ArticleBiology open2026
Is the developmental stage important for the plasticity of transgenerational immune priming?
Article in Biology open, 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
4 authors.
Funding
Abstract
Parental transfer of immune memory can increase offspring survival, although its benefits may vary across developmental stages. We investigated transgenerational immune priming in the fall armyworm (Spodoptera frugiperda) infected with the fungus Metarhizium brunneum. Using a split design, fathers and mothers were exposed to a low-dose fungal challenge at larval stages L5 or L6, and their offspring were subsequently challenged with a high dose at L5 or L6. We assessed survival, development, immune responses (phenoloxidase, lytic activity), and oxidative stress (total antioxidant capacity, catalase, superoxide dismutase, hydrogen peroxide). Parental immune activation at either instar had no significant effect on offspring survival. However, offspring responses were stage dependent: L5 larvae in the memory group (homologous challenge) showed higher survival than heterologous or L6-challenged larvae. No L6-challenged larvae reached adulthood. The L5 memory group developed more slowly than controls, while all L6 larvae failed to complete development. Immune response and oxidative stress were higher in L6 larvae, but immune priming effects did not differ. These results suggest that developmental constraints and self-inflicted damage from immune and oxidative responses limit immune priming efficiency at later stages. Our findings highlight that transgenerational immune priming is strongly influenced by the developmental stage at which offspring are challenged.
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.