Abstract

Flowers can be transmission platforms for parasites that impact bee health, yet bees share floral resources with other pollinator taxa, such as flies, that may be hosts or non-host vectors (i.e., mechanical vectors) of parasites. Here, we assessed whether the fecal-orally transmitted gut parasite of bees, Crithidia bombi, can infect Eristalis tenax flower flies. We also investigated the potential for two confirmed solitary bee hosts of C. bombi, Osmia lignaria and Megachile rotundata, as well as two flower fly species, Eristalis arbustorum and E. tenax, to transmit the parasite at flowers. We found that C. bombi did not replicate (i.e., cause an active infection) in E. tenax flies. However, 93% of inoculated flies defecated live C. bombi in their first fecal event, and all contaminated fecal events contained C. bombi at concentrations sufficient to infect bumble bees. Flies and bees defecated inside the corolla (flower) more frequently than other plant locations, and flies defecated at volumes comparable to or greater than bees. Our results demonstrate that Eristalis flower flies are not hosts of C. bombi, but they may be mechanical vectors of this parasite at flowers. Thus, flower flies may amplify or dilute C. bombi in bee communities, though current theoretical work suggests that unless present in large populations, the effects of mechanical vectors will be smaller than hosts.

Highlights

  • Recent analysis of long-term sampling data and biological records have shown that globally, wild insect pollinators, including solitary bees and flies, are experiencing population declines and range c­ ontractions[1,2,3,4]

  • There was no significant difference in C. bombi load between males vs. females (LRT, χ21 = 0.19, p = 0.66) and no C. bombi were found in the first defecation events of the control flies (n = 30; Table 1)

  • We found that C. bombi did not replicate and cause an active infection in E. tenax flies

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Summary

Introduction

Recent analysis of long-term sampling data and biological records have shown that globally, wild insect pollinators, including solitary bees and flies, are experiencing population declines and range c­ ontractions[1,2,3,4]. Honey bees (Apis spp.) and bumble bees (Bombus spp.) were previously thought to be the only host of certain viruses, microsporidians and trypanosomes, but recent studies have found many of these same parasites are present in and can infect wild solitary bee species, t­oo[16,17,18,19,20,21,22]. Brettell et al.[25] found bee-associated viruses in wild-caught flower flies after deep ­sequencing[25] While these studies suggest many bee parasites may be broad, multi-host parasites, they do not show whether infection (active replication of the parasites) is occurring in non-bee pollinators, nor how transmission occurs. This is important since flower flies occupy a similar ecological niche as bees because of their similar morphology, behaviors and foraging h­ abits[29,30]

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