Selective photoinactivation of Candida albicans in the non-vertebrate host infection model Galleria mellonella
- José Chibebe Junior†1, 2, 3,
- Caetano P Sabino†4, 5,
- Xiaojiang Tan†6, 2,
- Juliana C Junqueira1Email author,
- Yan Wang2, 7,
- Beth B Fuchs2,
- Antonio OC Jorge1,
- George P Tegos4, 8, 9,
- Michael R Hamblin4, 9, 10 and
- Eleftherios Mylonakis2, 11
© Chibebe Junior et al.; licensee BioMed Central Ltd. 2013
Received: 18 April 2013
Accepted: 17 September 2013
Published: 1 October 2013
Candida spp. are recognized as a primary agent of severe fungal infection in immunocompromised patients, and are the fourth most common cause of bloodstream infections. Our study explores treatment with photodynamic therapy (PDT) as an innovative antimicrobial technology that employs a nontoxic dye, termed a photosensitizer (PS), followed by irradiation with harmless visible light. After photoactivation, the PS produces either singlet oxygen or other reactive oxygen species (ROS) that primarily react with the pathogen cell wall, promoting permeabilization of the membrane and cell death. The emergence of antifungal-resistant Candida strains has motivated the study of antimicrobial PDT (aPDT) as an alternative treatment of these infections. We employed the invertebrate wax moth Galleria mellonella as an in vivo model to study the effects of aPDT against C. albicans infection. The effects of aPDT combined with conventional antifungal drugs were also evaluated in G. mellonella.
We verified that methylene blue-mediated aPDT prolonged the survival of C. albicans infected G. mellonella larvae. The fungal burden of G. mellonella hemolymph was reduced after aPDT in infected larvae. A fluconazole-resistant C. albicans strain was used to test the combination of aPDT and fluconazole. Administration of fluconazole either before or after exposing the larvae to aPDT significantly prolonged the survival of the larvae compared to either treatment alone.
G. mellonella is a useful in vivo model to evaluate aPDT as a treatment regimen for Candida infections. The data suggests that combined aPDT and antifungal therapy could be an alternative approach to antifungal-resistant Candida strains.
Candida albicans and other Candida species commonly colonize the epithelial surfaces of the human body . One-half of humans have oral cavities colonized by Candida species in a commensal relationship with the host . Although few healthy carriers develop clinical candidiasis, when the host becomes immunocompromised due to cancer, HIV/AIDS, diabetes, major surgery, transplantation of solid organs or hematopoietic stem cells, these opportunistic pathogens can cause superficial infections that may be cutaneous, subcutaneous or mucosal. In progressive cases, the fungus can penetrate the epithelial surface and be disseminated by the bloodstream with serious consequences [1, 3–7].
C. albicans is the most common species isolated from superficial and systemic candidiasis and it is considered the most pathogenic species of the Candida genus [5, 8–11]. In vitro investigations indicate that C. albicans expresses higher levels of putative virulence factors compared to other Candida species. It has been proposed that several virulence factors are involved in the pathogenicity of C. albicans, such as adhesion to host surfaces, hyphal formation and secretion of proteinases . In addition, C. albicans cells employ mechanisms that protect of the fungal cells from the host immune system, including an efficient oxidative stress response [12, 13]. When immunocompetent individuals are infected by fungi, macrophages and neutrophils generate reactive oxygen species (ROS), such as superoxide radicals and hydrogen peroxide that damage cellular components of C. albicans, inclusive of proteins, lipids and DNA. The production of ROS is an important mechanism of host defense against fungal pathogens , damaging cells enough to cause cell death of phagocytosed fungal cells [12, 14].
Treatment of fungal infections, especially invasive ones, is considered difficult due to the limited availability of antifungal drugs and by the emergence of drug-resistant strains. The development of new antifungal agents and new therapeutic approaches for fungal infections are therefore urgently needed [4, 8, 15]. Photodynamic therapy (PDT) is an innovative antimicrobial approach that combines a non-toxic dye or photosensitizer (PS) with harmless visible light of the correct wavelength. The activation of the PS by light results in the production of ROS, such as singlet oxygen and hydroxyl radicals, that are toxic to cells [6, 16]. PDT is a highly selective modality because the PS uptake occurs mainly in hyperproliferative cells and cell death is spatially limited to regions where light of the appropriate wavelength is applied. As microbial cells possess very fast growth rates, much like that of malignant cells, PDT has been widely used for microbial cell destruction . Several in vitro studies have shown that PDT can be highly effective in the inactivation of C. albicans and other Candida species. Therefore, antifungal PDT is a subject of increasing interest especially against Candida strains resistant to conventional antifungal agents .
Galleria mellonella (the greater wax moth) has been successfully used to study pathogenesis and infection by different fungal species, such as Candida albicans, Cryptococcus neoformans, Fusarium oxysporum, Aspergillus flavus and Aspergillus fumigatus . Recently, our laboratory was the first to describe G. mellonella as an alternative invertebrate model host to study antimicrobial PDT alone or followed by conventional therapeutic antimicrobial treatments . We demonstrated that after infection by Enterococcus faecium, the use of antimicrobial PDT prolonged larval survival. We have also found that aPDT followed by administration of a conventional antibiotic (vancomycin) was significantly effective in prolonging larval survival even when infected with a vancomycin-resistant E. faecium strain.
In this study, we go on to report the use of the invertebrate model G. mellonella as a whole animal host for the in vivo study of antifungal PDT, as well as the study of combined therapy using PDT and a conventional antifungal drug.
Microbial strains and culture conditions
The C. albicans strains used in this study were Can14 and Can37. C. albicans Can14 is a wild-type strain SC5314  and C. albicans Can37 is a fluconazole resistant clinical isolate from a patient with oropharyngeal candidiasis . C. albicans Can37 was identified by growth on Hicrome Candida (Himedia, Munbai, India), germ tube test, clamydospore formation on corn meal agar, and API20C for sugar assimilation (BioMerieux, Marcy Etoile, France). Susceptibility pattern to fluconazole was determined by the broth microdilution assay according to the Clinical and Laboratory Standards Institute (CLSI).
Strains were stored as frozen stocks with 30% glycerol at -80°C and subcultured on YPD agar plates (1% yeast extract, 2% peptone, and 2% dextrose) at 30°C. Strains were routinely grown in YPD liquid medium at 30°C in a shaking incubator.
Fungal inocula preparation
C. albicans cells were grown in YPD at 30°C overnight. Cells were collected with centrifugation and washed three times with PBS. Yeast cells were counted using a hemocytometer. The cell number was confirmed by determining colony-forming units per mL (CFU/mL) on YPD plates.
Inoculation of G. mellonella with C. albicansstrains
G. mellonella (Vanderhorst Wholesale, St. Marys, OH, USA) in the final larval stage were stored in the dark and used within 7 days from shipment. Sixteen randomly chosen G. mellonella larvae with similar weight and size (250-350 mg) were used per group in all assays. Two control groups were included: one group was inoculated with PBS to observe the killing due to physical trauma, and the other received no injection as a control for general viability.
A Hamilton syringe was used to inject 5 μL inoculum aliquots into the hemocoel of each larvae via the last left proleg containing 106 CFU/larvae of C. albicans cells suspended in PBS. After injection, larvae were incubated in plastic containers at 37°C and monitored for survival daily.
Chemicals and photosensitizer
Methylene blue (MB, Sigma, St Louis, MO) was used at a final working concentration of 1 mM. The dye was dissolved in distilled and deionized filter sterilized water (ddH2O). For each experiment, a new PS solution was prepared daily. Fluconazole (Sigma-Aldrich, Steinheim, Germany) was dissolved in ddH2O and injected in G. mellonella at a concentration of 14 mg/Kg.
Antimicrobial photodynamic therapy
The G. mellonella larvae were injected with 10 μL of a 1 mM solution of MB 90 min after the Candida infection and the PS was allowed to disperse for 30 min into the insect body in the dark, prior to the light irradiation.
A broad-band non coherent light source (LumaCare, Newport Beach, CA) was used for light delivery. This device was fitted with a 660 ± 15 nm band-pass filter probe that was employed to produce a uniform spot for illumination. The optical power was measured using a power meter (PM100D power/energy meter, Thorlabs, Inc., Newton, NJ).
For the study of aPDT combined with conventional antifungal drug, fluconazole (14 mg/kg) was injected immediately before or after the exposure of larvae to light. As a control, a group of the larvae received an injection containing PBS, in lieu of fluconazole.
G. mellonellasurvival assays
After aPDT or combined treatment of aPDT with fluconazole, larvae were observed every 24 h, and considered dead when they displayed no movement in response to touch. Survival curves were plotted and statistical analysis was performed by the Log-rank (Mantel-Cox) test using Graph Pad Prism statistical software. A P value <0.05 was considered statistically significant. All experiments were repeated at least twice, representative experiments are presented.
Persistence of C. albicans in the hemolymph of G. mellonella
The number of fungal cells recovered from the hemolymph of G. mellonella infected by C. albicans Can37 was measured immediately after larvae were exposed to aPDT and to combined treatment (aPDT and fluconazole). Three surviving larvae per group were bled by insertion of a lancet into the hemocoel. Hemolymph from 3 larvae was pooled into 1.5 ml Eppendorf tubes in a final volume of approximately 80 μL. Then, the hemolymph was serially diluted and plated on Sabouraud dextrose agar supplemented with chloramphenicol (100 mg/L). Plates were incubated aerobically at 37°C for 24 h, and colonies were counted in each pool (CFU/pool). The groups exposed to aPDT were compared to the control groups by Student t test. Difference in the number of CFUs were considered statistically significant at P < 0.05. The experiments were repeated at least twice and representative experiments are presented. Three polls per group were performed in each experiment.
We previously described the utility of the G. mellonella model host to assess antibacterial PDT efficacy against E. faecium . In this study we explored the potential of this model using antifungal therapy against one of the most common opportunistic fungal pathogens C. albicans. Briefly, after 90 min of Candida infection, G. mellonella larvae were treated with PDT mediated by MB and red light according to the methods described.
As a first step in exploring the optimal dose–response to MB mediated-PDT, we evaluated 10 groups of larvae that were infected with the wild-type strain of C. albicans (Can14) and received MB (1 mM) injection. We gradually increased the light exposure time. More specifically, eight groups were exposed to red light at different fluences (0.9, 1.8, 3.6, 5.4, 7.2, 10.8, 14.4 and 18 J/cm2, corresponding to 30, 60, 120, 180, 240, 360, 480 and 600 s of irradiation), while two control groups received injection of PBS or MB with no light exposure. After irradiation, the survival rate of G. mellonella was assessed 24 h post C. albicans infection. The best survival rate was reached with the lowest dose and 30 s of irradiation time (data not shown).
Discussion and conclusion
In this study we used the invertebrate model G. mellonella for the in vivo study of antifungal PDT. We verified that aPDT prolonged the survival of G. mellonella caterpillars infected by C. albicans and reduced the fungal burden in the hemolymph of these animals. In addition, we used a fluconazole-resistant C. albicans strain to test the combination of aPDT and fluconazole. The data presented here demonstrated that aPDT increased the susceptibility of C. albicans to fluconazole.
The increased numbers of fungal infections and the subsequent need for high-cost and time-consuming development of new antimicrobial strategies and anti-infectives has emerged as a major problem among infectious diseases researchers and clinicians [6, 26]. Antimicrobial PDT is one of the most promising alternative countermeasures for cutaneous or mucosal infections, caused by either bacteria or fungi [6, 26].
Antifungal PDT is an area of increasing interest, as research is advancing in answering fundamental questions regarding the photochemical and photophysical mechanisms involved in photoinactivation; producing new, potent and clinically compatible PS; and in understanding the effect of key microbial phenotypic multidrug resistance, virulence and pathogenesis determinants in photoinactivation. The novel concept of developing the non-vertebrate infection model in G. mellonella to explore the efficacy of antifungal PDT provides many competitive advantages .
The use of the invertebrate model host has significant benefits when compared to mammalian animals: there are no ethical or legal concerns, no need for specialized feeding or housing facilities, the management of the animal is very easy and no anesthesia is needed, animals are inexpensive, and the use of large sample numbers in the same group are possible [27–30]. G. mellonella has been used to study host-pathogen interactions as an alternative host model to small mammals such as mice and rats [9, 27–29, 31–40].
Our laboratory pioneered the use of G. mellonella as a suitable invertebrate model host to study aPDT against Enterococcus faecium . In the present study this approach to investigating aPDT was successfully expanded to include fungal pathogens. The optimal dose–response to MB mediated-PDT was evaluated and 0.9 J/cm2 showed the best survival of G. mellonella caterpillars, as was found in the E. faecium study. The same limited non-toxic dosage of aPDT to G. mellonella was applied to treat larvae infected by strains of Candida albicans.
During the G. mellonella killing assays, groups infected by C. albicans that received aPDT treatment demonstrated prolonged survival when compared to groups that did not received treatment. However a statistically significant difference between PDT and control groups was observed only for C. albicans Can14 wild-type strain. When the infection was induced by a fluconazole resistant strain (Can37), a statistically significant difference between these groups was not observed. Despite the fact that PDT has been described as a potent agent against both antimicrobial-resistant and sensitive microorganisms  we observed that a fluconazole-resistant C. albicans strain was less sensitive to aPDT.
This difference has also been described in an in vitro study performed by Dovigo et al. . These authors observed that fluconazole-resistant strains of C. albicans and C. glabrata showed reduced sensitivity to aPDT in comparison with reference strains susceptible to fluconazole, suggesting that resistance mechanisms of microorganisms to traditional antifungal drugs could reduce PDT effectiveness. According to Prates et al. , the resistance of Candida strains to fluconazole usually involves overexpression of cell membrane multidrug efflux systems belonging to the ATP-binding cassette (ABC) or the major facilitator superfamily (MFS) classes of transporters. The authors showed that the overexpression of both systems reduced MB uptake by fungal cells, as well as the killing effect of aPDT, suggesting that ABCs and MFSs are involved in the efficiency of aPDT mediated by MB and red light. In addition, Arana et al.  demonstrated that subinhibitory concentrations of fluconazole induced oxidative stress and a transcriptional adaptative response that was able to generate protection of C. albicans against subsequent challenges with oxidants. The mechanisms of protection against oxidative stress of fluconazole resistant C. albicans strain may have enhanced the resistance of C. albicans to oxidative damage caused by PDT.
In this study, we also evaluated the effects of aPDT on fungal cells in the hemolymph of G. mellonella larvae infected by fluconazole resistant C. albicans (Can37). Although this C. albicans strain had not shown a significant increase in survival rate in G. mellonella, it was observed that aPDT caused a reduction of the number of fungal cells in the hemolymph (0.2 Log) with a statistically significant difference between aPDT and control groups. In addition, these data demonstrated that aPDT was able to reduce fungal cell viability immediately upon light exposure, suggesting that C. albicans cells were sensitive to aPDT, by the lethal oxidative damage of the singlet oxygen pathway, in the experimental candidiasis in the G. mellonella model. At the moment, all the aPDT studies performed in vivo were developed in vertebrate models of rats and mice using fluences of light much higher than the dose used in our work [43–45]. Using an oral candidiasis mice model, Costa and colleagues  found a reduction of 0.73 Log in the fungal cells recovered after erythrosine- and LED-mediated aPDT when a fluence of 14 J/cm2 was applied. Dai et al.  also demonstrated that aPDT, with the combination of methylene blue and red light (78 J/cm2), reduced (0.77 Log of CFU) the fungal burden in skin abrasion wounds in mice infected with C. albicans.
Patients with fungal infections are often treated with azole antifungal drugs, however Candida resistance to azoles has been detected in recent years. Several mechanisms of resistance have been reported including the overexpression of cell membrane multidrug efflux pumps previously cited, an alteration in the chemical structure of the demethylase enzyme, and the incorporation of alternative sterols to ergosterol within the cell membrane [23, 24]. Giroldo et al.  suggested that MB-mediated aPDT caused damage to the cell membrane of the C. albicans cells. If the hypothesis that aPDT could affect the cell membrane is valid, the sequential use of aPDT with fluconazole could have a dual action on treating the infection. Conventional antimicrobial therapy could have aPDT as an adjunct or as an alternative . The combination of PDT with antimicrobials has been used with success when compared to either isolated approach [19, 26, 46]. Kato et al.  verified that after exposure to sublethal aPDT, the minimal inhibitory concentration (MIC) of fluconazole against C. albicans was reduced compared to non-aPDT treated strains.
Of note, we observed that the G. mellonella larvae survival after infection by the fluconazole resistant C. albicans strain, was prolonged when fluconazole was administered before or after aPDT, in comparison to the use of fluconazole or PDT alone. We believe that due to the permeabilization of the fungal cell membrane by the sublethal PDT dose, fungal cells become more susceptible to fluconazole action. In addition, it has been suggested that the use of azoles can increase the oxidative stress promoted by PDT by contributing to ROS formation themselves . Arana et al.  demonstrated that fluconazole was able to induce oxidative stress in C. albicans in a dose- and time-dependent manner, suggesting that ROS play a role in the mechanism of action of azoles. The exact mechanism involved in increasing the survival of larvae infected by the fluconazole resistant C. albicans strain and exposed to combined therapy of PDT and fluconazole remains to be clarified. Thus, comprehensive experiments are needed to better understand whether this process could be useful to treat antimicrobial resistant fungal infections.
In summary, the results obtained in this study showed that G. mellonella is a suitable model host to study the antifungal PDT in vivo. It is known that the G. mellonella model is not restricted to studies that examine aspects of the pathogenesis of fungal infections or antimicrobial therapies, but also can be used to the study of host defenses against fungal pathogens . The insect immune response demonstrates a number of strong structural and functional similarities to the innate immune response of mammals and, in particular, insect haemocytes and mammalian neutrophils have been shown to phagocytose and kill pathogens in a similar manner . Recent studies demonstrated that PDT can stimulate host defense mechanisms. Tanaka et al.  used a murine methicilin-resistant Staphylococcus aureus (MRSA) arthritis model and verified that the MB-mediated PDT exerted a therapeutic effect against a bacterial infection via the attraction and accumulation of neutrophils into the infected region. Neutrophils are among the first cells recruited to the illuminated area and their main function is to release enzymes for killing infectious organisms and secrete cytokines and other chemicals that promote inflammation . In this study, the effects of aPDT on the immune system of G. mellonella were not investigated. Therefore, future studies need to be developed to understanding the action of aPDT and methylene blue in the haemocyte density and in the expression of a variety of antimicrobial peptides involved in immune responses of G. mellonella.
The key conclusion is that the G. mellonela - C. albicans system is a suitable model to study antifungal PDT and to explore combinatorial aPDT-based treatments. Thus, this invertebrate animal model host provides a novel approach to assess the effects of in vivo PDT, alone or in combination with antifungal compounds, on fungal infections without the difficulties of mammalian models.
José Chibebe Junior thanks CAPES (PDEE 2507-11-0) for the scholarship during the PhD Program at Harvard Medical School. Xiaojiang Tan was supported by Science and Technology Planning Project of Guangdong Province, P.R. China (2011B080701091). Juliana C Junqueira thanks São Paulo Council of Research - FAPESP, Brazil (grant 12/19915-6). Research conducted in the Mylonakis Laboratory was supported by NIH (RO1 AI050875 to EM). Research conducted in the Hamblin Laboratory was supported by NIH (RO1 AI050875 to MRH) and US Air Force MFEL Program (FA9550-04-1-0079). George P Tegos was supported by the NIH (grant 5U54MH084690-02).
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