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Method Article

An Ex vivo Assay to Study Candida albicans Hyphal Morphogenesis in the Gastrointestinal Tract

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DOI:

10.3791/61488

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July 1st, 2020

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In This Article

Summary

The ex vivo assay described in this study using gut homogenate extracts and immunofluorescence staining represents a novel method to examine the hyphal morphogenesis of Candida albicans in the GI tract. This method can be utilized to investigate the environmental signals regulating morphogenetic transition in the gut.

Abstract

Candida albicans hyphal morphogenesis in the gastrointestinal (GI) tract is tightly controlled by various environmental signals, and plays an important role in the dissemination and pathogenesis of this opportunistic fungal pathogen. However, methods to visualize fungal hyphae in the GI tract in vivo are challenging which limits the understanding of environmental signals in controlling this morphogenesis process. The protocol described here demonstrates a novel ex vivo method for visualization of hyphal morphogenesis in gut homogenate extracts. Using an ex vivo assay, this study demonstrates that cecal contents from antibiotic treated mice, but not from untreated control mice, promote C. albicans hyphal morphogenesis in the gut content. Further, adding back specific groups of gut metabolites to the cecal contents from antibiotic-treated mice differentially regulates hyphal morphogenesis ex vivo. Taken together, this protocol represents a novel method to identify and investigate the environmental signals that control C. albicans hyphal morphogenesis in the GI tract.

Introduction

Candida albicans is an opportunistic, polymorphic fungal pathogen that is normally commensal, but can undergo a morphological change into a virulent form capable of causing life-threatening infections in immunocompromised individuals1,2,3,4,5,6,7,8,9,10,11,12

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Protocol

All animal protocols were approved by Midwestern University Institutional Animal Care and Use Committee (IACUC) as described before57. The Institutional Animal Care and Use Committee at Midwestern University approved this study under MWU IACUC Protocol #2894. The MWU animal care policies follow the Public Health Service (PHS) Policy on Humane Care and Use of Laboratory Animals and the policies laid out in the Animal Welfare Act (AWA).

1. Mice study standard protocol

  1. Use male and female C57BL/6J mice at least six weeks old. Supplement them with sterile water with or without cefoperazone (0.5 mg/mL).
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Results

These results along with previous findings from the Thangamani laboratory60 indicate that when C. albicans is grown ex vivo in gut homogenate extracts taken from the stomach, small intestines and large intestines of untreated control and antibiotic-treated mice, C. albicans generally develops with a yeast morphology (Figure 1B). However, when grown in the cecal extract from antibiotic-treated mice, C. albicans readily undergoes morphogenesis.......

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Discussion

The method described here presents a novel way to investigate the effect of antibiotic, dietary, xenobiotic and therapeutic impacts on C. albicans hyphal morphogenesis in the GI tract. Since the majority of systemic infections originate from the GI tract21,22,23,24,25,26,27,

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Disclosures

The authors have no competing financial interests or other conflicts of interest.

Acknowledgements

The authors acknowledge resources and support from Midwestern University Cellular and Molecular Core Research facility.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
1 - 10 µL Pipet TipsFisher Scientific02-707-454Misc
100 - 1000 µL Pipet TipsFisher Scientific02-707-400Misc
20 - 200 µL Pipet TipsFisher Scientific02-707-451Misc
2-methylbutyric acidSigma193070-25Ghyphal-inhibitory compound
488 goat anti-rabbit IgGInvitrogen (Fisher)A11008IF Staining secondary ab
AgarFisherBP1423-500YPD agar component
Automated Imaging MicroscopeKeyenceBZX700
Candida Albicans AntibodyInvitrogen (Fisher)PA1-27158IF Staining primary ab
cefoperazoneCayman16113antibiotic
deoxycholic acidSigma30960hyphal-inhibitory compound
D-GlucoseFisherD16-500hyphal-promoting compound
forcepsFisher08-885
lactic acidAlfa AesarAAAL13242-06hyphal-inhibitory compound
lithocholic acidSigmaL6250-10Ghyphal-inhibitory compound
palmitic acidSigmaP5585-10Ghyphal-inhibitory compound
ParaformaldehydeAlfa AesarA11313IF Staining fixative
Phosphate-buffered saline (PBS), 10xAlfa AesarJ62692PBS component
p-tolylacetic acidSCBTsc-257959hyphal-inhibitory compound
sebacic acidSigma283258-250Ghyphal-inhibitory compound
sharp ended scissorsFisher28301
sterile Milli-Q waterN/AN/AMisc
YPD BrothBD Biosciences242810YPD agar component

References

  1. Huffnagle, G. B., Noverr, M. C. The emerging world of the fungal microbiome. Trends in Microbiology. 21 (7), 334-341 (2013).
  2. Wisplinghoff, H., et al. Nosocomial bloodstream infections in US hospitals: analysis o....

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