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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 infectEristalis tenaxflower flies. We also investigated the potential for two confirmed solitary bee hosts ofC. bombi,Osmia lignariaandMegachile rotundata, as well as two flower fly species,Eristalis arbustorumandE. tenax,to transmit the parasite at flowers. We found thatC. bombidid not replicate (i.e., cause an active infection) inE. tenaxflies. However, 93% of inoculated flies defecated liveC. bombiin their first fecal event, and all contaminated fecal events containedC. bombiat 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 thatEristalisflower flies are not hosts ofC. bombi, but they may be mechanical vectors of this parasite at flowers. Thus, flower flies may amplify or diluteC. bombiin bee communities, though current theoretical work suggests that unless present in large populations, the effects of mechanical vectors will be smaller than hosts.
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Crithidia bombi can infect two solitary bee species while host survivorship depends on diet
Abstract Pathogens and lack of floral resources interactively impair global pollinator health. However, epidemiological and nutritional studies aimed at understanding bee declines have historically focused on social species, with limited evaluations of solitary bees. Here, we asked whether Crithidia bombi , a trypanosomatid gut pathogen known to infect bumble bees, could infect the solitary bees Osmia lignaria (females) and Megachile rotundata (males), and whether nutritional stress influenced infection patterns and bee survival. We found that C. bombi was able to infect both solitary bee species, with 59% of O. lignaria and 29% of M. rotundata bees experiencing pathogen replication 5–11 days following inoculation. Moreover, access to pollen resulted in O. lignaria living longer, although it did not influence M. rotundata survival. Access to pollen did not affect infection probability or resulting pathogen load in either species. Similarly, inoculating with the pathogen did not drive survival patterns in either species during the 5–11-day laboratory assays. Our results demonstrate that solitary bees can be hosts of a known bumble bee pathogen, and that access to pollen is an important contributing factor for bee survival, thus expanding our understanding of factors contributing to solitary bee health.
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- Award ID(s):
- 2010615
- PAR ID:
- 10249567
- Date Published:
- Journal Name:
- Parasitology
- Volume:
- 148
- Issue:
- 4
- ISSN:
- 0031-1820
- Page Range / eLocation ID:
- 435 to 442
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1017/S0031182020002218
