# Dysbiosis of the Gut–Lung Axis and Its Immune Correlates During Pulmonary Cryptococcus neoformans Infection

**Authors:** Jing Fan, Shujun Liu, Huijiao Zhang, Changzhong Jin, Nanping Wu

PMC · DOI: 10.3390/jof12030163 · 2026-02-25

## TL;DR

This study shows that infection with Cryptococcus neoformans disrupts the gut and lung microbiomes, linking these changes to immune responses and suggesting microbiome-based treatments.

## Contribution

The study reveals the coordinated dysbiosis of the gut–lung axis and its immune correlates during cryptococcosis in a mouse model.

## Key findings

- Pulmonary infection caused dysbiosis in both lung and gut microbiota, with reduced beneficial microbes and increased pathogens.
- Lung dysbiosis correlated with IL-17-driven inflammation, while gut dysbiosis linked to systemic immune activation in the spleen.
- Microbial metabolic pathways were disrupted, and lung and gut dysbiosis were positively correlated during infection.

## Abstract

Cryptococcus neoformans is a major fungal pathogen responsible for life-threatening meningitis, especially in immunocompromised individuals. Although the gut–lung axis is known to regulate immune responses in respiratory infections, its role in cryptococcosis remains unclear. This study aimed to define the dynamic changes in the gut and lung microbiota and their relationship with host immunity during C. neoformans infection. Using a mouse model, we found that pulmonary infection induced significant dysbiosis in both the lung and gut microbiota, marked by decreased beneficial commensals and increased opportunistic pathogens. Integrated analysis showed these microbial shifts were closely associated with distinct immune responses: lung dysbiosis correlated with a strong IL-17-mediated pulmonary inflammatory response, while gut dysbiosis was linked to systemic immune activation in the spleen. Functional metagenomic prediction further revealed widespread disruption in microbial metabolic pathways, including energy metabolism and biosynthesis, in both sites. Importantly, a positive correlation was observed between lung and gut dysbiosis, indicating an interconnected gut–lung axis during cryptococcosis. These findings demonstrate that C. neoformans infection causes coordinated disruptions in microbiota and immunity across the gut–lung axis, underscoring the microbiome as a critical modulator of host response and suggesting potential avenues for microbiome-targeted therapies.

## Linked entities

- **Diseases:** meningitis (MONDO:0021108), cryptococcosis (MONDO:0005724)
- **Species:** Cryptococcus neoformans (taxon 5207), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cd19 (CD19 antigen) [NCBI Gene 12478], Adgre1 (adhesion G protein-coupled receptor E1) [NCBI Gene 13733] {aka DD7A5-7, EGF-TM7, Emr1, F4/80, Gpf480, Ly71}, Ly6g (lymphocyte antigen 6 family member G) [NCBI Gene 546644] {aka Gr-1, Gr1, Ly-6G}, Itgax (integrin alpha X) [NCBI Gene 16411] {aka Cd11c, Cr4, N418}, Klrb1c (killer cell lectin-like receptor subfamily B member 1C) [NCBI Gene 17059] {aka CD161, Klrb1b, Ly-59, Ly55c, Ly59, NK-RP1}, Fcr (Fc receptor) [NCBI Gene 109615], Cd8a (CD8 subunit alpha) [NCBI Gene 12525] {aka Ly-2, Ly-35, Ly-B, Lyt-2}, Itgam (integrin alpha M) [NCBI Gene 16409] {aka CD11b/CD18, CR3, CR3A, Cd11b, F730045J24Rik, Ly-40}, Tcrb (T cell receptor beta chain) [NCBI Gene 21577] {aka TCRbeta, Tib}, Dnase1 (deoxyribonuclease I) [NCBI Gene 13419] {aka DNaseI, Dnl1}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Ptprc (protein tyrosine phosphatase receptor type C) [NCBI Gene 19264] {aka B220, CD45R, Cd45, L-CA, Ly-5, Lyt-4}, Nos2 (nitric oxide synthase 2, inducible) [NCBI Gene 18126] {aka MAC-NOS, NOS-II, Nos-2, Nos2a, i-NOS, iNOS}, Arg1 (arginase, liver) [NCBI Gene 11846] {aka AI, Arg-1, PGIF}
- **Diseases:** Infection (MESH:D007239), pulmonary infection (MESH:D012141), injury to (MESH:D014947), dislocation (MESH:D004204), meningoencephalitis (MESH:D008590), weight loss (MESH:D015431), pulmonary inflammation (MESH:D011014), deaths (MESH:D003643), tissue damage (MESH:D017695), meningitis (MESH:D008580), fungal (MESH:D009181), anorexia (MESH:D000855), cryptococcal (MESH:D016919), necrosis (MESH:D009336), Dysbiosis (MESH:D064806), C. neoformans Infection (MESH:D003453), granulomatous inflammation (MESH:D007249), impairment of gut homeostasis (MESH:C535334), granuloma (MESH:D006099), pulmonary inflammatory (MESH:D016726), gut (MESH:C536735), immunodeficiency (MESH:D007153)
- **Chemicals:** L-serine (MESH:D012694), sulfate (MESH:D013431), NAD (MESH:D009243), Chemicals (-), paraffin (MESH:D010232), tribromoethanol (MESH:C062527), coenzyme A (MESH:D003065), hydrogen sulfide (MESH:D006862), chloramphenicol (MESH:D002701), amino acids (MESH:D000596), PBS (MESH:D007854), fucose (MESH:D005643), purines (MESH:D011687), ethanol (MESH:D000431), carbon (MESH:D002244), lactate (MESH:D019344), paraformaldehyde (MESH:C003043), equol (MESH:D060754), fluconazole (MESH:D015725), L-tryptophan (MESH:D014364), dextrose (MESH:D005947), nitrogen (MESH:D009584), agar (MESH:D000362), butyrate (MESH:D002087), SCFA (MESH:D005232), rhamnose (MESH:D012210), TCA (MESH:D014238), glycine (MESH:D005998)
- **Species:** Bacillota (clostridial firmicutes, phylum) [taxon 1239], Staphylococcus aureus (species) [taxon 1280], Bifidobacterium (genus) [taxon 1678], Mus musculus (house mouse, species) [taxon 10090], Desulfovibrionaceae (family) [taxon 194924], Helicobacter (genus) [taxon 209], Adlercreutzia (genus) [taxon 447020], gut metagenome (species) [taxon 749906], Dubosiella (genus) [taxon 1937008], Lactobacillus (genus) [taxon 1578], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Rhizobium (genus) [taxon 379], Hyphomicrobium sp. 99 (species) [taxon 1163419], Escherichia coli (E. coli, species) [taxon 562], Homo sapiens (human, species) [taxon 9606], Streptococcus (genus) [taxon 1301], Acidovorax (genus) [taxon 12916], Cryptococcus neoformans (Cryptococcus neoformans serotype A, species) [taxon 5207], Shigella (genus) [taxon 620], Prevotella (genus) [taxon 838]
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027605/full.md

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Source: https://tomesphere.com/paper/PMC13027605