Pyflubumide is a novel selective carboxanilide acaricide that inhibits mitochondrial complex II of mainly spider species such as Tetranychus urticae. We explored the baseline toxicity and potential crossresistance risk of pyflubumide in a reference panel of T. urticae strains resistant to various acaricides with different modes of action. A cyenopyrafen resistant strain (JPR) was identified as the only strain with low-to-moderate level of cross-resistance to pyflubumide (LC50 = 49.07 mg/L). In a resistance risk assessment approach, JPR was subsequently selected which lead to two highly resistant strains JPR-R1 (LC50 = 1437.48 mg/L) and JPR-R2 (LC50 = 1893.67 mg/L). Interestingly, compared to adult females, resistance was much less pronounced in adult males and eggs of the two JPR-R strains. In order to elucidate resistance mechanisms, we first sequenced complex II subunits in susceptible and resistant strains, but target-site insensitivity could not be detected. In contrast, synergism/ antagonism experiments strongly suggested that cytochrome P450 monooxygenases are involved in pyflubumide resistance. We therefore conducted genome-wide gene expression experiments to investigate constitutive and induced expression patterns and documented the overexpression of five cytochrome P450 and four CCE genes in JPR-Rs after pyflubumide exposure. Together, we provide a thorough resistance risk assessment of a novel complex II inhibitor, and provide first evidence for metabolic resistance mediated by cytochrome P450s in T. urticae.