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Maes, J.

Publications and source records attributed to Maes, J..

4 recordsLinked to original sources

Eco-evolutionary feedback of adaptive evolution to a pesticide worsens the impact of a pesticide switch in a pivotal freshwater non-target species

Pest management often requires the switches of insecticides, sequentially exposing non-target populations to different compounds. In a two-phased experiment, we assessed whether exposure to the pesticide chlorpyrifos induces rapid evolution in the non-target species Daphnia magna, and quantified the response of control and pre-exposed populations to a second exposure to the same pesticide, another pesticide with the same mode of action (malathion), or a pesticide with another mode of action (deltamethrin). Chlorpyrifos selection induced rapid shifts in genotype composition and reduced genotype richness, and strongly influenced population development following the second exposure. Chlorpyrifos-selected populations outperformed control populations when subsequently exposed to chlorpyrifos and malathion, but underperformed when exposed to deltamethrin. Our results highlight an eco-evolutionary feedback in which rapid adaptive responses to a pesticide worsens the response when exposed to a different type of pesticide in non-target species, increasing vulnerability to common agricultural practices.

ecology↗

Phosphorylation on serine 72 modulates Rab7A palmitoylation and retromer recruitment

AbstractThe small GTPase Rab7A has a key role in regulating membrane trafficking at late endosomes. By interacting with several different effectors, this small GTPase controls late endosome mobility, orchestrates fusion events between late endosomes and lysosomes, and participates in the formation of and regulates the fusion between autophagosomes and lysosomes. Rab7A is also responsible for the spatiotemporal recruitment of retromer, which is required for the endosome-to-TGN retrieval of cargo-receptors such as sortilin and CI-MPR. Recently several post-translational modifications have been shown to modulate Rab7A functions, including palmitoylation, ubiquitination and phosphorylation. Here we show that phosphorylation of Rab7A at serine 72 is important to modulate its interaction with retromer, as the non-phosphorylatable Rab7AS72A mutant is not able to interact with and recruit retromer to late endosomes. We have previously shown that Rab7A palmitoylation is also required for efficient retromer recruitment. We found that palmitoylation of Rab7AS72A is reduced compared to the wild-type protein, suggesting an interplay between S72 phosphorylation and palmitoylation in regulating the Rab7A/retromer interaction. Finally, we identify NEK7 as the kinase required to phosphorylate Rab7A to promote retromer binding and recruitment.

cell biology↗

Biodiversity monitoring in Europe: user and policy needs

To implement the goals of the 2030 Global Biodiversity Framework, the European Biodiversity Strategy and the EU Green Deal, biodiversity monitoring is a pivotal instrument to achieve accountability and progress in conservation. Monitoring efforts in Europe, however, suffer from gaps and biases in taxonomy, spatial coverage, and temporal resolution, resulting in fragmented and disconnected data which does not provide sufficient evidence for policy making. To assess user and policy needs in biodiversity monitoring, we employed with EuropaBON a four-step user-centred stakeholder engagement process, including an international public stakeholder workshop, a standardised online survey, semi-structured interviews, and an expert meeting with representatives of EU member states, the European Commission and the European Environment Agency. The resulting insights into national and European biodiversity monitoring schemes identify policy needs, current challenges and potential solutions. Based on this in-depth policy and science stakeholder assessment, we recommend the establishment of a European Biodiversity Observation Network through a permanent Biodiversity Monitoring and Coordinating Centre to optimise existing observation efforts, harmonise data, and enhance our ability to predict and respond to key challenges related to biodiversity loss in a changing climate in Europe.

ecology↗

A robust human norovirus replication model in zebrafish larvae

Human noroviruses (HuNoVs) are an important cause of epidemic and endemic acute gastroenteritis worldwide; annually about 700 million people develop a HuNoV infection resulting in [~]219,000 deaths and a societal cost estimated at 60 billion US dollars 1. The lack of robust small animal models has significantly hindered the understanding of norovirus biology and the development of effective therapeutics against HuNoV. Here we report that HuNoV GI and GII replicate to high titers in zebrafish (Danio rerio) larvae; replication peaks at day 2 post infection and is detectable for at least 6 days. HuNoV is detected in cells of the hematopoietic lineage, the intestine, liver and pancreas. Antiviral treatment reduces HuNoV replication by >2 log10, showing that this model is suited for antiviral studies. Downregulation of fucosyltransferase 8 (fut8) in the larvae reduces HuNoV replication, highlighting a common feature with infection in humans. Zebrafish larvae constitute a simple and robust replication model that will largely facilitate studies of HuNoV biology and the development of antiviral strategies.

microbiology↗