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Real-time visualization of phagosomal pH manipulation by Cryptococcus neoformans in an immune signal-dependent way

Emmanuel J. Santiago-Burgos, Peter V. Stuckey, Felipe H. Santiago-Tirado
doi: https://doi.org/10.1101/2022.09.08.507177
Emmanuel J. Santiago-Burgos
1Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA
4Imanis Life Sciences, LLC, Rochester, MN, USA
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Peter V. Stuckey
1Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA
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Felipe H. Santiago-Tirado
1Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA
2Eck Institute for Global Health, University of Notre Dame, Notre Dame, IN, USA
3Warren Center for Drug Discovery, University of Notre Dame, Notre Dame, IN, USA
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  • For correspondence: fsantiago@nd.edu
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Abstract

Understanding of how intracellular pathogens survive in their host cells is important to improve management of their diseases. This has been fruitful for intracellular bacteria but it is an understudied area in fungal pathogens. Here we start elucidating and characterizing the strategies used by one of the commonest fungal pathogens, Cryptococcus neoformans, to survive intracellularly. The ability of the fungus to survive inside host cells is one of the main drivers of disease progression, yet it is unclear whether C. neoformans resides in a fully acidified, partially acidic, or neutral phagosome. Using a dye that only fluoresce under acidic conditions to stain C. neoformans, a hypha-defective Candida albicans mutant, and the nonpathogenic Saccharomyces cerevisiae, we characterized the fungal behaviors in infected macrophages by live microscopy. The main behavior in the C. albicans mutant strain and S. cerevisiae-phagosomes was rapid acidification after internalization, which remained for the duration of the imaging. In contrast, a significant number of C. neoformans-phagosomes exhibited alternative behaviors distinct from the normal phagosomal maturation: some phagosomes acidified with subsequent loss of acidification, and other phagosomes never acidified. Moreover, the frequency of these behaviors was affected by the immune status of the host cell. We applied the same technique to a flow cytometry analysis and found that a substantial percentage of C. neoformans-phagosomes showed impaired acidification, whereas almost 100% of the S. cerevisiae-phagosomes acidify. Lastly, using a membrane-damage reporter, we show phagosome permeabilization correlates with acidification alterations, but it is not the only strategy that C. neoformans uses to manipulate phagosomal acidification. The different behaviors described here provide an explanation to the confounding literature regarding cryptococcal-phagosome acidification and the methods can be applied to study other intracellular fungal pathogens.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted September 08, 2022.
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Real-time visualization of phagosomal pH manipulation by Cryptococcus neoformans in an immune signal-dependent way
Emmanuel J. Santiago-Burgos, Peter V. Stuckey, Felipe H. Santiago-Tirado
bioRxiv 2022.09.08.507177; doi: https://doi.org/10.1101/2022.09.08.507177
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Real-time visualization of phagosomal pH manipulation by Cryptococcus neoformans in an immune signal-dependent way
Emmanuel J. Santiago-Burgos, Peter V. Stuckey, Felipe H. Santiago-Tirado
bioRxiv 2022.09.08.507177; doi: https://doi.org/10.1101/2022.09.08.507177

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