Ross, Rachel, Hu, Chun, Castelli, Jack, Snider, Jamie, Palmeira, Bruna, Vaidya, Aditya, Lautens, Mark, Volpatti, Jonathan, Zasada, Inga, Stagljar, Igor, Kitner, Megan, Redman, Elizabeth, Dowling, James, MacParland, Sonya, Cowen, Leah, Xiao, Qi, Finney, Constance, Cutler, Sean, Marwah, Sagar, Burns, Andrew, Tiefenbach, Jens, Puumala, Emily, Krause, Henry, Meyer, Susan, MacDonald, Margaret, Chung, Sai, Roy, Peter, Gilleard, John
[
International Worm Meeting,
2021]
Global food security is threatened as the world amasses 10 billion people amid limited arable land. While nematode pests are a major barrier to agricultural intensification, most traditional nematicides are now banned because of poor nematode-selectivity, leaving farmers with inadequate controls. Here, we describe a screen carried out in the model nematode Caenorhabditis elegans that enriches for selective nematicides by identifying molecules that are bioactivated by cytochrome P450s, which are phylogenetically diverse. We identify a family of structures, called nemactivins, that are robustly bioactivated to a toxic metabolite selectively in nematodes. At low parts-per-million concentrations, nemactivins perform comparably well with commercial nematicides at controlling infection by the world's most destructive plant-parasitic nematode Meloidogyne incognita. Hence, nemactivins are first-in-class bioactivated nematicides that provide much needed nematode-selectivity.