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Life-history stage determines the diet of ectoparasitic mites on their honey bee hosts

Nature Communications 2024 78 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 70 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Bin Han, Jiangli Wu, Qiaohong Wei, Fengying Liu, Fengying Liu, Lihong Cui, Olav Rueppell, Shufa Xu

Summary

Researchers discovered that parasitic Varroa mites switch their diet depending on their life stage, feeding on the fat body of adult honey bees but primarily consuming hemolymph (blood) from bee pupae. While not directly about microplastics, this study matters because understanding threats to bee health, including parasites and environmental pollutants like microplastics, is essential for protecting pollinators that support our food supply.

Body Systems

Ectoparasitic mites of the genera Varroa and Tropilaelaps have evolved to exclusively exploit honey bees as food sources during alternating dispersal and reproductive life history stages. Here we show that the primary food source utilized by Varroa destructor depends on the host life history stage. While feeding on adult bees, dispersing V. destructor feed on the abdominal membranes to access to the fat body as reported previously. However, when V. destructor feed on honey bee pupae during their reproductive stage, they primarily consume hemolymph, indicated by wound analysis, preferential transfer of biostains, and a proteomic comparison between parasite and host tissues. Biostaining and proteomic results were paralleled by corresponding findings in Tropilaelaps mercedesae, a mite that only feeds on brood and has a strongly reduced dispersal stage. Metabolomic profiling of V. destructor corroborates differences between the diet of the dispersing adults and reproductive foundresses. The proteome and metabolome differences between reproductive and dispersing V. destructor suggest that the hemolymph diet coincides with amino acid metabolism and protein synthesis in the foundresses while the metabolism of non-reproductive adults is tuned to lipid metabolism. Thus, we demonstrate within-host dietary specialization of ectoparasitic mites that coincides with life history of hosts and parasites.

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