Red/Orange Autofluorescence in Selected Candida Strains Exposed to 405 nm Laser Light

Author:

Wiench Rafał1ORCID,Paliga Dariusz2,Mertas Anna3ORCID,Bobela Elżbieta3ORCID,Kuśka-Kiełbratowska Anna1ORCID,Bordin-Aykroyd Sonia4ORCID,Kawczyk-Krupka Aleksandra5ORCID,Grzech-Leśniak Kinga67ORCID,Lukomska-Szymanska Monika8ORCID,Lynch Edward4,Skaba Dariusz1ORCID

Affiliation:

1. Department of Periodontal Diseases and Oral Mucosa Diseases, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland

2. Dental Office Reanata and Dariusz Paliga, Aleja Niepodległości 3/lok 2, 35-303 Rzeszów, Poland

3. Department of Microbiology and Immunology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland

4. Photomedicine, Leicester School of Pharmacy, De Montfort University, The Gateway, Leicester LE1 9BH, UK

5. Department of Internal Diseases, Angiology and Physical Medicine, Center for Laser Diagnostics and Therapy, Medical University of Silesia in Katowice, 41-902 Bytom, Poland

6. Laser Laboratory, Dental Surgery Department, Wroclaw Medical University, 50-425 Wroclaw, Poland

7. Department of Periodontics, School of Dentistry, Virginia Commonwealth University, Richmond, VA 23284, USA

8. Department of General Dentistry, Medical University of Lodz, 251 Pomorska St., 92-213 Lodz, Poland

Abstract

Background: Candida albicans and similar species are significant pathogens in immunocompromised and hospitalized individuals, known for mucosal colonization and bloodstream/organ invasion. Many pathogenic fungi, including these species, exhibit autofluorescence (R/OF) under specific light conditions, a feature crucial for their detection. Aim: We investigated the use of a 405 nm diode laser for the direct observation of red/orange autofluorescence of Candida spp., common in the oral cavity, exploring its potential in health screenings. Methods: This study utilized cultures of Candida spp. on Sabouraud dextrose agar with Qdot 655 and 685 for fluorescence benchmarking, illuminated using a 405 nm diode laser (continuous wave, power 250 mW, 0.0425 J/cm² fluence, 0.0014 W/cm² power density). Images were captured using a yellow-filter camera at set intervals (48 to 144 h). Visual and computational analyses evaluated the R/OF in terms of presence, intensity, coloration, and intra-colony variation. Results: Most Candida strains displayed red/orange autofluorescence at all observation times, characterized by varied coloration and intra-colony distribution. Initially, there was an increase in R/OF intensity, which then stabilized in the later stages of observation. Conclusions: The majority of the Candida strains tested are capable of emitting R/OF under 405 nm laser light. This finding opens up new possibilities for integrating R/OF detection into routine dental screenings for Candida spp.

Publisher

MDPI AG

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