Sign In

A subscription to JoVE is required to view this content. Sign in or start your free trial.

In This Article

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

Summary

We propose an optimized Scanning Electron Microscopy protocol for visualizing highly heterogeneous and delicate samples containing plant and fungal biomass, together with microbiota and biofilm. This protocol allows describing the spatial dimensions of the microbiota organization.

Abstract

In macroscale ecosystems, such as rainforests or coral reefs, the spatial localization of organisms is the basis of our understanding of community ecology. In the microbial world, likewise, microscale ecosystems are far from a random and homogeneous mixture of organisms and habitats. Accessing the spatial distribution of microbes is fundamental for understanding the functioning and ecology of the microbiota, as cohabiting species are more likely to interact and influence each other's physiology.

An interkingdom microbial ecosystem is at the core of fungus-growing ant colonies, which cultivate basidiomycete fungi as a nutritional resource. Attine ants forage for diverse substrates (mostly plant-based), metabolized by the cultivated fungus while forming a spongy structure, a "microbial garden" that acts as an external gut. The garden is an intertwined mesh of fungal hyphae growing by metabolizing the substrate, opening niches for a characteristic and adapted microbiota to establish. The microbiota is thought to be a contributor to substrate degradation and fungal growth, though its spatial organization is yet to be determined.

Here, we describe how we employ Scanning Electron Microscopy (SEM) to investigate, with unprecedented detail, the microbiota and biofilm spatial organization across different fungiculture systems of fungus-growing ants. SEM imaging has provided a description of the microbiota spatial structure and organization. SEM revealed that microbiota commonly assemble in biofilms, a widespread structure of the microbial landscapes in fungiculture. We present the protocols employed to fix, dehydrate, dry, sputter coating, and image such a complex community. These protocols were optimized to deal with delicate and heterogeneous samples, comprising plant and fungal biomass, as well as the microbiota and the biofilm.

Introduction

Ecosystems are composed of organisms interconnected by processes in a specific geographical location (i.e., the environment). Organisms interact with their environment over time, from which complex and heterogeneous spatial patterns emerge. Spatial patterning determines ecological diversity and stability and, ultimately, ecosystem functioning1,2,3,4. In macroscale ecosystems, such as wetlands, savannas, coral reefs, and arid ecosystems, spatial patterns are correlated with resource flow and concentration. Permitting resource optimization, sp....

Protocol

1. Sampling field colonies

NOTE: When collecting ant colonies, certify that all the permissions required by local legislation are obtained before collecting. In our case, the collecting permit #74585 was issued by Instituto Chico Mendes de Conservação e Biodiversidade (ICMBio). When the samples come from a lab colony, go to section 2.

  1. Locate and mark the colony. Excavate a trench surrounding the nest area until the garden chamber is exposed (

Representative Results

Here, we presented a simplified protocol to visualize the components of attine garden and waste samples, such as fungal hyphae, substrate, microbiota, and biofilms. SEM has enhanced our understanding of how the garden and waste scaffold the microbiota structural patterns (Figure 3). In attine gardens, fungal hyphae are branch-like structures covering portions of the substrate surface. Since fungal hyphae tend to be very sensitive to dehydration and rupture, the user may be guided by the hyph.......

Discussion

SEM uses an electron beam to scan the sample, generating an enlarged image of it such that one can visualize three-dimensional microstructures in high resolution. As SEM operates under high vacuum, the removal of up to/more than 99% of water from samples is required. Inside the SEM vacuum chamber, partially hydrated samples may dehydrate and collapse, besides scattering electrons. For high-resolution imaging in SEM, sample preparation should include procedures for removing water while keeping the changes in volume and mo.......

Acknowledgements

The authors would like to thank Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) for providing financial support (Grant #2019/03746-0). MOB thanks for PhD scholarship received from FAPESP (process 2021/08013-0) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brazil (CAPES) - Finance Code 001. AR also thanks Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for a research fellowship (#305269/2018). The authors would like to thank Marcia Regina de Moura Aouada and Antonio Teruyoshi Yabuki for helping with pilot tests for sample preparation, to Renato B....

Materials

NameCompanyCatalog NumberComments
2 mL tubeAxygenMCT-200-C-BRATo fix and dehydrate samples
Calcium chloride anhydrousMerckC4901CaCl2 anhydrous to prepare Karnovsky’s fixative
Critical point dryerLeicaEM CPD 300For critical point drying
Double Sided Carbon Conductive Tape, 12 mm (W) X 5 M (L)Electron Microscopy Sciences77819-12For mounting samples
Entomological forcepsNo specific supplierTo manipulate garden samples
Ethyl alcohol (=ethanol), pure (≥99.5%)Sigma-Aldrich459836For dehydration
ForcepsNo specific supplierTo manipulate garden samples
Glass beakerNo specific supplierFor dehydration
Glass Petri dishNo specific supplierTo manipulate garden samples
Glass pipetteNo specific supplierTo fix and dehydrate samples
Glutaraldehyde (Aqueous Glutaraldehyde EM Grade 25%)Electron Microscopy Sciences16220To prepare Karnovsky’s fixative
Gold target Ted Pella, Inc.8071To sputter coat with gold
Hydrochloric acidSigma-Aldrich320331For adjusting solutions pH
Image editorPhotoshopany versionTo adjust images
Paraformaldehyde (Paraformaldehyde 20% Aqueous Solution EM Grade)Electron Microscopy Sciences15713To prepare Karnovsky’s fixative
Propilene recipientNo specific supplierFor maintaining alive ant colonies
Scanning Electron MicroscopeJEOL IT300 SEMFor sample imaging 
Sodium cacodylate trihydrateSigma-AldrichC0250For preparing sodium cacodylate buffer
SpatulaNo specific supplierTo manipulate garden samples
Specimen containers with 15 mm dia. x 10 mm highTed Pella, Inc.4591For critical point drying
Sputter coaterBaltec SCD 050To coat with gold
Stub (Aluminium mount, flat end pin) 12.7 mm x 8 mm Electron Microscopy Sciences75520For mounting samples

References

  1. Turner, M. G. Landscape ecology: the effect of pattern on process. Annu Rev Ecol Evol Syst. 20 (1), 171-197 (1989).
  2. Rietkerk, M., Van de Koppel, J. Regular pattern formation in real ecosystems. Trends Ecol Evol. 2....

Explore More Articles

Biology

This article has been published

Video Coming Soon

JoVE Logo

Privacy

Terms of Use

Policies

Research

Education

ABOUT JoVE

Copyright © 2024 MyJoVE Corporation. All rights reserved