Effects of human immunoglobulins on <i>Cryptococcus neoformans</i> morphology and proteome

<i>Cryptococcus neoformans</i> (Cn) is the main cause of fungal meningitis in people living with HIV. Perturbations in normal immunoglobulin (Ig) levels are observed in these individuals, but their association with Cn pathogenesis is unclear. Here, we investigated the physical and biological effects of normal (not elicited by known cryptococcal infection) human immunoglobulins (Igs), IgM, IgG, and IgA on Cn (strain H99). Each isotype affected the growth, surface morphology, and proteome of Cn. However, IgA had the most prominent effect. It induced growth inhibition after 24 h of co-culture with Cn, altered the structural organization of capsular fibers, and significantly reduced protein synthesis and proteins associated with intracellular glucuronoxylomannan (GXM) synthesis, such as those mediating transport of sugar precursors to Golgi and the cyclic AMP pathway. Together with prior data showing an association between reduced plasma IgA and HIV-associated cryptococcal meningitis (CM), our findings suggest that the influence of human IgA on Cn pathogenesis warrants further investigation.IMPORTANCECryptococcal meningitis (CM) causes approximately 1,200,000 deaths annually in people living with HIV and is also a threat to individuals with non-HIV-associated immune-compromising conditions, such as organ transplant recipients and other patients receiving immunosuppressants. Prior work has shown that normal human immunoglobulins (Igs) bind <i>Cryptococcus neoformans</i> (Cn) and that plasma levels of IgM, IgG, and IgA differ as a function of CM status. We investigated how human IgM, IgG, and IgA affect Cn growth, morphology, and protein synthesis. We found that IgA has major effects on these aspects of Cn biology and lends plausibility to the hypothesis that previously reported reductions in IgA levels in HIV-associated CM may influence Cn pathogenesis. Overall, our findings show that antibody immunity to Cn is more complex than previously thought.

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Journal
mBio
Published
2026-02-09
DOI
https://doi.org/10.1128/mbio.03827-25
Primary Topic
Fungal Infections and Studies
Type
article
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article

Effects of human immunoglobulins on Cryptococcus neoformans morphology and proteome

Joshua Daniel Nosanchuk, Antonio Nakouzi, Daniel Zamith‐Miranda, Haroldo César de Oliveira et al.
mBio
Fungal Infections and Studies
article

Effects of human immunoglobulins on Cryptococcus neoformans morphology and proteome

Joshua Daniel Nosanchuk, Antonio Nakouzi, Daniel Zamith‐Miranda, Haroldo César de Oliveira, Taiane Souza, M.H.Silla Santos, Marcio L. Rodrigues, Liise-Anne Pirofski
article en

Abstract

<i>Cryptococcus neoformans</i> (Cn) is the main cause of fungal meningitis in people living with HIV. Perturbations in normal immunoglobulin (Ig) levels are observed in these individuals, but their association with Cn pathogenesis is unclear. Here, we investigated the physical and biological effects of normal (not elicited by known cryptococcal infection) human immunoglobulins (Igs), IgM, IgG, and IgA on Cn (strain H99). Each isotype affected the growth, surface morphology, and proteome of Cn. However, IgA had the most prominent effect. It induced growth inhibition after 24 h of co-culture with Cn, altered the structural organization of capsular fibers, and significantly reduced protein synthesis and proteins associated with intracellular glucuronoxylomannan (GXM) synthesis, such as those mediating transport of sugar precursors to Golgi and the cyclic AMP pathway. Together with prior data showing an association between reduced plasma IgA and HIV-associated cryptococcal meningitis (CM), our findings suggest that the influence of human IgA on Cn pathogenesis warrants further investigation.IMPORTANCECryptococcal meningitis (CM) causes approximately 1,200,000 deaths annually in people living with HIV and is also a threat to individuals with non-HIV-associated immune-compromising conditions, such as organ transplant recipients and other patients receiving immunosuppressants. Prior work has shown that normal human immunoglobulins (Igs) bind <i>Cryptococcus neoformans</i> (Cn) and that plasma levels of IgM, IgG, and IgA differ as a function of CM status. We investigated how human IgM, IgG, and IgA affect Cn growth, morphology, and protein synthesis. We found that IgA has major effects on these aspects of Cn biology and lends plausibility to the hypothesis that previously reported reductions in IgA levels in HIV-associated CM may influence Cn pathogenesis. Overall, our findings show that antibody immunity to Cn is more complex than previously thought.

mBioVol. 17(3)
Universidade Federal do Rio de Janeiro (BR), Albert Einstein College of Medicine (US), Institut Pasteur de Montevideo (UY), Instituto de Investigaciones Biológicas Clemente Estable (UY), Fundação Oswaldo Cruz (BR), Universidade Federal de São Paulo (BR)
Good health and well-being
Openalex Percentile: Top 62%
Fungal Infections and Studies
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