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Memórias do Instituto Oswaldo Cruz

Print version ISSN 0074-0276

Mem. Inst. Oswaldo Cruz vol.107 no.1 Rio de Janeiro Feb. 2012 



Cellular characterisation of Candida tropicalis presenting fluconazole-related trailing growth



Marcos Dornelas-RibeiroI, II, III, IV; Eliane Olmo PinheiroIII; Carolina GuerraV; Lys Adriana Braga-SilvaVI, VII; Silvia Maia Faria de CarvalhoII; André Luis Souza dos SantosVI, VII; Sonia RozentalV; Sergio Eduardo Longo FracalanzzaIV, +

ILaboratório de Bacteriologia/Micologia, Instituto de Biologia do Exército, Rio de Janeiro, RJ, Brasil
IILaboratório de Bacteriologia/Micologia, Instituto Estadual de Hematologia, Rio de Janeiro, RJ, Brasil
IIILaboratório de Bacteriologia/Micologia, Hospital Adventista Silvestre, Rio de Janeiro, RJ, Brasil
IVLaboratório de Bacteriologia Médica, Departamento de Microbiologia Médica, Instituto de Microbiologia Paulo de Góes
VLaboratório de Biologia Celular de Fungos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brasil
VILaboratório de Estudos Integrados em Bioquímica Microbiana, Departamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes
VIIPrograma de Pós-Graduação em Bioquímica, Instituto de Química, Centro de Tecnologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brasil




We assessed fluconazole susceptibility in 52 Candida tropicalis clinical strains using seven antifungal susceptibility methods, including broth microdilution (BMD) [standard M27 A3 (with neutral and acid pH), ATB Fungus 3, Vitek 2 system and flow cytometric analysis] and agar-based methods (disk diffusion and E-test). Trailing growth, detection of cell-associated secreted aspartic proteases (Saps) and morphological and ultrastructural traits of these clinical strains were also examined. The ranges of fluconazole 24 h-minimum inhibitory concentration (MIC) values were similar among all methods. The essential agreement among the methods used for MIC determinations was excellent and all methods categorised all strains as susceptible, except for one strain that showed a minor error. The presence of the trailing effect was assessed by six methods. Trailing positivity was observed for 86.5-100% of the strains. The exception was the BMD-Ac method where trailing growth was not observed. Morphological and ultrastructural alterations were detected in C. tropicalis trailing cells, including mitochondrial swelling and cell walls with irregular shapes. We tested the production of Saps in 13 C. tropicalis strains expressing trailing growth through flow cytometry. Our results showed that all of the C. tropicalis strains up-regulated surface Sap expression after 24 h or 48 h of exposure to fluconazole, which was not observed in untreated yeast strains. We concluded that C. tropicalis strains expressing trailing growth presented some particular features on both biological and ultrastructural levels.

Key words: Candida tropicalis - antifungal susceptibility test - trailing growth - biological and ultrastructural alterations - aspartic protease production



The increased incidence of systemic mycoses caused by Candida species in hospitalised patients is an important cause of morbidity and mortality worldwide, especially in critically ill patients (Warnock 2007, Mimica et al. 2009, Ruan & Hsueh 2009). In this context, immunocompromised individuals and patients subjected to broad-spectrum antibiotics, using prostheses and access devices and experiencing prolonged stays in intensive care units are predisposed to Candida infections (Sandven 2000, Pfaller & Diekema 2004, 2007, Fridkin et al. 2006). More than 200 species of Candida have been described, but approximately 90% of human invasive fungal infections are caused by only five species: Candida albicans, Candida tropicalis, Candida parapsilosis, Candida glabrata and Candida krusei (Pfaller & Diekema 2004).

C. tropicalis is the second or third most abundant species of Candida non-albicans. This organism has been isolated in patients with cancer, particularly leukaemia, more frequently (Cantón et al. 2001, Colombo & Guimarães 2003). C. tropicalis is more invasive in relation to C. albicans and it is estimated that 50-60% of patients with predisposing conditions develop invasive candidiasis when they are colonised by this species (Cantón et al. 2001).

When tested against the azoles, some species of the genus Candida, mainly C. albicans and C. tropicalis, may express a trailing phenomenon, which is defined as a susceptible minimum inhibitory concentration (MIC) after 24 h of incubation with azole antifungal agents, but a resistant MIC after 48 h of exposure (Revankar et al. 1998, Arthington-Skaggs et al. 2000). As a consequence, the trailing phenotype results in a misinterpretation of the susceptibility profile for these drugs, reflecting a possible treatment failure. With this propose in mind, some studies have examined the methods to minimise the trailing effect and changes in the National Committee on Clinical Laboratory Standards/Clinical and Laboratory Standards Institute (NCCLS/CLSI) methodology, such as a more acid pH, addition of glucose to the medium and a cut-off criterion for the reading time have been proposed (Anaissie et al. 1996, Rodriguez-Tudela et al. 1996, Tornatore et al. 1997, Marr et al. 1999). Mechanisms have been proposed to explain the trailing effect, including the altered regulation of genes mediating resistance and virulence (Lee et al. 2004).

Pathogenic species of Candida spp produce many potential virulence factors and among them, the secreted aspartic proteases (Saps) have attracted the attention of many investigators (Naglik et al. 2003). A direct correlation exists between the virulence of these yeast strains and the secretion of Saps; consequently, these enzymes are becoming attractive targets for therapeutic drug design (Braga-Silva & Santos 2011). Ten different Saps, encoded by the SAP gene family, were described in C. albicans (Naglik et al. 2003) and four SAP genes were found in C. tropicalis (Zaugg et al. 2001). Moreover, immunological studies suggest the existence of common and specific antigenic domains among the Saps of these two clinically important Candida species (Odds 1985). At least in C. albicans, Saps participate in numerous facets of basic biological processes and directly participate in several interactions between fungal cells and host structures (Naglik et al. 2003).

In the present study we have aimed to characterise the trailing growth of 52 C. tropicalis clinical isolates using different antifungal susceptibility methods. In addition, the expression of surface Saps and the morphological/ultrastructural alterations in these strains were also reported.



Patients and strains - Of a total of 52 C. tropicalis clinical strains isolated from patients in three medical centres in the city of Rio de Janeiro, Brazil, 29 (55.7%) were from blood, eight (15.3%) from urine, five (9%) from faeces, three (6%) from skin material, three (6%) from secretion, two (4%) from sterile fluid, one (2%) from bronchoalveolar lavage and one (2%) from lymph node aspirate. Strains were isolated and identified by conventional methods and the identification was confirmed using the Vitek® 2 system (bioMérieux, Inc, France). Isolates were stored at -70ºC in Sabouraud dextrose broth with 20% glycerol and at room temperature in sterile distilled water (Lee et al. 2004).

Susceptibility testing - Testing of the susceptibility of C. tropicalis isolates to fluconazole and trailing growth characterisation were performed using seven methods. Three of these methods were standardised by CLSI [broth microdilution (BMD) tests in accordance with M27 A3 guideline at neutral pH (BMD-N) and acid pH (BMD-Ac)] (CLSI 2008) and NCCLS [disk diffusion test (DT) according to the M44-A guideline] (NCCLS 2004). The other four methods included commercial systems [ATB® Fungus 3 (ATBF3) (bioMérieux, Inc, France), Vitek 2 and E-test method (AB Biodisk, Solna, Sweden)] and the flow cytometric analysis (Ramani et al. 1997, Ramani & Chaturvedi 2000).

Inoculums - A suspension of five colonies, from up to 48 h-old cultures grown at 35ºC on Sabouraud dextrose agar, was prepared in 5 mL of sterile saline (0.85% NaCl). The cell density was standardised with a spectrophotometer, where diluent was added to the yeast suspension until it matched the value of a 0.5 McFarland standard at a 530 nm wavelength (1 x 106-5 x 106 yeast cells/mL). This standardised inoculum was used in the following methods: BMD-N and BMD-Ac, disk diffusion, E-test and flow cytometric analysis. For the ATBF3 and Vitek 2 methods, the inoculum was adjusted to 3-6 x 106 yeasts/mL.

CLSI reference procedure (M27-A3 guideline): BMD-N and BMD-Ac - Serial two-fold dilutions of fluconazole were prepared in Roswell Park Memorial Institute (RPMI)-1640 medium with L-glutamine and without bicarbonate (Sigma Chemical Co). The final concentrations of fluconazole ranged from 0.25-256 µg/mL and the pH value was adjusted to neutral (with a 165 mM morpholinepropanesulfonic acid buffer) or acid (pH 5.0, with HCl). A 100 µL aliquot of each drug dilution was dispensed into 96-well flat-bottom microdilution trays that were sealed and stored frozen at -70ºC until use. The standardised suspension was diluted 1:50 and then 1:20 in RPMI with L-glutamine and without sodium bicarbonate, resulting in 1 x 103-5 x 103 cells/mL. A 100 µL aliquot of the final suspension was put into each well of the microdilution plate and the plates were incubated at 35ºC for 48 h. As a viability, purity and concentration of inoculum control, aliquots (10 µL) of each suspension were inoculated on Sabouraud dextrose agar and incubated for 48 h at 35ºC. Endpoints were determined by visual reading. Before reading, the microdilution trays were agitated and the MIC was computed as the lowest concentration of fluconazole to cause at least 50% inhibition of growth relative to that of the drug-free control. The trailing growth was considered when a reduced but persistent growth of the strain was detected in high concentrations of fluconazole.

Disk diffusion and E-test methods - The two methods were performed on Mueller-Hinton agar plates supplemented with 2% glucose and 0.5 mg of methylene blue (GMB agar). For each isolate, two plates were inoculated by dipping two sterile cotton swabs into the standardised inoculum and evenly streaking the entire surface of the GMB agar in three directions, with a 60º angle between them. After drying for 15 min, one fluconazole E-test strip and one 25 µg fluconazole disk (Cecon, Ltd, São Paulo, Brazil) were applied to the medium. The plates were incubated at 35ºC and were read after 24 h and 48 h. The MIC was read as the lowest concentrations producing an 80% reduction in growth. In the E-test, the values of MIC were read at the point where the ellipse of the inhibition zone intersected the strip. The residual growth of yeast strains from the boundary of the inhibition zone, pointing towards the E-test strip, was considered to be trailing growth. In the DT, the inhibition zone diameter was measured to the nearest mm at a point where there was a prominent reduction of growth (80%). The CLSI inhibition zone diameter for fluconazole [susceptible (> 19 mm), S-DD (15-18 mm) and resistant (< 14 mm)] was used to categorise the disk diffusion results (NCCLS 2004). The yeast strains that showed a boundary of residual growth towards the disk of fluconazole were considered to exhibit trailing growth.

ATBF3 - An ATBF3 strip is composed of 32 wells that include a growth control and five antifungal drugs at different concentrations: 5-flucytosine from 4-16 µg/mL (log2 dilutions), amphotericin B from 0.5-16 µg/mL, fluconazole from 1-128 µg/mL, itraconazole from 0.125-4 µg/mL and voriconazole from 0.06-8 µg/mL. The ATBF3 test was performed according to the manufacturer's instructions. The strips were read either visually or automatically by the mini Api® instrument (bioMérieux, Inc, France) at 24-48 h for Candida species. MICs for azoles and 5-flucytosine were determined according to the following criteria: no reduction or a slight reduction in turbidity (scores 4 and 3) was considered to be "no inhibition", while a prominent decrease to no growth (scores 2-0) corresponded to "inhibition". Only samples that remained optically clear were considered to be susceptible to amphotericin B (Torres-Rodríguez & Alvarado-Ramírez 2007).

Vitek 2 system - Susceptibility testing with the Vitek 2 system (AST-YST card) was performed according to the manufacturer's instructions. From each strain, the standardised inoculum was placed in a Vitek 2 cassette, along with a sterile polystyrene test tube and a Vitek 2 card containing serial two-fold dilutions of fluconazole (1-64 µg/mL) and voriconazole (0.125-8 µg/mL). After the loaded cassettes were placed in the Vitek 2 instrument, the cards were filled with the diluted yeast suspensions, incubated for 24 h and read automatically. The MIC results were interpreted as described by the M27-A3 guideline.

Flow cytometric assay - This method was performed as previously described (Ramani et al. 1997). Briefly, 0.1 mL aliquots of the standardised yeast suspension were mixed with 0.1 mL of serial two-fold dilutions of fluconazole in 12 by 75-mm tubes (Falcon 2054, Becton Dickinson, Lincoln Park, NJ, USA). The growth control received 0.1 mL of the drug diluent (RPMI-1640 medium) without fluconazole. All of the tubes were incubated without agitation at 35ºC for 4 h. Then, each dilution was shaken gently and 200 µL of 25 mM sodium desoxycholate and 4 µL of 1% propidium iodide (Sigma) were added to each dilution, after which the tubes were carefully mixed again. Flow cytometry was performed on a FACS calibur cytometer (Becton Dickinson) on a sample volume of 75 µL with a flow rate of 10 µL/min. Cytometer parameters were as follows: forward scatter (linear gain 3.73), side scatter (gain 2.0), side scatter photomultiplier tubes (270 V) and log red fluorescence (FL2) 457 V log. Each flow cytometric susceptibility test analysed 10,000 yeast cells. MIC was computed as the lowest fluconazole concentration that resulted in a 50% increase in the mean channel fluorescence as compared to the growth control (Ramani et al. 1997, Ramani & Chaturvedi 2000, Chaturvedi et al. 2004). The results were analysed using the WinMDI 2.8 program for fluorescence intensity and dispersion of microorganisms.

Analysis and interpretation of results - Both on-scale and off-scale results obtained by all the methods were included in the analysis. The off-scale MICs were converted to the next highest or lowest concentration. The MIC values were considered to be in essential agreement (EA) between the two methods when they were within two dilutions. Categorical agreement (CA) was assigned to Candida spp susceptibility testing results that fell within the same interpretive categories. Results were analysed based on the interpretive breakpoints for fluconazole [susceptible (S), < 8 µg/mL; susceptible dose dependent (SDD), 16-32 µg/mL; resistant (R), > 64 µg/mL]. CA was assigned when both methods classified the susceptibilities of the isolates within the same interpretive categories (S, SDD or R). Discrepancies were considered "major" if an isolate classified as S by the reference method was classified as R by the commercial method and "very major" if an isolate classified as R by the reference method was classified as S by the commercial method. Errors were considered "minor" when there were discrepancies between the two methods in classifying SDD isolates as S or R or classifying S and R isolates as SDD.

Light and transmission electron microscopy analyses - In this set of experiments, the trailing positive C. tropicalis strain, 135, was used to investigate possible morphological alterations induced by fluconazole when compared to cells grown in its absence by both light microscopy and transmission electron microscopy.

For light microscopy analyses, aliquots of all dilutions of the BMD-N method, after a 24-h incubation, were placed on slides, stained by the Gram method and examined under a light microscope (Olympus, Japan) with a magnification of 1000X. For ultrastructural analyses, untreated and fluconazole-treated cells were fixed in a solution containing 2.5% glutaraldehyde and 4% freshly prepared formaldehyde in a 100 mM cacodylate buffer (pH 7.2) for 1 h and washed three times in the same buffer. Then, the yeast strains were post-fixed in a 100 mM cacodylate buffer (7.2 pH) containing 1% osmium tetroxide, 0.8% potassium ferrocyanide and 5 mM CaCl2 for 2 h. After that, the yeast strains were dehydrated in an ethanol-graded series and critical point-dried with CO2. The specimens were coated with 3 nm of gold in a Balzers apparatus and ultrathin sections were observed in a Jeol 1200 EX transmission electron microscope at 80 kV (Cunha et al. 2005).

Detection of Sap - Thirteen trailing-positive C. tropicalis strains were randomly chosen from among the 52 strains isolated in this work. The strains were grown in RPMI-1640 medium, with and without 128 µg/mL of fluconazole, for 24 and 48 h at 37ºC. All cultures were centrifuged to obtain concentrated cells, the yeast strains were washed in phosphate buffered saline (PBS) and a standardised inoculum (5 x 106 cells) was prepared. The suspensions used for these experiments were fixed at 4ºC in 4% paraformaldehyde in PBS (pH 7.2) for 20 min, followed by extensive washing in the same buffer. These fixed cells maintained their morphological integrity, as indicated by light microscope observation. They were incubated for 1 h at 25ºC with a 1:250 dilution of rabbit anti-Sap1-3 antibody (kindly provided by Dr Nina Agabian, University of California, San Francisco, CA, USA) and then incubated for an additional hour with a 1:200 dilution of fluorescein-isothiocyanate-labelled goat anti-rabbit IgG. For flow cytometric analysis, these cells were examined in an EPICS ELITE flow cytometer (Coulter Electronics, USA) equipped with a 15-mW argon laser emitting at 488 nm. Untreated cells and those treated only with the anti-Sap and secondary antibody were used as controls. Each experimental population was then mapped by using a two-parameter histogram of forward-angle light scatter versus side scatter. The mapped population (n = 10,000) was then analysed for log green fluorescence by using a single-parameter histogram (Braga-Silva et al. 2009).



In this study, the majority of the 52 C. tropicalis strains were isolated from clinical specimens collected from invasive infections, mainly blood (55%) and sterile fluids (24%), such as ascite and pleural effusions. Whereas, strains from noninvasive lesions were mainly isolated from urine (15%) and secretions (6%). The major invasive potential of C. tropicalis in relation to other species of Candida, particularly C. albicans, has been previously reported (Colombo & Guimarães 2003).

Susceptibility tests - We tested the susceptibility to fluconazole and the phenotypic expression of trailing growth for 52 C. tropicalis strains using the standard BMD-N method and six other methods for comparison (Table I). Data are shown as MIC ranges and the MIC50% and MIC90%, except for the M44-A method, where the area of the inhibition zone (mm) around the disk was considered.

The BMD-N method and most of the other methods could have a trailing effect so great as to make an isolate that appears susceptible after 24 h of incubation appear resistant after 48 h. Therefore, it is recommended that the test readings be conducted at 24 and 48 h for the azoles to avoid the interference of this effect on the outcome of the test and to determine the category of susceptibility. In this work, the BMD-N and BMD-Ac methods and the E-test were read at 24 and 48 h. ATBF3 was also examined after two incubation periods, but only the reading at 24 h was considered, while the flow cytometric, disk diffusion and Vitek 2 methods were read at 4 h, 24 h and up to 24 h, respectively.

The ranges of the 24 h-MIC results were similar among all methods. However, the readings were discrepant at 48 h compared to those at 24 h, particularly for the BMD-N and ATBF3 methods. No significant differences were noted for the BMD-Ac and E-test methods. The discrepancies reflect the presence of the trailing end. MIC50% and MIC 90% for fluconazole, as determined by six methods, were clearly concordant and ranged from < 1 µg/mL-2 µg/mL (MIC50%) and < 1-4 µg/mL (MIC90%) (Table I). The EA among all methods used for determining the MIC was excellent when compared with the BMD-N method, showing values of 98.1% for flow cytometry, 96.1% for Vitek 2 and ATBF3 and 92.3% for the BMD-Ac method. However, the E-test, which showed an EA of 80.8%, was an exception. Thirteen discrepancies were noted between the MIC values of each strain for each method tested in relation to BMD-N, including 10 with the E-test, four with the BMD-Ac, two with the ATBF3 and two with the Vitek 2. Of the discrepancies noted, the MIC values obtained by the BMD-N were always lower than those obtained by the other methods. Similar EA results for testing various methods against the standard method excluding the E-test have been reported in the literature (Pfaller et al. 2007, Torres-Rodríguez & Alvarado-Ramírez 2007, Cuenca-Estrella et al. 2010).

Previous studies also found similar EA results between E-test and BMD-N methods (Matar et al. 2003, Cuenca-Estrella et al. 2010). The results from the M44-A method were consistent with the categorisation of the strains as susceptible, in agreement with the other methods tested.

Despite of the discrepancies described, all methods identified all strains as susceptible to fluconazole, except for one strain that was SDD for the ATBF3 method and sensitive to other methods. Thus, although no major or very major error was defined, one minor error was defined. Table II shows the percentages of correlation between the different methods, in relation to EA. BMD-Ac and ATBF3 methods showed correlation values greater than 98% compared to three of the five other methods tested. Vitek 2 showed 100% correlation with BMD-Ac and flow cytometry, which suggests less of an influence on reading due to trailing growth, which has also been shown by other authors (Ramani & Chaturvedi 2000, Borghi et al. 2010). The lowest correlation rates were observed between flow cytometry and other methods, which is consistent with other previously reported results (Pfaller et al. 2007, Lee et al. 2009, Cuenca-Estrella et al. 2010). The presence of the trailing effect was assessed for all strains in relation to the seven methods tested (Table I). Percentages of the positivity of the strains ranging from 86.5-100% were detected for all methods, except for the BMD-Ac method, where trailing growth was not observed. This result agrees with the data of Marr et al. (1999). However, a previous study showed lower values for the presence of the trailing effect in C. tropicalis strains (Arthington-Skaggs et al. 2002). Ramani and Chaturvedi (2000) did not detect trailing growth in antifungal susceptibility testing performed using the flow cytometry method and suggested that the short incubation time was insufficient for the expression of this phenomenon. However, in our study we found a significant percentage of viable cells after 4 h, even at high concentrations of the antifungal agent, and we considered these cells to represent trailing cells. 

Morphological and ultrastructural changes - Several cellular and molecular mechanisms possibly responsible for trailing growth in Candida spp have been described (Lee et al. 2004, Vandeputte at al. 2005). Fluconazole, which is known to inhibit cell growth by disruption of sterol biosynthesis, increased cell size due to an apparently high porosity level of the cell wall. In consequence, these cells disintegrated, perhaps due to increased turgor pressure (Ramani & Chaturvedi 2000). Herein, we used two different approaches to analyse the morphological alterations in C. tropicalis (strain 135) after treatment with fluconazole: (i) staining yeast cells using the Gram method (Fig. 1) and (ii) visualisation of general ultrastructural alterations by transmission electron microscopy (Fig. 2). Light microscopy revealed that in the presence of fluconazole (8 µg/mL and 128 µg/mL) several cells showed an altered morphology, such as increased size with greater dye uptake. Furthermore, the number of yeasts containing buds and cells showing incomplete cell division was increased after exposure to fluconazole compared to the fluconazole-untreated cells (Fig. 1). The increase in cell size had already been suggested by studies using flow cytometry (Ramani et al. 1997) and implies that the azoles may significantly affect the outer cell envelope (Belanger et al. 1997). The fluconazole-treated cells, even when grown at a higher concentration (128 µg/mL), were viable and able to grow on Sabouraud dextrose agar similarly to the control cells. Studies suggest that in the presence of fluconazole, C. albicans cells up-regulate the transcription of genes encoding the azole drug target, lanosterol demethylase (ERG 11), the target terbinafine, squalene epoxidase (ERG 1) or the azole and terbinafine efflux transporters (CDR1, CDR2 and MDR1) (Smith & Edlind 2002). These same mechanisms and also point mutations in the ERG11 gene have been implicated as mechanisms of fluconazole resistance in C. albicans (Sanglard & Odds 2002). Therefore, trailing isolates, although susceptible to fluconazole, are capable of expressing the same molecular mechanisms as SDD and R isolates in the presence of fluconazole, but regulate them differently (Lee et al. 2004). In C. tropicalis, azole resistance mechanisms have been studied less, but the over-expression of the CtERG11 gene (not the CtMDR1 gene associated with a missense mutation in this gene) seemed to be responsible for the acquired azole resistance in a resistant clinical isolate of C. tropicalis (Vandeputte et al. 2005). However, the presence of trailing growth would have no greater significance in vivo because these strains were susceptible to the same concentrations of fluconazole used for susceptible strains (Arthington-Skaggs et al. 2000, Ostrosky-Zeichner et al. 2003).





The possible effect of trailing growth on ultrastructural changes in C. tropicalis was evaluated by transmission electron microscopy of yeast strains grown in concentrations of fluconazole above the MIC (Fig. 2). Electron micrographs of untreated C. tropicalis showed well-preserved yeast cells, presenting a compact cell wall (average thickness of 0.13 µm), a plasma membrane (with normal shape) and homogeneous cytoplasm (Fig. 2A and in the inset). However, yeast strains grown in the presence of 8 µg/mL of fluconazole and expressing trailing phenomenon showed important alterations, including mitochondrial swelling and a cell wall with an irregular shape and presenting wall thicknesses ranging from 0.14-0.28 µm (Fig. 2B). The highest concentration of fluconazole (128 µg/mL) induced more pronounced changes in the cytoplasm, such as the accumulation of several vacuoles and mitochondrial swelling. In addition, the cell wall showed an irregular shape and thicknesses ranging from 0.22-0.50 µm. Detachment and degradation of the cytoplasmic membrane was also evident (Fig. 2C). Previous works reported that Candida spp treated with azole agents or a synthetic arylquinucline derivate, exhibiting antifungal activity, presented similar ultrastructural alterations when examined under transmission electron microscopy (Belanger et al. 1997, Ishida et al. 2011).

Sap expression in trailing strains of C. tropicalis - A positive correlation between protease activity and antifungal susceptibility was already reported for C. albicans. In this sense, the C. albicans isolates from the human immunodeficiency virus-positive group that were characterised by higher levels of protease activity were also less susceptible to the widely used azole antifungal agents, ketoconazole and fluconazole (Ollert et al. 1995). C. albicans strains exposed to subinhibitory concentrations of antifungals belonging to the azole, echinocandin and pyrimidine analogue classes showed elevated activity of Sap2 in the culture filtrates (Wu et al. 2000, Ripeau et al. 2002). In addition, the expression of SAP2 and activity of the secreted Sap2 gene product was up-regulated in fluconazole-exposed yeast cells (Copping et al. 2005). In fact, Navarathna et al. (2005) showed that the virulence of C. albicans strains increases upon exposure to subinhibitory concentrations of fluconazole in animal experiments. Recently, Mores et al. (2011) described that biofilms of C. albicans challenged by sub-MICs of fluconazole tend to secrete higher quantities of Sap compared to non-treated cells.

With this task in mind, we assessed the production of Saps in 13 C. tropicalis strains, expressing trailing growth, through flow cytometry. The fluorescence intensity obtained with cells grown in the presence of fluconazole for 24 h or 48 h was compared to that obtained with control cells (cultured in the absence of antifungal) after staining with antibodies raised against Sap1-3 from C. albicans (Table III). Our results showed that all the C. tropicalis strains after exposure to fluconazole up-regulated on surface Sap expression, in relation to untreated yeast strains. In this context, yeast strains treated with fluconazole for 24 h had levels of surface Saps 1.67-44.3-fold higher than control cells (p < 0.05). Similarly, yeast strains under fluconazole pressure for 48 h presented 4.33-37.55-fold higher Sap levels in relation to untreated yeast strains (p < 0.05) (Table II). In addition, the majority of the strains (69.2%) showed an increased expression of Saps after 48 h of exposure to fluconazole when compared to a 24 h exposure. The significance of these findings in relation to C. tropicalis virulence in the presence of fluconazole in vivo is not clear, but experiments in vivo with C. albicans showed that Sap production may contribute to the pathogenesis of inflammatory mucosal lesions in a model of vaginal candidiasis (De Bernardis et al. 1999). Thus, the role of Saps of C. tropicalis in the pathogenicity of invasive or superficial infections caused by this species needs to be investigated. We demonstrated that even in the presence of high concentrations of fluconazole, C. tropicalis still produced significant levels of Saps, suggesting a possible role in the virulence characteristics of this species.



Taken together, our results show that C. tropicalis strains isolated from invasive and noninvasive infections were susceptible to fluconazole and all methods of antifungal susceptibility tested showed similar performance. Moreover, the strains of C. tropicalis had a high level of trailing growth and this phenomenon may have an influence on biological and structural properties of yeast cells. However, despite these physiological and structural alterations, several cells within the population maintained their viability and were able to multiply and produce, which are factors possibly involved in the pathogenesis of C. tropicalis.



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Received 7 April 2011
Accepted 16 August 2011



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