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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.
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.
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....
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.
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.......
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.......
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....
Name | Company | Catalog Number | Comments |
2 mL tube | Axygen | MCT-200-C-BRA | To fix and dehydrate samples |
Calcium chloride anhydrous | Merck | C4901 | CaCl2 anhydrous to prepare Karnovsky’s fixative |
Critical point dryer | Leica | EM CPD 300 | For critical point drying |
Double Sided Carbon Conductive Tape, 12 mm (W) X 5 M (L) | Electron Microscopy Sciences | 77819-12 | For mounting samples |
Entomological forceps | No specific supplier | To manipulate garden samples | |
Ethyl alcohol (=ethanol), pure (≥99.5%) | Sigma-Aldrich | 459836 | For dehydration |
Forceps | No specific supplier | To manipulate garden samples | |
Glass beaker | No specific supplier | For dehydration | |
Glass Petri dish | No specific supplier | To manipulate garden samples | |
Glass pipette | No specific supplier | To fix and dehydrate samples | |
Glutaraldehyde (Aqueous Glutaraldehyde EM Grade 25%) | Electron Microscopy Sciences | 16220 | To prepare Karnovsky’s fixative |
Gold target | Ted Pella, Inc. | 8071 | To sputter coat with gold |
Hydrochloric acid | Sigma-Aldrich | 320331 | For adjusting solutions pH |
Image editor | Photoshop | any version | To adjust images |
Paraformaldehyde (Paraformaldehyde 20% Aqueous Solution EM Grade) | Electron Microscopy Sciences | 15713 | To prepare Karnovsky’s fixative |
Propilene recipient | No specific supplier | For maintaining alive ant colonies | |
Scanning Electron Microscope | JEOL | IT300 SEM | For sample imaging |
Sodium cacodylate trihydrate | Sigma-Aldrich | C0250 | For preparing sodium cacodylate buffer |
Spatula | No specific supplier | To manipulate garden samples | |
Specimen containers with 15 mm dia. x 10 mm high | Ted Pella, Inc. | 4591 | For critical point drying |
Sputter coater | Baltec | SCD 050 | To coat with gold |
Stub (Aluminium mount, flat end pin) 12.7 mm x 8 mm | Electron Microscopy Sciences | 75520 | For mounting samples |
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