Prediction of fenpyroximate affinity to the NADH-ubiquinone oxidoreductase protein from complex I, for different bee species

Authors

  • Pedro Rodrigues CIIMAR - Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, Avenida General Norton de Matos, S/N, 4450-208 Matosinhos, Portugal https://orcid.org/0000-0002-6955-8868
  • Laura Guimarães CIIMAR - Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, Avenida General Norton de Matos, S/N, 4450-208 Matosinhos, Portugal
  • Nuno Gonçalo Ferreira CIIMAR - Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, Avenida General Norton de Matos, S/N, 4450-208 Matosinhos, Portugal; School of Biosciences - Cardiff University. Museum Avenue, Cardiff CF10 3AX, Wales (UK)

DOI:

https://doi.org/10.48797/sl.2024.238

Keywords:

Poster

Abstract

Background: Pesticide usage has several beneficial impacts on agricultural production. However, it also has negative environmental impacts on soil, water, and non-target species, which can potentially cause a decrease in biodiversity. A good example is the decline of bee populations due to pesticide use. Fenpyroximate (FEN) is a fungicide that acts by inhibiting mitochondrial complex I electron transport, focusing on the translocation of protons from NADH to ubiquinone oxidoreductase. It is among those detected in Caatinga crops and was already reported to have negative impacts on bees [1,2]. Objective: The main objective of this study is to understand the sensibility of different species of bees from the Caatinga biome to FEN using in silico analysis. Methods: A protein-ligand analysis was used to determine FEN's affinity and binding sites to the NADH-ubiquinone oxidoreductase complex I protein (NADH) for 26 bee species inhabiting the Caatinga biome. A phylogenetic tree was performed to determine the similarity and position of similar binding sites and pockets, and the protein-ligand docking was performed with Autodock (v4.2.6). Results: NADH sequences for the 26 bee species had a length between 438 and 566 bp, sharing 79% of pairwise residues for all sequences. Results show that the binding energy of FEN to NADH was between -8.39 and -10.28kcal/mol, inhibition constants between 28.98 and 713 nM, and ligand efficiency between 0.27 and 0.32. For all species, a minimum of 3 and a maximum of 10 ligand aminoacids were found. Conclusions: This bioinformatics analysis pipeline is a useful complementary tool to animal testing, giving important insights for determining the mechanisms underlying toxicity of pesticides in non-target bee species. Additionally, it was possible to determine a rank of species sensitivity to FEN that can be used as a policy-maker tool.

References

1. Bahreini, R., Nasr, M., Docherty, C., de Herdt, O., Muirhead, S., & Feindel, D. Evaluation of potential miticide toxicity to Varroa destructor and honey bees, Apis mellifera, under laboratory conditions. Scientific reports, (2020) 10(1), 21529.

2. Malhat, F., Abdallah, O., Anagnostopoulos, C., Hussien, M., Purnama, I., Helmy, R., ... & El-Hefny, D. Residue, dissipation, and dietary intake evaluation of fenpyroximate acaricide in/on guava, orange, and eggplant under open field condition. Frontiers in Nutrition (2022), 9, 939012.

Downloads

Published

2024-05-01

How to Cite

Rodrigues, P., Guimarães, L., & Ferreira, N. G. (2024). Prediction of fenpyroximate affinity to the NADH-ubiquinone oxidoreductase protein from complex I, for different bee species. Scientific Letters, 1(Sup 1). https://doi.org/10.48797/sl.2024.238

Issue

Section

Posters

Most read articles by the same author(s)

Similar Articles

<< < 6 7 8 9 10 11 12 13 14 15 > >> 

You may also start an advanced similarity search for this article.