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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Immunohistochemical methods are useful in honeybee research to detect and assess the level of apoptosis and necrosis in the midgut and hypopharyngeal glands of adult bees.

Abstract

Honeybees (Apis mellifera L.) inside the hive (nurse workers and other hive bees) and outside the hive (foragers) are exposed to climate and weather changes, various pesticides, pathogens, and malnutrition, mainly entering through the mouth and primarily affecting the digestive tracts of adult bees. To understand and prevent the effects of such external and internal stressors on honeybees, one useful research method is the immunohistochemical method. A basic protocol is described to prepare the midgut (ventriculus) and hypopharyngeal glands (HPGs) of adult bees for histological analysis. A detailed methodology is described to assess the level of cell damage and distinguish necrosis from programmed cell death (apoptosis) as a natural process of tissue regeneration. The results of adult honeybee treatment with oxalic acid and pesticides (insecticide and acaricide) and the determination of cell death in the ventriculus and HPGs are presented. The pros and cons of the methodology are also discussed.

Introduction

Honeybees (Apis mellifera L.) are, among other wild pollinators, the most important pollinators of agricultural plants. Over thousands of years, the changing environment has influenced bees to adapt their morphology, physiology, behavior, and tolerance to several pathogens and parasites. Therefore, honeybees have developed a highly diverse range of species and subspecies around the globe1. These results are consistent with previous findings, that there is genetic variation in the honeybee's digestive tract structure, but also suggest that alterations of the midgut are due to environmental factors2,

Protocol

1. Basic histology for honeybee research

  1. Dissection of honeybee tissue
    NOTE: For the dissection of worker bees, use a dissecting microscope with an LED light source. The most useful magnification is ~20x.
    1. Manipulation and dissection
      1. Carefully take a worker bee with forceps and put it on ice (or into the freezer at -20 °C) for 2 min to immobilize it22. Pin the bee on the Petri dish diagonally through the uppermost back portion of th.......

Representative Results

Cell death detection in the midgut
Newly emerged worker bees (Apis mellifera carnica) from the experimental apiary at the Agricultural Institute of Slovenia in Ljubljana were individually treated with 3% oxalic acid (OA)23. OA is frequently used in beekeeping for Varroa destructor control. After the treatment, the worker bees (three from each group) were immobilized on ice. The midgut was dissected and fixed it in 10% formalin. The tissue was then dehydrate.......

Discussion

In living organisms, cell death is defined as apoptosis or necrosis25 and can be accompanied by autophagy26. The difference between apoptotic and necrotic cells is that apoptosis is a form of programmed cell death and appears in normal cells, whereas necrosis occurs due to lethal conditions (e.g., accident, disease)27,28. Apoptosis can be detected using assay kits based on the TUNEL technique (detection ofDNA f.......

Acknowledgements

I gratefully acknowledge the support of the Slovenian Research Agency, grant no. P4-133.

....

Materials

NameCompanyCatalog NumberComments
2-Propanol
ApopTag Peroxidase kit (ApopTag Peroxidase In Situ Apoptosis Detection)Sigma-AldrichS7100Assay B, https://www.sigmaaldrich.com/SI/en/product/mm/s7100?gclid=CjwKCA
jw7vuUBhBUEiwAEdu2pPanI9SE
j81ZTl-nLHEoxXAv7ViKwPA_QRx
H7fciMRNcYwR7lbPQbhoCqcQQA
vD_BwE; Positive controls included in S7101
Covers
DeadEnd Colorimetric TUNEL systemPromegaG7360Assay A, https://worldwide.promega.com/products/cell-health-assays/apoptosis-assays/deadend-colorimetric-tunel-system/?catNum=G7360
Dissecting microscope  (for bee dissection)Zeiss
Distilled water
Embedding cassette
EnVision System alkaline phosphatase kitDako
Eosin Y SolutionSigma-Aldrichalcoholic
Ethanol95% (or less pure), 90%, 80%
Faramount mounting medium, aqueousDakomounting medium
Flattening tableLeicaHI1220
Forceps  (for bee dissection)Fine science tools11294-00Standard #4
Formalin 10%Formaldehyde
HematoxylinSigma-Aldrich
HistoChoice Clearing AgentSigma-Aldrichclearing agent
Hydrogen peroxidase 3%
IncubatorBioRad
Insect pins  (for bee dissection)Entosphinx44594Insect pins stainless steel – white, size 2
ISCDDK, AP (In Situ Cell Death Detecteion Kit, Alkaline Phosphatase)Roche11684809910Assay C, https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/362/737/11684809910b
ul.pdf
KH2PO4
Lab clock
Light microscopeLeica
Microscope slidesBox with the slides must be preserved in a plastic wrap to prevent dust
MicrotomeLeica
Modular tissue embedding stationLeica
Na2HPO4
NaCl
Paraformaldehyde 4%
ParaplastLeica
Pasteur pipettes1.5 mL; 3 mL
PBS
Petri dish  (for bee dissection)Filled with condensation silicon  (Xantoprene L blue and Universal liquid plus activator)
Proteinase KMerck21627
Ringers' solution  (for bee dissection)7.5 g NaCL, 2.38 g Na2HPO4, 2.72 g KH2PO4, 1 L distilled water
Scissors  (for bee dissection)Fine science tools1406-09, 14061-09Straight and curved, 9 cm
Universal liquid plus activator  (for bee dissection)Kulzer
Watchmaker’s forceps (for bee dissection)Fine science tools91100-12
Water bathLeica
Watercolor brush2x
Xantoprene L blue  (for bee dissection)Kulzer

References

  1. Ruttner, F. . Naturgeschichte der Honigbienen. , (1992).
  2. Jordan, R. Kleine Bienenkunde. Österreichischer Agrarverlag Wien München. , 41-45 (1964).
  3. Snodgrass, R. E.

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HistologyCell DeathHoneybee TissuePesticidesAcaricidesVarroa MitesWorker BeeMidgut DissectionHypopharyngeal Glands DissectionHematoxylin And Eosin StainingStereomicroscopeInsect SalineForcepsScissorsPinsPipette

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