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Deep Dermal Injection As a Model of Candida albicans Skin Infection for Histological Analyses
Published on: June 13, 2018
Cell aggregation mediated by ACE2 deletion in Candida auris modulates fungal colonization and host immune responses
Abishek Balakumar1, Abigail Cox1, Shankar Thangamani1,2
1Department of Comparative Pathobiology, College of Veterinary Medicine, Purdue University, West Lafayette, Indiana, USA.
Abstract:
Candida auris is an emerging multi-drug-resistant fungal pathogen that colonizes the skin and causes invasive infections in hospitalized patients. Multi-cellular aggregative phenotype is widely reported in the C. auris isolates, but its role in skin colonization and host immune response is not yet known. In this study, we generated aggregative phenotype by deleting the ACE2 gene in C. auris and determined the fungal colonization and host immune response using an intradermal mouse model of C. auris skin infection. Our results indicate that mice infected with ace2Δ strain had significantly lower fungal load after 3 and 14 days post-infections compared to the non-aggregative wild-type and the ACE2 reintegrated strain. The colonization of ace2Δ is associated with increased recruitment of CD11b+ Ly6G+ neutrophils and decreased accumulation of CD11b+ Ly6 Chi inflammatory monocytes and CD11b+ MHCII+ CD64+ macrophages. Furthermore, Th17 cells and type 3 innate lymphoid cells (ILCs) were significantly increased in the skin tissue of ace2Δ infected mice. Our findings suggest that aggregative phenotype mediated by ACE2 deletion in C. auris induces potent neutrophil and IL-17-mediated immune response and reduces fungal colonization in the skin.IMPORTANCEC. auris is a rapidly emerging fungal pathogen that can colonize hospitalized patients, especially in skin tissue, and cause invasive infections. C. auris isolates exhibit morphological heterogeneity, and the multicellular aggregative phenotype of C. auris is reported frequently in clinical settings. Understanding the role of fungal morphotypes in colonization, persistence, and immune response in the skin microenvironment will have potential applications in clinical diagnosis and novel preventive and therapeutic measures. Here, we utilized the murine model of intradermal infection and determined that the aggregative phenotype of C. auris as the result of ACE2 gene deletion elicits potential innate and adaptive immune responses in mice. These observations will help explain the differences in the skin colonization and immune responses of the aggregative morphotype of C. auris and open the door to developing novel antifungal therapeutics.
Insights
Candida auris aggregative phenotype, generated by ACE2 deletion, reduces fungal skin colonization. This phenotype enhances neutrophil and IL-17 immune responses, offering insights into antifungal strategies.
Area of Science:
- Mycology
- Immunology
- Infectious Diseases
Background:
- Candida auris is a multi-drug-resistant fungus causing invasive infections.
- The role of its aggregative phenotype in skin colonization and immune response is unknown.
Purpose of the Study:
- To investigate the role of the aggregative phenotype in Candida auris skin colonization and host immune response.
- To determine the impact of ACE2 gene deletion on fungal load and immune cell recruitment.
Main Methods:
- Generated aggregative phenotype by deleting the ACE2 gene in Candida auris.
- Utilized an intradermal mouse model for skin infection studies.
- Analyzed fungal load and host immune cell populations (neutrophils, monocytes, macrophages, Th17, ILCs).
Main Results:
- Mice infected with the ace2Δ strain showed significantly lower fungal loads.
- The aggregative strain induced increased neutrophils and Th17/ILC cells.
- Reduced accumulation of inflammatory monocytes and macrophages was observed with the aggregative strain.
Conclusions:
- The aggregative phenotype of Candida auris, mediated by ACE2 deletion, reduces fungal colonization in the skin.
- This phenotype elicits a potent neutrophil and IL-17-mediated immune response.
- Findings contribute to understanding fungal morphotypes and developing new antifungal therapies.

