Evaluation of APR1 Gene Expression in Candida albicans Strains Isolated From Patients With Multiple Sclerosis

Shahla Amri Saroukolaei1, Mojdeh Ghabaee2, Hojjatollah Shokri3

  • 1Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, University of Putra Malaysia, Selangor, Malaysia.

Abstract

Insights

Candida albicans APR1 gene expression is lower in multiple sclerosis (MS) patients compared to controls. This altered gene expression in MS patients may influence invasive candidiasis and disease progression.

Area of Science:

  • Medical Mycology
  • Neuroimmunology
  • Molecular Biology

Background:

  • The APR1 gene encodes intracellular aspartic proteinase A, crucial in Candida albicans systemic infections.
  • Candida albicans is implicated in opportunistic infections, particularly in immunocompromised individuals.

Purpose of the Study:

  • To investigate the expression levels of the APR1 gene in Candida albicans isolates from multiple sclerosis (MS) patients.
  • To compare APR1 gene expression between C. albicans strains from MS patients and healthy controls.

Main Methods:

  • C. albicans isolates were obtained from 135 MS patients and 100 healthy controls.
  • Isolates were cultured on sabouraud dextrose agar (SDA).
  • APR1 gene expression was quantified using reverse transcriptase-polymerase chain reaction (RT-PCR).

Main Results:

  • APR1 gene expression was significantly lower in C. albicans strains from MS patients (0.5208 ± 0.11518) compared to controls (0.7603 ± 0.11405) (P = 0.000).
  • A significant correlation was observed between APR1 gene expression and patient age and Expanded Disability Status Scale (EDSS) scores in MS patients (P = 0.000).
  • EDSS scores decreased after antifungal treatment (1.6074 ± 0.1081) compared to before treatment (2.2519 ± 0.1323) (P = 0.000).

Conclusions:

  • Lower APR1 gene expression in C. albicans from MS patients suggests a potential role in invasive candidiasis.
  • APR1 gene expression may be linked to the progression of multiple sclerosis.
  • Further research is warranted to elucidate the precise mechanisms.

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