Social Interaction is Unnecessary for Hindgut Microbiome Transmission in Honey Bees: The Effect of Diet and Social Exposure on Tissue-Specific Microbiome Assembly
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Department of Microbiology, School of Animal & Comparative Biomedical Sciences, University of ArizonaDepartment of Entomology and Center for Insect Science, University of Arizona
Issue Date
2022-05-02
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Springer Science and Business Media LLCCitation
Anderson, K. E., Ricigliano, V. A., Copeland, D. C., Mott, B. M., & Maes, P. (2022). Social Interaction is Unnecessary for Hindgut Microbiome Transmission in Honey Bees: The Effect of Diet and Social Exposure on Tissue-Specific Microbiome Assembly. Microbial Ecology.Journal
Microbial EcologyRights
This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2022. This article is licensed under a Creative Commons Attribution 4.0 International License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Honey bees are a model for host–microbial interactions with experimental designs evolving towards conventionalized worker bees. Research on gut microbiome transmission and assembly has examined only a fraction of factors associated with the colony and hive environment. Here, we studied the effects of diet and social isolation on tissue-specific bacterial and fungal colonization of the midgut and two key hindgut regions. We found that both treatment factors significantly influenced early hindgut colonization explaining similar proportions of microbiome variation. In agreement with previous work, social interaction with older workers was unnecessary for core hindgut bacterial transmission. Exposure to natural eclosion and fresh stored pollen resulted in gut bacterial communities that were taxonomically and structurally equivalent to those produced in the natural colony setting. Stressed diets of no pollen or autoclaved pollen in social isolation resulted in decreased fungal abundance and bacterial diversity, and atypical microbiome structure and tissue-specific variation of functionally important core bacteria. Without exposure to the active hive environment, the abundance and strain diversity of keystone ileum species Gilliamella apicola was markedly reduced. These changes were associated with significantly larger ileum microbiotas suggesting that extended exposure to the active hive environment plays an antibiotic role in hindgut microbiome establishment. We conclude that core hindgut microbiome transmission is facultative horizontal with 5 of 6 core hindgut species readily acquired from the built hive structure and natural diet. Our findings contribute novel insights into factors influencing assembly and maintenance of honey bee gut microbiota and facilitate future experimental designs.Note
Open access articleISSN
0095-3628EISSN
1432-184XVersion
Final published versionSponsors
Agricultural Research Serviceae974a485f413a2113503eed53cd6c53
10.1007/s00248-022-02025-5
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Except where otherwise noted, this item's license is described as This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2022. This article is licensed under a Creative Commons Attribution 4.0 International License.