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Updated: May 30, 2026

Visualizing Non-lytic Exocytosis of Cryptococcus neoformans from Macrophages Using Digital Light Microscopy
Published on: October 21, 2014
Dynamics of Cryptococcus neoformans-macrophage interactions reveal that fungal background influences outcome during
Alexandre Alanio1, Marie Desnos-Ollivier, Françoise Dromer
1Institut Pasteur, Molecular Mycology Unit, Paris, France.
Unlabelled:
Cryptococcosis is a multifaceted fungal infection with variable clinical presentation and outcome. As in many infectious diseases, this variability is commonly assigned to host factors. To investigate whether the diversity of Cryptococcus neoformans clinical (ClinCn) isolates influences the interaction with host cells and the clinical outcome, we developed and validated new quantitative assays using flow cytometry and J774 macrophages. The phenotype of ClinCn-macrophage interactions was determined for 54 ClinCn isolates recovered from cerebrospinal fluids (CSF) from 54 unrelated patients, based on phagocytic index (PI) and 2-h and 48-h intracellular proliferation indexes (IPH2 and IPH48, respectively). Their phenotypes were highly variable. Isolates harboring low PI/low IPH2 and high PI/high IPH2 values were associated with nonsterilization of CSF at week 2 and death at month 3, respectively. A subset of 9 ClinCn isolates with different phenotypes exhibited variable virulence in mice and displayed intramacrophagic expression levels of the LAC1, APP1, VAD1, IPC1, PLB1, and COX1 genes that were highly variable among the isolates and correlated with IPH48. Variation in the expression of virulence factors is thus shown here to depend on not only experimental conditions but also fungal background. These results suggest that, in addition to host factors, the patient's outcome can be related to fungal determinants. Deciphering the molecular events involved in C. neoformans fate inside host cells is crucial for our understanding of cryptococcosis pathogenesis.
Importance:
Cryptococcus neoformans is a life-threatening human fungal pathogen that is responsible for an estimated 1 million cases of meningitis/year, predominantly in HIV-infected patients. The diversity of infecting isolates is well established, as is the importance of the host factors. Interaction with macrophages is a major step in cryptococcosis pathogenesis. How the diversity of clinical isolates influences macrophages' interactions and impacts cryptococcosis outcome in humans remains to be elucidated. Using new assays, we uncovered how yeast-macrophage interactions were highly variable among clinical isolates and found an association between specific behaviors and cryptococcosis outcome. In addition, gene expression of some virulence factors and intracellular proliferation were correlated. While many studies have established that virulence factors can be differentially expressed as a function of experimental conditions, our study demonstrates that, under the same experimental conditions, clinical isolates behaved differently, a diversity that could participate in the variable outcome of infection in humans.
Insights
Cryptococcus neoformans clinical isolates show diverse interactions with host macrophages, influencing patient outcomes. Fungal genetic factors, not just host factors, contribute to cryptococcosis severity and treatment response.
Area of Science:
- Mycology
- Infectious Diseases
- Immunology
Background:
- Cryptococcosis, caused by Cryptococcus neoformans, presents with variable clinical outcomes.
- Host factors are traditionally considered the primary drivers of disease variability.
- Macrophage interaction is a critical step in cryptococcosis pathogenesis.
Purpose of the Study:
- To investigate if the diversity of clinical Cryptococcus neoformans isolates influences host cell interactions and clinical outcomes.
- To develop and validate quantitative assays for studying yeast-macrophage interactions.
- To correlate fungal isolate behavior with patient prognosis.
Main Methods:
- Developed and validated flow cytometry assays to quantify phagocytic index (PI) and intracellular proliferation (IPH2, IPH48).
- Phenotyped 54 clinical Cryptococcus neoformans isolates from cerebrospinal fluid.
- Analyzed intramacrophagic gene expression (LAC1, APP1, VAD1, IPC1, PLB1, COX1) in a subset of isolates.
Main Results:
- Significant variability in PI and IPH among clinical isolates was observed.
- Low PI/low IPH2 associated with non-sterilized CSF; high PI/high IPH2 associated with patient death.
- Intramacrophagic gene expression varied significantly among isolates and correlated with IPH48.
Conclusions:
- Fungal determinants, including variable virulence factor expression, contribute to the diverse outcomes in cryptococcosis.
- Beyond host factors, the intrinsic characteristics of Cryptococcus neoformans isolates play a role in disease progression.
- Understanding C. neoformans-host cell interactions is crucial for deciphering cryptococcosis pathogenesis.
Related Concept Videos
Cryptococcal Meningitis
Bacterial Meningitis II: Pathophysiology
Fungal Phylum Microsporidia

