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Antimicrobial Agents and Chemotherapy, March 2006, p. 1100-1103, Vol. 50, No. 3
0066-4804/06/$08.00+0     doi:10.1128/AAC.50.3.1100-1103.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Roles of Cellular Respiration, CgCDR1, and CgCDR2 in Candida glabrata Resistance to Histatin 5

Eva J. Helmerhorst,^1* Caterina Venuleo,¹ Dominique Sanglard,² and Frank G. Oppenheim¹

Department of Periodontology and Oral Biology, Goldman School of Dental Medicine, Boston University, 700 Albany Street, Boston, Massachusetts 02118,¹ Institute of Microbiology, University Hospital Lausanne (CHUV), Rue de Bugnon 48, CH-1011 Lausanne, Switzerland²

Received 13 September 2005/ Returned for modification 10 October 2005/ Accepted 4 January 2006

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Histatin 5, a human salivary protein with broad-spectrum antifungal activity, is remarkably ineffective against Candida glabrata. Fluconazole resistance in this fungus is due in most cases to upregulation of CgCDR efflux pumps. We investigated whether the distinct resistance of C. glabrata to histatin 5 is related to similar mechanisms.

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In the past decade, Candida glabrata has emerged as the second most common fungal pathogen in opportunistic fungal infections in humans. This increase is likely related to the widespread use of the antimycotic drug fluconazole, to which C. glabrata is inherently less sensitive than C. albicans, C. parapsilosis, and C. tropicalis (18). Resistance to azoles has been associated with the upregulation of the genes CgCDR1 and CgCDR2 (also designated PDH1) which encode proteins belonging to the ATP binding cassette family of multidrug resistance membrane-associated efflux pumps (1, 2, 12, 19, 20, 23). Other reported mechanisms of azole resistance in C. glabrata which may actually be related to CDR upregulation involve the generation or selection of respiratory-deficient petite mutants (3, 4). In the quest to develop new antimycotics with possibly different cellular targets, histatins, a group of salivary cationic proteins, have received special attention (5, 8, 16, 17, 21). While histatins are highly effective against diverse classes of fungi, they are significantly less effective against C. glabrata (9, 24). Furthermore, other, structurally unrelated, cationic antifungal peptides, belonging to the magainin and defensin family, also show a selectively reduced activity against this fungus (6, 9, 11). The cellular basis for the apparent insensitivity of C. glabrata to various antifungal agents as different as azoles and cationic antifungal proteins is as yet unknown. In the current study we evaluated the role of petite mutation, fermentation, and the activity of the efflux pumps CgCDR1 and CgCDR2 in the resistance of C. glabrata to histatin 5.

C. albicans (ATCC 10231) and C. glabrata (ATCC 90030) were cultured in 1:10 diluted Sabouraud dextrose broth (SDB; Difco, Becton Dickinson, Franklin Lakes, NJ) (9) and containing either 0, 56, 112, or 225 µg/ml of histatin 5. Assessment of the optical density at 620 nm (OD₆₂₀) after 48 h of incubation at 30°C showed that C. glabrata was able to grow even in the presence of the highest concentration of histatin 5, while the growth of C. albicans was inhibited by all three histatin concentrations (Fig. 1).

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FIG. 1. Assessment of growth (OD620) after 48 h of incubation of C. albicans and C. glabrata in diluted SDB containing three concentrations of histatin 5. Represented are the average values and standard errors of two independent experiments, each performed in duplicate.

Since C. glabrata resistance to fluconazole in some cases is explained by induction or selection of petite mutants (3, 4) and petite mutation in C. albicans is known to abolish sensitivity to histatin 5 (7), the respiratory competence of C. glabrata cells grown in the presence of histatin 5 was evaluated. Two experimental approaches were followed. First, 10-µl aliquots of cells grown for 48 h in the presence of the indicated three concentrations of histatin 5 were plated on glucose- or glycerol-limited agar (7), the latter strictly supporting cellular respiration. Second, since the C. glabrata petite phenotype may be a transient cellular characteristic caused by mitochondria that switch between states of respiratory competence and incompetence (12), we also measured directly the respiration of C. glabrata cells in the histatin 5-containing cell cultures. Plated C. albicans cell suspensions containing histatin 5 did not grow on agar (Fig. 2). In contrast, the histatin 5-grown C. glabrata cells grew well on glucose- and glycerol-limited agar, the latter indicating that the presence of histatin 5 during growth in diluted SDB broth had not induced "petite" characteristics. In addition, respiratory measurements using a biological oxygen monitor (Yellow Springs Instruments, Yellow Springs, Ohio) (7) of cells grown in the presence of 56, 112, or 225 µg/ml of histatin 5 indicated that the oxygen consumption of these cells in their respective supernatants was certainly not lower than that from cells that had been cultured in the absence of histatin 5 (10.6, 10.6, 10.2, and 9.0 nmol O₂/min/OD₆₂₀, respectively).

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FIG. 2. Determination of the viability and respiratory competence of aliquots of histatin-grown C. albicans and C. glabrata cell suspensions plated on glycerol or glucose-limited agar (7).

In previous studies it was demonstrated that cellular respiration is important in C. albicans sensitivity to histatin 5 (8). It was hypothesized that C. glabrata might escape histatin 5 activity by utilizing fermentative pathways, since theoretically dextrose (glucose) can either be fermented or assimilated. Furthermore, C. glabrata, but not C. albicans, is a Crabtree-positive fungus (22), and its respiration may be negatively affected by certain levels of glucose (15). To exclude the possibility of substrate fermentation by C. glabrata, growth inhibition assays were also conducted in broth containing only glycerol as the carbon source. C. glabrata was insensitive in either glycerol- or glucose-limited broth, exhibiting 50% inhibitory concentrations (IC₅₀s) higher than 225 µg/ml (Fig. 3). This result shows that the resistance of this fungus to histatin 5 is not explained by mitochondrial dysfunction or lack of respiration. In contrast, C. albicans was sensitive to histatin 5 in glycerol- and glucose-containing broths, exhibiting IC₅₀s of 13.8 ± 4.8 and 21.2 ± 2.5 µg/ml, respectively. The sensitivity of C. albicans in glucose broth is consistent with the fact that respiration of C. albicans is not suppressed by glucose (10).

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FIG. 3. Fungistatic activity of serially diluted histatin 5 toward C. albicans and three C. glabrata strains in diluted glycerol-limited broth (A), containing (per liter) 1 g peptone, 0.5 g yeast extract, 0.5 g glucose, and 0.5 g glycerol, and in glucose-limited broth (B), containing (per liter) 1 g peptone, 0.5 g yeast extract, 0.5 g glucose, and 0.5 g glycerol. Broth microdilution experiments were conducted as described previously (9). Graphs represent the averages of an experiment performed in duplicate and are representative of four independent experiments each performed in duplicate.

Previous studies have shown that the site-directed mutation in C. glabrata of CgCDR1, CgCDR2, or both affects sensitivity to fluconazole, in particular when both genes were disrupted simultaneously (20). Using the standardized antifungal susceptibility protocol M27-A2 of the National Committee for Clinical Laboratory Standards (NCCLS) (14), we confirmed published results (20) that strains in which either CgCDR1 or both CgCDR genes were abolished showed a marked increased sensitivity to fluconazole (Table 1). Since the intracellular accumulation of histatins is required for their activity toward C. albicans (8, 13, 25), it was hypothesized that C. glabrata resistance could be related to the fact that histatin 5 fails to accumulate intracellularly as a result of the activity of efflux pumps. While it is unknown whether histatin 5 could be transported by the CgCDR1 and CgCDR2 pumps that are so effective in exporting fluconazole, it was assessed whether the mutants lacking one or both of these genes would show an increased sensitivity to histatin 5. Growth inhibition assays with histatin 5 were conducted in diluted SDB (9), since salts in RPMI medium interfere with histatin activity (9). As indicated in Table 1, the efficacy of fluconazole in RPMI medium and in diluted SDB was in most cases comparable, allowing the comparison of C. glabrata sensitivities to fluconazole and histatin 5 in diluted SDB. The results indicated that while the various C. glabrata mutants showed differential sensitivities to fluconazole, all C. glabrata strains were resistant to histatin 5 growth inhibition (IC₅₀ > 225 µg/ml). Notably, the observed histatin 5 resistance was relative to the histatin 5 sensitivity of C. albicans, which displayed IC₅₀ values of 9.5 ± 0.5 µg/ml. In killing assays conducted in 5 mM potassium phosphate buffer, pH 7.0 (9), similar results of C. glabrata resistance were obtained, except that the ura3 C. glabrata strain (DSY 1029) was somewhat sensitive (Table 1). These results combined indicated that C. glabrata resistance to histatin 5 is independent of mutations in CgCDR1 or CgCDR2.

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TABLE 1. Comparison of fluconazole and histatin 5 sensitivity of CgCDR1 and CgCDR2 mutants of C. glabrataa

The data obtained here and in our previous study (9) reveal a seemingly fundamental and widespread resistance of C. glabrata to histatin 5. While the resistance of C. glabrata to fluconazole is known to occur in cells exhibiting petite mutations and/or overexpressing specific efflux pumps, the resistance to histatin 5 is not related to either of these two mechanisms. The absence of a correlation between the responses to fluconazole and histatin 5 of the various C. glabrata mutants evaluated suggests that the cellular characteristics providing resistance against azoles and cationic antifungal proteins in this fungus are not identical.

 
We thank Nerline Grand-Pierre and Ana S. Fraga for technical assistance.

This study is supported by NIH/NIDCR grants DE05672, DE07652, and DE14950.

 
* Corresponding author. Mailing address: Boston University, Goldman School of Dental Medicine, Department of Periodontology and Oral Biology, 700 Albany St., CABR W-201, Boston, MA 02118. Phone: (617) 414-1119. Fax: (617) 638-4924. E-mail: helmer{at}bu.edu.

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Antimicrobial Agents and Chemotherapy, March 2006, p. 1100-1103, Vol. 50, No. 3
0066-4804/06/$08.00+0     doi:10.1128/AAC.50.3.1100-1103.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

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