Are Efficient-Dose Mixtures a Solution to Reduce Fungicide Load and Delay Evolution of Resistance? An Experimental Evolutionary Approach

Pesticide resistance poses a critical threat to agriculture, human health and biodiversity. Mixtures of fungicides are recommended and widely used in resistance management strategies. However, the components of the efficiency of such mixtures remain unclear. We performed an experimental evolutionary study on the fungal pathogen Z. tritici to determine how mixtures managed resistance. We compared the effect of the continuous use of single active ingredients to that of mixtures, at the minimal dose providing full control of the disease, which we refer to as the “efficient” dose. We found that the performance of efficient-dose mixtures against an initially susceptible population depended strongly on the components of the mixture. Such mixtures were either as durable as the best mixture component used alone, or worse than all components used alone. Moreover, efficient dose mixture regimes probably select for generalist resistance profiles as a result of the combination of selection pressures exerted by the various components and their lower doses. Our results indicate that mixtures should not be considered a universal strategy. Experimental evaluations of specificities for the pathogens targeted, their interactions with fungicides and the interactions between fungicides are crucial for the design of sustainable resistance management strategies.

Climate warming promotes pesticide resistance through expanding overwintering range of a global pest

Climate change has the potential to change the distribution of pests globally and their resistance to pesticides, thereby threatening global food security in the 21st century. However, predicting where these changes occur and how they will influence current pest control efforts is a challenge. Using experimentally parameterised and field-tested models, we show that climate change over the past 50 years increased the overwintering range of a global agricultural insect pest, the diamondback moth (Plutella xylostella), by ~2.4 million km2 worldwide. Our analysis of global data sets revealed that pesticide resistance levels are linked to the species’ overwintering range: mean pesticide resistance was 158 times higher in overwintering sites compared to sites with only seasonal occurrence. By facilitating local persistence all year round, climate change can promote and expand pesticide resistance of this destructive species globally. These ecological and evolutionary changes would severely impede effectiveness of current pest control efforts and potentially cause large economic losses.

Experimental evolution of insect resistance to two pesticide classes reveals mechanistic diversity and context-dependent fitness costs

Does rapid adaptation to stressors evolve through similar underlying mechanisms among diverse populations, or are there many roads to a similar phenotype? The experimental evolution of pesticide resistance in insects provides a powerful model to study the diverse evolutionary signatures of adaptation and their associated costs. Here, we selected for resistance to two pesticides (organophosphates and pyrethroids) in six field-derived populations of the red flour beetle (Tribolium castaneum). After several generations of selection, we performed transcriptomic analyses and measured survival, development, and fecundity in the presence and absence of pesticides to detect fitness costs of resistance evolution. All pesticide-selected populations exhibited significantly improved survival after pesticide exposure without substantial fitness costs, compared to control populations. Populations that evolved to resist organophosphates had distinct gene expression in the presence and absence of organophosphates, supporting different detoxification mechanisms and cuticular modifications among populations. In contrast, pyrethroid resistant populations demonstrated common differential expression of cytochrome P450 transcripts. Furthermore, some populations evolved similar mechanisms against both pesticides while others showed little overlap in their evolved responses, suggesting variation in potential cross-resistance phenotypes. Overall, between populations, we observed both parallel and divergent patterns in gene expression associated with acquired pesticide resistance, without ubiquitous fitness costs.