Cellular heterogeneity of the developing worker honey bee (Apis mellifera) pupa: a single cell transcriptomics analysis

Author:

Patir Anirudh1,Raper Anna1,Fleming Robert1,Henderson Beth E P2,Murphy Lee3,Henderson Neil C24,Clark Emily L1,Freeman Tom C1,Barnett Mark W15

Affiliation:

1. The Roslin Institute, University of Edinburgh , Easter Bush, Midlothian EH25 9RG , UK

2. The Queen's Medical Research Institute, Centre for Inflammation Research, University of Edinburgh, Edinburgh BioQuarter, Edinburgh EH16 4TJ , UK

3. Edinburgh Clinical Research Facility, Western General Hospital, University of Edinburgh , Edinburgh EH4 2XU , UK

4. Institute of Genetics and Cancer, Western General Hospital, University of Edinburgh, Edinburgh EH4 2XU , UK

5. Beebytes Analytics CIC, The Roslin Innovation Centre, University of Edinburgh , The Charnock Bradley Building, Easter Bush, Midlothian EH25 9RG , UK

Abstract

Abstract It is estimated that animals pollinate 87.5% of flowering plants worldwide and that managed honey bees (Apis mellifera) account for 30–50% of this ecosystem service to agriculture. In addition to their important role as pollinators, honey bees are well-established insect models for studying learning and memory, behavior, caste differentiation, epigenetic mechanisms, olfactory biology, sex determination, and eusociality. Despite their importance to agriculture, knowledge of honey bee biology lags behind many other livestock species. In this study, we have used scRNA-Seq to map cell types to different developmental stages of the worker honey bee (prepupa at day 11 and pupa at day 15) and sought to determine their gene expression signatures. To identify cell-type populations, we examined the cell-to-cell network based on the similarity of the single-cells transcriptomic profiles. Grouping similar cells together we identified 63 different cell clusters of which 17 clusters were identifiable at both stages. To determine genes associated with specific cell populations or with a particular biological process involved in honey bee development, we used gene coexpression analysis. We combined this analysis with literature mining, the honey bee protein atlas, and gene ontology analysis to determine cell cluster identity. Of the cell clusters identified, 17 were related to the nervous system and sensory organs, 7 to the fat body, 19 to the cuticle, 5 to muscle, 4 to compound eye, 2 to midgut, 2 to hemocytes, and 1 to malpighian tubule/pericardial nephrocyte. To our knowledge, this is the first whole single-cell atlas of honey bees at any stage of development and demonstrates the potential for further work to investigate their biology at the cellular level.

Funder

Biotechnology and Biological Sciences Research Council (BBSRC) Institute

BBSRC

Wellcome Trust

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

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