ArticleVeterinary medicine and science2025
Successful Cryoprotectant-Free Vitrification of Honey Bee (Apis mellifera) Drone Sperm With Royal Jelly Supplemented Extender.
Article in Veterinary medicine and science, 2025. 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.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In trying to protect honey bee species and maintain genetic diversity, employing effective approaches for drone sperm conservation is crucial. Based on literature, drone sperm cryopreservation extenders and methods have not been fully optimized. Our research aim was to enhance drone bee sperm preservation by incorporating royal jelly (RJ) in the extender of the cryoprotectant-free vitrification method. Drone sperm was collected from adult drone bees (36 days old) using the manual inversion method. Different concentrations of RJ (0%, 0.5%, 1%, 2.5% and 5%) were added to the extender. Diluted sperm were cryopreserved using a cryoprotectant-free vitrification technique where 10 µL aliquots of the diluted sperm were directly dropped into the liquid nitrogen and then stored. Data were analysed based on a completely randomized design with ten replications. Sperm quality parameters, including motility, viability and DNA damage, were evaluated in vitro. Queens were artificially inseminated to measure the ability of motile sperm to reach the spermathecae. The results showed that 1% and 2.5% of RJ supplementation significantly enhanced sperm motility and viability and reduced DNA fragmentation compared to control and higher RJ concentrations. Specifically, the 1% RJ group resulted in the highest sperm viability, while both the 1% and 2.5% groups maintained lower DNA fragmentation rates. Queens inseminated with sperm treated with 1% and 2.5% RJ showed a notably higher number of motile sperm in their spermathecae. In conclusion, supplementation of 1% RJ to the cryoprotectant-free vitrification media may improve drone sperm quality parameters post-warming. Our findings provide valuable insights into optimizing drone bee sperm preservation, contributing to the conservation of these vital pollinators.
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.