Understanding the rapid evolution of agricultural pests can inform
mitigation efforts and provide comprehensive models for natural systems
and examples for the consequences of anthropogenic global change. It is
suspected that the practice of migratory beekeeping, in which beehives
are shipped great distances to meet pollination demands, increases
dispersal of honeybee (Apis melifera) pests and parasites, including the
highly virulent mite Varroa destructor. Given it has never been
explicitly examined in the United States, here we test this hypothesis
by studying the population genetics of Varroa mites sampled from
migratory and non-migratory hives across the western United States.
Using 3RAD to generate a genome-wide dataset for hundreds of samples, we
found very low genetic diversity and no population structure across more
than one thousand kilometers. Our findings are consistent with the
proposed large and fast mite admixture enabled by migratory pollination.
Furthermore, hives that avoid migratory pollination are not insulated
from the effects of this admixture, as there is evidence for extremely
high rates of gene flow into—and a resulting lack of isolation by
distance among—these sedentary populations. Our research suggests the
genetic variation of Varroa destructor in the western United States is a
result of its recent introduction to the region and shows clear signals
of high admixture, likely due to management practices. Moreover, it
demonstrates how an evolutionary, genetic perspective is crucial in
understanding host-parasite dynamics in agricultural systems and shaping
management decisions to protect key species