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CARD9 Mutations in Patients with Invasive Fungal Infections
Gizem Guner Ozenen1, Enise Avci Durmusalioglu2, Durdugul Ayyildiz Emecen2
1Division of Infectious Diseases, Department of Pediatrics, Medical School of Ege University, Izmir, Turkey.
Insights
Genetic analysis revealed CARD9 mutations in 6.6% of Turkish children with invasive fungal infections. This study highlights a novel pediatric case of Pseudallescheria boydii infection linked to a CARD9 mutation.
Area of Science:
- Immunology
- Medical Genetics
Background:
- Caspase-recruitment domain 9 (CARD9) mutations are linked to increased susceptibility to invasive fungal infections, especially Candida species.
- Understanding CARD9's role is crucial for managing these infections.
Purpose of the Study:
- To investigate the spectrum of CARD9 gene mutations in Turkish individuals, particularly children, with invasive fungal infections.
- To identify genetic predispositions to fungal infections in the Turkish pediatric population.
Main Methods:
- Sequencing analysis of all 12 exons and exon-intron junctions of the CARD9 gene.
- Inclusion of 30 patients diagnosed with invasive fungal infection or chronic mucocutaneous candidiasis between 2020-2023.
- Collection and analysis of demographic and clinical data.
Main Results:
- A disease-causing CARD9 mutation was identified in 2 out of 30 patients (6.6%).
- Diagnoses included fungal endocarditis, chronic mucocutaneous candidiasis, CNS infections, and candidemia.
- One patient with a Pseudallescheria boydii brain abscess had a detected CARD9 mutation.
Conclusions:
- CARD9 mutations were found in 6.6% of pediatric patients with invasive fungal infections in Turkey.
- This study reports the first pediatric case of Pseudallescheria boydii infection associated with a CARD9 mutation.
- Genetic screening for CARD9 mutations may aid in diagnosing and managing invasive fungal infections.
Background:
Homozygous mutations in the Caspase-associated recruitment domain 9 (CARD9) gene increase susceptibility to invasive fungal infections, particularly those caused by Candida species. This study aims to assess the spectrum of CARD9 gene mutations that predispose individuals in the Turkish population, especially children, to invasive fungal infections.
Methods:
Our study included 30 patients who were admitted to Ege University due to invasive fungal infection or chronic mucocutaneous candidiasis between 2020 and 2023. Demographic and clinical data of the patients were recorded, and a sequence analysis of the CARD9 gene was performed.
Results:
The median age of the patients was 1.8 years (interquartile range [IQR]: 11.8). Diagnoses included fungal endocarditis (n = 8, 26.6%), chronic mucocutaneous candidiasis (n = 7,23.3%), central nervous system (CNS) infections (n = 6,20%), candidemia (n = 4,13.3%), fungus ball in the kidney (n = 2, 6.7%), endophthalmitis ( n = 1, 3.3%), concurrent CNS and intra-abdominal infection (n = 1, 3.3%), and concurrent CNS infection and endophthalmitis (n = 1, 3.3%). All 12 exons and exon-intron junctions of the CARD9 (NM_052813.5) gene that encodes the CARD9 protein were analyzed. A disease-causing variant was detected in 2 patients (6.6%). One patient had a Pseudallescheria boydii brain abscess, and the other had an invasive fungal infection confirmed histopathologically.
Conclusions:
Among the 30 patients with invasive fungal infections, a disease-causing CARD9 mutation was identified in 2 (6.6%) patients. While CARD9 mutations are known to be associated with invasive candidiasis, this study reports the first pediatric case of P. boydii infection associated with a CARD9 mutation.
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