. Our results revealed that long non-coding RNA (lncRNA) and transcription factor (TF) played crucial roles in responding to A. veronii infection, particularly lncRNA LOC112842004 and TFs TFAP2B and SP2. The differentially expressed targets of these lncRNAs and TFs, along with other differentially expressed mRNAs, were predominantly enriched in immune-related pathways, progressively shifting from upstream genes to downstream genes within pathways as infection advanced. Additionally, specific pathways were activated at each time point, with the MAPK signaling pathway remaining continuously active during infection. These findings enhance our understanding of the molecular mechanisms underlying Nile tilapia's response to A. veronii infection and provide valuable insights for improving disease management strategies in aquaculture.
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.