1. Introduction
Candida spp. are the part of natural microbiota of healthy individuals. However, under conditions of host weakness, Candida isolates can become opportunist. The genotyping research of Brillowska-Dąbrowska et al. confirmed that endogenous isolates are the major cause of Candida infections [1]. Those infections are the fourth most common hospital-acquired systemic infections in the United States with mortality rates of up to 40% [2]. Progress of medicine paradoxically is a reason of increasing number of opportunistic Candida infections. The increasing number of immunocompromised patients, long-term stay at hospital, prolonging patients’ lives, using broad-spectrum antibiotics as prophylaxis and also health-care materials such as catheters and intravenous solutions have contributed to the increase of fungal infections [3]. Candida spp. facilitated its invasion and infections by expression of virulence factors (secretion of hydrolytic enzymes, adherence to surfaces, biofilm formation or morphological transition—Figure 1) and fitness attributes [4].
The first crucial step of Candida invasion is adherence to host cells. However, adhesion is also important to commensal carriage of these species. Adhesins play a role in facilizing adherence of Candida cells to other microorganisms or host cells and abiotic surfaces (medical devices) [5]. The best described adhesins of C. albicans are ALS (agglutinin-like sequence) proteins and Hwp1 (hypha-associated glycosylphosphatidylinositol (GPI)-linked) protein.
Candida spp. invade the host cell by invasins presented on the cell surface. These proteins facilitate the host cell to achieve endocytosis by binding to the host ligand. There are known two proteins responsible for invasion: Als3 (plays role of adhesin) and Ssa1 (heat shock protein—Hsp70) [6,7]. Those proteins bind to host E-cadherin and induce endocytosis. However, it has been proven that invasion of C. albicans into the host cell relies on active penetration. The molecular mechanism of active penetrations have been undefined yet. It has been established that this process requires viable C. albicans hyphae, but it seems that fungal adhesion and physical forces are crucial [8]. However, C. albicans hyphae formation mutants also do not express invasins, so it means that both active penetration and endocytosis are depended on hyphae formation [9].
Other virulence factors produced by Candida spp. are extracellular enzymes, responsible for tissue adhesion and penetration and thus host invasion. Four different classes of hydrolases (proteases, phospholipases, lipases, and hemolysins) have been so far identified in Candida spp. [5].
Proteases degrade different proteins of host cells, such as collagen, keratin, and mucin. These enzymes are also responsible for degradation of antibodies, complements and cytokines [4]. The best characterized proteases are Sap1–Sap10 aspartic proteases. These enzymes can bind to the cell surface or can be secreted to surrounding environment [5]. Aspartic proteases degrade the mucosal membranes of the host tissues and also facilities the degradation of the immunological defense proteins [6]. Moreover, it is considered that increased Sap gene expression level is associated with increasing Candida virulence and therefore related to clinical symptoms of candidiasis [3].
Phospholipases are responsible for disruption of the cell membrane by hydrolysis of the ester linkages in glycerophospholipids [4]. Four different classes have been so far identified (classes A–D), but only a few members of class B are secreted to the environment [5]. Moreover, the production of phospholipases is strain depending [10,11,12].
Hemolysins play a very important role in Candida virulence, because they are responsible for destroying red blood cells and iron acquisition. Inorganic elements, such as iron, are essential for the development of Candida cells and for the establishment of infection process [3,13].
Esterases are enzymes responsible for the hydrolysis of an ester group. However, information about esterases described in the literature are divergent. Esterase production was found among—C. albicans, C. tropicalis, C. parapsilosis, C. lipolytica—their low activity was also identified among C. parapsilosis [14]. The extracellular lipases play role in lipids digestion for nutrient acquisition, adhesion to host cells and influence on inflammatory process by lysing the competing microflora [3]. In C. albicans, 10 different lipases have been found. The research conducted on murine model, showed that inhibition of lipases expression in C. albicans and C. parapsilosis cells contributed to loss of virulence [15].
Biofilm is the prevalent growth form of microorganisms occurring on catheters, dentures, and mucosal cell surface [16,17]. Biofilm is a community of microorganisms embedded within an extracellular matrix and hyphal cells in the upper part [5]. Biofilm formation ability was identified in C. auris [18], C. albicans, C. glabrata, C. parapsilosis, and C. tropicalis [13]. Biofilm is an important virulence factor, responsible to prevent the antimycotic penetration through the matrix and therefore unregular antimycotics penetration into Candida cells [19,20], what leads to drug-tolerant and resistant mutants selection [20]. It has been proven that Candida biofilm contributes to development of resistance to azoles, polyenes, and pyrimidine analogues [21]. Planktonic cells are more sensitive to antimycotics than the biofilm cells [5]. Candida spp. grow budding yeast but they can also grow as pseudohyphae and hyphae [5]. Candida polymorphism facilitates host cell invasion due to active penetration by hyphae [17]. Candida mutants which are unable to hyphal grow, are less virulent. It was proven that hypha formation is associated with expression of genes encoding virulence factors, such as HWP1 (hyphal wall protein), ALS3, SAP4, SAP5, etc. [5]
A model organism for virulence studies of fungal infections should create response of immune system similar to response in human body. In biomedical research the gold standard are mammals (mice, rats, guinea pigs, or rabbits). However, using vertebrates is associated with ethical, logistical and economic considerations. What should be emphasize in virulence study most of the time a huge number of fungal isolates is tested. Those reasons enquired researchers to develop the alternative host models such as embryonated chicken eggs or zebra fish and also invertebrates: Drosophila melanogaster [22], Caenorhabditis elegans [23], Blattella germanica [24], Bombyx mori [25]. Recently, Galleria (G.) mellonella become used as host models for studying the molecular basis of virulence.
G. mellonella larvae are easy to house and breed on honeycomb or on culture media. The life cycle of G. mellonella lasts 6 weeks in optimal conditions. Moreover, the female moth is able to deposits about 1500 eggs [26]. The most important advantage, which is useful for virulence study is that larvae can be incubated in wide range of temperature up to 37 °C. The larvae are small (length approx. 2 cm) so it easy to keep them in laboratory, and the size is appropriate to perform precise application of defined amount of pathogens [27]. The experiments with G. mellonella allow to obtain the results during one or two weeks. Finally, G. mellonella larvae have ability to synthesize and secrete immune peptides, what allows to use the larvae as a host model [28]. Moreover, low price and ease in maintaining, lack of expensive equipment requirements and finally lack of requirement of ethical approval make G. mellonella a new alternative to mammalian models. However, this model has some disadvantages. The lack of defined G. mellonella lines and different quality of larvae deepens on distributors contributes to the need of performance detailed controls [29]. The different inoculation volume (10–40 µL) and concentration of pathogens (4 × 104–2 × 107), as well as different protocols and conditions of larvae maintenance make the data difficult to compare between experiments and laboratories. Nevertheless, the larvae of G. mellonella have been widely used as virulence models to examine fungal pathogens (Candida [30], Aspergillus [31], Histoplasma [32], Paracoccidioides [33], Fusarium [34] and Cryptococcus [35]) and to evaluate the efficacy of antimicrobial drugs or studies toxins [32,36]. G. mellonella larvae were also used to study C. albicans virulence [37,38]. What is very important, it was observed that the results obtained using G. mellonella are compatible with other model organisms, such as the murine model [31].
According to many research Candida virulence may vary depending on the species, geographical origin, host reaction and also the stage of infections. The aim of this study was to investigate the correlation between selected, extracellular virulence factors and survival of G. mellonella larvae infected with Candida isolates.
2. Results
2.1. Candida Virulence Investigation Using G. mellonella as Host Model
The presented research are based on the group of 25 Candida isolates (15 C. albicans, 1 C. glabrata, 1 C. inconspicua, 1 C. krusei, 3 C. palmioleophila, and 4 C. parapsilosis). Among tested isolates, C. albicans were the most virulent isolates. According to Kaplan–Meier analysis, 10 C. albicans isolates and 1 C. glabrata were highly virulent (total 11/25). The remaining 6 C. albicans isolates were moderately virulent. C. parapsilosis virulence was low, but one C. parapsilosis isolates (No. 441) was moderately virulent. We identified only three avirulent isolates: one C. krusei isolate and two out of four C. parapsilosis. C. palmioleophila isolates seemed to have moderate virulence, while C. inconspicua was also moderately virulent. Statistically significant differences were observed between the survival among isolates from each groups (p value < 0.05).
The survival distribution function of G. mellonella larvae after infections of Candida isolates is presented in Figure 2, Figure 3 and Figure 4. The survival of larvae after the second, fourth, and sixth day of infections and the standard deviation (SD) from two independent experiment were present in Table S1 (Supplementary Materials). The results of all performed controls are present in Table S1 (Supplementary Materials), while the control results are omitted in the Figures to simplify the picture.
The comparison of the virulence with echinocandin sensitivity suggested that C. albicans isolates characterized by the higher MIC values are the most virulent. Nevertheless, echinocandin sensitive C. albicans isolates in most cases were moderately or highly virulent. None of C. albicans isolates were avirulent. The non-albicans isolates with the high MIC values were most often of low virulence.
2.2. Examination of Virulence Factor Production
In Table 1 the comparison of enzymatic activity results and biofilm production with the results of larval survivals are presented according to the MIC values. The Person’s correlation of tested virulence factors are presented in Table S2 in the Supplementary Materials. The enzymatic activity results with their standard deviation are listed in Table S3 in the Supplementary Materials. The exemplary picture of the isolates growing on the specific medium for enzymatic activity testing are presented in Table S4.
Among 18 out of 24 (75%) Candida isolates the hemolytic activity was observed, two isolates exhibit low weak activity and one did not grow. The majority of isolates with hemolytic activity belong to the species C. albicans. Phospholipase activity was observed among 7/22 isolates (32%), four isolates exhibit a strong activity and three exhibit weak activity. Non phospholipases activity was observed among C. glabrata, C. krusei, C. inconspicua, and C. parapsilosis isolates. Proteases activity was identified among all tested isolates, with one exception, C. albicans isolate 1768 did not grow. Esterase activity was observed among 14/23 (61%) isolates. The majority of isolates producing esterase enzymes were C. albicans. Biofilm formation was observed among 18/25 (72% isolates), only 6 isolates had strong biofilm formation ability and 12 isolates had weak ability.
The distribution of virulence factors for the most virulent isolates of C. albicans seemed to be variable. C. inconspicua and C. palmioleophila both produced biofilm and proteases. Isolates with anidulafungin MIC values of ≥0.5 mg/l had less hemolysins and esterase activity.
Correlation analysis results with Person’s coefficient (Table S2 Supplementary Materials) revealed a positive correlation between the survival of larvae after the sixth day and following enzymes activity: esterase activity (r = 0.621, p value = 0.0016), hemolytic activity (r = 0.474, p value = 0.019), and protease activity (r = 0.505, p value = 0.012). Biofilm formation had a positive correlation with MIC values of anidulafungin (r = 0.502, p value = 0.0125), caspofungin (r = 0.422; p value 0.04), and micafungin (r = 0.504; r = 0.12). Moreover the positive correlation was observed between esterase activity and MIC values of caspofungin and micafungin.
3. Discussion
The virulence factors were identified in different Candida spp. such as: C. albicans [39], C. auris [40], C. parapsilosis complex [41], C. tropicalis [4], C. krusei, and C. glabrata [42]. However, the majority of studies were conducted on C. albicans isolates, which are considered the most pathogenic species of Candida [3]. In the literature, virulence factors among rare Candida species are not well-investigated.
Proteinase activity is observed among 70–100% of clinical C. albicans isolates [39,43]. The variable numbers of clinical C. parapsilosis isolates producing proteinases were reported (37% [44], 87% [41], and 100% [45]). The obtained data are in accordance with previous reports, due to demonstrate the high proteinase production among all tested isolates such as C. albicans, C. parapsilosis, and also rare species.
Phospholipase activity of C. albicans reported in the literature is variable. In one study, phospholipase activity was identified in 100% of C. albicans isolates [43] and in another research the production of these enzymes was observed among 29% [46], 48% [47] or 81% [48] of C. albicans isolates. Phospholipase activity was not detected within C. parapsilosis isolates [43,45]. In the presented study the phospholipase activity was reported among C. albicans, C. palmioleophila isolates and the range was the lowest (32%) among tested enzymes. In this research C. parapsilosis did not exhibit phospholipase activity what is in line with the literature data [45]. To the best knowledge of the authors’ there are no information about C. inconspicua virulence in the literature. However, in this study we reported that C. inconspicua isolate is able to produce this enzyme.
Esterase activity was reported among C. albicans, C. tropicalis, C. lipolytica, C. inconspicua, but only C. parapsilosis exhibited weak esterase activity [14]. In the other research esterase activity was identified as low as about 37% of Candida isolates [46]. On the other hand, esterase production among 87% of C. albicans, 47% of C. parapsilosis was detected by Pakshir et al. [49] and within 100% of C. albicans and C. tropicalis isolates by Slifkin et al. [50]. In our research, esterase activity was identified among 61% of tested isolates and the majority of those isolates were C. albicans (12/15).
Hemolysins production seems to be very prevalent and was reported in 100% [47] and 82% [46] of C. albicans. The low rate of hemolysins activity was identified among C. parapsilosis [4]. In this research hemolysins production was observed among 75% of isolates. Only one out of four isolates C. parapsilosis isolates and one of three C. palmioleophila isolates had hemolysins activity.
Another virulence factor contributed to development of Candida infections is biofilm formation. According to literature biofilm production contributed to 65% of all human infections. Biofilm formation was identified among 86% [47] or 67% [11] of C. albicans isolates. Data obtained during this research are in accordance with the literature, as 72% of all tested isolates produced biofilm. The weak biofilm formation ability was observed among C. palmioleophila, and the strong among C. inconspicua. The correlation between resistance to antifungals and pathogenicity is not well reported so far in the literature. However, Candida biofilm formation is considered to facilitate resistance to antifungal agents [3]. The correlation between fluconazole resistance among C. tropicalis and virulence factors as biofilm and phospholipase activity was proven [4]. For the other hand among C. albicans isolates negative correlation was identified between fluconazole MICs and biofilm formation [51]. In this research the positive correlation between biofilm formation and susceptibility to echinocandin was reported.
Virulence and pathogenicity potential of clinical Candida spp. collected from Polish hospital were investigated in vitro using G. mellonella larvae as a host model.
The literature reports on research conducted on Candida spp. using G. mellonella larvae as a host model is focused mainly on C. albicans virulence [52,53,54]. However, this host model was also used for virulence investigation among C. parapsilosis, C. krusei [36], C. glabrata, and C. tropicalis [55]. The virulence of Candida spp. tested in G. mellonella seems to be species dependent [53].
After infections of G. mellonella with 105 cells of C. albicans, C. dubliniensis, C. parapsilosis, and C. tropicalis the larvae mortality was 100% after 4 days of incubation at 37 °C. Lower mortality rates were observed among: C. lusitaniae (87%), C. norvegensis (37%), C. krusei (25%), and C. glabrata (20%). A different mortality rates were reported after 3 days of incubation at 30 °C (90% for C. albicans, 70% for C. tropicalis, 45% for C. parapsilosis and only 20% for C. krusei) [52].
The obtained results showed that data on G. mellonella survivals after infections can be employed to differentiate virulence between Candida species. The data obtained in this research presented the highest virulence among C. albicans isolates and the lowest among C. krusei isolates. This results are in line with literature—C. albicans was described as the most pathogenic species and C. krusei [36] as almost avirulent. According to the best knowledge of the authors this is the first examination report of the virulence of C. palmioleophila and C. inconspicua in the G. mellonella model. We identified C. inconspicua as moderately virulent, one C. palmioleophila isolate as low, and the remaining isolates of this species as moderately virulent. C. parapsilosis virulence was identified as varied, the majority of isolates were avirulent, only one isolate was moderately virulent. According to the literature virulence of the species from psilosis group is different—C. parapsilosis sensu stricto was the most virulent and C. metapsilosis was the weakest virulent species [56].
The correlation between mortality of the infected larvae and production of Candida virulence factors are not well investigated. This correlation was proven for biofilm [37,57] and proteases [58]. However, studies of 739 Candida isolates did not show the biofilm correlation with G. mellonella larval model [54]. Our research indicated that pathogenicity of Candida isolates examined in G. mellonella larvae is correlated with proteinase, hemolysins, and esterase activity but correlation between biofilm and larvae mortality were not confirmed.
4. Materials and Methods
4.1. Candida spp.
In presented studies 25 Candida isolates (15 C. albicans, 1 C. glabrata, 1 C. inconspicua, 1 C. krusei, 3 C. palmioleophila, and 4 C. parapsilosis) were tested. To exclude the contamination of another species, and cross contamination of Candida spp., all samples were cultured on CHROMagar medium (GRASO, Starograd Gdanski, Poland). The isolates that grew on the chromogenic medium in more than one color were regrown on SAB medium several times and the purities of the colony was investigated again. Species identification was carried out based on rRNA fragment sequencing, according to the procedure described by Mroczyńska [59].
Tested isolates were divided into three groups depending on the MIC values of anidulafungin to simplify data analysis. Echinocandins MIC values were determined according to European Committee on Antimicrobial Susceptibility Testing recommendation.
4.2. Candida spp. Virulence Investigation Using G. mellonella as Host Model
The protocol was based on Fuchs et al. procedure [27]. All tested isolates were grown overnight in 10 mL liquid Sabouraud (SAB) dextrose medium (BTL, Warszawa, Poland). Then 2 mL of inoculum was transferred to Eppendorf tubes and then centrifuged 1 min at 5000× g. The pellet of cells, after removed of the supernatant, was twice washed with PBS (Sigma Aldrich, Darmstadt, Germany). Then the pellet was suspended in 1 mL of PBS. Such prepared suspension was used to count the Candida cells with hemocytometer. The cell concentration was adjusted to appropriate amount of cell per microliter in sterile PBS.
Prepared inoculum of Candida isolate was injected into individual larva (Owadodajnia, Gdynia, Poland) in the last left proleg with final concentration 5 × 105 yeast cells/larva. For injection 10 µL of inoculum Hamilton syringe (Cat. No. 701RN 10 µL) was used. Before injections, the area of larvae was sterilized by ethanol. Every experiment was repeated twice and 10 larvae was used per one strain in one experiment. During experiments two control groups of 10 larvae were examined. The control experiments were performed to check the correctness of the injection process, the quality and sterility of PBS and to monitor the quality of delivered larvae. Moreover, also the control of injection of larva was performed (larva were only pierced).
After injection the larvae were transferred to a Petri dish containing a Whatman filter to recover (5–10 min). Groups of larvae injected with particular isolates were transferred to new separate Petri dishes. Infected larvae were maintain at 37 °C and scored for viability daily during seven days. Dead larvae and pupa were removed and the death and metamorphosis were noted. The remaining larvae were returned to the incubator. The endpoint of the experiment was when all larvae were death or transited from larva into pupa.
The results were presented as Kaplan–Meier survival plots and evaluated using Mann–Whitney (two-samples Wilcoxon) test. The p value < 0.05 was considered as statistically significant. All calculations were performed using XLSTAT computer program (demo version).
4.3. Examination of Virulence Factors Production
For determination of virulence factor production the following agar media were prepared. To determine the ability of phospholipase secretion the SAB medium (1.3%) supplemented by 1.17% NaCl (POCH, Gliwice, Poland), 0.011% CaCl2 (POCH, Gliwice, Poland), and 2% of the supernatant of egg yolk emulsion (Bio-maxima, Gdansk, Poland) was used. For positive phospholipase activity the appearance of a whitish zone of precipitation around colony was observed [39,60].
For detection of protease activity specific agar medium was prepared: 2% agar (BTL, Poland), 1.17% yeast carbon base (BTL, Warszawa, Poland), 0.01% yeast extract (BTL, Warszawa, Poland), and 0.2% bovine serum albumin (Sigma-Aldrich, Darmstadt, Germany). Yeast carbon base and BSA were sterilized by 0.22 µL filter. The presence of the opaque halo of degradation around the colonies indicate positive protease activity [61].
Hemolysin activity was examined on SAB medium with 3% glucose (A&A Biotechnology, Gdynia, Poland) and 7% sheep blood (pH = 5.6; Bio-maxima, Poland). The sheep blood was added when the autoclaved reagents were cooling to 50 °C. The presence of the translucent zone around colonies indicate the positive hemolytic activity [61,62].
Esterases activity was detected on medium which consist of 10% of peptone (BTL, Warszawa, Poland), 5% of NaCl, 0.1% of CaCl2 and 15% of agar with addition of Tween 80 (Pol-Aura, Gdansk, Poland) added after sterilization. The esterase production was determined by halo zones around the colony when observed against the transmitted light [50].
Culture were initiated on the surface of all mediums the 5 μL of Candida cell suspension in PBS (Sigma-Aldrich, Darmstadt, Germany) was placed. The density of culture were adjusted to 0.5 McFarland standard—1–5 × 106 CFU/mL yeast cells. The inoculated plates were incubate at 37 °C for 48 h. After incubation, the results were read visually as described above.
For all virulence factors the diameter of zone was measured and the activity were calculated used formula: Pz (precipitation zone): the phospholipase activity value (Pz) = (colony diameter)/(colony diameter with zone of precipitation). The results were classified as non-activity (Pz = 1), weak (0.64 < Pz < 0.99) and strong activity (Pz ≤ 0.63) [39,61]. The PRz index was determined as protease activity, Hz index as hemolytic activity and Ez index as esterase activity. Those values were determined and interpreted in the same way as phospholipase activity described above as example.
Candida biofilm investigation was based on the procedure described by Silva et al. [17]. Two hundred microliters of Candida cell suspension (0.5 McFarland standard—1–5 × 106 CFU/mL yeast cells) in SAB broth medium were transferred to each well of 96-well polystyrene microtiter plates (Medlab-Products, Raszyn, Poland). As negative control in empty wells medium without cells was placed. Next the plates were incubated at 37 °C on a shaker. After 24 h, 50 µL of the fresh SAB broth medium was added to the culture and then incubated for a further 24 h. After incubation the wells were washed twice with sterile water to remove the non-adherent cells. Biofilm was fixed by adding 200 µL of methanol (POCH, Gliwice, Poland) and incubated 15 min. Then the liquid was removed and the plates allowed to dry. Next, 200 µL of crystal violet (0.5% v/v; Sigma Aldrich, Darmstadt, Germany) were added to each well and incubated for further 5 min at room temperature. After removing of stain, wells were washed twice with sterile water. To release and dissolve the stain, 200 µl of acetic acid (POCH, Gliwice, Poland) was added into the wells. The absorbance of the solution was read at 600 nm using microtiter plate reader (Eppendorf BioSpectrometer® kinetic, Eppendorf, Hamburg, Germany). The absorbance of negative control were subtracted from all values for tested wells. All experiments were repeated three times and data are presented as the arithmetic mean and the standard deviation of the data. In the experiment the reference strain of C. albicans (ATCC 9028) was used, which is biofilm negative [63]. To determine if the isolates produce biofilm the cut off OD were define using the OD of reference strain. The results were classified as
OD ≤2 × OD reference − biofilm negative
2 × OD reference < OD <3 × OD reference − weak biofilm production
OD ≥3 × OD reference − strong biofilm production.
The correlation coefficient (Person’s r) was used to measure the correlation between virulence factors, survival of larvae and also MIC values. A perfect correlation is observed when r = 1. When r = 0 it means that there is no correlation and when r = −1, then the negative correlation is observed.
5. Conclusions
The most important conclusion of performed experiments are:
C. albicans isolates were the most virulent and produce the highest number of extracellular virulence factors;
A positive correlation between the biofilm formation and the MIC values of echinocandins was confirmed among the tested Candida isolates;
The virulence of Candida isolates is related to the expression of proteases, hemolysins, and esterases;
Supplementary Materials
The following are available online at
Author Contributions
Conceptualization, M.M. and A.B.-D.; Methodology, M.M.; Software, M.M.; Formal analysis, M.M., A.B.-D.; Investigation, M.M.; Writing—original draft preparation, M.M.; Writing—review and editing, A.B.-D. and M.M.; Funding acquisition, M.M. and A.B.-D. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Data sharing is not applicable to this article.
Conflicts of Interest
The authors declare no conflict of interest.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Figures and Table
Enlarge this image.Figure 2. Survival distribution function of G. mellonella infected with Candida isolates characterized by anidulafungin MIC values of ≤ 0.016 mg/L. The information on which number presented on figure represents what species—is described in Table 1.
Enlarge this image.Figure 3. Survival distribution of G. mellonella infected with Candida isolates characterized by anidulafungin MIC values between 0.031–0.25 mg/L. The information on which number presented on figure represents what species—is described in Table 1.
Enlarge this image.Figure 4. Survival distribution of G. mellonella infected with Candida isolates characterized by anidulafungin MIC values ≥ 0.5 mg/L. Information regarding number presented in the figure represents what species is described in Table 1.
Comparison of enzymatic activity and biofilm formation of Candida isolates with the larvae survival after six days of those isolates’ infection. Tested isolates were divided into three groups depending on the MIC values of anidulafungin.
| MIC Range | Candida spp. | Isolate No. | Hemolytic Activity | Phospholipase Activity | Protease Activity | Esterase Activity | Biofilm | Survival |
|---|---|---|---|---|---|---|---|---|
| Hz Value | Pz Value | PRz Value | Ez Value | Abs600 | 6th Day | |||
| MIC value ≤ 0.016 mg/L | C. albicans | 71 | 0.59 | 1.0 | 0.35 | 0.40 | 0.51 | 0.6 |
| C. albicans | 380 | 0.52 | 1.0 | 0.39 | 0.45 | 0.89 | 0.1 | |
| C. albicans | 389 | 0.48 | 1.0 | 0.36 | 1.0 | 1.89 | 0.54 | |
| C. albicans | 1010 | 0.48 | 0.48 | 0.39 | 0.44 | 1.27 | 0.50 | |
| C. albicans | 1296 | 0.44 | 0.80 | 0.48 | 0.55 | 0.80 | 0.26 | |
| C. albicans | 1768 | - * | - | - | - | 0.11 | 0.40 | |
| C. albicans | 2023 | 1.0 | 0.48 | 0.36 | 0.44 | 0.49 | 0.15 | |
| C. albicans | 2029 | 0.57 | 0.88 | 0.35 | 0.37 | 1.34 | 0.32 | |
| C. albicans | 2608 | 0.48 | 1.0 | 0.38 | 0.46 | 1.04 | 0.15 | |
| C. palmioleophila | 370 | 0.67 | 0.51 | 0.37 | 1.0 | 1.15 | 0.40 | |
| C. parapsilosis | 395 | 1.0 | 1.0 | 0.50 | 1.0 | 0.42 | 1.0 | |
| MIC value 0.31–0.25 mg/L | C. albicans | 40 | 0.44 | 1.0 | 0.37 | 0.53 | 0.97 | 0.16 |
| C. albicans | 49 | 0.56 | 1.0 | 0.34 | 0.48 | 0.24 | 0.40 | |
| C. albicans | 114 | 0.67 | - | 0.45 | 0.53 | 0.12 | 0.0 | |
| C. albicans | 125 | 0.61 | 0.81 | 0.36 | 0.39 | 1.05 | 0.056 | |
| C. albicans | 286 | 0.48 | 1.0 | 0.35 | 0.44 | 0.97 | 0.33 | |
| C. glabrata | 1150 | 0.50 | - | 0.35 | 1.0 | 0.81 | 0.21 | |
| MIC value ≥ 0.5 mg/L | C. albicans | 54 | 0.48 | 1.0 | 0.32 | - | 1.56 | 0.0 |
| C. krusei | 102 | 0.52 | 1.0 | 0.40 | 1.0 | 0.98 | 1.0 | |
| C. palmioleophila | 4 | 1.0 | 0.63 | 0.40 | 0.52 | 1.05 | 0.44 | |
| C. palmioleophila | 368 | 1.0 | 1.0 | 0.48 | 1.0 | 0.97 | 0.90 | |
| C. parapsilosis | 105 | 1.0 | 1.0 | 0.59 | 1.0 | 2.33 | 1.0 | |
| C. parapsilosis | 441 | 0.59 | 1.0 | 0.39 | 0.63 | 1.01 | 0.7 | |
| C. parapsilosis | 443 | 1.0 | 1.0 | 0.35 | 1.0 | 0.69 | 0.65 | |
| C. inconspicua | 1444 | 0.56 | 1.0 | 0.48 | 1.0 | 1.58 | 0.40 |
* The growth of isolates was not observed or was insufficient. Hz—index of hemolytic activity; Pz—index of phospholipase activity; PRz—index of protease activity; Ez—index of esterase; Abs600—absorbance (600 nm); 6th—larvae survival after 6 days of infection. Dark red marks a strong activity (≤0.63), light red marks a weak activity (0.64 < value < 0.99) and green marks a non—activity (value = 1) of extracellular enzymes. Violet marks a strong biofilm production (OD value ≥ 1.14), yellow weak biofilm production (0.76 < OD value < 1.14) and blue marks negative biofilm production (OD value ≤ 0.76). Dark red marks a survival of less than 0.4 (highly virulent), light red marks a survival rate between 0.4–0.7 (moderately virulent). The survival ≥ 0.7 to 0.95 (low virulence) is marked with green. The survival equal to 1 is marked in yellow.
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