# The pathogenicity and future treatment strategies of Candida albicans

**Authors:** Jiadi Wu, Chenyang Jiang, Hui Wang, Tongbin Chen, Xi Chen, Wenyue Da

PMC · DOI: 10.3389/fcimb.2026.1752304 · Frontiers in Cellular and Infection Microbiology · 2026-02-19

## TL;DR

This review explores how Candida albicans causes disease and suggests new treatment strategies to improve patient outcomes.

## Contribution

The paper provides a comprehensive overview of C. albicans pathogenicity and novel therapeutic approaches.

## Key findings

- C. albicans pathogenicity involves colonization, morphological transformation, and biofilm formation.
- Novel therapies include probiotics, antimicrobial peptides, and combination treatments with traditional antifungals.

## Abstract

Candida albicans (C. albicans) is a major pathogenic fungus that severely impacts on human health. This review systematically elaborates on the key pathogenic processes of C. albicans, starting with its colonization, morphological transformation and biofilm formation under different carbon sources. The interaction between C. albicans and host immunity, including the role of PRRs, host genetics and immune polymorphisms, and trained immunity. Candidalysin regulating cAMP/PKA signaling pathway of C. albicans hyphae-biofilm transformation, the interaction between C. albicans and bacteria, as well as mucosal and invasive C. albicans infections, persister cells in anti-C. albicans therapy, emerging biology and pathogenicity aspects, epigenetic and chromatin regulation of host-drug adaptation, and strain-specific heterogeneity in pathogenicity, biofilm traits and drug susceptibility. Additionally, it summarizes novel therapeutic strategies, emphasizing probiotics and antimicrobial peptides (AMPs), and combination strategies with novel targeted therapy and traditional anti-fungal therapy to improve the survival of patients with Candida albicans infection. It systematically and comprehensively summarizes the pathogenicity of C. albicans and the possible therapeutic targets, providing new ideas for the development of novel antifungal drugs in the future.

## Linked entities

- **Species:** Candida albicans (taxon 5476)

## Full-text entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}
- **Diseases:** critically ill (MESH:D016638), inflammation (MESH:D007249), liver diseases (MESH:D008107), systemic infection (MESH:D012141), pain (MESH:D010146), cancer (MESH:D009369), dysbiosis (MESH:D064806), denture stomatitis (MESH:D013282), candidemia (MESH:D058387), head and neck cancer (MESH:D006258), neurological diseases (MESH:D020271), hypoxic (MESH:D002534), oral diseases (MESH:D009059), tumorigenesis (MESH:D063646), hematological malignancies (MESH:D019337), osteoarticular infections (MESH:D014394), hypoxia (MESH:D000860), Clostridiodes difficile infection (MESH:D003015), nosocomial infections (MESH:D003428), neutrophil aggregation (MESH:C564275), CLRs (OMIM:211750), colitis (MESH:D003092), alcoholic hepatitis (MESH:D006519), immune (MESH:D007154), biofilm infection (MESH:D007239), Crohn's disease (MESH:D003424), allergic bronchopulmonary aspergillosis (MESH:D001229), CARD9 deficiency (MESH:C537979), weight loss (MESH:D015431), RVVC (MESH:D002181), cytotoxicity (MESH:D064420), endogenous endophthalmitis (MESH:D009877), CMC (MESH:D002179), gynecological disease (MESH:D005831), inflammatory bowel diseases (MESH:D015212), mucositis (MESH:D052016), IBS (MESH:D043183), vaginal candidiasis (MESH:D014627), C. albicans infection (MESH:D002177), hepatic injury (MESH:D056486), fungal (MESH:D009181), central nervous system infections (MESH:D002494), invasive (MESH:D009361), Candida bloodstream infection (MESH:D018805), aneuploidy (MESH:D000782), ulcerative colitis (MESH:D003093), tissue damage (MESH:D017695)
- **Chemicals:** Sodium New Houttuyfonate (MESH:C556396), methionine (MESH:D008715), pyruvate (MESH:D019289), Metal (MESH:D008670), zinc (MESH:D015032), oxygen (MESH:D010100), AMPs (MESH:D000089882), nitrogen (MESH:D009584), carboxylic acids (MESH:D002264), PG (MESH:D011453), lactate (MESH:D019344), polysaccharide (MESH:D011134), pentose phosphate (MESH:D010428), glucan (MESH:D005936), tricarboxylic acid (MESH:D014233), carbon (MESH:D002244), agar (MESH:D000362), chitin (MESH:D002686), beta-1,3 glucan (MESH:C033363), Azoles (MESH:D001393), Taurocholic acid (MESH:D013656), Iron (MESH:D007501), glycogen (MESH:D006003), acetyl coenzyme A (MESH:D000105), mannan (MESH:D008351), tunicamycin (MESH:D014415), Echinocandins (MESH:D054714), copper (MESH:D003300), Cyclic adenosine monophosphate (MESH:D000242), galactose (MESH:D005690), voriconazole (MESH:D065819), ethanol (MESH:D000431), bile acid (MESH:D001647), maltose (MESH:D008320), Als3p (-), Glycerol (MESH:D005990), GAG (MESH:D006025), sugar alcohols (MESH:D013402), heme (MESH:D006418), amino acid (MESH:D000596), proanthocyanidins (MESH:D044945), ergosterol (MESH:D004875), NADPH (MESH:D009249), amphotericin B (MESH:D000666), isavuconazole (MESH:C508735), rhamnose (MESH:D012210), beta-1,6 glucan (MESH:C064197), fatty acid (MESH:D005227), N-acetylglucosamine (MESH:D000117), carbohydrates (MESH:D002241), CoA (MESH:D003065), TCA (MESH:D014238), itraconazole (MESH:D017964), Polyenes (MESH:D011090), CO2 (MESH:D002245), Glutathione (MESH:D005978), DSS (MESH:D016264), fluconazole (MESH:D015725), fructose (MESH:D005632), arabinose (MESH:D001089)
- **Species:** Candida albicans (species) [taxon 5476], Aspergillus fumigatus (species) [taxon 746128], Candida tropicalis (species) [taxon 5482], Escherichia coli (E. coli, species) [taxon 562], Mus musculus (house mouse, species) [taxon 10090], Nakaseomyces glabratus (species) [taxon 5478], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Candidozyma auris (species) [taxon 498019], Enterococcus faecalis (species) [taxon 1351], Enterococcus (genus) [taxon 1350], Bacteroides thetaiotaomicron (species) [taxon 818], Galleria mellonella (greater wax moth, species) [taxon 7137], Penicillium (genus) [taxon 5073], Akkermansia muciniphila (species) [taxon 239935], Lodderomyces parapsilosis (species) [taxon 5480], Human immunodeficiency virus (species) [taxon 12721], Lactobacillus johnsonii (species) [taxon 33959], Rattus norvegicus (brown rat, species) [taxon 10116], Proteus mirabilis (species) [taxon 584], Homo sapiens (human, species) [taxon 9606], Faecalibacterium prausnitzii (species) [taxon 853], Bifidobacterium (genus) [taxon 1678], Clostridium (genus) [taxon 1485], Musca domestica (house fly, species) [taxon 7370], Metschnikowia (genus) [taxon 27320], Erysipelothrix sp. CE1 (species) [taxon 1856602], Bacillus (genus) [taxon 55087], Lactobacillus crispatus (species) [taxon 47770]
- **Mutations:** serine/threonine, Y238X

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960541/full.md

## References

201 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960541/full.md

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Source: https://tomesphere.com/paper/PMC12960541