1. Background
Dermatophytosis, one of the most common infectious diseases in the world, can be caused by dermatophyte fungal species of the genera Trichophyton, Microsporum and Epidermophyton. Onychomycosis is a fungal infection of the nails, which may be caused by many types of fungi, other dermatophytes or yeast species (1). Treatment of onychomycosis is a challenge and infections are typically more severe and difficult to treat in toenails than in fingernails (1). Optimal treatment of onychomycosis is extensively discussed. Treatment requires long-term therapy with oral antifungal medication (with the cure rates ranging from 48% to 76%) which may have side effects, and/or topical agents such as ciclopirox (34% cure rate) (2, 3). Oral therapies (terbinafine, itraconazole) provide access to the nail bed and matrix and are also used to treat concomitant skin infections such as tinea pedis. To prevent side effects prior to and periodically during oral therapy, liver function should be controlled. The newer imidazoles may lead to a higher cure rate (4), but these drugs are considerably more expensive than routine treatments. Topical therapies are associated with low rates of adverse events and mild localized reactions at the application site, but due to inadequate penetration, especially when the nails are thick, their efficacy is limited.
UV radiation induces DNA damage leading to inactivation of the pathogenic fungus commonly measured by viability count. UV-A with long wavelength (315 - 400 nm) rays has a slow effect on the skin and is poorly absorbed by the ozone layer. This ray is 1,000 times more common than UV-B with the middle-range of 290 - 320 nm that causes visible damage, commonly observed as redness and blistering and are a major cause of sunburn and skin cancer (5). UV-C with wavelengths less than 290 nm (100 - 280 nm) is the shortest and has the highest UV energy. It is filtered by the ozone layer; these wavelengths do not reach the earth surface and do not penetrate the atmosphere. Its rays are the most powerful, and do not damage human skin. UV-A radiation can penetrate glass and clouds. Thus, people are exposed to large doses of UV-A throughout their life, but UV-B rays do not penetrate glass (5). High doses of UV-A and UV-B radiation have significant inhibitory effects on dermatophytes (6). The antibacterial activity of UV-C radiation reduces the number of bacteria on environmental surfaces and vegetative bacteria including Mycobacterium tuberculosis, viruses and fungi (7, 8).
2. Objectives
The current study aimed to investigate the fungicidal effect of UV radiation on the growth of dermatophytes isolated from nails, considering the low efficacy of current treatment options and ease of exposing nails to UV light.
3. Patients and Methods
The sample comprised all the patients referred to the dermatology clinic (Shahid Faghihi hospital, Shiraz University of Medical Sciences, Iran) with suspected onychomycosis. The inclusion criteria were clinical manifestations such as distal or proximal sub ungula onychomycosis, white superficial onychomycosis, pitting, paronychia, onycholysis and nail plate discoloration. All diagnoses were confirmed by the mycology laboratory of Shahid Faghihi Hospital, Shiraz University of Medical Sciences, Iran. Since this procedure was part of the patients’ usual treatment protocol, informed consent for research purposes was not specifically sought. Fragments of nail plate and nail bed scrapes were inoculated onto Sabouraud dextrose agar (SDA) (Merck, Germany) with the antimicrobials cycloheximide (Sigma-Aldrich, Germany) and chloramphenicol (Merck, Germany) (9), and incubated at 30°C for 14 days. Isolated species were identified by macroscopic examination of colony morphology (size, color of the colonies from the top and bottom of the plate, and growth rate). Microscopic examinations were performed to identify dermatophyte species using lacto phenol-cotton blue and diagnostic methods such as growth on trichophyton agar media (Quelab, UK) and rice, and hair perforation test were performed to identify (9).
To determine the influence of different doses of UV light on the fungicidal effect, colony count and size, and growth rate of the isolated fungi were evaluated under laboratory conditions. Two strains of Trichophyton mentagrophytes and two strains of T. rubrum were isolated from the patients and used in the current study. Trichophyton rubrum type 1 was white and had fluffy colony with pink to burgundy on reverse. Type 2 was granular with powdery-velvet, radially folded and pale brown in color and the reverse was dark tan. T. mentagrophyte type 1 was downy, floccose and white in color with the fade yellow on reverse. Finally, type 2 was coarsely granular and light buff in color with the buff-tan color on reverse.
As in the skin samples from patients, only mycelium can be observed, in the current study mycelial colonies were harvested, suspended in Sabouraud dextrose broth (SDB) (Merck, Germany) and dispersed to small part suspensions using a sonic dismembrator (Dr. Hielscher GmbH, Stahnsdorf, Germany). Cell densities of the suspensions were counted in a Neubauer hemocytometer (Hausser Scientific, Horsham, PA, USA), and reached 105 pieces/mL. Fifty µL of suspension was inoculated onto SDA to observe macroscopic and microscopic colony characteristics. In each test, a 10 mL aliquot of the dermatophyte suspension was inoculated onto a petri dish. UV-A and UV-B lights were supplied by a Waldmann UV801KL apparatus (Waldmann, Villingen-Schwenningen, Germany) at 470 W, and UV-C light was supplied by an F30T8/GL apparatus (Young deungpo-Gu, Seoul, South Korea) at 30 W. Five different doses of UV light were used: UV-A (315 - 400) 3, 6, 9, 12, 15 J/cm2, UV-B (280 - 315) 0.5, 1, 1.5, 2, 2.5 J/cm2 and UV-C (100 - 280) 0.3, 0.6, 0.9, 1.2, 1.5 J/cm2. One positive control without exposure to UV light was cultured in each round with the test samples. The distance between the UV light source and the sample was 30 cm. This distance is widely used in dental and cosmetic fields to sterilize tools (10). In the current study, for UV-A and UV-B radiation, the lamps were utilized in the centers for dermatological diseases in order to obtain some practical implications.
Since radiation reduces the volume and raises the count because of evaporation, which may lead to errors, the specimen volumes were made up to the primary volume (10 mL) after irradiation, with SDB. For each irradiated specimen, the fungicidal effect of UV was evaluated by preparing five cultures to incubate at 30°C under laboratory conditions; therefore, 75 cultures for each fungus were prepared. Colony size, morphology and count, and growth rate of all isolates were checked in the plates every two days and mean values were calculated. Since most colony growth occurs during the first 14 days, the results were graphed after this period. All statistical analyses were conducted using Microsoft Excel software.The current research conformed to the Helsinki Declaration and local legislation, and was approved by the local ethics committee (91-5) in Clinical Microbiology Research Center, Shiraz University of Medical Sciences.
4. Results
In response to the UV treatments, compared with suspension control without irradiation, colony morphology for each dermatophyte remained unchanged, but colony count and size changed depending on the species and type of isolate. Of the two T. rubrum isolates (Figure 1), type 1 was less sensitive to UV-A and UV-C, and more sensitive to UV-B. Continuous irradiation with the UV-A and UV-B doses used in the study did not completely suppress the growth of the isolates, but higher intensities of UV-C light inhibited the growth of T. rubrum.
Mean colony counts at different intensities UV-A (315-400 nm), UV-B (290-320 nm) and UV-C (100-280nm).
Of the two T. mentagrophytes isolates (Figure 2), colony count in type 1 decreased as the dose of all three types of UV radiation increased. However, colony count in T. mentagrophytes type 2 showed different patterns as the dose of UV radiation increased. Type 2 strain was slightly responsive to UV-Abut compared to control cultures; there was no significant effect on colony count. Neither UV-B nor UV-C decreased the type 2 colony counts at low doses, but higher doses led to decreases in colony counts.
Mean colony counts at different intensities of UV-A (315-400 nm), UV-B (290-320 nm) and UV-C (100-280 nm).
According to Table 1, UV-A irradiation led to a slight increase in colony size in the four strains except T. mentagrophytes type 1, in which colony size increased with the lowest dose of irradiation and significantly decreased with increasing the doses. Irradiation with UV-B increased colony size in T. mentagrophytes type 2, but in type 1 UV ray increased colony size at the lowest dose and decreased colony size with increasing doses. UV-B irradiation decreased colony size in T. rubrum type 2 but had no significant effect on type 1 or either of the two strains of T. mentagrophytes. Irradiation with UV-C decreased colony size except for T. mentagrophytes type 2, in which higher doses increased colony size.
| UV light b | Trichophyton mentagrophyte 1 | T. mentagrophyte 2 | T. rubrum 1 | T. rubrum 2 |
|---|---|---|---|---|
| UVA 0 | 14 ± 1.1 | 13 ± 1.1 | 12 ± 1.1 | 23 ± 2 |
| UVA 3 | 20 ± 1.5 | 13 ± 1.1 | 13 ± 1.1 | 23 ± 1.9 |
| UVA 6 | 20 ± 1.6 | 13 ± 1.1 | 13 ± 1.1 | 23 ± 2 |
| UVA 9 | 7 ± 0.8 | 14 ± 1.1 | 13 ± 1.1 | 26 ± 2 |
| UVA 12 | 4 ± 0.5 | 15 ± 1.2 | 13 ± 1.1 | 26 ± 1.9 |
| UVA 15 | 3 ± 0.5 | 15 ± 1.2 | 13 ± 1.1 | 26 ± 1.9 |
| UVB 0 | 14 ± 1.1 | 13 ± 1.1 | 12 ± 1.1 | 23 ± 1.8 |
| UVB 0.5 | 22 ± 1.6 | 16 ± 1.2 | 13 ± 1.1 | 17 ± 1.3 |
| UVB 1 | 20 ± 1.6 | 16 ± 1.2 | 13 ± 1.1 | 16 ± 1.3 |
| UVB 1.5 | 9 ± 1 | 20 ± 1.9 | 12 ± 1.1 | 10 ± 1.0 |
| UVB 2 | 6 ± 0.5 | 20 ± 1.9 | 12 ± 1.1 | 10 ± 1.0 |
| UVB 2.5 | 5 ± 0.5 | 20 ± 2 | 11 ± 1.1 | 8 ± 0.9 |
| UVC 0 | 14 ± 1.1 | 13 ± 1.1 | 12 ± 1.1 | 23 ± 2 |
| UVC 0.3 | 12 ± 1.1 | 9 ± 0.9 | 8 ± 0.9 | 20 ± 1.9 |
| UVC 0.6 | 11 ± 1.0 | 9 ± 0.9 | 8 ± 0.9 | 20 ± 1.9 |
| UVC 0.9 | 10 ± 1.0 | 8 ± 0.9 | 8 ± 0.9 | 20 ± 1.9 |
| UVC 1.2 | 7 ± 0.9 | 20 ± 1.9 | 8 ± 0.9 | 20 ± 1.9 |
| UVC 1.5 | 6 ± 0.8 | 20 ± 1.9 | 7 ± 0.9 | 20 ± 2 |
Mean Diameter of Colony Size for the Fungi Isolated From Patients With Onychomycosis After 14 Days a
5. Discussion
According to obtained data, UV light can affect colony count and size of T. rubrum and T. mentagrophytes in the culture, the two fungal species frequently isolated from patients with onychomycosis. The estimated prevalence of onychomycosis caused by these species ranges from 10 to 21.3% in the general population in Australia, the United Kingdom and Iran (11, 12). This prevalence rate may increase to 30% in specific populations such as people over 70 years old (13-15). It is challenging to determine the optimal treatment and circumventing drug resistance in pathogenic fungi, including dermatophytes. Since the nails and skin are being exposed to sunlight, many photodynamic treatments are developed in dermatologic studies. For example, UV light therapy is investigated in diseases such as scleroderma (16) and onychomycosis (17).
The mechanism of UV radiation is the primary photochemical reaction, which damages DNA and affects survival and rate of germination (18). This molecular change makes the DNA unstable for essential biological processes such as transcription and replication. As a rule, the simpler the microorganism is in anatomical terms, the more easily it is inactivated by UV radiation. This is why viruses and prokaryotic cells such as bacteria are more easily destroyed than a complex of microorganisms such as eukaryotic cells, yeasts and vegetative fungi. In particular, fungal spores in which the DNA is protected by a concentrated cytoplasm and pigmented cell wall need high doses of UV energy to be destroyed.
Some data suggest that solar UV radiation can inhibit the growth of fungi on the soil surface in the antarctic terrestrial environment (19), and has disinfectant effects that can vary depending on the type and dosage of irradiation, condition of the surface and exposure time. The effective exposure time was reported to be 45 minutes for yeast and 75 minutes for mold (20). Different doses of UV-B light show different effects on the growth of Candida albicans. Increasing doses of UV-B strongly reduced hyphal growth in this fungus and triggered enhanced blastospore formation (21). The mechanism of resistance to UV radiation is not completely known, but intra hyphal growth and recolonization of old cells by new ones were observed in all the strains investigated by Gorbushina et al. (22).
In the present study, UV-C radiation affected T. rubrum type 1: as the dose increased, colony count decreased. However, supplementary therapy may still be needed (7, 8). Irradiation with UV-A and UV-B also decreased the colony count of some strains tested in the current study which was proportional to the dose. This finding may be due to the synthesis of new hyphae through the old hyphae not exposed to irradiation, or may be related to the age of the exposed hyphae (i.e. recolonization of older hyphae) in the suspension. Trichophyton rubrum is one of the most frequent causal agents in nail infections, and recurrence of the infection and resistance to therapy are the most important limitations to treatment success for this anthropophilic dermatophyte (22). This species was unaffected by infrared irradiation, responded with increased pigmentation to UV-A at13.5J/cm2 twice daily, and was inhibited by a single dose of UV-B at 15.1 J/cm2 (6).
Trichophyton mentagrophytes may be anthropophilic or zoophilic in nature. The anthropophilic type causes chronic infection but the zoophilic type causes inflammatory lesions. Growth rates, surface colony color and the texture of colony morphology are different in each strain. The current study compared two strains of T. mentagrophytes. According to Figure 2, UV-A, UV-B and UV-C had similar effects on T. mentagrophytes type 1, but affecting type 2 strains differently. The negative phototropism of dermatophytes were reported previously (6). Increasing pigmentation in response to UV-A (13.5 J/cm2 twice daily) was observed in T. rubrum (6). Electron microscopy studies showed a marked thickening and blurred contours of the cell walls grown with a brightener effect related to interference by optical brighteners with the formation of normal chitin fibrils and thickening of the cell walls (23).
In the present study, increasing doses of UV-A, UV-B and UV-C irradiation increased colony size in T. mentagrophytes type 2. It is well known that UV radiation damages human tissues, particularly the skin. UV-B irradiation of the skin is particularly well studied, and is accepted as the main cause of skin cancer. The depth of penetration of UV-C radiation into the human skin is very low; therefore, the risk of skin cancer associated with this type of treatment is low. There are studies which report the treatment of localized infections with multidrug-resistant microorganisms (24) and subungual onychomycosis (25) with UV-C light irradiation and favorable responses. As mentioned in these studies, the cases were limited and side effects should be taken into account more carefully. When UV irradiation is used to treat onychomycosis, it is important to minimize exposure by carefully masking the area with adhesive material. In addition, the dose of radiation must be minimized by careful dosimetery calculated with reference to the individual patient’s nails, the etiologic agent, and optical properties.
A potential limitation of this study was the limited availability of human nail samples. If there were enough samples, by using different types and doses of irradiation such as UV-A UV-B and UV-C for every single nail sample separately, the current study could directly examine the effects of radiation on them, but since the volume of samples was low, they were just cultured after the isolation of fungal strains and it was possible to evaluate different types and doses of irradiation in the isolated strains. UV-A, UV-B and UV-C seem to be effective in decreasing colony growth in some prevalent fungi, which caused onychomycosis in the patients. Further studies are needed to determine the efficacy of this therapy, identify possible side effects and establish appropriate dosages for the antifungal action of UV radiation therapy.
