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Wegener, J.

Publications and source records attributed to Wegener, J..

4 recordsLinked to original sources

Integrated risk assessment reveals low biological activity of RNA-based crop protection formulations across plant and non-target systems

RNA-based crop protection products are considered promising alternatives to conventional pesticides due to their high target specificity and selectivity profile. While current risk assessments mainly focus on sequence-dependent off-target effects, potential sequence-independent effects of RNA molecules and formulation components remain poorly understood. Here, we assessed the potential of naked and formulated RNA molecules to induce unintended biological responses in plants and non-target organisms using complementary plant stress and cellular toxicity assays. Single-stranded RNA (ssRNA), double-stranded RNA (dsRNA), circular RNA (circRNA), and chitosan-based RNA formulations were evaluated for their ability to induce early stress responses in plants and adverse effects in insect cells. Cytosolic Ca{superscript 2} signaling and reactive oxygen species (ROS) production were monitored in barley and Arabidopsis, while impedance-based phenotypic profiling (ECIS) was used to assess cellular responses in Spodoptera frugiperda (Sf21) cells. Neither naked nor formulated RNA preparations triggered pronounced Ca{superscript 2} influxes or ROS bursts, indicating an absence of substantial activation of early plant defense signaling. Likewise, RNA formulations caused only minor effects on insect cell attachment and spreading as a measure for cell viability. Observable responses occurred primarily at elevated concentrations of RNA formulations and were formulation-dependent rather than RNA-dependent. Overall, the investigated RNA molecules exhibited low biological activity across the tested non-target systems. Our results highlight the importance of evaluating RNA active ingredients and delivery matrices separately and demonstrate the value of integrated screening approaches for the early hazard assessment of RNA-based crop protection products.

Plant Biology↗

A SNP-based honey bee paternity assignment test for evaluating the effectiveness of mating stations and its application to the Ataun valley, Basque Country, Spain

Geographically isolated mating stations are deployed across Europe to facilitate controlled mating with selected drone-producing colonies. To assess the reliability of these stations, we developed a paternity assignment test using a custom Illumina genotyping chip with 6457 SNPs based on two metrics (number of mismatch alleles and kinship). The method demonstrated remarkable accuracy during validation with an independent dataset of known parent-offspring pairs, with an accuracy rate of 97.7%. We then applied the developed paternity assignment test to the Apis mellifera iberiensis mating station in the Ataun valley, Basque Country, Spain, in 2021. Drone-producing colonies in the valley were sampled and genotyped, as well as 156 worker offspring of queens mated at the station, and 56 drones collected in the drone congregation area. Out of the 156 worker samples, we could assign paternity of 120 (76.9%) to one of the drone-producing colonies in the valley, while 23.1% were of unknown patriline. Out of the 56 drones collected in the air, 52 (92.9%) were assigned to drone-producing colonies. We were also able to determine the colonies and apiaries that made the most significant contributions to the matings. This information aids in effective apiary management, including the selection of suitable mating station locations and the positioning of drone-producing colonies therein. Overall, our SNP-based paternity assignment test offers a valuable tool for evaluating mating station effectiveness across Europe, crucial for advancing breeding objectives in honey bee populations.

genetics↗

Direct monitoring of cAMP at the cardiac ryanodine receptor using a novel targeted fluorescence biosensor mouse

RationaleCyclic adenosine monophosphate (cAMP) is a ubiquitous second messenger which, upon {beta}-adrenergic receptor ({beta}-AR) stimulation, acts in microdomains to regulate cardiac excitation-contraction coupling by activating the cAMP-dependent protein kinase (PKA) phosphorylation of calcium handling proteins. One crucial microdomain is in vicinity of the cardiac ryanodine receptor type 2 (RyR2) which is associated with arrhythmogenic diastolic calcium leak from the sarcoplasmic reticulum (SR) often occurring upon RyR2 hyperphosphorylation by PKA and calcium/calmodulin-dependent kinase.\n\nObjectiveWe sought to establish a real time approach capable of directly visualizing cAMP and its pathological changes in the vicinity of RyR2 by generating a proper targeted biosensor and transgenic mouse model to express it in adult cardiomyocytes.\n\nMethods and ResultsWe generated transgenic mice expressing a novel targeted fluorescent biosensor for RyR2-associated cAMP in adult mouse cardiomyocytes. In healthy cardiomyocytes, {beta}1-AR but not {beta}2-AR stimulation strongly increased local RyR2-associated cAMP levels. However, in cardiac hypertrophy induced by aortic banding, there was a marked subcellular redistribution of phosphodiesterases (PDEs) 2, 3 and 4, which included a dramatic loss of the local pool of PDE4. This was also accompanied by measurable {beta}2-AR-induced cAMP signals, increased SR calcium leak and arrhythmia susceptibility.\n\nConclusionsOur new targeted biosensor expressed in transgenic mice can visualize cAMP levels in the vicinity of cardiac RyR2 in healthy and diseased cardiomyocytes. In the future, this novel biosensor can be used to better understand alterations of RyR2-associated cAMP in cardiovascular diseases and local actions of new therapies.

cell biology↗